ANALYTE SENSOR APPARATUSES HAVING INTERFERENCE REJECTION MEMBRANES AND METHODS FOR MAKING AND USING THEM

• US 20110082356A1
• Filed: 10/01/2009
• Published: 04/07/2011
• Est. Priority Date: 10/01/2009
• Status: Abandoned Application

• Current Assignee: Medtronic Minimed Incorporated (Medtronic Plc)
• Original Assignee: Medtronic Minimed Incorporated (Medtronic Plc)
• Inventors: Shah, Rajiv, Little, Megan E., Yang, Qingling, Chiu, Chia-Hung
• Application Number:
  US12/572,087
• Publication Number:
  US 20110082356A1
• Time in Patent Office: Days
• US Class Current: 600/345
• CPC Class Codes: C12Q 1/006 for glucose
• CPC Class Codes: Y02P 20/582 Recycling of unreacted starting or intermediate materials

Abstract

Embodiments of the invention provide amperometric analyte sensors having optimized elements such as interference rejection membranes as well as methods for making and using such sensors. While embodiments of the innovation can be used in a variety of contexts, typical embodiments of the invention include glucose sensors used in the management of diabetes.

Claims

1. An amperometric analyte sensor apparatus comprising:

a base layer;

a conductive layer disposed on the base layer and comprising a working electrode;

an interference rejection membrane disposed on an electroactive surface of the working electrode, wherein the interference rejection membrane comprises polymers crosslinked by a hydrophilic crosslinking agent; and

an analyte sensing layer.

2. The analyte sensor apparatus of claim 1, wherein the interference rejection membrane comprises crosslinked primary amine polymers or crosslinked methacrylate polymers.

3. The analyte sensor apparatus of claim 2, wherein the crosslinked methacrylate polymers comprise Poly(2-hydroxyethyl methacrylate) polymers having an average molecular weight between 100 and 1000 kilodaltons.

4. The analyte sensor apparatus of claim 2, wherein the crosslinked primary amine polymers comprise:

polylysine polymers;

poly(allylamine) polymers;

amine terminated poly(ethylene oxide) polymers;

poly(vinylamine) polymers;

or

polyethylenimine polymers;

having an average molecular weight between 4 and 500 kilodaltons.

5. The analyte sensor apparatus of claim 1, wherein the interference rejection membrane is between 0.1 μ

m and 1.0 μ

m thick.

6. The analyte sensor apparatus of claim 1, wherein the interference rejection membrane inhibits the diffusion therethrough of compounds having a molecular weight greater than 140 Daltons.

7. The analyte sensor apparatus of claim 1, wherein the interference rejection membrane inhibits the diffusion of acetaminophen therethrough in a manner that decreases a signal in the analyte sensor apparatus that results from a concentration of acetaminophen by at least 50% as compared to a control analyte sensor apparatus lacking the interference rejection membrane.

8. The analyte sensor apparatus of claim 1, wherein the hydrophilic crosslinking agent comprises:

a urea;

a hydrophilic organofunctional dipodal alkoxysilane;

or glutaraldehyde.

9. The analyte sensor apparatus of claim 1, wherein an electrochemically reactive surface of the working electrode comprises platinum black having an irregular surface structure.

10. The analyte sensor apparatus of claim 1, wherein:

the interference rejection membrane is in direct contact with an electrochemically reactive surface of the working electrode; and

the analyte sensing layer is in direct contact with the interference rejection membrane.

11. The analyte sensor apparatus of claim 1, wherein the analyte sensor apparatus is implantable within a mammal.

28. The analyte sensor apparatus of claim 1, further comprising at least one of:

a protein layer disposed on the analyte sensing layer;

an analyte modulating layer disposed on the analyte sensing layer or the protein layer, wherein the analyte modulating layer comprises a composition that modulates the diffusion of an analyte diffusing through the analyte modulating layer;

an adhesion promoting layer disposed on the analyte sensing layer, wherein the adhesion promoting layer promotes the adhesion between the analyte sensing layer and an analyte modulating layer;

or

a cover layer disposed on the analyte sensor apparatus, wherein the cover layer comprises an aperture positioned on the cover layer so as to facilitate an analyte present in the mammal contacting and diffusing through an analyte modulating layer; and

contacting the analyte sensing layer.

29. The analyte sensor apparatus of claim 1, wherein the conductive layer comprises a plurality of electrodes including the working electrode, a counter electrode and a reference electrode.

30. The analyte sensor of claim 29, wherein the conductive layer comprises a plurality of working electrodes, counter electrodes and reference electrodes;

and

the plurality of working, counter and reference electrodes are grouped together as a unit and positionally distributed on the conductive layer in a repeating pattern of units.

31. The analyte sensor apparatus of claim 1, wherein the analyte sensing layer comprises an oxidoreductase that generates hydrogen peroxide upon exposure to a substrate for the oxidoreductase, wherein the amount of hydrogen peroxide generated by the oxidoreductase is proportional to the amount of substrate exposed to the oxidoreductase.

32. The analyte sensor apparatus of claim 1, wherein the sensor is operatively coupled to:

a sensor input capable of receiving a signal from the sensor that is based on a sensed physiological characteristic value in the mammal; and

a processor coupled to the sensor input, wherein the processor is capable of characterizing one or more signals received from the sensor.

33. The analyte sensor of claim 1, wherein a pulsed voltage is used to obtain a signal from an electrode.

12. -27. (canceled)

34. A method of making a sensor apparatus for implantation within a mammal comprising the steps of:

providing a base layer;

forming a conductive layer on the base layer, wherein the conductive layer includes a working electrode;

forming an interference rejection membrane on the working electrode, wherein the interference rejection membrane comprises crosslinked methacrylate polymers or crosslinked primary amine polymers;

forming an analyte sensing layer on the conductive layer, wherein the analyte sensing layer includes an oxidoreductase;

optionally forming a protein layer on the analyte sensing layer;

forming an adhesion promoting layer on the analyte sensing layer or the optional protein layer;

forming an analyte modulating layer disposed on the adhesion promoting layer, wherein the analyte modulating layer includes a composition that modulates the diffusion of the analyte therethrough; and

forming a cover layer disposed on at least a portion of the analyte modulating layer, wherein the cover layer further includes an aperture over at least a portion of the analyte modulating layer.

35. The method of claim 34, wherein the crosslinked methacrylate polymers comprise Poly(2-hydroxyethyl methacrylate) (pHEMA) polymers having an average molecular weight of between 100 and 1000 kilodaltons.

36. The method of claim 34, wherein the polymers are crosslinked by a hydrophilic crosslinking agent.

37. The method of claim 35, wherein the interference rejection membrane is between 0.1 μ

m and 1.0 μ

m thick, and formed on the electrode by;

(1) a spray process using a solution comprising;

0.3 to 1% pHEMA; and

0.25% to 0.7% of a silane crosslinking agent;

(2) a spin process using a solution comprising;

1 to 3% pHEMA; and

0.3% to 0.7% of a silane crosslinking agent;

or

(3) a slot coating process using a solution comprising;

4% pHEMA; and

0.35% to 1.0% of a silane crosslinking agent.

38. The method of claim 37, wherein the silane crosslinking agent is bis[3-(triethoxysilyl)propyl]urea.

39. A polymeric composition comprising:

methacrylate polymers having a molecular weight between 100 and 1000 kilodaltons, wherein the methacrylate polymers are crosslinked by a hydrophilic organofunctional dipodal alkoxysilane;

or

primary amine polymers having a molecular weight between 4 and 500 kilodaltons, wherein the primary amine polymers are crosslinked by glutaraldehyde.

40. The polymeric composition of claim 39, wherein the composition coats a hydrogen peroxide transducing composition.

41. The polymeric composition of claim 39, wherein the crosslinked methacrylate polymers comprise Poly(2-hydroxyethyl methacrylate) polymers.

42. The polymeric composition of claim 39, wherein the crosslinked primary amine polymers comprise:

polylysine polymers;

poly(allylamine) polymers;

amine terminated poly(ethylene oxide) polymers;

poly(vinylamine) polymers;

or

polyethylenimine polymers.

43. The polymeric composition of claim 40, wherein the hydrogen peroxide transducing composition comprises an electrode;

and the polymeric composition is coated on the electrode in a layer between 0.1 μ

m and 1.0 μ

m thick.