Method for quantitative determination of glycated hemoglobin

• US 6,562,581 B2
• Filed: 08/31/2001
• Issued: 05/13/2003
• Est. Priority Date: 08/31/2001
• Status: Expired due to Fees

• Current Assignee: Portascience Incorporated
• Original Assignee: Portascience Incorporated
• Inventors: Nikolyukin, Yuri, Law, Wai Tak
• Primary Examiner(s): GITOMER, RALPH J
• Application Number:
  US09/943,674
• Publication Number:
  US 20030073243A1
• Time in Patent Office: 620 Days
• Field of Search: 435/14, 436/67, 436/172, 436/175, 436/524, 549/213
• US Class Current: 435/14
• CPC Class Codes: G01N 33/723 Glycosylated haemoglobin

Abstract

A method and a system for separating glycated hemoglobin from non-glycated hemoglobin, and a method for one-read quantitative determination of the glycated hemoglobin and % HbA_1c that does not require an additional measurement of total hemoglobin.

Claims

1. A method for quantitative determination of HbA_1c without using antibodies comprising:

a. incubating a diluted and lysed blood sample comprising a glycated hemoglobin (gHb) with a boronic acid derivative immobilized on a solid support to form a gHb-boronic acid conjugate;

b. separating the gHb-boronic conjugate from the sample;

c. adding a dye developing solution that is catalyzed by a peroxidase to form a dye and incubating the gHb-boronic conjugate with the dye developing solution to form a dye; and

d. measuring the dye concentration, which is directly proportional to the amount of bound glycated hemoglobin.

2. The method according to claim 1 wherein the boronic acid derivative is selected from the group consisting of arylboronic acids having a functional group which can be immobilized onto a solid support.

3. The method according to claim 2 wherein the functional group is selected from the group consisting of hydroxy, primary amino, secondary amino, aldehyde, and carboxylic groups.

4. The method according to claim 3 wherein the boronic acid derivative is m-aminophenylboronic acid.

5. The method according to claim 1 wherein the solid support is selected from the group consisting of beads, fabric sheets, polymer sheets, membranes, and magnetic particles coated with a polymer.

6. The method according to claim 1 wherein the incubation is conducted at a pH of from 7.5 to 10.0.

7. The method according to claim 1 wherein the dye developing solution contains a dye developing compound selected from the group consisting of monoamines, diamines, phenols, polyphenols, and leucodyes.

8. The method according to claim 7 wherein the dye developing compound is selected from the group consisting of triaryl methanes, xanthenes, styryl dyes, and azine dyes.

9. The method according to claim 1 wherein the dye developing solution comprises a color forming coupler and an oxidizable color-developing compound.

10. The method according to claim 9 wherein the color forming coupler is selected from the group consisting of N-substituted anilines.

11. The method according to claim 10 wherein the dye-developing compound is selected from the group consisting of 4-aminoantipyrine and 3-methylbenzothiazolone-2-hydrazone.

12. The method according to claim 1 wherein the boronic acid derivative is immobilized on a solid support selected from the group consisting of paper, porous particulates, cellulose, wood, glass fibers, membranes, woven fabrics, and nonwoven fabrics.

13. The method according to claim 1 wherein the peroxidase activity is obtained from the hemoglobin pseudo-peroxidase activity.

14. In a method for quantitative determination of HbA_1c without using antibodies, the improvement comprising formation of a detectable gHb-boronic acid conjugate.

15. The method according to claim 14 wherein the detectable gHb-boronic acid conjugate is detected by a dye developing solution that is catalyzed by a peroxidase to form a dye.

16. The method according to claim 15 wherein the dye developing solution comprises a color forming coupler and an oxidizable color-developing compound.

17. The method according to claim 16

wherein the dye developing solution contains a dye developing compound selected from the group consisting of monoamines, diamines, phenols, polyphenols, and leucodyes.

18. The method according to claim 17 wherein the dye developing compound is selected from the group consisting of triaryl methanes, xanthenes, styryl dyes, and azine dyes.

19. The method according to claim 14 wherein the gHb-boronic acid conjugate is formed with a boronic acid derivative having a functional group which can be immobilized onto a solid support.

20. The method according to claim 17 wherein the boronic acid derivative is immobilized on a solid support.

21. The method according to claim 20 wherein the solid support is selected from the group consisting of beads, nonwoven fabric sheets, woven fabric sheets, polymer sheets, membrane, magnetic particles coated with a polymer, paper, porous particulates, cellulose, wood, and glass fibers.