Peroxidase colloidal gold oxidase biosensors for mediatorless glucose determination

• US 5,334,296 A
• Filed: 06/28/1993
• Issued: 08/02/1994
• Est. Priority Date: 01/15/1992
• Status: Expired due to Term

• Current Assignee: ESA Biosciences, Inc. (Thermo Fisher Scientific Incorporated)
• Original Assignee: Andcare Incorporated
• Inventors: Zhao, Junguo, Henkens, Robert W., O'Daly, John P.
• Primary Examiner(s): Niebling, John
• Assistant Examiner(s): Bell, Bruce F.
• Application Number:
  US08/083,349
• Time in Patent Office: 400 Days
• Field of Search: 204/153.12, 204/403, 204/412, 204/415, 204/418, 204/435, 422/82.01, 422/82.03, 435/288, 435/817
• US Class Current: 205/777.5
• CPC Class Codes: C12Q 1/003 Functionalisation
• CPC Class Codes: C12Q 1/004 mediator-assisted
• 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: Y10S 435/817 Enzyme or microbe electrode

Abstract

Horseradish peroxidase (HRP) immobilized on colloidal gold and then deposited on an electrode surface can be reduced at a convenient rate at low voltage (Ag/AgCl) without an electron transfer mediator. Bioelectrodes combining both a colloidal gold-adsorbed oxidase and colloidal gold-adsorbed HRP located on an electrode surface are efficient biodetectors, particularly for the measurement of low glucose levels in samples when glucose oxidase is employed as the sensing enzyme. The biodetectors may be employed for mediatorless detection of a wide variety of analytyes depending on the oxidase employed.

Claims

1. A method of electrochemical determination of an analyte comprising:

obtaining a bioelectrode prepared from a colloidal gold adsorbed peroxidase and an oxidase in communication with a conducting surface; and

detecting current generated in the presence of the analyte when a sample containing the analyte is contacted with the bioelectrode.

2. The method of claim 1 wherein hydrogen peroxide from oxidase-catalyzed analyte conversion is selectively reduced by peroxidase on the conducting surface to produce a current.

3. The method of claim 1 wherein the sample is water, urine, blood, serum, plasma, sweat or tears.

4. The method of claim 1 wherein the oxidase is glucose oxidase, cholesterol oxidase, xanthine oxidase, amino acid oxidase, alcohol oxidase, lactic acid oxidase, sorbose oxidase, glycolate oxidase, gulonolactose oxidase, pyrodoxal-4-oxidase or galactose oxidase.

5. The method of claim 1 wherein the analyte is glucose, xanthine, cholesterol, galactose or lactic acid.

6. The method of claim 1 wherein the peroxidase is horseradish peroxidase.

7. The method of claim 1 wherein the current is measured amperometrically.

8. A method for mediatorless electrochemical determination of glucose, comprising the steps:

obtaining a bioelectrode prepared from colloidal gold adsorbed horseradish peroxidase and glucose oxidase in communication with a conducting surface; and

detecting current produced from reduction of hydrogen peroxide generated from glucose oxidase catalyzed glucose conversion.

9. The method of claim 8 wherein the detecting of hydrogen peroxide is conducted at a pH of about 4.5 to 7.5.

10. The method of claim 8 wherein the detecting of hydrogen peroxide is conducted at a pH of about 5.0.

11. The method of claim 8 wherein the current is measured amperometrically with a transducer comprising a reference/counter electrode component.

12. The method of claim 9 wherein the reference/counter electrode component is at 0 V/Ag Vs. Ag/AgCl which measures a current generated from direct electron transfer at the conducting electrode surface.

13. The method of claim 8 wherein current produced is proportional to glucose present in the sample from a range of about 1 to 250 μ

M glucose.

14. The method of claim 8 wherein the glucose is measured in a sample of water, blood, vaginal fluid, saliva or semen.

15. A method of determining glucose concentration wherein the glucose is electrochemically determined from a current generated from reduction of hydrogen peroxide produced by glucose oxidase catalyzed glucose conversion, the glucose oxidase being immobilized on a conducting surface with colloidal gold adsorbed horseradish peroxidase.

16. The method of claim 15 wherein the glucose oxidase is immobilized on top of a layer of horseradish peroxidase.

17. The method of claim 15 wherein the glucose oxidase is adsorbed to colloidal gold prior to deposition on the layer of horseradish peroxidase.

18. The method of claim 15 wherein the conducting surface is carbon.

19. The method of claim 15 wherein the conducting surface is glassy carbon.

20. The method of claim 15 wherein immobilization is be evaporative deposition on the conducting surface.