Creatinine biosensor

• US 6,861,232 B2
• Filed: 05/14/2001
• Issued: 03/01/2005
• Est. Priority Date: 05/16/2000
• Status: Expired due to Term

• Current Assignee: Roche Diagnostics Operations Incorporated (Roche Holding AG)
• Original Assignee: Roche Diagnostics Operations Incorporated (Roche Holding AG)
• Inventors: Schaffar, Berhard Peter Harald
• Primary Examiner(s): Witz, Jean C.
• Assistant Examiner(s): HANLEY, SUSAN MARIE
• Application Number:
  US10/031,516
• Publication Number:
  US 20030027239A1
• Time in Patent Office: 1,387 Days
• Field of Search: 435/7.91, 435/24, 435/175, 435/176, 435/212, 435/817
• US Class Current: 435/7.91
• CPC Class Codes: A61K 31/415 1,2-Diazoles
• CPC Class Codes: Y10S 435/817 Enzyme or microbe electrode

Abstract

The present invention generally relates to a method for producing biosensors and a biosensor for determination of creatinine. The biosensor comprises at least two enzymes, for the amperometric determination of enzymatically degradable substances in biological liquids, the enzymes being immobilized on a working electrode.

Claims

1. A method for producing biosensors comprising at least two enzymes for the amperometric determination of enzymatically degradable substances in biological liquids wherein the enzymes are immobilized on a working electrode, comprising applying an enzyme together with one or more surface-active substances in an aqueous solution on the working electrode, allowing said enzyme together with the one or more surface-active substances in the aqueous solution to dry, and chemically immobilizing the at least second enzyme thereupon.

2. The method according to claim 1, wherein polyalcohols, detergents, or a combination thereof are used as surface-active substances.

3. The method according to claim 2, wherein non-ionic tensides are used as surface-active substances.

4. The method according to claim 2, further comprising applying a cover membrane after immobilization.

5. The method according to claim 1, wherein the at least second enzyme is immobilized by crosslinking, covalent binding or matrix inclusion.

6. The method according to claim 5, wherein the at least second enzyme is immobilized by glutardialdehyde.

7. The method according to claim 5, further comprising applying a cover membrane after immobilization.

8. The method according to claim 2, wherein the at least second enzyme is immobilized by crosslinking, covalent binding or matrix inclusion.

9. The method according to claim 8, further comprising applying a cover membrane after immobilization.

10. A biosensor comprising a working, a reference and a counter electrode, produced by means of the method according claim 1, wherein the reference electrode is an Ag/AgCl electrode and the counter electrode is a carbon electrode and the working electrode consists of carbon, metal, metal oxides or a mixture of carbon and metal or metal oxides, the electrodes being applied on a nonconducting substrate.

11. A biosensor according to claim 10 for the determination of creatinine, wherein sarcosine oxidase is adsorbed on the working electrode and creatininase and creatinase are immobilized thereupon.

12. A biosensor according to claim 11, wherein it is made up of two three-electrodes systems, the first electrode system comprising the enzymes creatininase, creatinase and sarcosine oxidase and serving for the determination of the sum of creatinine and creatine and the second electrode system comprising the enzymes crease and sarcosine oxidase and serving for the determination of creatine, whereby the two results are subtracted for the determination of creatinine.

13. A biosensor according to claim 12 which comprises a further electrode system serving for the elimination of electrochemical interferences.