IP Library Granted Patent US 6,939,682
Granted Patent B2
US 6,939,682 · App. 10/415,726 · Granted Sep 6, 2005

Test piece for assaying high density lipoprotein (HDL) cholesterol

Assignees: Arkray, Inc.; Daiichi Pure Chemicals Co., Ltd.
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Quick Facts
Patent No.
US 6,939,682
App. No.
10/415,726
Granted
Sep 6, 2005
Kind
B2
Abstract

The present invention relates to a test piece having a simple structure, by which HDL cholesterol can be measured easily using a small amount of specimen. A reagent layer ( 2 ) is formed on a support ( 1 ), and an enzyme reagent for measuring cholesterol, a first surfactant that makes a solubility of a high-density lipoprotein (HDL) higher than that of a lipoprotein other than the HDL, and a second surfactant that inhibits the lipoprotein other than the HDL from dissolving are contained in the reagent layer ( 2 ).

Claims (20)

1. A test piece for measuring high-density lipoprotein (HDL) cholesterol comprising:

an enzyme reagent for measuring cholesterol;

a first surfactant that makes a solubility of HDL higher than that of a lipoprotein other than the HDL; and

a second surfactant that inhibits the lipoprotein other than the HDL from dissolving, wherein a reagent layer is formed on a support, and the enzyme reagent, the first surfactant, and the second surfactant are contained in the reagent layer.

2. The test piece according to claim 1 , wherein the reagent layer includes a sample supply layer and a detecting layer, the first surfactant and the second surfactant are contained in the sample supply layer, and the enzyme reagent is contained in the detecting layer.

3. The test piece according to claim 2 , wherein the second surfactant is contained in an upper portion of the sample supply layer and the first surfactant is contained in a lower portion of the sample supply layer.

4. The test piece according to claim 2 , wherein the first surfactant, the second surfactant, and a part of the enzyme reagent are contained in the sample supply layer, and the rest of the enzyme reagent is contained in the detecting layer.

5. The test piece according to claim 1 , wherein the first surfactant is at least one surfactant selected from polyoxyethylene alkylene phenyl ether and polyoxyethylene alkylene tribenzyl phenyl ether.

6. The test piece according to claim 1 , wherein the second surfactant is at least one surfactant selected from the group consisting of polyoxyethylene alkylether, polyoxyethylene alkyl phenyl ether, a polyoxyethylene-polyoxypropylene condensation product, polyoxyethylene alkylether sulfate, and alkyl benzenesulphonate.

7. The test piece according to claim 1 , wherein the enzyme reagent contains cholesterol esterase and cholesterol oxidase.

8. The test piece according to claim 1 , wherein the enzyme reagent contains cholesterol esterase and cholesterol dehydrogenase.

9. The test piece according to claim 1 , wherein a proportion of the first surfactant in all the components during an enzyme reaction is in a range from 1 to 10 wt %.

10. The test piece according to claim 1 , wherein a proportion of the second surfactant in all the components during an enzyme reaction is in a range from 1 to 20 wt %.

11. The test piece according to claim 1 , wherein a weight ratio (A/B) of the first surfactant (A) to the second surfactant (B) is in a range from 1/10 to 1/1.

12. The test piece according to claim 1 , wherein a reaction pH during an enzyme reaction is adjusted to be in a range from 6 to 9.

13. The test piece according to claim 4 , wherein the second surfactant is contained in an upper portion of the sample supply layer, the first surfactant and the part of the enzyme reagent are contained in a lower portion of the sample supply layer, and the rest of the enzyme reagent is contained in the detecting layer.

14. The test piece according to claim 4 , wherein cholesterol elastase and cholesterol oxidase are contained in the sample supply layer as the part of the enzyme reagent, and a peroxidase and a substrate that develops color by oxidation are contained in the detecting layer as the rest of the enzyme reagent.

15. The test piece according to claim 9 , wherein a proportion of the first surfactant in all the components during an enzyme reaction is in a range from 3 to 7 wt %.

16. The test piece according to claim 10 , wherein a proportion of the second surfactant in all the components during an enzyme reaction is in a range from 7 to 13 wt %.

17. The test piece according to claim 11 , wherein a weight ratio (A/B) of the first surfactant (A) to the second surfactant (B) is in a range from 1/3 to 2/3.

Assignments (2)
CHANGE OF NAME Recorded Jun 11, 2010
From: DAIICHI PURE CHEMICALS CO., LTD.
To: SEKISUI MEDICAL CO., LTD.
Reel/Frame 024523/0811 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 1, 2003
From: TAMURA, HIROSHI; NISHINO, SUSUMU; YAMAGUCHI, TAKEHIRO; HINO, KOICHI
To: ARKRAY, INC.; DAIICHI PURE CHEMICALS CO., LTD.
Reel/Frame 014395/0847 →
Priority Claims (1)
JP 2000-340751 · Nov 8, 2000 · national
Continuity (1)
Related Publication 20040023400A1 · Feb 5, 2004