US20160209409A1 - Device and Method for Detecting Analyte by Movement of Particles - Google Patents

Device and Method for Detecting Analyte by Movement of Particles Download PDF

Info

Publication number
US20160209409A1
US20160209409A1 US14/915,206 US201414915206A US2016209409A1 US 20160209409 A1 US20160209409 A1 US 20160209409A1 US 201414915206 A US201414915206 A US 201414915206A US 2016209409 A1 US2016209409 A1 US 2016209409A1
Authority
US
United States
Prior art keywords
analyte
chamber
particles
detection
sample
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.)
Abandoned
Application number
US14/915,206
Other languages
English (en)
Inventor
Suk-Jung Choi
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.)
Industry Academy Cooperation Foundation of Gangneung Wonju National University
Amo Lifescience Co Ltd
Original Assignee
Amogreentech Co Ltd
Industry Academy Cooperation Foundation of Gangneung Wonju National University
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 Amogreentech Co Ltd, Industry Academy Cooperation Foundation of Gangneung Wonju National University filed Critical Amogreentech Co Ltd
Assigned to Gangneung-Wonju National University Industry Academy Cooperation Group, AMOGREENTECH CO., LTD. reassignment Gangneung-Wonju National University Industry Academy Cooperation Group ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CHOI, SUK-JUNG
Publication of US20160209409A1 publication Critical patent/US20160209409A1/en
Assigned to AMOLIFESCIENCE CO., LTD. reassignment AMOLIFESCIENCE CO., LTD. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: AMOGREENTECH CO., LTD.
Abandoned legal-status Critical Current

Links

Images

Classifications

    • 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
    • B01L3/502761—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 specially adapted for handling suspended solids or molecules independently from the bulk fluid flow, e.g. for trapping or sorting beads, for physically stretching molecules
    • 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
    • G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
    • G01N33/54366—Apparatus specially adapted for solid-phase testing
    • G01N33/54386—Analytical elements
    • 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
    • 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
    • B01L3/502738—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 integrated valves
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03C—MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03C1/00—Magnetic separation
    • B03C1/005—Pretreatment specially adapted for magnetic separation
    • B03C1/01—Pretreatment specially adapted for magnetic separation by addition of magnetic adjuvants
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03C—MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03C1/00—Magnetic separation
    • B03C1/02—Magnetic separation acting directly on the substance being separated
    • B03C1/28—Magnetic plugs and dipsticks
    • B03C1/288—Magnetic plugs and dipsticks disposed at the outer circumference of a recipient
    • 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
    • G01N33/536—Immunoassay; Biospecific binding assay; Materials therefor with immune complex formed in liquid phase
    • 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
    • G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
    • G01N33/54313—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals the carrier being characterised by its particulate form
    • G01N33/54326—Magnetic particles
    • 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
    • G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
    • G01N33/54393—Improving reaction conditions or stability, e.g. by coating or irradiation of surface, by reduction of non-specific binding, by promotion of specific binding
    • 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
    • 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
    • G01N35/08—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor using a stream of discrete samples flowing along a tube system, e.g. flow injection analysis
    • G01N35/085—Flow Injection Analysis
    • 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
    • B01L2200/0647—Handling flowable solids, e.g. microscopic beads, cells, particles
    • 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
    • B01L2200/0647—Handling flowable solids, e.g. microscopic beads, cells, particles
    • B01L2200/0668—Trapping microscopic beads
    • 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
    • B01L2200/0673—Handling of plugs of fluid surrounded by immiscible fluid
    • 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
    • B01L2200/10—Integrating sample preparation and analysis in single entity, e.g. lab-on-a-chip concept
    • 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
    • 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
    • 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
    • B01L2300/0803—Disc shape
    • 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
    • B01L2300/0877—Flow chambers
    • 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
    • B01L2300/12—Specific details about materials
    • 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
    • B01L2400/0409—Moving fluids with specific forces or mechanical means specific forces centrifugal 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
    • B01L2400/0403—Moving fluids with specific forces or mechanical means specific forces
    • B01L2400/043—Moving fluids with specific forces or mechanical means specific forces magnetic 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
    • B01L2400/0403—Moving fluids with specific forces or mechanical means specific forces
    • B01L2400/0457—Moving fluids with specific forces or mechanical means specific forces passive flow or gravitation
    • 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
    • B01L2400/0481—Moving fluids with specific forces or mechanical means specific mechanical means and fluid pressure squeezing of channels or chambers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03C—MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03C2201/00—Details of magnetic or electrostatic separation
    • B03C2201/18—Magnetic separation whereby the particles are suspended in a liquid
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03C—MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
    • B03C2201/00—Details of magnetic or electrostatic separation
    • B03C2201/26—Details of magnetic or electrostatic separation for use in medical applications
    • 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
    • G01N2035/00158—Elements containing microarrays, i.e. "biochip"

Definitions

  • the present invention relates to a device and method for detecting an analyte by movement of particles.
  • Immunoassays such as ELISA (enzyme-linked immunosorbent assay) are antibody-based detection methods and are widely used in disease diagnosis or research.
  • a sandwich ELISA method uses two kinds of antibodies that bind to different sites of an analyte. Of the two antibodies, one antibody is immobilized on a solid phase such as an immunoplate and used as a capture antibody, and the other antibody is linked to an enzyme and used as a labeled antibody.
  • a sample containing an analyte is added to and reacted with the solid phase having the capture antibody immobilized thereon, the analyte binds to the antibody.
  • the enzyme binds to the solid phase in proportion to the amount of the analyte.
  • the amount of the analyte can be measured by measuring the activity of the enzyme.
  • the reason why the antibody is immobilized on the solid phase is because substances remaining in the liquid phase without binding to the solid phase can be easily removed.
  • a secondary antibody or protein G capable of binding to the antibody may be immobilized on the solid phase, or an antigen may also be immobilized on the solid phase.
  • a plastic surface such as an immunoplate is frequently used, but particles may also be used due to its advantages such as a large surface area.
  • magnetic particles have an advantage in that they can be captured or moved using a magnet, and thus are frequently used in a pretreatment process for separating an analyte from a sample containing a large amount of impurities.
  • an antibody for an analyte when magnetic particles having immobilized thereon an antibody for an analyte are added to and reacted with a sample, the analyte binds to the antibody immobilized on the magnetic particles.
  • a magnetic force is applied to the wall of a tube containing the sample, the magnetic particles all adhere to the tube wall, and impurities can all be removed by removing the remaining solution.
  • the present invention is intended to provide an analyte detection device and method, which can easily detect an analyte by moving the analyte from a sample chamber to a detection chamber.
  • the present invention provides an analyte detection device comprising: a sample chamber configured to contain a mixed solution of a reactant comprising particles and a sample containing an analyte; a detection chamber configured to contain a detection solution; and a channel located between the sample chamber and the detection chamber so as to prevent the mixed solution and the detection solution from mixing with each other, wherein the analyte is detected by moving the particles from the sample chamber to the detection chamber using moving means.
  • the present invention also provides a method for detecting an analyte using an analyte detection device, the analyte detection device comprising: a sample chamber configured to contain a mixed solution of a reactant comprising particles and a sample containing the analyte; a detection chamber configured to contain a detection solution; and a channel located between the sample chamber and the detection chamber so as to prevent the mixed solution and the detection solution from mixing with each other; the method comprising the steps of mixing and reacting the sample containing the analyte with the reactant comprising the particles in the sample chamber; moving the particles to the detection chamber by moving means; and detecting the analyte in the detection chamber.
  • the present invention also provides a method for detecting an analyte using an analyte detection device, the analyte detection device comprising: a sample chamber configured to contain a mixed solution of a reactant comprising capture particles and labeling particles and a sample containing the analyte; a detection chamber configured to contain a detection solution; and a channel located between the sample chamber and the detection chamber so as to prevent the mixed solution and the detection solution from mixing with each other; the method comprising the steps of: mixing the reactant with the sample in the sample chamber to form a capture particle-analyte-labeling particle complex; moving the capture particle-analyte-labeling particle complex to the detection chamber by moving means; and detecting the analyte in the detection chamber.
  • the present invention also provides a method for detecting an analyte using analyte detection device, the analyte detection device comprising: a sample chamber configured to contain a mixed solution of a sample containing the analyte and a reactant comprising capture particles having immobilized thereon a primary receptor specific for the analyte and a labeled standard material having a label linked to a standard material; a detection chamber configured to contain a detection solution; and a channel located between the sample chamber and the detection chamber so as to prevent the mixed solution and the detection solution from mixing with each other; the method comprising the steps of mixing the reactant and the sample in the sample chamber to form a capture particle-analyte complex and a capture particle-labeled standard material complex; moving the capture particle-analyte complex and the capture particle-labeled standard material complex to the detection chamber by moving means; and detecting the analyte in the detection chamber by use of the label linked to the labeled standard material, wherein the standard material
  • the present invention also provides a method for detecting an analyte using an analyte detection device, the analyte detection device comprising: a sample chamber configured to contain a mixed solution of a sample containing the analyte and a reactant which comprises capture particles having immobilized thereon a primary receptor specific for the analyte and a secondary receptor specific for the primary receptor and which also comprises a labeled standard material having a label linked to a standard material; a detection chamber configured to contain a detection solution; and a channel located between the sample chamber and the detection chamber so as to prevent the mixed solution and the detection solution from mixing with each other; the method comprising the steps of: mixing the reactant and the sample in the sample chamber to form a capture particle-primary receptor-analyte complex and a capture particle-primary receptor-labeled standard material complex; moving the capture particle-primary receptor-analyte complex and the capture particle-primary receptor-labeled standard material complex to the detection chamber by moving means; and
  • the present invention also provides a method for detecting an analyte using an analyte detection device, the analyte detection device comprising: a sample chamber configured to contain a mixed solution of a sample containing an analyte and a reactant comprising capture particles having immobilized thereon a first receptor specific for the analyte and a labeled receptor having a label attached to a second receptor specific for the analyte; a detection chamber configured to contain a detection solution; and a channel located between the sample chamber and the detection chamber so as to prevent the mixed solution and the detection solution from mixing with each other; the method comprising the steps of mixing the reactant and the sample in the sample chamber to form a capture particle-analyte-labeled receptor complex; moving the capture particle-analyte-labeled receptor complex to the detection chamber by moving means; and detecting the analyte using the label attached to the labeled receptor, wherein the first receptor and the second receptor are capable of binding non-competit
  • the present invention also provides a system for detecting an analyte using gravity, comprising: an analyte detection device comprising a sample chamber configured to contain a mixed solution of a reactant comprising particles and a sample containing an analyte, a detection chamber formed below the sample chamber and configured to contain a detection solution, and a channel located between the sample chamber and the detection chamber so as to prevent the mixed solution and the detection solution from mixing with each other; and at least one valve between the sample chamber and the channel, wherein the particles have a specific gravity greater than that of the mixed solution and the detection solution of the sample.
  • the present invention also provides a method for detecting an analyte using gravity, which uses the system for detecting the analyte using gravity and comprises the steps of: reacting the reactant with the sample in the sample chamber in a state in which the valve is closed; opening the valve to move the particles to the detection chamber; and detecting the analyte in the detection chamber.
  • the present invention also provides a system for detecting an analyte using gravity, the system comprising an analyte detection device comprising: a sample chamber configured to contain a mixed solution of a reactant comprising particles and a sample containing the analyte; a detection chamber configured to contain a detection solution; and a channel located between the sample chamber and the detection chamber so as to prevent the mixed solution and the detection solution from mixing with each other, wherein the channel is configured to connect the upper portion of the sample chamber with the upper portion of the detection chamber in a state in which the sample chamber and the detection chamber are horizontally positioned, and the particles have a specific gravity greater than that of each of the mixed solution and the detection solution of the sample.
  • the present invention also provides a method for detecting an analyte using gravity, which uses the system for detecting the analyte using gravity and comprises the steps of reacting the reactant with the sample in the sample chamber; inclining the analyte detection device at an angle of 20-70° such that the channel faces downward, thereby moving the particles to the detection. chamber; and detecting the analyte in the detection chamber.
  • the present invention also provides a system for detecting an analyte using a centrifugal force, comprising: an analyte detection device comprising a sample chamber configured to contain a mixed solution of a reactant comprising particles and a sample containing the analyte, a detection chamber configured to contain a detection solution, and a channel located between the sample chamber and the detection chamber so as to prevent the mixed solution and the detection solution from mixing with each other; a disc which includes a plurality of the analyte detection devices and is rotatable; and at least one detector ted near the disc, wherein the sample chamber is disposed toward the center of the disc, and the detection chamber is disposed outward from the center of the disc.
  • the present invention also provides a method for detecting an analyte using a centrifugal force, which uses the system for detecting the analyte using the centrifugal force and comprises the steps of reacting the reactant with the sample in the sample chamber; rotating the disc to open the valve and the channel; moving the particles to the detection chamber; and stopping the rotation, and then rotating the disc at an angle of 10-180° such that the detection chambers of the detection devices sequentially face toward the detector, and detecting the analyte in each of the detection chambers.
  • the present invention also provides a system for detecting an analyte using a magnetic force, the system comprising: an analyte detection device comprising a sample chamber configured to contain a mixed solution of a sample containing the analyte and a reactant comprising labeling capture particles which comprises a label attached to magnetic particles and have immobilized thereon a receptor for the analyte, a detection chamber configured to contain a detection solution, and a channel located between the sample chamber and the detection chamber so as to prevent the mixed solution and the detection solution from mixing each other; a filter disposed on the bottom inside the analyte detection device; and at least one magnetic force application unit disposed on the outer wall of the bottom of the analyte detection device and configured to apply a magnetic force to the labeling capture particles, wherein the channel is configured to connect the bottom of the sample chamber with the bottom of the detection chamber in a state in which the sample chamber and the detection chamber are horizontally disposed.
  • the present invention also provides a method for detecting an analyte using a magnetic force, which uses the system for detecting the analyte using the magnetic force and comprises the steps of reacting the reactant with the sample in the sample chamber; applying a magnetic force from the detection chamber to the sample chamber using the magnetic force application unit disposed on one side of the detection chamber, thereby moving the magnetic particles from the sample chamber to the detection chamber; and detecting the analyte in the detection chamber.
  • the present invention also provides a method for detecting an analyte using a magnetic force, which uses the system for detecting the analyte using the magnetic force and comprises the steps of: reacting the reactant with the sample in the sample chamber; moving the magnetic force application unit from the sample chamber to the detection chamber in a state in which the magnetic force application unit is located on the outside of the analyte detection device, thereby moving the magnetic particles from the sample chamber to the detection chamber; and detecting the analyte in the detection chamber.
  • the present invention also provides a system for detecting an analyte using a magnetic force, the system comprising: an analyte detection device comprising a sample chamber configured to contain a mixed solution of a sample containing the analyte and a reactant comprising labeling capture magnetic particles which have a label attached thereto and have immobilized thereon a receptor for the analyte, a detection chamber configured to contain a detection solution, and a channel located between the sample chamber and the detection chamber so as to prevent the mixed solution and the detection solution from mixing with each other; a filter disposed on the bottom inside the analyte detection device; and at least one magnetic farce application unit disposed on the outer wall of the bottom of the analyte detection device and configured to apply a magnetic force to the labeling capture magnetic particles, wherein the channel is configured to connect the bottom of the sample chamber with the bottom of the detection chamber in a state in which the sample chamber and the detection chamber are horizontally disposed.
  • the present invention also provides a method for detecting an analyte using a magnetic force, which uses the system for detecting the analyte using the magnetic force and comprises the steps of: reacting the reactant with the sample in the sample chamber to form a labeling capture particle-analyte complex; moving the magnetic force application unit from the sample chamber to the detection chamber, thereby discharging labeling capture particles unbound to the analyte to the bottom of the filter and moving the labeling capture particle-analyte complex to the detection chamber; and detecting the analyte in the detection chamber by use of the label attached to the labeling capture particles.
  • the present invention also provides a system for detecting an analyte using a magnetic force and a centrifugal force, the system comprising: an analyte detection device comprising a sample chamber configured to contain a mixed solution of a sample containing the analyte and a reactant comprising labeling capture particles which comprise a label attached to magnetic particles and have immobilized thereon a receptor for the analyte, a detection chamber configured to contain a detection solution, and a channel located between the sample chamber and the detection chamber so as to prevent the mixed solution and the detection solution from mixing with each other; a filter disposed on the bottom inside the analyte detection device; at least one magnetic force application unit disposed on the outer wall of the bottom of the analyte detection device and configured to apply a magnetic three to the labeling capture particles; a disc which includes a plurality of the analyte detection devices and is rotatable; and at least one detector located near the disc, wherein the sample chamber is disposed toward the center of
  • the present invention also provides a method for detecting an analyte using a magnetic force and a centrifugal force, which uses the system for detecting the analyte using the magnetic force and the centrifugal force and comprises the steps of: reacting the reactant with the sample in the sample chamber to form a labeling capture particle-analyte complex; rotating the disc in a state in which the magnetic force application unit is fixed to the bottom of the sample chamber, thereby discharging labeling capture particles unbound to the analyte to the bottom of the filter and moving the labeling capture particle-analyte complex to the detection chamber; and detecting the analyte in the detection chamber by use of the label attached to the labeling capture particles.
  • the analyte detection device does not require units fix moving solutions, and thus is highly economical.
  • FIG. 1 illustrates an analyte detection device according to the present invention.
  • FIG. 2 illustrates that a labeling chamber is additionally provided between a sample chamber and a detection chamber according to the present invention.
  • FIG. 3 illustrates that a waste chamber is additionally provided in a detection chamber according to the present invention.
  • FIG. 4 illustrates that a reactant chamber connected to a sample chamber according to the present invention is additionally disposed.
  • FIG. 5 illustrates a method in which a reactant is injected by moving a reactant chamber plug using a fixing cover having a protrusion formed thereon according to the present invention.
  • FIG. 6 illustrates a method in which a dried reactant is dissolved using a solvent stored in a reactant chamber and is injected into a sample chamber according to the present invention.
  • FIG. 7 illustrates a method in which a washing buffer is injected by moving a washing buffer chamber plug using a fixing cover having a protrusion formed thereon according to the present invention.
  • FIG. 8 illustrates a system for detecting an analyte using gravity according to the present invention.
  • FIG. 9 illustrates a system for detecting an analyte using gravity according to the present invention.
  • FIG. 10 illustrates a system for detecting an analyte using a centrifugal three according to the present invention.
  • FIG. 11 illustrates a system for detecting an analyte using a centrifugal force according to the present invention.
  • FIG. 12 illustrates a valve that is opened or closed by a centrifugal force using a cam having a weigh connected thereto in a system for detecting an analyte using a centrifugal force according to the present invention.
  • FIG. 13 illustrates a valve that is opened or closed by a centrifugal force using a horizontally movable clamp in a system for detecting an analyte using a centrifugal force according to the present invention.
  • FIG. 14 illustrates a method in which magnetic particles are moved from a sample chamber to a sample direction by applying a magnetic force in a direction from the detection chamber to the sample chamber in a system for detecting an analyte using a magnetic force according to the present invention.
  • FIG. 15 illustrates a method in which magnetic particles are moved by moving a magnet.
  • FIG. 16 illustrates a method in which different kinds of particles are separated from each other using a magnetic force together with a centrifugal force according to the present invention.
  • FIG. 17 illustrates a method in which bacteria are detected using capture particles (capture magnetic particles) having immobilized thereon a receptor for the bacteria and labeling particles (labeling receptor particles) which have immobilized thereon a receptor for the bacteria and have a labeling function, according to the present invention.
  • FIG. 18 illustrates a method in which magnetic particles unbound to bacteria are removed by disposing a filter on an inner surface opposite an outer surface with which a magnet comes into contact, and moving the magnet, according to the present invention.
  • FIG. 19 illustrates a method in which magnetic particles unbound to bacteria are removed by using a centrifugal force together with a magnetic force in a state in which a filter is disposed on an inner surface opposite an outer surface with which a magnet comes into contact, according to the present invention.
  • FIG. 20 illustrates a method in which an analyte is detected by a sandwich ELISA method using capture particles having a capture antibody immobilized thereon and a labeled antibody according to the present invention.
  • FIG. 21 illustrates a method in which the analyte kinase is detected by immobilizing on particles a receptor for a material produced by the analyte according to the present invention.
  • FIG. 22 illustrates a method in which the analyte protease is detected by immobilizing on particles a receptor for a material dissociated by the analyte according to the present invention.
  • FIG. 23 illustrates a principle according to which paralytic shellfish toxin (STX) is detected by a competitive immunoassay using magnetic particles as a solid phase in a detection device according to the present invention.
  • STX paralytic shellfish toxin
  • FIG. 24 shows the structure of a detection device used in Example 1.
  • FIG. 25 is a graph showing the results of detecting paralytic shellfish toxin (STX) by a competitive immunoassay in Example 1.
  • FIG. 26 shows the LOC structure of a detection device used in Example 2.
  • FIG. 27A and 27B show the structure and operating principle of a measurement device used in Example 2.
  • FIG. 28A and 28B are a graph showing the results of detecting the paralytic shellfish toxin STX by a competitive immunoassay in Example 2.
  • FIG. 29 shows the LOC structure of a detection device used in Example 3.
  • FIG. 30 shows the structure and operating principle of a magnetic particle moving device used in Example 3.
  • FIG. 31 is a graph showing the results of an experiment performed in Example 3 to confirm whether or not solutions of the sample chamber and detection chamber of an LOC are mixed with each other and whether or not other materials of the sample chamber also move during movement of particles of the sample chamber.
  • FIG. 32 is a graph showing the results of detecting paralytic shellfish toxin GTX 2&3 by a competitive immunoassay in Example 3.
  • FIG. 33 shows a principle according to bacteria are detected using capture particles (capture magnetic particles) and labeling particles (labeling particles) in Example 4.
  • FIG. 34 is a photograph showing a measurement device used in Example 4.
  • FIG. 35 is a graph showing the results of detecting Salmonella bacteria in Example 4.
  • FIG. 1 illustrates an analyte detection device according to the present invention
  • FIG. 2 illustrates that a labeling chamber is additionally provided between a sample chamber and a detection chamber according to the present invention
  • FIG. 3 illustrates that a waste chamber is additionally provided in a detection chamber according to the present invention
  • FIG. 4 illustrates that a reactant chamber connected to a sample chamber according to the present invention is additionally disposed
  • FIG. 5 illustrates a method in which a reactant is injected by moving a reactant chamber plug using a fixing cover having a protrusion formed thereon according to the present invention
  • FIG. 6 illustrates a method in which a dried reactant is dissolved using a solvent stored in a reactant chamber and is injected into a sample chamber according to the present invention
  • FIG. 1 illustrates an analyte detection device according to the present invention
  • FIG. 2 illustrates that a labeling chamber is additionally provided between a sample chamber and a detection chamber according to the present invention
  • FIG. 3 illustrates that a
  • FIG. 7 illustrates a method in which a washing buffer is injected by moving a washing buffer chamber plug using a fixing cover having a protrusion formed thereon according to the present invention
  • FIG. 8 illustrates a system for detecting an analyte using gravity according to the present invention
  • FIG. 9 illustrates a system for detecting an analyte using gravity according to the present invention
  • FIG. 10 illustrates a system for detecting an analyte using a centrifugal force according to the present invention
  • FIG. 11 illustrates a system for detecting an analyte using a centrifugal force according to the present invention
  • FIG. 12 illustrates a valve that is opened or closed by a centrifugal force using a cam having a weight connected thereto in a system for detecting an analyte using a centrifugal three according to the present invention
  • FIG. 13 illustrates a valve that is opened or closed by a centrifugal force using a horizontally movable clamp in a system for detecting an analyte using a centrifugal force according to the present invention
  • FIG. 14 illustrates a method in which magnetic particles are moved from a sample chamber to a sample direction by applying a magnetic force in a direction from the detection chamber to the sample chamber in a system for detecting an analyte using a magnetic force according to the present invention
  • FIG. 15 illustrates a method in which magnetic particles are moved by moving a magnet
  • FIG. 16 illustrates a method in which different kinds of particles are separated from each other using a magnetic force together with a centrifugal force according to the present invention
  • FIG. 17 illustrates a method in which bacteria are detected using capture particles (capture magnetic particles) having immobilized thereon a receptor for the bacteria and labeling particles (labeling receptor particles) which have immobilized thereon a receptor for the bacteria and have a labeling function, according to the present invention
  • FIG. 18 illustrates a method in which magnetic particles unbound to bacteria are removed by disposing a filter on an inner surface opposite an outer surface with which a magnet comes into contact, and moving the magnet, according to the present invention
  • FIG. 19 illustrates a method in which magnetic particles unbound to bacteria am removed by using a centrifugal force together with a magnetic force in a state in which a filter is disposed on an inner surface opposite an outer surface with which a magnet comes into contact, according to the present invention
  • FIG. 20 illustrates a method in which an analyte is detected by a sandwich ELISA method using capture particles having a capture antibody immobilized thereon and a labeled antibody according to the present invention
  • FIG. 21 illustrates a method in which the analyte kinase is detected by immobilizing on particles a receptor for a material produced by the analyte according to the present invention
  • FIG. 22 illustrates a method in which the analyte protease is detected by immobilizing on particles a receptor for a material dissociated by the analyte according to the present invention
  • FIG. 23 illustrates a principle according to which paralytic shellfish toxin (STX) is detected by a competitive immunoassay using magnetic particles as a solid phase in a detection device according to the present invention
  • FIG. 24 shows the structure of a detection device used in Example 1;
  • FIG, 25 is a graph showing the results of detecting paralytic shellfish toxin (STX) by a competitive immunoassay in Example 1;
  • FIG. 26 shows the LOC structure of a detection device used in Example 2;
  • FIG. 27 shows the structure and operating principle of a measurement device used in Example 2;
  • FIG. 28 is a graph showing the results of detecting the paralytic shellfish toxin SIX by a competitive immunoassay in Example 2;
  • FIG. 29 shows the LOC structure of a detection device used in Example 3;
  • FIG. 30 shows the structure and operating principle of a magnetic particle moving device used in Example 3;
  • FIG. 31 is a graph showing the results of an experiment performed in Example 3 to confirm whether or not solutions of the sample chamber and detection chamber of an LOC are mixed with each other and whether or not other materials of the sample chamber also move during movement of particles of the sample chamber;
  • FIG. 32 is a graph showing the results of detecting paralytic shellfish toxin GTX 2&3 by a competitive immunoassay in Example 3;
  • FIG. 33 shows a principle according to bacteria are detected using capture particles (capture magnetic particles) and labeling particles (labeling particles) in Example 4;
  • FIG. 34 is a photograph showing a measurement device used in Example 4;
  • FIG. 35 is a graph showing the results of detecting Salmonella bacteria in Example 4.
  • an analyte detection device 100 comprises a sample chamber 110 and a detection chamber 120 , and may comprise a channel 130 between the sample chamber 110 and the detection chamber 120 .
  • the sample chamber 110 may receive a mixed solution of a reactant comprising particles 200 and a sample containing an analyte 210
  • the detection chamber 120 may receive a detection solution.
  • the diameter of the channel 130 may be smaller than the diameter of each of the sample chamber 110 and the detection chamber 120 in order to prevent the mixed solution and the detection from mixing with each other.
  • the particles 200 may be a material that is bound to the analyte 210 or a product produced by the analyte 210 to form a particle-analyte complex or a particle-product complex.
  • a receptor specific for the analyte 210 or a receptor specific for a product produced by the analyte 210 may be immobilized on the particles 200 .
  • the particles 200 may function to move the analyte 210 or a product produced by the analyte 210 from the sample chamber 110 to the detection chamber 120 , and may also function to attach a label to the analyte 210 .
  • the particles 200 may be at least one kind of particles selected from the group consisting of silica particles, polystyrene particles, polycarbonate particles, glass particles, alumina particles, gold particles, silver particles, palladium particles, platinum particles, titania particles, zirconium particles, and core-shell particles.
  • the receptor immobilized on the particles may be a receptor capable of binding directly to the analyte 210 .
  • the analyte 210 is one of substances such as proteins, organic molecules, viruses, bacteria, plant cells or animal cells, for which antibodies can be formed, an antibody for each analyte 210 may be used as the receptor.
  • the analyte 210 is lectin, a carbohydrate may be used as the receptor, and on the contrary, if the analyte 210 comprises a carbohydrate, lectin may be used as the receptor.
  • the analyte 210 is nucleic acid such as DNA or RNA
  • a DNA or PNA peptide nucleic acid having a nucleotide sequence complementary thereto
  • any substances including aptamers obtained from nucleic acids, peptide ligands obtained from peptide libraries, protein ligands obtained from affibody libraries, etc., may be used as the receptor, as long as the analyte 210 may bind specifically thereto.
  • a receptor capable of binding a receptor that binds directly to the analyte may be immobilized on the particles.
  • the receptor that binds directly to the analyte is referred herein to as the primary receptor
  • the receptor that binds to the primary receptor is referred herein to as the secondary receptor.
  • the primary receptor is an antibody
  • the secondary receptor used may be a secondary antibody or protein G.
  • the primary receptor is DNA or PNA (peptide nucleic acid)
  • a DNA or PNA complementary to a portion of the nucleotide sequence of the primary receptor may be used as the secondary receptor.
  • the secondary antibody used may be, for example, an anti-rabbit immunoglobulin G antibody, if the primary antibody is of rabbit origin.
  • the receptor may be a receptor capable of binding to a substance produced by the analyte 210 , and the analyte 210 may be an enzyme. More specifically, the receptor may be a receptor for a substance that is produced in proportion to the amount of the analyte 210 . For example, if the analyte 210 is an enzyme, the receptor may be a receptor for the product. As another example, a receptor for a molecule that is dissociated or structurally changed in response to the analyte 210 may also be used.
  • the present invention is characterized in that the mixed solution and the detection solution am received in a stationary state, and the detection chamber 210 may be closed other than the portion collected to the channel 130 .
  • the expression “the mixed solution and the detection are stationary” does not mean that the solutions do not move, but means that analysis can be performed by moving the solid phase instead of moving the liquid phase in a main analysis step, unlike a conventional method in which the liquid phase is moved.
  • the term “solid phase” may refer to particles.
  • the detection solution may be filled in the channel 130 .
  • a washing buffer may be filled in the channel 130 .
  • washing buffer refers to a buffer containing components that assist in removing nonspecifically adsorbed substances from the particles, such as an appropriate. concentration of detergent or salt.
  • the analyte detection device 100 may further comprise a labeling chamber 140 containing a labeling solution.
  • the labeling chamber 140 may be connected between the sample chamber 110 and the detection chamber 120 by the channel 130 , and the labeling solution 230 may comprise a labeled receptor 230 .
  • the labeled receptor 230 means one having a label attached to a receptor capable of binding to the analyte 210 , and the label may be at least one selected from the group consisting of color development, luminescence, fluorescence, catalytic activity, magnetic force, and radioactivity.
  • the labeling chamber 140 may be used in a sandwich method in which capture particles having immobilized thereon a receptor capable of binding to the analyte 210 are added to a sample containing the analyte 210 to bind the analyte 210 to the capture particles which are then washed, after which the labeled receptor 230 is added thereto to bind the analyte 210 .
  • the reason why the particles used are referred to as the capture particles 220 is because these particles serve to capture and move the analyte.
  • the receptor immobilized on the capture particles 220 and the receptor used in the labeled receptor should be able to simultaneously bind non-competitively to different sites of the analyte.
  • the two receptors are referred herein to as the first receptor and the second receptor, respectively, in order to distinguish from the above-described primary receptor and secondary receptor.
  • the analyte 210 when a sample containing the analyte 210 and the capture particles 220 are added to the sample chamber 110 and reacted with each other, the analyte 210 can be bound to the capture particles 220 .
  • the capture particles 220 are moved to the labeling chamber 140 , substances unbound to the capture particles 220 can be washed out during passage through the channel 130 , and the labeled receptor 230 can bind to the analyte 210 in the labeling chamber 140 , and thus a sandwich form can be obtained.
  • the capture particles 220 and the labeled receptor 230 may be added to the detection device of FIG. 1 and reacted with one another, and then the capture particles 200 may be moved to the detection chamber 120 , thereby detecting the analyte.
  • the detection chamber 120 may contain, on at least one side, a receptor to which the particles 200 can bind, and the analyte detection device of the present invention may further comprise a waste chamber 150 configured to receive particles 200 unbound to the receptor 200 .
  • the waste chamber 150 may be connected to one side of the detection chamber 120 .
  • the detection device shown in FIG. 3 may be used to detect the analyte 210 by a sandwich method using the labeling capture particles 220 which have immobilized thereon a is receptor and function as a label.
  • the first receptor may be placed in the detection chamber 120 as described above, and the second receptor may be immobilized on the particles 200 .
  • the two receptors should be receptors that bind to different sites of the analyte so as not to overlap each other.
  • the enzyme together with the first receptor may be bound to the particles 200 .
  • the receptor may be immobilized on particles 200 capable of emitting fluorescence.
  • the analyte detection device may further comprise a reactant chamber 160 connected to one side of the sample chamber 110 and containing a reactant 113 .
  • the reactant chamber 160 may be connected to one side of the sample chamber 110 through a first connection passage 131 , and the diameter of the first connection passage 131 may be smaller than that of each of the reaction chamber 160 and the sample chamber 110 .
  • the reaction chamber 160 comprises a first cavity formed therein, and a reactant chamber plug 112 disposed in the upper portion of the first cavity so as to be movable up and down by external pressure, wherein the reactant 113 is placed in the lower portion of the first cavity so that it will be discharged to the first connection passage 131 by movement of the reactant chamber plug 112 .
  • the reactant 113 can be stored for a long period of time without losing its activity when it is stored in a dried state in the sample chamber 110 or the reactant chamber 160 .
  • the reactant 113 can be dried after its absorption into fiber.
  • reaction chamber may further comprise, above the dried reactant 114 , a solvent 115 for dissolving the dried reactant 114 .
  • the analyte detection device of the present invention may further comprise a buffer chamber.
  • the buffer chamber may be connected between the sample chamber 110 and the detection chamber 120 , or between the sample chamber 110 and the labeling chamber 140 , or between the labeling chamber 140 and the detection chamber 120 .
  • the buffer chamber is disposed is because, when the channel 130 is filled with a washing buffer, the washing buffer can be diffused to and mixed with other solution during storage of the analyte detection device 100 .
  • the channel 130 be filled with air, and then filled with a washing buffer when the analyte detection device 100 is used.
  • the buffer chamber may be connected to the channel 130 through second connection passage 132 , and the diameter of the second connection passage 132 may be smaller than that of each of the buffer chamber and the sample chamber 110 .
  • the buffer chamber comprises a second cavity formed therein, and a butler chamber plug 112 disposed in the upper portion of the second cavity so as to be movable up and down by external pressure, wherein the buffer is contained in the lower portion of the second cavity so that it will be discharged to the sample chamber 110 through the second connection passage 132 and the channel 130 by up-and-down movement of the buffer chamber plug.
  • the analyte detection device 100 of the present invention may comprise a fixing cover 170 . More specifically, the analyte detection device 100 comprises: a fixing cover 170 provided at the top of the analyte detection device 100 ; a first protrusion 171 formed on the fixing cover 170 at a position corresponding to the reactant chamber plug 112 ; and a second protrusion 171 formed on the fixing cover 170 at a position corresponding to the buffer chamber plug, wherein the first protrusion 171 and the second protrusion 171 can move the reactant chamber plug 112 and the buffer chamber plug downward by external pressure.
  • the analyte detection device 100 may further comprise, in the fixing cover 170 , a sample inlet 111 tor injecting a sample.
  • the reactant 113 may also be stored in the sample chamber without being stored in a separate reactant chamber 160 .
  • the reactant 113 may be a dried reactant 114 , and the dried reactant 114 may be obtained by absorbing a liquid-state reactant into a fiber substrate and drying the absorbed reactant.
  • the receptor may be a primary receptor capable of binding directly to the analyte 210 .
  • the analyte 210 is one of substances such as proteins, organic molecules, viruses, bacteria, plant cells or animal cells, for which antibodies can be formed, an antibody for each analyte 210 may be used as the receptor.
  • the analyte 210 is lectin, a carbohydrate may be used as the receptor, and on the contrary, if the analyte 210 comprises a carbohydrate, lectin may be used as the receptor.
  • the analyte 210 is nucleic acid such as DNA or RNA
  • a DNA or PNA peptide nucleic acid having a nucleotide sequence complementary thereto
  • any substances including aptamers obtained from nucleic acids, peptide ligands obtained from peptide libraries, protein ligands obtained from affibody libraries, etc., may be used as the receptor, as long as the analyte 210 may bind specifically thereto.
  • the receptor may be a secondary receptor capable of binding to the primary receptor, and the primary receptor may be a receptor capable of binding directly to the analyte 210 . More specifically, if the primary receptor is an antibody, the secondary receptor used may be a secondary antibody or protein G. As another example, if the primary receptor is DNA or PNA (peptide nucleic acid), a DNA or PNA complementary to a portion of the nucleotide sequence of the primary receptor may be used as the secondary receptor.
  • the primary receptor is DNA or PNA (peptide nucleic acid)
  • a DNA or PNA complementary to a portion of the nucleotide sequence of the primary receptor may be used as the secondary receptor.
  • the secondary antibody used may be, for example, an anti-rabbit immunoglobulin G antibody, if the primary antibody is of rabbit origin.
  • the receptor may be a receptor capable of binding to a substance produced by the analyte 210 , and the analyte 210 may be an enzyme. More specifically, the receptor may be a receptor for a substance that is produced in proportion to the amount of the analyte 210 . For example, if the analyte 210 is an enzyme, the receptor may be a receptor for the product. As another example, a receptor for a molecule that is dissociated or structurally changed in response to the analyte 210 may also be used.
  • the analyte detection device 100 of the present invention is characterized in that the particles 200 are moved from the sample chamber 110 to the detection chamber 120 by moving means.
  • the moving means may be a centrifugal force, gravity, or a magnetic force.
  • the particles 200 may be composed of two or more types of particles.
  • the particles 200 may be composed of magnetic particles and nonmagnetic particles, or may composed of particles having a specific gravity lower than that of the detection solution and particles having a specific gravity higher than that of the detection solution.
  • a centrifugal force and a magnetic force may be used together to move the two or more types of particles. This will be described in detail later.
  • the analyte detection device 100 of the present invention may comprise at least one vibrating unit in order to react a sample with the reactant 113 or to promote movement of the particles 200 .
  • the vibrating unit may be a vibrator.
  • the label is not specifically limited, as long as it includes measurable properties, including magnetic properties, optical properties such as fluorescence, luminescence or absorbance, catalytic activities such as enzymes or metal catalysts, radioactivity, electrical conductivity, mass, and the like.
  • catalytic activity may serve as a label. If catalytic activity serves as a label, the production or dissipation of a fluorescent product, the production or dissipation of a light-absorbing substance, the generation of light, a change in pH, a change in electrical conductivity, a change in potential difference, a change in mass, or the like, which results from the catalytic reaction, may be measured.
  • a light-absorbing property may serve as a label.
  • two opposite sides in the detection chamber are preferably transparent in order to measure absorbance.
  • one side of the detection chamber may be transparent, and the remaining sides of e detection chamber may be white or silver in color so that they can more easily reflect light.
  • fluorescence may serve as a label.
  • one side of the detection chamber 120 may be transparent, and the remaining sides of the detection chamber 120 may be black in color so that they can easily absorb light.
  • the two non-opposite sides of the detection chamber 120 may be transparent, and the remaining sides may be black in color so that they can easily absorb light.
  • Methods for detecting the analyte 210 using the analyte detection device 100 as described above are as follows.
  • the present invention is directed to a method for detecting an analyte using the analyte detection device 100 , the analyte detection device 100 comprising: a sample chamber 110 configured to contain a mixed solution of a reactant 113 comprising the particles 200 and a sample containing the analyte 210 ; a detection chamber 120 configured to contain a detection solution; and a channel 130 located between the sample chamber 110 and the detection chamber 120 so as to prevent the mixed solution and the detection solution from mixing with each other; the method comprising the steps of mixing and reacting the sample containing the analyte 210 with the reactant 113 comprising the particles 200 in the sample chamber 110 ; moving the particles 200 to the detection chamber 120 by moving means; and detecting: the analyte 210 in the detection chamber 120 .
  • the present invention is also directed to a method for detecting an analyte using the analyte detection device 100 , the analyte detection device 100 comprising: a sample chamber 110 configured to contain a mixed solution of a reactant comprising capture particles 200 and labeling particles 250 and a sample containing the analyte 210 ; a detection chamber 120 configured to contain a detection solution; and a channel 130 located between the sample chamber 110 and the detection chamber 120 so as to prevent the mixed solution and the detection solution from mixing with each other; the method comprising the steps of: mixing the reactant 113 and the sample in the sample chamber 110 to form a capture particle-analyte-labeling particle conjugate; moving the capture particle-analyte-labeling particle conjugate to the detection chamber 120 by moving means; and detecting the analyte 210 in the detection chamber 120 .
  • the capture particles 220 may be magnetic particles having immobilized thereon a to primary receptor specific for the analyte 210
  • the labeling particles 250 may be nonmagnetic particles having the primary receptor specific for the analyte 210 and comprising a label.
  • the capture particles 220 may be particles having immobilized thereon a primary receptor specific for the analyte 210 and having a specific gravity greater than that of the detection solution
  • the labeling particles may be particles having immobilized. thereon the primary receptor specific for the analyte 210 and comprising a label and having a specific gravity smaller than that of the detection solution.
  • the receptors that are immobilized on the capture particles 220 and the labeling particles 250 may be the same primary receptor or may be two kinds of primary receptors that bind to different sites. In other words, the first receptor and the second receptor may also be used.
  • the analyte 210 may be at least one selected from among viruses, bacteria and eukaryotic cells, which have a plurality of binding sites.
  • the present invention is also directed to a method for detecting an analyte using the analyte detection device 100 , the analyte detection device 100 comprising: a sample chamber 110 configured to contain a mixed solution of a sample containing the analyte 210 and a reactant 113 comprising capture particles 220 having immobilized thereon a primary receptor specific for the analyte 210 and a standard material having a label attached thereto; a detection chamber 120 configured to contain a detection solution; and a channel 130 located between the sample chamber 110 and the detection chamber 120 so as to prevent the mixed solution and the detection solution from mixing with each other; the method comprising the steps of mixing the reactant 113 and the sample in the sample chamber 110 to form a capture particle-analyte complex and a capture particle-standard material complex; moving the capture particle-analyte complex and the capture particle-standard material complex to the detection chamber 120 by moving means; and detecting the analyte in the detection chamber 120 by use of the label linked to
  • the present invention is also directed to a method for detecting an analyte using the analyte detection device 100 , the analyte detection device 100 comprising: a sample chamber 110 configured to contain a mixed solution of a sample containing the analyte 210 and a reactant comprising capture particles 220 having immobilized thereon a primary receptor specific for the analyte 210 and a secondary receptor specific for the primary receptor, and a labeled receptor 230 having a label attached thereto; a detection chamber 120 configured to contain a detection solution; and a channel 130 located between the sample chamber 110 and the detection chamber 120 so as to prevent the mixed solution and the detection solution from mixing with each other; the method comprising the steps of: mixing the reactant 113 and the sample in the sample chamber 110 to form a capture particle-primary receptor-analyte complex and a capture particle-primary receptor-standard material complex; moving the capture particle-primary receptor-analyte complex and the capture particle-primary receptor-standard material complex
  • the present invention is also directed to a method for detecting an analyte using the analyte detection device 100 , the analyte detection device 100 comprising: a sample chamber 110 configured to contain a mixed solution of a sample containing the analyte 210 and a reactant 113 comprising a capture particles having immobilized thereon a first receptor specific for the analyte 210 and a labeled receptor 230 comprising a label attached to a second receptor specific for the analyte 210 ; a detection chamber 120 configured to contain a detection solution; and a channel 130 located between the sample chamber 110 and the detection chamber 120 so as to prevent the mixed solution and the detection solution from mixing with each other; the method comprising the steps of mixing the reactant 113 and the sample in the sample chamber 110 to form a capture particle-analyte-labeled receptor complex; moving the capture particle-analyte-labeled receptor complex to the detection chamber 120 by moving means; and detecting the analyte
  • the present invention is directed to a system 300 for detecting an analyte using gravity
  • the system 300 comprising: an analyte detection device comprising a sample chamber 110 configured to contain a mixed solution of a reactant 113 comprising particles 200 and a sample containing the analyte, a detection chamber 120 disposed below the sample chamber and configured to contain a detection solution, and a channel 130 located between the sample chamber 110 and the detection chamber 120 so as to prevent the mixed solution and the detection solution from mixing with each other; and at least one valve 310 between the sample chamber 110 and the channel 130 , wherein the particles 200 have a specific gravity greater than that of each of the mixed solution and the detection solution.
  • at least one selected from the group consisting of glycerol, sugar and Ficoll may be added to the detection solution in order to increase the specific gravity of the detection solution.
  • the present invention is directed to a method for detecting analyte using gravity, which uses the system 300 for detecting the analyte using gravity and comprises the steps of: reacting the reactant 113 with the sample in the sample chamber 110 in a state in which the valve 310 is closed; opening the valve 310 to move the particles 200 to the detection chamber 120 ; and detecting the analyte in the detection chamber 120 .
  • the channel 130 is made of a soft tube, the channel 130 can be simply closed using a clamp 452 , and the stopcock-type valve 310 may also be disposed.
  • the particles 200 used can be heavy so that they can precipitate in the sample vibe detection solution.
  • a system for detecting an analyte 210 using gravity comprises an analyte detection device 100 comprising: a sample chamber 110 configured to contain a mixed solution of a reactant 113 comprising particles 200 and a sample containing the analyte 210 ; a detection chamber 120 configured to contain a detection solution; and a channel 130 located between the sample chamber 110 and the detection chamber 120 so as to prevent the mixed solution and the detection solution from mixing with each other, wherein the channel 130 is configured to connect the upper portion of the sample chamber 110 with the upper portion of the detection chamber 120 in a state in which the sample chamber 110 and the detection chamber 120 are horizontally positioned, and the particles 200 have a specific gravity greater than that of each of the mixed solution and the detection solution.
  • at least one selected from the group consisting of glycerol, sugar and Ficoll may be added to the detection solution in order to increase the specific gravity of the detection solution.
  • a method for detecting an analyte using the system 300 for detecting the analyte using gravity comprises the steps of: reacting the reactant 113 with the sample in the sample chamber 110 ; inclining the analyte detection device 100 at an angle of 20-70° such that the channel 130 faces downward, thereby moving the particles 200 to the detection chamber 120 ; and detecting the analyte in the detection chamber 120 .
  • the method for detecting an analyte using gravity has advantages in that it does not require a separate device to move the particles 200 , and thus is highly economical and is conveniently used on site.
  • the present invention is directed to a system 400 for detecting an analyte using a centrifugal force
  • the system 400 comprising: an analyte detection device comprising a sample chamber 110 configured to contain a mixed solution of a reactant 113 comprising particles 200 and a sample containing an analyte 210 , a detection chamber 120 configured to contain a detection solution, and a channel 130 located between the sample chamber 110 and the detection chamber 120 so as to prevent the mixed solution and the detection from mixing with each other; a disc 410 which includes a plurality of the analyte detection devices 100 and is rotatable; and at least one detector 420 located near the disc 410 , wherein the detection chamber 120 is disposed outward from the center of the disc 410 .
  • the channel 130 may comprise a single valve 440 .
  • the valve 440 comprises a rotatable shaft configured to open or close the channel 130 , and a weight connected to the rotatable shaft. The weight can be rotated by a centrifugal force caused by rotation of the disc 410 , thereby opening the channel 130 .
  • the valve 450 comprises a valve body 451 , and a clamp 452 located on the valve body 451 so as to open or close the channel 130 .
  • the clamp 452 is movable horizontally by rotation of the disc 410 to thereby open the channel 130 .
  • the particles 200 may have a specific gravity greater than that of each of the mixed solution comprising the sample and the detection solution.
  • the present invention is also directed to a method for detecting an analyte using a centrifugal force, which uses the system 400 for detecting the analyte using a centrifugal force and comprises the steps of reacting the reactant 113 and the sample in the sample chamber 110 ; rotating the disc 410 to open the valve 440 or 450 to thereby open the channel 130 ; moving the particles 200 to the detection chamber 120 ; and stopping the rotation, and then rotating the disc 410 at an angle of 10-180° such that the detection chambers 120 of the detection devices sequentially face the detector 420 , thereby detecting the analyte in the detection chamber 120 .
  • analyte detection devices 100 may be disposed in the disc 410 .
  • the analyte 210 in the detection chamber 120 can be analyzed by the single detector 420 while the disc 410 is rotated at an angle of 45°.
  • the moving speed of the particles 200 toward the detection chamber 120 can be controlled according to the rotating speed of the disc 410 .
  • the particles 200 may be a particle-analyte complex.
  • the sample may contain solid dregs, and thus when the mixed solution containing: the sample is likely to move to the detection chamber 120 or to be mixed with the detection solution due to the high specific gravity of the mixed solution containing the sample, a substance, such as glycerol, sugar, Ficoll or the like, which increases specific gravity, may be added to the detection.
  • a filter 520 for filtering dregs may be disposed in the sample inlet.
  • the analyte 210 can be detected by the method for detecting the analyte 210 using the centrifugal force according to the present invention without using separate particles 200 .
  • the labeled receptor 230 having a function of labeling a receptor for bacteria is bound to bacteria and then a centrifugal force is applied thereto, only a bacteria-labeled receptor complex can move to the detection chamber 120 , and thus the number of the bacteria can be evaluated by measuring the signal of the label in the detection chamber 120 .
  • particles 200 having low buoyant density may be labeled, and a receptor for bacteria may be immobilized on the particles 200 .
  • a receptor for bacteria may be immobilized on the particles 200 .
  • polystyrene nanoparticles having a size of several tens of nanometers have a specific gravity of about 1.0 and a small size, and thus are not easily settled down by the centrifugal force.
  • the particles are referred to as the labeling particles 250 , because these particles do not contribute to movement.
  • labeling particles 250 When the labeling particles 250 are mixed and reacted with a sample and a centrifugal three is applied thereto, labeling particles 250 unbound to bacteria will not move, and only a complex comprising the labeling particles 250 bound to bacteria will move to the detection chamber 120 , and thus the number of the bacteria can be evaluated by measuring the signal of the label in the detection chamber 120 .
  • the present invention is directed to a system for detecting an analyte using a magnetic force, comprising: an analyte detection device comprising a sample chamber 110 configured to contain a mixed solution of a reactant 113 comprising magnetic particles and a sample containing an analyte 210 , a detection chamber 120 configured to contain a detection solution, and a channel 130 located between the sample chamber 110 and the detection chamber 120 so as to prevent the mixed solution and the detection solution from mixing with each other; and at least one magnetic force application unit 510 disposed on the outer wall of the analyte detection device 100 and configured to apply a magnetic force to the magnetic particles 250 , wherein the sample chamber 110 and the detection chamber 120 are horizontally disposed.
  • the present invention is also directed to a method for detecting an analyte using a magnetic force, which uses the system for detecting the analyte using the magnetic force and comprises the steps of reacting the reactant 113 with the sample in the sample chamber 110 ; applying a magnetic force from the detection chamber 120 to the sample chamber 110 using a magnetic force application unit 510 disposed on one side of the detection chamber 120 , thereby moving the magnetic particles from the sample chamber 110 to the detection chamber 120 ; and detecting the analyte in the detection chamber 120 .
  • the present invention is directed to a method for detecting an analyte using a magnetic force, which uses the system for detecting the analyte using the magnetic force and comprises the steps of reacting the reactant 113 with the sample in the sample chamber 110 ; moving the magnetic force application unit 510 , located on the outside of the analyte detection device 100 , from the sample chamber 110 to the detection chamber, thereby moving the magnetic particles from the sample chamber 110 to the detection chamber 120 ; and detecting the analyte 210 in the detection chamber 120 .
  • the position of the magnetic particles is determined by the position of the magnetic force application unit, and thus the moving direction or moving speed of the magnetic particles 250 can be easily controlled.
  • the particles 200 when the particles 200 are moved by the magnetic force, the particles 200 move along the wall surface of the device 100 for detecting the analyte 210 . For this reason, in order to facilitate the movement of the particles 200 , at least one surface of the device 100 for detecting the analyte 210 should be smooth without irregularities.
  • the sample chamber 110 , the channel 130 and the detection chamber 120 may be horizontally disposed, and the channel 130 may be configured to connect the lower portion of the sample chamber 110 with the lower portion of the detection chamber 120 .
  • the bacteria can be detected using two kinds of particles 200 having different properties. More specifically, only a receptor for bacteria may be immobilized on the magnetic particles so that the particles can be used as capture particles 220 , and a receptor for bacteria may be immobilized on other nonmagnetic particles which are then labeled so that the nonmagnetic particles can be used as labeling particles 250 .
  • the receptors that are immobilized on two kinds of particles may be the same receptor, but may also be two kinds of receptors that bind to different sites.
  • the capture particles 220 move to the detection chambers 220 .
  • the labeling particles 250 can also bind to the bacteria.
  • the number of the bacteria can be evaluated by measuring the label signal of the bacteria-bound labeling particles 250 that moved to the detection chamber 120 .
  • the above-described method that uses two kinds of particles having different properties may applied to, in addition to bacteria, any analytes having several binding sites, such as cells or viruses.
  • a system for detecting the analyte 210 using a magnetic force comprises: an analyte detection device 100 comprising a sample chamber 110 configured to a mixed solution of a sample containing the analyte 210 and a reactant 113 comprising labeling capture particles 240 which have a label attached to magnetic particles and have immobilized thereon a receptor for the analyte, a detection chamber 120 configured to contain a detection solution, and a channel 130 located between the sample chamber 110 and the detection chamber 120 so as to prevent the mixed solution and the detection solution from mixing with each other; a filter 520 disposed on the bottom inside the analyte detection device 100 ; and at least one magnetic force application unit 510 disposed on the outer wall of the bottom of the analyte detection device 100 and configured to apply a magnetic force to the labeling capture particles 240 , wherein the channel 130 is configured to connect the bottom of the sample chamber 110 with the bottom of the detection chamber 120 in a state in Which the sample chamber 110 and the detection
  • the system may further comprise a porous filter 520 support for supporting the filter 520 , and the filter 520 may be a filter capable of filtering the magnetic particles 250 .
  • the filter 520 may be a filter through which labeling capture particles 240 unbound to the analyte 210 pass and a labeling capture particle-analyte complex does not pass.
  • the filter 520 may be negatively or positively charged.
  • the present invention is directed to a method for detecting analyte using a magnetic three, which uses the system for detecting analyte using the magnetic force and comprises the steps of reacting the reacting the reactant 113 with the sample in the sample chamber 110 to form a labeling capture particle-analyte complex; moving the magnetic force application unit 510 from the sample chamber 110 to the detection chamber 120 , thereby discharging labeling capture particles 240 unbound to the analyte 210 and moving the labeling capture particle-analyte complex to the detection chamber 120 ; and detecting the analyte 210 in the detection chamber 120 by use of the label attached to the labeling capture particles 240 .
  • the present invention is also directed to a system for detecting an analyte using a magnetic force and a centrifugal force, which comprises an analyte detection device 100 comprising a sample chamber 110 configured to contain a mixed solution of a sample containing the analyte 210 and a reactant 113 comprising labeling capture particles 240 which have a label attached thereto and have immobilized thereon a receptor for the analyte 210 , a detection chamber 120 configured to contain a detection solution, and a channel 130 located between the sample chamber 110 and the detection chamber 120 so as to prevent the mixing solution and the detection solution from mixing with each other; a filter 520 disposed on the bottom inside the analyte detection device 100 ; at least one magnetic force application unit 510 disposed on the outer wall of the bottom of the analyte detection device 100 and configured to apply a magnetic force to the labeling capture particles 240 ; a disc 410 which includes a plurality of the analyte detection devices 100 and is
  • the filter 520 may be a filter 520 through which labeling capture particles 240 unbound to the analyte 210 pass and the labeling capture particle-analyte complex does not pass.
  • the present invention is also directed to a method for detecting an analyte using a magnetic force and a centrifugal force, which uses the system for the analyte using the magnetic force and the centrifugal force and comprises the steps of reacting the reactant 113 with the sample in the sample chamber 110 to form a labeling capture particle-analyte complex; rotating the disc 410 in a state in which the magnetic three application unit 510 is fixed to the bottom of the sample chamber 110 , thereby discharging labeling capture particles 240 unbound to the analyte 210 to the bottom of the filter 520 and moving the labeling capture particle-analyte complex to the detection chamber 120 ; and detecting the analyte in the detection chamber 120 by use of the label attached to the labeling capture particles 240 .
  • a high-molecular-weight substance such as a protein, a nucleic acid, a carbohydrate or the like
  • it can be detected by a sandwich method using two kinds of receptors (i.e., the first receptor and the second receptor) that are capable of simultaneously binding non-competitively to different sites of the analyte (see FIGS. 2 and 3 ).
  • the sandwich method is performed using an analyte detection device comprising: a sample chamber configured to contain a mixed solution of a sample containing an analyte and a reactant comprising capture particles 220 having immobilized thereon a first receptor specific for the analyte and a labeled receptor 230 having a label attached to a second receptor specific for the analyte; a detection chamber configured to contain a detection solution; and a channel located between the sample chamber and the detection chamber so as to prevent the mixed solution and the detection solution from mixing with each other.
  • the sandwich method uses the analyte detection device, and comprises the steps of mixing the reactant and the sample in the sample chamber to than a capture particle-analyte-labeled receptor complex; moving the capture particle-analyte-labeled receptor complex to the detection chamber by moving means; and detecting the analyte by use of the label attached to the labeled receptor ( FIG. 20 ).
  • a sample containing an analyte is reacted only with capture particles 220 in the sample chamber to form a capture particle-analyte complex, and then the particles are moved to the labeling chamber.
  • a labeled receptor is additionally bound to the capture particle-analyte complex to form a capture particle-analyte-labeled receptor complex.
  • the capture particle-analyte-labeled receptor complex is moved to the detection chamber, and then the analyte can be detected using the labeling function of the labeled receptor.
  • capture particles 220 and labeling particles 250 as two kinds of particles having different properties, as described above with respect to the detection of bacteria.
  • different receptors that is, the first receptor and the second receptor, should be immobilized on the two kinds of particles.
  • a competitive immunoassay is used, because it is difficult to make two kinds of antibodies that bind to different sites.
  • a receptor is immobilized on particles 200 to make capture particles, and a standard material for the analyte is labeled to make a labeled standard material.
  • standard material for the analyte 210 means either an analyte 210 which has already been purified to have a known concentration, or a material capable of binding to a receptor for the analyte 210 , and refers to a material that can be used as a standard for evaluating the amount of the analyte contained in the sample.
  • capture particles and a labeled standard material When capture particles and a labeled standard material is added to and reacted with a sample containing the analyte 210 , the labeled standard material will bind to the capture particles in an amount inversely proportional to the amount of the analyte 210 contained in the sample.
  • the amount of the analyte 210 can be evaluated by moving the capture particles to the detection chamber and measuring the signal of the label bound to the capture particles.
  • a second receptor may also be immobilized instead of immobilizing the receptor for the analyte 210 on the particles 200 .
  • the primary receptor is an antibody
  • a secondary antibody or protein G may be used as the secondary receptor.
  • the secondary receptor is immobilized on the capture particles, the capture particles, the primary receptor for the analyte 210 , and the labeled standard are added to and reacted with the sample, after which the particles 200 are moved.
  • the standard material for the analyte 210 may also be immobilized on the particles 200 to make capture particles instead of immobilizing the receptor on the particles 200 .
  • the receptor should be labeled to make a labeled receptor 230 .
  • the capture particles having the standard material immobilized thereon and the labeled receptor 230 are added to and reacted with the sample, the labeled receptor 230 will bind to the capture particles in an amount inversely proportional to the amount of the analyte contained in the sample.
  • the amount of the analyte 210 can be evaluated by moving the particles to the detection chamber and measuring the signal of the label bound to the particles 200 .
  • the amount of the analyte 210 can be evaluated by detecting a material that is produced in proportional to the amount of the analyte 210 .
  • a receptor for the material that is produced in the amount of the analyte 210 should be to immobilized on the particles 200 , and if the analyte 210 is an enzyme, the receptor may be a receptor for the product of the enzyme.
  • a receptor for a molecule that is dissociated or structurally changed in response to the analyte 210 may also be immobilized on the particles 200 .
  • the receptor for the product is immobilized on the particles 200
  • the product itself preferably has a labeling function.
  • the receptor for the molecule that is dissociated or structurally changed in response to the analyte 210 is immobilized on the particles, the molecule may be labeled.
  • examples of detachable materials that are produced in the amount of the analyte 210 include kinase enzyme.
  • kinase has an activity of phosphorylating its substrate protein, and antibodies are known, which do not bind to unphosphorylated substrate proteins and can bind only to phosphorylated substrate proteins.
  • the substrate protein is labeled and the receptor capable of binding only to the phosphorylated substrate protein is immobilized to the particles 200 , the amount of kinase in the sample can be measured.
  • examples of detectable materials that are dissociated in response to the analyte 210 include protease.
  • a material capable of functioning as a label is immobilized on a stationary solid phase using a peptide, which can act as a substrate for protease, as a linker.
  • the stationary solid phase can be the sample chamber wall or a stationary particle.
  • a receptor for the label material is immobilized on movable particles to make capture particles.
  • the present invention can be used to detect analytes 210 , including organic materials, proteins, nucleic acids, cells, or the like.
  • Paralytic shellfish toxin is composed of various toxins, and an antibody (STX Ab) against saxitoxin (STX) that is the most important toxin among the toxins was used as a primary antibody.
  • STX Ab an antibody against saxitoxin
  • STX saxitoxin
  • horseradish peroxidase (HRP)-conjugated SIX STX-HRP
  • STX Ab solution and STX-HRP solution were purchased from Beacon Analytical Systems (USA) and used without changes.
  • ABTS solution Sigma
  • a substrate for HRP was filled in a detection chamber 120 and used as a detection solution.
  • a 2-way stopcock (purchased from Bio-Rad) for syringe use was connected to a immunoplate well (purchased from Corning) using a silicon tube, and a 3 ml syringe was then connected thereto ( FIG. 24 ).
  • the immunoplate well serves as the detection chamber
  • the syringe serves as the sample chamber
  • the 2-way stopcock serves as the channel 130 .
  • First ABTS solution was filled from the immunoplate well up to the valve 310 of the 2-way stopcock, and the valve 310 was closed.
  • 50 ⁇ l of STX Ab solution, 50 ⁇ l of STX-HRP solution, 50 ⁇ l of a sample containing STX, 30 ⁇ l of G-MB and 320 ⁇ l of PBS buffer were placed in the syringe and reacted for 30 minutes with shaking.
  • the syringe was carefully put into the 2-way stopcock such that no bubbles would be formed in the middle portion of the 2-way stopcock, and swinging bucket.
  • the syringe was centrifuged in a centrifuge equipped with a swinging bucket at 1000 rpm for 5 minutes.
  • the immunoplate well was separated, and the absorbance at 405 nm was measured with a microplate reader.
  • Lumigen PS-atto reagent Liigen
  • a structure as shown in FIG. 26 was prepared using PDMS.
  • the total size of this structure was 41 mm (W) ⁇ 26 mm (L) ⁇ 7 mm (H); the diameter of the detection chamber was 5 mm; the size of the sample chamber was 10 mm (W) ⁇ 10 mm (L); and the channel 130 had a length of 10 mm, a width of 1 mm and a height of 1 mm.
  • Glass having a thickness of 1 mm was attached to the bottom of the structure to form each chamber and the channel 130 .
  • a detection solution was placed in the detection chamber and the channel 130 , and then the top of the detection chamber was sealed with a transparent tape.
  • the device for measurement was manufactured in a light-shieldable box as shown in FIG. 27 .
  • a photodetector and a magnet were disposed above and below an LOC holder, respectively, such that the photodetector and the magnet were located immediately above and below the detection chamber of the LOC when the LOC was introduced.
  • the LOC holder was disposed above a vibrator.
  • the IDC was placed in the measurement device, and the box was covered with a lid. In this state, the intensity of light detected by the photodector was measured while vibration was applied. As a result, as shown in FIG. 28(A) , the intensity of light increased progressively with time, and the rate of the increase was inversely proportional to the concentration of STX contained in the sample.
  • FIG. 28(B) shows the intensity of light as a function of the concentration of STX contained in the sample.
  • a structure for manufacturing a lab-on-a-chip (LOC) was manufactured as shown in FIG. 29 by slightly modifying the structure of Example 2.
  • the shape of the detection chamber was changed to a rectangular shape (5 mm ⁇ 10 mm), and in order to prevent a solution in the sample chamber and a solution in the detection chamber from mixing with each other, the length of the channel 130 was made longer (15 mm), and each of the width and height of the channel 130 were made smaller (0.5 mm).
  • the total size of the LOC was also made smaller (41 mm (W) ⁇ 20 (L) ⁇ 5 mm (H)).
  • a device for moving magnetic particles 250 was manufactured using a syringe pump as shown in FIG. 30 .
  • a vibrator was fixed to one end of the pump, and an LOC holder was disposed thereon.
  • a magnet was fixed ID the moving portion of the pump so as to be located on the bottom of each LOC. Also, when the moving portion of the pump moved, each magnet moved from the sample chamber of each LOC to the detection chamber. In addition, vibration was applied during movement of the magnet so that the magnetic particles 250 would effectively move.
  • the mixture was allowed to react for 30 minutes while it was shaken at 350 rpm.
  • HRP-Ab did bind to GMB, but HRP remained in the solution without binding.
  • the magnetic particles 250 were not moved, and the solution of the sample chamber and the solution of the detection chamber were taken and transferred to microtubes.
  • the magnet was moved from the bottom of the sample chamber to the bottom of the detection chamber at a speed of 2 cm/min, thereby moving the magnetic particles 250 .
  • the solutions in the two chambers were also taken and transferred to microtubes.
  • the magnetic particles 250 were recovered from the four solutions, and then the activity of HRP enzyme remaining in the solutions and the activity of HRP enzyme present on the magnetic particles 250 were measured.
  • the magnetic particles 250 were present only in the sample chamber before movement of the magnet (SC-MB, light gray color) and were not present in the detection chamber (DC-MB, light gray color). However, after movement of the magnet, it could be seen that the magnetic particles 250 did not remain in the sample chamber (SC-MB, dark gray color) and were present in the detection chamber (DC-MB, dark gray color). This suggests that the magnetic particles 250 remained in the sample chamber without moving to the detection chamber during the first 30 minutes of shaking, and then were moved to the detection chamber by movement of the magnet. In addition, the activity of HRP enzyme in the solutions was found only in the sample chamber before or after movement of the magnet (SC-sol; light gray color and dark gray color).
  • GTX 2&3 a kind of paralytic shellfish poison, was detected using this system. Because GTX 2&3 can hind to STX-Ab due to its structure similar to that of STX, it could be detected by the same competitive immunoassay.
  • the detection chamber and channel 130 of the LOC were filled with 150 ⁇ l of a solution of 3,3′,5,5′-Tetratmethylbenzidine (TMB) that is a color development substrate for HRP enzyme. This solution was purchased from Sigma.
  • TMB 3,3′,5,5′-Tetratmethylbenzidine
  • the top side of the detection chamber was sealed with a transparent tape, and 20 ⁇ g of G-MB, 75 ⁇ g of STX-Ab, Ab, 75 ⁇ l of STX-HRP, and 20 g of a sample containing GTX 2&3 were added to the sample chamber which was then sealed with a transparent tape.
  • the contents in the sample chamber were subjected to a binding reaction in a shaker at 350 rpm for 30 minutes, and the magnet particles 250 were moved from the sample chamber to the detection chamber by use of the magnet moving unit while vibration was applied.
  • the LOC was shaken at 350 rpm for 30 minutes so that a reaction with HRP enzyme in the detection chamber would occur.
  • bacteria were detected by a method of moving the particles 200 by movement of a magnet.
  • Capture particles 220 are magnetic particles having immobilized thereon an antibody specific for bacteria
  • labeling particles are nonmagnetic panicles having immobilized thereon an antibody specific for bacteria and an enzyme label.
  • the capture particles 220 and the labeling panicles are added to a sample containing bacteria and allowed to react in the sample chamber, the two kinds of particles all bind to the bacteria.
  • the capture particles 220 are moved from the sample chamber to the detection chamber using a magnet, the bacteria bound to the capture particles 220 also move to the detection chamber.
  • labeling particles bound to the bacteria move to the detection chamber 120 together with the bacteria, but labeling particles unbound to the bacteria remain in the sample chamber 110 . Accordingly, because the amount of labeling particles that moved to the detection chamber 120 is proportional to the number of the bacteria, the number of the bacteria can be evaluated by measuring the activity of the enzyme label in the detection chamber 120 .
  • capture particles 220 were prepared by immobilizing biotin-anti-Salmonella antibody (biotin-Salmonella Ab; purchased from Thermo) on 1 ⁇ m-diameter Streptavidin magnetic beads (SA-MB; purchased from Dynabead), Labeling particles were prepared by immobilizing streptavidin-HRP on 100-nm-diameter COOH-silica nanoparticles (purchased from Microspheres-Nanospheres) by a chemical method using EDC, and then immobilizing biotin-Salmonella Ab thereon. Whether streptavidin-HRP was immobilized was confirmed by directly measuring the activity of HRP enzyme. Whether biotin-Salmonella Ab was immobilized was confirmed by alkaline phosphate-conjugated anti-rabbit immunoglobulin G antibody.
  • a measurement device disposed in a dark room as shown in FIG. 34 was used.
  • An LOC holder was disposed over a vibrator so that vibration could be applied during movement of particles.
  • a magnet could be moved by a magnet pulling wire below the LOC, and the wire was connected to an external syringe pump so that it could be pulled at a certain speed.
  • a photodetector was disposed immediately above the detection chamber of the LOC so that it could detect light immediately the particles 200 moved.
  • the detection chamber 120 of the LOC was filled with Lumigen PS-atto, and a mixture of 10 ⁇ g of the capture particles 220 , 10 ⁇ g of the labeling particles and a sample containing Salmonella bacteria was added to the sample chamber 110 .
  • the LOC was placed in a measurement device, and the magnet was moved from the sample chamber 110 to the detection chamber 120 at a speed of cm/min while vibration was applied. During movement of the magnet, the intensity of light was measured. As a result, as shown in FIG. 35 , light started to be emitted from about 100 seconds after the start of movement of the magnet, and the intensity of light reached a constant value after 250 seconds. In addition, the final intensity of light was proportional to the number of Salmonella bacteria, From the above results, it could be seen that bacteria could be detected using two kinds of particles, that is, magnetic capture particles 220 and nonmagnetic labeling particles.
  • first connection passage 132 : second connection passage
  • 140 labeling chamber
  • 150 waste chamber
  • 210 analyte
  • 220 capture particles
  • 300 system for detecting analyte using gravity
  • valve body valve body
  • 452 clamp
  • 500 system for detecting analyte using magnetic force

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Immunology (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Analytical Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Urology & Nephrology (AREA)
  • Molecular Biology (AREA)
  • Biomedical Technology (AREA)
  • General Physics & Mathematics (AREA)
  • Biochemistry (AREA)
  • Pathology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Food Science & Technology (AREA)
  • Biotechnology (AREA)
  • Cell Biology (AREA)
  • Microbiology (AREA)
  • Medicinal Chemistry (AREA)
  • Clinical Laboratory Science (AREA)
  • Dispersion Chemistry (AREA)
  • Fluid Mechanics (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)
  • Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
US14/915,206 2013-08-29 2014-08-27 Device and Method for Detecting Analyte by Movement of Particles Abandoned US20160209409A1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
KR20130102944 2013-08-29
KR10-2013-0102944 2013-08-29
KR10-2013-0166909 2013-12-30
KR20130166909A KR101398764B1 (ko) 2013-08-29 2013-12-30 입자의 이동에 의해 분석물질을 검출하는 장치 및 방법
PCT/KR2014/007976 WO2015030485A1 (ko) 2013-08-29 2014-08-27 입자의 이동에 의해 분석물질을 검출하는 장치 및 방법

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
PCT/KR2014/007976 A-371-Of-International WO2015030485A1 (ko) 2013-08-29 2014-08-27 입자의 이동에 의해 분석물질을 검출하는 장치 및 방법

Related Child Applications (1)

Application Number Title Priority Date Filing Date
US15/785,272 Division US10859570B2 (en) 2013-08-29 2017-10-16 Methods for detecting an analyte using an analyte detection device

Publications (1)

Publication Number Publication Date
US20160209409A1 true US20160209409A1 (en) 2016-07-21

Family

ID=50895090

Family Applications (2)

Application Number Title Priority Date Filing Date
US14/915,206 Abandoned US20160209409A1 (en) 2013-08-29 2014-08-27 Device and Method for Detecting Analyte by Movement of Particles
US15/785,272 Active 2035-02-08 US10859570B2 (en) 2013-08-29 2017-10-16 Methods for detecting an analyte using an analyte detection device

Family Applications After (1)

Application Number Title Priority Date Filing Date
US15/785,272 Active 2035-02-08 US10859570B2 (en) 2013-08-29 2017-10-16 Methods for detecting an analyte using an analyte detection device

Country Status (4)

Country Link
US (2) US20160209409A1 (zh)
KR (1) KR101398764B1 (zh)
CN (1) CN105683761B (zh)
WO (1) WO2015030485A1 (zh)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107796939A (zh) * 2016-08-30 2018-03-13 希森美康株式会社 试样分析用盒及其制造方法、以及其用途
EP3325976A4 (en) * 2015-07-17 2019-07-24 Genobio Corp. SYSTEM FOR SEPARATING MAGNETIC IRON PARTICLES
WO2020094780A3 (de) * 2018-11-08 2020-07-02 Hahn-Schickard-Gesellschaft für angewandte Forschung e.V. Vorrichtung und verfahren zum transport magnetischer partikel
US11099182B2 (en) 2016-06-30 2021-08-24 Sysmex Corporation Detection apparatus and detection method
WO2021230821A1 (en) * 2020-05-12 2021-11-18 National University Of Singapore A method for virus and biomarker detection
EP3881934A4 (en) * 2018-11-15 2022-07-27 Daegu Gyeongbuk Institute Of Science and Technology MICROFLUIDIC DEVICE AND METHOD FOR SEPARATION OF TARGET CELLS USING THE SAME
US11480525B2 (en) 2016-06-30 2022-10-25 Sysmex Corporation Chemiluminescence measurement apparatus
US11660615B2 (en) * 2016-07-19 2023-05-30 Jun Seok Lee Centrifugal separation container, and method for moving substances inside centrifugal separation container

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11754563B2 (en) * 2014-11-20 2023-09-12 Global Life Sciences Solutions Operations UK Ltd Porous membranes with a polymer grafting, methods and uses thereof
KR101643477B1 (ko) 2014-12-26 2016-07-28 강릉원주대학교산학협력단 정지 액체상 랩온어칩 분석장치
KR20160101775A (ko) 2015-02-17 2016-08-26 강릉원주대학교산학협력단 수직형 정지액체상 랩온어칩, 이를 이용한 분석물질 검출장치 및 검출방법
KR101811134B1 (ko) 2016-06-29 2017-12-22 강릉원주대학교산학협력단 정지액체상 랩온어칩을 이용한 박테리아 검출 방법
KR101871042B1 (ko) 2016-06-29 2018-06-26 강릉원주대학교산학협력단 정지액체상 랩온어칩을 이용한 핵산 시료의 제조 방법
JP6479730B2 (ja) * 2016-06-30 2019-03-06 シスメックス株式会社 化学発光測定装置
JP6457451B2 (ja) * 2016-06-30 2019-01-23 シスメックス株式会社 検出装置および検出方法
KR101949128B1 (ko) * 2017-02-08 2019-02-18 강릉원주대학교산학협력단 박테리아 검출 시스템 및 검출 방법
KR101895597B1 (ko) 2017-02-20 2018-09-07 강릉원주대학교산학협력단 정지 액체상 랩온어튜빙
KR101988233B1 (ko) * 2018-01-22 2019-06-12 강릉원주대학교산학협력단 세포 검출장치 및 이를 이용한 세포 검출방법
KR102020369B1 (ko) 2018-02-23 2019-09-10 강릉원주대학교산학협력단 분자진단 장치 및 이를 이용한 분자진단 방법
KR102244375B1 (ko) 2019-02-20 2021-04-27 강릉원주대학교산학협력단 입자와 용액의 동시 이동에 의한 분석물질을 검출하는 장치 및 이를 이용한 검출방법
KR102328372B1 (ko) * 2019-02-26 2021-11-23 강릉원주대학교산학협력단 분석물질을 검출하는 장치 및 이를 이용한 검출방법
KR102155218B1 (ko) * 2019-04-17 2020-09-11 아주대학교산학협력단 생체물질의 분석 방법
KR102450943B1 (ko) * 2020-07-30 2022-10-04 아주대학교산학협력단 바이오 센서, 이의 제조방법 및 이를 이용한 분석 방법
KR102634939B1 (ko) * 2020-10-28 2024-02-07 주식회사 퀀타매트릭스 항생제 감수성 검사 장치, 및 이의 항생제 감수성 검사 방법, 및 이를 포함하는 시스템
KR20230057939A (ko) 2021-10-22 2023-05-02 강릉원주대학교산학협력단 중력을 이용하는 자성입자 기반 바이오칩 및 이를 이용한 분석물질 검출 방법

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090221431A1 (en) * 2005-05-06 2009-09-03 Jae Chern Yoo Digital bio disc (dbd), dbd driver apparatus, and assay method using the same
US20100144558A1 (en) * 2006-08-25 2010-06-10 Frederic Zenhausern Systems and methods for biodosimetry with biochip using gene expression signatures

Family Cites Families (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5945281A (en) * 1996-02-02 1999-08-31 Becton, Dickinson And Company Method and apparatus for determining an analyte from a sample fluid
US20050214276A9 (en) 2002-05-03 2005-09-29 Myette James R Delta 4, 5 glycuronidase and uses thereof
US7094354B2 (en) 2002-12-19 2006-08-22 Bayer Healthcare Llc Method and apparatus for separation of particles in a microfluidic device
CN1568999A (zh) 2003-07-14 2005-01-26 南宁枫叶药业有限公司 稳定的医药用河豚毒素冷冻干燥制剂
US20050074796A1 (en) 2003-07-31 2005-04-07 Stephen Yue Unsymmetrical cyanine dimer compounds and their application
WO2005042504A1 (en) 2003-10-31 2005-05-12 Molecular Probes, Inc. Fluorinated resorufin compounds and their application in detecting hydrogen peroxide
EP1692275B1 (en) 2003-11-04 2010-12-29 Biomaster, Inc. Method and system for preparing stem cells from fat tissue
US7776529B2 (en) 2003-12-05 2010-08-17 Life Technologies Corporation Methine-substituted cyanine dye compounds
CN101301632B (zh) * 2004-11-10 2010-12-29 横河电机株式会社 化学反应盒、其制造方法和化学反应盒驱动系统
FR2878850B1 (fr) 2004-12-02 2008-10-31 Cis Bio Internat Sa Derives de l'inositol-1-phosphate
US20060228734A1 (en) * 2005-03-18 2006-10-12 Applera Corporation Fluid processing device with captured reagent beads
DK2239327T3 (en) 2005-08-11 2015-05-18 Synthetic Genomics Inc A method for in vitro recombination
US8158801B2 (en) 2005-09-26 2012-04-17 Life Technologies Corporation Violet laser excitable dyes and their method of use
JP5288718B2 (ja) 2006-03-31 2013-09-11 日産自動車株式会社 電気化学セル用電極触媒、その製造方法、電気化学セル、燃料電池セル及び燃料電池
CN101149376B (zh) * 2006-09-19 2012-07-25 财团法人工业技术研究院 磁珠式检体分离装置
CA2668417A1 (en) 2006-11-03 2008-05-15 Alphavax, Inc. Alphavirus and alphavirus replicon particle formulations and methods
DK2829282T3 (en) 2007-03-22 2018-01-02 Univ Colorado Regents Process for preparing an immunologically active adjuvant-linked dried vaccine composition
KR101228308B1 (ko) * 2007-05-23 2013-01-31 삼성전자주식회사 미세유동 칩을 이용한 디스크형 미세유동장치 및 생체물질마이크로어레이 칩을 이용한 디스크형 미세유동장치
US8304203B2 (en) 2007-12-05 2012-11-06 Zyomyx, Inc. Cell assay kit and method
US7927561B2 (en) * 2008-01-10 2011-04-19 Becton, Dickinson And Company Rapid particle detection assay
CN102138075B (zh) * 2008-10-01 2014-05-28 三星电子株式会社 离心式微流体设备、制造微流体设备的方法以及使用微流体设备测试样品的方法
KR101335725B1 (ko) * 2008-10-02 2013-12-04 삼성전자주식회사 다중분석용 미세유동 구조물 및 이를 포함하는 미세유동 장치
WO2010041174A1 (en) * 2008-10-06 2010-04-15 Koninklijke Philips Electronics N.V. Microfluidic device
KR101217572B1 (ko) 2009-09-16 2013-01-03 한국전자통신연구원 바이오 칩 및 바이오 칩 리더기
GB0919159D0 (en) * 2009-11-02 2009-12-16 Sec Dep For Environment Food A Device and apparatus
EP2552443B1 (en) 2010-04-01 2021-07-14 Oncorena Ab Improved treatment of renal cell carcinoma
CN102893151B (zh) 2010-04-14 2015-06-03 荣研化学株式会社 标记化探针-水溶性载体复合物
KR101519379B1 (ko) 2010-04-29 2015-05-12 삼성전자 주식회사 원심력 기반의 미세유동장치 및 이를 이용한 면역분석방법
KR20120080765A (ko) * 2011-01-10 2012-07-18 삼성전자주식회사 미세유동장치 및 이를 이용한 검체검사방법
JP5850915B2 (ja) 2011-03-14 2016-02-03 国立大学法人北海道大学 肺送達のためのベクター、導入剤及び使用
CN105102979B (zh) * 2013-01-29 2017-05-03 生物辐射海法有限公司 利用磁性纳米粒子的检测测定法

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090221431A1 (en) * 2005-05-06 2009-09-03 Jae Chern Yoo Digital bio disc (dbd), dbd driver apparatus, and assay method using the same
US20100144558A1 (en) * 2006-08-25 2010-06-10 Frederic Zenhausern Systems and methods for biodosimetry with biochip using gene expression signatures

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3325976A4 (en) * 2015-07-17 2019-07-24 Genobio Corp. SYSTEM FOR SEPARATING MAGNETIC IRON PARTICLES
US11099182B2 (en) 2016-06-30 2021-08-24 Sysmex Corporation Detection apparatus and detection method
US11480525B2 (en) 2016-06-30 2022-10-25 Sysmex Corporation Chemiluminescence measurement apparatus
US11660615B2 (en) * 2016-07-19 2023-05-30 Jun Seok Lee Centrifugal separation container, and method for moving substances inside centrifugal separation container
CN107796939A (zh) * 2016-08-30 2018-03-13 希森美康株式会社 试样分析用盒及其制造方法、以及其用途
WO2020094780A3 (de) * 2018-11-08 2020-07-02 Hahn-Schickard-Gesellschaft für angewandte Forschung e.V. Vorrichtung und verfahren zum transport magnetischer partikel
CN113272063A (zh) * 2018-11-08 2021-08-17 哈恩席卡德应用研究协会 用于输送磁性粒子的设备和方法
EP3881934A4 (en) * 2018-11-15 2022-07-27 Daegu Gyeongbuk Institute Of Science and Technology MICROFLUIDIC DEVICE AND METHOD FOR SEPARATION OF TARGET CELLS USING THE SAME
US11772094B2 (en) 2018-11-15 2023-10-03 Daegu Gyeongbuk Institute Of Science And Technology Microfluidic apparatus and method for separating target cells using the same
WO2021230821A1 (en) * 2020-05-12 2021-11-18 National University Of Singapore A method for virus and biomarker detection

Also Published As

Publication number Publication date
CN105683761B (zh) 2018-11-02
WO2015030485A1 (ko) 2015-03-05
KR101398764B1 (ko) 2014-05-27
US10859570B2 (en) 2020-12-08
US20180038854A1 (en) 2018-02-08
CN105683761A (zh) 2016-06-15

Similar Documents

Publication Publication Date Title
US10859570B2 (en) Methods for detecting an analyte using an analyte detection device
Liu et al. Liposomes in biosensors
CA1304290C (en) Orthographic flow immunoassays and devices
US8753574B2 (en) Systems for immunoassay tests
JP5423200B2 (ja) 分析チップおよび検体の分析方法
Hartwell et al. Flow based immuno/bioassay and trends in micro-immuno/biosensors
KR101608598B1 (ko) 정지 액체상 랩온어칩
US20120021934A1 (en) Methods and Devices for Active Bioassay
US6593085B1 (en) Assay method and apparatus
EP2473595A1 (en) Integrated sample preparation and analyte detection
JP2012514204A (ja) 磁場の適用によるチェンバー中の粒子分散
US11879901B2 (en) Cartridges for immunoassay tests and methods of using the same
Nevídalová et al. Capillary electrophoresis–based immunoassay and aptamer assay: A review
WO2007026731A1 (ja) バイオチップ及び免疫分析方法
NO337444B1 (no) Analysemetode
CN114923886A (zh) 一种基于光栅与磁阵列式的单分子荧光检测方法
US5098845A (en) Device and procedure for automated solid-phase immunoassay
WO1993010455A1 (en) Improved centrifuge vessel for automated solid-phase immunoassay
KR101895597B1 (ko) 정지 액체상 랩온어튜빙
US7381374B2 (en) Immunoassay devices and methods of using same
KR102244375B1 (ko) 입자와 용액의 동시 이동에 의한 분석물질을 검출하는 장치 및 이를 이용한 검출방법
KR20200144459A (ko) 분석물질 검출장치 및 이를 이용한 검출방법
KR102220357B1 (ko) 면역진단 키트 및 이를 이용한 면역진단 방법
KR20230057939A (ko) 중력을 이용하는 자성입자 기반 바이오칩 및 이를 이용한 분석물질 검출 방법
KR910001313B1 (ko) 면역 분석 방법 및 장치

Legal Events

Date Code Title Description
AS Assignment

Owner name: AMOGREENTECH CO., LTD., KOREA, REPUBLIC OF

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:CHOI, SUK-JUNG;REEL/FRAME:037854/0891

Effective date: 20160224

Owner name: GANGNEUNG-WONJU NATIONAL UNIVERSITY INDUSTRY ACADE

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:CHOI, SUK-JUNG;REEL/FRAME:037854/0891

Effective date: 20160224

AS Assignment

Owner name: AMOLIFESCIENCE CO., LTD., KOREA, REPUBLIC OF

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:AMOGREENTECH CO., LTD.;REEL/FRAME:041229/0650

Effective date: 20170208

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION