Measurement method using oxidase

• US 8,722,355 B2
• Filed: 10/20/2011
• Issued: 05/13/2014
• Est. Priority Date: 10/22/2010
• Status: Active Grant

• Current Assignee: ARKRAY, Inc
• Original Assignee: ARKRAY, Inc
• Inventors: Kaneda, Hisashi
• Primary Examiner(s): NOAKES, SUZANNE MARIE
• Application Number:
  US13/277,473
• Publication Number:
  US 20120100567A1
• Time in Patent Office: 936 Days
• Field of Search: None
• US Class Current: 435/25
• CPC Class Codes: C12Q 1/005 involving specific analytes or enzymes including groups of enzymes, e.g. oxydases; C12Q1/004 takes precedence
• CPC Class Codes: C12Q 1/006 for glucose
• CPC Class Codes: C12Q 1/26 involving oxidoreductase
• CPC Class Codes: G01N 27/3274 Corrective measures, e.g. error detection, compensation for temperature or hematocrit, calibration coding of calibration information G01N33/48771

Abstract

A method for measuring a target object in a sample by using an oxidase, wherein the influence of dissolved oxygen in the sample can be corrected, is provided. The method comprises: obtaining measurement values by causing the target object in the sample to react with the oxidase under different conditions of two or more types; and performing a correction based on the obtained two or more measurement values and a correction method preliminarily set so as to correct the influence of dissolved oxygen in the sample.

Claims

1. A method for providing a corrected measurement of a target object in a sample, wherein the sample comprises dissolved oxygen, the method comprising:

obtaining separate measurement values of the target object in the sample by reacting the target object with an oxidase under two or more different types of conditions; and

performing a correction based on the measurement values obtained from the two or more different types of conditions to correct for the influence of the dissolved oxygen in the sample on the accuracy of the measurement value of the target object.

2. The method according to claim 1, wherein the reaction between the target object and the oxidase is performed in a biosensor that comprises

two independent electrode systems, where each electrode system comprises a working electrode and a counter electrode, and

a reagent layer comprising the oxidase provided on each of the two electrode systems.

3. The method according to claim 2, wherein the reagent layer further comprises a mediator.

4. The method according to claim 2, wherein the biosensor comprises more than two independent electrode systems.

5. The method according to claim 1, wherein the sample is selected from the group consisting of blood, plasma, serum and urine.

6. The method according to claim 5, wherein the sample is blood.

7. The method according to claim 1, wherein the target object is selected from the group consisting of glucose, lactic acid, bilirubin, cholesterol and ascorbic acid.

8. The method according to claim 7, wherein the target object is glucose.

9. The method according to claim 1, wherein the oxidase is selected from the group consisting of glucose oxidase, lactate oxidase, bilirubin oxidase, cholesterol oxidase, ascorbic acid oxidase, uric acid oxidase, peroxidase, sulfurous acid oxidase, amine oxidase, lysyl oxidase, lysine oxidase, amino acid oxidase, diamine oxidase, pyridoxine phosphate oxidase, protein-lysine 6-oxidase, acyl-CoA oxidase, alcohol oxidase, choline oxidase, pyruvic acid oxidase, sarcosine oxidase, tyramine oxidase and glycerophosphate oxidase.

10. The method according to claim 9, wherein the oxidase is glucose oxidase.

11. The method according to claim 1, wherein the mediator is selected from the group consisting of potassium ferricyanide, sodium ferricyanide, p-benzoquinone, phenazine methosulfate, indophenol, potassium β

-naphthoquinone-4-sulfonate, 2,6-dichlorophenol indophenol, methylene blue, nitrotetrazolium blue, ferrocene, an osmium complex, a ruthenium complex, NAD⁺, NADP⁺ and pyrroloquinoline quinone (PQQ).

12. The method according to claim 11, wherein the mediator is a ruthenium complex.

13. The method according to claim 3, wherein the reagent layer further comprises at least one selected from the group consisting of a hydrophilic polymer, a surfactant and a saccharide.