Device, systems, methods and tools for continuous glucose monitoring

• US 20080154107A1
• Filed: 12/20/2006
• Published: 06/26/2008
• Est. Priority Date: 12/20/2006
• Status: Abandoned Application

• Current Assignee: ArKal Medical, Inc.
• Original Assignee: ArKal Medical, Inc.
• Inventors: Jina, Arvind N.
• Application Number:
  US11/642,196
• Publication Number:
  US 20080154107A1
• Time in Patent Office: Days
• US Class Current: 600/347
• 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 5/14865 invasive, e.g. introduced into the body by a catheter or needle or using implanted sensors

Abstract

The present invention includes methods and apparatus for continuous glucose monitoring of a patient. In one aspect a glucose monitor includes a plurality of substantially cylindrical tissue piercing elements adapted to pierce the stratum corneum and enter the epidermis, allowing for the diffusion of glucose from the interstitial fluid into the glucose monitors described herein. In another aspect of the invention, a glucose monitor includes a deformed substrate layer defining a plurality of tissue piercing elements.

Claims

1. A glucose monitor, comprising:

at least one substantially cylindrical tissue piercing element having a distal opening, proximal opening, and an interior lumen extending between the distal and proximal openings;

a sensing area in fluid communication with the proximal opening of the at least one substantially cylindrical tissue piercing element;

sensing fluid extending from the sensing area into substantially the entire interior lumen of the at least one substantially cylindrical tissue piercing element; and

a glucose sensor adapted to detect glucose in the sensing fluid within the sensing area.

2. The glucose monitor of claim 1 further comprising a substrate coupled to and supporting the at least one substantially cylindrical tissue piercing element.

3. The glucose monitor of claim 2 wherein the substrate comprises a lumen in fluid communication with the proximal opening of the tissue piercing element and the sensing area.

4. The glucose monitor of claim 1 wherein the at least one tissue piercing element is made of a metal or alloy.

5. The glucose monitor of claim 4 wherein the metal or alloy is a stainless steel.

7. The glucose monitor of claim 1 wherein the at least one substantially cylindrical tissue piercing element is configured to pierce only as deep as into the epidermis.

8. The glucose monitor of claim 1 further comprising a sensing fluid reservoir in fluid communication with the sensing area, wherein the sensing fluid reservoir is adapted to house a reservoir of sensing fluid with a known glucose concentration.

9. The glucose monitor of claim 8 further comprising an actuator configured to move fresh sensing fluid from the at least one sensing fluid reservoir into the sensing area.

10. The glucose monitor of claim 9 further comprising a waste reservoir in fluidic communication with the sensing area adapted to receive sensing fluid from the sensing area when the fresh sensing fluid is moved into the sensing area.

11. The glucose monitor of claim 9 wherein the actuator comprises a pump and/or a valve.

12. The glucose monitor of claim 9 wherein the actuator is configured to be manually actuated.

13. The glucose monitor of claim 9 wherein the actuator is configured to be automatically actuated.

14. The glucose monitor of claim 13 wherein the monitor further comprises a programmable component in communication with the actuator wherein the programmable component is programmed to automatically actuate the actuator.

15. The glucose monitor of claim 14 wherein the programmable component is configured to be programmed using a device that is not housed with the sensor.

16. The glucose monitor of claim 8 wherein the known glucose concentration is between about 0 mg/dl and about 400 mg/dl.

17. The glucose monitor of claim 8 wherein the sensing fluid reservoir is a first sensing fluid reservoir adapted to house a first sensing fluid with a first known glucose concentration, the glucose monitor further comprising a second sensing fluid reservoir adapted to house a second sensing fluid with a second known glucose concentration, wherein the first and second known glucose concentrations are not the same.

18. The glucose monitor of claim 17 wherein the first known glucose concentration is between about 0 mg/dl and about 100 mg/dl and the second known glucose concentration is between about 100 mg/dl and about 400 mg/dl.

19. The glucose monitor of claim 8 further comprising a housing comprising a first part and a second part, the first part of the housing being adapted to support the at least one substantially cylindrical tissue piercing elements, the sensing fluid reservoir, the sensing area, and at least part of the glucose sensor, the second part of the housing comprising an electrical connection to the at least part of the glucose sensor in the first part of the housing, the housing further comprising a connector adapted to connect and disconnect the first part of the housing from the second part of the housing.

20. The glucose monitor of claim 1 further comprising a removable cover extending over the distal opening of the at least one substantially cylindrical tissue piercing element.

21. The glucose monitor of claim 1 further comprising a display adapted to display a glucose concentration sensed by the sensor.

22. The glucose monitor of claim 21 wherein the sensor is housed in a first housing and the display is housed in a second housing separate from the first housing, wherein the first housing comprises a transmitter to wirelessly transmit information indicative of the glucose concentration sensed by the sensor to a receiver in the second housing.

23. The glucose monitor of claim 22 wherein the second housing is adapted to determine the glucose concentration in the blood of the subject based on the information indicative of the glucose concentration sensed by the sensor.

24. The glucose monitor of claim 1 further comprising an adhesive element adapted to attach the glucose monitor to the skin of a subject.

25. The glucose monitor of claim 1 wherein the glucose monitor is further adapted to detect a concentration of glucose in the sensing fluid with the sensing area without extracting interstitial fluid through the distal opening into the interior lumen.

26. The glucose monitor of claim 1 further comprising a body temperature sensor adapted to sense the body temperature of the subject.

27. The glucose monitor of claim 1 further comprising a vibration assembly adapted to vibrate at least part of the glucose monitor such that the at least one tissue piercing element penetrates the stratum corneum.

6. The glucose monitor of clam 1 wherein the at least one substantially cylindrical tissue piercing element is tapered near its distal opening.

28. A method of in vivo monitoring of an individual'"'"'s interstitial fluid glucose concentration comprising:

inserting a distal end of at least one substantially cylindrical tissue piercing element through a stratum corneum area of the individual'"'"'s skin, the at least one tissue piercing element comprising a distal opening, a proximal opening, an interior lumen extending between the distal and proximal openings, and a sensing fluid filling substantially the entire interior lumen; and

sensing a glucose concentration of the sensing fluid.

29. The method of claim 28 wherein a glucose sensor senses the glucose concentration, the method further comprising calibrating the glucose sensor prior to the sensing step.

30. The method of claim 29 wherein the glucose sensor is in fluid communication with a sensing area which is in fluid communication with the interior lumen of the at least one tissue piercing element.

31. The method of claim 29 wherein the sensing fluid has a known glucose concentration, and calibrating the glucose sensor comprises determining an output from the glucose sensor based on the known glucose concentration.

32. The method of claim 31 wherein calibrating the glucose sensor further comprises moving fresh sensing fluid with the known glucose concentration into the sensing area and determining the output from the glucose sensor based on the known glucose concentration of the fresh sensing fluid.

33. The method of claim 32 wherein the calibrating further comprises moving the sensing fluid from the sensing area as the fresh sensing fluid is moved into the sensing area.

34. The method of claim 32 wherein calibrating comprises actuating an actuator which moves the fresh sensing fluid into the sensing area.

35. The method of claim 34 wherein actuating comprises manually actuating the actuator.

36. The method of claim 34 wherein actuating comprises automatically actuating the actuator.

37. The method of claim 36 wherein the actuator is adapted to be programmed to be automatically actuated.

38. The method of claim 28 further comprising adhering the monitor to the subject'"'"'s skin with adhesive.

39. The method of claim 30 further comprising permitting glucose to diffuse from interstitial fluid of the subject into the sensing area without extracting interstitial fluid through the distal opening in the interior lumen.

40. The method of claim 28 further comprising sensing the subject'"'"'s body temperature.

41. The method of claim 28 further comprising determining a glucose concentration of the interstitial fluid of the subject wherein the determined glucose concentration is based on the sensed glucose concentration.

42. The method of claim 41 wherein an output from the sensor indicative of the sensed concentration is transmitted to an external device separate from the sensor, and the external device determines the glucose concentration of the interstitial fluid based on the output from the sensor.

43. The method of claim 42 further comprising displaying the determined glucose concentration of the interstitial fluid.

44. The method of claim 42 wherein the external device determines the concentration of glucose in the patient'"'"'s blood based on the glucose concentration of the interstitial fluid.

45. A glucose monitor, comprising:

a deformed substrate layer defining a plurality of tissue piercing elements each having a distal opening, a proximal opening and a lumen extending between the distal and proximal openings;

a sensing area in fluid communication with the proximal openings of the plurality of metal tissue piercing elements;

sensing fluid extending from the sensing area into substantially the entire interior space of the plurality of tissue piercing elements; and

a glucose sensor adapted to detect glucose in the sensing fluid within the sensing area.

46. The monitor of claim 45 wherein the deformed substrate layer is made of metal or an alloy.

47. The monitor of claim 46 wherein the deformed substrate layer is an alloy and is a stainless steel.

48. The monitor of claim 45 wherein the deformed substrate layer has been deformed by an external actuator.

49. The monitor of claim 48 wherein the external actuator comprises a plate having a plurality of pins extending therefrom, wherein the pins are adapted to pass through the substrate layer thereby deforming the substrate layer and creating the tissue piercing elements, the distal and proximal openings, and the lumens.

50. The monitor of claim 45 wherein the plurality of tissue piercing elements have a substantial volcano shape.

51. The monitor of claim 45 wherein at least one of the plurality of tissue piercing elements has a distal opening with a smaller radius than the radius of the proximal opening.

52. The monitor of claim 45 wherein the distal end of the plurality of tissue piercing elements comprise a plurality of protrusions.

53. The monitor of claim 45 wherein the plurality of tissue piercing element are configured to pierce only as deep as into the epidermis.

54. The monitor of claim 45 further comprising a sensing fluid reservoir in fluid communication with the sensing area, wherein the sensing fluid reservoir is adapted to house a reservoir of sensing fluid with a known glucose concentration.

55. The monitor of claim 54 further comprising an actuator configured to move fresh sensing fluid from the at least one sensing fluid reservoir into the sensing area.

56. The monitor of claim 55 further comprising a waste reservoir in fluidic communication with the sensing area adapted to receive sensing fluid from the sensing area when the fresh sensing fluid is moved into the sensing area.

57. The monitor of claim 55 wherein the actuator comprises a pump and/or a valve.

58. The monitor of claim 55 wherein the actuator is configured to be manually actuated.

59. The monitor of claim 55 wherein the actuator is configured to be automatically actuated.

60. The monitor of claim 54 wherein the known glucose concentration is between about 0 mg/dl and about 400 mg/dl.

61. The monitor of claim 54 wherein the sensing fluid reservoir is a first sensing fluid reservoir adapted to house a first sensing fluid with a first known glucose concentration, the glucose monitor further comprising a second sensing fluid reservoir adapted to house a second sensing fluid with a second known glucose concentration, wherein the first and second known glucose concentrations are not the same.

62. The monitor of claim 61 wherein the first known glucose concentration is between about 0 mg/dl and about 100 mg/dl and the second known glucose concentration is between about 100 mg/dl and about 400 mg/dl.

63. The glucose monitor of claim 55 further comprising a housing comprising a first part and a second part, the first part of the housing being adapted to support the at least one substantially cylindrical tissue piercing elements, the sensing fluid reservoir, the sensing area, and at least part of the glucose sensor, the second part of the housing comprising an electrical connection to the at least part of the glucose sensor in the first part of the housing, the housing further comprising a connector adapted to connect and disconnect the first part of the housing from the second part of the housing.

64. The monitor of claim 45 further comprising a removable cover extending over the distal opening of the at least one substantially cylindrical tissue piercing element.

65. The monitor of claim 45 further comprising a display adapted to display a glucose concentration sensed by the sensor.

66. The monitor of claim 65 wherein the sensor is housed in a first housing and the display is housed in a second housing, wherein the first housing comprises a transmitter to wirelessly transmit information indicative of the glucose concentration sensed by the sensor to a receiver housed in the second housing.

67. The monitor of claim 66 wherein the second housing is adapted to determine the glucose concentration in the blood of the subject based on the information indicative of the glucose concentration sensed by the sensor.

68. The monitor of claim 45 further comprising an adhesive element adapted to attach the glucose monitor to the skin of a subject.

69. The monitor of claim 45 wherein the glucose monitor is further adapted to detect a concentration of glucose in the sensing fluid with the sensing area without extracting interstitial fluid through the distal opening into the interior lumen.

70. The monitor of claim 45 further comprising a body temperature sensor adapted to sense the body temperature of the subject.

71. The monitor of claim 45 further comprising a vibration assembly adapted to vibrate at least part of the glucose monitor to allow the at least one tissue piercing element to penetrate the stratum corneum.

72. A method of in vivo monitoring of a patient'"'"'s interstitial fluid glucose concentration comprising:

inserting distal ends of a plurality of tissue piercing elements defined by a deformed substrate layer through a stratum corneum area of a patient'"'"'s skin, the at least one tissue piercing element comprising a distal opening, a proximal opening,

an interior lumen extending between the distal and proximal openings, and a sensing fluid filling substantially the entire interior lumen; and

sensing a glucose concentration of the sensing fluid.

73. The method of claim 72 wherein a glucose sensor senses the glucose concentration, the method further comprising calibrating the glucose sensor prior to the sensing step.

74. The method of claim 73 wherein the glucose sensor is in fluid communication with a sensing area which is in fluid communication with the interior lumen of the plurality of tissue piercing elements.

75. The method of claim 73 wherein the sensing fluid has a known glucose concentration, and calibrating the glucose sensor comprises determining an output from the glucose sensor based on the known glucose concentration.

76. The method of claim 75 wherein calibrating the glucose sensor further comprises moving fresh sensing fluid with the known glucose concentration into the sensing area and determining the output from the glucose sensor based on the known glucose concentration of the fresh sensing fluid.

77. The method of claim 76 wherein the calibrating further comprises moving the sensing fluid from the sensing area as the fresh sensing fluid is moved into the sensing area.

78. The method of claim 76 wherein calibrating comprises actuating an actuator which moves the fresh sensing fluid into the sensing area.

79. The method of claim 78 wherein actuating comprises manually actuating the actuator.

80. The method of claim 78 wherein actuating comprises automatically actuating the actuator.

81. The method of claim 80 wherein the actuator is adapted to be programmed to be automatically actuated.

83. The method of claim 74 further comprising permitting glucose to diffuse from interstitial fluid of the patient into the sensing area without extracting interstitial fluid through the distal opening in the interior lumen.

84. The method of claim 72 further comprising sensing the subject'"'"'s body temperature.

85. The method of claim 72 further comprising determining a glucose concentration of the interstitial fluid of the subject wherein the determined glucose concentration is based on the sensed glucose concentration.

86. The method of claim 85 wherein an output from the sensor indicative of the sensed concentration is transmitted to an external device separate from the sensor, and the external device determines the glucose concentration of the interstitial fluid based on the output from the sensor.

87. The method of claim 86 further comprising displaying the determined glucose concentration of the interstitial fluid.

88. The method of claim 86 wherein the external device determines the concentration of glucose in the patient'"'"'s blood based on the glucose concentration of the interstitial fluid.

82. The method of claim further comprising adhering the monitor to the subject'"'"'s skin with adhesive.