Electrode and method for the detection of hydrogen peroxide

• US 5,320,725 A
• Filed: 05/08/1992
• Issued: 06/14/1994
• Est. Priority Date: 08/02/1989
• Status: Expired due to Fees

• Current Assignee: Therasense Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: E. Heller & Company
• Inventors: Gregg, Brian A., Heller, Adam
• Primary Examiner(s): TUNG, TA HSUNG
• Application Number:
  US07/880,759
• Time in Patent Office: 767 Days
• Field of Search: 204/153.12, 204/403, 204/415, 204/416, 204/418, 435/28, 435/817, 436/528, 436/531, 436/533, 436/535, 436/806
• US Class Current: 205/777.5
• CPC Class Codes: C12Q 1/002 Electrode membranes
• 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
• CPC Class Codes: Y10S 436/806 Electrical property or magnetic property

Abstract

An amperometric biosensor and method for the detection of hydrogen peroxide, NADH, or NADPH with high sensitivity includes an electrode having on its testing surface a three-dimensional redox polymer network in which peroxidase is immobilized.

Claims

1. An electrode for the detection of hydrogen peroxide comprising:

an electrode having a testing surface; and

a transducing film substantially covering the testing surface of the electrode, the film comprising a cross-linked redox polymer network, the network comprising a redox compound having multiple redox centers and a peroxidase having redox centers wherein the redox centers of the peroxidase are electrically connected, in the absence of diffusional electron shuttles, to the electrode.

2. The electrode of claim 1, wherein the peroxidase is chemically bonded to the redox polymer network.

3. The electrode of claim 2, wherein the peroxidase is covalently bonded to the redox polymer network.

4. The electrode of claim 1, wherein the peroxidase is horseradish peroxidase.

5. The electrode of claim 1, wherein the peroxidase is fungal peroxidase of Arthoromyces ramosus.

6. The electrode of claim 1, wherein said peroxidase is a heme-containing molecule.

7. The electrode of claim 1, wherein the redox centers of the redox compound contain osmium.

8. The electrode of claim 7, wherein the redox compound is poly(vinyl pyridine) complexed with osmium bis(2,2'"'"'-bipyridine).

9. The electrode of claim 7, wherein the redox compound is poly (N-vinyl imidazole) complexed with osmium bis(2,2'"'"'-bipyridine).

10. The electrode of claim 1, further comprising an enzyme fixed to the network, which enzyme catalyzes a substrate-enzyme reaction generating H₂ O₂, NADPH, or NADP, and wherein the enzyme is isolated from the peroxidase.

11. The electrode of claim 10, wherein the enzyme is physically isolated from the peroxidase.

12. The electrode of claim 11, wherein the enzyme is electrically isolated from the peroxidase.

13. A method for analyzing the presence of hydrogen peroxide in a test sample comprising the steps of:

contacting a test sample with an electrode having a test surface substantially covered with a transducing film comprising a cross-linked redox polymer network having multiple redox centers and peroxidase immobilized in the network;

generating electrons at the electrode;

transferring electrons from the electrode through the cross-linked polymer network to the peroxidase;

electroreducing hydrogen peroxide at the peroxidase;

generating an electrical current by electroreduction of hydrogen peroxide within the cross-linked redox polymer network; and

measuring the generated current.

14. The method of claim 13 wherein the peroxidase is covalently bound to the redox polymer network.

15. The method of claim 13, wherein the H₂ O₂ present in the test sample is generated by a substrate-enzyme reaction such that the generated current is directly related to the amount of the substrate in the test sample.

16. A method for analyzing the presence of NADPH or NADH in a test sample comprising the steps of:

reacting NADPH or NADH with dissolved molecular oxygen in the presence of a quinoid in the test sample;

contacting the reacted test solution with an electrode having a testing surface substantially covered with a transducing film comprising a cross-linked redox polymer network having multiple redox centers and peroxidase immobilized in the network;

generating electrons at the electrode;

transferring electrons from the electrode through the cross-linked polymer network to the peroxidase;

electroreducing hydrogen peroxide at the immobilized peroxidase;

generating an electrical current by the transfer of electrons and electroreduction of hydrogen peroxide; and

quantifying the generated current.

17. The method of claim 16, wherein said NADPH or NADP present in the test sample is generated by substrateenzyme reaction such that the generated current is directly related to the amount of the substrate in the test sample.