Immunochromato device and method for measuring samples using the same

• US 20020146754A1
• Filed: 04/04/2002
• Published: 10/10/2002
• Est. Priority Date: 04/06/2001
• Status: Abandoned Application

• Current Assignee: Matsushita Electric Industrial Company Limited (Panasonic Holdings Corporation)
• Original Assignee: Matsushita Electric Industrial Company Limited (Panasonic Holdings Corporation)
• Inventors: Shigeto, Nobuyuki, Kitawaki, Fumihisa
• Application Number:
  US10/116,407
• Publication Number:
  US 20020146754A1
• Time in Patent Office: Days
• US Class Current: 435/7.93
• CPC Class Codes: G01N 33/543 with an insoluble carrier for immobilising immunochemicals
• CPC Class Codes: G01N 33/54388 based on lateral flow
• CPC Class Codes: G01N 33/558 using diffusion or migration of antigen or antibody immunochromatographic test strips G01N33/54387
• CPC Class Codes: G01N 33/726 Devices

Abstract

An immunochromatographic device includes a sample application section; a determination section; and a capillary-flow section. The determination section has an immobilization section including one type of first antibody specifically reacting with all the types of target substances, or a plurality of types of first antibodies each specifically reacting with a corresponding type of target substance, the one type of first antibody or the plurality of types of first antibodies being immobilized. The sample application section or the capillary-flow section has a plurality of types of second antibodies each specifically reacting with all the types of target substances or a corresponding type of target substance. The plurality of types of second antibodies can be eluted. At least one type of second antibody specifically reacts with one type of target substance among the plurality of types of target substances. The plurality of types of second antibodies are labeled with different labeling substances.

Claims

1. An immunochromatographic device for detecting or measuring a plurality of types of target substances contained in a liquid sample, the immunochromatographic device comprising:

a sample application section;

a determination section; and

a capillary-flow section,

wherein;

the sample application section, the determination section and the capillary-flow section are located so that the liquid sample introduced to the sample application section is transferred to the determination section via the capillary-flow section,

the determination section has an immobilization section including one type of first antibody specifically reacting with all the plurality of types of target substances, or a plurality of types of first antibodies each specifically reacting with a corresponding type of target substance, the one type of first antibody or the plurality of types of first antibodies being immobilized,

the sample application section or the capillary-flow section has a plurality of types of second antibodies each specifically reacting with all the plurality of types of target substances or a corresponding type of target substance, wherein the plurality of types of second antibodies can be eluted,

at least one type of second antibody specifically reacts with one type of target substance among the plurality of types of target substances, and

the plurality of types of second antibodies are labeled with different labeling substances.

2. An immunochromatographic device according to claim 1, wherein:

the plurality of target substances are glycohemoglobin and hemoglobin,

the one type of first antibody is a first anti-hemoglobin monoclonal antibody specifically reacting with both glycohemoglobin and hemoglobin, and

the plurality of types of second antibodies include a second anti-hemoglobin monoclonal antibody specifically reacting with both glycohemoglobin and hemoglobin, and an anti-glycohemoglobin monoclonal antibody specifically reacting with glycohemoglobin.

3. An immunochromatographic device according to claim 1, wherein the labeling substances have different absorbance wavelengths from each other.

4. An immunochromatographic device according to claim 1, wherein the labeling substances have different fluorescence wavelengths from each other.

5. An immunochromatographic device according to claim 1, wherein the labeling substances have different phosphorescence wavelengths from each other.

6. A method for measuring a plurality of types of target substances using an immunochromatographic device according to claim 3, the method comprising the steps of:

(A) introducing a liquid sample to a sample application section;

(B) measuring, in a determination section, one of hue, clarity, or brightness of complexes generated by reaction of the plurality of types of target substances, and a second antibody and a first antibody corresponding to each type of target substance; and

(C) finding an absolute amount of each of the plurality of types of target substances or an amount ratio of the plurality of types of target substances contained in the liquid sample based on the measurements obtained in step (B).