Small volume in vitro analyte sensor with diffusible or non-leachable redox mediator

• US 6,338,790 B1
• Filed: 04/21/1999
• Issued: 01/15/2002
• Est. Priority Date: 10/08/1998
• Status: Expired due to Term

• Current Assignee: Abbott Diabetes Care Incorporated (Abbott Laboratories Incorporated)
• Original Assignee: Therasense Incorporated (Abbott Laboratories Incorporated)
• Inventors: Funderburk, Jeffrey V., Krishnan, Rajesh, Heller, Ephraim, Heller, Adam, Colman, Fredric C., Feldman, Benjamin J., Mao, Fei, Vivolo, Joseph A.
• Primary Examiner(s): Tung, T.
• Assistant Examiner(s): NOGUEROLA, ALEXANDER STEPHAN
• Application Number:
  US09/295,962
• Time in Patent Office: 1,000 Days
• Field of Search: 204/403, 205/777.5
• US Class Current: 205/777.5
• 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

A sensor utilizing a non-leachable or diffusible redox mediator is described. The sensor includes a sample chamber to hold a sample in electrolytic contact with a working electrode, and in at least some instances, the sensor also contains a non-leachable or a diffusible second electron transfer agent. The sensor and/or the methods used produce a sensor signal in response to the analyte that can be distinguished from a background signal caused by the mediator. The invention can be used to determine the concentration of a biomolecule, such as glucose or lactate, in a biological fluid, such as blood or serum, using techniques such as coulometry, amperometry, and potentiometry. An enzyme capable of catalyzing the electrooxidation or electroreduction of the biomolecule is typically provided as a second electron transfer agent.

Claims

1. A sensor for determining the concentration of an analyte in a sample fluid, the sensor comprising:

an electrode pair comprising a working electrode and a counter electrode, wherein at least a portion of the working electrode is within a distance of no more than 200 m of a portion of the counter electrode;

a measurement zone positioned adjacent to the working electrode and counter electrode, wherein the measurement zone is sized to contain a volume of no more than about 1 μ

L of sample;

a reference electrode disposed in contact with the measurement zone; and

an analyte-responsive enzyme and a diffusible redox mediator disposed in the measurement zone;

wherein the sensor is configured and arranged so that the redox mediator oxidizes the analyte and the half-wave potential of the redox mediator, as measured by cyclic voltammetry in 0.1 M NaCl at pH 7, is no more than about +100 millivolts relative to the potential of the reference electrode.

2. The sensor of claim 1, wherein the sensor is configured and arranged so that a background signal generated by the diffusible redox mediator is the same or less than the signal generated by oxidation or reduction of the average normal physiological amount of analyte.

3. The sensor of claim 1, wherein the sensor is configured and arranged so that a background signal generated by the diffusible redox mediator is no more than 25% of the signal generated by oxidation or reduction of the expected amount of analyte.

4. The sensor of claim 1, wherein the sensor is configured and arranged so that a background signal generated by the diffusible redox mediator is no more than 5% of the signal generated by oxidation or reduction of the expected amount of analyte.

5. The sensor of claim 1, further comprising a sample chamber for holding the sample in electrolytic contact with the working electrode, wherein the measurement zone is part of the sample chamber.

6. The sensor of claim 5, wherein the sample chamber is sized to contain a volume of no more than about 1 μ

L of sample.

7. The sensor of claim 5, wherein the measurement zone comprises at least about 80% of the sample chamber volume.

8. The sensor of claim 5, wherein the measurement zone and the sample chamber have the same volume.

9. The sensor of claim 1, wherein the measurement zone is sized to contain a volume of no more than about 0.1 μ

L of sample.

10. The sensor of claim 1, wherein a portion of the working electrode is within 50 μ

m of a portion of the counter electrode.

11. The sensor of claim 1, wherein the analyte is glucose.

12. The sensor of claim 1, wherein the working electrode and counter electrode form a facing electrode pair with the measurement zone positioned between the working electrode and the counter electrode.

13. The sensor of claim 1, further comprising sorbent material disposed in the measurement zone.

14. The sensor of claim 1, wherein the measurement zone is bounded on at least two sides by the working electrode and the counter electrode.

15. The sensor of claim 1, further comprising a first substrate upon which the working electrode is disposed and a second substrate upon which the counter electrode is disposed, wherein a distance between the first and second substrates is less than a nearest distance between the working electrode and counter electrode.

16. The sensor of claim 1, wherein the sensor is configured and arranged so that a background signal generated by the diffusible redox mediator is no more than five times the signal generated by oxidation or reduction of the average normal physiological amount of analyte.

17. The sensor of claim 1, wherein the counter electrode is also the reference electrode.

18. The sensor of claim 1, wherein the half-wave potential of the redox mediator, as measured by cyclic voltammetry in 0.1 M NaCl at pH 7, is about the same as the potential of the reference electrode.

19. The sensor of claim 1, wherein the half-wave potential of the redox mediator, as measured by cyclic voltammetry in 0.1 M NaCl at pH 7, is no more than about −

150 millivolts relative to the potential of the reference electrode.

20. A method for determining a concentration of an analyte in a sample, comprising the steps of:

contacting a sample with an electrochemical sensor comprising

an electrode pair comprising a working electrode and a counter electrode, wherein at least a portion of the working electrode is within a distance of no more than 200 μ

m of a portion of the counter electrode;

a measurement zone positioned adjacent to the working electrode and counter electrode, wherein the measurement zone is sized to contain a volume of no more than about 1 μ

L of sample; and

an analyte-responsive enzyme and a diffusible redox mediator disposed in the measurement zone;

deterring transport of the diffusible redox mediator between the working electrode and the counter electrode;

generating a sensor signal at the working electrode, wherein a background signal that is generated by the diffusible redox mediator is no more than five times a signal generated by oxidation or reduction of an average normal physiological amount of analyte, and

determining the concentration of the analyte using the sensor signal.

21. The method of claim 20, wherein determining the concentration of the analyte comprises determining the concentration of the analyte by coulometry using the sensor signal.

22. The method of claim 20, wherein determining the concentration of the analyte comprises determining the concentration of the analyte by amperometry using the sensor signal.

23. The method of claim 20, further comprising:

providing calibration data on a batch of electrodes to the measurement instrument, said calibration data comprising information related to a magnitude of a background charge for the batch of electrodes;

wherein the step of determining the concentration of the analyte comprises determining the concentration of the analyte using the sensor signal and the calibration data.

24. The method of claim 20, wherein determining the concentration of the analyte comprises determining the concentration of the analyte by potentiometry using the sensor signal.

25. The method of claim 20, wherein generating a sensor signal comprises operating the sensor at an applied potential of no more than about +100 mV between the working electrode and the counter electrode when the redox mediator is reduced at the counter electrode.

26. The method of claim 20, wherein generating a sensor signal comprises operating the sensor at an applied potential of about 0 mV between the working electrode and the counter electrode when the redox mediator is reduced at the counter electrode.

27. The method of claim 20, wherein generating a sensor signal comprises operating the sensor at an applied potential of no more than about −

100 mV between the working electrode and the counter electrode when the redox mediator is reduced at the counter electrode.

28. A sensor for determining the concentration of glucose in a sample fluid, the sensor comprising:

an electrode pair comprising a working electrode and a counter electrode, wherein at least a portion of the working electrode is within a distance of no more than 200 μ

m of a portion of the counter electrode;

a measurement zone positioned adjacent to the working electrode and counter electrode, wherein the measurement zone is sized to contain a volume of no more than about 1 μ

L of sample; and

a glucose-responsive enzyme and a diffusible redox mediator disposed in the measurement zone;

means for maintaining a background signal generated by the diffusible redox mediator at no more than five times a signal generated by oxidation or reduction of 5 mM glucose.

29. A sensor for determining the concentration of an analyte in a sample fluid, the sensor comprising:

an electrode pair comprising a working electrode and a counter electrode, wherein at least a portion of the working electrode is within a distance of no more than 200 μ

m of a portion of the counter electrode;

a measurement zone positioned adjacent to the working electrode and counter electrode, wherein the measurement zone is sized to contain a volume of no more than about 1 μ

L of sample; and

an analyte-responsive enzyme and a diffusible redox mediator disposed in the measurement zone;

means for maintaining a background signal generated by the diffusible redox mediator at no more than five times a signal generated by oxidation or reduction of an average normal physiological amount of analyte.

30. The sensor of claim 29, wherein said means comprises the redox mediator having an effective diffusion coefficient, within the sensor, of no more than about 1×

10<sup>−

6</sup> cm/sec in the sample fluid.

31. The sensor of claim 29, wherein said means comprises a barrier disposed between the working electrode and the counter electrode to retard a flow of the diffusible redox mediator to the counter electrode.

32. The sensor of claim 29, wherein said means comprises, within the sensor, the effective diffusion coefficient of the redox mediator through the sample fluid is less than the effective diffusion coefficient of the analyte through the sample fluid.

33. The sensor of claim 29, wherein said means comprises, within the sensor, the effective diffusion coefficient of the redox mediator through the sample fluid is at least ten times less than the effective diffusion coefficient of the analyte through the sample fluid.

34. The sensor of claim 29, wherein said means comprises the diffusible mediator having a molecular weight of at least 5,000 daltons.

35. The sensor of claim 29, wherein said means comprises the sensor being configured and arranged so that the redox mediator is more readily electrolyzed on the working electrode than the counter electrode.

36. The sensor of claim 29, wherein said means comprises a molar amount of the redox mediator that is, on a stoichiometric basis, no more than an average normal physiological amount of the analyte.

37. The sensor of claim 29, wherein said means comprises a molar amount of the redox mediator that is, on a stoichiometric basis, no more than 20% of an average normal physiological amount of the analyte.

38. The sensor of claim 29, wherein said means comprises the working electrode having a surface area of no more than about 0.01 cm² exposed in the measurement zone.

39. The sensor of claim 29, wherein said means comprises the working electrode having a surface area of no more than about 0.001cm² exposed in the measurement zone.

40. The sensor of claim 29, wherein said means comprises the activity of the enzyme being no more than 1 unit/cm³.

41. The sensor of claim 29, wherein said means comprises the sensor being configured and arranged so that the diffusible redox mediator precipitates when reacted at the counter electrode.

42. The sensor of claim 29, wherein said means comprises the sensor being configured and arranged so that a mathematical product of the effective diffusion coefficient of the redox mediator and the concentration of the redox mediator is no more than 1×

10<sup>−

12</sup> moles cm<sup>−

1</sup> sec<sup>−

1</sup> when sample fluid fills the measurement zone.

43. The sensor of claim 29, further comprising a reference electrode disposed in contact with the measurement zone.

44. The sensor of claim 43, wherein said means comprises the sensor configured and arranged so that the redox mediator oxidizes the analyte and the half-wave potential of the redox mediator, as measured by cyclic voltammetry in 0.1 M NaCl at pH 7, is no more than about +100 millivolts relative to the potential of the reference electrode.

45. The sensor of claim 44, wherein the half-wave potential of the redox mediator, as measured by cyclic voltammetry in 0.1 M NaCl at pH 7, is about the same as the potential of the reference electrode.

46. The sensor of claim 44, wherein the half-wave potential of the redox mediator, as measured by cyclic voltammetry in 0.1 M NaCl at pH 7, is no more than about −

150 millivolts relative to the potential of the reference electrode.

47. The sensor of claim 43, wherein said means comprises the sensor configured and arranged so that the redox mediator reduces the analyte and the half-wave potential of the redox mediator, as measured by cyclic voltammetry in 0.1 M NaCl at pH 7, is no less than about −

100 millivolts relative to the potential of the reference electrode.

48. The sensor of claim 47, wherein the half-wave potential of the redox mediator, as measured by cyclic voltammetry in 0.1 M NaCl at pH 7, is about the same as the potential of the reference electrode.

49. The sensor of claim 47, wherein the half-wave potential of the redox mediator, as measured by cyclic voltammetry in 0.1 M NaCl at pH 7, is no less than about +200 millivolts relative to the potential of the reference electrode.

50. The sensor of claim 43, wherein the counter electrode is also the reference electrode.

51. The sensor of claim 29, wherein said means maintains a background signal generated by the diffusible redox mediator at the same level or less than the signal generated by oxidation or reduction of the average normal physiological amount of analyte.

52. The sensor of claim 29, wherein said means maintains a background signal generated by the diffusible redox mediator at no more than 25% of the signal generated by oxidation or reduction of the expected amount of analyte.

53. The sensor of claim 29, further comprising a sample chamber for holding the sample in electrolytic contact with the working electrode, wherein the measurement zone is part of the sample chamber.

54. The sensor of claim 53, wherein the sample chamber is sized to contain a volume of no more than about 1 μ

L of sample.

55. The sensor of claim 53, wherein the measurement zone comprises at least about 80% of the sample chamber volume.

56. The sensor of claim 53, wherein the measurement zone and the sample chamber have a same volume.

57. The sensor of claim 29, wherein the measurement zone is sized to contain a volume of no more than about 0.1 μ

L of sample.

58. The sensor of claim 29, wherein a portion of the working electrode is within 50 μ

m of a portion of the counter electrode.

59. The sensor of claim 29, wherein the analyte is glucose.

60. The sensor of claim 29, wherein the working electrode and counter electrode form a facing electrode pair with the measurement zone positioned between the working electrode and the counter electrode.

61. A sensor for determining the concentration of an analyte in a sample fluid, the sensor comprising:

an electrode pair comprising a working electrode and a counter electrode, wherein at least a portion of the working electrode is within a distance of no more than 200 m of a portion of the counter electrode;

a measurement zone positioned adjacent to the working electrode and counter electrode, wherein the measurement zone is sized to contain a volume of no more than about 1 μ

L of sample;

a reference electrode disposed in contact with the measurement zone; and

an analyte-responsive enzyme and a diffusible redox mediator disposed in the measurement zone;

wherein the sensor is configured and arranged so that the redox mediator reduces the analyte and the half-wave potential of the redox mediator, as measured by cyclic voltammetry in 0.1 M NaCl at pH 7, is no less than about −

100 millivolts relative to the potential of the reference electrode.

62. The sensor of claim 61, wherein the sensor is configured and arranged so that a background signal generated by the diffusible redox mediator is the same or less than the signal generated by oxidation or reduction of the average normal physiological amount of analyte.

63. The sensor of claim 61, wherein the sensor is configured and arranged so that a background signal generated by the diffusible redox mediator is no more than 25% of the signal generated by oxidation or reduction of the expected amount of analyte.

64. The sensor of claim 61, wherein the sensor is configured and arranged so that a background signal generated by the diffusible redox mediator is no more than 5% of the signal generated by oxidation or reduction of the expected amount of analyte.

65. The sensor of claim 61, further comprising a sample chamber for holding the sample in electrolytic contact with the working electrode, wherein the measurement zone is part of the sample chamber.

66. The sensor of claim 65, wherein the sample chamber is sized to contain a volume of no more than about 1 μ

L of sample.

67. The sensor of claim 65, wherein the measurement zone comprises at least about 80% of the sample chamber volume.

68. The sensor of claim 65, wherein the measurement zone and the sample chamber have a same volume.

69. The sensor of claim 67, wherein the measurement zone is sized to contain a volume of no more than about 0.1 μ

L of sample.

70. The sensor of claim 61, wherein a portion of the working electrode is within 50 μ

m of a portion of the counter electrode.

71. The sensor of claim 61, wherein the analyte is glucose.

72. The sensor of claim 61, wherein the working electrode and counter electrode form a facing electrode pair with the measurement zone positioned between the working electrode and the counter electrode.

73. The sensor of claim 61, wherein the half-wave potential of the redox mediator, as measured by cyclic voltammetry in 0.1 M NaCl at pH 7, is about the same as the potential of the reference electrode.

74. The sensor of claim 61, wherein the half-wave potential of the redox mediator, as measured by cyclic voltammetry in 0.1 M NaCl at pH 7, is no less than about +200 millivolts relative to the potential of the reference electrode.