Biosensors and methods of making

• US 7,811,430 B2
• Filed: 02/28/2006
• Issued: 10/12/2010
• Est. Priority Date: 02/28/2006
• Status: Active Grant

• Current Assignee: Abbott Diabetes Care Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: Abbott Diabetes Care Incorporated (Abbott Laboratories Incorporated)
• Inventors: Hector, Simon Andrew, Petyt, Adrian
• Primary Examiner(s): Neckel; Alexa D
• Assistant Examiner(s): DIETERLE, JENNIFER M
• Application Number:
  US11/276,432
• Publication Number:
  US 20070199818A1
• Time in Patent Office: 1,687 Days
• Field of Search: 204/403.01, 204/412, 204/411, 204/403.1, 204/403.14, 204/409, 204/403.04, 204/777.5, 204/779, 205/775
• US Class Current: 204/403.01
• CPC Class Codes: C12Q 1/005 involving specific analytes or enzymes including groups of enzymes, e.g. oxydases; C12Q1/004 takes precedence
• 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 33/5438 Electrodes
• CPC Class Codes: G01N 33/66 involving blood sugars, e.g. galactose

Abstract

Devices and methods for determining the concentration of an analyte in a sample of liquid are provided.

Claims

1. A biosensor comprising:

(a) a first and a second substrate;

(b) a sample chamber positioned between the first substrate and the second substrate;

(c) an incompressible element, wherein the incompressible element is a monofilament, a thread or a yarn, positioned within a portion of the sample chamber, wherein the incompressible element defines the structure of the sample chamber in the absence of a spacer layer, and wherein the first substrate is deformable and deforms due to the incompressible element; and

(d) wherein the biosensor comprises a proximal end, a distal end that engages with a meter, a first side extending between the proximal end and the distal end of the sensor, and a second side extending between the proximal end and the distal end of the sensor, and wherein the incompressible element extends from an edge of the first side to an edge of the second side of the biosensor.

2. The biosensor of claim 1, further comprising sensing chemistry proximate the incompressible element.

3. The biosensor of claim 2, wherein the sensing chemistry comprises an enzyme.

4. The biosensor of claim 3, wherein the sensing chemistry further comprises a redox mediator.

5. The biosensor of claim 1, wherein the sample chamber has a volume of no more than about 1 microliter.

6. The biosensor of claim 5, wherein the sample chamber has a volume of no more than about 0.5 microliter.

7. The biosensor of claim 6, wherein the sample chamber has a volume of no more than about 0.1 microliter.

8. The biosensor of claim 1, wherein the incompressible element provides at least a first opening extending into the sample chamber.

9. The biosensor of claim 8, wherein the opening is a vent.

10. The biosensor of claim 8, wherein the opening is a sample inlet.

11. The biosensor of claim 8, wherein the incompressible element provides a second opening extending into the sample chamber, the first opening being a vent and the second opening being a sample inlet.

12. A biosensor strip for determining the concentration of an analyte in a sample, the biosensor strip having a first side and a second side comprising:

(a) a first substrate;

(b) a second substrate in covering relation to the first substrate;

(c) a sample chamber present between the first substrate and the second substrates;

(d) an electrode arrangement present between the first substrate and the second substrate and in the sample chamber;

(e) an incompressible element, wherein the incompressible element is a monofilament, a thread or a yarn, extending between an edge of the first side and an edge of the second side of the sensor in the sample chamber which forms an opening between the first substrate and the second substrate at one of the first side edge and the second side edge, wherein the incompressible element defines the structure of the sample chamber in the absence of a spacer layer, and wherein the first substrate is deformable and deforms due to the incompressible element; and

(f) sensing chemistry proximate the incompressible element.

13. The biosensor of claim 12, wherein the incompressible element forms the first opening at the first side edge and forms a second opening between the first substrate and the second substrate at the second side edge.

14. The biosensor of claim 13, wherein the first opening is an inlet and the second opening is a vent.

15. The biosensor of claim 12, wherein the sensing chemistry comprises an enzyme.

16. The biosensor of claim 15, wherein the sensing chemistry further comprises a redox mediator.

17. The biosensor of claim 12, wherein the sample chamber has a volume of no more than about 1 microliter.

18. The biosensor of claim 17, wherein the sample chamber has a volume of no more than about 0.5 microliter.

19. The biosensor of claim 18, wherein the sample chamber has a volume of no more than about 0.1 microliter.

20. The biosensor of claim 12, wherein the second substrate comprises a backing having a layer of adhesive on one major surface thereof.

21. The biosensor of claim 12, wherein the electrode arrangement comprises at least one working electrode and at least one counter electrode.

22. The biosensor of claim 21, wherein the at least one working electrode and the at least one counter electrode are facing electrodes.

23. The biosensor of claim 21, wherein the at least one working electrode and the at least one counter electrode are co-planar electrodes.

24. A method of manufacturing a sensor, the method comprising:

(a) positioning an incompressible element on a first substrate, wherein the incompressible element is a monofilament, a thread or a yarn;

(b) overlying a second substrate over the first substrate and incompressible element to form a layered construction having at least one sample chamber, wherein the incompressible element is positioned within a portion of the sample chamber and defines the structure of the sample chamber in the absence of a spacer layer, and wherein the second substrate is deformable and deforms due to the incompressible element; and

(c) converting the layered construction into at least one sensor, each of the at least one sensor having a sample chamber.

25. The method of claim 24, wherein converting the layered construction into at least one sensor comprises:

(a) separating the layered construction into a plurality of sensors, wherein each sensor comprises a first substrate, a second substrate overlying the first substrate, and an incompressible element.

26. The method of claim 24, further comprises:

(a) providing sensing chemistry on the incompressible element.

27. The method of claim 24, wherein overlying a second substrate comprises:

(a) overlying a second substrate comprising an adhesive surface.