WO2002011888A9 - Fluidic mixer in microfluidic system - Google Patents
Fluidic mixer in microfluidic systemInfo
- Publication number
- WO2002011888A9 WO2002011888A9 PCT/US2001/024521 US0124521W WO0211888A9 WO 2002011888 A9 WO2002011888 A9 WO 2002011888A9 US 0124521 W US0124521 W US 0124521W WO 0211888 A9 WO0211888 A9 WO 0211888A9
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- channel
- sheet
- microfluidic device
- microfluidic
- sheets
- Prior art date
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D17/00—Separation of liquids, not provided for elsewhere, e.g. by thermal diffusion
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D17/00—Separation of liquids, not provided for elsewhere, e.g. by thermal diffusion
- B01D17/02—Separation of non-miscible liquids
- B01D17/0208—Separation of non-miscible liquids by sedimentation
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D17/00—Separation of liquids, not provided for elsewhere, e.g. by thermal diffusion
- B01D17/08—Thickening liquid suspensions by filtration
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F25/00—Flow mixers; Mixers for falling materials, e.g. solid particles
- B01F25/40—Static mixers
- B01F25/42—Static mixers in which the mixing is affected by moving the components jointly in changing directions, e.g. in tubes provided with baffles or obstructions
- B01F25/421—Static mixers in which the mixing is affected by moving the components jointly in changing directions, e.g. in tubes provided with baffles or obstructions by moving the components in a convoluted or labyrinthine path
- B01F25/422—Static mixers in which the mixing is affected by moving the components jointly in changing directions, e.g. in tubes provided with baffles or obstructions by moving the components in a convoluted or labyrinthine path between stacked plates, e.g. grooved or perforated plates
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01F—MIXING, e.g. DISSOLVING, EMULSIFYING OR DISPERSING
- B01F33/00—Other mixers; Mixing plants; Combinations of mixers
- B01F33/30—Micromixers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
- B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B81—MICROSTRUCTURAL TECHNOLOGY
- B81B—MICROSTRUCTURAL DEVICES OR SYSTEMS, e.g. MICROMECHANICAL DEVICES
- B81B1/00—Devices without movable or flexible elements, e.g. microcapillary devices
- B81B1/002—Holes characterised by their shape, in either longitudinal or sectional plane
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/08—Geometry, shape and general structure
- B01L2300/0809—Geometry, shape and general structure rectangular shaped
- B01L2300/0816—Cards, e.g. flat sample carriers usually with flow in two horizontal directions
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/08—Geometry, shape and general structure
- B01L2300/0861—Configuration of multiple channels and/or chambers in a single devices
- B01L2300/0864—Configuration of multiple channels and/or chambers in a single devices comprising only one inlet and multiple receiving wells, e.g. for separation, splitting
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/08—Geometry, shape and general structure
- B01L2300/0861—Configuration of multiple channels and/or chambers in a single devices
- B01L2300/0867—Multiple inlets and one sample wells, e.g. mixing, dilution
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/08—Geometry, shape and general structure
- B01L2300/0861—Configuration of multiple channels and/or chambers in a single devices
- B01L2300/0874—Three dimensional network
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/08—Geometry, shape and general structure
- B01L2300/0887—Laminated structure
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/16—Surface properties and coatings
- B01L2300/161—Control and use of surface tension forces, e.g. hydrophobic, hydrophilic
- B01L2300/165—Specific details about hydrophobic, oleophobic surfaces
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2400/00—Moving or stopping fluids
- B01L2400/04—Moving fluids with specific forces or mechanical means
- B01L2400/0403—Moving fluids with specific forces or mechanical means specific forces
- B01L2400/0406—Moving fluids with specific forces or mechanical means specific forces capillary forces
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2400/00—Moving or stopping fluids
- B01L2400/04—Moving fluids with specific forces or mechanical means
- B01L2400/0475—Moving fluids with specific forces or mechanical means specific mechanical means and fluid pressure
- B01L2400/0487—Moving fluids with specific forces or mechanical means specific mechanical means and fluid pressure fluid pressure, pneumatics
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
- B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
- B01L3/502707—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by the manufacture of the container or its components
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B81—MICROSTRUCTURAL TECHNOLOGY
- B81B—MICROSTRUCTURAL DEVICES OR SYSTEMS, e.g. MICROMECHANICAL DEVICES
- B81B2201/00—Specific applications of microelectromechanical systems
- B81B2201/05—Microfluidics
- B81B2201/051—Micromixers, microreactors
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N2035/00178—Special arrangements of analysers
- G01N2035/00237—Handling microquantities of analyte, e.g. microvalves, capillary networks
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N2035/00465—Separating and mixing arrangements
- G01N2035/00534—Mixing by a special element, e.g. stirrer
- G01N2035/00544—Mixing by a special element, e.g. stirrer using fluid flow
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T137/00—Fluid handling
- Y10T137/206—Flow affected by fluid contact, energy field or coanda effect [e.g., pure fluid device or system]
- Y10T137/218—Means to regulate or vary operation of device
- Y10T137/2191—By non-fluid energy field affecting input [e.g., transducer]
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T137/00—Fluid handling
- Y10T137/206—Flow affected by fluid contact, energy field or coanda effect [e.g., pure fluid device or system]
- Y10T137/2224—Structure of body of device
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T137/00—Fluid handling
- Y10T137/794—With means for separating solid material from the fluid
- Y10T137/8122—Planar strainer normal to flow path
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24479—Structurally defined web or sheet [e.g., overall dimension, etc.] including variation in thickness
- Y10T428/24562—Interlaminar spaces
-
- Y—GENERAL 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
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24744—Longitudinal or transverse tubular cavity or cell
Definitions
- the present invention relates to microfluidic devices and the control of fluid flow within those devices. These devices are useful in various biological and chemical systems, as well as in combination with other liquid-distribution devices.
- microfluidic systems for the acquisition of chemical and biological information.
- microfluidic systems allow complicated biochemical reactions to be carried out using very small volumes of liquid. These miniaturized systems increase the response time of the reactions, minimize sample volume, and lower reagent cost.
- microfluidic systems have been constructed in a planar fashion using silicon fabrication techniques. Representative systems are described, for example, by Manz et al. (Trends in Anal. Chem. (1990) 10(5): 144-149; Advances in Chromatography (1993) 33: 1-66). These publications describe microfluidic devices constructed using photolithography to define channels on silicon or glass substrates and etching techniques to remove material from the substrate to form the channels. A cover plate is bonded to the top of this device to provide closure.
- a number of methods have been developed that allow microfluidic devices to be constructed from plastic, silicone or other polymeric materials.
- a negative mold is first constructed, and plastic or silicone is then poured into or over the mold.
- the mold can be constructed using a silicon wafer (see, e.g., Duffy et al., Analytical Chemistry (1998) 70: 4974-4984; McCormick et al, Analytical Chemistry (1997) 69: 2626-2630), or by building a traditional injection molding cavity for plastic devices.
- Some molding facilities have developed techniques to construct extremely small molds.
- microfluidic mixing devices have been constructed in substantially planar microfluidic systems where the fluids are allowed to mix through diffusion (see Bokenkamp et al, Analytical Chemistry (1998) 70( 2): 23 2-236. In these systems, the fluids only mix at the interface of the fluids, which is commonly small relative to the overall volume of the fluids. Thus, very little mixing occurs.
- One object of the present invention is to provide an inexpensive and robust microfluidic device that can control the mixing of two or more fluids.
- An additional object of the present invention is to provide a microfluidic mixing device that can accommodate the use of a vast array of liquid reagents or solutions. Different types of solvents and samples can be mixed, including but not limited to water- based systems, organic-based systems, biological materials solvated or dispersed within solvent, chemical systems, and others known by those skilled in the art.
- the microfluidic devices of the present invention are constructed using a combination of traditional manufacturing techniques and novel chemistry and alignment procedures.
- Microfluidic mixing devices have at least two inlet channels on different substantially planar layers of the device.
- the layers are horizontally disposed, such that a channel is substantially in a horizontal plane, and a channel in an adjacent layer can be above or below the first channel.
- the layers containing the inlet channels can be adjacent or can be separated by one or more layers.
- the inlet channels meet at an overlap region. Where the inlet channels are separated by more than one intervening layer, apertures in the intervening layers can extend the inlet channel to form the overlap region.
- An outlet channel is provided that is in fluid communication with the overlap region, such that fluids introduced from the inlet channels must proceed into the outlet channel.
- Channels have at least one dimension less than about 500 microns. Channels also have an aspect ratio that maximizes surface to surface contact between fluid streams.
- a channel of the invention can have a depth from about I to about 500 microns, preferably from about 10 to about 100 microns, and a width of about 10 to about 10,000 microns such that the aspect ratio (width/depth) of the channel cross section is at least about 2, preferably at least about 10, at the overlap region where the channels meet.
- the two or more inlet channels are in fluid communication at an overlap region.
- the overlap region is also in fluid communication with an outlet channel.
- the outlet channel can be on the same layer as one of the inlet channels or can be on a different layer.
- the outlet channel is on a layer intermediate between the inlet channels.
- channel as used herein is to be interpreted in a broad sense. Thus, it is not intended to be restricted to elongated configurations where the transverse or longitudinal dimension greatly exceeds the diameter or cross-sectional dimension. Rather, such terms are meant to comprise cavities or tunnels of any desired shape or configuration through which liquids may be directed.
- a fluid cavity may, for example, comprise a flow-through cell where fluid is to be continually passed or, alternatively, a chamber for holding a specified, discrete amount of fluid for a specified amount of time.
- Channels may be filled or may contain internal structures comprising valves or equivalent components.
- microfluidic as used herein is to be understood, without any restriction thereto, to refer to structures or devices through which fluid(s) are capable of being passed or directed, wherein one or more of the dimensions is less than 500 microns.
- Figure 1 is a figure of a basic microfluidic mixing device.
- Figure 2 is a schematic of various ways to control the microfluidic mixing.
- Figure 3 is a schematic of a microfluidic mixing device next to three prior art devices where minimal mixing occurs.
- Figure 4 is a photograph of a prior art microfluidic mixing device where mixing does not occur, and a mixing device where complete mixing occurs.
- Figure 5 is a schematic of a microfluidic mixer where three separate fluids can be mixed.
- Figure 6 is a schematic of a combinatorial microfluidic mixer system.
- Figure 7 is a microfluidic mixer constructed from etched silicon devices. DETAILED DESCRIPTION OF THE INVENTION
- the invention is directed to microfluidic mixing devices that provide rapid mixing of two or more fluids and includes microfluidic systems that are capable of mixing various fluids in a controlled manner based on the design and construction of the devices.
- these devices contain microfluidic channels that are formed in various layers of a three dimensional structure. The various channels intersect in certain areas in order to produce mixing of the fluids in the various channels.
- the amount of overlap, geometry of the overlaps, surface chemistry of the overlaps, fluid used and flow rate of the fluids all have a controllable effect on the amount of mixing.
- a microfluidic device of the invention has at least two inlet channels on different substantially planar, horizontally disposed, layers of the device.
- Such layers can be flexible, such that the overall device does not lie in a plane.
- the layers containing the inlet channels can be adjacent or can be separated by one or more layers.
- the inlet channels meet at an overlap region. Where the layers are stencil layers, and the channels are cut through the layers, the inlet channels must not overlap vertically until the overlap region, unless an intermediate layer is used.
- An outlet channel may be provided that is in fluid communication with the overlap region, such that fluid flowing through the inlet channels must enter the overlap region and exit through the outlet channel.
- the inlet channels are in fluid communication at the overlap region.
- the overlap region is also in fluid communication with an outlet channel, if an outlet channel is provided.
- the outlet channel can be on the same layer as one of the inlet channels or can be on a different layer. In a preferred embodiment, the outlet channel is on a layer intermediate between the inlet channels.
- the present invention is a microfluidic device comprising a plurality of microfluidic inlet channels and an overlap region within which said inlet channels are in fluid communication with each other.
- at least one inlet channel is formed in a first sheet of a first material and at least another inlet channel is formed in a second sheet of a second material. The materials of the sheets may or may not be the same.
- one sheet may be made of hydrophobic materials whereas the other sheet may be made of hydrophilic materials.
- the sheets may be made of materials that expedite fluid flow through the channels.
- the material of individual sheets may be selected depending on the composition and chemical nature of the fluid flowing through individual channels.
- the invention is a microfluidic device comprising a first inlet channel which is substantially parallel to the top and the bottom surfaces of the first sheet, a second inlet channel which is substantially parallel to the top and the bottom surfaces of the second sheet, and an overlap region within which said first and second inlet channels are in fluid communication with each other.
- the microfluidic device can further comprise an outlet channel in fluid communication with the inlet channels through the overlap region.
- the outlet channel is formed in the first sheet or the second sheet.
- the first sheet and the second sheet are joined together such that the plane of the joint is substantially parallel to the top and bottom surfaces of the sheets.
- a further embodiment of the invention is a device wherein the outlet channel is formed in a third sheet of the material such that the outlet channel is in a plane that is substantially parallel to the top and bottom surfaces of the third sheet. Further, the first, second and third sheets are joined together such that the planes of the joints are substantially parallel to the top and bottom surfaces of the sheets. Alternatively, the third sheet is joined to both the first sheet and the second sheet.
- the invention is a microfluidic mixer comprising a first sheet having a first channel through which a first fluid flows, a second sheet having a second channel through which a second fluid flows, and an overlap region formed by the first and second channels such that the first fluid and the second fluid enter the overlap region and mix therein.
- This embodiment may further comprise an outlet channel in fluid communication with the inlet channels through the overlap region.
- Such an outlet channel for example, is formed in the first sheet or the second sheet.
- the outlet channel is formed by in a substantially flat third sheet of the material such that the outlet channel is in a plane that is substantially parallel to the top and bottom surfaces of the third sheet.
- the invention is a microfluidic mixer comprising a first channel through which a first fluid flows, a second channel through which a second fluid flows, and an overlap region formed by the first and second channels such that the first fluid and the second fluid enter the overlap region and mix therein to form a mixture of the first and second fluids.
- a mixer may further comprise an outlet channel connected to the overlap region such that the mixture from the overlap region may flows through the outlet channel.
- the mixer may be such that the first and second fluids are substantially the same or may differ in one or more of their properties, such as, viscosities, temperatures, flow rates, compositions.
- the device has two or more microfluidic inlet channels that are located within different layers of a three-dimensional device.
- the inlet channels are designed such that the flows of the fluids overlap, with a membrane separating the fluids from each other, and the flows run substantially in the same direction.
- the inlet channels end at an overlap region.
- the combined fluid flow then continues into the outlet channel that begins at the same overlap region.
- This outlet channel is in a layer between the two inlet channels, and is designed such that the direction of the resulting combined fluid flows in the same direction as the inlet fluids.
- the outlet channel can simply be an extension of one of the inlet channels.
- a microfluidic device contains one or more of these fluidic overlaps.
- all of the fluidic mixers are identical.
- the mixers differ within a single device in order to produce preferential mixing.
- the mixers are multiplexed within a device to perform various applications.
- the mixers are multiplexed within a device to create the possibility for combinatorial, synthesis of various types of materials.
- microfluidic devices of the invention also act as phase separators.
- a microfluidic device is constructed that has one inlet channel. The inlet channel terminates in an overlap region. A channel in the layer above the inlet channel and a channel in the layer below the inlet channel overlap the termination of the inlet channel as described above in the mixer embodiment.
- a fluid enters the inlet area. Phase separation may occur in the inlet channel so that at the outlet channels two phases are separated into the two outlet channels. Examples of phase separation could be from oil/water mixtures where the oil rises to the top half of the inlet region and the water goes to the bottom portion. The oil then is withdrawn through the top inlet channel and the water exits out the bottom channel, resulting in separated phase streams.
- the top portion of the inlet channel can be constructed from a different polymer than the bottom portion so as to expedite the phase separation.
- the top half could be constructed from a hydrophobic material and the bottom half from a hyderphilic material.
- the fluid within the channel will rearrange with the organic portion in the top half near the hydrophobic region and the aqueous portion in the bottom half near the hydrophilic region.
- the exit channels can be made of different materials as well to enhance this phase separation.
- the invention may be a microfluidic separator comprising a first channel formed by removing a volume of material equal to the volume of the first channel from a substantially flat first sheet of the material such that the channel is substantially parallel to the top and the bottom surfaces of the first sheet, a second channel formed by removing a volume of material equal to the volume of the second channel from a substantially flat second sheet of the material such that the channel is substantially parallel to the top and the bottom surfaces of the second sheet, a third channel formed by removing a volume of material equal to the volume of the third channel from a substantially flat third sheet of the material such that the channel is substantially parallel to the top and the bottom surfaces of the third sheet, and an overlap region within which said first, second and third inlet channels are in fluid communication with each other.
- the first sheet is sandwiched between the second and third sheets whereby the second channel is in fluid communication with the top half of the overlap region and the third channel is in fluid communication with the bottom half of the overlap region.
- a fluid comprising a two-phase mixture is fed to the first channel under conditions sufficient to separate the two phases with the separated phases entering the overlap region such that one of the separated phases is withdrawn through the second channel and another of the separated phases is withdrawn through the third channel.
- This embodiment may be such that the materials of the first, second and third sheets are substantially the same. Further, the materials of the second and third sheets can be selected such that the separation of the phases is expedited. For example, in one embodiment, the materials of the of the second and third sheets are selected such that the material of one of the sheets is hydrophobic and the material of another of the sheets is hydrophilic.
- the above separator can be used in a method for separating phases of a multi-phase mixture.
- the method comprises the steps of feeding a fluid comprising a multi-phase mixture to the first channel under conditions sufficient to separate the two phases such that the separated phases enter the overlap region, withdrawing one of the separated phases through the second channel, and withdrawing another of the separated phases through the third channel.
- the invention is a method of manufacturing a microfluidic mixing device comprising the steps of removing a volume of material equal to the volume of a first channel from a substantially flat sheet of the material such that the channel is substantially parallel to the top and bottom surfaces of the sheet, removing a volume of material equal to the volume of a second channel from a substantially flat sheet of the material such that the channel is substantially parallel to the top and bottom surfaces of the sheet, and forming an overlap region within which said first and second channels are in fluid communication with each other.
- the invention is a method for mixing two or more fluids comprising transporting a first fluid at a first flow rate and a second fluid at a second flow rate through said first and second inlet channels of the various microfluidic devices described above.
- This method may be implemented under conditions such that the flow rates are substantially the same.
- the flow rates are controlled to change the composition in the overlap region of the devices described above.
- Each of the inlet and outlet channels of the above devices and mixers are formed, for example, by removing a volume of material equal to the volume of the channel from a substantially flat sheet of the material. Examples of methods for removing the materials are set forth in co-pending applications, United States Patent Application Serial Nos. 09/550,184 and 09/453,029, the entire contents of which are herein incorporated by reference.
- Examples of the microfluidic devices of the invention are devices wherein the volume of the inlet channels is between about I nanoliter to about 50 microliters per centimeter length of the inlet channel.
- the inlet channels have a rectangular or a square cross section with the length of each side between about 1 and about 500 microns.
- the inlet channels have a circular cross section with the diameter of the inlet channels between about 10 microns to about 1000 microns.
- channels have at least one dimension less than about 500 microns.
- Channels also have an aspect ratio that maximizes surface to surface contact between fluid streams.
- a channel of the invention can have a depth from about 1 to about 500 microns, preferably from about 10 to about 100 microns, and a width of about 10 to about 10,000 microns such that the aspect ratio (width/depth) of the channel cross section is at least about 2, preferably at least about 10, at the overlap region where the channels meet.
- a channel can be molded into a layer, etched into a layer, or can be cut through a layer. Where a channel is cut through a layer, the layer is referred to as a stencil layer.
- the nature of these microfluidic mixers is tuned for particular applications. Some of the parameters that affect the design of these systems include the type of fluid to be used, flow rate, and material composition of the devices.
- the microfluidic mixers described in the present invention can be constructed in a microfluidic device by controlling the geometry and chemistry of junction points.
- microfluidic mixing devices have fluidic channels on a single substantially planar layer of a microfluidic device.
- the aspect ratio of these channels is 10:1 or greater.
- the width of the channels is typically 10 to 500 times greater than the height of the channels.
- two coplanar inlet channels are brought together into a common outlet channel. The fluids meet at the intersection and proceed down the outlet channel.
- all fluid flow is laminar (no turbulent flow occurs); thus, any mixing in this outlet channel occurs through diffusional mixing at the interface between the inputted liquid streams.
- fluidic channels are located on different vertical layers of a three-dimensional device.
- the interface between the two fluids is along the horizontal dimension of the channels, which is the larger dimension of the perpendicular cross-section of the fluid streams.
- the larger interface maximizes the diffusion area between the fluids.
- the majority of the volume of the fluids is in very close proximity to the diffusion interface of the mixing fluids and mixing occurs very rapidly.
- the nature of these overlap regions must be carefully controlled in order to optimize the mixing, as will be described below.
- the overlap region comprises one or more sheets containing apertures in fluid communication with the inlet channels.
- the devices may further comprise an upper sheet, wherein said upper sheet provides the top surface of one inlet channel. Further, the devices may comprise a lower sheet, wherein said lower sheet provides the bottom surface of another inlet channel. These upper and lower sheets in certain embodiments are substantially rigid.
- the material of the microfluidic devices of the invention is, for example, is paper, foil or a plastic.
- plastics are plastics selected from the group consisting of polytetrafluoroethylenes, polycarbonates, polypropylenes, polyimide and polyesters.
- the sheets of the invention can be made of plastic, paper or foil.
- the sheets of the invention can be joined together such that the plane of the joint is substantially parallel to the top and bottom surfaces of the sheets.
- the first, second and third sheets are joined together such that the planes of the joints are substantially parallel to the top and bottom surfaces of the sheets.
- the third sheet is joined to both the first sheet and the second sheet such that it is sandwiched between the first and the second sheet.
- these devices are constructed using stencil layers to define channels and/or chambers.
- a stencil layer is substantially planar and has a channel cut through it, such that in the final device, the top and bottom surfaces of the microfluidic channel within the stencil layer are formed from the bottom and top, respectively, of adjacent stencil or substrate layers.
- the stencils are preferably sandwiched between substrates, wherein the substrates are preferably substantially planar.
- Stencil layers are bonded by any technique that results in substantially liquid-tight channels within the device.
- the stencil can, for example, be self-adhesive to form a seal between adjacent substrates.
- an adhesive coating can be applied to the stencil layers.
- the stencil layers may be held together using gaskets and or mechanical force.
- microfluidic devices from stencil layers and substrates are described in co-pending applications, United States Patent Application Serial Nos. 09/550,184 and 09/453,029 the entire contents of which are herein incorporated by reference.
- the stencil layers are comprised of single- or double-sided adhesive tape.
- a portion of the tape (of the desired shape and dimensions) can be cut and removed to form channels, chambers and apertures.
- the tape stencil can then be placed on a supporting substrate or between layers of tape.
- stencil layers can be stacked on each other.
- the thickness or height of the channels can be varied by simply varying the thickness of the stencil (e.g., the tape carrier and the adhesive or glue thereon) or by using multiple identical stencil layers stacked on top of one another.
- tapes are useful in the above embodiment.
- Single- or double-sided adhesive tape is preferred.
- the type of glue or adhesive can be varied to accommodate the application, as can the underlying carrier's thickness and composition.
- Such tapes may have various methods of curing, including pressure sensitive tapes, temperature-curing tapes, chemically-curing tapes, optical-curing tapes, and other types of curing tapes. Examples include tapes that use rubber-based adhesive, acrylic-based adhesive, and other types of adhesive.
- the materials used to carry the adhesive are also numerous. Examples of suitable tape carrier materials include polyesters, polycarbonates, polytetrafluoroethylenes, polypropylenes, polyimides (e.g., KAPTONTTM) and polyesters (e.g., MYLARTM). The thickness of these carriers can be varied.
- the layers are formed from silicon or similar materials, with channels etched therein.
- a set of channels is etched or created into the top surface of a silicon or glass substrate.
- a second set of channels is etched or created into a second substrate. The two substrates are adhered together in such a way that the channel surfaces are facing one another and certain regions are overlapping to form the mixing area.
- Such a device is described infra.
- the layers are not discrete, but a layer describes a substantially planar section through such a device.
- a device can be constructed using photopolyraerization techniques such as those described in Cumpston B.H. et al. (1999) Nature 398:51-54.
- a microfluidic mixing device is constructed by sandwiching stencil layers on top of one another.
- a microfluidic mixer is constructed by sandwiching four stencil layers 21-24 and adhering them to a substrate 20.
- the stencils have various channels 25-27 and apertures.
- Inlet ports 30, 31 and an outlet port 32 are in the top stencil layer 24.
- the assembled device is shown in Figure IB.
- a first fluid is injected into inlet port 30, passes through through-holes in layers 23 and 22 and enters channel 25.
- a second fluid enters entry port 31 and passes through channel 27.
- the two fluids meet at the overlap region 33 shown in Figure IB. At this point, the fluids are forced to converge into a single channel 26 located in stencil layer 22.
- the top half of the channel is fluid two and the bottom half is fluid one.
- the height of these channels is relatively small (between 100 nm and 500 microns), so diffusional mixing quickly occurs and a homogenous material is transported off board at exit port 32. It has been discovered that the majority of the mixing occurs right at the junction point 33, with a slight amount of mixing occurring within channel 26 immediately after the junction point 34. The amount that mixing occurs after the junction point 33 depends on a number of factors, including geometry of the channels, chemical make-up of the channels and samples, flow rate, etc.
- the three channels that converge at point 32 are all the same width. Surprisingly, it has been discovered that if the layers containing the channels are not well aligned, proper mixing does not occur.
- the fluid entering outlet channel 26 is a mixture of the two input fluids only at points where channels 25, 26 and 27 all overlap. If, for example, inlet channel 25 is misaligned laterally such that for a small portion of the overlap there is an area where only inlet channel 27 and outlet channel 26 overlap, then in this region only the fluid from inlet channel 27 will enter outlet channel 26.
- FIG. 2 Preferred mixer embodiments are shown in Figure 2. These embodiments do not suffer from the same strict alignment parameters that the mixer shown in Figure 1 has.
- FIG 2A three different microfluidic mixers are built into a single device. The device is constructed from five stencil layers 40-44. Stencil layers have channels 45-53, through holes, entry ports 54,55 and exit ports 56 removed. The stencil layers are adhered together to form the completed device, shown in Figure 2B. Notice that the shapes of the overlap regions in these mixer devices 60-62 are shaped so that slight misalignment of layers during construction will not have a great effect on fluid flow and mixing. It has been found that mixers such as in Figure 2 are far superior to the mixer shown in Figure 1, for the above outlined reason.
- changing the chemical nature in the overlap region alters the overlap junction.
- This can be accomplished by forming the stencil from a different material, or altering the surface chemistry of this stencil layer.
- the surface chemistry can be altered in many ways, as one skilled in the art will realize. These methods of altering the surface chemistry include chemical derivatization as well as surface modification techniques such as plasma cleaning or chemical etching.
- the chemical derivatization is preferably chosen such that fluids flow through the channels and overlap region occurs smoothly and without bubble formation.
- One surprising aspect of the present invention is that the optimal parameters for a given overlap are greatly affected by the nature of the sample that is to be used within the device. It has been found that the optimal geometry for these overlaps changes depending upon the solution used.
- the mixing between two or more fluid channels can be adjusted to give a tremendous range of different ratios. The main or easiest way to do this is to hold the flow rate of one channel constant, while adjusting the flow rate of the other channel. In this way, different mixture ratios are formed by virtue of different quantities of each liquid entering the mixing chamber/ overlap area in a given time period.
- Another method is to alter the size of the channels leading into the mixing region; this has the effect of changing the flow rate internally. This would be useful for arrays, where different ratios are desired without the hassle of using different external flow rates.
- a single device is constructed that contains four independent microfluidic devices.
- the device is constructed from five stencil layers 80-84 that have channels 85-90 and through holes 91 cut into them.
- the stencils are constructed from layers of single sided tape (3 mil polypropylene carrier with water based adhesive on one side) and the channels are all 45 mils wide.
- the bottom stencil 80 is an 1/4" thick block of acrylic. Inlet ports 92,93 and outlet ports 94,95 are placed in the upper most stencil layer. All of the holes are 60 mils in diameter. The stencils are adhered together to form the completed device, shown in Figure 3B.
- microfluidic devices are constructed in a 2-dimensional fashion such as the completed devices on the right of Figure 3B 97-99. If two different fluids are injected into the 2 inlet ports 92,93 of device 99, the fluids travel down their independent channels and meet at the central section of channel 90. In the central region, all of the flow is laminar. The fluids travel down their respective sides of the central channel until they reach the outlet channel areas 100,101. Surprisingly, the fluid that entered into inlet port 93 exits almost completely out of exit channel 100 and exit port 95. The fluid that entered 92, exits out of channel area 101 and exit port 94 almost exclusively. The only mixing that occurred in the central area of channel 90 is through diffusional mixing at the relatively small interface of the liquids.
- the prior art microfluidic mixers can be improved slightly by making the channel longer and thereby extending the interfacial contact area between the two fluids as in device 97 and 98.
- the length of the mixing region is extended.
- very little mixing occurs even in these devices.
- a slower flow-rate allows more time for the diffusion process to occur.
- this also results in incomplete mixing over any reasonable time period.
- inlet channels 85,87 were constructed on different layers of a three dimensional structure.
- the inlet channels are in fluid communication at overlap region 102 where the two fluids to be mixed are forced to enter into outlet channel 86, in this case located on a layer intermediate to the layers containing the two inlet channels.
- the interfacial contact area between the two fluids extends all the way across the width of the channel and is 15 times greater than in the previous device 99.
- the average distance that the molecules need to diffuse in order for mixing to occur is now 2 mils, rather than 30 mils as in the previous device 99.
- the reaction was also performed with a 0.1 M HC1 solution mixing with a 0.2M NaOH solution, in which the indicator was first dissolved in the acidic solution.
- the clear NaOH solution and yellow HC1 solution mixed to create a dark purple fluid (in this case, the weaker acid is neutralized by the stronger base, resulting in a mixture that is weakly basic).
- a device of the prior art was also tested using these same solutions. In this device, little or no mixing occurred at the interface of the two liquids.
- the solutions that came out of the outlets on either side were the same color and pH as the solutions that were inputted at the corresponding inlet side.
- the two fluids were then injected into the microfluidic mixer described in this invention. Again, a clear NaOH solution was input at inlet 92 and a yellow HCI solution (containing indicator) at inlet 93. The two fluids begin to mix at the overlap region 102 and the mixing is nearly complete just after this region 103. Dark fluid color was observed within the exit channel 86 and at the outlet ports 106,107, which was indicative of the acid-base reaction going to completion.
- FIG. 5 a microfluidic mixer that brings in three different fluids and mixes them is shown.
- Figure 5A shows seven stencil layers 120-126 that have channels 127-129 and through regions 130,131 and through holes 132. All of the channels are 60 mils wide and the holes are all 80 mils in diameter.
- the stencil layers are all constructed from single sided tape (3 mil thick polypropylene backing with water based adhesive).
- the bottom stencil 120 is a 1/4" thick block of acrylic.
- the top stencil layers 126 has inlet ports 133 and an exit port 134 in it.
- the assembled device is shown in Figure 5B. In use, three different fluids are injected at the inlet ports 133.
- the fluid from channel 129 is forced into the top third of channel region 136
- the fluid from 128 occupies the middle third of region 136
- the fluid from 127 occupies the bottom third of 136.
- the interfacial contact area between the two fluids is now maximized in the channel area 136 between the three fluids and diffusional mixing occurs very rapidly, so that the fluid that exits port 134 is fully mixed.
- This device also allows for a tremendous range in the mixing ratios.
- the flow rates of each of the fluids can be adjusted to allow a greater or lesser amount of each fluid to be added to the mixture.
- a combinatorial microfluidic mixer is shown in Figure 6. This device brings in two different fluids and mixes them in four different stoichiometries.
- a combinatorial microfluidic mixer is constructed from five stencil layers 150 - 154 that has channels 155-159 and through-holes 160,161. Inlet ports 162,163 and outlet ports 164-167 are located in the top stencil layer 154. Channels 157 and 158 are 45 mils wide, channels 155, 156 and 159 are 30 mils wide and the overlap regions are 15 mils. All of the round areas and holes are 70 mils in diameter.
- the stencil layers are all constructed from single sided tape (3 mil thick polypropylene backing with water based adhesive).
- the bottom stencil 150 is a 1/4" thick block of acrylic. In use, fluid A is injected at port 162 and fluid B at port 163. The fluids are split in the division sections of channel 158.
- microfluidic mixer region 168 fluids A and B mix to form A+B.
- the fluids move on to the splitter channels 157 to the next set of microfluidic; mixer regions.
- region 169 the mixture of A+B meets with pure A.
- the output is 3 A+B.
- region 170 A+B meets with pure B, outputting 3B+A.
- the outputs of the combinatorial microfluidic mixer are as follows: 164 is pure B, 165 is 3B+A, 166 is 3 A+B, 167 is pure A. Other combinations can be constructed.
- the amounts of fluid mixing at each of the output is dependent on a number of factors, including flow rate, fluid properties and device geometry and chemistry.
- a microfluidic device of the invention were constructed using silicon fabrication techniques. Referring to Figure 7A, a channel 181 is patterned in (110) Si substrate 180 using an oxide mask and etched in 70°C KOH. The channel 181 is etched so that it is 100 microns wide and 3 microns deep. A second channel 183 is similarly patterned and etched in another (110) Si substrate 182. Holes 184-186 are drilled all the way through the second substrate 182. These holes are 800 microns in diameter.
- the two substrates 180 and 182 are aligned face-to-face and the two surface
- two different fluids are injected at inlet ports 184 and 185. They each travel down their respective channels and meet at the junction point 189. Again, the interfacial contact area between the two fluids is maximized in the channel area 189 between the two fluids and diffusional mixing occurs very rapidly, so that once the fluid reached region 190 is it fully mixed.
Abstract
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU2001281076A AU2001281076A1 (en) | 2000-08-07 | 2001-08-03 | Fluidic mixer in microfluidic system |
EP01959530A EP1309404A2 (en) | 2000-08-07 | 2001-08-03 | Fluidic mixer in microfluidic system |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US63268100A | 2000-08-07 | 2000-08-07 | |
US09/632,681 | 2000-08-07 |
Publications (3)
Publication Number | Publication Date |
---|---|
WO2002011888A2 WO2002011888A2 (en) | 2002-02-14 |
WO2002011888A3 WO2002011888A3 (en) | 2003-01-03 |
WO2002011888A9 true WO2002011888A9 (en) | 2003-10-02 |
Family
ID=24536489
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2001/024521 WO2002011888A2 (en) | 2000-08-07 | 2001-08-03 | Fluidic mixer in microfluidic system |
Country Status (4)
Country | Link |
---|---|
US (2) | US6676835B2 (en) |
EP (1) | EP1309404A2 (en) |
AU (1) | AU2001281076A1 (en) |
WO (1) | WO2002011888A2 (en) |
Families Citing this family (165)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6890093B2 (en) * | 2000-08-07 | 2005-05-10 | Nanostream, Inc. | Multi-stream microfludic mixers |
DE50113383D1 (en) * | 2000-09-07 | 2008-01-24 | Gesim Ges Fuer Silizium Mikros | METHOD FOR PRODUCING A 3-D MICROFLOW CELL AND 3-D MICROFLOW CELL |
US20050032204A1 (en) * | 2001-04-10 | 2005-02-10 | Bioprocessors Corp. | Microreactor architecture and methods |
FR2823995B1 (en) * | 2001-04-25 | 2008-06-06 | Alfa Laval Vicarb | IMPROVED DEVICE FOR EXCHANGING AND / OR REACTING BETWEEN FLUIDS |
US6814938B2 (en) * | 2001-05-23 | 2004-11-09 | Nanostream, Inc. | Non-planar microfluidic devices and methods for their manufacture |
JP3694877B2 (en) * | 2001-05-28 | 2005-09-14 | 株式会社山武 | Micro mixer |
US7128876B2 (en) * | 2001-07-17 | 2006-10-31 | Agilent Technologies, Inc. | Microdevice and method for component separation in a fluid |
GB2380528B (en) * | 2001-10-05 | 2003-09-10 | Minebea Co Ltd | A bearing assembly and method of manufacturing a bearing assembly |
DE10150549A1 (en) * | 2001-10-12 | 2003-04-17 | Roche Diagnostics Gmbh | Separation module, useful for the separation of corpuscles from blood, comprises two channels from a junction with a faster flow in one channel taking most of the particles, and a slower flow with few particles through the other channel |
US7069952B1 (en) | 2001-11-14 | 2006-07-04 | Caliper Life Sciences, Inc. | Microfluidic devices and methods of their manufacture |
US20030098661A1 (en) * | 2001-11-29 | 2003-05-29 | Ken Stewart-Smith | Control system for vehicle seats |
US6848462B2 (en) * | 2001-12-06 | 2005-02-01 | Nanostream, Inc. | Adhesiveless microfluidic device fabrication |
US6845787B2 (en) * | 2002-02-23 | 2005-01-25 | Nanostream, Inc. | Microfluidic multi-splitter |
US7223371B2 (en) | 2002-03-14 | 2007-05-29 | Micronics, Inc. | Microfluidic channel network device |
GB0208766D0 (en) * | 2002-04-02 | 2002-05-29 | Univ Surrey | Liquid-liquid separation |
US7517440B2 (en) * | 2002-07-17 | 2009-04-14 | Eksigent Technologies Llc | Electrokinetic delivery systems, devices and methods |
US7364647B2 (en) * | 2002-07-17 | 2008-04-29 | Eksigent Technologies Llc | Laminated flow device |
US7235164B2 (en) * | 2002-10-18 | 2007-06-26 | Eksigent Technologies, Llc | Electrokinetic pump having capacitive electrodes |
DE10238825A1 (en) * | 2002-08-23 | 2004-03-11 | Roche Diagnostics Gmbh | Microfluidic systems with a high aspect ratio |
JP3824160B2 (en) * | 2002-08-28 | 2006-09-20 | 株式会社島津製作所 | High-speed liquid chromatograph mixer |
US6806543B2 (en) * | 2002-09-12 | 2004-10-19 | Intel Corporation | Microfluidic apparatus with integrated porous-substrate/sensor for real-time (bio)chemical molecule detection |
EP1403209A1 (en) * | 2002-09-24 | 2004-03-31 | The Technology Partnership Limited | Fluid routing device |
WO2004034436A2 (en) * | 2002-10-09 | 2004-04-22 | Cellectricon Ab | Method for interfacing macroscale components to microscale devices |
AU2003284055A1 (en) * | 2002-10-09 | 2004-05-04 | The Board Of Trustees Of The University Of Illinois | Microfluidic systems and components |
DE10302720A1 (en) * | 2003-01-23 | 2004-08-05 | Steag Microparts Gmbh | Microfluidic switch for stopping the flow of fluid during a time interval |
DE10302721A1 (en) * | 2003-01-23 | 2004-08-05 | Steag Microparts Gmbh | Microfluidic arrangement for dosing liquids |
DE10320870A1 (en) * | 2003-05-09 | 2004-12-09 | Evotec Technologies Gmbh | Particle injector for a cell sorter |
CA2526965C (en) * | 2003-05-16 | 2011-10-11 | Velocys Inc. | Process for forming an emulsion using microchannel process technology |
US7485671B2 (en) * | 2003-05-16 | 2009-02-03 | Velocys, Inc. | Process for forming an emulsion using microchannel process technology |
KR100509254B1 (en) * | 2003-05-22 | 2005-08-23 | 한국전자통신연구원 | Micro-fluidic device to control flow time of micro-fluid |
JP4348676B2 (en) * | 2003-06-03 | 2009-10-21 | 富士フイルム株式会社 | Micro chemical equipment |
US7344681B1 (en) | 2003-06-06 | 2008-03-18 | Sandia Corporation | Planar micromixer |
US20050112634A1 (en) * | 2003-09-19 | 2005-05-26 | Woudenberg Timothy M. | High density sequence detection methods and apparatus |
US20050069462A1 (en) * | 2003-09-30 | 2005-03-31 | International Business Machines Corporation | Microfluidics Packaging |
US20050069949A1 (en) * | 2003-09-30 | 2005-03-31 | International Business Machines Corporation | Microfabricated Fluidic Structures |
US6994245B2 (en) * | 2003-10-17 | 2006-02-07 | James M. Pinchot | Micro-reactor fabrication |
US8066955B2 (en) * | 2003-10-17 | 2011-11-29 | James M. Pinchot | Processing apparatus fabrication |
US20050084072A1 (en) * | 2003-10-17 | 2005-04-21 | Jmp Industries, Inc., An Ohio Corporation | Collimator fabrication |
EP1525917A1 (en) * | 2003-10-23 | 2005-04-27 | F. Hoffmann-La Roche Ag | Microfluidic device with feed-through |
KR100613398B1 (en) * | 2003-11-25 | 2006-08-17 | 한국과학기술연구원 | Element detecting system using cantilever, method for fabrication of the same system and method for detecting micro element using the same system |
US20050133437A1 (en) * | 2003-12-17 | 2005-06-23 | Intel Corporation | Sieving media from planar arrays of nanoscale grooves, method of making and method of using the same |
EP1718409B1 (en) * | 2004-02-17 | 2018-12-26 | ibidi GmbH | Device for microfluidic analyses |
US7588724B2 (en) | 2004-03-05 | 2009-09-15 | Bayer Healthcare Llc | Mechanical device for mixing a fluid sample with a treatment solution |
US7507380B2 (en) * | 2004-03-19 | 2009-03-24 | State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University | Microchemical nanofactories |
US7559356B2 (en) | 2004-04-19 | 2009-07-14 | Eksident Technologies, Inc. | Electrokinetic pump driven heat transfer system |
US7674615B2 (en) | 2004-05-04 | 2010-03-09 | Bayer Healthcare Llc | Mechanical cartridge with test strip fluid control features for use in a fluid analyte meter |
US7419639B2 (en) * | 2004-05-12 | 2008-09-02 | The Board Of Trustees Of The Leland Stanford Junior University | Multilayer microfluidic device |
ATE427213T1 (en) * | 2004-06-23 | 2009-04-15 | Tesa Ag | MEDICAL BIOSENSOR USING BIOLOGICAL LIQUIDS ARE EXAMINED |
US7264206B2 (en) * | 2004-09-30 | 2007-09-04 | The Boeing Company | Leading edge flap apparatuses and associated methods |
JP5643474B2 (en) | 2004-10-01 | 2014-12-17 | ヴェロシス,インク. | Multiphase mixing process using microchannel process technology |
US7955504B1 (en) | 2004-10-06 | 2011-06-07 | State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University | Microfluidic devices, particularly filtration devices comprising polymeric membranes, and method for their manufacture and use |
CA2587546C (en) * | 2004-11-16 | 2013-07-09 | Velocys Inc. | Multiphase reaction process using microchannel technology |
WO2006057895A2 (en) * | 2004-11-17 | 2006-06-01 | Velocys Inc. | Process for making or treating an emulsion using microchannel technology |
WO2006088427A1 (en) * | 2005-02-15 | 2006-08-24 | Agency For Science, Technology And Research | Microfluidics package and method of fabricating the same |
FR2882939B1 (en) * | 2005-03-11 | 2007-06-08 | Centre Nat Rech Scient | FLUIDIC SEPARATION DEVICE |
DE102005013916B4 (en) * | 2005-03-24 | 2016-06-09 | Leibniz-Institut Für Polymerforschung Dresden E.V. | Microfluidic device for separation of emulsions |
US20070021411A1 (en) * | 2005-05-11 | 2007-01-25 | Cloyd James C | Supersaturated benzodiazepine solutions and their delivery |
US20060285433A1 (en) * | 2005-06-20 | 2006-12-21 | Jing-Tang Yang | Fluidic mixer of serpentine channel incorporated with staggered sudden-expansion and convergent cross sections |
US7846489B2 (en) | 2005-07-22 | 2010-12-07 | State of Oregon acting by and though the State Board of Higher Education on behalf of Oregon State University | Method and apparatus for chemical deposition |
US20070047388A1 (en) * | 2005-08-25 | 2007-03-01 | Rockwell Scientific Licensing, Llc | Fluidic mixing structure, method for fabricating same, and mixing method |
DK1957794T3 (en) | 2005-11-23 | 2014-08-11 | Eksigent Technologies Llc | Electrokinetic pump designs and drug delivery systems |
US8679587B2 (en) * | 2005-11-29 | 2014-03-25 | State of Oregon acting by and through the State Board of Higher Education action on Behalf of Oregon State University | Solution deposition of inorganic materials and electronic devices made comprising the inorganic materials |
US8647590B2 (en) * | 2006-03-16 | 2014-02-11 | Agilent Technologies, Inc. | Optical detection cell with micro-fluidic chip |
US20070218454A1 (en) * | 2006-03-16 | 2007-09-20 | Brennen Reid A | Optical detection cell for micro-fluidics |
WO2007136057A1 (en) * | 2006-05-24 | 2007-11-29 | Kyoto University | Microchannel for separating blood plasma |
US7771655B2 (en) * | 2006-07-12 | 2010-08-10 | Bayer Healthcare Llc | Mechanical device for mixing a fluid sample with a treatment solution |
US20080108122A1 (en) * | 2006-09-01 | 2008-05-08 | State of Oregon acting by and through the State Board of Higher Education on behalf of Oregon | Microchemical nanofactories |
US8247464B2 (en) | 2006-09-28 | 2012-08-21 | University Of Washington | Method of selective foaming for porous polymeric material |
JP2010505393A (en) * | 2006-09-28 | 2010-02-25 | ユニヴァーシティ オブ ワシントン | 3D microscale artificial tissue model system |
US8403557B2 (en) * | 2006-09-28 | 2013-03-26 | University Of Washington | Micromixer using integrated three-dimensional porous structure |
CN101578520B (en) | 2006-10-18 | 2015-09-16 | 哈佛学院院长等 | Based on formed pattern porous medium cross flow and through biometric apparatus, and preparation method thereof and using method |
US7867592B2 (en) | 2007-01-30 | 2011-01-11 | Eksigent Technologies, Inc. | Methods, compositions and devices, including electroosmotic pumps, comprising coated porous surfaces |
US20080237044A1 (en) * | 2007-03-28 | 2008-10-02 | The Charles Stark Draper Laboratory, Inc. | Method and apparatus for concentrating molecules |
WO2008130618A1 (en) | 2007-04-19 | 2008-10-30 | The Charles Stark Draper Laboratory, Inc. | Method and apparatus for separating particles, cells, molecules and particulates |
EP2191897B1 (en) | 2007-06-21 | 2014-02-26 | Gen-Probe Incorporated | Instrument and receptacles for performing processes |
US8206025B2 (en) * | 2007-08-07 | 2012-06-26 | International Business Machines Corporation | Microfluid mixer, methods of use and methods of manufacture thereof |
US7837379B2 (en) * | 2007-08-13 | 2010-11-23 | The Charles Stark Draper Laboratory, Inc. | Devices for producing a continuously flowing concentration gradient in laminar flow |
US8251672B2 (en) | 2007-12-11 | 2012-08-28 | Eksigent Technologies, Llc | Electrokinetic pump with fixed stroke volume |
KR100912540B1 (en) | 2007-12-14 | 2009-08-18 | 한국전자통신연구원 | Chip of micro-channel network for increasing washing effect |
US8397762B2 (en) * | 2008-02-04 | 2013-03-19 | Bioscale, Inc. | Fluidic system with improved flow characteristics |
US20090211977A1 (en) * | 2008-02-27 | 2009-08-27 | Oregon State University | Through-plate microchannel transfer devices |
JP5470642B2 (en) * | 2008-03-25 | 2014-04-16 | 国立大学法人 岡山大学 | Micro droplet preparation device |
WO2009121043A2 (en) * | 2008-03-27 | 2009-10-01 | President And Fellows Of Harvard College | Cotton thread as a low-cost multi-assay diagnostic platform |
CN102016595B (en) * | 2008-03-27 | 2014-08-06 | 哈佛学院院长等 | Three-dimensional microfluidic devices |
US9829488B2 (en) * | 2008-03-27 | 2017-11-28 | President And Fellows Of Havard College | Paper-based cellular arrays |
WO2009121041A2 (en) * | 2008-03-27 | 2009-10-01 | President And Fellows Of Harvard College | Paper-based microfluidic systems |
KR101541458B1 (en) * | 2008-07-03 | 2015-08-04 | 삼성전자주식회사 | Method for Mixing Micro-fluids and Micro-fluidic Mixing Device |
US8764279B2 (en) * | 2008-07-18 | 2014-07-01 | 3M Innovation Properties Company | Y-cross mixers and fluid systems including the same |
US8846314B2 (en) * | 2009-03-03 | 2014-09-30 | The Board Of Trustees Of The Leland Stanford Junior University | Isotachophoretic focusing of nucleic acids |
PL2403645T3 (en) | 2009-03-06 | 2017-05-31 | President And Fellows Of Harvard College | Microfluidic, electrochemical devices |
US8236599B2 (en) | 2009-04-09 | 2012-08-07 | State of Oregon acting by and through the State Board of Higher Education | Solution-based process for making inorganic materials |
US8801922B2 (en) | 2009-06-24 | 2014-08-12 | State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University | Dialysis system |
ES2635219T3 (en) * | 2009-06-24 | 2017-10-02 | Oregon State University | Microfluidic devices for dialysis |
US9599407B2 (en) | 2009-07-29 | 2017-03-21 | Tokitae Llc | System and structure for heating or sterilizing a liquid stream |
US9930898B2 (en) * | 2009-07-29 | 2018-04-03 | Tokitae Llc | Pasteurization system and method |
US20110189048A1 (en) * | 2009-12-05 | 2011-08-04 | Curtis James R | Modular dialysis system |
US8753515B2 (en) | 2009-12-05 | 2014-06-17 | Home Dialysis Plus, Ltd. | Dialysis system with ultrafiltration control |
EP2531300A1 (en) | 2010-02-03 | 2012-12-12 | President and Fellows of Harvard College | Devices and methods for multiplexed assays |
DE102010003642A1 (en) * | 2010-03-15 | 2011-09-15 | Fresenius Medical Care Deutschland Gmbh | Cassette with a sensor for determining the difference between a first and a second liquid flow |
US9125305B2 (en) * | 2010-03-17 | 2015-09-01 | Delta Design, Inc. | Devices with pneumatic, hydraulic and electrical components |
DE102010018981B3 (en) * | 2010-05-03 | 2011-07-21 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V., 80686 | Process for the plasma-assisted treatment of inner surfaces of a hollow body, fluid separator and its use |
US8580161B2 (en) | 2010-05-04 | 2013-11-12 | State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University | Fluidic devices comprising photocontrollable units |
US8501009B2 (en) | 2010-06-07 | 2013-08-06 | State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University | Fluid purification system |
JP5892551B2 (en) * | 2010-06-30 | 2016-03-23 | 株式会社メタボスクリーン | Microchemical chip, method for producing the same, and method for using the same |
US9004001B2 (en) | 2010-12-17 | 2015-04-14 | Palo Alto Research Center Incorporated | Interdigitated finger coextrusion device |
US9589692B2 (en) | 2010-12-17 | 2017-03-07 | Palo Alto Research Center Incorporated | Interdigitated electrode device |
CA2834708A1 (en) | 2011-05-05 | 2012-11-08 | Eksigent Technologies, Llc | Gel coupling for electrokinetic delivery systems |
US9291547B2 (en) * | 2011-07-15 | 2016-03-22 | Nanyang Technological University | Immersion refractometer |
WO2013052680A2 (en) | 2011-10-07 | 2013-04-11 | Home Dialysis Plus, Ltd. | Heat exchange fluid purification for dialysis system |
US10221442B2 (en) | 2012-08-14 | 2019-03-05 | 10X Genomics, Inc. | Compositions and methods for sample processing |
US10400280B2 (en) | 2012-08-14 | 2019-09-03 | 10X Genomics, Inc. | Methods and systems for processing polynucleotides |
US10752949B2 (en) | 2012-08-14 | 2020-08-25 | 10X Genomics, Inc. | Methods and systems for processing polynucleotides |
US10323279B2 (en) | 2012-08-14 | 2019-06-18 | 10X Genomics, Inc. | Methods and systems for processing polynucleotides |
US11591637B2 (en) | 2012-08-14 | 2023-02-28 | 10X Genomics, Inc. | Compositions and methods for sample processing |
US10273541B2 (en) | 2012-08-14 | 2019-04-30 | 10X Genomics, Inc. | Methods and systems for processing polynucleotides |
US9951386B2 (en) | 2014-06-26 | 2018-04-24 | 10X Genomics, Inc. | Methods and systems for processing polynucleotides |
AU2013302756C1 (en) | 2012-08-14 | 2018-05-17 | 10X Genomics, Inc. | Microcapsule compositions and methods |
US9701998B2 (en) | 2012-12-14 | 2017-07-11 | 10X Genomics, Inc. | Methods and systems for processing polynucleotides |
US10533221B2 (en) | 2012-12-14 | 2020-01-14 | 10X Genomics, Inc. | Methods and systems for processing polynucleotides |
EP3567116A1 (en) | 2012-12-14 | 2019-11-13 | 10X Genomics, Inc. | Methods and systems for processing polynucleotides |
US9899669B2 (en) | 2012-12-27 | 2018-02-20 | Palo Alto Research Center Incorporated | Structures for interdigitated finger co-extrusion |
US9337471B2 (en) | 2012-12-27 | 2016-05-10 | Palo Alto Research Center Incorporated | Co-extrusion print head for multi-layer battery structures |
US9012090B2 (en) | 2012-12-27 | 2015-04-21 | Palo Alto Research Center Incorporated | Advanced, high power and energy battery electrode manufactured by co-extrusion printing |
US10923714B2 (en) | 2012-12-27 | 2021-02-16 | Palo Alto Research Center Incorporated | Structures for interdigitated finger co-extrusion |
US9590232B2 (en) | 2012-12-27 | 2017-03-07 | Palo Alto Research Center Incorporated | Three dimensional co-extruded battery electrodes |
KR102190198B1 (en) | 2013-02-08 | 2020-12-14 | 10엑스 제노믹스, 인크. | Polynucleotide barcode generation |
US9506934B2 (en) * | 2013-04-29 | 2016-11-29 | Honeywell International Inc. | Polymer test cartridge mixer for cell lysis |
US10800086B2 (en) | 2013-08-26 | 2020-10-13 | Palo Alto Research Center Incorporated | Co-extrusion of periodically modulated structures |
US9751071B2 (en) | 2013-12-27 | 2017-09-05 | State Of Oregon Acting By And Through The State Board Of Higher Education On Behalf Of Oregon State University | Continuous microwave-assisted segmented flow reactor for high-quality nanocrystal synthesis |
DE202015009494U1 (en) | 2014-04-10 | 2018-02-08 | 10X Genomics, Inc. | Fluidic devices and systems for encapsulating and partitioning reagents, and their applications |
WO2015168280A1 (en) | 2014-04-29 | 2015-11-05 | Outset Medical, Inc. | Dialysis system and methods |
MX2016016902A (en) | 2014-06-26 | 2017-03-27 | 10X Genomics Inc | Methods of analyzing nucleic acids from individual cells or cell populations. |
US9882200B2 (en) | 2014-07-31 | 2018-01-30 | Palo Alto Research Center Incorporated | High energy and power Li-ion battery having low stress and long-term cycling capacity |
JP6346298B2 (en) * | 2014-10-14 | 2018-06-20 | アルプス電気株式会社 | Fluid mixing device |
CN107002128A (en) | 2014-10-29 | 2017-08-01 | 10X 基因组学有限公司 | The method and composition being sequenced for target nucleic acid |
US9975122B2 (en) | 2014-11-05 | 2018-05-22 | 10X Genomics, Inc. | Instrument systems for integrated sample processing |
SG11201705615UA (en) | 2015-01-12 | 2017-08-30 | 10X Genomics Inc | Processes and systems for preparing nucleic acid sequencing libraries and libraries prepared using same |
EP3262407B1 (en) | 2015-02-24 | 2023-08-30 | 10X Genomics, Inc. | Partition processing methods and systems |
AU2016222719B2 (en) | 2015-02-24 | 2022-03-31 | 10X Genomics, Inc. | Methods for targeted nucleic acid sequence coverage |
US20160322131A1 (en) | 2015-04-29 | 2016-11-03 | Palo Alto Research Center Incoporated | Co-extrusion printing of filaments for superconducting wire |
US9755221B2 (en) | 2015-06-26 | 2017-09-05 | Palo Alto Research Center Incorporated | Co-extruded conformal battery separator and electrode |
US11071956B2 (en) * | 2015-08-17 | 2021-07-27 | Ton Duc Thang University | Device and process for a micromixer having a trapezoidal zigzag channel |
DK3882357T3 (en) | 2015-12-04 | 2022-08-29 | 10X Genomics Inc | Methods and compositions for the analysis of nucleic acids |
EP3408389B1 (en) | 2016-01-29 | 2021-03-10 | Purigen Biosystems, Inc. | Isotachophoresis for purification of nucleic acids |
US10107726B2 (en) * | 2016-03-16 | 2018-10-23 | Cellmax, Ltd. | Collection of suspended cells using a transferable membrane |
DE102016108258A1 (en) | 2016-05-03 | 2017-11-09 | Plan Optik Ag | Phase separation chamber and method for separation of two phases |
WO2017197338A1 (en) | 2016-05-13 | 2017-11-16 | 10X Genomics, Inc. | Microfluidic systems and methods of use |
EP3500317B1 (en) | 2016-08-19 | 2022-02-23 | Outset Medical, Inc. | Peritoneal dialysis system and methods |
US10011872B1 (en) | 2016-12-22 | 2018-07-03 | 10X Genomics, Inc. | Methods and systems for processing polynucleotides |
US10550429B2 (en) | 2016-12-22 | 2020-02-04 | 10X Genomics, Inc. | Methods and systems for processing polynucleotides |
US10815525B2 (en) | 2016-12-22 | 2020-10-27 | 10X Genomics, Inc. | Methods and systems for processing polynucleotides |
EP4029939B1 (en) | 2017-01-30 | 2023-06-28 | 10X Genomics, Inc. | Methods and systems for droplet-based single cell barcoding |
GB201703233D0 (en) * | 2017-02-28 | 2017-04-12 | Ge Healthcare Bio Sciences Ab | A modular bio-processing unit and a bio-processing system employing plural units |
CN109526228B (en) | 2017-05-26 | 2022-11-25 | 10X基因组学有限公司 | Single cell analysis of transposase accessible chromatin |
US10844372B2 (en) | 2017-05-26 | 2020-11-24 | 10X Genomics, Inc. | Single cell analysis of transposase accessible chromatin |
US11041150B2 (en) | 2017-08-02 | 2021-06-22 | Purigen Biosystems, Inc. | Systems, devices, and methods for isotachophoresis |
EP3625361A1 (en) | 2017-11-15 | 2020-03-25 | 10X Genomics, Inc. | Functionalized gel beads |
US10829815B2 (en) | 2017-11-17 | 2020-11-10 | 10X Genomics, Inc. | Methods and systems for associating physical and genetic properties of biological particles |
EP3775271A1 (en) | 2018-04-06 | 2021-02-17 | 10X Genomics, Inc. | Systems and methods for quality control in single cell processing |
US20220146400A1 (en) * | 2019-02-27 | 2022-05-12 | Kyocera Corporation | Particle separating and measuring device and particle separating and measuring apparatus |
JP6761153B1 (en) * | 2019-03-20 | 2020-09-23 | 京セラ株式会社 | Particle measurement device and particle separation measurement device and particle separation measurement device |
WO2020189572A1 (en) * | 2019-03-20 | 2020-09-24 | 京セラ株式会社 | Particle measuring device, particle separating and measuring device, and particle separating and measuring apparatus |
CN111085281B (en) * | 2020-01-08 | 2021-05-14 | 西安交通大学 | Surface acoustic wave regulated high-flux micro-droplet generation device and method |
CN113063779A (en) * | 2021-03-15 | 2021-07-02 | 埃妥生物科技(杭州)有限公司 | Sampler and mixing device of sample and reagent |
WO2023196418A1 (en) * | 2022-04-06 | 2023-10-12 | AtlasXomics Inc. | Microfluidic chip |
Family Cites Families (69)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK429682A (en) | 1982-09-28 | 1984-03-29 | Inflow Aps | INTEGRATED MICRO-ROOM SYSTEMS FOR CONTINUOUS FLOW ANALYSIS |
US4946795A (en) * | 1987-08-27 | 1990-08-07 | Biotrack, Inc. | Apparatus and method for dilution and mixing of liquid samples |
JPS6487187A (en) * | 1987-09-26 | 1989-03-31 | Kokusan Kogyo Kk | Continuous cutter for flexible blank elongated by tensile force |
US5070606A (en) | 1988-07-25 | 1991-12-10 | Minnesota Mining And Manufacturing Company | Method for producing a sheet member containing at least one enclosed channel |
US5858188A (en) | 1990-02-28 | 1999-01-12 | Aclara Biosciences, Inc. | Acrylic microchannels and their use in electrophoretic applications |
US6176962B1 (en) | 1990-02-28 | 2001-01-23 | Aclara Biosciences, Inc. | Methods for fabricating enclosed microchannel structures |
GB2244135B (en) | 1990-05-04 | 1994-07-13 | Gen Electric Co Plc | Sensor devices |
SE470347B (en) | 1990-05-10 | 1994-01-31 | Pharmacia Lkb Biotech | Microstructure for fluid flow systems and process for manufacturing such a system |
SE9100392D0 (en) | 1991-02-08 | 1991-02-08 | Pharmacia Biosensor Ab | A METHOD OF PRODUCING A SEALING MEANS IN A MICROFLUIDIC STRUCTURE AND A MICROFLUIDIC STRUCTURE COMPRISING SUCH SEALING MEANS |
US5698299A (en) | 1991-02-28 | 1997-12-16 | Dyconex Patente Ag | Thin laminated microstructure with precisely aligned openings |
US5230866A (en) | 1991-03-01 | 1993-07-27 | Biotrack, Inc. | Capillary stop-flow junction having improved stability against accidental fluid flow |
US5262127A (en) | 1992-02-12 | 1993-11-16 | The Regents Of The University Of Michigan | Solid state chemical micro-reservoirs |
US5222808A (en) | 1992-04-10 | 1993-06-29 | Biotrack, Inc. | Capillary mixing device |
US5545367A (en) | 1992-04-15 | 1996-08-13 | Soane Technologies, Inc. | Rapid prototype three dimensional stereolithography |
US5726026A (en) | 1992-05-01 | 1998-03-10 | Trustees Of The University Of Pennsylvania | Mesoscale sample preparation device and systems for determination and processing of analytes |
US5639423A (en) | 1992-08-31 | 1997-06-17 | The Regents Of The University Of Calfornia | Microfabricated reactor |
US5534328A (en) * | 1993-12-02 | 1996-07-09 | E. I. Du Pont De Nemours And Company | Integrated chemical processing apparatus and processes for the preparation thereof |
JP3512186B2 (en) | 1993-03-19 | 2004-03-29 | イー・アイ・デユポン・ドウ・ヌムール・アンド・カンパニー | Integrated structures and methods for chemical processing and manufacturing, and methods of using and manufacturing the same |
US5595712A (en) * | 1994-07-25 | 1997-01-21 | E. I. Du Pont De Nemours And Company | Chemical mixing and reaction apparatus |
US5658413A (en) | 1994-10-19 | 1997-08-19 | Hewlett-Packard Company | Miniaturized planar columns in novel support media for liquid phase analysis |
US5640995A (en) | 1995-03-14 | 1997-06-24 | Baxter International Inc. | Electrofluidic standard module and custom circuit board assembly |
DE19511603A1 (en) | 1995-03-30 | 1996-10-02 | Norbert Dr Ing Schwesinger | Device for mixing small amounts of liquid |
US5932100A (en) | 1995-06-16 | 1999-08-03 | University Of Washington | Microfabricated differential extraction device and method |
TW293783B (en) | 1995-06-16 | 1996-12-21 | Ciba Geigy Ag | |
US5856174A (en) | 1995-06-29 | 1999-01-05 | Affymetrix, Inc. | Integrated nucleic acid diagnostic device |
US5872010A (en) | 1995-07-21 | 1999-02-16 | Northeastern University | Microscale fluid handling system |
US5849208A (en) | 1995-09-07 | 1998-12-15 | Microfab Technoologies, Inc. | Making apparatus for conducting biochemical analyses |
US6130098A (en) | 1995-09-15 | 2000-10-10 | The Regents Of The University Of Michigan | Moving microdroplets |
US5658515A (en) | 1995-09-25 | 1997-08-19 | Lee; Abraham P. | Polymer micromold and fabrication process |
DE19536856C2 (en) | 1995-10-03 | 1997-08-21 | Danfoss As | Micromixer and mixing process |
DE19541266A1 (en) | 1995-11-06 | 1997-05-07 | Bayer Ag | Method and device for carrying out chemical reactions using a microstructure lamella mixer |
EP0910474B1 (en) | 1996-06-14 | 2004-03-24 | University of Washington | Absorption-enhanced differential extraction method |
WO1998000705A1 (en) | 1996-06-28 | 1998-01-08 | Caliper Technologies Corporation | Electropipettor and compensation means for electrophoretic bias |
US5921678A (en) | 1997-02-05 | 1999-07-13 | California Institute Of Technology | Microfluidic sub-millisecond mixers |
DE19708472C2 (en) * | 1997-02-20 | 1999-02-18 | Atotech Deutschland Gmbh | Manufacturing process for chemical microreactors |
GB2337113B (en) | 1997-02-28 | 2001-03-21 | Burstein Lab Inc | Laboratory in a disk |
US5904824A (en) | 1997-03-07 | 1999-05-18 | Beckman Instruments, Inc. | Microfluidic electrophoresis device |
US6235471B1 (en) | 1997-04-04 | 2001-05-22 | Caliper Technologies Corp. | Closed-loop biochemical analyzers |
US5932315A (en) | 1997-04-30 | 1999-08-03 | Hewlett-Packard Company | Microfluidic structure assembly with mating microfeatures |
US5869004A (en) | 1997-06-09 | 1999-02-09 | Caliper Technologies Corp. | Methods and apparatus for in situ concentration and/or dilution of materials in microfluidic systems |
US5882465A (en) | 1997-06-18 | 1999-03-16 | Caliper Technologies Corp. | Method of manufacturing microfluidic devices |
US5771810A (en) | 1997-06-25 | 1998-06-30 | Eastman Kodak Company | Continuous tone microfluidic display and printing |
US5932799A (en) | 1997-07-21 | 1999-08-03 | Ysi Incorporated | Microfluidic analyzer module |
US6007775A (en) | 1997-09-26 | 1999-12-28 | University Of Washington | Multiple analyte diffusion based chemical sensor |
US6136272A (en) | 1997-09-26 | 2000-10-24 | University Of Washington | Device for rapidly joining and splitting fluid layers |
US5842787A (en) | 1997-10-09 | 1998-12-01 | Caliper Technologies Corporation | Microfluidic systems incorporating varied channel dimensions |
US5945203A (en) | 1997-10-14 | 1999-08-31 | Zms Llc | Stratified composite dielectric and method of fabrication |
US6803019B1 (en) | 1997-10-15 | 2004-10-12 | Aclara Biosciences, Inc. | Laminate microstructure device and method for making same |
US6074725A (en) | 1997-12-10 | 2000-06-13 | Caliper Technologies Corp. | Fabrication of microfluidic circuits by printing techniques |
US6050719A (en) | 1998-01-30 | 2000-04-18 | Affymetrix, Inc. | Rotational mixing method using a cartridge having a narrow interior |
EP1046032A4 (en) * | 1998-05-18 | 2002-05-29 | Univ Washington | Liquid analysis cartridge |
US6494614B1 (en) * | 1998-07-27 | 2002-12-17 | Battelle Memorial Institute | Laminated microchannel devices, mixing units and method of making same |
US6482306B1 (en) | 1998-09-22 | 2002-11-19 | University Of Washington | Meso- and microfluidic continuous flow and stopped flow electroösmotic mixer |
US6572830B1 (en) | 1998-10-09 | 2003-06-03 | Motorola, Inc. | Integrated multilayered microfludic devices and methods for making the same |
BR9914554A (en) | 1998-10-13 | 2001-06-26 | Biomicro Systems Inc | Fluid circuit components based on passive fluid dynamics |
US6193471B1 (en) | 1999-06-30 | 2001-02-27 | Perseptive Biosystems, Inc. | Pneumatic control of formation and transport of small volume liquid samples |
AU7808800A (en) | 1999-10-20 | 2001-04-30 | University Of Sheffield, The | Fluidic mixer |
US6537506B1 (en) * | 2000-02-03 | 2003-03-25 | Cellular Process Chemistry, Inc. | Miniaturized reaction apparatus |
CA2404008A1 (en) | 2000-03-31 | 2001-10-11 | Jurgen Sygusch | Protein crystallization in microfluidic structures |
US6561208B1 (en) * | 2000-04-14 | 2003-05-13 | Nanostream, Inc. | Fluidic impedances in microfluidic system |
US20010048637A1 (en) | 2000-05-24 | 2001-12-06 | Weigl Bernhard H. | Microfluidic system and method |
WO2001090614A2 (en) | 2000-05-24 | 2001-11-29 | Micronics, Inc. | Surface tension valves for microfluidic applications |
CN100394171C (en) | 2000-08-02 | 2008-06-11 | 卡钳技术有限公司 | High throughput analysis system based on separation |
WO2002022267A2 (en) | 2000-09-18 | 2002-03-21 | Micronics, Inc. | Externally controllable surface coatings for microfluidic devices |
WO2002023161A1 (en) | 2000-09-18 | 2002-03-21 | University Of Washington | Microfluidic devices for rotational manipulation of the fluidic interface between multiple flow streams |
US7223363B2 (en) | 2001-03-09 | 2007-05-29 | Biomicro Systems, Inc. | Method and system for microfluidic interfacing to arrays |
US6418968B1 (en) * | 2001-04-20 | 2002-07-16 | Nanostream, Inc. | Porous microfluidic valves |
US6919046B2 (en) * | 2001-06-07 | 2005-07-19 | Nanostream, Inc. | Microfluidic analytical devices and methods |
US20030123322A1 (en) | 2001-12-31 | 2003-07-03 | Industrial Technology Research Institute | Microfluidic mixer apparatus and microfluidic reactor apparatus for microfluidic processing |
-
2001
- 2001-08-03 WO PCT/US2001/024521 patent/WO2002011888A2/en not_active Application Discontinuation
- 2001-08-03 AU AU2001281076A patent/AU2001281076A1/en not_active Abandoned
- 2001-08-03 EP EP01959530A patent/EP1309404A2/en not_active Withdrawn
-
2002
- 2002-04-23 US US10/131,969 patent/US6676835B2/en not_active Expired - Fee Related
-
2003
- 2003-05-21 US US10/444,041 patent/US6935772B2/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
US20020113009A1 (en) | 2002-08-22 |
US6676835B2 (en) | 2004-01-13 |
US6935772B2 (en) | 2005-08-30 |
EP1309404A2 (en) | 2003-05-14 |
US20030198130A1 (en) | 2003-10-23 |
AU2001281076A1 (en) | 2002-02-18 |
WO2002011888A3 (en) | 2003-01-03 |
WO2002011888A2 (en) | 2002-02-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US6676835B2 (en) | Microfluidic separators | |
US6890093B2 (en) | Multi-stream microfludic mixers | |
US6877892B2 (en) | Multi-stream microfluidic aperture mixers | |
CA2304572C (en) | Microfluidic systems incorporating varied channel depths | |
Fidalgo et al. | Surface-induced droplet fusion in microfluidic devices | |
US6851846B2 (en) | Mixing method, mixing structure, micromixer and microchip having the mixing structure | |
Kim et al. | A serpentine laminating micromixer combining splitting/recombination and advection | |
US6729352B2 (en) | Microfluidic synthesis devices and methods | |
KR100540143B1 (en) | Microfluidic control device and method for controlling microfluidic | |
US6481453B1 (en) | Microfluidic branch metering systems and methods | |
EP1453606B1 (en) | Microfluidic devices with distributing inputs | |
US8226907B2 (en) | Microfluidic devices and methods of making the same | |
KR100666500B1 (en) | Serpentine laminating chaotic micromixer | |
US20020023841A1 (en) | Electrohydrodynamic convection microfluidic mixer | |
EP1392436B1 (en) | Microfluidic fraction collectors | |
KR101113727B1 (en) | Vertical lamination micromixer | |
KR20100004262A (en) | Method for mixing micro-fluids and micro-fluidic mixing device | |
Schmidt et al. | Open flow microreactors | |
KR100860872B1 (en) | A fault type micro channel | |
Wu et al. | A novel microdroplet cassette for biochemical screening |
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 BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ PL PT RO RU SD SE SG SI SK SL TJ TM TR TT TZ UA UG UZ VN YU ZA ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A2 Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZW AM AZ BY KG KZ MD RU TJ TM AT BE CH CY DE DK ES FI FR GB GR IE IT LU MC NL PT SE 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 | ||
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2001959530 Country of ref document: EP |
|
WWP | Wipo information: published in national office |
Ref document number: 2001959530 Country of ref document: EP |
|
REG | Reference to national code |
Ref country code: DE Ref legal event code: 8642 |
|
NENP | Non-entry into the national phase |
Ref country code: JP |
|
WWW | Wipo information: withdrawn in national office |
Ref document number: 2001959530 Country of ref document: EP |