Method of manufacturing in vitro analyte sensors

• US 8,272,125 B2
• Filed: 09/29/2009
• Issued: 09/25/2012
• Est. Priority Date: 10/08/1998
• Status: Expired due to Fees

• Current Assignee: Abbott Diabetes Care Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: Abbott Diabetes Care Incorporated (Abbott Laboratories Incorporated)
• Inventors: Feldman, Benjamin J., Heller, Adam, Heller, Ephraim, Mao, Fei, Vivolo, Joseph A., Funderburk, Jeffery V., Colman, Fredric C., Krishnan, Rajesh
• Primary Examiner(s): Nguyen, Donghai D.
• Application Number:
  US12/569,179
• Publication Number:
  US 20100019407A1
• Time in Patent Office: 1,092 Days
• Field of Search: 204/403.01, 204/403.03, 204/403.04, 204/409, 204/416, 205/777.5, 427/2.13, 435/287.5, 435/287.8, 435/287.9, 600/345, 600/347, 294/15, 29593-595, 298/30, 298/31, 298/74, 298/76, 298/77, 298/84
• US Class Current: 29/842
• CPC Class Codes: C12Q 1/001 Enzyme electrodes
• CPC Class Codes: C12Q 1/006 for glucose
• CPC Class Codes: C12Q 1/32 involving dehydrogenase
• 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 27/3272 Test elements therefor, i.e. disposable laminated substrates with electrodes, reagent and channels optical biosensors G01N33/52
• CPC Class Codes: G01N 27/3274 Corrective measures, e.g. error detection, compensation for temperature or hematocrit, calibration coding of calibration information G01N33/48771
• CPC Class Codes: Y10T 156/1052 with cutting, punching, tearing or severing
• CPC Class Codes: Y10T 29/49002 Electrical device making
• CPC Class Codes: Y10T 29/49004 including measuring or testing of device or component part
• CPC Class Codes: Y10T 29/49007 Indicating transducer
• CPC Class Codes: Y10T 29/49126 Assembling bases
• CPC Class Codes: Y10T 29/49128 Assembling formed circuit to base
• CPC Class Codes: Y10T 29/4913 Assembling to base an electrical component, e.g., capacitor, etc.
• CPC Class Codes: Y10T 29/49147 Assembling terminal to base
• CPC Class Codes: Y10T 29/49155 Manufacturing circuit on or in base
• CPC Class Codes: Y10T 29/49204 Contact or terminal manufacturing
• CPC Class Codes: Y10T 29/49208 by assembling plural parts
• CPC Class Codes: Y10T 29/4921 with bonding
• CPC Class Codes: Y10T 29/49794 Dividing on common outline

Abstract

Provided are methods of manufacturing a plurality of electrochemical sensors. The methods include forming a plurality of working electrodes on a first electrode region of a substrate, forming a plurality of counter electrodes on a second electrode region of the substrate, disposing a spacer layer on one of the first and second electrode regions, folding the substrate with the spacer layer between the first electrode region and the second electrode region to form a layered structure, and separating or cutting the layered structure to form individual electrochemical sensors.

Claims

1. A method of manufacturing a plurality of electrochemical sensors for use in determining a concentration of an analyte in a sample of bodily fluid, the method comprising the steps of:

(a) forming a plurality of working electrodes on a first electrode region of a substrate;

(b) forming a plurality of counter electrodes on a second electrode region of the substrate;

(c) disposing a spacer layer on one of the first and the second electrode regions;

(d) removing a portion of the spacer layer to define sample chamber regions;

(e) folding the substrate with the spacer layer between the first electrode region and the second electrode region to form a layered structure; and

(f) separating the layered structure into a plurality of electrochemical sensors, each electrochemical sensor comprising at least one working electrode, at least one counter electrode, and at least one sample chamber region,

wherein each electrochemical sensor comprises a proximal end having a width and a distal end having a width, the distal end being configured for insertion into a sensor reader, wherein the width of the distal end is greater than the width of the proximal end.

2. The method according to claim 1, wherein the working electrodes comprise a material selected from the group consisting of gold, carbon, platinum, ruthenium dioxide, and palladium.

3. The method according to claim 1, wherein the counter electrodes comprise a material selected from the group consisting of gold, carbon, platinum, ruthenium dioxide, and palladium.

4. The method according to claim 1, wherein the step of forming a plurality of working electrodes comprises printing a plurality of working electrodes, and wherein the step of forming a plurality of counter electrodes comprises printing a plurality of counter electrodes.

5. The method according to claim 4, wherein printing a plurality of working electrodes comprises printing a carbon ink.

6. The method according to claim 4, wherein printing a plurality of counter electrodes comprises printing a Ag/AgCl ink.

7. The method according to claim 1, further comprising forming a plurality of indicator electrodes on the substrate, wherein the step of separating the layered structure into a plurality of electrochemical sensors comprises separating the layered structure into a plurality of electrochemical sensors, each electrochemical sensor comprising at least one working electrode, at least one counter electrode, at least one indicator electrode, and at least one sample chamber.

8. The method according to claim 1, further comprising depositing an enzyme over a portion of the working electrodes.

9. The method according to claim 8, wherein the analyte is glucose, and wherein the enzyme is selected from the group consisting of glucose dehydrogenase, and glucose oxidase.

10. The method according to claim 8, wherein the analyte is a ketone and the enzyme is a ketone-responsive enzyme.

11. The method according to claim 1, further comprising depositing a redox mediator over a portion of the working electrodes.

12. The method according to claim 11, wherein the redox mediator comprises a transition metal complex comprising a metal selected from the group consisting of osmium, ruthenium, iron, and cobalt.

13. The method according to claim 12, wherein the transition metal complex comprises osmium.

14. The method according to claim 1, wherein each electrochemical sensor comprises a first and second lateral extension flanking the sample chamber region.

15. A method of manufacturing a plurality of electrochemical sensors for use in determining a concentration of an analyte in a sample of bodily fluid, the method comprising the steps of:

(a) forming a plurality of working electrodes on a first electrode region of a first substrate;

(b) forming a plurality of counter electrodes on a second electrode region of the first substrate;

(c) disposing a spacer layer on one of the first electrode region and the second electrode region, the spacer layer defining sample chamber regions;

(d) folding the substrate with the spacer layer between the first electrode region and the second electrode region to form a layered structure; and

(e) cutting the layered structure to provide individual electrochemical sensors, each electrochemical sensor comprising at least one working electrode, at least one counter electrode, and at least one sample chamber region, wherein at least one end of the at least one sample chamber region is defined by a cut,

wherein each electrochemical sensor comprises a proximal end having a width and a distal end having a width, the distal end being configured for insertion into a sensor reader, wherein the width of the distal end is greater than the width of the proximal end.

16. The method according to claim 15, wherein the working electrodes comprise a material selected from the group consisting of gold, carbon, platinum, ruthenium dioxide, and palladium.

17. The method according to claim 15, wherein the counter electrodes comprise a material selected from the group consisting of gold, carbon, platinum, ruthenium dioxide, and palladium.

18. The method according to claim 15, wherein the step of forming a plurality of working electrodes comprises printing a plurality of working electrodes, and wherein the step of forming a plurality of counter electrodes comprises printing a plurality of counter electrodes.

19. The method according to claim 18, wherein printing a plurality of working electrodes comprises printing a carbon ink.

20. The method according to claim 18, wherein printing a plurality of counter electrodes comprises printing a Ag/AgCl ink.

21. The method according to claim 15, further comprising forming a plurality of indicator electrodes on the substrate, wherein the step of separating the layered structure into a plurality of electrochemical sensors comprises separating the layered structure into a plurality of electrochemical sensors, each electrochemical sensor comprising at least one working electrode, at least one counter electrode, at least one indicator electrode, and at least one sample chamber.

22. The method according to claim 15, further comprising depositing an enzyme over a portion of the working electrodes.

23. The method according to claim 22, wherein the analyte is glucose, and wherein the enzyme is selected from the group consisting of glucose dehydrogenase, and glucose oxidase.

24. The method according to claim 22, wherein the analyte is a ketone and the enzyme is a ketone-responsive enzyme.

25. The method according to claim 15, further comprising depositing a redox mediator over a portion of the working electrodes.

26. The method according to claim 25, wherein the redox mediator comprises a transition metal complex comprising a metal selected from the group consisting of osmium, ruthenium, iron, and cobalt.

27. The method according to claim 26, wherein the transition metal complex comprises osmium.

28. The method according to claim 15, wherein each electrochemical sensor comprises a first and second lateral extension flanking the sample chamber region.