Method for production of coated electrode

• US 4,894,253 A
• Filed: 08/08/1988
• Issued: 01/16/1990
• Est. Priority Date: 08/12/1986
• Status: Expired due to Fees

• Current Assignee: University of Cincinnati
• Original Assignee: University of Cincinnati
• Inventors: Galiatsatos, Christos, Decastro, Emory S., Heineman, William R., Mark, James E.
• Primary Examiner(s): PIANALTO, BERNARD D
• Application Number:
  US07/229,720
• Time in Patent Office: 526 Days
• Field of Search: 427/36, 427/35, 427/38, 427/44, 427/54.1, 427/58, 427/409, 427/388.2, 427/346, 427/421, 427/435
• US Class Current: 427/498
• CPC Class Codes: C12Q 1/002 Electrode membranes
• CPC Class Codes: G01N 27/3271 Amperometric enzyme electrodes for analytes in body fluids, e.g. glucose in blood amperometry per se G01N27/49; aspects concerning the enzyme reagent C12Q1/001
• CPC Class Codes: G01N 33/5438 Electrodes
• CPC Class Codes: H01M 4/60 of organic compounds
• CPC Class Codes: Y02E 60/10 Energy storage using batteries

Abstract

An electrode having a coating comprising at least two layers, at least one layer being a polymer network cross-linked by high energy radiation or chemically, and a method of producing such an electrode. The electrode is useful as a sensor for molecular oxygen, or as an ampermometric sensor with an enzyme or antibody immobilized in the cross-linked polymer layer.

Claims

1. A method of producing an electrode which comprises applying to an electroconductive core a liquid inner layer and a liquid outer layer by dipping, spraying or spin coating at a temperature not higher than about 100°

C., said inner and outer layers being different materials, at least said outer layer being polymerizable, cross-linking said outer polymerizable layer in situ into a network, and controlling the pore size of said layer to obtain a permeable polymer network.

2. The method claimed in claim 1, wherein cross-linking is effected by high energy radiation.

3. The method claimed in claim 1, wherein cross-linking is effected chemically by means of end linkers to obtain functionally terminated chains having a length not exceeding a Dp of 25.

4. The method claimed in claim 1, wherein cross-linking is effected chemically by means of reactive functional groups located as side chains.

5. The method claimed in claim 1, wherein cross-linking is effected chemically by generation of free radicals from unstable organic compounds by thermal decomposition.

6. The method claimed in claim 5, wherein said unstable organic compounds are peroxides.

7. The method claimed in claim 1, wherein said inner layer is polymerizable, wherein said inner layer is cross-linked by high energy radiation, and thereafter said outer layer is applied.

8. The method claimed in claim 5, wherein said outer layer is cross-linked after application by high energy radiation.

9. The method claimed in claim 8, wherein cross-linking is effected by gamma ray irradiation.

10. The method claimed in claim 7, wherein said outer layer is poly (dimethyl siloxane).

11. The method claimed in claim 7, wherein said inner layer is poly (vinylbenzyl trimethyl ammonium chloride).

12. The method claimed in claim 11, wherein a redox couple is dispersed in said inner layer.

13. The method claimed in claim 7, wherein said inner layer is poly (vinyl alcohol) having one of an enzyme and an antibody dispersed therein.

14. The method of claim 13, wherein said radiation is of a dose capable of completely cross-linking the polymer and entrapping the enzyme in the polymer network, but not capable of destroying the activity of the enzyme.

15. The method claimed in claim 13, wherein said enzyme is glucose oxidase.

16. The method claimed in claim 13, wherein said outer layer functions as a selective chemical film capable of retarding fouling of said electrode.

17. The method claimed in claim 1, wherein said outer layer is a gas permeable, liquid impermeable material.

18. The method claimed in claim 1, wherein said inner layer is poly (vinylbenzyl trimethyl ammonium chloride).

19. The method claimed in claim 1, wherein said outer layer is a poly (dimethyl siloxane).