Implantable glucose sensor

• US 6,815,186 B2
• Filed: 01/28/2002
• Issued: 11/09/2004
• Est. Priority Date: 09/14/1999
• Status: Expired due to Term

• Current Assignee: Arbmetrics, LLC
• Original Assignee: Implanted Biosystems Incorporated
• Inventors: Clark, Leland C Jr.
• Primary Examiner(s): Lankford, Jr., Leon B.
• Application Number:
  US10/058,453
• Publication Number:
  US 20020068860A1
• Time in Patent Office: 1,016 Days
• Field of Search: 435/183, 435/188, 435/189, 435/176, 435/180, 435/182, 600/347, 600/377, 600/300
• US Class Current: 435/183
• CPC Class Codes: A61B 5/14865 invasive, e.g. introduced into the body by a catheter or needle or using implanted sensors
• CPC Class Codes: C12Q 1/002 Electrode membranes
• CPC Class Codes: C12Q 1/006 for glucose

Abstract

The sensitivity of enzyme-based polarographic electrodes to oxygen concentration can be significantly reduced or eliminated by providing an oxygen-reservoir in intimate contact with the oxidative enzyme. This is achieved by making a stabilized emulsion between the enzyme and a compound in which oxygen is extremely soluble. An aqueous glucose oxidase solution is emulsified with a perfluorocarbon liquid, and the resulting emulsion is stabilized by chemically crosslinking the mixture to form a gel. Thin layers of the emulsion are fabricated by spreading a layer of the liquid emulsion before gelation occurs. Additional carrier proteins such as albumin may be added to the enzyme prior to crosslinking to protect enzymatic activity and enhance gel strength. Additional electron transport compounds may be added to further reduce sensitivity to oxygen concentration.

Claims

1. A method for producing a stabilized enzyme emulsion for use with a polarographic or amperometric sensor comprising the steps of:

making an aqueous solution of a protein, either water soluble enzyme that oxidizes an organic substrate to produce hydrogen peroxide or a carrier protein;

emulsifying a volume of a water immiscible oxygen dissolving substance selected from the group consisting of perfluorocarbons, silicone oils, fluorosilicone oils, aromatic and aliphatic hydrocarbon oils or solids, carotenoids and steroids into the aqueous solution to form an emulsion;

contacting the emulsion with a protein crosslinking agent; and

spreading a mixture of the protein crosslinking agent and the emulsion into a uniform layer whereby the crosslinking agent crosslinks the protein within the emulsion to form a solid gel.

2. The method of claim 1, wherein the aqueous solution contains a carrier protein so that when the emulsion is contacted with the protein crosslinking agent the carrier protein becomes crosslinked.

3. The method of claim 2, wherein the aqueous solution contains the water soluble carrier protein and the water soluble enzyme and is added to the emulsion prior to contacting with the protein crosslinking agent.

4. The method of claim 1, wherein the oxygen dissolving substance is a perfluorocarbon liquid selected from the group consisting of perfluorooctyl bromide, perfluorodichlorooctane, perfluorodecalin, perfluoroindane, perfluorophenanthrene, perfluorotetramethylcyclohexane, perfluoropolyalkylether oil, perfluoromethyldecalin, perfluorodimethylethylcyclohexane, perfluorodimethyldecalin, perfluorotrimethyldecalin, perfluoroisopropyldecalin, perfluoropentamethyldecalin, perfluorodiisopropyl decalin, perfluorodiethyldecalin, perfluoromethyladamantane, perfluorodimethyladamantane, perfluoro-di-xylethane, and perfluoro-6,7 H-undec-6-ene.

10. The method of claim 2, wherein an aqueous solution of water soluble enzyme that oxidizes an organic substrate to produce hydrogen peroxide is added to the emulsion following the step of contacting with the protein crosslinking agent.

5. A method for producing a stabilized enzyme emulsion for use with a polarographic sensor comprising the steps of:

making an aqueous solution of a carrier protein;

emulsifying a volume of a perfluorocarbon liquid into the aqueous solution to form an emulsion;

contacting the emulsion with a water soluble enzyme that oxidizes an organic substrate to produce hydrogen peroxide to form a mixture;

contacting the mixture with a protein crosslinking agent; and

spreading a mixture of the protein crosslinking agent and the emulsion into a uniform layer whereby the crosslinking agent crosslinks at least the carrier protein within the emulsion becomes to form a solid gel.

6. The method of claim 5, wherein the oxygen dissolving substance is a perfluorocarbon liquid selected from the group consisting of perfluorooctyl bromide, perfluorodichlorooctane, perfluorodecalin, perfluoroindane, perfluorophenanthrene, perfluorotetramethylcyclohexane, perfluoropolyalkylether oil, perfluoromethyldecalin, perfluorodimethylethylcyclohexane, perfluorodimethyldecalin, perfluorotrimethyldecalin, perfluoroisopropyldecalin, perfluoropentamethyldecalin, perfluorodiisopropyl decalin, perfluorodiethyldecalin, perfluoromethyladamantane, perfluorodimethyladamantane, perfluoro-di-xylethane, and perfluoro-6,7 H-undec-6-ene.

7. The method of claim 5, wherein the step of contacting the emulsion with a water soluble enzyme follows the step of contacting the mixture with a protein crosslinking agent.

8. The method of claim 5, wherein the protein crosslinking agent is selected from the group consisting of glutaraldehyde, carbodiimide, pyrocarbonate, imidoesters, N-hydroxysuccinimid esters and multifunctional epoxides.

9. The method of claim 5, wherein the protein crosslinking agent is selected from the group consisting of glutaraldehyde, carbodiimide, pyrocarbonate, imidoesters, N-hydroxysuccinimid esters and multifunctional epoxides.