Electrode materials, systems and methods for the electrochemical detection of nitric oxide

• US 6,280,604 B1
• Filed: 03/10/2000
• Issued: 08/28/2001
• Est. Priority Date: 03/10/2000
• Status: Expired due to Fees

• Current Assignee: Duke University
• Original Assignee: Duke University
• Inventors: Allen, Barry W., Coury, Louis A., Piantadosi, Claude A.
• Primary Examiner(s): Bell, Bruce F.
• Application Number:
  US09/523,645
• Time in Patent Office: 536 Days
• Field of Search: 205/777.5, 205/778, 205/781, 205/792, 205/793, 204/403, 204/415, 204/291, 600/309, 600/345, 600/353
• US Class Current: 205/777.5
• CPC Class Codes: G01N 27/4045 for gases other than oxygen

Abstract

Nitric oxide-specific electrodes are useful for in situ detection of nitric oxide in biomedical applications and have at least a surface region capable of forming complexes with nitric oxide. The nitric oxide complexes formed at the surface of the electrodes apparently increase the concentration of nitric oxide available for detection, leading to significantly improved relative responses as compared to other known nitric oxide electrode materials. The electrode has at least an exterior surface region which contains ruthenium and/or at least one oxide of ruthenium. The electrodes are pre-conditioned at a potential, or potentials, different than the working potential of the electrode, followed by further conditioning at the working potential. Direct response to nitric oxide has been observed for ruthenium electrodes at or below potentials about +675 mV vs. Ag/AgCl, while ruthenium electrodes paradoxical response to nitric oxide has been observed at potentials above +675 mV vs. Ag/Cl.

Claims

1. An electrode for detecting nitric-oxide having a surface region formed of a material which, at an electrochemical working potential thereof, complexes with nitric oxide when exposed to a nitric oxide-containing fluid, and which exhibits maximal nitric oxide response after being held, prior to nitric oxide exposure, at a pre-conditioning potential different from the working potential thereof, followed by subsequent conditioning at the working potential thereof.

2. The electrode of claim 1, wherein the material is at least one selected from the group consisting of metals, metaloids, electrically-conducting or electrically semiconducting oxides, and mixtures thereof.

3. The electrode of claim 1, wherein the electrode does not exhibit a maximal response to nitric oxide after being conditioned at its working potential, but does exhibit a maximal response to nitric oxide after being conditioned at both said pre-conditioning potential and said working potential.

4. The electrode of claim 1, wherein the pre-conditioning potential is greater than the working potential thereof.

5. The electrode of claim 1, wherein the pre-conditioning potential is less than the working potential thereof.

6. The electrode of claim 1, wherein the pre-conditioning potential is alternately changed between a first potential which is less than the working potential thereof, and a second potential which is greater than the working potential thereof.

7. The electrode subjected to a preconditioning potential according to one or more preconditioning profiles as in any one of claims 4-6.

8. A method for the in vivo detection of nitric oxide comprising placing an electrode according to any one of claims 1-6 at a site within a patient or other living organism, and then determining the nitric oxide present at said site by the electrochemical response of said electrode.

9. The method of claims 8, wherein said step of determining the nitric oxide present at said site includes subjecting the electrode to a predetermined fixed potential which causes said electrode to electrochemically respond directly to the presence of nitric oxide at said site.

10. The method of claim 9, wherein said predetermined fixed potential is less than about +675 mV vs. Ag/AgCl.

11. The method of claim 8, wherein said step of determining the nitric oxide present in said sample includes subjecting the electrode to a predetermined fixed potential which causes said electrode to electrochemically respond indirectly to the presence of nitric oxide at said site.

12. The method of claim 11, wherein said predetermined fixed potential is greater than about +675 mV vs. Ag/AgCl.

13. The method of claim 8, wherein said step of determining the presence of nitric oxide at said site includes subjecting the electrode to a fixed potential sufficient to suppress oxidative background current.

14. The method of claim 13, wherein said background current is suppressed by allowing a film consisting essentially of nitrosyl complexes or any structural isomers thereof to form on said electrode surface.

15. A method of detecting nitric oxide in a biological sample comprising bringing an electrode according to any one of claims 1-6 into contact with the biological sample, and then determining the nitric oxide present in said sample by the electrochemical response of said electrode.

16. The method of claim 15, wherein said step of determining the nitric oxide present in said sample includes subjecting the electrode to a predetermined fixed potential which causes said electrode to electrochemically respond directly to the presence of nitric oxide in said sample.

17. The method of claim 16, wherein said predetermined fixed potential is less than about +675 mV vs. Ag/AgCl.

18. The method of claim 15, wherein said step of determining the nitric oxide present in said sample includes subjecting the electrode to a predetermined fixed potential which causes said electrode to electrochemically respond indirectly to the presence of nitric oxide in said sample.

19. The method of claim 18, wherein said predetermined fixed potential is greater than about +675 mV vs. Ag/AgCl.

20. The method of claim 15, wherein said step of determining the presence of nitric oxide at said site includes subjecting the electrode to a fixed potential sufficient to suppress oxidative background current.

21. The method of claim 20, wherein said background current is suppressed by allowing a film consisting essentially of nitrosyl complexes (or any structural isomers thereof) to form on said electrode surface.

22. The electrode of claim 1, wherein said complex is a nitrosyl complex or any structural isomer thereof.

23. The electrode of claim 1, wherein at least the surface region consists essentially of ruthenium and/or at least one oxide of ruthenium.

24. The electrode of claim 1, wherein at least the surface region includes at least one oxide of ruthenium having the formula RuO_x, where x is a number greater than 0.

25. The electrode of claim 24, wherein x is a number greater than 0 up to and including about 2.

26. The electrode of claim 1, wherein the electrode response to nitric oxide is enhanced by the presence of a chloride-containing species on said electrode surface region thereof.

27. The electrode of claim 1, wherein the electrode response to nitric oxide is enhanced by the formation on the electrode surface region of an electrically-conductive oxide.

28. The electrode of claim 1, wherein the elctrode is comprised of ruthenium and/or at least one oxide of ruthenium.

29. An electrode for the detection of nitric oxide in a biological sample having a surface region formed of a material which, at an electrochemical working potential thereof, complexes with nitric oxide when exposed to a nitric oxide-containing fluid, and which exhibits maximal nitric oxide response after being held, prior to nitric oxide exposure, at a pre-conditioning potential different from the working potential thereof, followed by subsequent conditioning at the working potential thereof.

30. The electrode of claim 29, wherein the material is at least one selected from the group consisting of metals, metaloids, electrically-conducting or electrically semiconducting oxides, and mixtures thereof.

31. The electrode of claim 29, wherein the electrode does not exhibit a maximal response to nitric oxide after being conditioned at its working potential, but does exhibit a maximal response to nitric oxide after being held at both said pre-conditioning potential and said working potential.

32. The electrode of claim 29, wherein the pre-conditioning potential is greater than the working potential thereof.

33. The electrode of claim 29, wherein the pre-conditioning potential is less than the working potential thereof.

34. The electrode of claim 29, wherein the pre-conditioning potential is alternately changed between a first potential which is less than the working potential thereof, and a second potential which is greater than the working potential thereof.

35. The electrode subjected to a preconditioning potential according to one or more preconditioning profiles as in any one of claims 32-34.

36. The electrode of claim 29, wherein said complex is a nitrosyl complex or any structural isomer thereof.

37. The electrode of claim 29, wherein at least the surface region consists essentially of ruthenium and/or at least one oxide of ruthenium.

38. The electrode of claim 37, wherein at least the surface region includes at least one oxide of ruthenium having the formula RuO_x, where x is a number greater than 0.

39. The electrode of claim 38, wherein x is a number greater than 0 up to and including about 2.

40. The electrode of claim 29, wherein the electrode is comprised of ruthenium and/or at least one oxide of ruthenium.

41. A method of making an electrode for the detection of nitric oxide having a surface region formed of a material which, at an electrochemical working potential thereof, complexes with nitric oxide when exposed to a nitric oxide-containing fluid, which method comprises conditioning at least the surface region of the electrode by (i) subjecting the surface region to one or more pre-conditioning potential(s) different from the working potential, and then subsequently (ii) subjecting the surface region to conditioning at the working potential.

42. The method of claim 41, wherein the material is at least one selected from the group consisting of metals, metaloids, electrically-conducting or electrically semiconducting oxides, and mixtures thereof.

43. The method of claim 41, wherein the pre-conditioning potential is greater than the working potential thereof.

44. The method of claim 41, wherein the pre-conditioning potential is less than the working potential thereof.

45. The method of claim 41, wherein the pre-conditioning potential is alternately changed between a first potential which is less than the working potential thereof, and a second potential which is greater than the working potential thereof.

46. A method of making an electrode which comprises subjecting the electrode to a preconditioning potential according to one or more preconditioning profiles as in any one of claims 43-45.

47. An electrode for the detection of nitric oxide made according to any one of claims 41-45.

48. A nitric oxide detector system comprising an electrode having a surface region formed of a material which complexes with nitric oxide when exposed to a nitric oxide-containing fluid, a mechanical support for the electrode, and electrical conductors to electrically connect the electrode to an electrochemical instrument.

49. The system of claim 48, wherein the material is at least one selected from the group consisting of metals, metaloids, electrically-conducting or electrically semiconducting oxides, and mixtures thereof.

50. The system of claim 48 or 49, comprising plural electrodes, at least one of which has a surface region formed of said material which complexes with nitric oxide when exposed to a nitric oxide-containing fluid.

51. The system of claim 50, wherein said mechanical support includes a support tube sleeved over said plural electrodes.

52. The system of claim 51, further comprising a temperature probe adjacent to said plural electrodes.

53. The system of claim 50, further comprising a catheter adjacent to said plural electrodes.

54. The system of claim 50 wherein said support tube is sleeved over said plural electrodes, said temperature probe and said catheter.

57. The system of claim 48 or 55, wherein said at least one electrode has a surface region formed of said material which, at an electrochemical working potential thereof, complexes with nitric oxide when exposed to a nitric oxide-containing fluid, and which exhibits maximal nitric oxide response after being held, prior to nitric oxide exposure, at a pre-conditioning potential different from the working potential thereof, followed by subsequent conditioning at the working potential thereof.

58. The system of claim 57, wherein the electrode does not exhibit a maximal response to nitric oxide after being conditioned at its working potential, but does exhibit a maximal response to nitric oxide after being conditioned at both said pre-conditioning potential and said working potential.

59. The system of claim 57, wherein the pre-conditioning potential is greater than the working potential thereof.

60. The system of claim 57, wherein the pre-conditioning potential is less than the working potential thereof.

61. The system of claim 57, wherein the pre-conditioning potential is alternately changed between a first potential which is less than the working potential thereof, and a second potential which is greater than the working potential thereof.

55. A nitric oxide detector system comprising a probe assembly which includes a plurality of individual electrodes, at least one of which is formed of a material which complexes with nitric oxide in response to contact with a nitric oxide-containing fluid and generates a signal in response thereto, an electrochemical instrument which receives said signal and outputs a signal indicative of nitric oxide presence in said fluid, and instrument cabling which operatively connects the individual electrodes to said electrochemical instrument.

56. The system of claim 55, wherein the material is at least one selected from the group consisting of metals, metaloids, electrically-conducting or electrically semiconducting oxides, and mixtures thereof.

62. A method of detecting a pathological condition which produces or suppresses nitric oxide comprising bringing an electrode which complexes with nitric oxide into nitric oxide detecting proximity of a biological sample, measuring nitric oxide present in the sample, whereby a pathological condition which produces or suppresses nitric oxide can be determined.

63. The method of claim 62, wherein said electrode has a surface region formed of a material which, at an electrochemical working potential thereof, complexes with nitric oxide when exposed to a nitric oxide-containing fluid, and which exhibits maximal nitric oxide response after being held, prior to nitric oxide exposure, at a pre-conditioning potential different from the working potential thereof, followed by subsequent conditioning at the working potential thereof.

64. The method of claim 62 or 63, wherein the material is at least one selected from the group consisting of metals, metaloids, electrically-conducting or electrically semiconducting oxides, and mixtures thereof.

65. The method of claim 64, wherein the electrode does not exhibit a maximal response to nitric oxide after being conditioned at its working potential, but does exhibit a maximal response to nitric oxide after being conditioned at both said pre-conditioning potential and said working potential.

66. The method of claim 62 or 63, wherein the pre-conditioning potential is greater than the working potential thereof.

67. The method of claim 62 or 63, wherein the pre-conditioning potential is less than the working potential thereof.

68. The method of claim 62 or 63, wherein the pre-conditioning potential is alternately changed between a first potential which is less than the working potential thereof, and a second potential which is greater than the working potential thereof.