Process for preparing enzyme electrodes

• US 4,971,901 A
• Filed: 01/20/1988
• Issued: 11/20/1990
• Est. Priority Date: 01/24/1987
• Status: Expired due to Term

• Current Assignee: New Oji Paper Co., Ltd. (Oji Holdings Corporation)
• Original Assignee: Kanzaki Paper Manufacturing Co., Ltd.
• Inventors: Hayashi, Ryuzo, Kariyone, Akio
• Primary Examiner(s): Naff, David M.
• Application Number:
  US07/146,202
• Time in Patent Office: 1,035 Days
• Field of Search: 435/176, 435/177, 435/288, 435/817, 435/14, 435/25, 204/403
• US Class Current: 435/176
• 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

An enzyme electrode is prepared by a process wherein an albumin solution containing 0.05 to 0.5% by weight of a multifunctional aldehyde is applied onto the surface of an electroconductive substrate while maintaining the atmospheric temperature at 0° to 20° C. to thereby form a crosslinked albumin layer on the surface of the electroconductive substrate. Thereafter a solution containing 0.5% by weight or less of a multifunctional aldehyde and a predetermined amount of an oxidase capable of producing hydrogen peroxide (H₂ O₂) is applied on the surface of the previously formed crosslinked albumin layer to form a H₂ O₂ productive oxidase containing layer.

Claims

1. A process for preparing an enzyme electrode consisting essentially of the steps of:

(a) applying an albumin solution containing 0.05 to 0.5% by weight of a multifunctional aldehyde onto the surface of an electroconductive substrate to form a coat comprised of said solution,

(b) maintaining the atmospheric temperature of 0°

C. to 20°

C. to thereby form a permselective crosslinked albumin layer, and

(c) applying a solution containing a hydrogen peroxide productive oxidase and greater than 0 up to 0.5% by weight of a multifunctional aldehyde onto the surface of the above permselective crosslinked albumin layer to form a hydrogen peroxide productive oxidase containing layer thereon.

2. The process according to claim 1, wherein the albumin solution in the step (a) contains 0.1 to 0.5% by weight of a multifunctional aldehyde.

3. The process of claim 1, wherein the step (b) is carried out at a temperature of 0 to 10°

C.

4. The process according to claim 1, wherein the electroconductive substrate is platinum.

5. The process according to claim 4, wherein the platinum substrate has a surface treated with a silane coupling reagent.

6. The process according to claim 5, wherein the silane coupling reagent is one or more members selected from the group consisting of γ

-aminopropyltriethoxy silane, 4-aminobutyldimethylmethoxy silane and 4-aminobutyltriethoxy silane.

7. The process according to claim 5, wherein prior to subjecting to the silane coupling reagent treatment, the platinum substrate is subjected to electrolytic treatment using the platinum substrate as the working electrode at an electric potential of +1.0 to +1.5 V ν

s Ag/AgCl electrode for a period of more than 30 seconds.

8. The process according to claim 1, wherein the multifunctional aldehyde is glutaraldehyde.

9. The process according to claim 1, wherein the albumin is bovine serum albumin.

10. The process according to claim 1, wherein the step (b) is carried out at a temperature of 0 to 10°

C. for a period of 20 minutes to 24 hours.

11. The process according to claim 10, wherein the period is 30 minutes to 4 hours.

12. The process according to claim 1, wherein the hydrogen peroxide productive oxidase is selected from glucoseoxidase and galactoseoxidase.

13. The process according to claim 1, wherein the solution in the step (c) further contains a protein other than an enzyme.

14. The process according to claim 13, wherein the protein is albumin.

15. An enzyme electrode produced in accordance with the process according to claim 1.