IP Library Granted Patent US 9,939,436
Granted Patent B2
US 9,939,436 · App. 14/389,277 · Granted Apr 10, 2018

Immunological analysis method and reagent

Inventors: Mayumi Kano (Gosen, JP); Ritsuko Tachibana (Gosen, JP); Masayuki Iizuka (Gosen, JP)
Assignee: DENKA SEIKEN CO., LTD.
G01N33/54393C08F210/14C08F222/02G01N33/5306G01N33/54313
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Quick Facts
Patent No.
US 9,939,436
App. No.
14/389,277
Granted
Apr 10, 2018
Kind
B2
Abstract

Disclosed are an immunoassay method which can measure an antigen with high sensitivity and accuracy; and a reagent therefor. In the immunoassay method, an antigen-antibody reaction and/or a measurement is(are) carried out in the presence of a polycarboxylic acid type surfactant. The immunoassay reagent for use in the method is characterized by comprising the polycarboxylic acid type surfactant. By employing such a simple means that the polycarboxylic acid type surfactant is allowed to be present in the reaction and/or measurement system, non-specific reactions can be suppressed effectively even in a highly sensitive immunoassay, and an antigen can be measured accurately and specificity can be improved in the immunoassay.

Claims (18)

1. An optical immunoagglutination measurement method for detecting an antigen in a sample, said method comprising:

carrying out an immunoagglutination antigen-antibody reaction in the presence of a polycarboxylic acid type surfactant, said polycarboxylic acid type surfactant being in a reaction system at a concentration of 0.001% to 3% by mass, said reaction system inclusive of the sample; and

measuring optically the immunoglutinnated sample with a portion of the reaction system to detect the presence of the antigen in the sample;

wherein said polycarboxylic acid type surfactant is a copolymer of (1) maleic acid and/or maleic anhydride and (2) diisobutylene; and/or a salt thereof, and wherein said immunoagglutination antigen-antibody reaction is a latex agglutination.

2. The method according to claim 1 , wherein the concentration of said polycarboxylic acid type surfactant in the reaction system is 0.005% to 1%.

3. The method according to claim 1 , wherein said polycarboxylic acid type surfactant is allowed to be present during from beginning of the antigen-antibody reaction to completion of the measurement.

4. The method according to claim 1 , wherein the polycarboxylic acid type surfactant is dissolved in a solution.

5. The method according to claim 1 , wherein the immunoagglutination antigen-antibody reaction and measurement is carried out on a sample from urine.

6. An optical immunoagglutination measurement method for detecting an antigen in a sample comprising:

carrying out an immunoagglutination antigen-antibody reaction in the presence of a polycarboxylic acid type surfactant, said polycarboxylic acid type surfactant being in a reaction system at an effective amount and said reaction system inclusive of the sample; and

measuring optically the immunoglutinnated sample with a portion of the reaction system to detect the presence of the antigen in the sample;

wherein said polycarboxylic acid type surfactant is a copolymer of (1) maleic acid and/or maleic anhydride and (2) diisobutylene; and/or a salt thereof, and wherein said immunoagglutination antigen-antibody reaction is a latex agglutination.

7. An immunoagglutination measurement method for detecting an antigen in a sample comprising:

carrying out an immunoagglutination antigen-antibody reaction in the presence of a polycarboxylic acid type surfactant, said polycarboxylic acid type surfactant being in a reaction system at an effective amount and said reaction system inclusive of the sample; and

measuring the immunoglutinnated sample with a portion of the reaction system to detect the presence of the antigen in the sample;

wherein said polycarboxylic acid type surfactant is a copolymer of (1) maleic acid and/or maleic anhydride and (2) diisobutylene; and/or a salt thereof, and wherein said immunoagglutination antigen-antibody reaction is a latex agglutination.

8. The method according to claim 1 , wherein the antigen is a protein marker, immunoglobulin, viral antigen, bacterial antigen, peptide hormone, bioactive amine, vitamin, prostaglandin, antibiotic, pesticide or environmental hormone.

9. The method according to claim 1 , wherein the test sample does not comprise LDL.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE PATENT NUMBERS 10007286 AND 10415007 PREVIOUSLY RECORDED AT REEL: 054513 FRAME: 0142. ASSIGNOR(S) HEREBY CONFIRMS THE MERGER. Recorded Dec 14, 2020
From: DENKA SEIKEN CO., LTD.
To: DENKA COMPANY LIMITED
Reel/Frame 055437/0045 →
MERGER Recorded Nov 24, 2020
From: DENKA SEIKEN CO., LTD.
To: DENKA COMPANY LIMITED
Reel/Frame 054513/0142 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 30, 2014
From: KANO, MAYUMI; TACHIBANA, RITSUKO; IIZUKA, MASAYUKI
To: DENKA SEIKEN CO., LTD.
Reel/Frame 033856/0204 →
Priority Claims (1)
JP 2012-078449 · Mar 30, 2012 · national
Continuity (1)
Related Publication 20150086975A1 · Mar 26, 2015