|Publication number||US3759374 A|
|Publication date||Sep 18, 1973|
|Filing date||Jun 30, 1970|
|Priority date||Jul 3, 1969|
|Also published as||DE1933689A1|
|Publication number||US 3759374 A, US 3759374A, US-A-3759374, US3759374 A, US3759374A|
|Inventors||Baumer W, Hartel A, Helger R, Stein A|
|Original Assignee||Merck Patent Gmbh|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (10), Referenced by (36), Classifications (13)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent 1191 Helger et al.
[ Sept. 18, 1973 CUVETTE  Inventors: Roland Helger; Arnold l-lartel;
Alfred Stein; Wilhelm Baumer, all of Darmstadt, Germany  Assignee: Merck Patent Gesellschatt mit beschankter Hattung, Darmstadt, Germany 22 Filed: June 30,1970 211 Appl. No.: 51,048
 Foreign Application Priority Data July 3, 1969 Germany P 19 33 689.1
 References Cited UNITED STATES PATENTS 10/1941 Stevens 356/246 3,579,306 5/1971 Crane 206/47 A 3,673,302 6 1972 Halsall 264 334 2,783,908 3/1957 Winfield 215 37 R 3,503,493 3/1970 Nagy 206/56 AB 2,138,241 11 1938 Koch et al. 206 4534 2,018,005 10 1935 Barnby 206 65 E 2,549,574 4/1951 condirf 356/246 2,949,710 8/1960 Wheeler 264/334 FOREIGN PATENTS OR APPLICATIONS 9/1965 Great Britain 206 65 R Primary Examiner-William T. Dixson, Jr. Attorney-Milieu, Raptes and White  ABSTRACT 9 Claims, 3 Drawing Figures PATENTEU 31973 INVENTORS ROLAND HELGIER ARNOLD HARTEL ALFRED STEIN WILHELM BAUMER wz nm ATTORNEYS BACKGROUND OF THE INVENTION This invention relates to a cuvette for holding solids or liquids adaptable for the optical measurement of analytical samples.
The rapid growth of analytical chemistry favored two directions of development in recent years, viz., on the one hand, the manufacture of automatic analyzers which automatically conduct even the complicated working steps of specimen processing, and, on the other hand, the development of simple methods and techniques which enable even unskilled personnel to conduct reliable analyses. Particularly suitable for such developments are photometric measurements, wherein it is often merely necessary to mix a measured amount of sample with a measured volume of reagent, and introduce the mixture into the measuring cuvette of a photometer.
There has been a great number of attempts to simplify the operating steps during the photometric measuring procedure and to relieve the analyst of as much work as possible by mechanically produced, convenient forms of the reagents. For example, the reagent solution required for a single determination can be supplied in individual small bottles which are made available to the analyst ready for use. When the shelf life of the solution is too short, the reagent mixtures can be supplied in individual, single use small bottles or plastic capsules, either by introducing the solid substances directly, or by metering the solution into the individual containers and then freeze-drying the. solution therein In the last-mentioned form, such finished reagents have found wide application.
Particularly useful are cuvettes which can serve both as a storage vessel for the reagent as well as a container for measuring the analysis sampleshSu ch cuvettes can be manufactured in good quality at very low prices from transparent and dimensionally stable material, especially plastics, so that it is economically feasible to use them only once. In addition to the fact that the analyst saves the expense of buying expensive glass or quartz cuvettes and the time required to fill them with the reagents, one-time usage offers the advantage that the cleaning and the drying (or the intermediate rinsing) of the cuvette after each measuring step arefeliminated. For these reasons, disposable single-use plastic cuvettes are presently employed in most of the discontinuousautomatic analyzers.
In the manual technique, the plastic cuvette has not received widespread acceptance heretofore, especially those which are adapted to serve both as the storage container for the reagents for a single determination and for the optical measurement or the visual evaluation of the analytical sample. The reason apparently is v the lack of a simple closure device. Because of the measuring techniques employed, rectangular or square internal cross sections or basal surfaces arepreferred.
Because of the molding techniques employed in injection molding, the aperture cross section must not be smaller than the internal cross section, so that the inner surfaces of the cuvette form a truncated pyramid with an inclination of the side wall of -5. Consequently, rectangular or square apertures are produced which are difficult to seal. To solve this problem, it has been suggested, for example, to glue to the normal square opening of the cuvette ahead portion of plastic having device. Furthermore, both of these sealing possibilities either require very complicated special machines to attach the plugs or caps, or they require manual labor to do so, which makes the sealing process even more expensive.
OBJECTS OF THE INVENTION It is therefore an object of this; invention to provide 7 novel inexpensive disposable rectangular and square cuvettes. It is another object to providesuch cuvettes adapted to be used as the container for an analytical sample during photometric analysis thereof. It is another object to provide such cuvettes also adapted to be used as a storage vessel for a reagent employed in such photometric analysis. It is another object to provide a method for sealing such cuvettes; It is still another object to provide a method for producing a plurality of such sealed cuvettes which are separablyjoined together. Other objects will be apparent to those skilled in the art to which this invention pertains.
SUMMARY OF THE INVENTION According to this invention, thesealing of filled cuvette s having a rectangular or square aperture is accomplished in a simple and inexpensive manner by bonding, e.g., gluing, welding or sealing a film or foil to the upper edges of the side walls defining the aperture.
Although closing apertures of containers by gluing film or paper thereon has, for a long period of time, conventionally been employed, for example, in the packaging of foodstuffs, it was surprising such means could be employed to seal cuvettes having a square or rectangular aperture which would meet the high. requirements of leakproofness, chemiccal stability, impermeability and pressureinsensitivity, which must be satisfied by a cuvette seal despite the narrow bonding area provided by the thin upper edge of the vertical walls of the cuvette- DRAWINGS With reference to the drawings: FIG. 1 is a perspective invention;
FIG. 2 is a side elevation of a plurality of cuvettes of this invention joined together by the sealing means;*and FIG. 3'is a perspective view of a plurality of cuvettes shown'in FIG. 2 joined by a common sealing means.
DETAILED DISCUSSION in arr-aperture which is sealed, after the desired subview of a single cuvette of this stance or substances have been added thereto, with a film or foil 3 by gluing, welding or sealing.
The outer surface of the upper end of each of the four side walls 2 of cuvette 10 have a recessed portion 4 of reduced thickness extending to the upper edge of the side wall and forming a shoulder in the outer surface of the side wall. As shown in FIGS. 2 and 3, when the apertures of a plurality of cuvettes 2 in closely packed proximity with each other are sealed by a large common film or foil 3a, the indented portions 4 and shoulders 5 of adjacent cuvettes and the portion of the film or foil 3a above form a cavity 6 which facilitates separating the cuvettes by cutting the film or foil with a knife, pencil or other sharp or pointed utensil. Cutting of the common web 3a can be facilitated by optional score or printed guidelines 7. The upper surface of the film or foil 3a is printed with indicia identifying the contents of the cuvette.
The cuvettes of this invention can be formed of glass, quartz, or, preferably, plastic and are transparent, at least in the zone of the beam path, in the wavelength range to be measured, e.g., 200-800 nanometersor a partial range thereof.
Preferred materials are plastics which can be formed into cuvettes by injection molding, for example, polystyrene or polymethacrylates and, in particular, polymethacrylates formed from lower-alkyl methacrylates, e.g., polymethyl, ethyl, propyl, isopropyl, n-butyl or tert.-butyl methacrylate, or mixed polymeric esters of methacrylic acid with various, especially lower, alcohols. Polymethyl methacrylate and polyethyl methacrylate are especially suitable, since they have good transmissibility in the ultraviolet range and thus permit measurements in the UV range without large loss of energy. The novel cuvette can also be formed from cellulose esters, such as for example, cellulose or butyrate, or mixed esters of cellulose with various, especially lower, carboxylic acids, especially cellulose acetates/butyrates, for example, those sold under the tradename Acetobutyrat. Also suitable are ionic carboxylgroup-containing ethylene copolymers which can optionally be cross-linked, for example, polymers of ethylene and other unsaturated monomers, e.g., acrylic acid derivatives, especially those polymers sold under the trademark Surlyn A." Polymeric carbonic acid esters of aromatic bisphenols, e.g., those sold under the trademark Makrolon, can also be used.
The plan form of the cuvette, i.e., its base cross section and aperture, is preferably square with an optical path length inner edge length of the plan form) of 10 mm. The cuvette preferably has a height of 30-60 mm. The outer walls of the cuvette are preferably plane-parallel. However, they can also beformed into other shapes suitable for optical measurement. For example, the outer surfaces of the side walls can form an angle with the vertical, for instance of the same order of magnitude as the inner surfaces thereof. The wall thickness of the cuvette is preferably 0.3 10 mm., especially l 5 mm. The dimensions of the square or rectangular aperture preferably corresponds to the entire inner cross section of the cuvette.
To seal the cuvettes, a metal or metal alloy foil, preferably aluminum, or film (plastic or paper) can be employed. The foil or film can be rigid, self-supporting or non-self-supporting and can be of a thickness of 5 1,000 n, preferably 20-50 lb. Laminated foils and films (which term includes sheets of paper) can also be em- 4 ployed. If the film or foil is not self-bonding, it can be provided with a layer of adhesive on one face thereof, preferably adhesives of the hot glue type which, at
, room temperature, establish a very tight bond between the cuvette and the foil and are inert at the non-bonded area. Suitable foils provided with a layer of hot glue are commercially available. Especially tight bonds between aluminum foils and polymethacrylate cuvettes are obtained, for example, by applying the commercial adhesive V 274/6 (producer: Ardal-Klebstoffwerke, Mainz) to the foil, either in a molten condition or dissolved in a solvent. A uniform layer can be obtained by spreading the solution, applying it by a roller, or, best of all, by spraying. Thereafter, the solvent is allowed to evaporate, optionally at a higher temperature. Before or after applying the adhesive layer to the foil, the opposite face of the foils can be subjected to a continuous printing process in accordance with the conventional methods, suitably in such a manner that, later on, each cuvette seal bears at least once the text describing the contents. It is also possible to apply the layer of adhesive to the upper edge of the sides of the cuvette which define the aperture, rather than to the foil, or to both.
When using a foil or film formed of a material which, when heated, will bond itself to the upper edge of the side walls of the cuvette by softening the film or foil or the upper edge of the side walls, or both, the adhesive can be omitted.
The cuvette can be sealed by placing the surface of the film or foil coated with the adhesive layer in contact with the upper edges of the side walls 2 of the cuvette 10 and pressing it into place with a planar plate. When a hot glue is employed, the plate is heated to the temperature required to soften the glue, e.g., C. For example, when a small number of cuvettes is involved, a normal household iron can be used as the heated plate. When a plurality of cuvettes are sealed simultaneously, the sealing step is conducted analogously to the sealing of a single cuvette, viz., with a heatable metallic plate. However, when a large number of cuvettes must be sealed simultaneously, they are preferably disposed on a planar surface. It is advantageous to employ a slightly resilient plate, or a plate covered with foam material, so that the cuvettes during sealing areresiliently pressed against the foil, and small differences in height canbe compensated for. In order to be able to arrange the cuvettes readily in rows, they are advantageously placed in a wood, metal, or plastic frame. Because of the satisfactory alignment thereby attained, the film or foil 3a can later readily be severed to separate the cuvettes into single units, as shown in FIG. 1.
In a special embodiment of the method of making the cuvettes of this invention, the cuvette is first provided with a temporary seal. Such a seal is of interest when the reagent in the cuvette is to be freeze-dried and must be sealed, for preservation reasons, under a nitrogen atmosphere in the lyophilizing chamber. In this case, the film or foil can be attached to the plates disposed above the plates supporting the. cuvettes. After the freeze-drying step, dry nitrogen is introduced into the chamber. Due to the sealing hydraulics, with the chamber closed, the foil is pressed so firmly against the cuvettes that a temporary seal is obtained. The permanent or final seal is achieved with the aid of a heated metal plate in the manner described above after the chamber has been'opened.
The cuvette seals produced in this manner provide a very good seal. They can withstand an internal pressure of about 2 atmospheres gauge or more. Yet, later on, the'sealing foil or film can very easily be removed during use by tearing off the film or foil. Alternatively, it is also possible to simply penetrate the foil, to put the cuvette to use, using the tip of the measuring pippette used to introduce the liquid sample into the cuvette.
The many advantages resulting from the use of the plastic cuvette of this invention, which considerably enhance the economical use thereof, could not be foreseen. These advantages become particularly apparent when large individual numbers (100 100,000, especially 1,000 10,000 per batch) must be sealed. It is not necessary, as with conventional closures, to apply the plugs individually. instead, the foil to which the adhesive has been applied is simply placed, as described above, on the cuvettes which are disposed closely adjacent to one another in a frame. By pressing a planar metall plate thereon, all cuvettes are simultaneously glued with their upper edges to the foil. Only after the sealing step is the foil severed between the cuvettes, for example, by' cutting.
As described above, the cuvettes are expediently provided on the outer upper edge, with a recessed portion 4 which acts as a guide for a blade during the cutting process which separates the cuvettes joined by a common film or foil 3a. The shoulder 5 advantageously has a width of about 0.2 1 mm. and the recessed portion 4 has a height of about 0.2 mm. However, the width of this recessed portion-must be dimensioned so that the upper edges of the side walls 2 defining the aperture of the cuvette have a minimum thickness of about 0.2 mm, and preferably thickness of 0.8 1.2 mm. It is, of course, also possible to employ cuvettes having, in place of a recessed outer face, an outwardly beveled or an outwardly rounded upper edge to provide the cavity which guides the'cutting means.
Since single-use cuvettes are advantageously sold packaged in a bundle, it is advantageous not to separate all the cuvettes which are sealed by a common foil or film 3a from each other, but instead first cut the cuvettes into bundles required for packaging reasons, as shown in FIG. 2. Thus, contrary to conventional processes, the sorting of individual cuvettes into packaged bundles is eliminated. A still further working step is omitted, viz., the labeling of each individual cuvette, since it is possible without difficultieswto employ preprinted foils for sealing the cuvettes. Furthermore, contrary to conventional processes,complicated machines for applying the plugs, for labeling, and for sorting of individual cuvettes into packaged bundles is likewise eliminated. FIG. 2 of the drawings shows such a packaged bundle in a lateral view.
The advantages of the novel single use one-way cuvette" becomes abundantly apparent when it serves simultaneously as the supply'and storage container for a measured amount of reagent, for example when the cuvette contains'a substrate/buffer mixture for kinetic enzyme determinations. Examples of such substratelbuffer mixtures are:
a. Potassium phosphate, monobasic; potassium phosphate, dibasic; sodium pyruvate; NADH, (dihydronicotinic acid amide adenine dinucleotide, which, when dissolved in water, is a reagent for lactate dehydrogenase determination). T
b. Potassium phosphate, monobasic; potassium phosphate, dibasic; DL-alanine; NADH,; and lactate dehydrogenase (for determining glutamatepyruvate transaminase); and t I c. Potassium phosphate, monobasic; potassium phosphate, dibasic; sodium-L-asparaginate; NADH,; and malate dehydrogenase (for the determination of glutamate-oxalacetate transaminase).
After the solution to be tested has been added, the measurement can immediately be conducted, without danger of contamination or loss of reagent during refill ing. When a mixture of several reagents are required which, as a mixture are stable for only a short period of time, the novel cuvette can be provided with a partition separating the lower portion of the cuvette into two chambers. The mutually incompatible auxiliary substances can be introduced in metered quantities into these chambers, e.g., in the form of solutions, with subsequent freeze-drying. After the measured amount of solution has been added, the reactants can be combined by shaking.
The cuvettes, or bundles of cuvettes, are preferably packed into a metal container or in a metallic foil, op-. tionally in the form of packaged bundles, optionally with the addition of a drying agent.
Without further elaboration, it is believed that one skilled in the art can, using the preceding description, utilize the present invention to itsfullest extent. The following preferred specific embodiments are, therefore, to be construed as'merely illustrative, and not limitative of the remainder of the disclosure in any way whatsoever.
' I EXAMPLE 1 a. Coating the Sealing Foil with a Layer of a Hot Glue Two-hundred grams of Ardal V 274/6 contact cement is dissolved in 2 liters of chloroform, and applied by spraying to one side of a commercial alumi'numfoil of 30p. thickness, the other side of which has been pro vided with a continuous imprint of the text of the identifying label. Thereafter, the foil is heated for about 10 minutes to 110 C.
b. Preparation of the Cuvettes for Sealing The plastic cuvettes, filled with reagent, are placed upright on a mat of foam material having a thickness of 5 mm., which mat is disposed on a planar surface. With the aid of a frame, the cuvettes are pushed together until they are packed closely adjacent one another, so that the idented portion 4 (grooves) of the cuvettes form continuous channels.
c. Sealing Process and Cutting I The side of the foil coated with the layer of hot glue,
' is placed face down on the cuvettes and, to protect the labeling from being scratched, a second, uncoated aluminum foil is placed thereover. Then, pressure and heat are applied to the upper face of the foil for about 15 seconds with a household iron adjusted to 150 C. (wool). Thereafter, the foil is cut in the channels formed by the indented portion (grooves) of the cuvettes with a nife.
EXAMPLE 2 One kg. of Ardal V274/6 contact cement is melted and mixed with ml. of chloroform. The solution is introduced into a foil spreading machine wherein the solution runs, without the use of rolls, directly onto the aluminum foil disposed underneath the storage tank.
The foil moves at a speed of cm./min. beneath the applicator blade, and is coated during this procedure with a thin film of adhesive. After passing a drying channel and cooling, the foil is again reeled up on a drum, suitably with the interposition of a separating paper (e.g., siliconized paper), to prevent the foil from sticking together.
The cuvettes are sealed as described in Examples 1(b) and 1(c).
EXAMPLE 3 Production of a Reagent Preparation for the Quantitative Determination of Glutamate-Oxalacetate Transaminase (GOT).
Approximately 6,000 plastic cuvettes are packed as densely as possible in three metallic frames and rigidly mounted thereon with setscrews. Then the cuvettes in the frames are rinsed. The cuvettes are allowed to dripdry, and then each are filled with a filling machine at a rate of 50/minute with 1 ml. of a solution containing the following components per 500 ml.:
0.05 M of ethylenediaminetetraacetic acid 0.10 M of phosphate buffer (NaI-l PO /Na,HPO
0.25 M of aspartic acid 0.01 M of ketoglutaric acid 2 X 10 M of dihydronicotinic acid amide adenine dinucleotide (NADH 10 mg. of malate dehydrogenase (MDH) 10 mg. of lactate dehydrogenase (LDH) For the subsequent freeze-drying step, a device is utilized having four temperature-controllable plates. The uppermost plate serves as radiation protection, and the lower three plates serve as supporting plates. The arrangement also contains a hydraulic unit with which the plates can later be pressed together.
The adhesive coated aluminum foil, produced as described in Example 2, is attached to the undersides of the upper three plates so that the printed side is oriented upwardly and the side having the coating of hot glue is directed downwardly. The three frames with the filled cuvettes are placed on the three lower plates, and a freeze-drying process is conducted in a conventional manner. After introducing a nitrogen atmosphere, but before opening the chamber, the plates and thus also the cuvettes positioned between the plates and the foil, are pressed one to the other with the aid of the hydrau-- lic unit for a short period of time. When the frames with the cuvettes are withdrawn from the chamber, the foil adheres to the cuvettes so tightly that the nitrogen cannot escape. Thereafter, a plate heated to 150 C. is pressed for 30 seconds against the foil, which tightly seals the foil to the upper rim of the cuvette. The foil between the cuvettes is cut by guiding ablade along in the channels formed by the indented upper portion 4 of adjacent cuvettes. Not all of the cuvettes are separated from one another. Instead, the foil is cut so as to leave, e.g., 25 cuvettes together in a bundle. -After releasing the setscrews, the bundles of cuvettes, filled with reagent, sealed, and labeled, can be withdrawn from the frame and further packaged.
For use purposes, a single cuvette is separated from the bundle, simultaneously removing the foil closure. Two ml. of water and 0.5 ml. of the serum to be examined are added thereto, the components are mixed, and the reduction of extinction (A E per minute) is measured at 366 nanometers (1 cm. layer thickness). The
GOT concentration is calculated in accordance with the following-formula:
GOT Concentration A E/min. X1.515 U/ml.
(U international enzyme unit) Analogously, a reagent preparation for determining glutamate-pyruvate transaminase concentration is produced from a solution which, prior to the freeze-drying step, contains the following components (per 500 ml.):
0.1 M of phosphate buffer, pH 7.4
0.8 M of DL-alanine 0.01 M of a-ketoglutaric acid 2 X 10 M of NADH, and
10 mg. of LDH To measure the LDH concentration, the solution contains 2 X 10 M of NADH in 0.02 M of bicarbonate buffer, pH 9.5. In this case, the freeze-dried product is dissolved in a 6 X 10" M of pyruvate solution in 0.l M of phosphate buffer, pH 7.4, rather than in water.
EXAMPLE 4 A commercial hot melt film (silicon paper with a coating of hot glue) is pressed, with the aid of an iron, heated roll or other suitable heated device, for a few seconds onto printed paper at about C. After cooling, the silicon paper can be readily pulled from the printed paper, to which the hot glue adheres completely. The printed paper, provided with a layer of this hot glue, is employed for sealing the cuvettes in accordance with Examples 1(b) and 1(0).
The preceding examples can be repeated with similar success by substituting the generically or specifically described reactants and/or operating conditions of this invention for those used in the preceding examples.
From the foregoing description, one skilled in the art can easily ascertain the essential characteristics of this invention, and without departing from the spirit and scope thereof, can make various changes and modifica tions of the invention to adapt it to various usages and conditions.
What is claimed is:
1. A sealed cuvette having a rectangular or square basal surface and side walls whose inner surfaces form a truncated pyramid having a side wall inclination of 0-5 and whose upper edges form a rectangular or square aparature corresponding in dimensions to the inner cross section of the cuvette and whose side walls have a recessed outer face at their upper end which forms a shoulder in said side walls extending to their upper edge, formed of a transparent and dimensionally stable plastic which is light-permeable in at least a portion of the wavelength range from 200-800 nanometers and adapted for string solids and liquids and for the optical measurement of analytical samples, said aperture being sealed by a foil or film bonded to said upper edge of said side walls.
2. A cuvette according toclaim 1, formed of polystyrene.
3. A cuvette according to claim 1, formed of polymethyl methacrylate.
4. A cuvette according to claim 1, whose aperture is sealed with aluminum foil.
5. A cuvette according to claim 1 wherein said foil or film bears identifying indicia on its outer surface.
6. A cuvette according to claim 5 whose aperture is sealed with aluminum foil.
7. A plurality of cuvettes according to claim 1 whose film bears identifying indicia on its outer surface. side walls are in face-to-face contact and which are 9. A cuvette according to claim 2 whose aperture is joined together by the film or foil sealing their aperture. sealed with aluminum foil.
8. A cuvette according to claim 7 wherein said foil or
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US2018005 *||Nov 17, 1933||Oct 22, 1935||Owens Illinois Glass Co||Sealing means for empty containers|
|US2138241 *||Aug 9, 1935||Nov 29, 1938||Koch Herman||Sealed package|
|US2258073 *||Jan 12, 1939||Oct 7, 1941||Daniel S Stevens||Disposable colorimeter cell|
|US2549574 *||Jul 8, 1948||Apr 17, 1951||Archer Daniels Midland Co||Apparatus for making fluorophotometric measurements|
|US2783908 *||Feb 9, 1954||Mar 5, 1957||Glaxo Lab Ltd||Closures for bottles, vials and the like|
|US2949710 *||Sep 16, 1958||Aug 23, 1960||Airkem Inc||Gel packaging method and resulting package|
|US3503493 *||Jan 8, 1968||Mar 31, 1970||Hoffmann La Roche||Medicament packaging device|
|US3579306 *||Jan 22, 1969||May 18, 1971||Organon||Diagnostic test device|
|US3673302 *||Aug 19, 1968||Jun 27, 1972||Globe Union Inc||Method for fabricating battery cases|
|GB1004176A *||Title not available|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US3968876 *||Mar 19, 1975||Jul 13, 1976||Brookfield Richard A||Sealed container with a sterilized hypodermic needle within it and method for effecting the sealing thereof|
|US4154795 *||Jul 21, 1977||May 15, 1979||Dynatech Holdings Limited||Microtest plates|
|US4198484 *||Jul 26, 1978||Apr 15, 1980||Abbott Laboratories||Cuvette ampule for use with automatic analyzer apparatus|
|US4249826 *||Jul 19, 1978||Feb 10, 1981||Laboratoires Biotrol S.A.||Method and device for analyzing and measuring out constituents of solid or liquid media|
|US4251159 *||Jan 15, 1979||Feb 17, 1981||American Hospital Supply Corporation||Disposable multi-chamber cuvette|
|US4472357 *||Nov 18, 1981||Sep 18, 1984||Medical Laboratory Automation, Inc.||Blood bank cuvette cassette and label therefor|
|US4751186 *||Feb 15, 1985||Jun 14, 1988||Eppendorf Geratebau Netheler & Hinz Gmbh||Process for performing sample analyses and rack for performing the process|
|US5401465 *||May 5, 1992||Mar 28, 1995||Chiron Corporation||Luminometer with reduced sample crosstalk|
|US5514343 *||Jun 22, 1994||May 7, 1996||Nunc, As||Microtitration system|
|US5716583 *||Mar 28, 1995||Feb 10, 1998||Smethers; Rick T.||Luminometer with reduced sample crosstalk|
|US5720924 *||Mar 1, 1996||Feb 24, 1998||Boehringer Mannheim Gmbh||Storage system for test elements|
|US5863800 *||Sep 22, 1997||Jan 26, 1999||Boehringer Mannheim Gmbh||Storage system for test elements|
|US6328164||Nov 10, 1997||Dec 11, 2001||Kone Instruments Oy||Multicell cuvette package, method of loading multicell cuvettes into a measurement instrument and a dispensing device for loading cuvettes|
|US6333008 *||Sep 28, 1999||Dec 25, 2001||Stratec Eletronik Gnbh||Measuring system and method for performing luminometric series analyses as well as multiple cuvette for receiving liquid samples therefor|
|US7098035||Nov 16, 2001||Aug 29, 2006||Thermo Electron Oy||Multicell cuvette package, method of loading multicell cuvettes into a measurement instrument and a dispensing device for loading cuvettes|
|US7353953 *||Sep 21, 2004||Apr 8, 2008||Ortho-Clinical Diagnostics, Inc.||Packaging of multiple fluid receptacles|
|US7517499 *||Sep 25, 2002||Apr 14, 2009||Ibidi Gmbh||Flow chamber|
|US7674433 *||Mar 18, 2004||Mar 9, 2010||The Automation Partnership (Cambridge) Limited||Tube for storing fluid|
|US8197776 *||May 27, 2009||Jun 12, 2012||Thermo Fisher Scientific Oy||Reaction vessel and method for the handling thereof|
|US20020009397 *||Jun 6, 2001||Jan 24, 2002||Taisuke Hirono||Cuvette stand and stand with cuvettes|
|US20020027093 *||Nov 16, 2001||Mar 7, 2002||Konelab Corporation||Multicell cuvette package, method of loading multicell cuvettes into a measurement instrument and a dispensing device for loading cuvettes|
|US20040226984 *||Mar 18, 2004||Nov 18, 2004||Smith Philip Russel James||Tube for storing fluid|
|US20050019231 *||Sep 25, 2002||Jan 27, 2005||Kahl Johan Valentin||Flow chamber|
|US20050079622 *||Sep 21, 2004||Apr 14, 2005||Davis Freeman||Packaging of multiple fluid receptacles|
|US20110064543 *||May 27, 2009||Mar 17, 2011||Thermo Fisher Scientific Oy||Reaction vessel and method for the handling thereof|
|US20120292220 *||Feb 22, 2011||Nov 22, 2012||Vesa Nuotio||Handling package of cuvettes|
|USRE30391 *||Feb 23, 1976||Sep 2, 1980||Abbott Laboratories||Chemical analysis cuvette|
|USRE34133 *||Jun 30, 1988||Nov 24, 1992||Dynatech Holdings, Ltd.||Microtest plates|
|DE2711853A1 *||Mar 18, 1977||Sep 21, 1978||Eppendorf Geraetebau Netheler||Gefaessverbund mit einer mehrzahl von kuevetten oder reaktionsgefaessen und haltevorrichtung fuer einen solchen verbund|
|DE4217868A1 *||May 29, 1992||Dec 2, 1993||Univ Schiller Jena||Temp.-controlled multiple test tube for optical study of liquids - has upper and lower aluminium plates having openings into which test tubes are placed at least one plate has surface foil heating element|
|DE4405375A1 *||Feb 19, 1994||Aug 24, 1995||Fritz Nerbe Nachfolger Juergen||Mikrotiterplatte|
|DE19736630A1 *||Aug 22, 1997||Mar 11, 1999||Schott Glas||Microtitration plate comprising adhered assembly of glass vessels|
|EP0843171A2 *||Nov 6, 1997||May 20, 1998||KONE Instruments Oy|
|EP1234614A1 *||Feb 27, 2001||Aug 28, 2002||Pentapharm Gmbh||Metering vessel subdivided by ribs for receiving reagents, its fabrication and use|
|EP1524036A2 *||Oct 13, 2004||Apr 20, 2005||Ortho-Clinical Diagnostics, Inc.||Packaging of multiple fluid receptacles|
|EP1550853A1 *||May 19, 2003||Jul 6, 2005||Nippon Sheet Glass Co.,Ltd.||Biochemical container|
|U.S. Classification||206/431, 206/459.5, 206/504, 220/665, 356/246|
|International Classification||G01N33/53, G01N35/02, B01L3/00, G01N21/03|
|Cooperative Classification||G01N21/03, G01N33/5304|
|European Classification||G01N33/53B2, G01N21/03|