Interstitial fluid analyzer

• US 20060058602A1
• Filed: 08/17/2004
• Published: 03/16/2006
• Est. Priority Date: 08/17/2004
• Status: Abandoned Application

• Current Assignee: Lynntech Incorporated
• Original Assignee: Lynntech Incorporated
• Inventors: Kwiatkowski, Krzysztof C., Magnuson, James W.
• Application Number:
  US10/920,036
• Publication Number:
  US 20060058602A1
• Time in Patent Office: Days
• US Class Current: 600/407
• CPC Class Codes: A61B 5/14514 using means for aiding extraction of interstitial fluid, e.g. microneedles or suction
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/14546 for measuring analytes not otherwise provided for, e.g. ions, cytochromes
• CPC Class Codes: A61B 5/1486 using enzyme electrodes, e.g. with immobilised oxidase
• CPC Class Codes: A61N 1/303 Constructional details electrodes for external use A61N1/0428

Abstract

A device useful for measuring an analyte in the interstitial fluid of an animal comprising an array chamber having an array of one or more microprojections and a detection compartment comprising a sensor in selective fluid communication with the array chamber. Also included are two extraction electrodes for inducing electrotransport of the interstitial fluid from the animal into the array chamber. A method includes the steps of forming a plurality of microchannels through a stratum corneum layer of an epidermis of the animal, inducing electrotransport of interstitial fluid containing the analyte through the microchannels and mixing one or more materials with the interstitial fluid to form a mixture, contacting the mixture with detection electrodes and analyzing the mixture with the detection electrodes.

Claims

1. An apparatus for measuring an analyte in interstitial fluid of an animal, comprising:

an array chamber comprising an array of one or more microprojections;

a detection compartment comprising a sensor in selective fluid communication with the array chamber;

two extraction electrodes for inducing electrotransport of the interstitial fluid from the animal to the array chamber; and

an electronic control module.

2. The apparatus of claim 1, further comprising:

means for the array to transiently perforate an epidermis of the animal.

3. The apparatus of claim 2, wherein the means for the array to transiently perforate the epidermis comprises a piezoelectric stack attached to the array.

4. The apparatus of claim 2, wherein the means for the array to transiently perforate the epidermis comprises a spring and an electromagnet attached to the array, wherein the spring pushes the array to perforate the epidermis and the electromagnet pulls the array from the epidermis.

5. The apparatus of claim 2, wherein the means for the array to transiently perforate the epidermis comprises a spring and an electromagnet attached to the array, wherein the electromagnet pushes the array to perforate the epidermis and the spring pulls the array from the epidermis.

6. The apparatus of claim 2, wherein the means for the array to transiently perforate the epidermis are adapted to provide perforation of the epidermis to a depth of between about 50 μ

m and about 150 μ

m.

7. The apparatus of claim 1, wherein the tip of the microprojections have a diameter of between about 0.5 μ

m and about 5 μ

m.

8. The apparatus of claim 1, wherein the tip of the microprojections have a diameter of between about 1 μ

m and about 2 μ

m.

9. The apparatus of claim 1, wherein the microprojections are adapted to transiently perforate the epidermis to a depth greater than the thickness of a stratum corneum layer of the epidermis but less than a total thickness of the epidermis.

10. The apparatus of claim 1, wherein the microprojections are made of materials selected from tungsten, platinum, silicon, gold or silver.

11. The apparatus of claim 1, wherein the microprojections are made of etched tungsten wire plated with platinum.

12. The apparatus of claim 1, wherein the microprojections are made of etched silicon block plated with platinum.

13. The apparatus of claim 1, wherein each of the arrays have a density of microprojections between about 3 microprojections per square centimeter and about 1000 microprojections per square centimeter.

14. The apparatus of claim 1, wherein each of the arrays have a density of microprojections between about 50 microprojections per square centimeter and about 500 microprojections per square centimeter.

15. The apparatus of claim 1, further comprising:

a salt bridge for providing electrical resistance between one of the extraction electrodes and the array chamber.

16. The apparatus of claim 15, wherein the salt bridge comprises agarose gel.

17. The apparatus of claim 1, further comprising:

a power source for applying a potential across the extraction electrodes.

18. The apparatus of claim 17, wherein the power source is a battery.

19. The apparatus of claim 17, wherein the power source provides a pulsed current to the extraction electrodes.

20. The apparatus of claim 19, wherein the pulsed current is selected from a sine wave, a triangle wave or combinations thereof.

21. The apparatus of claim 19, wherein the pulsed current is an exponential decay.

22. The apparatus of claim 1, wherein a first of the two extraction electrodes is made of platinum.

23. The apparatus of claim 1, wherein a second of the two extraction electrodes is made of a material selected from gold, platinum, silver, palladium, graphite, or glassy carbon.

24. The apparatus of claim 1, wherein the first, extraction electrode is in electrical communication with the array chamber.

25. The apparatus of claim 24, wherein the two extraction electrodes provide an electric potential across a sampling site of the animal.

26. The apparatus of claim 1, wherein the sensor comprises a working electrode, a reference electrode and a counter electrode that are each in electrical communication with the electronic control module.

27. The apparatus of claim 26, wherein the counter electrode is platinum.

28. The apparatus of claim 26, wherein the counter electrode is selected from gold, graphite or glassy carbon.

29. The apparatus of claim 26, wherein the working electrode is platinum.

30. The apparatus of claim 26, wherein the working electrode is selected from gold, graphite or glassy carbon.

31. The apparatus of claim 26, wherein the reference electrode is an Ag/AgCl electrode.

32. The apparatus of claim 1, wherein the electronic control module comprises a potentiostat.

33. The apparatus of claim 1, further comprising:

one or more reservoirs in selective fluid communication with the array chamber and the detection compartment.

34. The apparatus of claim 1, further comprising:

one or more micropumps for pumping a contents of the one or more reservoirs to the array chamber, the detection compartment, or combinations thereof.

35. The apparatus of claim 34, wherein the one or more micropumps are started and stopped by control signals generated by the electronic control module.

36. The apparatus of claim 1, further comprising one or more waste reservoirs in selective fluid communication with the array chamber, the detection compartment, or combinations thereof.

37. The apparatus of claim 1, further comprising a switch to selectively alternate the current between the two extraction electrodes, wherein each extraction electrode selectively operates as a cathode or an anode.

38. The apparatus of claim 1, further comprising:

two or more array chambers, each array chamber comprising an array having one or more microprojections and each of the array chambers in electrical communication with either the first or the second of the two extraction electrodes.

39. The apparatus of claim 38, further comprising:

two or more detection compartments, each comprising a sensor in selective communication with one or more of the array chambers.

40. A method for measuring an analyte in interstitial fluid of an animal, comprising forming a plurality of microchannels through a stratum corneum layer of an epidermis of the animal;

inducing electrotransport of interstitial fluid containing the analyte through the microchannels;

mixing one or more materials with the interstitial fluid to form a mixture;

contacting the mixture with detection electrodes; and

conducting amperometric analysis on the mixture with the detection electrodes.

41. The method of claim 40, wherein the step of inducing electrotransport of interstitial fluid causes electroosmosis.

42. The method of claim 40, wherein the step of inducing electrotransport of interstitial fluid causes reverse iontophoresis.

43. The method of claim 40, wherein the step of forming a plurality of microchannels comprises:

transiently perforating the stratum corneum with microprojections.

44. The method of claim 43, wherein the microprojections are arranged in two arrays, wherein each array has one or more microprojections.

45. The method of claim 40, wherein the microchannels are formed to a depth less than a thickness of the epidermis.

46. The method of claim 40, wherein the microchannels are formed with a diameter less than about 5 μ

m.

47. The method of claim 40, wherein the microchannels are formed with a diameter less than about 1 μ

m.

48. The method of claim 40, further comprising:

separating a cathode electrode and an anode electrode from the epidermis of the animal with salt bridges, wherein the cathode electrode and the anode electrode are used in the step of electrokinetically inducing a flow of interstitial fluid; and

reversing polarity of the cathode electrode and the anode electrode after a performance of the step of conducting amperometric analysis.

49. The method of claim 40, wherein the step of inducing electrotransport of interstitial fluid comprises:

inducing a voltage potential across the plurality of microchannels.

50. The method of claim 40, wherein the analyte is glucose, the one or more materials comprises glucose oxidase and (dimethylaminomethyl)ferrocene.

51. The method of claim 50, wherein the one or more materials further comprises phosphate buffer.

52. The method of claim 50, wherein the step of conducting amperometric analysis comprises:

measuring the oxidation peak of (dimethylaminomethyl)ferrocene to determine glucose concentration in the interstitial fluid.

53. The method of claim 40, wherein the analyte is albumin.

54. The method of claim 40, wherein the analyte is cholesterol.

55. The method of claim 40, wherein the analyte is urea.

56. The method of claim 40, wherein the analyte is tumor metabolite.

57. The method of claim 40, wherein the analyte is an unbound cancer drug.