Biosensor membrane and methods related thereto

• US 8,679,308 B2
• Filed: 03/15/2006
• Issued: 03/25/2014
• Est. Priority Date: 03/15/2006
• Status: Active Grant

• Current Assignee: Honeywell International Inc.
• Original Assignee: Honeywell International Inc.
• Inventors: Gu, Yuandong
• Primary Examiner(s): Van, Luan
• Assistant Examiner(s): Kaur, Gurpreet
• Application Number:
  US11/375,910
• Publication Number:
  US 20070215465A1
• Time in Patent Office: 2,932 Days
• Field of Search: 204/400, 204403-40306, 204/403.14, 204/418, 204/419, 205/777, 205/777.5, 205/792, 205/778
• US Class Current: 204/403.01
• CPC Class Codes: C12Q 1/002 Electrode membranes

Abstract

Embodiments of the present invention relate to a sensor membrane. The sensor membrane comprises one or more conversion layers wherein the one or more conversion layers are capable of converting a non-charged analyte into a charged species, one or more polymeric layers wherein the one or more polymeric layers act as matrices to host the one or more conversion layers and wherein the one or more conversion layers and one or more polymeric layers create oppositely charged regions within the membrane.

Claims

1. A sensor to detect an analyte in a physiological fluid, comprising:

a sensor having a surface

a membrane, in contact with the sensor surface, the membrane comprising;

an outer layer;

a plurality of alternating layers of conversion layers comprising an enzyme capable of converting an analyte in a physiological fluid sample into a charged species and polyelectrolyte layers, the polyelectrolyte layers acting as matrices to host the conversion layers, wherein the polyelectrolyte comprises repeating units having an electrolyte group which dissociates in the physiological fluid, making the polyelectrolyte layer negatively charged, wherein the polyelectrolyte layers have a pKa value that differs by two pH units or more than the operating pH of the sensor; and

wherein the conversion layers and the polyelectrolyte layers are selected to control the exclusion of a negatively charged physiological buffer species found in the physiological fluid sample, thereby enhancing the rate or sensitivity of the conversion of the analyte into a charged species, and wherein the outer layer of the membrane is negatively charged; and

a transducer adapted to detect the presence or amount of the charged species, thereby detecting the presence or amount of the analyte in a physiological fluid sample.

2. The sensor of claim 1 wherein the selection of the one or mere conversion layers and the polyelectrolyte layers enhances the rate of the conversion of the analyte into a charged species.

3. The sensor of claim 1, wherein the total charge of the combination of conversion layers, the polyelectrolyte layers and mobile ions attracted to the layers in solution is neutral.

4. The sensor of claim 1, wherein the conversion layers and the polyelectrolyte layers comprise a polyelectrolyte.

5. The sensor of claim 1, wherein the polyelectrolyte comprises poly(sodium styrene sulfonate) (PSS), poly(acrylic acid) (PAA), or combinations thereof.

6. The sensor of claim 1, wherein the polyelectrolyte layers have a pKa value lower than about 4.5.

10. The sensor of claim 1 wherein the physiological buffer species is carbonate ion.

14. The sensor of claim 1, wherein the analyte is glucose or urea.

7. A method of detecting a selected analyte in a physiological fluid, the method comprising:

contacting a physiological fluid sample comprising the analyte and the physiological fluid having a negatively charged buffering species with a layered membrane, sufficient to create an analyte in a buffer selective environment;

controlling the exclusion of the negatively charged buffering species within the layered membrane thereby enhancing the rate or sensitivity of the conversion of the analyte into a charged species;

and

detecting with a sensor the conversion of the analyte, sufficient to provide analyte concentration measurements;

wherein the layered membrane comprises

an outer layer;

a plurality of alternating layers of conversion layers comprising an enzyme capable of converting an analyte into a charged species and polyelectrolyte layers, the polyelectrolyte layers acting as matrices to host the conversion layers, wherein the polyelectrolyte comprises repeating units having an electrolyte group which dissociates in the physiological fluid, making the polyelectrolyte layer negatively charged, wherein the polyelectrolyte layers have a pKa value that differs by two pH units or more than the operating pH of the sensor; and

wherein the conversion layers and polyelectrolyte layers are selected to control the exclusion of the negatively charged physiological buffer species, and wherein the outer layer of the membrane is negatively charged.

8. The method of claim 7, wherein detecting the conversion of the analyte comprises detection by calorimetric, amperometric, potentiometric, optical, piezo-electric means or combinations thereof.

9. The method of claim 7 wherein the combination of the conversion layers and the polyelectrolyte layers enhances the sensitivity of the conversion.

11. The method of claim 7 wherein the buffering species is carbonate ion.

12. The method of claim 7, wherein the polyelectrolyte comprises poly(sodium styrene sulfonate) (PSS), poly(acrylic acid) (PAA), or combinations thereof.

13. The method of claim 7, wherein the polyelectrolyte layers have a pKa value lower than about 4.5.

15. The method of claim 7, wherein the analyte is glucose or urea.