WO2005124297A2 - Apparatus and method for producing or processing a product or sample - Google Patents

Apparatus and method for producing or processing a product or sample Download PDF

Info

Publication number
WO2005124297A2
WO2005124297A2 PCT/US2005/020390 US2005020390W WO2005124297A2 WO 2005124297 A2 WO2005124297 A2 WO 2005124297A2 US 2005020390 W US2005020390 W US 2005020390W WO 2005124297 A2 WO2005124297 A2 WO 2005124297A2
Authority
WO
WIPO (PCT)
Prior art keywords
carrier substrates
liquid
machine
dispensing
image
Prior art date
Application number
PCT/US2005/020390
Other languages
French (fr)
Other versions
WO2005124297A3 (en
Inventor
Allan J. Clarke
David George Doughty
Frederick H. Fiesser
David R. Rudd
David A. Tainsh
David S. Wagner
Original Assignee
Smithkline Beecham Corporation
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Smithkline Beecham Corporation filed Critical Smithkline Beecham Corporation
Priority to MXPA06014533A priority Critical patent/MXPA06014533A/en
Priority to EP05760285.6A priority patent/EP1756535A4/en
Priority to CA2570037A priority patent/CA2570037C/en
Priority to JP2007527750A priority patent/JP5346466B2/en
Publication of WO2005124297A2 publication Critical patent/WO2005124297A2/en
Publication of WO2005124297A3 publication Critical patent/WO2005124297A3/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61JCONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J3/00Devices or methods specially adapted for bringing pharmaceutical products into particular physical or administering forms
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05CAPPARATUS FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05C11/00Component parts, details or accessories not specifically provided for in groups B05C1/00 - B05C9/00
    • B05C11/10Storage, supply or control of liquid or other fluent material; Recovery of excess liquid or other fluent material
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61JCONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J3/00Devices or methods specially adapted for bringing pharmaceutical products into particular physical or administering forms
    • A61J3/005Coating of tablets or the like
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61JCONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J3/00Devices or methods specially adapted for bringing pharmaceutical products into particular physical or administering forms
    • A61J3/007Marking tablets or the like
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C16/00Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes
    • C23C16/44Chemical coating by decomposition of gaseous compounds, without leaving reaction products of surface material in the coating, i.e. chemical vapour deposition [CVD] processes characterised by the method of coating
    • C23C16/52Controlling or regulating the coating process
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/25Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
    • G01N21/31Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
    • G01N21/35Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light
    • G01N21/3563Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light for analysing solids; Preparation of samples therefor
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/25Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
    • G01N21/31Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry
    • G01N21/35Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light
    • G01N21/359Investigating relative effect of material at wavelengths characteristic of specific elements or molecules, e.g. atomic absorption spectrometry using infrared light using near infrared light
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/84Systems specially adapted for particular applications
    • G01N21/88Investigating the presence of flaws or contamination
    • G01N21/93Detection standards; Calibrating baseline adjustment, drift correction
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/84Systems specially adapted for particular applications
    • G01N21/88Investigating the presence of flaws or contamination
    • G01N21/95Investigating the presence of flaws or contamination characterised by the material or shape of the object to be examined
    • G01N21/9508Capsules; Tablets
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61JCONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
    • A61J3/00Devices or methods specially adapted for bringing pharmaceutical products into particular physical or administering forms
    • A61J3/10Devices or methods specially adapted for bringing pharmaceutical products into particular physical or administering forms into the form of compressed tablets
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41PINDEXING SCHEME RELATING TO PRINTING, LINING MACHINES, TYPEWRITERS, AND TO STAMPS
    • B41P2200/00Printing processes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B41PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
    • B41PINDEXING SCHEME RELATING TO PRINTING, LINING MACHINES, TYPEWRITERS, AND TO STAMPS
    • B41P2200/00Printing processes
    • B41P2200/30Heliography
    • B41P2200/31Pad printing
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/62Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light
    • G01N21/63Systems in which the material investigated is excited whereby it emits light or causes a change in wavelength of the incident light optically excited
    • G01N21/64Fluorescence; Phosphorescence
    • G01N2021/6417Spectrofluorimetric devices
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00Chemistry: analytical and immunological testing
    • Y10T436/11Automated chemical analysis
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00Chemistry: analytical and immunological testing
    • Y10T436/11Automated chemical analysis
    • Y10T436/113332Automated chemical analysis with conveyance of sample along a test line in a container or rack
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00Chemistry: analytical and immunological testing
    • Y10T436/12Condition responsive control
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00Chemistry: analytical and immunological testing
    • Y10T436/25Chemistry: analytical and immunological testing including sample preparation
    • Y10T436/2575Volumetric liquid transfer

Definitions

  • the present invention relates to the manufacture or processing of products or samples. More particularly, the present invention relates to an apparatus and process for manufacturing or processing a product or sample by dispensing.
  • soldering methods have been developed for connecting integrated circuit chips to the printed circuit board.
  • One such method includes applying a small amount of solder to the bottom surface of the chip, aligning the solder with a bond pad on the surface of the printed circuit board, and heating the solder until -it reflows.
  • Another such method includes applying solder to bonding pads on the printed circuit board and then bonding electrical components to the printed circuit boards by positioning the components over the solder and by heating and reflowing the solder.
  • chips are bonded to a patterned layer of solder created by applying a thin layer of solder paste to a printed circuit board through holes in a stencil, leaving a selected solder pattern on the printed circuit board.
  • a monitoring system for a machine that produces a plurality of products by dispensing droplets of liquid on one or more carrier substrates.
  • the monitoring system comprises an inspection system having a microprocessor, a first camera or video recording device, in communication with the microprocessor and a trigger operably connected to the first camera or video recording device.
  • the inspection system determines an amount of the liquid that is being added to each of the carrier substrates.
  • the trigger actuates the first camera or video recording device to obtain a first image of each of the droplets in-flight.
  • the microprocessor determines the amount of the liquid based upon the first image.
  • Camera means herein a video/digital recording device.
  • an apparatus for producing a plurality of products has a carrier substrate and a dispensed liquid thereon.
  • the apparatus comprises a dispensing system for dispensing the dispensed liquid as a droplet onto each of the carrier substrates and a monitoring system comprising an inspection system that determines an amount of the dispensed liquid that is being added to each of the carrier substrates by the dispensing system.
  • the inspection system comprises a microprocessor, a first camera or video recording device in communication with the microprocessor and a trigger operably connected to the first camera or video recording device. The trigger actuates the first camera or video recording device to " obtain a first image of the droplet in-flight.
  • the microprocessor determines the amount of the dispensed liquid based upon the first image.
  • an apparatus for producing a plurality of products that each have a carrier substrate and a dispensed liquid comprises a dispensing system that adds the dispensed liquid to each of the carrier substrates; and a monitoring system that performs real-time monitoring of the dispensing system to determine an amount of the dispensed liquid on each of the carrier substrates.
  • a monitoring system for a machine that produces a plurality of products where the plurality of products each have a carrier substrate and a dispensed liquid.
  • the monitoring system comprises a confirmation system operably connected to the machine that determines an amount of the dispensed liquid that has been added to each of the carrier substrates by the machine.
  • the confirmation system performs optical profilometry on each of the carrier substrates to determine the amount of the dispensed liquid.
  • a machine which produces a plurality of products where each has a carrier substrate and a dispensed liquid is provided.
  • the machine comprises a dispensing system for adding the dispensed liquid to each of the carrier substrates and a confirmation system for determining an amount of the dispensed liquid that has been added to each of the carrier substrates.
  • the confirmation system performs optical profilometry on each of the carrier substrates to determine the amount of the dispensed liquid.
  • a method of monitoring a machine produces a plurality of products by dispensing a droplet of liquid on a carrier substrate.
  • the method comprises actuating a camera based upon dispensing of the droplet; obtaining a first image of the droplet in-flight; and determining a volume of the droplet based upon the first image.
  • a method of producing a plurality of products that each have a carrier substrate and a dispensed liquid thereon comprises dispensing the dispensed liquid as a droplet onto each of the carrier substrates; and determining an amount of the dispensed liquid that is being added to each of the carrier substrates by the dispensing system by obtaining a first image of the droplet in-flight and determining the amount of the dispensed liquid based upon the first image.
  • Each of the carrier substrates can continue to move along the apparatus as the inspection system determines the amount of the dispensed liquid.
  • the monitoring system may further comprise a confirmation system having a probe that performs spectroscopy on the dispensed liquid that has been added to each of the carrier substrates.
  • a confirmation system having a probe that performs spectroscopy on the dispensed liquid that has been added to each of the carrier substrates.
  • Each of the carrier substrates can continue to move along the apparatus as the probe performs spectroscopy.
  • the spectroscopy may be taken from the group consisting of near infrared, mid-infrared, ultraviolet/visible, fluorescence, laser-induced fluorescence, Raman, terahertz, and any combinations thereof.
  • the monitoring system can further comprise a confirmation system having a second camera or video recording device that obtains a second image of the dispensed liquid on each of the carrier substrates.
  • the confirmation system determines a position of the dispensed liquid for each of the carrier substrates based on the second image.
  • Each of the carrier substrates may continue to move along the apparatus as the second camera or video recording device obtains the second image.
  • the apparatus can further comprise a temperature conditioning system that changes the temperature of the dispensed liquid to facilitate its formation on the carrier substrate.
  • the temperature conditioning system may monitor environmental parameters for each of the carrier substrates, wherein the environmental parameters are taken from the group consisting of temperature, airflow rate, humidity, radiation, product surface temperature, or any combinations thereof.
  • the apparatus can further comprise a printing system for applying an identification marker to each of the carrier substrates.
  • the printing system may have a third camera or video recording device for obtaining a third image of the identification marker for inspection.
  • Each of the carrier substrates can continue to move along the apparatus as the third camera or video recording device obtains the third image.
  • the apparatus can further comprise a control system for performing real-time control of the dispensing system based on the real-time monitoring.
  • the real-time control may comprise adjusting an amount of dispensing from the dispensing system.
  • the dispensing system may have a nozzle, wherein the real-time control comprises adjusting a position of the nozzle with respect to each of the carrier substrates thereby adjusting the position of the dispensed liquid on each of the carrier substrates.
  • the confirmation system can perform optical profilometry on each of the carrier substrates to determine the amount of the dispensed liquid. Each of the carrier substrates may continue to move along the apparatus as the optical profilometry is performed.
  • FIG. 1 is a perspective view of a preferred embodiment of a machine of the present invention
  • FIG. 2 is a schematic representation of the automation components of the machine of FIG. 1;
  • FIG. 2a is a representation of a path of continuous movement of the dispensing module of the machine of FIG. 1;
  • FIG. 2b is a representation of another path of continuous movement of the dispensing module of the machine of FIG. 1;
  • FIG. 2c is a perspective view of a dispenser assembly of the machine of FIG. 1;
  • FIG. 2d is a perspective cross-sectional view of the dispenser assembly of FIG. 2c;
  • FIG. 2e is a perspective view of the pump module of the dispenser assembly of FIG. 2c;
  • FIG. 2f is a perspective view of the motor module of the dispenser assembly of FIG. 2c;
  • FIG. 2g is a perspective cross-sectional view of another embodiment of a nozzle of the machine of FIG. 1;
  • FIG. 2h is a schematic representation of another embodiment of a dispensing assembly of the machine of FIG. 1;
  • FIG. 2i shows the range of droplets that can be dispensed from the assembly of FIG. 2h;
  • FIG. 2j shows the dispensing assembly of FIG. 2h with multiple nozzles or apertures;
  • FIG. 3 is a high speed video image of a droplet dispensed by the machine of FIG. 1;
  • FIG. 4 is a perspective view of an alternative embodiment of a machine of the present invention.
  • FIG. 5 is a perspective view of another alternative embodiment of a machine of the present invention.
  • FIG. 6 is a schematic representation of components of the machine of FIG. 4.
  • FIG. 7 is a schematic representation of the communication between the components of the machine of FIG. 4.
  • the machine 10 has a plurality of components that are operably connected to manufacture a product or process a sample, and preferably a batch of products or samples, as will be described later in greater detail.
  • a batch is a quantity of product, which has been produced or processed during a defined cycle, such as, for example, a fixed number or one or more runs over a fixed time period.
  • the machine 10 has various components arranged along a straight or substantially straight line.
  • the present invention contemplates other arrangements and positionings of the various components, such as, for example, in circular or rectangular paths.
  • the exemplary embodiment describes the manufacture of a product via dispensing, the present invention contemplates other processes being performed by the machines described herein, such as, for example, testing or processing of samples via dispensing.
  • Machine 10 can have components stacked on each other or at differing heights to take advantage of vertical space, as well as facilitating operation, such as, for example, enabling the use of gravity in the process performed by the machine.
  • the machine 10 has a loading system 100, a holding system 200, a conveyor system 300, a dispensing system 400, a coating system 600, a printing system 700, a product acception-rejection system 800, and a control system 900.
  • Each of these systems 100 through 900 are operably connected to each other to efficiently and ergonomically provide products that are ready for packaging, and which have each undergone real-time monitoring, and preferably real-time feedback and adjustment or control.
  • the machine 10 delivers the product, which is a combination of a substrate 1000 and a liquid 2000.
  • the liquid 2000 is dispensed by dispensing system 400 in the form of a droplet 2100 (shown in FIG. 3) that is dispensed onto the substrate 1000.
  • the liquid 2000 can have a variety of properties, such as, for example, low-viscosity, high-viscosity, such that the term liquid is not intended to be limiting.
  • the liquid 2000 can be anything that is dispensable onto the substrate 1000, such as, for example, solder onto an IC chip or a therapeutic active agent onto a carrier tablet.
  • the present invention could utilize the present invention for processing a variety of substrates 1000 with a variety of liquids 2000. Additionally, the dispensing of liquid 2000 onto substrate 1000 is not limited to droplets 2100, but can also include other flow patterns, such as, for example, a partial or continuous stream. It should be further understood that the present invention contemplates the substrate 1000 being a variety of substances upon which the liquid 2000 can be dispensed and having a variety of properties. Such a substance for substrate 1000 may also include another liquid.
  • the droplet 2100 is dispensed onto the outer surface or substantially along the outer surface of the substrate 1000, such as, for example, solder that is heated and then dispensed onto the substrate.
  • the substrate 1000, the liquid 2000 and the resulting product undergo real-time monitoring, feedback and adjustment, which improve quality control.
  • loading system 100 has a loading container or hopper 110 in communication with a loading chute 120.
  • Hopper 110 is preferably movable so that one or more substrates 1000 can be loaded into the hopper and then the hopper can be moved into communication with the loading chute 120.
  • Loading chute 120 is in communication with holding system 200 and conveyor system 300 so that the substrates 1000 can be moved from the hopper 110 into the holding system 200 for movement along and through machine 10 by way of conveyor system 300.
  • the hopper 110 and loading chute 120 can use various devices and methods, such as, for example, powered wheels or wedges, powered belts, or gravity, to move each of the substrates 1000 into their designated positions in holding system 200.
  • a portion of loading system 100 is preferably disposed above a portion of conveyor system 300 to take advantage of gravity, in combination with a mechanical loading device.
  • holding system 200 has a plurality of holding members or trays 210 with substrate positions 220 having a size and shape that allows for holding of each of the substrates 1000.
  • each of the holding trays 210 is rectangular, and the substrate positions 220 are arranged in an array of equi-distantly spaced rows and columns. As will be explained later, this array facilitates operation of .the dispensing system 400 in adding the droplets 2100 to the substrates 1000.
  • the present invention contemplates the use of other structures and methods for securing each of the substrates 1000 and the resulting products as they travel along machine 10.
  • the holding trays 210 may simply be a mechanism for temporarily connecting the substrate 1000 with the conveyor system 300 so that the substrate travels along the machine 10, such as, for example, a large substrate receiving multiple dispensings thereon.
  • Holding system 200 tracks individual substrates 1000 by their designation in each of the substrate positions 220. This allows machine 10 to perform various real-time monitoring, feedback and adjustment activities upon each of the substrates 1000, droplets 2100 and products, and also to make determinations as to whether each of the substrates, droplets or resulting products have met the quality control standards that are designated for a particular product.
  • the tracking of each of the substrates 1000, droplets 2100 and/or products throughout the process carried out by machine 10 allows for acceptance or rejection during the process.
  • the present invention also contemplates tracking of unacceptable substrates 1000 for removal by acception-rejection system 800 based on the real-time monitoring.
  • holding system 200 for each of the substrates 1000.
  • holding trays 210 have a bar code 230 that can be scanned to provide identification and information to control system 900, and which can also be used to track and monitor the individual substrates 1000, droplets 2100 and/or products throughout the process.
  • control system 900 the data compiled throughout the process is stored by control system 900. The data is based upon the individual substrates 1000, droplets 2100 and/or products, as opposed to contemporary quality control methods that use batch-sampling.
  • holding system 200 positions each of the substrates 1000 so that dispensing system 400 can add the droplet 2100 to the outer surface of the substrate, which is facing away from the holding tray 210.
  • the present invention contemplates the dispensing system 400 also adding the droplet 2100 to the opposing outer surface of the substrate 1000. This would allow for a greater capacity of liquid 2000 being carried by the substrate 1000 (on both of its outer surfaces) .
  • Dispensing onto both sides of the substrate 1000 would also provide the ability for different liquids 2000, to be dispensed upon a single substrate, such as, for example, where the different liquids are incompatible and cannot be mixed together in liquid form or where the different liquids cannot be layered on top of each other.
  • the present invention contemplates dispensing system 400 adding one or more different liquids 2000 to substrates 1000 through layering, through depositing on opposing outer surfaces and/or both.
  • the present invention also contemplates dispensing system 400 adding a plurality of different liquids 2000 to substrates 1000, where the liquids are simultaneously on one or both of the outer surfaces of the substrate.
  • Machine 10 can also be used to re-process the substrates 1000 any number of times through the dispensing system 400 in order to add each of the different liquids 2000.
  • Machine 10 may have additional dispensing systems 400 in series that will add each of the different liquids 2000 to the substrates 1000.
  • Holding system 200 can alternatively provide for dispensing the liquid 2000 (or different liquids) on both sides of the substrates 1000 by providing dispensing system 400 with access to both sides of the substrate.
  • alternative methods of dispensing include, but are not limited to, inverting holding tray 210 so that each of the substrates 1000 are transferred into a second holding tray 210 so that the opposing outer surfaces are now facing away from the second holding tray or using a holding tray that holds each of the substrates around their perimeters or outer circumferences so that both outer surfaces are simultaneously accessible.
  • each of the carrier substrates 1000 or their holding tray 210 can be done near the end of the process so that the opposing outer surface is re-processed by the same components or a second set of components could be added to machine 10 to continue the process with respect to the opposing outer surface. Additionally, the inverting of each of the substrates 1000 or their holding tray 210, can be done by holding system 200 to allow for other operations or processes to be performed on the opposing outer surface, such as, for example, coating or printing on both sides of the products .
  • Conveyor system 300 provides for movement of holding trays 210 along machine 10 and through the various stages or systems of the machine.
  • conveyor system 300 provides for movement of holding trays 210 along a substantially horizontal path.
  • the present invention contemplates movement of the holding trays 210 in other directions, such as, for example, in a vertical path, where spacial economy, the use of gravity or other reasons suggest or dictate such a direction of movement.
  • Conveyor system 300 has a drive conveyor 310.
  • Drive conveyor 310 is controlled by control system 900, shown in FIG. 1, and is preferably variable speed.
  • Holding trays 210 are preferably removably connected to drive conveyor 310. Holding trays 210 are securely connected to the drive conveyor 310 so that each of the substrate positions 220 remains constant with respect to the drive conveyor in order to provide accuracy in dispensing and monitoring of the substrates 1000, droplets 2100 and products.
  • drive conveyor 310 is a circulating conveyor belt that traverses the length of machine 10 and, more preferably, is a serial real-time communications system drive unit.
  • the present invention contemplates other types and methods of moving the holding trays 210, such as, for example, parallel drive chains, tracks, belts or wheels to which the holding trays can be removably connected.
  • the present invention also contemplates the use of a number or series of holding trays 210 that are pivotally secured to each other to form a belt-like structure or tray belt, which can be operably connected to the drive conveyor 310.
  • Machine 10 can have a plurality of tray belts with different sizes and/or shapes of substrate positions 220 to accommodate different sizes and/or shapes of substrates 1000.
  • the tray belt is a length or line of holding trays 210 that is connectable at opposing ends to form a loop.
  • the tray belt is fed along the drive conveyor 310 and then secured at its opposing ends to form the belt along the machine 10.
  • the second tray belt can preferably be connected to the end of the first tray belt that is being removed, as that first tray belt is driven along and off of the drive conveyor.
  • the present invention also contemplates the use of any number of drive conveyors 310.
  • different systems of machine 10 can have independent drive conveyors 310 that allow for independent control of the speed of the drive conveyors, such as, for example, to more rapidly remove the products from the end of the process.
  • control system 900 would preferably control the various independent drive conveyors 310, and be able to coordinate their movement .
  • dispensing system 400 provides for the addition of the liquid 2000 to each of the substrates 1000, and provides for real-time monitoring, feedback and adjustment.
  • dispensing system 400 has a gantry 410 that laterally spans above and across drive conveyor 310, and is longitudinally movable with respect to the drive conveyor. The movement of gantry 410, including speed and position, is controlled by control system 900.
  • the gantry 410 has a dispensing module 420 movably connected thereto.
  • the dispensing module 420 is movable along the longitudinal axis of the gantry 410, which laterally traverses across the drive conveyor 310.
  • the movement of the dispensing module 420, including speed and position, is also controlled by the control system 900.
  • the dispensing module 420 is capable of movement along X and Y axes with respect to the drive conveyor 310 and the holding trays 210. Additionally, the present invention contemplates movement of the gantry 410, the dispensing module 420, and/or both, along a Z-axis with respect to the drive conveyor 310 and the holding trays 210. The movement of the dispensing module 420 allows it to accurately dispense the droplet 2100 on each of the substrates 1000 that are in the array of substrate positions 220 on holding tray 210. Control system 900 can also adjust the movement of the dispensing module 420 and the gantry 410 to accommodate different sizes and shapes of holding trays 210, as well as different arrays of substrate positions 220 on the holding trays.
  • the use of the gantry 410 to move the dispensing module 420 along X and Y axes (and the Z axis if desired) provides for smooth movement and accurate alignment of the dispensing module with each of the substrates 1000. This is especially significant in the preferred embodiment of machine 10 where the drive conveyor 310 continues to move the holding tray 210 through the dispensing system 400 as the droplets 2100 are being dispensed.
  • the continuous movement of each of the substrates 1000 along machine 10 as the dispensing step is occurring speeds up the manufacturing process.
  • Dispensing module 420 preferably moves in an X-like path to accurately dispense on each of the substrates 1000.
  • the size and shape of the X-like path depends upon the dispensing speed and the spacing of substrate positions 220, as shown in FIGS. 2a and 2b. It should be further understood by one of ordinary skill in the art that the dispensing module 420 can be moved along alternative paths that preferably allow for continuous movement of the substrates 1000 during dispensing.
  • the accuracy of the alignment of the dispensing module 420 with each of the substrates 1000, and the efficiency of the movement of the module, is facilitated by the use of the rectangular array of substrate positions 220 along holding tray 210 and the control of the movement of the module and gantry 410 in a rectangular coordinate system.
  • the present invention contemplates the use of other structures and methods that could also be used to move the dispensing module 420 with respect to each of the substrates 1000, as the drive conveyor 310 continues to move through the dispensing system 400, such as, for example, a multiple axis robotic arm and/or along different coordinate systems.
  • the dispensing system 400 has a pair of dispensing modules 420 connected to gantry 410.
  • the use of more than one dispensing module 420 provides for increased speed and efficiency in dispensing of the liquid 2000. Additionally, the use of more than one dispensing module 420 would allow the dispensing system 400 to add different liquids 2000 to a substrate 1000 without cleaning or replacing the module, such as, for example, in layering or on opposing outer surfaces through re-processing the substrate back through the dispensing system.
  • Dispensing module 420 dispenses a desired amount of liquid 2000 onto the substrate 1000.
  • the dispensing module 420 has a pump 425, a flow cell or meter 430, and a dispensing head 435.
  • the present invention contemplates a single dispensing module 420 that has duplicate components, such as, for example, a pump 425 and a flow cell 430 that are in fluid communication with a pair of dispensing heads 435, and/or other combinations or numbers of components for any number of dispensing modules.
  • the pump 425 is connected to a liquid source 440.
  • the liquid source 440 is a movable container 445 that is connected to the pump 425 via removably connectable conduit 447, so that the liquid 2000 can be quickly and efficiently replaced.
  • the liquid source 440 can have a heater (not shown) to facilitate flow of the liquid 2000 from the container 445 to the pump 425, such as, for example, where the liquid is a solder or other type of material that is generally in a solid state at room temperature.
  • the present invention contemplates the use of a liquid source 440 with replaceable cartridges, containers or canisters (not shown) that can be easily inserted in, or connected to, the liquid source.
  • a liquid source 440 that is held in replaceable cartridges, containers or canisters is especially useful for facilitating operation of machine 10.
  • the pump 425 is preferably a metered, positive displacement pump (shown in FIGS. 2c through 2f) , which causes the dispensing head 435 to dispense a single droplet 2100.
  • the metered, positive displacement pump 425 is controlled by the control system 900, and facilitates the accuracy and control of dispensing a single droplet 2100 of the desired size so that the proper amount of liquid 2000 is added to the substrate 1000.
  • the present invention contemplates the use of other types of pumps, such as, for example, a time-pressure pump or reciprocating piston pump connected to a dispensing module that can provide the same degree of accuracy and speed in adding the liquid 2000 to the substrate 1000.
  • Pump 425 has a motor module 4250 and a piston module 4280, as shown in FIGS. 2e and 2f.
  • the motor module 4250 has a motor 4255, a connection port 4260 and an adjustment mechanism 4265.
  • the piston module 4280 has a piston assembly 4285 and a cylinder 4290.
  • the piston module 4260 is operably connected to the motor module 4250 through connection port 4260, the piston on piston assembly 4285 is driven which imparts both reciprocating and rotary motion to the piston.
  • the magnitude of the piston stroke is manually adjustable by the adjustment mechanism 4265.
  • the present invention contemplates automatic adjustment through use of the real time monitoring, feedback and control as described herein.
  • Pump 425 as controlled by the control system 900, can skip select substrate positions 220, where the substrates 1000 contained therein have been designated as rejected.
  • Machine 10 provides for inspection of the substrates 1000 before they undergo the dispensing process described above.
  • the substrate inspection is performed by a video camera 426 and gantry assembly (not shown) , which provide images of each of the substrates 1000 for inspection by control system 900.
  • Camera means herein a video/digitial recording device.
  • Alternative inspection devices and methods can be used which determine the condition of the substrate, as well as ensure that it is properly positioned in substrate position 220.
  • Selective dispensing by pump 425 improves efficiency by not wasting any liquid 2000 on any substrates 1000 that have already been deemed to not meet the required tolerances of the products or are not properly positioned for receiving the droplet 2100.
  • the pump 425 is connected to the flow cell 430.
  • the flow cell 430 determines the amount of liquid 2000 contained in container 445 that is going to be dispensed through the dispensing head 435, which will be used in the real-time monitoring of the droplets 2100.
  • the dispensing head 435 has a dispensing nozzle 450 (shown in FIG. 2d) through which the pressurized, metered amount of liquid 2000 is dispensed, and forms the droplet 2100.
  • the droplet 2100 dispenses onto the outer surface of the substrate 1000.
  • Nozzle 450 provides for exact amounts of liquid 2000 being dispensed.
  • the liquid 2000 is preferably dispensed by a very precise, positive displacement, piston pump 425 that pumps the liquid through tubing to the nozzle 450.
  • the proper selection of liquid composition, viscosity, the materials of construction and orifice size of the nozzle 450 are significant and/or critical parameters to the reproducibility of droplets formed.
  • Nozzle 450 can also be made from a hydrophobic material and/or have a hydrophobic coating to facilitate formation and dispensing of droplet 2100 by compensating for liquid vehicle composition/formulation and surface tension.
  • nozzle 450 has an internal plunger 4510 that is retracted to allow the exact amount of liquid 2000 to enter the dispensing chamber 4520 under pressure of pump 425.
  • plunger 4510 is spring-loaded by a spring 4530, or other biasing device, and can be retracted by air pressure, such as, for example, by a solenoid driven pressure source.
  • the liquid 2000 is dispensed as a result of the retraction of the plunger 4510.
  • the time that the plunger 4510 is in the open position, the pressure maintained on the reservoir of liquid and the vehicle composition are significant and/or critical parameters to the reproducibility of the droplets formed.
  • Chamber 4520 is preferably selectively sealed so that the chamber and liquid 2000 contained therein remain under pressure.
  • a heater 4540 may be utilized to facilitate the ejection process.
  • Nozzle 450 may have a micro-adjuster 4550 or other adjustment mechanism, manual or automatic (such as being controlled by control system 900 with real-time monitoring, feedback and control) , that provides for adjustment of the amount of liquid 2000 that is allowed to exit the dispensing chamber 4520.
  • Nozzle 4560 may be a co-axial air exhaust 4560 that further facilitates dispensing of liquid 2000.
  • the dispensing system 400 uses a pump and nozzle assembly to form and dispense the droplet 2100. This is advantageous due to the accuracy of the components as described above, and the ability to perform real-time monitoring of their activities. Also, the dispensing system 400, through use of nozzle 450, can preferably provide a spherical or substantially spherical droplet 2100, which reduces or prevents splashing and overspray. Additives can be provided to liquid 2000 to facilitate dispensing where appropriate.
  • the dispensing system 400 and the use of a liquid 2000 and droplet 2100 that are dispensed onto the substrate 1000, is advantageous over contemporary systems and processes in that the production facilities or sites where the machine 10 is located can centrally process the liquid. This reduces the steps of the production, such as eliminating off-site production and delivery, which decreases production time and saves on costs. Where harmful compounds are being used in the liquid 2000, this is especially advantageous in reducing the handling of the compounds by the workers .
  • Dispensing system 400 can alternatively have a nozzle-plate assembly 4600 (a portion of which is schematically represented in FIGS. 2h through 2j) to form and dispense the droplet 2100.
  • the assembly 4600 has a plate 4610 with an aperture or nozzle opening 4620 therethrough.
  • the plate 4610 is capable of movement with respect to the supply of liquid 2000, as indicated by arrows 4630. Such movement includes, but is not limited to, vibration of the plate 4610 in order to actuate the dispensing.
  • the liquid 2000 is dispensed through nozzle opening 4620 when the plate 4610 is selectively moved towards the supply of the liquid.
  • the size of nozzle opening 4620 can be adjusted or changed to provide for a range of different sizes or volumes for droplet 2100.
  • the ability to accurately size very. small openings in plate 4610 and the dispensing dynamics of the assembly 4600 allow for dispensing of very small amounts of liquid 2000.
  • a number of nozzle openings 4620 can also be used in the plate 4610 so that array dispensing can be done.
  • Nozzle-plate assembly 4600 is advantageous due to its minimization of components so that there are fewer materials in contact with the liquid 2000.
  • the dispensing operation of the assembly 4600 is reliable since there are no narrow channels and the design is insensitive to air entrapment. Dispensing through the movement of plate 4610 makes the assembly 4600 easy to load and easy to clean. Dead volume for the supply of liquid 2000 is minimized or eliminated due to the planar or substantially planar shape of plate 4610.
  • the present invention further contemplates the use of other structures and methods of dispensing the liquid 2000 onto the substrate 1000, such as, for example, by a pad-printing device where the liquid 2000 is loaded into the ink cartridge.
  • Dispensing system 400 has a dispensing inspection system 460 that provides real-time monitoring of each droplet 2100 that is to be added to the substrates 1000.
  • dispensing inspection system 460 uses high-speed imaging of the droplet 2100 to determine the volume of the droplet.
  • Dispensing inspection system 460 has a high-speed digital camera 465 that is connected to gantry 410 and which is able to take a high-speed image 470 (shown in FIG. 3) of each droplet 2100.
  • two high-speed digital cameras 465 are used, which correspond to each of the two dispensing modules 420.
  • the image 470 of the droplet 2100 is preferably taken in-flight after the droplet has left the nozzle 450 but before it makes contact with substrate 1000.
  • the machine 10 uses a laser detector to trigger the camera 465 to obtain the image 470 due to the high speed of the droplet 2100 (shown generally in FIG. 2d) .
  • the present invention contemplates the use of other triggering devices and methods for triggering camera 465 and obtaining image 470.
  • Image 470 is used by the control system 900 to calculate a volume of each of the droplets 2100.
  • the calculated volume of the droplet 2100 is used to determine the amount of liquid 2000 that is being dispensed onto the substrate 1000. Any amount of liquid 2000 that does not meet tolerances will be marked with an error code by control system 900 so that the substrate 1000 having that particular droplet 2100 can be rejected.
  • dispensing module 420 may dispense a number of droplets 2100 or a stream of liquid. Dispensing inspection system 460 still has the ability to capture the image 470 of the stream of liquid 2000, and the volume calculations can be made therefrom.
  • Dispensing system 400 has a temperature conditioning system 475 that performs cooling/heating/drying of the droplet 2100 on the substrate 1000 depending upon the particular liquid 2000 that has been dispensed, such as, for example, solder may be subjected to cooling to transform it to its solid state while a therapeutic active agent may be subjected to drying to form a film on a carrier tablet.
  • temperature conditioning system 475 has a temperature conditioner 480 and temperature conditioner sensors or monitors 482 (not shown in detail) .
  • the temperature conditioner 480 provides a temperature change to the droplet 2100 and substrate 1000, such as, for example, heating, cooling, and/or air flow.
  • temperature conditioner 480 such as, for example, an oven, refrigeration/cooling device and/or fan.
  • the temperature conditioner sensors 482 monitor the conditions or environmental parameters of each of the dispensed droplets 2100 and substrates 1000 to ensure that the products meet the required tolerances.
  • Conditions such as, for example, temperature, air-flow and humidity are monitored by the temperature conditioner sensors 482, and a number of such sensors are used to account for any variance along the temperature conditioner 480.
  • the data gathered by the sensors is provided to control system 900 for evaluation of the quality of the substrates 1000 and droplets 2100 in each of the holding trays 220.
  • the drying conditions are monitored for the entire holding tray 220, and error codes can be assigned to the individual substrates 1000 and droplets 2100 contained therein, based upon a holding tray being affected by a condition of the temperature conditioner 480 that does not meet the required tolerances.
  • portions of trays can be monitored for drying conditions by placing more sensors 482 in the temperature conditioner 480 in strategic positions.
  • the present invention contemplates the monitoring of other conditions or criteria related to the temperature conditioning process, such as, for example, conditions that may be more significant to particular products.
  • Temperature conditioning system 475 can include sensors to detect conditions, such as, for example, the surface temperature of the substrates 1000, or IR radiation. Temperature conditioning system 475 may also include a sensor for turning on the temperature conditioner, such as, for example, a photo-cell triggered by holding trays 210 entering the temperature conditioner 480. Additionally, temperature conditioner 480 can be utilized for heating of the substrate 1000 to cause reflow, such as for dispensed solder.
  • IR infrared
  • Dispensing system 400 has a dispensing confirmation system 500 that provides real-time monitoring, feedback and adjustment for the liquid 2000 that has been added to the substrate 1000.
  • the dispensing confirmation system 500 monitors the positioning of the liquid 2000 on the substrate 1000 and the amount of the liquid contained thereon. Additionally, the dispensing confirmation system 500 can monitor for other substances, such as, for example, identifying contaminants present on the substrate 1000, as well as the amount of such other substances .
  • the data obtained by the dispensing confirmation system 500 is provided to the control system 900.
  • the control system 900 will assign error codes to individual substrates 1000 and their liquids 2000 that do not meet the required tolerances of the product.
  • dispensing confirmation system 500 has a gantry 510 (similar to gantry 410 described above) with a pair of charge coupled device (CCD) cameras 520 that obtain images 525 of each of the substrates 1000.
  • the images 525 are provided to control system 900 for a determination of the position of the liquid 2000 with respect to the substrate 1000.
  • the position of solder on an IC chip can be analyzed via image 525 to determine the strength of the bond, as well as short circuits or the potential risk of short circuits.
  • Dispensing confirmation system 500 can also have a probe 530 (shown in FIG. 2) that is used for determining the amount, type and/or distribution of the liquid 2000 on the substrate 1000.
  • the probe 530 uses chemical imaging to determine the amount of the liquid 2000 present on the substrate 1000.
  • the present invention contemplates dispensing confirmation system 500 providing other analysis for the liquid 2000, such as, for example, mechanical stress, crystallinity, crystal orientation, composition, crystal phase, and/or doping.
  • Probe 530 has components that carry out chemical imaging on each of the substrates 1000 in holding tray 210, such as, for example, fiber optics, focal plane array (FPA) detectors, and/or charge coupled device (CCD) detectors. Additionally, liquid crystal tunable filters can be used as wavelength selectors for the chemical imaging. The chemical imaging provides good penetration into the liquid 2000 and upper surface of the substrate 1000 for an accurate measurement of the quantity of the liquid.
  • FPA focal plane array
  • CCD charge coupled device
  • probe 530 uses a focal plane array detector to obtain a signal from every point in the sample area.
  • the sample area preferably includes the entire holding tray 210 so that all of the substrates 1000 are being simultaneously measured, which further improves the efficiency of the process.
  • the focal plane detector is able to obtain simultaneous spectral information at every frequency for the sample area.
  • Probe 530 can rapidly and non- destructively measure the liquid 2000 for various characteristics including, but not limited to, amount, formulation and/or distribution, as well as monitor or detect other substances contained in or on the substrate 1000.
  • the present invention contemplates the use of various methods and devices for determining the presence, type, distribution, amount or other characteristics of a particular liquid 2000 on the substrate 1000, such as, for example, spectroscopy and/or chemical imaging utilizing Raman and UV reflectance, and/or various other types of imaging, chemical imaging and/or spectroscopy, such as, for example, UV/visible absorption, fluorescence, laser- induced fluorescence, luminescence, photoluminescence, terahertz, NIR, and/or mid-IR.
  • various methods and devices for determining the presence, type, distribution, amount or other characteristics of a particular liquid 2000 on the substrate 1000 such as, for example, spectroscopy and/or chemical imaging utilizing Raman and UV reflectance, and/or various other types of imaging, chemical imaging and/or spectroscopy, such as, for example, UV/visible absorption, fluorescence, laser- induced fluorescence, luminescence, photoluminescence, terahertz, NIR, and/or mid-IR.
  • the present invention contemplates the use of various devices or components that facilitate the use of spectroscopy and/or chemical imaging for analysis of the products, such as, for example, lasers (e.g., pulse lasers), beam splitters, water-vapor free environments (e.g., nitrogen shrouds), optical delays (e.g., variable optical delays), antennas and/or semiconductors.
  • lasers e.g., pulse lasers
  • beam splitters e.g., water-vapor free environments (e.g., nitrogen shrouds), optical delays (e.g., variable optical delays), antennas and/or semiconductors.
  • optical delays e.g., variable optical delays
  • antennas and/or semiconductors e.g., variable optical delays
  • the present invention contemplates the use of room temperature solid state detectors and/or pulsed time- gated techniques and components.
  • the present invention contemplates the use of techniques for analysis of the products that are non-ionizing, non-invasive, nondestructive, and/or require low power
  • the present invention contemplates the use of any regions of the electromagnetic spectrum that allow for analysis of the substrate 1000 and liquid 2000, as well as various techniques and sources for excitation in using the particular type of spectroscopy.
  • the present invention also contemplates the use of other techniques and components for digital imaging to allow for use of chemical imaging of the substrate 1000 and liquid 2000.
  • dispensing confirmation system 500 also contemplates the use of surrogate detection in any of the spectral ranges.
  • the coating system 600 of machine 10 provides for a coating (not shown) to be placed on the substrate 1000 and/or over the liquid 2000, or some portion thereof.
  • the coating 2300 may be a sealant or a protective layer.
  • Coating system 600 has a coating device 610, a coating source 620 and a coating dryer 630 (if necessary depending upon the particular coating being used) .
  • the coating device 610 transfers the coating to the upper surface of the substrate 1000.
  • a pad-printing device can be used for coating device 610 and is advantageous because of its efficient transfer of the coating to the substrate without any waste, e.g., no overspray.
  • Alternative devices can also be used, such as, for example, a spray device (not shown) or ink jet device, to spray the coating upon the substrate 1000.
  • the spray device could also be movably connected to gantry 615 to pass over each of the substrate positions 220.
  • the present invention contemplates the use of other devices and methods for applying a coating to the substrate 1000, such as, for example, an ultrasonic atomizer.
  • the coating system 600 can use intermittent, low volume atomized sprayers to locally apply the coating over the all or a portion (s) of the surface of substrate 1000.
  • the sprayer may use volumetric pumps to intermittently supply coating materials.
  • a two fluid air- liquid atomization sprayer may also be used to generate a fine spray.
  • coating device 610 is connected to or is positioned adjacent to the machine 10 to coat an array of substrates with each reciprocating stroke.
  • Coating device 610 can be movably connected to a gantry 615 or other similar device to facilitate movement of the coating device with respect to the holding tray 220.
  • the holding tray 220 continues to move as the coating is being applied by the coating device 610.
  • the present invention contemplates the use of other devices and methods of positioning the coating device 610 with respect to each of the substrate positions 220 so that the coating is accurately applied.
  • the coating device 610 is releasably connected to the coating source 620.
  • the coating source 620 is a movable container 625 that is connected to the coating device 610 via removably connectable conduit 627, so that the coating can be quickly and efficiently replaced.
  • the coating system can provide the necessary coating depending upon how the liquid 2000 has been added to the substrate, such as, for example, on both sides or between layers. This can facilitate the use of higher volumes of liquid 2000.
  • Coating dryer 630 can be used to perform drying of the coating (where appropriate) that has been applied to the substrate 1000 and/or over the liquid 2000.
  • the coating dryer 630 preferably has an oven 640 and one or more oven sensors 650 (not shown in detail) .
  • the oven 640 provides heat and air flow to the coating.
  • the oven sensors 650 similar to the temperature conditioner sensors 482 discussed above, monitor the drying conditions of the coatings to ensure that the products meet the required tolerances.
  • the printing system 700 of machine 10 provides an identification marker on the substrate 1000.
  • the printing system preferably has a pad-printing device 710 that transfers the marker to the substrate 1000 and a pair of video cameras 720 that obtain an image 730 of each of the identification markers to verify the quality of the image. Unacceptable substrates 1000 will be identified by the control system 900 for subsequent rejection by system 800.
  • pad- printing device 710 and cameras 720 are movably connected to a gantry 735 (similar to gantries 410, 510 and 615) to facilitate movement of the pad-printing device with respect to the holding tray 210 that continues to move as the identification marker is being applied.
  • a gantry 735 similar to gantries 410, 510 and 615) to facilitate movement of the pad-printing device with respect to the holding tray 210 that continues to move as the identification marker is being applied.
  • the present invention contemplates the use of other devices and/or methods, for positioning the pad-printing device 710 or alternative device with respect to each of the substrate positions 220 for accurate application of the identification markers, such as, for example, lasermarking, inkjet, and/or rotogravure.
  • Each of the marker images 730 is provided to control system 900 for inspection and to determine if the printed identification marker meets the required tolerances of the products.
  • the present invention contemplates machine 10 having an ink dryer (not shown) , such as, for
  • the acception-rejection system 800 provides products that have undergone real-time monitoring and adjustment for quality control to ensure that each of the products meets the required tolerances. Based upon the real-time monitoring being continuously performed at various stages of the process by machine 10, control system 900 has designated each and every product as either acceptable or rejected.
  • Acceptable products pass through to the delivery area (not shown in detail) , preferably under bias that is selectively controlled by the control system 900, while rejected product drop into a scrap area, preferably under the force of gravity.
  • the present invention contemplates the use of other structures and methods of separating those products that are designated by control system 900 as acceptable from those products that have been designated by the control system as rejected.
  • control system 900 coordinates and synchronizes the various stages and systems of the machine 10.
  • control system 900 is a distributed process control system that has a number of microprocessors 910 that control the different systems of machine 10.
  • the microprocessors 910 are preferably coordinated through a workstation 920.
  • the present invention contemplates other types of system control including central and regional control, such as, for example, a single microprocessor 910 controlling all of the systems or similar systems being controlled by one of several microprocessors 910.
  • the microprocessors 910 and workstation 920 are in communication with each other, preferably through a network 930 using an Ethernet switch 935, which allows for the real-time monitoring, feedback and adjustment of the process being performed by the machine 10.
  • the present invention contemplates the use of other structures and methods for communication, such as, for example, hardwiring.
  • the control system 900 also has an archive microprocessor or historian 940, which is used to centrally store the large amount of data that is compiled for each and every product that is processed by the machine 10.
  • the present invention contemplates other methods of storage of the process data, such as, for example, microprocessors 910 individually storing the data that they have compiled.
  • the control system 900 preferably has a number of monitors 950 that provide displays of the data, portions of the data, summaries of the data, and/or calculations and conclusions based upon the data, so that the workers can monitor and/or adjust the process as it is occurring. More preferably, the monitors 950, through use of the various microprocessors 910 and/or workstation 920, can selectively display the data, portions of the data, summaries of the data, calculations based upon the data, and conclusions based upon the data. Preferably, control system 900 records data for every product, which includes most, an preferably all, of the following: time, initial substrate status, droplet volume, temperature conditioner temperature, temperature conditioner humidity, temperature conditioner air flow, liquid location on substrate, liquid quantity and acceptability.
  • the present invention also contemplates dispensing inspection system 460 utilizing optical profilometry for real-time monitoring and feedback control.
  • the components utilized by dispensing inspection system 460 to carry out the optical profilometry are known to one skilled in the art, such as, for example, a laser and camera.
  • the technique of optical profilometry is especially useful for larger volumes of liquid 2000, such as, for example, greater than 10 microliters , where the dispensing system 400 is dispensing a stream, as opposed to the droplet 2100.
  • dispensing inspection system 460 performs a first scan of the substrate 1000 prior to dispensing of the liquid 2000 in order to obtain a first profile of the substrate. A second scan is then performed by the dispensing inspection system 460 to obtain a second profile of the substrate 1000 with the liquid 2000 thereon. The difference in the first and second profiles provides the measurement of the volume of liquid 2000 that has been dispensed onto the substrate 1000.
  • the present invention further contemplates the use of optical profilometry of the substrate 1000 after the liquid 2000 has been dried on the substrate.
  • the first profile may be based upon a predetermined value for the same substrates 1000 to expedite the process and eliminate the need for two scans.
  • the present invention also contemplates the use of real-time monitoring to provide real-time feedback and adjustment to the conveyor and dispensing systems 300 and 400, such as, for example, adjusting the speed for better positioning of the droplet 2100 on the substrate 1000 or adjusting the pump 425 and/or nozzle 450 to increase or decrease the volume of the droplet, which increases or decreases the amount of liquid 2000 that is ultimately dried on the substrate.
  • the use of real-time monitoring of the droplet 2100 both before and after contact with the substrate 1000 also would allow for more efficient accounting for any losses occurring during the process.
  • FIGS. 4, 6 and 7, another embodiment of an apparatus or machine of the present invention is shown and generally referred to by reference numeral 20.
  • the machine 20 has components that are similar to the components described above with respect to the preferred embodiment of FIG. 1 and are similarly numbered, such as, conveyor system 300, dispensing system 400 and control system 900.
  • Machine 20 is a scaled-down version of the preferred embodiment but still provides real-time monitoring for the process.
  • Each of these systems 300, 400 and 900 are operably connected to each other to efficiently and ergonomically provide products that have each undergone real-time monitoring, and, preferably, real-time feedback and adjustment.
  • Holding trays 210 are manually placed on drive conveyor 310 where the substrates 1000 begin their descent through machine 20. Each holding tray 210 is identified through use of the bar code 230 on the tray and a scanner
  • the holding trays 210 continue to move along machine
  • a dispensing module 420 which is mounted to gantry 410, dispenses droplets 2100 on each of the substrates 1000.
  • Video camera 465 takes an image of each droplet being dispensed and, in conjunction with the flow cell 430, the real-time monitoring of the amount of liquid being dispensed occurs.
  • each of the substrates undergoes real-time monitoring of the position and amount of the liquid.
  • Video camera 520 which is mounted on gantry 510, obtains an image 525 of each of the substrates 1000 and liquids 2000 thereon. The images 525 are processed by control system 900 for the location and quantity of the liquid 2000.
  • camera 520 captures the image 525 of the deposition spot left after dispensing and drying.
  • Image analysis software uses gray scale to tabulate the number of pixels and relative intensity of the pixel to develop an image of the dried spot left behind. Based on this information, the amount of the liquid 2000 on the substrate 1000 is determined.
  • FIG. 5 A second alternative embodiment of the apparatus of the present invention is shown in FIG. 5 and is generally represented by reference numeral 20' . Similar to the embodiment described above with respect to FIGS. 4, 6 and 7, machine 20' is a scaled down version of the preferred embodiment of machine 10 shown in FIG. 1.
  • Machine 20' has many features similar to machines 10 and 20 and such features are similarly numbered, such as, conveyor system 300, and dispensing system 400.
  • Machine 20' exemplifies the modularity of the present invention as it includes the features of machine 20 and additionally has gantry 510, which is readily available for connection with dispensing confirmation system 500.
  • Control system 900 will synchronize the other systems based upon the lack of use of certain systems, which will further maximize the efficiency of the process, such as, for example, where drying of substrate 1000 and liquid 2000 is minimal or not required, the other activities can be greatly sped up.
  • the present invention contemplates machines 10, 20 and 20' , and the various components and systems therein, being modular. This will allow machines 10, 20 and 20' to carry out only the necessary activities for particular products by removing selected unnecessary components, and will provide time saving, such as, for example, avoiding passing holding trays 220 through the coating temperature conditioner 630 where no coating is being applied.
  • the present invention contemplates the interchangeability of different components to perform the various activities of machines 10, 20 and 20', such as, for example, probe 530 that performs chemical imaging being interchangeable with other probes that perform other types of analysis, such as, for example, spectroscopy and chemical imaging, such as, for example, utilizing Raman, UV reflectance, fluorescence, and/or terahertz.
  • Machines 10, 20 and 20' can utilize the type of analysis, and hence the components that perform that analysis, which are most efficient and accurate for a particular product.
  • the present invention also contemplates control system 900 indicating which types of analysis and their corresponding components are to be used for a particular product.
  • the present invention further contemplates the process performed by machines 10, 20 and 20' including a packaging step so that the end result is a product that is ready for shipping, especially where real-time release of products is utilized.
  • the design and modularity of machines 10, 20 and 20' facilitates the addition of a packaging step to the process (where appropriate) .
  • Machines 10, 20 and 20' also provide the ability to change production to a different product in a fraction of the time that it takes to make a similar adjustment to a contemporary machine. The cleaning of the machines 10,
  • Dispensing modules 420 are relatively low-cost which allows for their replacement rather than a time-consuming repair.
  • Machines 10, 20 and 20' improve efficiency in manufacturing the products based upon the manufacturing steps as well as the quality control steps. The continuity of the process quickly and efficiently provides the products that are directly ready for packaging, without the need for any other quality control testing being performed on them. Also, machines 10, 20 and 20' provide a process that can be run continuously without the need for stopping as in contemporary devices and techniques .
  • the real-time monitoring, feedback and adjustment of the present invention avoids unnecessary manufacturing steps (e.g., dispensing on rejected substrates) and provides quality control based on the individual properties of each of the substrates.
  • the present invention is cost effective because it only discards the defective product identified by control system 900, rather than discarding all of the products in a batch that has a significant number of defective substrates, as by contemporary methods of product sampling.
  • the present invention contemplates the use of individual systems or combinations of systems of machines 10, 20 and 20' in combination with other devices, to provide one or more of the steps described herein. It should be further understood by one of ordinary skill in the art that the degree of real-time monitoring and/or feedback can be varied depending upon the particular product being manufactured and/or based upon other factors. For example, but not limited to, the machine 10, 20 and 20' may only utilize the high-speed imaging for detection of whether the droplet 2100 has accurately been dispensed upon carrier substrate 1000. Preferably, the volume calculation of dispensing inspection system 460 is also utilized to calculate the amount of liquid 2000 in the droplet 2100. However, the use of contemporary quality control techniques is also contemplated, such as batch sampling. Also, the present invention contemplates the use of contemporary quality control techniques, such as, for example, batch sampling, in parallel with the real-time monitoring and/or feedback described herein for machines 10, 20 and 20' .
  • machines 10, 20 and 20' can be utilized by themselves or in combination with one or more of the other systems of machines 10, 20 and 20' or in combination with contemporary devices for manufacturing products.
  • the high-speed imaging and volume calculation of dispensing inspection system 460 may be followed by a contemporary batch sampling technique for quality control of the resulting products.
  • the video imaging and volume calculation of dispensing inspection system 460 provides versatile realtime monitoring and feedback control for the products. This type of quality control is not dependent on the particular formulation of the liquid 2000, as opposed to some forms of chemical imaging which have such dependency.
  • the terms "first”, “second”, “third”, “fourth”, “upper”, “lower”, and the like, are used herein to modify various elements. These modifiers do not imply a spatial, sequential, or hierarchical order to the modified elements unless specifically stated.

Abstract

An apparatus and method are provided for producing a plurality of products or processing a plurality of samples via dispensing. The apparatus and method provide real-time monitoring of the products/samples and can provide real-time control. The apparatus and method can monitor the liquid both before and after it has been added to a carrier substrate. The apparatus and method can provide monitoring of each product/sample that is processed.

Description

APPARATUS AND METHOD FOR PRODUCING OR PROCESSING A PRODUCT OR SAMPLE
BACKGROUND OF THE INVENTION
Field of the Invention
[0001] The present invention relates to the manufacture or processing of products or samples. More particularly, the present invention relates to an apparatus and process for manufacturing or processing a product or sample by dispensing.
Description of Related Art
[0002] Manufacturing processes often require the combination of different materials, such as solder onto a printed circuit board or an active agent onto a pharmaceutical substrate. Various methods have been developed for the combining of such materials. For example, soldering methods have been developed for connecting integrated circuit chips to the printed circuit board. One such method includes applying a small amount of solder to the bottom surface of the chip, aligning the solder with a bond pad on the surface of the printed circuit board, and heating the solder until -it reflows.
Another such method includes applying solder to bonding pads on the printed circuit board and then bonding electrical components to the printed circuit boards by positioning the components over the solder and by heating and reflowing the solder. In other methods, chips are bonded to a patterned layer of solder created by applying a thin layer of solder paste to a printed circuit board through holes in a stencil, leaving a selected solder pattern on the printed circuit board.
[0003] Such methods suffer from drawbacks as to efficiency and quality. Accordingly, there is a need for an apparatus and process for manufacturing products via dispensing that reduces or eliminates these manufacturing and quality control drawbacks of the contemporary devices and techniques .
SUMMARY OF THE INVENTION
[0004] It is an object of the present invention to provide a more efficient process and/or apparatus for manufacturing or processing products or samples that comprise a dispensed component.
[0005] It is another object of the present invention to provide such a process and/or apparatus that provides real-time process monitoring.
[0006] It is yet another object of the present invention to provide such a process and/or apparatus that provides real-time feedback and control of the process and product quality.
[0007] It is still another object of the present invention to provide such a process and/or apparatus that provides monitoring of each of the products or samples that are manufactured or processed. [0008] It is yet still another object of the present invention to provide such a process and/or apparatus that minimizes or eliminates off-line quality control inspection and facilitates real-time release of the products .
[0009] It is yet a further object of the present invention to provide such a process and/or apparatus that facilitates change over to production of a different product.
[0010] These and other objects and advantages of the present invention are provided by a monitoring system for a machine that produces a plurality of products by dispensing droplets of liquid on one or more carrier substrates. The monitoring system comprises an inspection system having a microprocessor, a first camera or video recording device, in communication with the microprocessor and a trigger operably connected to the first camera or video recording device. The inspection system determines an amount of the liquid that is being added to each of the carrier substrates. The trigger actuates the first camera or video recording device to obtain a first image of each of the droplets in-flight. The microprocessor determines the amount of the liquid based upon the first image. Camera means herein a video/digital recording device.
[0011] In another aspect, an apparatus for producing a plurality of products is provided. Each of the plurality of products has a carrier substrate and a dispensed liquid thereon. The apparatus comprises a dispensing system for dispensing the dispensed liquid as a droplet onto each of the carrier substrates and a monitoring system comprising an inspection system that determines an amount of the dispensed liquid that is being added to each of the carrier substrates by the dispensing system. The inspection system comprises a microprocessor, a first camera or video recording device in communication with the microprocessor and a trigger operably connected to the first camera or video recording device. The trigger actuates the first camera or video recording device to " obtain a first image of the droplet in-flight. The microprocessor determines the amount of the dispensed liquid based upon the first image.
[0012] In another aspect, an apparatus for producing a plurality of products that each have a carrier substrate and a dispensed liquid is provided. The apparatus comprises a dispensing system that adds the dispensed liquid to each of the carrier substrates; and a monitoring system that performs real-time monitoring of the dispensing system to determine an amount of the dispensed liquid on each of the carrier substrates.
[0013] In another aspect, a monitoring system for a machine that produces a plurality of products is provided where the plurality of products each have a carrier substrate and a dispensed liquid. The monitoring system comprises a confirmation system operably connected to the machine that determines an amount of the dispensed liquid that has been added to each of the carrier substrates by the machine. The confirmation system performs optical profilometry on each of the carrier substrates to determine the amount of the dispensed liquid. [0014] In another aspect, a machine which produces a plurality of products where each has a carrier substrate and a dispensed liquid is provided. The machine comprises a dispensing system for adding the dispensed liquid to each of the carrier substrates and a confirmation system for determining an amount of the dispensed liquid that has been added to each of the carrier substrates. The confirmation system performs optical profilometry on each of the carrier substrates to determine the amount of the dispensed liquid.
[0015] In another aspect, a method of monitoring a machine is provided. The machine produces a plurality of products by dispensing a droplet of liquid on a carrier substrate. The method comprises actuating a camera based upon dispensing of the droplet; obtaining a first image of the droplet in-flight; and determining a volume of the droplet based upon the first image.
[0016] In another aspect, a method of producing a plurality of products that each have a carrier substrate and a dispensed liquid thereon is provided. The method comprises dispensing the dispensed liquid as a droplet onto each of the carrier substrates; and determining an amount of the dispensed liquid that is being added to each of the carrier substrates by the dispensing system by obtaining a first image of the droplet in-flight and determining the amount of the dispensed liquid based upon the first image. Each of the carrier substrates can continue to move along the apparatus as the inspection system determines the amount of the dispensed liquid. The monitoring system may further comprise a confirmation system having a probe that performs spectroscopy on the dispensed liquid that has been added to each of the carrier substrates. Each of the carrier substrates can continue to move along the apparatus as the probe performs spectroscopy. The spectroscopy may be taken from the group consisting of near infrared, mid-infrared, ultraviolet/visible, fluorescence, laser-induced fluorescence, Raman, terahertz, and any combinations thereof.
[0017] The monitoring system can further comprise a confirmation system having a second camera or video recording device that obtains a second image of the dispensed liquid on each of the carrier substrates. The confirmation system determines a position of the dispensed liquid for each of the carrier substrates based on the second image. Each of the carrier substrates may continue to move along the apparatus as the second camera or video recording device obtains the second image.
[0018] The apparatus can further comprise a temperature conditioning system that changes the temperature of the dispensed liquid to facilitate its formation on the carrier substrate. The temperature conditioning system may monitor environmental parameters for each of the carrier substrates, wherein the environmental parameters are taken from the group consisting of temperature, airflow rate, humidity, radiation, product surface temperature, or any combinations thereof.
[0019] The apparatus can further comprise a printing system for applying an identification marker to each of the carrier substrates. The printing system may have a third camera or video recording device for obtaining a third image of the identification marker for inspection. Each of the carrier substrates can continue to move along the apparatus as the third camera or video recording device obtains the third image.
[0020] The apparatus can further comprise a control system for performing real-time control of the dispensing system based on the real-time monitoring. The real-time control may comprise adjusting an amount of dispensing from the dispensing system. The dispensing system may have a nozzle, wherein the real-time control comprises adjusting a position of the nozzle with respect to each of the carrier substrates thereby adjusting the position of the dispensed liquid on each of the carrier substrates. The confirmation system can perform optical profilometry on each of the carrier substrates to determine the amount of the dispensed liquid. Each of the carrier substrates may continue to move along the apparatus as the optical profilometry is performed.
[0021] Other and further objects, advantages and features of the present invention will be understood by reference to the following:
BRIEF DESCRIPTION OF THE DRAWINGS
[0022] FIG. 1 is a perspective view of a preferred embodiment of a machine of the present invention;
[0023] FIG. 2 is a schematic representation of the automation components of the machine of FIG. 1; [0024] FIG. 2a is a representation of a path of continuous movement of the dispensing module of the machine of FIG. 1;
[0025] FIG. 2b is a representation of another path of continuous movement of the dispensing module of the machine of FIG. 1;
[0026] FIG. 2c is a perspective view of a dispenser assembly of the machine of FIG. 1;
[0027] FIG. 2d is a perspective cross-sectional view of the dispenser assembly of FIG. 2c;
[0028] FIG. 2e is a perspective view of the pump module of the dispenser assembly of FIG. 2c;
[0029] FIG. 2f is a perspective view of the motor module of the dispenser assembly of FIG. 2c;
[0030] FIG. 2g is a perspective cross-sectional view of another embodiment of a nozzle of the machine of FIG. 1;
[0031] FIG. 2h is a schematic representation of another embodiment of a dispensing assembly of the machine of FIG. 1;
[0032] FIG. 2i shows the range of droplets that can be dispensed from the assembly of FIG. 2h;
[0033] FIG. 2j shows the dispensing assembly of FIG. 2h with multiple nozzles or apertures; [0034] FIG. 3 is a high speed video image of a droplet dispensed by the machine of FIG. 1;
[0035] FIG. 4 is a perspective view of an alternative embodiment of a machine of the present invention;
[0036] FIG. 5 is a perspective view of another alternative embodiment of a machine of the present invention;
[0037] FIG. 6 is a schematic representation of components of the machine of FIG. 4; and
[0038] FIG. 7 is a schematic representation of the communication between the components of the machine of FIG. 4.
DETAILED DESCRIPTION OF THE INVENTION
[0039] Referring to the drawings, and in particular FIGS. 1 through 3, a preferred embodiment of the apparatus or machine of the present invention is shown and generally referred to by reference numeral 10. The machine 10 has a plurality of components that are operably connected to manufacture a product or process a sample, and preferably a batch of products or samples, as will be described later in greater detail. A batch is a quantity of product, which has been produced or processed during a defined cycle, such as, for example, a fixed number or one or more runs over a fixed time period. The machine 10 has various components arranged along a straight or substantially straight line. However, the present invention contemplates other arrangements and positionings of the various components, such as, for example, in circular or rectangular paths. While the exemplary embodiment describes the manufacture of a product via dispensing, the present invention contemplates other processes being performed by the machines described herein, such as, for example, testing or processing of samples via dispensing.
[0040] The arrangement and positioning of the components of machine 10 provide a smaller footprint for space savings, as well as providing a more efficient and ergonomic machine that facilitates operation. Machine 10 can have components stacked on each other or at differing heights to take advantage of vertical space, as well as facilitating operation, such as, for example, enabling the use of gravity in the process performed by the machine.
[0041] The machine 10 has a loading system 100, a holding system 200, a conveyor system 300, a dispensing system 400, a coating system 600, a printing system 700, a product acception-rejection system 800, and a control system 900. Each of these systems 100 through 900 are operably connected to each other to efficiently and ergonomically provide products that are ready for packaging, and which have each undergone real-time monitoring, and preferably real-time feedback and adjustment or control.
[0042] The machine 10 delivers the product, which is a combination of a substrate 1000 and a liquid 2000. As will be described later in greater detail, the liquid 2000 is dispensed by dispensing system 400 in the form of a droplet 2100 (shown in FIG. 3) that is dispensed onto the substrate 1000. It should be understood that the liquid 2000 can have a variety of properties, such as, for example, low-viscosity, high-viscosity, such that the term liquid is not intended to be limiting. The liquid 2000 can be anything that is dispensable onto the substrate 1000, such as, for example, solder onto an IC chip or a therapeutic active agent onto a carrier tablet. One of ordinary skill in the art could utilize the present invention for processing a variety of substrates 1000 with a variety of liquids 2000. Additionally, the dispensing of liquid 2000 onto substrate 1000 is not limited to droplets 2100, but can also include other flow patterns, such as, for example, a partial or continuous stream. It should be further understood that the present invention contemplates the substrate 1000 being a variety of substances upon which the liquid 2000 can be dispensed and having a variety of properties. Such a substance for substrate 1000 may also include another liquid.
[0043] The droplet 2100 is dispensed onto the outer surface or substantially along the outer surface of the substrate 1000, such as, for example, solder that is heated and then dispensed onto the substrate. The substrate 1000, the liquid 2000 and the resulting product undergo real-time monitoring, feedback and adjustment, which improve quality control.
[0044] In the preferred embodiment shown in FIG. 1, loading system 100 has a loading container or hopper 110 in communication with a loading chute 120. Hopper 110 is preferably movable so that one or more substrates 1000 can be loaded into the hopper and then the hopper can be moved into communication with the loading chute 120. Loading chute 120 is in communication with holding system 200 and conveyor system 300 so that the substrates 1000 can be moved from the hopper 110 into the holding system 200 for movement along and through machine 10 by way of conveyor system 300.
[0045] The hopper 110 and loading chute 120 can use various devices and methods, such as, for example, powered wheels or wedges, powered belts, or gravity, to move each of the substrates 1000 into their designated positions in holding system 200. In machine 10, a portion of loading system 100 is preferably disposed above a portion of conveyor system 300 to take advantage of gravity, in combination with a mechanical loading device.
[0046] In the preferred embodiment, holding system 200 has a plurality of holding members or trays 210 with substrate positions 220 having a size and shape that allows for holding of each of the substrates 1000. Preferably, each of the holding trays 210 is rectangular, and the substrate positions 220 are arranged in an array of equi-distantly spaced rows and columns. As will be explained later, this array facilitates operation of .the dispensing system 400 in adding the droplets 2100 to the substrates 1000. However, the present invention contemplates the use of other structures and methods for securing each of the substrates 1000 and the resulting products as they travel along machine 10.
[0047] One of ordinary skill in the art can vary the sizes, capacities and shapes of the holding trays 210 and the substrate positions 220 to accommodate different shapes and/or sizes of substrates 1000 and to increase efficiency. Additionally, the holding trays 210 may simply be a mechanism for temporarily connecting the substrate 1000 with the conveyor system 300 so that the substrate travels along the machine 10, such as, for example, a large substrate receiving multiple dispensings thereon.
[0048] Holding system 200 tracks individual substrates 1000 by their designation in each of the substrate positions 220. This allows machine 10 to perform various real-time monitoring, feedback and adjustment activities upon each of the substrates 1000, droplets 2100 and products, and also to make determinations as to whether each of the substrates, droplets or resulting products have met the quality control standards that are designated for a particular product. The tracking of each of the substrates 1000, droplets 2100 and/or products throughout the process carried out by machine 10, allows for acceptance or rejection during the process. The present invention also contemplates tracking of unacceptable substrates 1000 for removal by acception-rejection system 800 based on the real-time monitoring.
[0049] Various tracking or identification methods can be used by holding system 200 for each of the substrates 1000. In the preferred embodiment of machine 10, holding trays 210 have a bar code 230 that can be scanned to provide identification and information to control system 900, and which can also be used to track and monitor the individual substrates 1000, droplets 2100 and/or products throughout the process. As will be discussed later in greater detail', the data compiled throughout the process is stored by control system 900. The data is based upon the individual substrates 1000, droplets 2100 and/or products, as opposed to contemporary quality control methods that use batch-sampling.
[0050] In the embodiment of machine 10, holding system 200 positions each of the substrates 1000 so that dispensing system 400 can add the droplet 2100 to the outer surface of the substrate, which is facing away from the holding tray 210. The present invention contemplates the dispensing system 400 also adding the droplet 2100 to the opposing outer surface of the substrate 1000. This would allow for a greater capacity of liquid 2000 being carried by the substrate 1000 (on both of its outer surfaces) .
[0051] Dispensing onto both sides of the substrate 1000 would also provide the ability for different liquids 2000, to be dispensed upon a single substrate, such as, for example, where the different liquids are incompatible and cannot be mixed together in liquid form or where the different liquids cannot be layered on top of each other. The present invention contemplates dispensing system 400 adding one or more different liquids 2000 to substrates 1000 through layering, through depositing on opposing outer surfaces and/or both. The present invention also contemplates dispensing system 400 adding a plurality of different liquids 2000 to substrates 1000, where the liquids are simultaneously on one or both of the outer surfaces of the substrate.
[0052] Machine 10 can also be used to re-process the substrates 1000 any number of times through the dispensing system 400 in order to add each of the different liquids 2000. Machine 10 may have additional dispensing systems 400 in series that will add each of the different liquids 2000 to the substrates 1000.
[0053] Holding system 200 can alternatively provide for dispensing the liquid 2000 (or different liquids) on both sides of the substrates 1000 by providing dispensing system 400 with access to both sides of the substrate. Examples of such alternative methods of dispensing include, but are not limited to, inverting holding tray 210 so that each of the substrates 1000 are transferred into a second holding tray 210 so that the opposing outer surfaces are now facing away from the second holding tray or using a holding tray that holds each of the substrates around their perimeters or outer circumferences so that both outer surfaces are simultaneously accessible.
[0054] The flipping or inverting of each of the carrier substrates 1000 or their holding tray 210 can be done near the end of the process so that the opposing outer surface is re-processed by the same components or a second set of components could be added to machine 10 to continue the process with respect to the opposing outer surface. Additionally, the inverting of each of the substrates 1000 or their holding tray 210, can be done by holding system 200 to allow for other operations or processes to be performed on the opposing outer surface, such as, for example, coating or printing on both sides of the products .
[0055] Conveyor system 300 provides for movement of holding trays 210 along machine 10 and through the various stages or systems of the machine. In the preferred embodiment of machine 10, conveyor system 300 provides for movement of holding trays 210 along a substantially horizontal path. However, the present invention contemplates movement of the holding trays 210 in other directions, such as, for example, in a vertical path, where spacial economy, the use of gravity or other reasons suggest or dictate such a direction of movement.
[0056] Conveyor system 300 has a drive conveyor 310. Drive conveyor 310 is controlled by control system 900, shown in FIG. 1, and is preferably variable speed. Holding trays 210 are preferably removably connected to drive conveyor 310. Holding trays 210 are securely connected to the drive conveyor 310 so that each of the substrate positions 220 remains constant with respect to the drive conveyor in order to provide accuracy in dispensing and monitoring of the substrates 1000, droplets 2100 and products. In the preferred embodiment of machine 10, drive conveyor 310 is a circulating conveyor belt that traverses the length of machine 10 and, more preferably, is a serial real-time communications system drive unit. However, the present invention contemplates other types and methods of moving the holding trays 210, such as, for example, parallel drive chains, tracks, belts or wheels to which the holding trays can be removably connected.
[0057] The present invention also contemplates the use of a number or series of holding trays 210 that are pivotally secured to each other to form a belt-like structure or tray belt, which can be operably connected to the drive conveyor 310. Machine 10 can have a plurality of tray belts with different sizes and/or shapes of substrate positions 220 to accommodate different sizes and/or shapes of substrates 1000. The tray belt is a length or line of holding trays 210 that is connectable at opposing ends to form a loop. When the holding trays 210 are to be replaced for a different products, the tray belt is fed along the drive conveyor 310 and then secured at its opposing ends to form the belt along the machine 10. To expedite the connection of the second tray belt to drive conveyor 310, the second tray belt can preferably be connected to the end of the first tray belt that is being removed, as that first tray belt is driven along and off of the drive conveyor.
[0058] The present invention also contemplates the use of any number of drive conveyors 310. For example, different systems of machine 10 can have independent drive conveyors 310 that allow for independent control of the speed of the drive conveyors, such as, for example, to more rapidly remove the products from the end of the process. In such an alternative embodiment, control system 900 would preferably control the various independent drive conveyors 310, and be able to coordinate their movement .
[0059] In the preferred embodiment, dispensing system 400 provides for the addition of the liquid 2000 to each of the substrates 1000, and provides for real-time monitoring, feedback and adjustment. To dispense the liquid 2000, dispensing system 400 has a gantry 410 that laterally spans above and across drive conveyor 310, and is longitudinally movable with respect to the drive conveyor. The movement of gantry 410, including speed and position, is controlled by control system 900.
[0060] The gantry 410 has a dispensing module 420 movably connected thereto. The dispensing module 420 is movable along the longitudinal axis of the gantry 410, which laterally traverses across the drive conveyor 310. The movement of the dispensing module 420, including speed and position, is also controlled by the control system 900.
[0061] Based upon the movement of the gantry 410, and its own movement with respect to the gantry, the dispensing module 420 is capable of movement along X and Y axes with respect to the drive conveyor 310 and the holding trays 210. Additionally, the present invention contemplates movement of the gantry 410, the dispensing module 420, and/or both, along a Z-axis with respect to the drive conveyor 310 and the holding trays 210. The movement of the dispensing module 420 allows it to accurately dispense the droplet 2100 on each of the substrates 1000 that are in the array of substrate positions 220 on holding tray 210. Control system 900 can also adjust the movement of the dispensing module 420 and the gantry 410 to accommodate different sizes and shapes of holding trays 210, as well as different arrays of substrate positions 220 on the holding trays.
[0062] The use of the gantry 410 to move the dispensing module 420 along X and Y axes (and the Z axis if desired) , provides for smooth movement and accurate alignment of the dispensing module with each of the substrates 1000. This is especially significant in the preferred embodiment of machine 10 where the drive conveyor 310 continues to move the holding tray 210 through the dispensing system 400 as the droplets 2100 are being dispensed. The continuous movement of each of the substrates 1000 along machine 10 as the dispensing step is occurring speeds up the manufacturing process. Additionally, smooth continuous movement of the holding tray 210 and the substrates 1000 thereon, as opposed to dispensing onto the substrates via indexing or discontinuous movement, provides for less wear and tear on the machine 10 and its components, particularly the drive conveyor 310. Dispensing module 420 preferably moves in an X-like path to accurately dispense on each of the substrates 1000. The size and shape of the X-like path depends upon the dispensing speed and the spacing of substrate positions 220, as shown in FIGS. 2a and 2b. It should be further understood by one of ordinary skill in the art that the dispensing module 420 can be moved along alternative paths that preferably allow for continuous movement of the substrates 1000 during dispensing.
[0063] The accuracy of the alignment of the dispensing module 420 with each of the substrates 1000, and the efficiency of the movement of the module, is facilitated by the use of the rectangular array of substrate positions 220 along holding tray 210 and the control of the movement of the module and gantry 410 in a rectangular coordinate system. However, the present invention contemplates the use of other structures and methods that could also be used to move the dispensing module 420 with respect to each of the substrates 1000, as the drive conveyor 310 continues to move through the dispensing system 400, such as, for example, a multiple axis robotic arm and/or along different coordinate systems.
[0064] In the preferred embodiment of machine 10, the dispensing system 400 has a pair of dispensing modules 420 connected to gantry 410. The use of more than one dispensing module 420 provides for increased speed and efficiency in dispensing of the liquid 2000. Additionally, the use of more than one dispensing module 420 would allow the dispensing system 400 to add different liquids 2000 to a substrate 1000 without cleaning or replacing the module, such as, for example, in layering or on opposing outer surfaces through re-processing the substrate back through the dispensing system.
[0065] Dispensing module 420 dispenses a desired amount of liquid 2000 onto the substrate 1000. In the preferred embodiment of machine 10, the dispensing module 420 has a pump 425, a flow cell or meter 430, and a dispensing head 435. The present invention contemplates a single dispensing module 420 that has duplicate components, such as, for example, a pump 425 and a flow cell 430 that are in fluid communication with a pair of dispensing heads 435, and/or other combinations or numbers of components for any number of dispensing modules.
[0066] The pump 425 is connected to a liquid source 440. In the preferred embodiment of the machine 10, the liquid source 440 is a movable container 445 that is connected to the pump 425 via removably connectable conduit 447, so that the liquid 2000 can be quickly and efficiently replaced. The liquid source 440 can have a heater (not shown) to facilitate flow of the liquid 2000 from the container 445 to the pump 425, such as, for example, where the liquid is a solder or other type of material that is generally in a solid state at room temperature.
[0067] The present invention contemplates the use of a liquid source 440 with replaceable cartridges, containers or canisters (not shown) that can be easily inserted in, or connected to, the liquid source. For lower amounts of the liquid 2000 to be dispensed, having a liquid source 440 that is held in replaceable cartridges, containers or canisters is especially useful for facilitating operation of machine 10.
[0068] The pump 425 is preferably a metered, positive displacement pump (shown in FIGS. 2c through 2f) , which causes the dispensing head 435 to dispense a single droplet 2100. The metered, positive displacement pump 425 is controlled by the control system 900, and facilitates the accuracy and control of dispensing a single droplet 2100 of the desired size so that the proper amount of liquid 2000 is added to the substrate 1000. However, the present invention contemplates the use of other types of pumps, such as, for example, a time-pressure pump or reciprocating piston pump connected to a dispensing module that can provide the same degree of accuracy and speed in adding the liquid 2000 to the substrate 1000.
[0069] Pump 425 has a motor module 4250 and a piston module 4280, as shown in FIGS. 2e and 2f. The motor module 4250 has a motor 4255, a connection port 4260 and an adjustment mechanism 4265. The piston module 4280 has a piston assembly 4285 and a cylinder 4290. When the piston module 4260 is operably connected to the motor module 4250 through connection port 4260, the piston on piston assembly 4285 is driven which imparts both reciprocating and rotary motion to the piston. The magnitude of the piston stroke is manually adjustable by the adjustment mechanism 4265. The present invention contemplates automatic adjustment through use of the real time monitoring, feedback and control as described herein.
Pump 425, as controlled by the control system 900, can skip select substrate positions 220, where the substrates 1000 contained therein have been designated as rejected. Machine 10 provides for inspection of the substrates 1000 before they undergo the dispensing process described above. In the preferred embodiment, the substrate inspection is performed by a video camera 426 and gantry assembly (not shown) , which provide images of each of the substrates 1000 for inspection by control system 900. Camera means herein a video/digitial recording device.
[0070] Alternative inspection devices and methods can be used which determine the condition of the substrate, as well as ensure that it is properly positioned in substrate position 220. Selective dispensing by pump 425 improves efficiency by not wasting any liquid 2000 on any substrates 1000 that have already been deemed to not meet the required tolerances of the products or are not properly positioned for receiving the droplet 2100.
[0071] The pump 425 is connected to the flow cell 430. The flow cell 430 determines the amount of liquid 2000 contained in container 445 that is going to be dispensed through the dispensing head 435, which will be used in the real-time monitoring of the droplets 2100.
[0072] The dispensing head 435 has a dispensing nozzle 450 (shown in FIG. 2d) through which the pressurized, metered amount of liquid 2000 is dispensed, and forms the droplet 2100. The droplet 2100 dispenses onto the outer surface of the substrate 1000.
[0073] Nozzle 450 provides for exact amounts of liquid 2000 being dispensed. The liquid 2000 is preferably dispensed by a very precise, positive displacement, piston pump 425 that pumps the liquid through tubing to the nozzle 450. The proper selection of liquid composition, viscosity, the materials of construction and orifice size of the nozzle 450 are significant and/or critical parameters to the reproducibility of droplets formed.
[0074] Nozzle 450 can also be made from a hydrophobic material and/or have a hydrophobic coating to facilitate formation and dispensing of droplet 2100 by compensating for liquid vehicle composition/formulation and surface tension.
[0075] In an alternative embodiment shown in FIG. 2g, nozzle 450 has an internal plunger 4510 that is retracted to allow the exact amount of liquid 2000 to enter the dispensing chamber 4520 under pressure of pump 425. Preferably, plunger 4510 is spring-loaded by a spring 4530, or other biasing device, and can be retracted by air pressure, such as, for example, by a solenoid driven pressure source. The liquid 2000 is dispensed as a result of the retraction of the plunger 4510. Under automatic control, the time that the plunger 4510 is in the open position, the pressure maintained on the reservoir of liquid and the vehicle composition are significant and/or critical parameters to the reproducibility of the droplets formed.
[0076] Chamber 4520 is preferably selectively sealed so that the chamber and liquid 2000 contained therein remain under pressure. A heater 4540 may be utilized to facilitate the ejection process. Nozzle 450 may have a micro-adjuster 4550 or other adjustment mechanism, manual or automatic (such as being controlled by control system 900 with real-time monitoring, feedback and control) , that provides for adjustment of the amount of liquid 2000 that is allowed to exit the dispensing chamber 4520. Nozzle 4560 may be a co-axial air exhaust 4560 that further facilitates dispensing of liquid 2000.
[0077] The dispensing system 400 uses a pump and nozzle assembly to form and dispense the droplet 2100. This is advantageous due to the accuracy of the components as described above, and the ability to perform real-time monitoring of their activities. Also, the dispensing system 400, through use of nozzle 450, can preferably provide a spherical or substantially spherical droplet 2100, which reduces or prevents splashing and overspray. Additives can be provided to liquid 2000 to facilitate dispensing where appropriate.
[0078] The dispensing system 400, and the use of a liquid 2000 and droplet 2100 that are dispensed onto the substrate 1000, is advantageous over contemporary systems and processes in that the production facilities or sites where the machine 10 is located can centrally process the liquid. This reduces the steps of the production, such as eliminating off-site production and delivery, which decreases production time and saves on costs. Where harmful compounds are being used in the liquid 2000, this is especially advantageous in reducing the handling of the compounds by the workers .
[0079] Dispensing system 400 can alternatively have a nozzle-plate assembly 4600 (a portion of which is schematically represented in FIGS. 2h through 2j) to form and dispense the droplet 2100. The assembly 4600 has a plate 4610 with an aperture or nozzle opening 4620 therethrough. The plate 4610 is capable of movement with respect to the supply of liquid 2000, as indicated by arrows 4630. Such movement includes, but is not limited to, vibration of the plate 4610 in order to actuate the dispensing. The liquid 2000 is dispensed through nozzle opening 4620 when the plate 4610 is selectively moved towards the supply of the liquid.
[0080] As shown in FIG. 2i, the size of nozzle opening 4620 can be adjusted or changed to provide for a range of different sizes or volumes for droplet 2100. The ability to accurately size very. small openings in plate 4610 and the dispensing dynamics of the assembly 4600 allow for dispensing of very small amounts of liquid 2000. As shown in FIG. 2j, a number of nozzle openings 4620 can also be used in the plate 4610 so that array dispensing can be done.
[0081] Nozzle-plate assembly 4600 is advantageous due to its minimization of components so that there are fewer materials in contact with the liquid 2000. The dispensing operation of the assembly 4600 is reliable since there are no narrow channels and the design is insensitive to air entrapment. Dispensing through the movement of plate 4610 makes the assembly 4600 easy to load and easy to clean. Dead volume for the supply of liquid 2000 is minimized or eliminated due to the planar or substantially planar shape of plate 4610.
[0082] The present invention further contemplates the use of other structures and methods of dispensing the liquid 2000 onto the substrate 1000, such as, for example, by a pad-printing device where the liquid 2000 is loaded into the ink cartridge.
[0083] Dispensing system 400 has a dispensing inspection system 460 that provides real-time monitoring of each droplet 2100 that is to be added to the substrates 1000. In the preferred embodiment of the machine 10, dispensing inspection system 460 uses high-speed imaging of the droplet 2100 to determine the volume of the droplet. Dispensing inspection system 460 has a high-speed digital camera 465 that is connected to gantry 410 and which is able to take a high-speed image 470 (shown in FIG. 3) of each droplet 2100. In the preferred embodiment of machine 10, two high-speed digital cameras 465 are used, which correspond to each of the two dispensing modules 420.
[0084] The image 470 of the droplet 2100 is preferably taken in-flight after the droplet has left the nozzle 450 but before it makes contact with substrate 1000. The machine 10 uses a laser detector to trigger the camera 465 to obtain the image 470 due to the high speed of the droplet 2100 (shown generally in FIG. 2d) . However, the present invention contemplates the use of other triggering devices and methods for triggering camera 465 and obtaining image 470.
[0085] Image 470 is used by the control system 900 to calculate a volume of each of the droplets 2100. The calculated volume of the droplet 2100 is used to determine the amount of liquid 2000 that is being dispensed onto the substrate 1000. Any amount of liquid 2000 that does not meet tolerances will be marked with an error code by control system 900 so that the substrate 1000 having that particular droplet 2100 can be rejected.
[0086] Where larger amounts of liquid 2000 are required in a product, dispensing module 420 may dispense a number of droplets 2100 or a stream of liquid. Dispensing inspection system 460 still has the ability to capture the image 470 of the stream of liquid 2000, and the volume calculations can be made therefrom.
[0087] Dispensing system 400 has a temperature conditioning system 475 that performs cooling/heating/drying of the droplet 2100 on the substrate 1000 depending upon the particular liquid 2000 that has been dispensed, such as, for example, solder may be subjected to cooling to transform it to its solid state while a therapeutic active agent may be subjected to drying to form a film on a carrier tablet. In the preferred embodiment of the machine 10, temperature conditioning system 475 has a temperature conditioner 480 and temperature conditioner sensors or monitors 482 (not shown in detail) . The temperature conditioner 480 provides a temperature change to the droplet 2100 and substrate 1000, such as, for example, heating, cooling, and/or air flow. Various components can be used for temperature conditioner 480, such as, for example, an oven, refrigeration/cooling device and/or fan. The temperature conditioner sensors 482 monitor the conditions or environmental parameters of each of the dispensed droplets 2100 and substrates 1000 to ensure that the products meet the required tolerances. [0088] Conditions, such as, for example, temperature, air-flow and humidity are monitored by the temperature conditioner sensors 482, and a number of such sensors are used to account for any variance along the temperature conditioner 480. The data gathered by the sensors is provided to control system 900 for evaluation of the quality of the substrates 1000 and droplets 2100 in each of the holding trays 220.
[0089] In the preferred embodiment, the drying conditions are monitored for the entire holding tray 220, and error codes can be assigned to the individual substrates 1000 and droplets 2100 contained therein, based upon a holding tray being affected by a condition of the temperature conditioner 480 that does not meet the required tolerances. Alternatively, portions of trays can be monitored for drying conditions by placing more sensors 482 in the temperature conditioner 480 in strategic positions. Additionally, the present invention contemplates the monitoring of other conditions or criteria related to the temperature conditioning process, such as, for example, conditions that may be more significant to particular products.
[0090] The present invention also contemplates temperature conditioner 480 being an infrared (IR) temperature conditioner and/or having a combination of IR, convection, conduction, and/or microwave heating. Temperature conditioning system 475 can include sensors to detect conditions, such as, for example, the surface temperature of the substrates 1000, or IR radiation. Temperature conditioning system 475 may also include a sensor for turning on the temperature conditioner, such as, for example, a photo-cell triggered by holding trays 210 entering the temperature conditioner 480. Additionally, temperature conditioner 480 can be utilized for heating of the substrate 1000 to cause reflow, such as for dispensed solder.
[0091] Dispensing system 400 has a dispensing confirmation system 500 that provides real-time monitoring, feedback and adjustment for the liquid 2000 that has been added to the substrate 1000. In particular, the dispensing confirmation system 500 monitors the positioning of the liquid 2000 on the substrate 1000 and the amount of the liquid contained thereon. Additionally, the dispensing confirmation system 500 can monitor for other substances, such as, for example, identifying contaminants present on the substrate 1000, as well as the amount of such other substances .
[0092] The data obtained by the dispensing confirmation system 500 is provided to the control system 900. The control system 900 will assign error codes to individual substrates 1000 and their liquids 2000 that do not meet the required tolerances of the product.
[0093] In the preferred embodiment of the machine 10, dispensing confirmation system 500 has a gantry 510 (similar to gantry 410 described above) with a pair of charge coupled device (CCD) cameras 520 that obtain images 525 of each of the substrates 1000. The images 525 are provided to control system 900 for a determination of the position of the liquid 2000 with respect to the substrate 1000. For example, the position of solder on an IC chip can be analyzed via image 525 to determine the strength of the bond, as well as short circuits or the potential risk of short circuits.
[0094] Dispensing confirmation system 500 can also have a probe 530 (shown in FIG. 2) that is used for determining the amount, type and/or distribution of the liquid 2000 on the substrate 1000. In the preferred embodiment of machine 10, the probe 530 uses chemical imaging to determine the amount of the liquid 2000 present on the substrate 1000. The present invention contemplates dispensing confirmation system 500 providing other analysis for the liquid 2000, such as, for example, mechanical stress, crystallinity, crystal orientation, composition, crystal phase, and/or doping.
[0095] Probe 530 has components that carry out chemical imaging on each of the substrates 1000 in holding tray 210, such as, for example, fiber optics, focal plane array (FPA) detectors, and/or charge coupled device (CCD) detectors. Additionally, liquid crystal tunable filters can be used as wavelength selectors for the chemical imaging. The chemical imaging provides good penetration into the liquid 2000 and upper surface of the substrate 1000 for an accurate measurement of the quantity of the liquid.
[0096] In the preferred embodiment of machine 10, probe 530 uses a focal plane array detector to obtain a signal from every point in the sample area. The sample area preferably includes the entire holding tray 210 so that all of the substrates 1000 are being simultaneously measured, which further improves the efficiency of the process. The focal plane detector is able to obtain simultaneous spectral information at every frequency for the sample area. Probe 530 can rapidly and non- destructively measure the liquid 2000 for various characteristics including, but not limited to, amount, formulation and/or distribution, as well as monitor or detect other substances contained in or on the substrate 1000.
[0097] The present invention contemplates the use of various methods and devices for determining the presence, type, distribution, amount or other characteristics of a particular liquid 2000 on the substrate 1000, such as, for example, spectroscopy and/or chemical imaging utilizing Raman and UV reflectance, and/or various other types of imaging, chemical imaging and/or spectroscopy, such as, for example, UV/visible absorption, fluorescence, laser- induced fluorescence, luminescence, photoluminescence, terahertz, NIR, and/or mid-IR. The present invention contemplates the use of various devices or components that facilitate the use of spectroscopy and/or chemical imaging for analysis of the products, such as, for example, lasers (e.g., pulse lasers), beam splitters, water-vapor free environments (e.g., nitrogen shrouds), optical delays (e.g., variable optical delays), antennas and/or semiconductors. The present invention contemplates the use of room temperature solid state detectors and/or pulsed time- gated techniques and components. The present invention contemplates the use of techniques for analysis of the products that are non-ionizing, non-invasive, nondestructive, and/or require low power.
[0098] The present invention contemplates the use of any regions of the electromagnetic spectrum that allow for analysis of the substrate 1000 and liquid 2000, as well as various techniques and sources for excitation in using the particular type of spectroscopy. The present invention also contemplates the use of other techniques and components for digital imaging to allow for use of chemical imaging of the substrate 1000 and liquid 2000. It should be further understood that dispensing confirmation system 500 also contemplates the use of surrogate detection in any of the spectral ranges.
[0099] The coating system 600 of machine 10 provides for a coating (not shown) to be placed on the substrate 1000 and/or over the liquid 2000, or some portion thereof. The coating 2300 may be a sealant or a protective layer. Coating system 600 has a coating device 610, a coating source 620 and a coating dryer 630 (if necessary depending upon the particular coating being used) . The coating device 610 transfers the coating to the upper surface of the substrate 1000. A pad-printing device can be used for coating device 610 and is advantageous because of its efficient transfer of the coating to the substrate without any waste, e.g., no overspray. Alternative devices can also be used, such as, for example, a spray device (not shown) or ink jet device, to spray the coating upon the substrate 1000. The spray device could also be movably connected to gantry 615 to pass over each of the substrate positions 220. The present invention- contemplates the use of other devices and methods for applying a coating to the substrate 1000, such as, for example, an ultrasonic atomizer. The coating system 600 can use intermittent, low volume atomized sprayers to locally apply the coating over the all or a portion (s) of the surface of substrate 1000. The sprayer may use volumetric pumps to intermittently supply coating materials. A two fluid air- liquid atomization sprayer may also be used to generate a fine spray.
[00100] In the preferred embodiment of machine 10, coating device 610 is connected to or is positioned adjacent to the machine 10 to coat an array of substrates with each reciprocating stroke. Coating device 610 can be movably connected to a gantry 615 or other similar device to facilitate movement of the coating device with respect to the holding tray 220. The holding tray 220 continues to move as the coating is being applied by the coating device 610. However, the present invention contemplates the use of other devices and methods of positioning the coating device 610 with respect to each of the substrate positions 220 so that the coating is accurately applied.
[00101] The coating device 610 is releasably connected to the coating source 620. In the preferred embodiment of the machine 10, the coating source 620 is a movable container 625 that is connected to the coating device 610 via removably connectable conduit 627, so that the coating can be quickly and efficiently replaced.
[00102] As described above with respect to the dispensing of the substrate 1000 in layers or on opposing sides, the coating system can provide the necessary coating depending upon how the liquid 2000 has been added to the substrate, such as, for example, on both sides or between layers. This can facilitate the use of higher volumes of liquid 2000.
[00103] Coating dryer 630 can be used to perform drying of the coating (where appropriate) that has been applied to the substrate 1000 and/or over the liquid 2000. The coating dryer 630 preferably has an oven 640 and one or more oven sensors 650 (not shown in detail) . The oven 640 provides heat and air flow to the coating. The oven sensors 650, similar to the temperature conditioner sensors 482 discussed above, monitor the drying conditions of the coatings to ensure that the products meet the required tolerances.
[00104] The printing system 700 of machine 10 provides an identification marker on the substrate 1000. The printing system preferably has a pad-printing device 710 that transfers the marker to the substrate 1000 and a pair of video cameras 720 that obtain an image 730 of each of the identification markers to verify the quality of the image. Unacceptable substrates 1000 will be identified by the control system 900 for subsequent rejection by system 800.
[00105] In the preferred embodiment of machine 10, pad- printing device 710 and cameras 720 are movably connected to a gantry 735 (similar to gantries 410, 510 and 615) to facilitate movement of the pad-printing device with respect to the holding tray 210 that continues to move as the identification marker is being applied. However, the present invention contemplates the use of other devices and/or methods, for positioning the pad-printing device 710 or alternative device with respect to each of the substrate positions 220 for accurate application of the identification markers, such as, for example, lasermarking, inkjet, and/or rotogravure. Each of the marker images 730 is provided to control system 900 for inspection and to determine if the printed identification marker meets the required tolerances of the products. Also, the present invention contemplates machine 10 having an ink dryer (not shown) , such as, for example, an oven, that applies heat and/or air-flow to the identification marker to dry it.
[00106] The acception-rejection system 800 provides products that have undergone real-time monitoring and adjustment for quality control to ensure that each of the products meets the required tolerances. Based upon the real-time monitoring being continuously performed at various stages of the process by machine 10, control system 900 has designated each and every product as either acceptable or rejected.
[00107] Acceptable products pass through to the delivery area (not shown in detail) , preferably under bias that is selectively controlled by the control system 900, while rejected product drop into a scrap area, preferably under the force of gravity. However, the present invention contemplates the use of other structures and methods of separating those products that are designated by control system 900 as acceptable from those products that have been designated by the control system as rejected.
[00108] The control system 900 coordinates and synchronizes the various stages and systems of the machine 10. In the preferred embodiment, control system 900 is a distributed process control system that has a number of microprocessors 910 that control the different systems of machine 10. The microprocessors 910 are preferably coordinated through a workstation 920. However, the present invention contemplates other types of system control including central and regional control, such as, for example, a single microprocessor 910 controlling all of the systems or similar systems being controlled by one of several microprocessors 910.
[00109] The microprocessors 910 and workstation 920 are in communication with each other, preferably through a network 930 using an Ethernet switch 935, which allows for the real-time monitoring, feedback and adjustment of the process being performed by the machine 10. The present invention contemplates the use of other structures and methods for communication, such as, for example, hardwiring. The control system 900 also has an archive microprocessor or historian 940, which is used to centrally store the large amount of data that is compiled for each and every product that is processed by the machine 10. However, the present invention contemplates other methods of storage of the process data, such as, for example, microprocessors 910 individually storing the data that they have compiled.
[00110] The control system 900 preferably has a number of monitors 950 that provide displays of the data, portions of the data, summaries of the data, and/or calculations and conclusions based upon the data, so that the workers can monitor and/or adjust the process as it is occurring. More preferably, the monitors 950, through use of the various microprocessors 910 and/or workstation 920, can selectively display the data, portions of the data, summaries of the data, calculations based upon the data, and conclusions based upon the data. Preferably, control system 900 records data for every product, which includes most, an preferably all, of the following: time, initial substrate status, droplet volume, temperature conditioner temperature, temperature conditioner humidity, temperature conditioner air flow, liquid location on substrate, liquid quantity and acceptability.
[00111] The present invention also contemplates dispensing inspection system 460 utilizing optical profilometry for real-time monitoring and feedback control. The components utilized by dispensing inspection system 460 to carry out the optical profilometry are known to one skilled in the art, such as, for example, a laser and camera. The technique of optical profilometry is especially useful for larger volumes of liquid 2000, such as, for example, greater than 10 microliters , where the dispensing system 400 is dispensing a stream, as opposed to the droplet 2100.
[00112] For the optical profilometry technique, dispensing inspection system 460 performs a first scan of the substrate 1000 prior to dispensing of the liquid 2000 in order to obtain a first profile of the substrate. A second scan is then performed by the dispensing inspection system 460 to obtain a second profile of the substrate 1000 with the liquid 2000 thereon. The difference in the first and second profiles provides the measurement of the volume of liquid 2000 that has been dispensed onto the substrate 1000. The present invention further contemplates the use of optical profilometry of the substrate 1000 after the liquid 2000 has been dried on the substrate. Also, the first profile may be based upon a predetermined value for the same substrates 1000 to expedite the process and eliminate the need for two scans.
[00113] The present invention also contemplates the use of real-time monitoring to provide real-time feedback and adjustment to the conveyor and dispensing systems 300 and 400, such as, for example, adjusting the speed for better positioning of the droplet 2100 on the substrate 1000 or adjusting the pump 425 and/or nozzle 450 to increase or decrease the volume of the droplet, which increases or decreases the amount of liquid 2000 that is ultimately dried on the substrate. The use of real-time monitoring of the droplet 2100 both before and after contact with the substrate 1000, also would allow for more efficient accounting for any losses occurring during the process.
[00114] Referring to FIGS. 4, 6 and 7, another embodiment of an apparatus or machine of the present invention is shown and generally referred to by reference numeral 20. The machine 20 has components that are similar to the components described above with respect to the preferred embodiment of FIG. 1 and are similarly numbered, such as, conveyor system 300, dispensing system 400 and control system 900. Machine 20 is a scaled-down version of the preferred embodiment but still provides real-time monitoring for the process. Each of these systems 300, 400 and 900 are operably connected to each other to efficiently and ergonomically provide products that have each undergone real-time monitoring, and, preferably, real-time feedback and adjustment.
[00115] Holding trays 210 are manually placed on drive conveyor 310 where the substrates 1000 begin their descent through machine 20. Each holding tray 210 is identified through use of the bar code 230 on the tray and a scanner
235. The holding trays 210 continue to move along machine
20 and pass through to the dispensing system 400 where a dispensing module 420, which is mounted to gantry 410, dispenses droplets 2100 on each of the substrates 1000. Video camera 465 takes an image of each droplet being dispensed and, in conjunction with the flow cell 430, the real-time monitoring of the amount of liquid being dispensed occurs.
[00116] After passing through temperature conditioner 480, where the liquid 2000 is formed on the outer surface or substantially along the outer surface of the substrate 1000, each of the substrates undergoes real-time monitoring of the position and amount of the liquid. Video camera 520, which is mounted on gantry 510, obtains an image 525 of each of the substrates 1000 and liquids 2000 thereon. The images 525 are processed by control system 900 for the location and quantity of the liquid 2000.
[00117] Using spectroscopy, camera 520 captures the image 525 of the deposition spot left after dispensing and drying. Image analysis software uses gray scale to tabulate the number of pixels and relative intensity of the pixel to develop an image of the dried spot left behind. Based on this information, the amount of the liquid 2000 on the substrate 1000 is determined.
[00118] The holding tray 210 is then manually removed from the drive conveyor 310. Data has been compiled for each product regarding dispensing position, quantity of liquid 2000, and drying conditions. This data is used by control system 900 to provide a designation for each of the products as either acceptable or rejected. The machine 20 uses separate scanners 235 at different stages of the machine for identification of the individual substrates 1000. [00119] A second alternative embodiment of the apparatus of the present invention is shown in FIG. 5 and is generally represented by reference numeral 20' . Similar to the embodiment described above with respect to FIGS. 4, 6 and 7, machine 20' is a scaled down version of the preferred embodiment of machine 10 shown in FIG. 1. Machine 20' has many features similar to machines 10 and 20 and such features are similarly numbered, such as, conveyor system 300, and dispensing system 400. Machine 20' exemplifies the modularity of the present invention as it includes the features of machine 20 and additionally has gantry 510, which is readily available for connection with dispensing confirmation system 500.
[00120] It should further be understood that some of the components and/or systems described with respect to machines 10, 20 and 20' may not need to be utilized for certain products. For example, but not limited to, products that are highly regulated may require rigorous quality control. Control system 900 will synchronize the other systems based upon the lack of use of certain systems, which will further maximize the efficiency of the process, such as, for example, where drying of substrate 1000 and liquid 2000 is minimal or not required, the other activities can be greatly sped up.
[00121] The present invention contemplates machines 10, 20 and 20' , and the various components and systems therein, being modular. This will allow machines 10, 20 and 20' to carry out only the necessary activities for particular products by removing selected unnecessary components, and will provide time saving, such as, for example, avoiding passing holding trays 220 through the coating temperature conditioner 630 where no coating is being applied.
The present invention contemplates the interchangeability of different components to perform the various activities of machines 10, 20 and 20', such as, for example, probe 530 that performs chemical imaging being interchangeable with other probes that perform other types of analysis, such as, for example, spectroscopy and chemical imaging, such as, for example, utilizing Raman, UV reflectance, fluorescence, and/or terahertz. Machines 10, 20 and 20' can utilize the type of analysis, and hence the components that perform that analysis, which are most efficient and accurate for a particular product. The present invention also contemplates control system 900 indicating which types of analysis and their corresponding components are to be used for a particular product.
[00122] The present invention further contemplates the process performed by machines 10, 20 and 20' including a packaging step so that the end result is a product that is ready for shipping, especially where real-time release of products is utilized. The design and modularity of machines 10, 20 and 20' facilitates the addition of a packaging step to the process (where appropriate) .
[00123] Machines 10, 20 and 20' also provide the ability to change production to a different product in a fraction of the time that it takes to make a similar adjustment to a contemporary machine. The cleaning of the machines 10,
20 and 20' for a change of production to a different product requires only the cleaning of the dispensing module 420, which can be quickly disassembled. Dispensing modules 420 are relatively low-cost which allows for their replacement rather than a time-consuming repair.
[00124] Machines 10, 20 and 20' improve efficiency in manufacturing the products based upon the manufacturing steps as well as the quality control steps. The continuity of the process quickly and efficiently provides the products that are directly ready for packaging, without the need for any other quality control testing being performed on them. Also, machines 10, 20 and 20' provide a process that can be run continuously without the need for stopping as in contemporary devices and techniques .
[00125] The real-time monitoring, feedback and adjustment of the present invention avoids unnecessary manufacturing steps (e.g., dispensing on rejected substrates) and provides quality control based on the individual properties of each of the substrates. The present invention is cost effective because it only discards the defective product identified by control system 900, rather than discarding all of the products in a batch that has a significant number of defective substrates, as by contemporary methods of product sampling.
[00126] The present invention contemplates the use of individual systems or combinations of systems of machines 10, 20 and 20' in combination with other devices, to provide one or more of the steps described herein. It should be further understood by one of ordinary skill in the art that the degree of real-time monitoring and/or feedback can be varied depending upon the particular product being manufactured and/or based upon other factors. For example, but not limited to, the machine 10, 20 and 20' may only utilize the high-speed imaging for detection of whether the droplet 2100 has accurately been dispensed upon carrier substrate 1000. Preferably, the volume calculation of dispensing inspection system 460 is also utilized to calculate the amount of liquid 2000 in the droplet 2100. However, the use of contemporary quality control techniques is also contemplated, such as batch sampling. Also, the present invention contemplates the use of contemporary quality control techniques, such as, for example, batch sampling, in parallel with the real-time monitoring and/or feedback described herein for machines 10, 20 and 20' .
[00127] It should be further understood by one of ordinary skill in the art that the various devices, techniques and/or systems described herein for machines 10, 20 and 20' can be utilized by themselves or in combination with one or more of the other systems of machines 10, 20 and 20' or in combination with contemporary devices for manufacturing products. For example, but not limited to, the high-speed imaging and volume calculation of dispensing inspection system 460 may be followed by a contemporary batch sampling technique for quality control of the resulting products.
[00128] The video imaging and volume calculation of dispensing inspection system 460 provides versatile realtime monitoring and feedback control for the products. This type of quality control is not dependent on the particular formulation of the liquid 2000, as opposed to some forms of chemical imaging which have such dependency. [00129] It should also be noted that the terms "first", "second", "third", "fourth", "upper", "lower", and the like, are used herein to modify various elements. These modifiers do not imply a spatial, sequential, or hierarchical order to the modified elements unless specifically stated.
[00130] While the present invention has been described with reference to one or more exemplary embodiments, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted for elements thereof without departing from the scope of the present invention . In addition, many modifications may be made to adapt a particular situation or material to the teachings of the disclosure without departing from the scope thereof. Therefore, it is intended that the present invention not be limited to the particular embodiment (s) disclosed as the best mode contemplated, but that the invention will include all embodiments falling within the scope of the appended claims .

Claims

WHAT IS CLAIMED IS:
1. A monitoring system for a machine that produces a plurality of products by dispensing droplets of liquid on carrier substrates, the monitoring system comprising: an inspection system having a microprocessor, a first camera or video recording device, in communication with said microprocessor and a trigger operably connected to said first camera or video recording device, wherein said inspection system determines an amount of the liquid that is being added to each of the carrier substrates, wherein said trigger actuates said first camera or video recording device to obtain a first image of each of the droplets inflight, and wherein said microprocessor determines said amount of the liquid based upon said first image.
2. The system of claim 1, wherein each of the carrier substrates continues to move along the machine as said inspection system determines said amount of the liquid.
3. The system of claim 1, further comprising a confirmation system having a probe that performs spectroscopy on the liquid that has been added to each of the carrier substrates.
4. The system of claim 3, wherein each of the carrier substrates continues to move along the machine as said probe performs said spectroscopy.
5. The system of claim 3, wherein said spectroscopy is taken from the group consisting of near infrared, mid- infrared, ultraviolet/visible, fluorescence, laser induced fluorescence, Raman, terahertz, and any combinations thereof.
6. The system of claim 1, further comprising a confirmation system having a second camera or video recording device that obtains a second image of the liquid on each of the carrier substrates, and wherein said confirmation system determines a position of the liquid for each of the carrier substrates based on said second image .
7. The system of claim 6, wherein each of the carrier substrates continues to move along the machine as said second camera or video recording device obtains said second image.
8. An apparatus for producing a plurality of products, each of the plurality of products having a carrier substrate and a dispensed liquid thereon, the apparatus comprising: a dispensing system for dispensing the dispensed liquid as a droplet onto each of the carrier substrates; and a monitoring system having an inspection system that determines an amount of the dispensed liquid that is being added to each of the carrier substrates by said dispensing system, wherein said inspection system comprises a microprocessor, a first camera or video recording device in communication with said microprocessor and a trigger operably connected to said first camera or video recording device, wherein said trigger actuates said first camera or video recording device to obtain a first image of said droplet in-flight, and wherein said microprocessor determines said amount of the dispensed liquid based upon said first image.
9. The apparatus of claim 8, wherein each of the carrier substrates continues to move along the apparatus as said inspection system determines said amount of the dispensed liquid.
10. The apparatus of claim 8, wherein said monitoring system further comprises a confirmation system having a probe that performs spectroscopy on the dispensed liquid that has been added to each of the carrier substrates .
11. The apparatus of claim 10, wherein each of the carrier substrates continues to move along the apparatus as said probe performs said spectroscopy.
12. The apparatus of claim 10, wherein said spectroscopy is taken from the group consisting of near infrared, mid-infrared, ultraviolet/visible, fluorescence, laser induced fluorescence, Raman, terahertz, and any combinations thereof.
13. The apparatus of claim 8, wherein said monitoring system further comprises a confirmation system having a second camera or video recording device that obtains a second image of the dispensed liquid on each of the carrier substrates, and wherein said confirmation system determines a position of the dispensed liquid for each of the carrier substrates based on said second image.
14. The apparatus of claim 13, wherein each of the carrier substrates continues to move along the apparatus as said second camera or video recording device obtains said second image.
15. The apparatus of claim 8, further comprising a temperature conditioning system that changes a temperature of the dispensed liquid to facilitate formation on the carrier substrate.
16. The apparatus of claim 15, wherein said temperature conditioning system monitors environmental parameters for each of the carrier substrates, and wherein the environmental parameters are taken from the group consisting of temperature, air-flow rate, humidity, radiation, product surface temperature, and any combinations thereof.
17. The apparatus of claim 8, further comprising a printing system for applying an identification marker to each of the carrier substrates, and a third camera or video recording device for obtaining a third image of said identification marker for inspection.
18. The apparatus of claim 17, wherein each of the carrier substrates continues to move along the apparatus as said third camera or video recording device obtains said third image.
19. An apparatus for producing a plurality of products, each of the plurality of products having a carrier substrate and a dispensed liquid, the apparatus comprising: a dispensing system that adds the dispensed liquid to each of the carrier substrates; and a monitoring system that performs real-time monitoring of said dispensing system to determine an amount of the dispensed liquid on each of the carrier substrates .
20. The apparatus of claim 19, further comprising a control system for performing real-time control of said dispensing system based on said real-time monitoring, wherein said real-time control comprises adjusting an amount of dispensed liquid being dispensing from said dispensing system.
21. The apparatus of claim 19, wherein said dispensing system has a nozzle, and wherein said real-time control comprises adjusting a position of said nozzle with respect to each of the carrier substrates thereby adjusting the position of the dispensed liquid on each of the carrier substrates.
22. A monitoring system for a machine that produces a plurality of products, each of the plurality of products having a carrier substrate and a dispensed liquid, the system comprising: a confirmation system operably connected to the machine, said confirmation system determining an amount of the dispensed liquid that has been added to each of the carrier substrates by the machine, wherein said confirmation system performs optical profilometry on each of the carrier substrates to determine said amount of the dispensed liquid.
23. The system of claim 22, wherein said confirmation system performs said optical profilometry while each of the carrier substrates continues to move along the machine.
24. A machine which produces a plurality of products, each of the plurality of products having a carrier substrate and a dispensed liquid, the machine comprising: a dispensing system for adding the dispensed liquid to each of the carrier substrates; and a confirmation system for determining an amount of the dispensed liquid that has been added to each of the carrier substrates, wherein said confirmation system performs optical profilometry on each of the carrier substrates to determine said amount of the dispensed liquid.
25. The machine of claim 24, wherein said confirmation system performs said optical profilometry while each of the carrier substrates continues to move along the machine.
26. A method of monitoring a machine that produces a plurality of products by dispensing a droplet of liquid on a carrier substrate, the method comprising: actuating a camera or video recording device based upon dispensing of the droplet; obtaining a first image of the droplet in-flight; and determining a volume of the droplet based upon said first image.
27. The method of claim 26, further comprising continuously moving each of the carrier substrates along the machine as said first image is being obtained.
28. The method of claim 26, further comprising performing spectroscopy on the liquid that has been added to each of the carrier substrates.
29. The method of claim 28, further comprising continuously moving each of the carrier substrates along the machine as said spectroscopy is being performed.
30. The method of claim 26, further comprising obtaining a second image of the liquid on each of the carrier substrates and determining a position of the liquid for each of the carrier substrates based on said second image.
31. The method of claim 30, further comprising continuously moving each of the carrier substrates along the machine as said second image is being obtained.
32. A method of producing a plurality of products thateach have a carrier substrate and a dispensed liquid thereon, the method comprising: dispensing the dispensed liquid as a droplet onto each of the carrier substrates; and determining an amount of the dispensed liquid that is being added to each of the carrier substrates by said dispensing system by obtaining a first image of said droplet in-flight and determining said amount of the dispensed liquid based upon said first image.
33. The method of claim 32, further comprising continuously moving each of the carrier substrates along the machine as said first image is being obtained.
34. The method of claim 32, further comprising performing spectroscopy on the dispensed liquid that has been added to each of the carrier substrates.
35. The method of claim 34, further comprising continuously moving each of the carrier substrates along the machine as said spectroscopy is being performed.
36. The method of claim 32, further comprising obtaining a second image of the dispensed liquid on each of the carrier substrates and determining a position of the dispensed liquid for each of the carrier substrates based on said second image.
37. The method of claim 36, further comprising continuously moving each of the carrier substrates along the machine as said second image is being obtained.
38. The method of claim 32, further comprising changing a temperature of the dispensed liquid to facilitate formation on the carrier substrate.
39. The method of claim 32, further comprising applying an identification marker to each of the carrier substrates .
40. The method of claim 39, further comprising obtaining a third image of said identification marker for inspection.
41. The method of claim 40, further comprising continuously moving each of the carrier substrates along the machine as said third image is being obtained.
PCT/US2005/020390 2004-06-09 2005-06-09 Apparatus and method for producing or processing a product or sample WO2005124297A2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
MXPA06014533A MXPA06014533A (en) 2004-06-09 2005-06-09 Apparatus and method for producing or processing a product or sample.
EP05760285.6A EP1756535A4 (en) 2004-06-09 2005-06-09 Apparatus and method for producing or processing a product or sample
CA2570037A CA2570037C (en) 2004-06-09 2005-06-09 Apparatus and method for producing or processing a product or sample
JP2007527750A JP5346466B2 (en) 2004-06-09 2005-06-09 Apparatus and method for manufacturing or processing products or samples

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US57824504P 2004-06-09 2004-06-09
US60/578,245 2004-06-09
US62199204P 2004-10-25 2004-10-25
US60/621,992 2004-10-25

Publications (2)

Publication Number Publication Date
WO2005124297A2 true WO2005124297A2 (en) 2005-12-29
WO2005124297A3 WO2005124297A3 (en) 2008-09-25

Family

ID=35510312

Family Applications (2)

Application Number Title Priority Date Filing Date
PCT/US2005/020390 WO2005124297A2 (en) 2004-06-09 2005-06-09 Apparatus and method for producing or processing a product or sample
PCT/US2005/020319 WO2005123569A2 (en) 2004-06-09 2005-06-09 Apparatus and method for pharmaceutical production

Family Applications After (1)

Application Number Title Priority Date Filing Date
PCT/US2005/020319 WO2005123569A2 (en) 2004-06-09 2005-06-09 Apparatus and method for pharmaceutical production

Country Status (28)

Country Link
US (3) US8122849B2 (en)
EP (3) EP2638891B1 (en)
JP (5) JP4917034B2 (en)
KR (4) KR101313374B1 (en)
CN (3) CN104622694A (en)
AR (1) AR049080A1 (en)
AU (1) AU2005254510B2 (en)
BR (1) BRPI0511937A (en)
CA (4) CA2814857C (en)
DK (2) DK1773708T3 (en)
ES (2) ES2427169T3 (en)
HK (2) HK1108152A1 (en)
HR (2) HRP20130849T1 (en)
HU (1) HUE024497T2 (en)
IL (3) IL179752A (en)
MA (1) MA28665B1 (en)
MX (3) MXPA06014533A (en)
MY (1) MY165810A (en)
NO (1) NO340856B1 (en)
NZ (3) NZ588256A (en)
PE (2) PE20060130A1 (en)
PH (2) PH12014502612A1 (en)
PL (2) PL2638891T3 (en)
PT (2) PT2638891E (en)
RU (1) RU2449771C2 (en)
SI (2) SI1773708T1 (en)
TW (3) TWI356036B (en)
WO (2) WO2005124297A2 (en)

Families Citing this family (129)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7776314B2 (en) 2002-06-17 2010-08-17 Grunenthal Gmbh Abuse-proofed dosage system
DE10336400A1 (en) 2003-08-06 2005-03-24 Grünenthal GmbH Anti-abuse dosage form
DE102005005446A1 (en) 2005-02-04 2006-08-10 Grünenthal GmbH Break-resistant dosage forms with sustained release
US20070048228A1 (en) 2003-08-06 2007-03-01 Elisabeth Arkenau-Maric Abuse-proofed dosage form
DE10361596A1 (en) 2003-12-24 2005-09-29 Grünenthal GmbH Process for producing an anti-abuse dosage form
US7799273B2 (en) 2004-05-06 2010-09-21 Smp Logic Systems Llc Manufacturing execution system for validation, quality and risk assessment and monitoring of pharmaceutical manufacturing processes
US7444197B2 (en) * 2004-05-06 2008-10-28 Smp Logic Systems Llc Methods, systems, and software program for validation and monitoring of pharmaceutical manufacturing processes
TWI356036B (en) * 2004-06-09 2012-01-11 Smithkline Beecham Corp Apparatus and method for pharmaceutical production
US20050288906A1 (en) * 2004-06-29 2005-12-29 Drennen James K Iii Spectroscopic pharmacy verification and inspection system
DE102004032049A1 (en) 2004-07-01 2006-01-19 Grünenthal GmbH Anti-abuse, oral dosage form
EP1794575A4 (en) * 2004-09-28 2011-06-22 Glaxo Group Ltd Luminescense sensor apparatus and method
US9710866B2 (en) 2005-09-30 2017-07-18 Edge Medical, Llc System and method for processing a multiple prescription order
US9238518B2 (en) 2004-10-01 2016-01-19 Edge Medical Properties, Llc Inspection system and method with a control process that inspects different medications
US9334096B2 (en) 2004-10-01 2016-05-10 Edge Medical Properties, Llc Multiple inspection system and method that inspects different medications
US9141764B2 (en) 2010-11-12 2015-09-22 Edge Medical Properties, Llc System and method for online integrated multiple tablet ordering
US8123036B2 (en) 2004-10-01 2012-02-28 Edge Medical Properties, Llc Pill assembly for pill packaging and delivery systems
US10315450B1 (en) 2006-10-24 2019-06-11 Edge Medical Properties, Llc System and method for generating an integrated label for container housing multi-script pouches
US8266878B2 (en) * 2004-10-01 2012-09-18 Edge Medical Properties, Llc System and method for verifying and assembling a multiple prescription package
US8022032B2 (en) * 2004-11-19 2011-09-20 Smithkline Beecham Corporation Method for customized dispensing of variable dose drug combination products for individualizing of therapies
KR20130115401A (en) * 2004-11-19 2013-10-21 글락소스미스클라인 엘엘씨 Pharmaceutical product
DE102005005449A1 (en) * 2005-02-04 2006-08-10 Grünenthal GmbH Process for producing an anti-abuse dosage form
GB0504284D0 (en) * 2005-03-02 2005-04-06 Boc Group Plc Conveyor system
US8802183B2 (en) 2005-04-28 2014-08-12 Proteus Digital Health, Inc. Communication system with enhanced partial power source and method of manufacturing same
EP3827747A1 (en) 2005-04-28 2021-06-02 Otsuka Pharmaceutical Co., Ltd. Pharma-informatics system
PL2404919T3 (en) 2005-11-08 2014-01-31 Vertex Pharma Heterocyclic compound useful as a modulator of ATP-binding cassette transporters.
WO2008001785A1 (en) * 2006-06-26 2008-01-03 Toshiba Solutions Corporation Specimen inspecting apparatus, and specimen inspecting method
US20100148091A1 (en) * 2006-09-29 2010-06-17 Glaxo Group Limited Method and system for rapid phase luminescense spectroscopy analysis
DE102006048433B3 (en) * 2006-10-12 2008-06-26 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Analysis method for investigation of interaction between foreign matter and polymers, monitoring production process and quality or stability control, involves analyzing time-dependent change of condition of mixture by terahertz spectroscopy
GB2465896B (en) * 2007-01-29 2011-12-07 Teraview Ltd A pharmaceutical analysis method and apparatus
WO2008103622A1 (en) * 2007-02-21 2008-08-28 Smithkline Beecham Corporation Continuous coating of pellets
CL2008000597A1 (en) * 2007-03-01 2008-09-05 Glaxo Group Ltd DOSAGE FORM INCLUDING 6- (3-CYCLLOBUTIL-2,3,4,5-TETRAHYDRO-1H-BENZO [D] AZEPIN-7-IL OXI) -N-METHYL NICOTINAMIDE, A STABILIZER AND A EXCIPIENT; PREPARATION PROCEDURE; AND ITS USE TO TREAT NEUROLOGICAL DISEASES.
CA2587805C (en) 2007-04-25 2014-02-18 The Procter & Gamble Company Improved vitamin d content uniformity in pharmaceutical dosage forms
CA2708318C (en) * 2007-07-27 2016-12-20 Glaxosmithkline Llc Temperature telemetry in processing of materials
AU2008308686B2 (en) 2007-10-02 2015-01-22 Labrador Diagnostics Llc Modular point-of-care devices and uses thereof
CA2706920C (en) 2007-12-07 2018-02-13 Vertex Pharmaceuticals Incorporated Solid forms of 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)cyclopropanecarboxamido)-3-methylpyridin-2-yl)benzoic acid
EP2249811A1 (en) * 2008-01-25 2010-11-17 Grünenthal GmbH Pharmaceutical dosage form
HUE030803T2 (en) * 2008-05-09 2017-06-28 Gruenenthal Gmbh Process for the preparation of an intermediate powder formulation and a final solid dosage form under usage of a spray congealing step
TW201036606A (en) * 2009-01-06 2010-10-16 Proteus Biomedical Inc High-throughput production of ingestible event markers
MX2011011506A (en) 2009-04-28 2012-05-08 Proteus Biomedical Inc Highly reliable ingestible event markers and methods for using the same.
AU2010248978C1 (en) * 2009-05-15 2014-04-17 Glaxosmithkline Llc Using thermal imaging for control of a manufacturing process
DE102009021843B4 (en) * 2009-05-19 2011-02-24 Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. Method for determining a quantity of a flowable substance added to a body to be filled
PE20120572A1 (en) * 2009-07-22 2012-06-06 Gruenenthal Chemie HANDLING RESISTANT STABILIZED OXIDATION DOSAGE FORM
EP2456427B1 (en) 2009-07-22 2015-03-04 Grünenthal GmbH Hot-melt extruded controlled release dosage form
US20130053446A1 (en) * 2009-11-06 2013-02-28 Rutgers, The State University Of New Jersey Pharmaceutical preparations having individualized dosage and structure
EP2531176B1 (en) * 2010-02-03 2016-09-07 Grünenthal GmbH Preparation of a powdery pharmaceutical composition by means of an extruder
EP2552607B1 (en) * 2010-03-26 2016-04-20 Monsanto Technology LLC Automated small object sorting systems and methods
ES2604480T5 (en) 2010-04-07 2020-03-17 Vertex Pharma 3- (6- (1- (2,2-Difluorobenzo [d] [1,3] dioxol-5-yl) cyclopropanecarboxamido) -3-methylpyridin-2-yl) benzoic acid pharmaceutical compositions and administration thereof
WO2011127252A2 (en) 2010-04-07 2011-10-13 Proteus Biomedical, Inc. Miniature ingestible device
DE102010028715A1 (en) * 2010-05-07 2011-11-10 Robert Bosch Gmbh Device and method for checking objects for pharmaceutical applications
PE20131126A1 (en) 2010-09-02 2013-10-21 Gruenenthal Chemie ALTERATION RESISTANT DOSAGE FORM INCLUDING AN ANIONIC POLYMER
NZ607392A (en) 2010-09-02 2015-03-27 Gruenenthal Chemie Tamper resistant dosage form comprising inorganic salt
US20120107402A1 (en) * 2010-10-29 2012-05-03 Monosol Rx, Llc Process for analyzing and establishing dosage size in an ingestible film
EP2642983A4 (en) 2010-11-22 2014-03-12 Proteus Digital Health Inc Ingestible device with pharmaceutical product
WO2012087492A2 (en) 2010-12-23 2012-06-28 Tailorpill Technologies, Llc System and methods for personalized pill compounding
AR085087A1 (en) * 2011-01-21 2013-09-11 Theranos Inc SYSTEMS AND METHODS TO MAXIMIZE THE USE OF SAMPLES
US10435192B2 (en) 2011-05-16 2019-10-08 Edge Medical Properties, Llc Multiple inspection system and method that inspects different medications
CN102853649A (en) * 2011-07-01 2013-01-02 康准电子科技(昆山)有限公司 Drying oven and drying system adopting same
JP4954345B1 (en) * 2011-07-06 2012-06-13 アピ株式会社 Drug substance aseptic purification equipment
WO2015112603A1 (en) 2014-01-21 2015-07-30 Proteus Digital Health, Inc. Masticable ingestible product and communication system therefor
JP5718749B2 (en) * 2011-07-13 2015-05-13 日立アロカメディカル株式会社 Drug audit support device
US10723497B2 (en) * 2014-11-03 2020-07-28 Vanrx Pharmasystems Inc. Apparatus and method for monitoring and controlling the filling of a container with a pharmaceutical fluid in an aseptic environment
EP2736495B1 (en) 2011-07-29 2017-08-23 Grünenthal GmbH Tamper-resistant tablet providing immediate drug release
DK2736497T3 (en) 2011-07-29 2017-11-13 Gruenenthal Gmbh Shock-resistant tablet that provides an immediate release of a drug.
KR101246554B1 (en) * 2011-08-12 2013-03-25 (주)아모레퍼시픽 Device for customizing cosmetics having contents absorbent process for contents absorbent members
US20140170735A1 (en) 2011-09-25 2014-06-19 Elizabeth A. Holmes Systems and methods for multi-analysis
US9664702B2 (en) 2011-09-25 2017-05-30 Theranos, Inc. Fluid handling apparatus and configurations
US8475739B2 (en) 2011-09-25 2013-07-02 Theranos, Inc. Systems and methods for fluid handling
US9632102B2 (en) 2011-09-25 2017-04-25 Theranos, Inc. Systems and methods for multi-purpose analysis
US10012664B2 (en) 2011-09-25 2018-07-03 Theranos Ip Company, Llc Systems and methods for fluid and component handling
US9810704B2 (en) 2013-02-18 2017-11-07 Theranos, Inc. Systems and methods for multi-analysis
MX356421B (en) 2012-02-28 2018-05-29 Gruenenthal Gmbh Tamper-resistant dosage form comprising pharmacologically active compound and anionic polymer.
LT2838512T (en) 2012-04-18 2018-11-12 GrĆ¼nenthal GmbH Tamper resistant and dose-dumping resistant pharmaceutical dosage form
WO2013161300A1 (en) * 2012-04-24 2013-10-31 株式会社マイクロジェット Discharge system and method for discharging by discharge system
US10064945B2 (en) 2012-05-11 2018-09-04 Gruenenthal Gmbh Thermoformed, tamper-resistant pharmaceutical dosage form containing zinc
WO2014013974A1 (en) * 2012-07-19 2014-01-23 大塚製薬株式会社 Printer and tablet
US11110648B2 (en) * 2012-07-31 2021-09-07 Makerbot Industries, Llc Build material switching
US11149123B2 (en) 2013-01-29 2021-10-19 Otsuka Pharmaceutical Co., Ltd. Highly-swellable polymeric films and compositions comprising the same
JP6195052B2 (en) 2013-03-08 2017-09-13 セイコーエプソン株式会社 Specimen inspection equipment
US10175376B2 (en) 2013-03-15 2019-01-08 Proteus Digital Health, Inc. Metal detector apparatus, system, and method
JP6378310B2 (en) 2013-03-15 2018-08-22 ディバーシー・インコーポレーテッド Adjustable dosing cap
GB2513581A (en) * 2013-04-30 2014-11-05 Res Ct Pharmaceutical Engineering Gmbh A device and a method for monitoring a property of a coating of a solid dosage form during a coating process forming the coating of the solid dosage form
MX2015016254A (en) 2013-05-29 2016-04-20 Gruenenthal Gmbh Tamper resistant dosage form with bimodal release profile.
US10154966B2 (en) 2013-05-29 2018-12-18 Grünenthal GmbH Tamper-resistant dosage form containing one or more particles
KR20160031526A (en) 2013-07-12 2016-03-22 그뤼넨탈 게엠베하 Tamper-resistant dosage form containing ethylene-vinyl acetate polymer
EP3023187B1 (en) * 2013-07-16 2020-02-12 Qualicaps Co., Ltd. Apparatus and method for marking edible object
US9796576B2 (en) 2013-08-30 2017-10-24 Proteus Digital Health, Inc. Container with electronically controlled interlock
US9606054B2 (en) * 2013-09-30 2017-03-28 Advantest Corporation Methods, sampling device and apparatus for terahertz imaging and spectroscopy of coated beads, particles and/or microparticles
US10084880B2 (en) 2013-11-04 2018-09-25 Proteus Digital Health, Inc. Social media networking based on physiologic information
KR102280372B1 (en) 2013-11-12 2021-07-22 버텍스 파마슈티칼스 인코포레이티드 Process of preparing pharmaceutical compositions for the treatment of cftr mediated diseases
USD746137S1 (en) 2013-11-15 2015-12-29 Diversey, Inc. Dosing cap
CA2931553C (en) 2013-11-26 2022-01-18 Grunenthal Gmbh Preparation of a powdery pharmaceutical composition by means of cryo-milling
US9417181B2 (en) 2014-05-08 2016-08-16 Advantest Corporation Dynamic measurement of density using terahertz radiation with real-time thickness measurement for process control
EP3142646A1 (en) 2014-05-12 2017-03-22 Grünenthal GmbH Tamper resistant immediate release capsule formulation comprising tapentadol
ES2551809B1 (en) 2014-05-21 2016-05-17 Kiro Robotics Sl Intravenous substance preparation machine
US9872835B2 (en) 2014-05-26 2018-01-23 Grünenthal GmbH Multiparticles safeguarded against ethanolic dose-dumping
RU2691136C2 (en) * 2014-11-18 2019-06-11 Вертекс Фармасьютикалз Инкорпорейтед High-performance test high-performance liquid chromatography method
WO2016170097A1 (en) 2015-04-24 2016-10-27 Grünenthal GmbH Tamper-resistant dosage form with immediate release and resistance against solvent extraction
WO2016194761A1 (en) * 2015-05-29 2016-12-08 芝浦メカトロニクス株式会社 Tablet printing device and tablet printing method
US11051543B2 (en) 2015-07-21 2021-07-06 Otsuka Pharmaceutical Co. Ltd. Alginate on adhesive bilayer laminate film
JP6546815B2 (en) * 2015-09-02 2019-07-17 株式会社Screenホールディングス Tablet printing apparatus and tablet printing method
WO2017042325A1 (en) 2015-09-10 2017-03-16 Grünenthal GmbH Protecting oral overdose with abuse deterrent immediate release formulations
KR101740146B1 (en) * 2015-10-30 2017-05-26 주식회사 프로텍 Pump Position Feedback Type Dispenser and Dispensing Method
US10365229B2 (en) * 2015-12-31 2019-07-30 Kaiser Optical Systems, Inc. Real-time characterization of pharmaceutical tablet coatings using Raman spectroscopy
EP3439612B1 (en) * 2016-04-05 2020-04-01 Jan Franck Device and method for the dosing of active substances for the preparation of medicaments
USD809576S1 (en) * 2016-07-08 2018-02-06 Ackley Machine Corporation Carrier link for longitudinally compressed tablet
US10583089B2 (en) 2016-07-19 2020-03-10 Johnson & Johnson Consumer Inc. Tablets having discontinuous coated regions
BR112019001076A8 (en) 2016-07-19 2022-08-09 Currahee Holding Company Inc DOSAGE FORM, MANUFACTURING METHOD OF A DOSAGE FORM AND APPARATUS FOR APPLYING A CIRCUMFERENTIAL BATCH COATED REGION ON A SURFACE OF A TABLET-FORMED SUBSTRATE
CN109843149B (en) 2016-07-22 2020-07-07 普罗秋斯数字健康公司 Electromagnetic sensing and detection of ingestible event markers
JP2019535377A (en) 2016-10-26 2019-12-12 プロテウス デジタル ヘルス, インコーポレイテッド Method for producing capsules with ingestible event markers
DE202017102645U1 (en) * 2017-05-03 2018-08-06 Romaco Kilian Gmbh Drainage device for compacts of a rotary tablet press and rotary tablet press with drain device
JP7057730B2 (en) * 2017-09-19 2022-04-20 芝浦メカトロニクス株式会社 Tablet printing device and tablet printing method
US10991264B2 (en) * 2017-11-23 2021-04-27 Omnicell, Inc. Multi-camera imaging for IV compounding
US10596319B2 (en) 2017-11-23 2020-03-24 Aesynt Incorporated Compounding device system
US11335444B2 (en) 2017-11-30 2022-05-17 Omnicell, Inc. IV compounding systems and methods
IT201800004265A1 (en) 2018-04-06 2019-10-06 Apparatus and method for the automated production of customizable dosage forms.
JP7191455B2 (en) * 2018-06-19 2022-12-19 Ckd株式会社 Tablet filling machine and PTP packaging machine
KR20210045625A (en) 2019-10-17 2021-04-27 주식회사 엘지화학 Electrode slurry coating device and method forming active material double layers
CN109530167B (en) * 2018-09-29 2021-01-15 领益智造科技(东莞)有限公司 Glue amount detection device used after glue dispensing in concave space
CN109283154B (en) * 2018-11-02 2020-12-01 河北大学 System and method for detecting volatile organic molecules in exhaled air
SG11202105479RA (en) * 2018-12-19 2021-07-29 Agency Science Tech & Res A non-destructive system and method for determining the quality of chinese herb using terahertz time-domain spectroscopy
US10824822B2 (en) * 2019-02-05 2020-11-03 International Business Machines Corporation Magnetic tracking for medicine management
WO2020218310A1 (en) 2019-04-22 2020-10-29 ニプロ株式会社 Method for producing pharmaceutical formulation
EP4289289A3 (en) * 2019-05-06 2024-03-06 Transport Authority, Inc. Systems and methods for manufacturing cannabis edibles, and resulting edible products
KR20200138921A (en) * 2019-06-03 2020-12-11 삼성전자주식회사 Apparatus and method for identifying pharmaceutical
JP6832986B2 (en) * 2019-06-24 2021-02-24 株式会社Screenホールディングス Tablet printing device and tablet printing method
USD939600S1 (en) * 2019-07-23 2021-12-28 ACG PAM Pharma Technologies Pvt. Ltd. Cartoning machine
US11250874B2 (en) 2020-05-21 2022-02-15 Bank Of America Corporation Audio quality enhancement system
US20220008330A1 (en) * 2020-07-10 2022-01-13 Nova Thin Film Pharmaceuticals Llc Method and System for Manufacturing Oral Soluble Films, Compositions of Oral Soluble Films, Oral Soluble Films Made by Thereby, and Methods of Use Thereof
WO2023200954A1 (en) 2022-04-13 2023-10-19 Aprecia Pharmaceuticals LLC System and method for additive manufacturing using an omnidirectional magnetic movement apparatus

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5711989A (en) * 1992-11-19 1998-01-27 Nordson Corporation Computer controlled method for dispensing viscous fluid

Family Cites Families (229)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US678579A (en) * 1899-06-27 1901-07-16 Oliver Typewriter Co Tabulating attachment for type-writers.
NL24712C (en) 1928-05-01
US3333031A (en) * 1963-06-14 1967-07-25 American Cyanamid Co Surface dyeing and pigment marking of gelatin capsules
US3272118A (en) * 1965-02-04 1966-09-13 Hartnett Co R W Article marking machine
CH543306A (en) 1971-10-13 1973-10-31 Hoffmann La Roche Micropipettor
US3837590A (en) * 1972-06-26 1974-09-24 Johns Manville Cable reel assembly
US3834590A (en) 1972-10-24 1974-09-10 Drummond Scient Co Microliter fluid delivery apparatus
JPS5314227Y2 (en) * 1973-03-29 1978-04-15
US3871295A (en) * 1973-09-04 1975-03-18 Hartnett Co R W Capsule orienting apparatus and method of spin printing
US3884143A (en) 1973-09-04 1975-05-20 Hartnett Co R W Conveyor link for tablet printing apparatus
US4136145A (en) 1974-07-05 1979-01-23 Schering Aktiengesellschaft Medicament carriers in the form of film having active substance incorporated therein
IT1033533B (en) 1974-11-06 1979-08-10 Gamberini E TRANSPORT FOR CAPSULE FILLING MACHINES
US4349531A (en) 1975-12-15 1982-09-14 Hoffmann-La Roche Inc. Novel dosage form
US4197289A (en) * 1975-12-15 1980-04-08 Hoffmann-La Roche Inc. Novel dosage forms
DE2658486C3 (en) 1976-12-23 1980-04-24 Beckman Instruments Gmbh, 8000 Muenchen Pipetting and dilution device for small amounts of liquid with direct digital setting of their volumes in milliliter and microliter units and with exchangeable piston pump modules
US4218433A (en) * 1977-03-03 1980-08-19 Nippon Kayaku Kabushiki Kaisha Constant-rate eluting tablet and method of producing same
DE2741321C3 (en) 1977-09-14 1981-05-27 Wibau Industrie und Verwaltung GmbH, 6466 Gründau Method for determining the particle size distribution of a falling or flowing stream of material by recording and evaluating video images
GB1572226A (en) * 1977-11-03 1980-07-30 Hoechst Uk Ltd Pharmaceutical preparations in solid unit dosage form
US4257267A (en) 1978-10-18 1981-03-24 Bohr Scientific Corporation Dispenser unit with lockable actuating lever
DE2849495C3 (en) 1978-11-15 1982-05-13 Voss, Gunther M., 8918 Diessen Use of an inkjet printer to write on or print on pharmaceutical formulations
US4548825A (en) * 1978-11-15 1985-10-22 Boehringer Ingelheim Gmbh Method for ink-jet printing on uncoated tablets or uncoated tablet cores
DE2849494A1 (en) * 1978-11-15 1980-05-29 Voss Gunter M METHOD FOR THE PRODUCTION OF MEDICINAL FORMS
JPS55119782A (en) * 1979-03-09 1980-09-13 Daihen Corp Pattern automatic inspection method
DE2935812A1 (en) 1979-09-05 1981-03-12 Fa. Carl Zeiss, 7920 Heidenheim METHOD FOR TESTING MATERIAL
US4308942A (en) * 1979-10-29 1982-01-05 Michael Ackley Single drum material orientation apparatus and method
JPS56163656A (en) 1980-05-22 1981-12-16 Nippon Elanco Device for filling hard gelatin capsule with viscous substance
SU952254A1 (en) * 1980-10-02 1982-08-23 Ленинградский научно-исследовательский институт вакцин и сывороток Apparatus for manufacturing epicutaneous bacterial samples
SU943100A1 (en) * 1980-11-14 1982-07-15 Опытно-Конструкторское Технологическое Бюро Расфасовочного И Упаковочного Оборудования Apparatus for packaging articles into web material
IT1158388B (en) * 1982-05-25 1987-02-18 Mg 2 Spa MACHINE FOR FILLING CONTAINER WITH PHARMACEUTICAL PRODUCTS PASTA SUBFORMATION
US4489026A (en) * 1982-09-07 1984-12-18 The Upjohn Company Process for preparing solid unit dosage forms of ultra-low dose drugs
US4485387A (en) 1982-10-26 1984-11-27 Microscience Systems Corp. Inking system for producing circuit patterns
DE3239955A1 (en) 1982-10-28 1984-05-03 Gunther Meinhardt 8918 Dießen Voss Manipulation-secured medicament capsule and process for its production
DE3246453A1 (en) 1982-12-15 1984-06-20 Gunther Meinhardt 8918 Dießen Voss Shaped pharmaceutical objects provided with coloured patterns, and process for the production thereof
LU84911A1 (en) * 1983-07-14 1985-04-17 Cockerill Sambre Sa METHOD AND INSTALLATION FOR COOKING AN ORGANIC COATING APPLIED TO A SUPPORT
US4866906A (en) 1983-09-02 1989-09-19 Capsule Technology International, Ltd. Device for producing tamper evident capsules
US5310687A (en) * 1984-10-31 1994-05-10 Igen, Inc. Luminescent metal chelate labels and means for detection
US5655453A (en) * 1987-02-06 1997-08-12 Ackley; E. Michael Method and apparatus for marking pellet shaped articles
SE457480B (en) 1987-05-06 1988-12-27 Gedevelop Electronics Ab SET AND DEVICE FOR DETERMINING SIZE AND / OR FORM OF A FREE FALLING ITEM
US4936828A (en) 1987-06-02 1990-06-26 Kophu Chiang Liquid drop image sensor
DE3721404A1 (en) * 1987-06-29 1989-01-12 Kopperschmidt Mueller & Co DEVICE FOR ELECTROSTATIC SPRAY COATING OF PLATE-SHAPED WORKPIECES
US4784582A (en) 1987-10-02 1988-11-15 Creative Automation Company Fluid dispensing pump
JP2573969B2 (en) * 1987-10-21 1997-01-22 帝國製薬株式会社 Drug Intermittent Release Oral Formulation
JPH0782542B2 (en) * 1988-01-29 1995-09-06 株式会社スキャンテクノロジー Print inspection method, print inspection device, and automatic printed matter distribution system
US4859064A (en) * 1988-05-09 1989-08-22 Spectra-Tech, Inc. Diffuse reflectance spectroscopy system and method
US4900379A (en) * 1988-05-20 1990-02-13 The Boeing Company Method for producing composite materials
US5016196A (en) * 1988-05-24 1991-05-14 Battelle Memorial Institute Rain sampling device
US4927062A (en) 1988-09-22 1990-05-22 Walsh James W Precision micro-liter drop dispenser
US4935261A (en) * 1988-10-17 1990-06-19 Micro Robotics Systems Inc. Method for controlling accurate dispensing of adhesive droplets
EP0388159A3 (en) 1989-03-15 1991-06-12 Seiko Instruments Inc. Apparatus for sealing liquid within cavities
CA2057047A1 (en) * 1989-07-27 1991-01-28 Chris R. Redford Combined ink laser printing of tablets
US5049721A (en) * 1989-09-18 1991-09-17 American Telephone And Telegraph Company Laser marking apparatus and method for providing markings of enhanced readability in an outer jacket of a moving cable
US5040353A (en) * 1990-07-26 1991-08-20 Glaxo Inc. System for inspecting and recycling goods from defective packages on a blister packaging machine
US5085510A (en) 1990-08-28 1992-02-04 Pfizer Inc. Pharmaceutical tablet vision inspection system
DE4203273A1 (en) 1991-02-05 1992-08-27 Voss Gunter M Coating surface with substance dispersed in evaporable liq. - with nozzle providing intermittent supply of liq. and continuous supply of gas, for lubrication of medical tablet prodn. equipment
GB2253164B (en) * 1991-02-22 1994-10-05 Hoechst Uk Ltd Improvements in or relating to electrostatic coating of substrates of medicinal products
IE67345B1 (en) * 1991-03-12 1996-03-20 Akzo Nv Low dose dry pharmaceutical preparations
FR2674747B1 (en) 1991-04-05 1993-07-30 Step Soc Tech Pulverisation DEVICE FOR DISPENSING DROPS OF SMALL VOLUME, PARTICULARLY FOR OPHTHALMOLOGICAL CARE.
US5223225A (en) 1991-05-17 1993-06-29 Bio 101 Scale-marked pipet tip for precision dispensing of fluids over a large range of volumes
US5195656A (en) 1991-09-03 1993-03-23 Motorola, Inc. Accurately controlled fluid dispenser with upper and lower stroke adjusters
US5278626A (en) 1991-09-05 1994-01-11 Amherst Process Instruments, Inc. Non-volatile residue system for monitoring impurities in a liquid
NL9101825A (en) 1991-10-30 1993-05-17 Academisch Ziekenhuis Vrije Un METHOD FOR ACCURATE FLOW FLOW DETERMINATION OF LIQUIDS AND AN APPARATUS FOR CARRYING OUT THAT METHOD
US5312233A (en) 1992-02-25 1994-05-17 Ivek Corporation Linear liquid dispensing pump for dispensing liquid in nanoliter volumes
US5324359A (en) * 1992-02-25 1994-06-28 Nouvas Manufacturing Technology Co. Material deposition device
US5194297A (en) * 1992-03-04 1993-03-16 Vlsi Standards, Inc. System and method for accurately depositing particles on a surface
USRE36529E (en) * 1992-03-06 2000-01-25 The United States Of America As Represented By The Department Of Health And Human Services Spectroscopic imaging device employing imaging quality spectral filters
CN1035716C (en) * 1992-03-23 1997-08-27 中国人民解放军第一一八医院 Automatic compounding and split charging machine for medicine liquid
DE4210970C2 (en) * 1992-04-02 1996-10-17 Markus Dipl Chem Sauer Process for the simultaneous optical qualitative and quantitative detection of different molecules of a mixture marked with fluorochromes or fluorogens by means of laser spectroscopy
RU2015744C1 (en) * 1992-09-14 1994-07-15 Акционерное общество "Сорбполимер" Device for applying the coating on moving base
IT1255522B (en) * 1992-09-24 1995-11-09 Ubaldo Conte COMPRESSED FOR THERAPEUTIC USE SUITABLE FOR SELLING ONE OR MORE ACTIVE SUBSTANCES WITH DIFFERENT SPEEDS
GB2272389B (en) * 1992-11-04 1996-07-24 Bespak Plc Dispensing apparatus
JP3123626B2 (en) * 1992-11-06 2001-01-15 シオノギクオリカプス株式会社 Solid preparation printing equipment
US5525515A (en) 1993-02-03 1996-06-11 Blattner; Frederick R. Process of handling liquids in an automated liquid handling apparatus
US5334353A (en) 1993-02-03 1994-08-02 Blattner Frederick R Micropipette device
DE4330412A1 (en) 1993-09-08 1995-03-09 Boehringer Mannheim Gmbh Method and device for dosing liquids
JP2937710B2 (en) * 1993-09-22 1999-08-23 日本電気株式会社 Print inspection device for inkjet printer
US6280771B1 (en) * 1997-02-20 2001-08-28 Therics, Inc. Dosage forms exhibiting multi-phasic release kinetics and methods of manufacture thereof
US5568186A (en) * 1993-11-15 1996-10-22 The United States Of America As Represented By The Secretary Of The Army Focal plane filtered multispectral multidetector imager
US5442892A (en) 1994-01-14 1995-08-22 Glaxo Inc. System for facilitate recycling goods from defective packages on a blister packaging machine
JPH0821805A (en) * 1994-07-08 1996-01-23 Datsuku Eng Kk Appearance inspecting method and device thereof
JP3015677B2 (en) * 1994-08-10 2000-03-06 ファイザー製薬株式会社 Divided tablets with film coating
ATE251433T1 (en) * 1994-08-30 2003-10-15 Pharmacia Ab LIQUID CAN PACKAGING, EYE TREATMENT DEVICE AND USE THEREOF
US5560543A (en) 1994-09-19 1996-10-01 Board Of Regents, The University Of Texas System Heat-resistant broad-bandwidth liquid droplet generators
US5900634A (en) 1994-11-14 1999-05-04 Soloman; Sabrie Real-time on-line analysis of organic and non-organic compounds for food, fertilizers, and pharmaceutical products
US5593290A (en) * 1994-12-22 1997-01-14 Eastman Kodak Company Micro dispensing positive displacement pump
US5683718A (en) * 1995-04-04 1997-11-04 Time-Cap Labs, Inc. Enteric coated tablet with raised identification character and method of manufacture
TR199701323T1 (en) * 1995-05-09 1998-02-21 Colorcon Limited Powder coating composition for electrostatic coating of pharmaceutical substrates.
US5604130A (en) 1995-05-31 1997-02-18 Chiron Corporation Releasable multiwell plate cover
DE19535010C2 (en) 1995-09-21 1998-01-22 Pelikan Produktions Ag Use of a drop generator in a medical device for the metered delivery of a medicament to a fluid stream
DE69631428T2 (en) * 1995-10-13 2004-12-02 Nordson Corp., Westlake SYSTEM AND METHOD FOR COATING THE BASE OF FLIP CHIPS
GB9525065D0 (en) * 1995-12-07 1996-02-07 Smithkline Beecham Plc Packaging system
US6040578A (en) * 1996-02-02 2000-03-21 Instrumentation Metrics, Inc. Method and apparatus for multi-spectral analysis of organic blood analytes in noninvasive infrared spectroscopy
US5753302A (en) * 1996-04-09 1998-05-19 David Sarnoff Research Center, Inc. Acoustic dispenser
DE19617014C2 (en) * 1996-04-27 1998-04-09 Uhlmann Pac Systeme Gmbh & Co Method and device for refilling filling material in the wells of a film web
US6083762A (en) * 1996-05-31 2000-07-04 Packard Instruments Company Microvolume liquid handling system
US6174497B1 (en) * 1997-06-04 2001-01-16 Euro-Celtique, S.A. Detection systems and methods for predicting the dissolution curve of a drug from a pharmaceutical dosage form
AU735071B2 (en) * 1996-06-17 2001-06-28 Janssen Pharmaceutica N.V. Marking rapidly disintegrating dosage forms
US5743960A (en) * 1996-07-26 1998-04-28 Bio-Dot, Inc. Precision metered solenoid valve dispenser
US5916524A (en) 1997-07-23 1999-06-29 Bio-Dot, Inc. Dispensing apparatus having improved dynamic range
FR2754177B1 (en) * 1996-10-07 1999-08-06 Sanofi Sa PHARMACEUTICAL MICROSPHERES OF VALPROIC ACID FOR ORAL ADMINISTRATION
FR2754900B1 (en) 1996-10-23 1998-11-27 Elf Antar France METHOD FOR MONITORING AND MONITORING A MANUFACTURING UNIT AND / OR A NEAR INFRARED SPECTROMETER USING AT LEAST ONE INDICATOR
US5781289A (en) * 1996-11-05 1998-07-14 Sabsabi; Mohamad Method and apparatus for rapid in situ analysis of preselected components of homogeneous solid compositions, especially pharmaceutical compositions
GB9623634D0 (en) * 1996-11-13 1997-01-08 Bpsi Holdings Inc Method and apparatus for the coating of substrates for pharmaceutical use
JP3245813B2 (en) * 1996-11-27 2002-01-15 東京エレクトロン株式会社 Coating film forming equipment
US6330351B1 (en) * 1996-11-29 2001-12-11 Kabushiki Kaisha Yuyama Seisakusho Drug inspection device and drug packaging device
US6007631A (en) * 1997-11-10 1999-12-28 Speedline Technologies, Inc. Multiple head dispensing system and method
US5964381A (en) 1997-11-12 1999-10-12 Ljl Biosystems, Inc. Device for projectile dispensing of small volume liquid samples
TW419376B (en) 1997-12-05 2001-01-21 Yung Shin Pharm Ind Co Ltd The process for preparing the rapid-function pharmaceutical composition
US6063339A (en) * 1998-01-09 2000-05-16 Cartesian Technologies, Inc. Method and apparatus for high-speed dot array dispensing
US5997518A (en) * 1998-01-14 1999-12-07 Laibovitz; Robert A. Apparatus and method for delivery of small volumes of liquid
GB9803487D0 (en) * 1998-02-20 1998-04-15 Inst Of Food Research Nuclear magnetic resonance spectroscopy
IL128818A0 (en) * 1998-03-12 2000-01-31 Akzo Nobel Nv Making dosage units using low shear granulation
US6159186A (en) 1998-03-13 2000-12-12 Wft Projects (Proprietary) Limited Infusion delivery system
US6350470B1 (en) * 1998-04-29 2002-02-26 Cima Labs Inc. Effervescent drug delivery system for oral administration
NZ508402A (en) * 1998-06-10 2003-08-29 Delsys Pharmaceutical Corp Dry powder deposition apparatus for electrostatic deposition of a pharmaceutical powder
US6287595B1 (en) * 1998-06-10 2001-09-11 Delsys Pharmaceuticals Corporation Biomedical assay device
US6063194A (en) 1998-06-10 2000-05-16 Delsys Pharmaceutical Corporation Dry powder deposition apparatus
US6303143B1 (en) * 1998-06-10 2001-10-16 Sarnoff Corporation Pharmaceutical product
JP2000042089A (en) 1998-07-27 2000-02-15 Shionogi Qualicaps Kk Method for printing oral administration product and printing ink
DE19844011C1 (en) * 1998-09-25 2000-03-09 Bosch Gmbh Robert Pressurized pharmaceutical filling apparatus comprises primary pipe, distribution unit, filling valves, pressure sensor and housing
DE19852947A1 (en) 1998-11-12 2000-05-18 Univ Schiller Jena Micro-liter automatic dispensing apparatus comprises needle moving vertically to penetrate cover over micro-titration plate, to dispense liquid into cells
DE19856147A1 (en) * 1998-12-04 2000-06-08 Knoll Ag Divisible solid dosage forms and methods for their preparation
JP4072268B2 (en) 1998-12-24 2008-04-09 キヤノン株式会社 Skin absorption type chemical solution administration device
US6690464B1 (en) * 1999-02-19 2004-02-10 Spectral Dimensions, Inc. High-volume on-line spectroscopic composition testing of manufactured pharmaceutical dosage units
WO2000070331A1 (en) * 1999-05-14 2000-11-23 Gunther Krieg Method and device for detecting and differentiating between contaminations and accepts as well as between different colors in solid particles
JP4366757B2 (en) * 1999-05-27 2009-11-18 東レ株式会社 Coating apparatus, coating method, and method for manufacturing plasma display or display member
DE19930729A1 (en) 1999-07-05 2001-01-11 Achim Goepferich Block copolymers for the production of biomimetic surfaces
AU765526B2 (en) * 1999-08-17 2003-09-18 Novartis Consumer Health S.A. Rapidly dissolving dosage form and process for making same
DE19940242A1 (en) 1999-08-25 2001-03-01 Lohmann Therapie Syst Lts Applying a preparation in liquid phase containing active substances to a substrate constituting an adhesive therapeutic system involves use of a free jet similarly to bubble jet printing
DE19940241A1 (en) 1999-08-25 2001-03-01 Lohmann Therapie Syst Lts Method for applying at least one active substance to a thin substrate forming a carrier layer involves use of liquid active substances which are applicable by bubble jet printing techniques
BE1013128A6 (en) 1999-09-21 2001-10-02 Volder L De Device for printing objects of the type of tablets with special medical tablets.
DE19947878C1 (en) * 1999-10-05 2001-04-05 Hahn Schickard Ges Apparatus useful for empirical quality control of microdroplets on transparent substrate, especially microarrays on biochips, comprises focuses and analyses droplet image patterns
WO2001029539A1 (en) * 1999-10-20 2001-04-26 Massachusetts Institute Of Technology Systems and methods for analyzing mixtures using fluorescence
US6440669B1 (en) 1999-11-10 2002-08-27 Agilent Technologies, Inc. Methods for applying small volumes of reagents
ATE328670T1 (en) 1999-11-11 2006-06-15 Trinity College Dublin DEVICE AND METHOD FOR ADMINISTRATION OF DROPS
DE19955240A1 (en) 1999-11-17 2001-05-23 Henkel Kgaa Production of laundry and other detergent tablets, useful in washing machine or dishwasher, or bleach or water softener tablets by pressing detergent composition(s), uses ink-jet printing for marking tablets
US6149815A (en) 1999-11-23 2000-11-21 Sauter; Andrew D. Precise electrokinetic delivery of minute volumes of liquid(s)
US6331438B1 (en) * 1999-11-24 2001-12-18 Iowa State University Research Foundation, Inc. Optical sensors and multisensor arrays containing thin film electroluminescent devices
BR0008018B1 (en) * 1999-12-03 2010-07-27 process and apparatus for mixing control in a pharmaceutical combiner.
US6806017B2 (en) * 1999-12-17 2004-10-19 Phoqus Limited Electrostatic application of powder material to solid dosage forms
US6213354B1 (en) * 1999-12-29 2001-04-10 Elite Engineering Corporation System and method for dispensing fluid droplets of known volume and generating very low fluid flow rates
SE0000090D0 (en) * 2000-01-13 2000-01-13 Astrazeneca Ab Method and apparatus for monitoring
US6399591B1 (en) 2000-01-19 2002-06-04 Yung-Shin Pharmaceutical Ind. Co., Ltd. Chargeable pharmaceutical tablets
JP4029252B2 (en) 2000-02-24 2008-01-09 セイコーエプソン株式会社 Microcapsule manufacturing method and display device manufacturing method
DE10022398B4 (en) 2000-04-28 2011-03-17 Eppendorf Ag Gas cushion micro-dosing system
CA2409093C (en) 2000-05-16 2009-07-21 Regents Of The University Of Minnesota High mass throughput particle generation using multiple nozzle spraying
CA2408956C (en) * 2000-05-18 2011-07-12 Therics, Inc. Method and form of a drug delivery device,such as encapsulating a toxic core within a non-toxic region in an oral dosage form
US20010050294A1 (en) 2000-05-25 2001-12-13 Plattner Edward Michael Adhesive dispensing and vision system for an automatic assembly system
DE10032456A1 (en) * 2000-07-04 2002-01-31 Lohmann Therapie Syst Lts Rapidly disintegrating dosage form for the release of active substances in the mouth or in the body cavities
AU2001292618A1 (en) 2000-09-12 2002-03-26 Massachusetts Institute Of Technology Methods and products related to low molecular weight heparin
SE521383C2 (en) * 2000-10-31 2003-10-28 Nordson Corp Apparatus and method for monitoring the operation of a fluid distributor gun
NL1016532C1 (en) * 2000-11-02 2002-05-07 Arnold Wilhelm Heinrich Toonen Adhesive inspection device for gluing and folding machine, comprises intelligent camera system operated using program structure design software package
CH695544A5 (en) 2000-11-17 2006-06-30 Tecan Trading Ag Apparatus for dispensing or aspirating / dispensing liquid samples.
RS50414B (en) 2000-12-14 2009-12-31 Ortho-Mcneil Pharmaceutical I.N.C., Steroid hormone products and methods for preparing them
US20030206945A1 (en) 2000-12-20 2003-11-06 Giulio Tarro Sticking plaster for controlled release of natural interferon
US6386396B1 (en) 2001-01-31 2002-05-14 Hewlett-Packard Company Mixing rotary positive displacement pump for micro dispensing
US6667802B2 (en) 2001-02-12 2003-12-23 Analytical Spectral Devices, Inc. System and method for self-referencing calibration
US6765212B2 (en) 2001-02-12 2004-07-20 Analytical Spectral Devices, Inc. System and method for combining reflectance data
JP2002239434A (en) * 2001-02-14 2002-08-27 Tokyo Electron Ltd Apparatus and method for forming coating film
WO2002066002A2 (en) * 2001-02-14 2002-08-29 Glaxo Wellcome S.A. Pharmaceutical formulation
US20040172169A1 (en) 2001-03-02 2004-09-02 Curtis Wright Method and apparatus for compouding individualized dosege forms
US20030050312A1 (en) * 2001-03-12 2003-03-13 Hjorth Thyge Borup Novel tablets and capsules and a process for its preparation
US6431694B1 (en) * 2001-04-24 2002-08-13 Hewlett-Packard Company Pump for recirculating ink to off-axis inkjet printheads
DE10121471A1 (en) 2001-05-02 2002-11-07 Beiersdorf Ag Plaster for controlled release of active agent to skin or wounds, comprising adsorbent, pressure-sensitive adhesive matrix surface-doped with active agent, e.g. dexpanthenol
US7247338B2 (en) 2001-05-16 2007-07-24 Regents Of The University Of Minnesota Coating medical devices
US20040231594A1 (en) 2001-06-01 2004-11-25 Edwards Charles O. Microdeposition apparatus
US7244310B2 (en) 2001-06-01 2007-07-17 Litrex Corporation Over-clocking in a microdeposition control system to improve resolution
KR20040024558A (en) * 2001-06-01 2004-03-20 리트렉스 코오포레이션 Formation of printed circuit board structures using piezo microdeposition
US20050016451A1 (en) 2001-06-01 2005-01-27 Edwards Charles O. Interchangeable microdesition head apparatus and method
JP4492775B2 (en) * 2001-06-07 2010-06-30 大日本スクリーン製造株式会社 Substrate processing equipment
US6962715B2 (en) * 2001-10-24 2005-11-08 Hewlett-Packard Development Company, L.P. Method and dosage form for dispensing a bioactive substance
US20040173147A1 (en) * 2001-06-07 2004-09-09 Figueroa Iddys D. Application of a bioactive agent to a delivery substrate
US6623785B2 (en) 2001-06-07 2003-09-23 Hewlett-Packard Development Company, L.P. Pharmaceutical dispensing apparatus and method
US20040173146A1 (en) * 2001-06-07 2004-09-09 Figueroa Iddys D. Application of a bioactive agent to a delivery substrate
US6702894B2 (en) 2001-10-24 2004-03-09 Hewlett-Packard Development Company, L.P. Fluid ejection cartridge and system for dispensing a bioactive substance
US20020187564A1 (en) 2001-06-08 2002-12-12 Caliper Technologies Corp. Microfluidic library analysis
SE0102511D0 (en) * 2001-07-12 2001-07-12 Astrazeneca Ab Method and device for coating
GB2377661B (en) 2001-07-20 2005-04-20 Univ Newcastle Methods of manufacturing particles
US20030032198A1 (en) 2001-08-13 2003-02-13 Symyx Technologies, Inc. High throughput dispensing of fluids
JP3844670B2 (en) * 2001-09-14 2006-11-15 東京エレクトロン株式会社 Coating film forming device
US20030054025A1 (en) 2001-09-14 2003-03-20 3M Innovative Properties Company Non-contact printing method for making a medical pressure sensitive adhesive article
US6723077B2 (en) 2001-09-28 2004-04-20 Hewlett-Packard Development Company, L.P. Cutaneous administration system
JP2005509605A (en) * 2001-09-28 2005-04-14 マクニール−ピーピーシー・インコーポレイテッド A dosage form comprising an edible composition and an edible skin
GB0125492D0 (en) * 2001-10-24 2001-12-12 Astrazeneca Ab Formulation
CA2463481A1 (en) 2001-10-29 2003-05-22 Therics, Inc. Three-dimensional suspension printing of dosage forms
US6976639B2 (en) 2001-10-29 2005-12-20 Edc Biosystems, Inc. Apparatus and method for droplet steering
US6684880B2 (en) 2001-12-04 2004-02-03 Hewlett-Packard Development Company, L.P. Applicator for dispensing bioactive compositions and methods for using the same
NZ552514A (en) 2001-12-24 2008-08-29 Teva Pharma Dosage form with a core tablet of active ingredient sheathed in a compressed annular body of powder or granular material, and process and tooling for producing it
US6682759B2 (en) 2002-02-01 2004-01-27 Depomed, Inc. Manufacture of oral dosage forms delivering both immediate-release and sustained-release drugs
WO2003068604A1 (en) * 2002-02-13 2003-08-21 Weibel Michael K Drug dose-form and method of manufacture
US6561224B1 (en) 2002-02-14 2003-05-13 Abbott Laboratories Microfluidic valve and system therefor
GB2385415B (en) * 2002-02-15 2005-09-14 Teraview Ltd An analysis apparatus and method
US6919556B1 (en) 2002-02-22 2005-07-19 Monocle Technologies, Inc. System and method for monitoring and evaluating solid and semi-solid materials
US20030175410A1 (en) 2002-03-18 2003-09-18 Campbell Phil G. Method and apparatus for preparing biomimetic scaffold
SG109494A1 (en) 2002-04-08 2005-03-30 Inst Of High Performance Compu Liquid ejection pump system
DE60323482D1 (en) 2002-05-06 2008-10-23 Massachusetts Inst Technology DIFFUSION CONTROLLED MEDICAMENT AND METHOD OF MANUFACTURE THROUGH THREE-DIMENSIONAL PRINTING
US7118010B2 (en) * 2002-05-10 2006-10-10 Oriel Therapeutics, Inc. Apparatus, systems and related methods for dispensing and /or evaluating dry powders
US6886610B2 (en) 2002-06-05 2005-05-03 Techelan Liquid dispenser
JP2004041464A (en) 2002-07-12 2004-02-12 Canon Inc Wearable dosing appliance of cutaneous absorption chemical
JP2004069484A (en) * 2002-08-06 2004-03-04 Canon Inc Liquid discharge head, and droplet amount measuring method therefor, check system, liquid discharging device, manufacturing system, and droplet amount measuring device
ITBS20020078A1 (en) * 2002-09-02 2004-03-03 Paoli Ambrosi Gianfranco De COMPOSITION BASED ON TRIETYL CITRATE IN THE TREATMENT OF INFECTIONS OF BACTERIAL ORIGIN OF THE SKIN.
KR100681237B1 (en) 2002-09-27 2007-02-09 시마쯔 코퍼레이션 Liquid portioning method and device
US7807197B2 (en) * 2002-09-28 2010-10-05 Mcneil-Ppc, Inc. Composite dosage forms having an inlaid portion
US7582872B2 (en) 2002-10-11 2009-09-01 Malvern Instruments Incorporated Volumetric spectral imaging
US20040081689A1 (en) 2002-10-24 2004-04-29 Dunfield John Stephen Pharmaceutical dosage form and method of making
US7154102B2 (en) 2002-11-21 2006-12-26 Cdex, Inc. System and methods for detection and identification of chemical substances
US6786579B2 (en) 2002-12-18 2004-09-07 Xerox Corporation Device for dispensing particulate matter and system using the same
KR20040056430A (en) * 2002-12-23 2004-07-01 주식회사 하이닉스반도체 Method of manufacturing a flash memory device
US20040241872A1 (en) * 2003-03-17 2004-12-02 Qiagen Operon, Inc. Optical detection liquid handling robot system
GB0308258D0 (en) 2003-04-10 2003-05-14 Central Science Lab Representi Marking system and method
US6772801B1 (en) 2003-05-14 2004-08-10 Shire Laboratories, Inc. Fluidization of particles for encapsulation in oral dosage pharmaceutical products
US7294367B2 (en) * 2003-06-06 2007-11-13 The United States Of America As Represented By The Secretary Of The Navy Biological laser printing via indirect photon-biomaterial interactions
SE0301663D0 (en) 2003-06-10 2003-06-10 Oncolog Medical Qa Ab Method of analysis for infusion drugs
US7267278B2 (en) * 2003-06-23 2007-09-11 Robert Lammle Method and system for providing pharmaceutical product information to a patient
US20050118246A1 (en) * 2003-10-31 2005-06-02 Wong Patrick S. Dosage forms and layered deposition processes for fabricating dosage forms
US7166154B2 (en) * 2003-11-06 2007-01-23 Hewlett-Packard Development Company, L.P. System and a method for an edible, optically invisible ink
US8080097B2 (en) * 2003-11-06 2011-12-20 Hewlett-Packard Development Company, L.P. System and a method for the creation of edible, optically invisible images
US7727576B2 (en) 2004-04-16 2010-06-01 Hewlett-Packard Development Company, L.P. System and a method for producing layered oral dosage forms
US7900577B2 (en) 2004-04-27 2011-03-08 Hewlett-Packard Development Company, L.P. System and a method for starch-based, slow-release oral dosage forms
US20050257738A1 (en) 2004-05-21 2005-11-24 Semiconductor Energy Laboratory Co., Ltd. Manufacturing apparatus of semiconductor device and pattern-forming method
TWI356036B (en) * 2004-06-09 2012-01-11 Smithkline Beecham Corp Apparatus and method for pharmaceutical production
US20060008507A1 (en) 2004-07-06 2006-01-12 Gore Makarand P System for generating a bioactive dosage form
US8609198B2 (en) * 2004-07-21 2013-12-17 Hewlett-Packard Development Company, L.P. Pharmaceutical dose form with a patterned coating and method of making the same
EP1812079A4 (en) 2004-10-15 2012-07-25 Spectral Dimensions Inc Pharmaceutical mixture evaluation
KR100827453B1 (en) 2004-12-29 2008-05-07 엘지디스플레이 주식회사 Electro-Luminescence Display Device And Driving Method thereof
US7729750B2 (en) 2005-01-20 2010-06-01 The Regents Of The University Of California Method and apparatus for high resolution spatially modulated fluorescence imaging and tomography
US7749553B2 (en) 2005-01-31 2010-07-06 Boston Scientific Scimed, Inc. Method and system for coating a medical device using optical drop volume verification
US20060190137A1 (en) 2005-02-18 2006-08-24 Steven W. Free Chemometric modeling software
EP1752213A1 (en) 2005-08-12 2007-02-14 Samsung Electronics Co., Ltd. Device for printing droplet or ink on substrate or paper
US7867998B2 (en) 2005-09-12 2011-01-11 Hong Kong Jockey Club Institute Of Chinese Medicine Limited Method of making antitussive medicine and relieving cough

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5711989A (en) * 1992-11-19 1998-01-27 Nordson Corporation Computer controlled method for dispensing viscous fluid

Also Published As

Publication number Publication date
CA2570037C (en) 2013-11-12
JP5346466B2 (en) 2013-11-20
US20060017916A1 (en) 2006-01-26
EP1773708B1 (en) 2013-06-12
TWI547431B (en) 2016-09-01
JP2011229928A (en) 2011-11-17
TWI356036B (en) 2012-01-11
CA2570037A1 (en) 2005-12-29
BRPI0511937A (en) 2008-01-22
JP5690662B2 (en) 2015-03-25
US20060000470A1 (en) 2006-01-05
MY165810A (en) 2018-04-27
WO2005124297A3 (en) 2008-09-25
IL179752A0 (en) 2007-05-15
NZ551729A (en) 2010-11-26
CA2814857C (en) 2016-12-13
JP2008506531A (en) 2008-03-06
TW201107224A (en) 2011-03-01
PT2638891E (en) 2015-03-19
MX338155B (en) 2016-04-04
PE20100623A1 (en) 2010-09-25
CA2569976A1 (en) 2005-12-29
IL217917A (en) 2015-09-24
PH12014502629A1 (en) 2015-08-03
AR049080A1 (en) 2006-06-21
WO2005123569A2 (en) 2005-12-29
JP2011235111A (en) 2011-11-24
KR101238518B1 (en) 2013-03-04
PL2638891T3 (en) 2015-05-29
CA2814904C (en) 2015-08-18
IL217916A0 (en) 2012-03-29
JP5335859B2 (en) 2013-11-06
MXPA06014474A (en) 2007-03-01
AU2005254510B2 (en) 2011-04-28
NZ597658A (en) 2013-10-25
MA28665B1 (en) 2007-06-01
US8122849B2 (en) 2012-02-28
JP2008516639A (en) 2008-05-22
KR101244090B1 (en) 2013-03-19
NZ588256A (en) 2012-07-27
EP1773708A2 (en) 2007-04-18
IL217917A0 (en) 2012-03-29
JP5335860B2 (en) 2013-11-06
ES2427169T3 (en) 2013-10-29
KR20120088693A (en) 2012-08-08
DK1773708T3 (en) 2013-09-08
EP2638891A1 (en) 2013-09-18
IL179752A (en) 2014-03-31
RU2449771C2 (en) 2012-05-10
TW201434730A (en) 2014-09-16
KR20120079465A (en) 2012-07-12
EP1773708A4 (en) 2011-09-28
ES2531323T3 (en) 2015-03-13
KR20070034572A (en) 2007-03-28
CN101912344A (en) 2010-12-15
SI1773708T1 (en) 2013-10-30
US20060016830A1 (en) 2006-01-26
DK2638891T3 (en) 2015-03-02
EP2638891B1 (en) 2014-12-17
CA2569976C (en) 2015-07-21
HRP20130849T1 (en) 2013-10-11
KR20120087913A (en) 2012-08-07
CA2814904A1 (en) 2005-12-29
MXPA06014533A (en) 2007-03-23
SI2638891T1 (en) 2015-04-30
PL1773708T3 (en) 2013-11-29
PT1773708E (en) 2013-09-13
EP1756535A2 (en) 2007-02-28
KR101313374B1 (en) 2013-10-14
WO2005123569A3 (en) 2010-01-28
TWI428271B (en) 2014-03-01
US8252234B2 (en) 2012-08-28
CA2814857A1 (en) 2005-12-29
PH12014502612A1 (en) 2015-05-18
EP1756535A4 (en) 2015-11-18
CN104622694A (en) 2015-05-20
HUE024497T2 (en) 2016-01-28
HK1185534A1 (en) 2014-02-21
PE20060130A1 (en) 2006-03-05
JP2012001542A (en) 2012-01-05
KR101253940B1 (en) 2013-04-17
NO20066051L (en) 2007-03-02
CN104606152A (en) 2015-05-13
NO340856B1 (en) 2017-07-03
HK1108152A1 (en) 2008-05-02
RU2006146063A (en) 2008-07-20
TW200611871A (en) 2006-04-16
JP4917034B2 (en) 2012-04-18
AU2005254510A1 (en) 2005-12-29
HRP20150252T1 (en) 2015-06-05

Similar Documents

Publication Publication Date Title
CA2570037C (en) Apparatus and method for producing or processing a product or sample
US8101244B2 (en) Apparatus and method for producing or processing a product or sample
US20060002594A1 (en) Method for producing a pharmaceutical product
US20060002986A1 (en) Pharmaceutical product
AU2011204851B2 (en) Apparatus and method for pharmaceutical production
AU2011204852B2 (en) Apparatus and method for pharmaceutical production
AU2011204848B2 (en) Apparatus and method for pharmaceutical production

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A2

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KM KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NG NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SM SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A2

Designated state(s): BW GH GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
WWE Wipo information: entry into national phase

Ref document number: 2570037

Country of ref document: CA

Ref document number: 2007527750

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: PA/a/2006/014533

Country of ref document: MX

NENP Non-entry into the national phase

Ref country code: DE

WWW Wipo information: withdrawn in national office

Country of ref document: DE

WWE Wipo information: entry into national phase

Ref document number: 2005760285

Country of ref document: EP

WWP Wipo information: published in national office

Ref document number: 2005760285

Country of ref document: EP

DPE1 Request for preliminary examination filed after expiration of 19th month from priority date (pct application filed from 20040101)