Method for reducing measurement error in latex agglutination immunoassay

US11668708B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11668708-B2
Application numberUS-201716651872-A
CountryUS
Kind codeB2
Filing dateSep 29, 2017
Priority dateSep 29, 2017
Publication dateJun 6, 2023
Grant dateJun 6, 2023

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A method for avoiding the influence of a blood sample on a measurement error in a latex agglutination immunoassay. The measurement error caused by a blood sample in a latex agglutination immunoassay can be reduced by a method which includes a step of bringing the sample into contact, in a liquid phase, with latex particles carrying a substance having a specific affinity for an analyte in the presence of imidazole.

First claim

Opening claim text (preview).

The invention claimed is: 1. A method for measuring an analyte in a chylous plasma or chylous serum by a latex agglutination immunoassay, comprising the following steps: (1) bringing a chylous plasma or chylous serum containing chyle into contact with imidazole or an imidazole derivative, or a salt thereof in a liquid phase; (2) adding latex particles carrying a substance having a specific affinity for the analyte to the liquid phase sequentially after the step (1); and (3) measuring an agglutination reaction between the analyte and the latex particles after the step (2), without performing a cleaning or separation step during or after the step (2), wherein the concentration of imidazole or an imidazole derivative, or a salt thereof in the step (3) of measuring the agglutination reaction of the latex particles is not less than 100 mM and not more than 375 mM. 2. A method for measuring an analyte in a chylous plasma or chylous serum by a latex agglutination immunoassay, comprising the following steps: (1) bringing a chylous plasma or chylous serum into contact with imidazole or an imidazole derivative, or a salt thereof in a liquid phase; (2) adding latex particles carrying a substance having a specific affinity for the analyte to the liquid phase after the step (1); and (3) measuring an agglutination reaction between the analyte and the latex particles after the step (2), without performing a cleaning or separation step prior to the measurement step (3), wherein the concentration of imidazole or an imidazole derivative, or a salt thereof in the step (3) of measuring the agglutination reaction of the latex particles is not less than 100 mM and not more than 375 mM. 3. The method according to claim 1 , wherein said step of bringing a chylous plasma or chylous serum into contact with imidazole or an imidazole derivative, or a salt thereof in a liquid phase is a step of adding a first reagent to a chylous plasma or chylous serum, thereby producing a first mixture, wherein said first reagent contains a buffer solution containing imidazole or an imidazole derivative, or a salt thereof; and wherein said step of adding latex particles carrying a substance having a specific affinity for the analyte to the liquid phase is a step of adding a second reagent to the first mixture, wherein said second reagent contains latex particles carrying a substance having a specific affinity for the analyte. 4. The method according to claim 3 , wherein said first reagent is a buffer solution containing imidazole or an imidazole derivative, or a salt thereof. 5. The method according to claim 4 , wherein said second reagent is a suspension of latex particles carrying a substance having a specific affinity for the analyte. 6. The method according to claim 5 , wherein the step of measuring an agglutination reaction between the analyte and the latex particles is a step of measuring an agglutination reaction between an analyte and latex particles without performing a cleaning or separation step during or after the step of adding a suspension of latex particles carrying a substance having a specific affinity for the analyte to the first mixture. 7. The method according to claim 1 , wherein said imidazole or imidazole derivative or salt thereof is selected from the group consisting of imidazole, 1-methylimidazole, 1-ethylimidazole, 1-propylimidazole, 1-butylimidazole, 1-phenylimidazole, 1-vinylimidazole, 1-allylimidazole, 1-benzyl-2-methylimidazole, 1-benzyl-2-formylimidazole, 1-benzyl-4-hydroxymethylimidazole, 1-benzyl-5-hydroxymethylimidazole, 1-(2-hydroxyethyl)-imidazole, 1-(2-hydroxyethyl)-2-methylimidazole, 2-methylimidazole, 2-ethylimidazole, 2-propylimidazole, 2-butylimidazole, 2-phenylimidazole, 2-formylimidazole, 2-hydroxymethylimidazole, 2-methyl-1-vinylimidazole, 2-butyl-4-formylimidazole, 2-butyl-4-hydroxymethylimidazole, 2-butyl-4-chloro-5-formylimidazole, 2-hydroxymethyl-1-benzylimidazole, 2-hydroxymethyl-2-methylimidazole, 2-ethyl-4-methylimidazole, 4-butylimidazole, 4-formylimidazole, 4-formyl-1-methylimidazole, 4-formyl-1-tritylimidazole, 5-formyl-1-methylimidazole, 4-formyl-5-methylimidazole, 4-hydroxymethylimidazole hydrochloride, methylimidazole-4-carboxylate, ethylimidazole-4-carboxylate, 1,2-dimethylimidazole, 1,2,4-trimethylimidazole and a salt of any of said imidazole or imidazole derivatives. 8. The method according to claim 6 , wherein said imidazole or imidazole derivative or salt thereof is selected from the group consisting of imidazole, 1-methylimidazole, 1-ethylimidazole, 1-propylimidazole, 1-butylimidazole, 1-phenylimidazole, 1-vinylimidazole, 1-allylimidazole, 1-benzyl-2-methylimidazole, 1-benzyl-2-formylimidazole, 1-benzyl-4-hydroxymethylimidazole, 1-benzyl-5-hydroxymethylimidazole, 1-(2-hydroxyethyl)-imidazole, 1-(2-hydroxyethyl)-2-methylimidazole, 2-methylimidazole, 2-ethylimidazole, 2-propylimidazole, 2-butylimidazole, 2-phenylimidazole, 2-formylimidazole, 2-hydroxymethylimidazole, 2-methyl-1-vinylimidazole, 2-butyl-4-formylimidazole, 2-butyl-4-hydroxymethylimidazole, 2-butyl-4-chloro-5-formylimidazole, 2-hydroxymethyl-1-benzylimidazole, 2-hydroxymethyl-2-methylimidazole, 2-ethyl-4-methylimidazole, 4-butylimidazole, 4-formylimidazole, 4-formyl-1-methylimidazole, 4-formyl-1-tritylimidazole, 5-formyl-1-methylimidazole, 4-formyl-5-methylimidazole, 4-hydroxymethylimidazole hydrochloride, methylimidazole-4-carboxylate, ethylimidazole-4-carboxylate, 1,2-dimethylimidazole, 1,2,4-trimethylimidazole and a salt of any of said imidazole or imidazole derivatives. 9. The method according to claim 2 , wherein step (1) comprises bringing the chylous plasma or chylous serum into contact with a buffer solution containing imidazole or an imidazole derivative, or a salt thereof. 10. The method according to claim 9 , wherein the latex particles are added in the form of a suspension of latex particles carrying a substance having a specific affinity for the analyte. 11. The method according to claim 10 , wherein the step of measuring an agglutination reaction between the analyte and the latex particles is a step of measuring an agglutination reaction between an analyte and latex particles without performing a cleaning or separation step during or after the step of adding a suspension of latex particles carrying a substance having a specific affinity for the analyte to the first mixture. 12. The method according to claim 2 , wherein said imidazole or imidazole derivative or salt thereof is selected from the group consisting of imidazole, 1-methylimidazole, 1-ethylimidazole, 1-propylimidazole, 1-butylimidazole, 1-phenylimidazole, 1-vinylimidazole, 1-allylimidazole, 1-benzyl-2-methylimidazole, 1-benzyl-2-formylimidazole, 1-benzyl-4-hydroxymethylimidazole, 1-benzyl-5-hydroxymethylimidazole, 1-(2-hydroxyethyl)-imidazole, 1-(2-hydroxyethyl)-2-methylimidazole, 2-methylimidazole, 2-ethylimidazole, 2-propylimidazole, 2-butylimidazole, 2-phenylimidazole, 2-formylimidazole, 2-hydroxymethylimidazole, 2-methyl-1-vinylimidazole, 2-butyl-4-formylimidazole, 2-butyl-4-hydroxymethylimidazole, 2-butyl-4-chloro-5-formylimidazole, 2-hydroxymethyl-1-benzylimidazole, 2-hydroxymethyl-2-methylimidazole, 2-ethyl-4-methylimidazole, 4-butylimidazole, 4-formylimidazole, 4-formyl-1-methylimidazole, 4-formyl-1-tritylimidazole, 5-formyl-1-methylimidazole, 4-formyl-5-methylimidazole, 4-hydroxymethylimidazole hydrochloride, methylimidazole-4-carboxylate, ethylimidazole-4-carboxylate, 1,2-dimethylimidazole, 1,2,4-trimethylimidazole and a salt of any of said imidazole or imidazole derivatives. 13. The method according to claim 11 , wherein said imidazole or imidazole derivative or salt thereof is selected from the group

Assignees

Inventors

Classifications

  • with immune complex formed in liquid phase · CPC title

  • Improving reaction conditions, e.g. reduction of non-specific binding, promotion of specific binding · CPC title

  • G01N33/543Primary

    with an insoluble carrier for immobilising immunochemicals · CPC title

  • Labels used in chemical analysis of biological material · CPC title

  • Synthetic resin · CPC title

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What does patent US11668708B2 cover?
A method for avoiding the influence of a blood sample on a measurement error in a latex agglutination immunoassay. The measurement error caused by a blood sample in a latex agglutination immunoassay can be reduced by a method which includes a step of bringing the sample into contact, in a liquid phase, with latex particles carrying a substance having a specific affinity for an analyte in the pr…
Who is the assignee on this patent?
Sekisui Medical Co Ltd
What technology area does this patent fall under?
Primary CPC classification G01N33/5306. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Jun 06 2023 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).