IP Library Granted Patent US 10,571,424
Granted Patent B2
US 10,571,424 · App. 15/251,418 · Granted Feb 25, 2020

Sensor, sensor system, method of manufacturing sensor, and method of measuring concentration of target substance

Inventors: Motonori Uchiyama (Ehime, JP); Takuo Kouno (Ehime, JP)
Assignee: PHC HOLDINGS CORPORATION
G01N27/3272C12Q1/004C12Q1/006C12Q1/26C12Q1/32G01N2333/904
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Quick Facts
Patent No.
US 10,571,424
App. No.
15/251,418
Granted
Feb 25, 2020
Kind
B2
Abstract

The present invention provides: a reagent composition having higher storage stability; a sensor involving the reagent composition; and others. According to the present invention, a specific heterocyclic compound is added to a reagent composition to improve the storage stability of the reagent composition and reduce the degree of fluctuation in current values in a sensor that utilizes reagent composition.

Claims (62)

1. A sensor comprising:

a sample chamber having an opening configured to receive therein a liquid sample;

at least one pair of electrodes disposed in the sample chamber; and

a reagent layer being disposed in the sample chamber,

wherein the reagent layer comprises:

an oxidoreductase;

an electron acceptor; and

a heterocyclic compound represented by one of the following general formulae (I-1) to (I-5):

wherein:

R 1 represents a hydrogen atom;

R 2 to R 5 , if present, each independently represent a hydrogen atom, an amino group, a hydroxyl group, or a C 1-12 hydrocarbon group;

the C 1-12 hydrocarbon group may have at least one substituent selected from the group consisting of an amino group, a hydroxyl group, and a carboxyl group;

at least one of R 2 to R 5 of the heterocyclic compound is an amino group; and

the heterocyclic compound is not histidine or histamine.

2. The sensor according to claim 1 , wherein the heterocyclic compound has five nitrogen atoms.

3. The sensor according to claim 1 , wherein the heterocylic compound is at least one compound selected from the group consisting of 2-amino-imidazole, 3-amino-1,2,4-triazole, 4-amino-1,2,4-triazole, and 3,5-diamino-1,2,4-triazole.

4. The sensor according to claim 1 , wherein the reagent layer contains glucose dehydrogenase as the oxidoreductase.

5. The sensor according to claim 4 , further comprises a coenzyme operable with the oxidoreductase.

6. The sensor according to claim 5 , wherein the oxidoreductase has pyrroloquinoline quinone (PQQ) dependency or flavin adenine dinucleotide (FAD) dependency.

7. The sensor according to claim 1 , wherein the reagent layer is solid.

8. The sensor according to claim 1 , wherein the reagent layer is disposed so as to be in contact with both electrodes of the at least one pair of electrodes.

9. A sensor system comprising:

the sensor according to claim 1 ;

a measurement section that measures a current value between electrodes of the at least one pair of electrodes; and

a calculation section that calculates a concentration of a target substance in the liquid sample based on a measurement result obtained by the measurement section.

10. A sensor comprising:

a sample chamber having an opening configured to receive therein a liquid sample;

at least one pair of electrodes disposed in the sample chamber; and

a reagent layer being disposed in the sample chamber,

wherein the reagent layer comprises:

an oxidoreductase;

an electron acceptor; and

a heterocyclic compound,

wherein the heterocyclic compound is at least one compound selected from the group consisting of 2-amino-imidazole, 4,5-bis(hydroxymethyl)imidazole, 2-methylimidazole, 1,2-dimethylimidazole, 3-amino-1,2,4-triazole, 4-amino-1,2,4-triazole, and 3,5-diamino-1,2,4-triazole.

11. A method of manufacturing a sensor, comprising:

(a) providing at least one pair of electrodes on a substrate;

(b) applying on the substrate a reagent composition; and

(c) drying the reagent composition applied in the step (b) to form a reagent layer,

wherein the reagent layer comprises:

an oxidoreductase;

an electron acceptor; and

a heterocyclic compound represented by one of the following general formulae (I-1) to (I-5):

wherein:

R 1 represents a hydrogen atom;

R 2 to R 5 , if present, each independently represent a hydrogen atom, an amino group, a hydroxyl group, or a C 1-12 hydrocarbon group;

the C 1-12 hydrocarbon group may have at least one substituent selected from the group consisting of an amino group, a hydroxyl group, and a carboxyl group;

at least one of R 2 to R 5 of the heterocyclic compound is an amino group; and

the heterocyclic compound is not histidine or histamine.

12. A method of measuring a concentration of a target substance, comprising:

(a) bringing a reagent composition into contact with a liquid sample;

(b) detecting a current generated in the step (a); and

(c) measuring the concentration of the target substance based on a detection result obtained in the step (b),

wherein the reagent composition comprises:

an oxidoreductase;

an electron acceptor; and

a heterocyclic compound represented by one of the following general formulae (I-1) to (I-5):

wherein:

R 1 represents a hydrogen atom;

R 2 to R 5 , if present, each independently represent a hydrogen atom, an amino group, a hydroxyl group, or a C 1-12 hydrocarbon group;

the C 1-12 hydrocarbon group may have at least one substituent selected from the group consisting of an amino group, a hydroxyl group, and a carboxyl group;

at least one of R 2 to R 5 of the heterocyclic compound is an amino group; and

the heterocyclic compound is not histidine or histamine.

Assignments (1)
CHANGE OF NAME Recorded May 17, 2018
From: PANASONIC HEALTHCARE HOLDINGS CO., LTD.
To: PHC HOLDINGS CORPORATION
Reel/Frame 046179/0658 →
Priority Claims (1)
JP 2010-222142 · Sep 30, 2010 · national
Continuity (2)
Continuation 13821365
Related Publication 20160376626A1 · Dec 29, 2016