Electrolytic analytical methods

• US 5,545,519 A
• Filed: 06/05/1995
• Issued: 08/13/1996
• Est. Priority Date: 09/13/1990
• Status: Expired due to Fees

• Current Assignee: The Victoria University of Manchester
• Original Assignee: The Victoria University of Manchester
• Inventors: Jones, Malcolm N., Rosenberg, Mark F., Vadgama, Pankaj M.
• Primary Examiner(s): Weimar, Elizabeth C.
• Assistant Examiner(s): Mohamed, Abdel A.
• Application Number:
  US08/465,601
• Time in Patent Office: 435 Days
• Field of Search: 435/4, 435/14, 435/25, 435/26, 435/28, 435/183, 435/190, 435/192, 436/63, 436/71, 424/450
• US Class Current: 435/4
• CPC Class Codes: C12Q 1/002 Electrode membranes

Abstract

Enzyme electrodes having the enzyme enclosed within liposomes supported on, or in a membrane and immobilized therein are provided. The liposomes may be made using lipids and conveniently by "reverse phase evaporation". The enzyme electrodes incorporate conventional electrode elements, e.g., THE Clark electrode pair (Platinum/Silver) and additional membranes or screens, and used particularly in amperometric measurements. The enzyme can be an oxidase and is useful for measurement, directly or indirectly, of low molecular weight species generated by enzymic action, and effective for study of biological fluids.

Claims

1. Enzyme electrodes, having at least one active electrode component appropriate for the performance of an electrolytic measuring function, in association with an enzyme, wherein the enzyme is enclosed within liposomes and the liposomes, within which the enzyme is enclosed, are incorporated on or in a supporting carrier.

2. Enzyme electrodes as claimed in claim 1 wherein the supporting carrier is a membrane.

3. Enzyme electrodes as claimed in claim 1 or claim 2 wherein the liposomes comprise a bi-polar lipid exterior enclosing the enzyme.

4. Enzyme electrodes as claimed in claim 3 wherein the bi-polar lipid is a phospholipid.

5. Enzyme electrodes as claimed in claim 4 wherein the lipid is phosphatidyl inositol, dimyristoylphosphatidylcholine, dipalmitoyl-phosphatidylcholine or distearoyl-phosphatidylcholine.

6. Enzyme electrodes as claimed in claim 1 or claim 2 wherein the size of the liposomes is in the range of 25 to 1000 nm.

7. Enzyme electrodes as claimed in claim 6 wherein the size of the liposomes is in the range of 100 to 200 nm.

8. Enzyme electrodes as claimed in claim 1 or claim 2 wherein the enzyme is an enzyme which catalyses an oxidative process in which hydrogen peroxide is generated as a co-product.

9. Enzyme electrodes as claimed in claim 8 wherein the enzyme is glucose oxidase.

10. Enzyme electrodes as claimed in claim 1 or claim 2 wherein the supporting carrier on which the liposomes are immobilized comprises a polycarbonate or a cellulose derivative.

11. Enzyme electrodes as claimed in claim 10 wherein the cellulose derivative is an ester of cellulose.

12. Enzyme electrodes as claimed in claim 11 wherein the ester of cellulose is a cellulose acetate or a cellulose nitrate.

13. In a method for electro-analysis of solutions containing substances which interact with an enzyme in an enzyme electrode, the improvement which comprises enclosing the enzyme within liposomes.

14. A method according to claim 13 wherein the liposomes in which the enzyme is enclosed are incorporated on or in a supporting carrier.

15. A method according to claim 14 wherein the carrier is a membrane.