CA2250212A1 - Device and method for multiple analyte detection - Google Patents

Device and method for multiple analyte detection

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Publication number
CA2250212A1
CA2250212A1 CA002250212A CA2250212A CA2250212A1 CA 2250212 A1 CA2250212 A1 CA 2250212A1 CA 002250212 A CA002250212 A CA 002250212A CA 2250212 A CA2250212 A CA 2250212A CA 2250212 A1 CA2250212 A1 CA 2250212A1
Authority
CA
Canada
Prior art keywords
analyte
detection
sample
specific
chambers
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.)
Granted
Application number
CA002250212A
Other languages
French (fr)
Other versions
CA2250212C (en
Inventor
Timothy W. Woudenberg
Michael Albin
Reid B. Kowallis
Yefim Raysberg
Robert. P. Ragusa
Emily S. Winn-Deen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Applied Biosystems LLC
Original Assignee
The Perkin-Elmer Corporation
Timothy W. Woudenberg
Michael Albin
Reid B. Kowallis
Yefim Raysberg
Robert. P. Ragusa
Emily S. Winn-Deen
Pe Corporation (Ny)
Applera Corporation
Applied Biosystems Inc.
Applied Biosystems, Llc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by The Perkin-Elmer Corporation, Timothy W. Woudenberg, Michael Albin, Reid B. Kowallis, Yefim Raysberg, Robert. P. Ragusa, Emily S. Winn-Deen, Pe Corporation (Ny), Applera Corporation, Applied Biosystems Inc., Applied Biosystems, Llc filed Critical The Perkin-Elmer Corporation
Publication of CA2250212A1 publication Critical patent/CA2250212A1/en
Application granted granted Critical
Publication of CA2250212C publication Critical patent/CA2250212C/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/5302—Apparatus specially adapted for immunological test procedures
    • G01N33/5304—Reaction vessels, e.g. agglutination 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
    • B01L3/502—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
    • 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
    • B01L3/50273—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 means or forces applied to move the fluids
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/02—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving viable microorganisms
    • C12Q1/04—Determining presence or kind of microorganism; Use of selective media for testing antibiotics or bacteriocides; Compositions containing a chemical indicator therefor
    • C12Q1/06—Quantitative determination
    • C12Q1/08—Quantitative determination using multifield media
    • 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
    • B01L2200/026—Fluid interfacing between devices or objects, e.g. connectors, inlet details
    • B01L2200/027—Fluid interfacing between devices or objects, e.g. connectors, inlet details for microfluidic devices
    • 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
    • B01L2200/06—Fluid handling related problems
    • B01L2200/0642—Filling fluids into wells by specific techniques
    • 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
    • B01L2200/14—Process control and prevention of errors
    • B01L2200/141—Preventing contamination, tampering
    • 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
    • B01L2300/06—Auxiliary integrated devices, integrated components
    • B01L2300/0627—Sensor or part of a sensor is integrated
    • B01L2300/0636—Integrated biosensor, microarrays
    • 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
    • B01L2300/18—Means for temperature control
    • B01L2300/1805—Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks
    • B01L2300/1827—Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks using resistive heater
    • 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
    • B01L2400/049—Moving fluids with specific forces or mechanical means specific mechanical means and fluid pressure fluid pressure, pneumatics vacuum
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L7/00—Heating or cooling apparatus; Heat insulating devices
    • B01L7/52—Heating or cooling apparatus; Heat insulating devices with provision for submitting samples to a predetermined sequence of different temperatures, e.g. for treating nucleic acid samples
    • 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
    • G01N35/00029—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor provided with flat sample substrates, e.g. slides
    • G01N2035/00099—Characterised by type of test elements
    • G01N2035/00148—Test cards, e.g. Biomerieux or McDonnel multiwell test cards
    • 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
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/973—Simultaneous determination of more than one analyte
    • 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
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S436/00—Chemistry: analytical and immunological testing
    • Y10S436/807—Apparatus included in process claim, e.g. physical support structures

Abstract

The invention is directed to a method and device for simultaneously testing a sample for the presence, absence, and/or amounts of one or more a plurality of selected analytes. The invention includes, in one aspect, a device for detecting or quantitating a plurality of different analytes in a liquid sample. The device includes a substrate which defines a sample-distribution network having (i) a sample inlet, (ii) one or more detection chambers, and (iii) channel means providing a dead-end fluid connection between each of the chambers and the inlet. Each chamber may include an analyte-specific reagent effective to react with a selected analyte that may be present in the sample, and detection means for detecting the signal. Also disclosed are methods utilizing the device.

Claims (40)

1. A device for detecting or quantitating a plurality of different analytes in a liquid sample, said device comprising a substrate defining a sample-distribution network having (i) a sample inlet, (ii) one or more detection chambers, and (iii) channel means providing a dead-end fluid connection between each of said chambers and said inlet, wherein each of said chambers includes an analyte-specific reagent effective to react with a selected analyte that may be present in such sample, to produce a detectable signal, said substrate providing, for each chamber, detection means for detecting such signal, whereby evacuation of said network, followed by application of the sample to said inlet, is effective to draw sample by vacuum into each of said chambers.
2. The device of claim 1, wherein said channel means includes a single channel to which said detection chambers are connected by said fluid connections.
3. The device of claim 1, wherein said channel means includes a first channel to which a first group of detection chambers are connected by such dead-end fluid connections, and a second channel to which a second group of detection chambers are connected by such dead-end fluid connections.
4. The device of claim 1, wherein said channel means includes an individual channel for each detection chamber, for providing a dead-end fluid connection between said inlet and each detection chamber.
5. The device of claim 1, which further includes a vacuum port connected to said channel means at a site in fluid communication with the sample inlet and detection chambers.
6. The device of claim 5, wherein said vacuum port is connected to said channel means at a site that is downstream of said detection chambers.
7. The device of claim 1, which further includes a non-flowthrough vacuum reservoir in fluid communication with said channel means.
8. The device of claim 1, wherein said detection means includes an optically transparent window associated with each detection chamber, through which such signal can be optically detected.
9. The device of claim 1, wherein the analytes are polynucleotides, and at least two of said detection chambers each contain detection reagents for detecting different polynucleotide analytes.
10. The device of claim 9, wherein the analyte-specific detection reagents include first and second oligonucleotide primers having sequences effective to hybridize to opposite end regions of complementary strands of a selected polynucleotide analyte segment, for amplifying the segment by primer-initiated polymerase chain reaction.
11. The device of claim 10, wherein said analyte-specific detection reagents further include a fluorescer-quencher oligonucleotide capable of hybridizing to the analyte segment in a region downstream of one of the primers, for producing a detectable fluorescent signal when the analyte is present in the sample.
12. The device of claim 9, wherein the analyte-specific detection reagents include first and second oligonucleotides effective to bind to adjacent, contiguous regions of a target sequence in the selected analyte, for oligonucleotide ligation assay detection of the analyte.
13. The device of claim 12, wherein the analyte-specific detection reagents include a second pair of oligonucleotides which are effective to bind to adjacent, contiguous regions complementary to the regions bound by the first pair of oligonucleotides, for amplification of the polynucleotide analyte by ligase chain reaction.
14. The device of claim 9, wherein the analyte-specific deotection reagents include a binding polymer effective to hybridize to a selected sequence in the polynucleotide analyte, and the binding polymer includes a fluorescent dye moiety which produces a detectable signal upon hybridizing to the selected sequence.
15. The device of claim 9, wherein the analyte-specific reagents additionally include an intercalating compound which produces an optically detectable signal upon intercalating a double-stranded polynucleotide.
16. The device of claim 1, wherein the analyte-specific reagents in each chamber include an antibody specific for a selected antigen which may be present in the sample.
17. The device of claim 1, wherein the analyte-specific reagents in each chamber include an antigen for reacting with a selected analyte antibody which may be present in the sample.
18. The device of claim 1, wherein said substrate further includes temperature regulating means for controlling the temperature of each detection chamber.
19. The device of claim 1, wherein said substrate defines at least two such sample-distribution networks.
20. The device of claim 1, wherein the interior of said network is under vacuum.
21. A method for detecting or quantitating one or more of a plurality of analytes in a liquid sample, said method comprising providing a device in accordance with claim 1, wherein the interior of the network is under vacuum, applying a liquid sample to the sample inlet and allowing the sample to be drawn into the network by vacuum action to deliver the sample to the detection chambers, allowing the delivered sample to react with the analyte-specific reagents in each detection chamber under conditions effective to produce a detectable signal in each detection chamber when the selected analyte is present in the sample, and measuring the signals produced in the reaction chambers to determine which selected analytes are present in the sample.
22. The method of claim 21, wherein said channel means includes a single channel to which said detection chambers are connected by said fluid connections.
23. The method of claim 21, wherein said channel means includes a first channel to which a first group of detection chambers are connected by such fluid connections, and a second channel to which a second group of detection chambers are connected.
24. The method of claim 21, wherein said channel means includes an individual channel for each detection chamber, for providing a dead-end fluid connection between said inlet and each detection chamber.
25. The method of claim 21, wherein said device further includes a vacuum port connected to the channel means at a site in fluid communication with the sample inlet and detection chambers, and prior to said applying, said network is evacuated by applying a vacuum to the vacuum port.
26. The method of claim 25, wherein said vacuum port is connected to the channel means at a site that is downstream of said sample inlet and said detection chambers.
27. The method of claim 21, wherein said device further includes a non-flowthrough vacuum reservoir in fluid communication with said channel means.
28. The method of claim 21, wherein the analytes are polynucleotides, and at least two of said detection chambers each contain detection reagents for detecting different polynucleotide analytes.
29. The method of claim 28, wherein the analyte-specific reagents include an oligonucleotide primer pair suitable for amplifying, by polymerase chain reaction, an analyte segment which is flanked by sequences complementary to the primer pair.
30. The method of claim 29, wherein said analyte-specific detection reagents further include a fluorescer-quencher oligonucleotide capable of hybridizing to the analyte segment in a region downstream of one of the primers, for producing a detectable fluorescent signal when the analyte is present in the sample.
31. The method of claim 28, wherein the analyte-specific detection reagents include first and second oligonucleotides effective to bind to adjacent contiguous regions of a target sequence in the selected analyte, for oligonucleotide ligation assay detection of the analyte.
32. The method of claim 31, wherein the analyte-specific detection reagents include a second pair of oligonucleotides which are effective to bind to adjacent, contiguous regions complementary to the regions bound by the first pair of oligonucleotides, for amplification of the polynucleotide analyte by ligase chain reaction.
33. The method of claim 28, wherein the analyte-specific detection reagents include a binding polymer effective to hybridize to a selected sequence in the polynucleotide analyte, and the binding polymer includes a fluorescent dye moiety which produces a detectable signal upon hybridizing to the selected sequence.
34. The method of claim 28, wherein the analyte-specific reagents additionally include an intercalating compound which produces an optically detectable signal upon intercalating a double-stranded polynucleotide.
35. The method of claim 21, wherein the analyte-specific reagents in each chamber include an antibody specific for a selected antigen which may be present in the sample.
36. The method of claim 21, wherein the analyte-specific reagents in each chamber include an antigen for reacting with a selected analyte antibody which may be present in the sample.
37. The method of claim 21, wherein said substrate further includes temperature regulating means for controlling the temperature of each detection chamber.
38. The method of claim 21, wherein said substrate defines at least two such sample-distribution networks.
39. The method of claim 21, wherein said providing includes filling said network with carbon dioxide gas, prior to placing said network under vacuum.
40. The method of claim 21, wherein the analyte is a drug candidate, and the detection reagents include a drug target.
CA2250212A 1996-04-03 1997-04-02 Device and method for multiple analyte detection Expired - Fee Related CA2250212C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US1471296P 1996-04-03 1996-04-03
US60/014712 1996-04-03
PCT/US1997/005458 WO1997036681A1 (en) 1996-04-03 1997-04-02 Device and method for multiple analyte detection

Publications (2)

Publication Number Publication Date
CA2250212A1 true CA2250212A1 (en) 1997-10-09
CA2250212C CA2250212C (en) 2010-02-09

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
CA2250212A Expired - Fee Related CA2250212C (en) 1996-04-03 1997-04-02 Device and method for multiple analyte detection

Country Status (7)

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US (2) US6126899A (en)
EP (1) EP0889751B1 (en)
JP (3) JP4912517B2 (en)
AU (1) AU706862B2 (en)
CA (1) CA2250212C (en)
DE (1) DE69700499T2 (en)
WO (1) WO1997036681A1 (en)

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