Peroxidase colloidal gold oxidase biosensors for mediatorless glucose determination

• US 5,225,064 A
• Filed: 03/06/1992
• Issued: 07/06/1993
• Est. Priority Date: 01/15/1992
• Status: Expired due to Term

• Current Assignee: ESA Biosciences, Inc. (Thermo Fisher Scientific Incorporated)
• Original Assignee: Enzyme Technology Research Group, Inc.
• Inventors: Zhao, Junguo, Henkens, Robert W., O'Daly, John P.
• Primary Examiner(s): Niebling, John
• Assistant Examiner(s): Bell, Bruce F.
• Application Number:
  US07/846,229
• Time in Patent Office: 487 Days
• Field of Search: 204/403, 204/415, 435/817
• US Class Current: 204/403.1
• 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 analytes depending on the oxidase employed.

Claims

1. A bioelectrode comprising:

a conducting surface;

a peroxidase adsorbed in a monolayer or close to a monolayer onto colloidal gold particles wherein the colloidal gold-adsorbed peroxidase is deposited on the conducting surface; and

an oxidase layer atop the deposited colloidal gold adsorbed peroxidase wherein direct electron transfer to the conducting surface occurs in the presence of an analyte when the bioelectrode is suitably coupled with a reference/counter electrode.

2. The biooelectrode of claim 1 wherein the peroxidase is horseradish peroxidase.

3. The bioelectrode of claim 1 wherein colloidal gold adsorbed oxidase is deposited atop the peroxidase.

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

5. The bioelectrode of claim 1 wherein the oxidase is glucose oxidase.

6. The bioelectrode of claim 1 wherein the oxidase is immobilized in a matrix at the conducting surface of the electrode.

7. The bioelectrode of claim 6 wherein the matrix is a hydrophilic polymer.

8. The bioelectrode of claim 7 wherein the hydrophilic polymer is carrageenan.

12. The bioelectrode of claim 1 further comprising depositing at least two oxidase enzymes atop the deposited monolayer-coated colloidal gold peroxidase layer.

15. An instrument for measuring concentrations of oxidase substrate comprising the bioelectrode of claim 1.

9. A bioelectrode for mediatorless electrochemical detection of glucose comprising a conducting surface having a first deposited layer of monolayer-coated colloidal gold-adsorbed horseradish peroxidase and a second deposited layer of colloidal gold-adsorbed glucose oxidase atop said first layer.

10. The bioelectrode of claim 9 wherein the conducting electrode surface is glassy carbon.

11. The bioelectrode of claim 9 wherein the first layer of colloidal gold-adsorbed horseradish peroxidase is evaporatively deposited onto the electrode surface prior to evaporative deposition of the second layer of colloidal gold-adsorbed glucose oxidase.

13. A process for preparing a bioelectrode comprising depositing a coating thickness of between 10 to 20 monolayers of a colloidal gold-adsorbed monolayer of peroxidase onto a conducting surface.

14. A bioelectrode prepared by the process of claim 13.