EP1214147A1 - Dispositif et procede permettant de manipuler et de traiter des echantillons et/ou des melanges reactionnels de petit volume - Google Patents
Dispositif et procede permettant de manipuler et de traiter des echantillons et/ou des melanges reactionnels de petit volumeInfo
- Publication number
- EP1214147A1 EP1214147A1 EP00957213A EP00957213A EP1214147A1 EP 1214147 A1 EP1214147 A1 EP 1214147A1 EP 00957213 A EP00957213 A EP 00957213A EP 00957213 A EP00957213 A EP 00957213A EP 1214147 A1 EP1214147 A1 EP 1214147A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- format
- microtitre plate
- well
- adapter
- well format
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 238000000034 method Methods 0.000 title claims description 19
- 239000011541 reaction mixture Substances 0.000 title claims description 11
- 239000003153 chemical reaction reagent Substances 0.000 claims abstract description 27
- 238000006243 chemical reaction Methods 0.000 claims abstract description 19
- 238000005119 centrifugation Methods 0.000 claims abstract description 4
- 230000000994 depressogenic effect Effects 0.000 claims 1
- 238000004458 analytical method Methods 0.000 description 11
- 239000000523 sample Substances 0.000 description 10
- 238000013537 high throughput screening Methods 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 230000008901 benefit Effects 0.000 description 4
- 230000006835 compression Effects 0.000 description 4
- 238000007906 compression Methods 0.000 description 4
- 239000013618 particulate matter Substances 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 230000018109 developmental process Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- 239000002033 PVDF binder Substances 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000011324 bead Substances 0.000 description 2
- 238000005842 biochemical reaction Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 238000009509 drug development Methods 0.000 description 2
- 229920001903 high density polyethylene Polymers 0.000 description 2
- 239000004700 high-density polyethylene Substances 0.000 description 2
- 239000013610 patient sample Substances 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- -1 polypropylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 238000012742 biochemical analysis Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000000356 contaminant Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000012864 cross contamination Methods 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- 238000004512 die casting Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003344 environmental pollutant Substances 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000001900 immune effect Effects 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002991 molded plastic Substances 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
- G01N21/25—Colour; Spectral properties, i.e. comparison of effect of material on the light at two or more different wavelengths or wavelength bands
- G01N21/251—Colorimeters; Construction thereof
- G01N21/253—Colorimeters; Construction thereof for batch operation, i.e. multisample apparatus
-
- 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
- B01L3/508—Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above
- B01L3/5085—Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above for multiple samples, e.g. microtitration plates
-
- 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
- B01L3/508—Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above
- B01L3/5085—Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above for multiple samples, e.g. microtitration plates
- B01L3/50855—Containers for the purpose of retaining a material to be analysed, e.g. test tubes rigid containers not provided for above for multiple samples, e.g. microtitration plates using modular assemblies of strips or of individual wells
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/01—Arrangements or apparatus for facilitating the optical investigation
- G01N21/03—Cuvette constructions
- G01N21/07—Centrifugal type cuvettes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
- B01L2200/02—Adapting objects or devices to another
- B01L2200/021—Adjust spacings in an array of wells, pipettes or holders, format transfer between arrays of different size or geometry
-
- 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
- B01L2300/0893—Geometry, shape and general structure having a very large number of wells, microfabricated wells
Definitions
- the present invention concerns a device and a method for the simultaneous handling of a multitude of small volume samples, and in particular novel means and a method for compressing or condensing a set of samples such as a set of samples on a microtitre plate from one format to a less space-demanding one.
- Biochemical reactions are routinely carried out in so-called microtitre plates - sheets of moulded plastic that typically contain eight rows and twelve columns of tiny wells, each of which capable of holding a few millilitres or less of the reaction rnixture. This is known as the 8 by 12 or 96-well format.
- the 96-well format is widely used, not only in biochemical operations, such as analysis, diagnostics, small scale synthesis and the like, but also in fields like high throughput screening and combinatorial chemistry.
- the receiving microtitre plate cannot have too high resolution.
- a very dense format will become physically unmanageable from the user's point of view and the risk of mix-ups and contamination increases.
- the 96-well format is widely used and accepted by the laboratories, both in research and other applications. Auxiliary equipment has been designed to accommodate this format.
- the historical and wide-spread use of the 96-well format means that vast amounts of old patient samples, compounds for drug development etc are stored in the 96-well format.
- the format has to be compressed. Presently, such reformation, compression or condensation is done by pipetting robots.
- the above problem is solved by the device and method as defined in the attached claims.
- the inventive device allows easy conversion between different microtitre plate formats, thus adding flexibility and making possible the sequential use of apparatuses designed for different formats.
- Other applications and benefits of the invention will be described in or become evident from the description and examples below.
- FIG. 1 shows schematically the compression steps from the 96-well format to the
- Fig. 2 shows an adapter according to claim X in perspective
- Fig. 3 shows the above adapter in cross section along the line IJJ;
- Fig. 4 shows the above adapter in cross section along line TV; and Fig. 5 shows schematically how four adapters, two of each (denoted A and B, respectively) are assembled together.
- microtitre plates in general, which is hereby defined as comprising any device capable of receiving a multitude of samples in separate and/or discrete locations or so called wells.
- grid is used to define the spatial distribution of said wells, e.g. their distribution in rows and columns, on the microtitre plate.
- upper is used to define the surface of the adapter having a grid corresponding to the less dense format. Consequently, the term “lower” is used to define the surface of the adapter having a grid corresponding to the more dense format
- small volume reactions includes any chemical reaction conducted in volumes below 100 ⁇ l.
- Typical biochemical reactions are immunological determinations, histological determinations, enzymatic determinations, biochemical diagnosis of diseases, determinations of paternity, various determinations in forensic medicine, various operations in analysis and synthesis applications.
- Typical chemical reactions intended to fall within this definition are reactions in the screening and synthesis of pharmaceuticals, for example high throughput screening, combinatorial chemistry, analysis, determination of environmental pollutants etc.
- the adapter according to the invention is a three-dimensional body having openings on one surface, said openings spaced according to the less dense donating format, and a corresponding amounts of openings on its reverse surface, said openings being connected by individual channels.
- the relative position of each opening on one surface is identical to the position of the corresponding opening on the reverse surface.
- the grid of the wells on the upper surface corresponds to the grid of microtitre plates of this less dense format, which is subject of compression.
- the grid of the openings on the lower surface in its turn corresponds to the grid of the more dense, receiving format.
- An adapter for compressing the 96-well format into the 384-well format typically has 24 wells, arranged in 6 rows and 4 columns, on its upper surface. Correspondingly, there are 24 openings on its lower surface, arranged in 6 rows and 4 columns.
- the grid on the upper surface is identical to the grid of a 96-well microtitre plate, and the grid on the lower surface is identical to the grid of a 384-well microtitre plate.
- the adapter is designed to fit tightly to the openings of the donating microtitre plate.
- the individual wells on the adapter will be designed to fit to the wells of the donating microtitre plate, sufficiently well to prevent leakage or cross-contamination when the combined adapter and donating plate is turned up-side-down. This can be achieved by providing the adapter with protruding rims, around each well, protruding cylinders that fit into the donating wells, gaskets, flanges etc.
- the adapter can consist of a full 8 by 12 upper surface in the 96-well format and a corresponding 8 by 12 lower surface in the 384-well format.
- the adapter is manufactured in two parts being a mirror image of each other. When put into use, two of each part are assembled as shown in Fig. 3. In order to compress a conventional 8 by 12 microtitre plate (the 96-well format) into a more dense format, e.g. a 16 by 24 plate (the 384-well format) four adapters are assembled as illustrated in Fig. 3. The set of four adapters can be arranged on top of a receiving microtitre plate, e.g. one comer or a quarter of a microtitre plate in the 384-well format. The samples and reagents, as desired, are then dispensed in the wells of the adapters, either manually or using equipment developed for the 96-well format.
- the adapters together with the receiving microtitre plate or quarter thereof, are then placed in a centrifuge and subjected to a centrifugal force sufficient to transfer all the contents of the upper wells, through the channels, into the receiving denser format.
- the adapters can then be removed and discarded and the samples, being in the 384-well format, processed further or analysed using equipment adapted to this format.
- Possible further steps for the contents transferred to the denser format include analysis, storage or emptying or a combination thereof. Analysis steps may include the addition of a further reagent and the analysis itself can encompass photometric determinations, such as measuring the fluorescence intensity of the mixture.
- the channels connecting the upper and lower openings on an adapter are made so narrow, that the sample and/or reaction mixture cannot pass the channels unless the adapter is subjected to a certain centrifugal force.
- the channels can be closed by an inert substance which is either solid or viscous at normal analysis temperature, but which melts or turns less viscous at an increased temperature within a range, tolerable for the sample and reagents. In this way the user can have control over the reaction, for example by adding a sample plus reagent in the less dense format and, at a desired moment, end the reaction by centrifuging the mixture into the receiving format, possibly containing an agent quenching the reaction.
- the channels connecting the upper and lower openings on the adapter are provided with constrictions or filter means for separating the sample and reagent mixture from auxiliary components, such as particulate matter or reagent capillaries.
- Particulate matter e.g. silica particles, glass beads, latex beads etc is frequently used in extraction, purification and separation operations.
- An adapter provided with constrictions or filter means would therefor function as a convenient means for separating the particulate matter from the reaction mixture, simultaneously as the separate samples are transferred to a denser format.
- the filter means constitute a convenient way to simultaneously separate the particulate matter from the reaction mixture and emptying the contents into a denser format for further analysis or subsequent reactions.
- the adapter itself can function as a microtitre plate, being the receptacle of samples and reagents, with the further benefit of allowing the reaction mixture to be transferred into a denser format at any time desired by the user.
- the adapter or device according to the invention is preferable made of a suitable thermoplastic.
- suitable materials include, but are not limited to, polypropylene (PP), polystyrene (PS), polyethylene (PE), high density polyethylene (HDPE), polycarbonate (PC), polyacetate (PA), poly-methyleene-methacrylate (PMMA) and poly-vinylidene-fluoride (PVDF).
- PP polypropylene
- PS polystyrene
- PE polyethylene
- HDPE high density polyethylene
- PC polycarbonate
- PA polyacetate
- PMMA poly-methyleene-methacrylate
- PVDF poly-vinylidene-fluoride
- the choice of material is not only governed by thermal and chemical considerations, but also economic considerations such as material costs, production technology etc.
- One suitable method of production is injection moulding. Vacuum die-casting is another possible method of production.
- the adapter is of course manufactured under conditions rendering it sterile and free from
- the device comprises physical characteristics aiding in the correct positioning of the device in relation to surrounding devices and in relation to the receiving microtitre plate.
- Such physical characteristic can comprise veits, grooves, colour codes and pins, with corresponding members in the adjacent device. In practise this can be realised by coloured fields, forming a pre-determined pattern when the devices are correctly assembled.
- hte device is equipped with pins on at least one side, said pins fitting in corresponding holes on at least one side of the adjacent device, when the devices are correctly assembled.
- velts or raised details can be provided, said velts or raised details fitting in corresponding grooves or depressions on the adjacent device when correctly assembled.
- the device according to the invention comprises predispensed reagents, preferably in reagent cartridges or capillaries which are emptied by c ⁇ ntrifugation.
- reagents can be single- or multi-compartment cartridges or single- or multi-lumen capillaries.
- reagents can be added to the samples or reaction mixtures before or during the compression or transferral to a denser format. This is achieved through the fact, that reagent cartridges and capillaries can be made to release their content at predefined temperatures or centrifugal forces.
- reagent cartridges see e.g. WO 98/10866.
- a method according to the present invention includes both the possibility, that the adapter is delivered with suitable reagent cartridges or capillaries in place and the possibility, that these are added to the wells of the adapter after addition of the sample or reagent mixture that is to be compressed to a denser format.
- the channels in the adapter, connecting the openings at the upper surface, corresponding to a less dense format, and the openings at the lower surface, corresponding to a more dens format are designed not to allow the passage of the reagent cartridge or the reagent capillary.
- the devices according to the invention fits into a frame, said frame also being part of the invention.
- the frame is designed to fit the receiving microtitre plate and to hold the devices in an orientation and position in relation to each other and in relation to the receiving microtitre plate as to guarantee flawless transfer of the sample or reagents from one format to the other.
- the adapter and methods of its use, according to the present invention, offer the user numerous benefits.
- the device functions as an interface between manual handling of the traditional 96-well format and the automated handling of the newer 384-well format and more dense formats.
- the device makes it possible to transfer samples and reaction mixtures from one format into a more dense one with little or no risk for error, as the alignment of the corresponding wells is an automatic, "built-in" feature of the adapters.
- the possibility of conducting an exactly determinable part of a reaction in the adapter, after which the reaction mixture is transferred into the receiving format offers many advantages.
- the inventive device and method is superior, both in regard of the initial costs and sample economy.
- the inventive device and method is particularly suited for supplying old samples, stored in serial format or on 96-well plates, to the newly developed methods and apparatuses used in high throughput screening and combinatorial chemistry.
- the device and method of the present invention constitute a convenient interface between manual and automated operations in all types of small volume reactions, e.g. in fields like diagnostic analysis, biochemical analysis and high throughput screening and combinatorial chemistry.
- Example 1 Four devices according to the invention are assembled in a frame, and placed over the first quadrant of a 16 by 24 microtitre plate. Samples are manually pipetted into the wells of the devices, now resembling a conventional 8 by 12 microtitre plate. This way the first 96-samples are compressed to the 384-well format. The process is repeated by first assembling four devices over the second, third and fourth quadrant of the receiving 16 by 24 plate.
- Four 96-well microtitre plates are filled with samples and reagents in a conventional manner and subjected to temperation in a thermo shaker, built for this format.
- Four devices according to the invention are assembled in a frame and placed over the first quadrant of a 16 by 24 microtitre plate.
- the first 96-well plate is emptied in the assembled devices and the reaction mixtures thus transferred and compressed to the 384-well format
- the process is repeated with new devices, assembled in lots of four, corresponding to the second, third and fourth quadrant of the receiving 16 by 24 plate.
- Example 3 Four adapters assembled to form a 96-well grid on their combined upper surfaces, are supplied with reagent cartridges, for example single- or multilumen capillaries, containing one or several reagents.
- the adapters are connected, up-side-down to a conventional 96-well microtitre plate, forming a tight seal between the openings of the wells on the 96-well microtitre plate and the openings of the adapter.
- This combination is then turned and connected to the receiving, denser format, e.g. a 384-well microtitre plate and placed in a centrifuge.
- the receiving, denser format e.g. a 384-well microtitre plate and placed in a centrifuge.
- the reagent cartridge or single- or multilumen capillaries are emptied of their contents and at another, predetermined speed, the entire content of the former 96-well plate and the reagents are transferred into the receiving, 384-well plate.
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Analytical Chemistry (AREA)
- Physics & Mathematics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Hematology (AREA)
- Clinical Laboratory Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Automatic Analysis And Handling Materials Therefor (AREA)
- Sampling And Sample Adjustment (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
Abstract
A l'aide d'un dispositif tel qu'un adaptateur on peut comprimer le format d'une plaque de microtitration classique à 96 cupules pour constituer un format à 384 cupules ou bien des formats encore plus denses. L'adaptateur peut également faire office de cuve à réaction dans une forme de réalisation dans laquelle il est vidé par centrifugation pour produire le format de réception plus dense. En outre, cet adaptateur peut comprendre des réactifs, qui se présentent de préférence sous forme de capillaires réactifs qui sont vidés lorsque la centrifugation a atteint un niveau prédéterminé.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE9903002 | 1999-08-25 | ||
| SE9903002A SE9903002D0 (sv) | 1999-08-25 | 1999-08-25 | Device and method for handling small volume samples and/or reaction mixtures |
| PCT/SE2000/001632 WO2001014063A1 (fr) | 1999-08-25 | 2000-08-24 | Dispositif et procede permettant de manipuler et de traiter des echantillons et/ou des melanges reactionnels de petit volume |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP1214147A1 true EP1214147A1 (fr) | 2002-06-19 |
Family
ID=20416746
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP00957213A Withdrawn EP1214147A1 (fr) | 1999-08-25 | 2000-08-24 | Dispositif et procede permettant de manipuler et de traiter des echantillons et/ou des melanges reactionnels de petit volume |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP1214147A1 (fr) |
| JP (1) | JP2003531358A (fr) |
| AU (1) | AU6886600A (fr) |
| SE (1) | SE9903002D0 (fr) |
| WO (1) | WO2001014063A1 (fr) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003055589A2 (fr) * | 2001-12-31 | 2003-07-10 | Institut für Physikalische Hochtechnologie e.V. | Plaque de microtitration pour l'execution en parallele de plusieurs microsyntheses, en particulier a temperatures elevees |
| US7459127B2 (en) | 2002-02-26 | 2008-12-02 | Siemens Healthcare Diagnostics Inc. | Method and apparatus for precise transfer and manipulation of fluids by centrifugal and/or capillary forces |
| US7125711B2 (en) | 2002-12-19 | 2006-10-24 | Bayer Healthcare Llc | Method and apparatus for splitting of specimens into multiple channels of a microfluidic device |
| US7094354B2 (en) | 2002-12-19 | 2006-08-22 | Bayer Healthcare Llc | Method and apparatus for separation of particles in a microfluidic device |
| US7435381B2 (en) | 2003-05-29 | 2008-10-14 | Siemens Healthcare Diagnostics Inc. | Packaging of microfluidic devices |
| US7347617B2 (en) | 2003-08-19 | 2008-03-25 | Siemens Healthcare Diagnostics Inc. | Mixing in microfluidic devices |
| FR3033409B1 (fr) * | 2015-03-03 | 2017-04-14 | Nicolas Ugolin | Electrodot : procede d'analyse d'echantillons biologiques en matrice de spots fixes par l'action d'un courant electrique conjuguee a une difference de pression |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5840256A (en) * | 1996-04-09 | 1998-11-24 | David Sarnoff Research Center Inc. | Plate for reaction system |
| US6054325A (en) * | 1996-12-02 | 2000-04-25 | Glaxo Wellcom Inc. | Method and apparatus for transferring and combining distinct chemical compositions with reagents |
| DE19712195B4 (de) * | 1997-03-22 | 2007-12-27 | Friedrich-Schiller-Universität Jena | Verfahren und Vorrichtung zur Bereitstellung von Proben für den off-line Nachweis von Analyten nach der MALDI-Massenspektrometrie |
| EP0955084B1 (fr) * | 1998-04-27 | 2006-07-26 | Corning Incorporated | Procédé pour le dépôt d'échantillons biologiques avec un réservoir capillaire refilé |
-
1999
- 1999-08-25 SE SE9903002A patent/SE9903002D0/xx unknown
-
2000
- 2000-08-24 WO PCT/SE2000/001632 patent/WO2001014063A1/fr not_active Ceased
- 2000-08-24 JP JP2001518192A patent/JP2003531358A/ja active Pending
- 2000-08-24 AU AU68866/00A patent/AU6886600A/en not_active Abandoned
- 2000-08-24 EP EP00957213A patent/EP1214147A1/fr not_active Withdrawn
Non-Patent Citations (1)
| Title |
|---|
| See references of WO0114063A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2003531358A (ja) | 2003-10-21 |
| SE9903002D0 (sv) | 1999-08-25 |
| WO2001014063A1 (fr) | 2001-03-01 |
| AU6886600A (en) | 2001-03-19 |
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