Non-invasive measurement of blood glucose using retinal imaging

• US 20050245796A1
• Filed: 07/07/2005
• Published: 11/03/2005
• Est. Priority Date: 06/10/2003
• Status: Abandoned Application

• Current Assignee: Fovioptics Incorporated
• Original Assignee: Fovioptics Incorporated
• Inventors: Messerschmidt, Robert G., Routt, Wilson, Ou, Junli, Woods, Joe W., Smith, John L., Rice, Mark J.
• Application Number:
  US11/177,015
• Publication Number:
  US 20050245796A1
• Time in Patent Office: Days
• US Class Current: 600/315
• CPC Class Codes: A61B 3/10 Objective types, i.e. instruments for examining the eyes independent of the patients' perceptions or reactions
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/1455 using optical sensors, e.g. spectral photometrical oximeters
• CPC Class Codes: A61B 5/6821 Eye

Abstract

An apparatus carries out measurements of blood glucose in a repeatable, non-invasive manner by measurement of the rate of regeneration of retinal visual pigments, such as cone visual pigments. The rate of regeneration of visual pigments is dependent upon the blood glucose concentration, and by measuring the visual pigment regeneration rate, blood glucose concentration can be accurately determined. This apparatus exposes the retina to light of selected wavelengths in selected distributions and subsequently analyzes the reflection (as color or darkness) from a selected portion of the exposed region of the retina, preferably from the fovea.

Claims

1. A method for use in the determination of blood glucose concentration of an individual comprising:

projecting a first light into retina of an eye of the individual;

directing a second light into the retina;

detecting light reflected from the retina from the second light;

measuring a visual pigment regeneration rate in the retina using the light reflected from the retina; and

determining the blood glucose concentration using the visual pigment regeneration rate.

2. The method of claim 1, wherein the second light has a second intensity level, and wherein the second intensity level is lower than the first intensity level.

3. The method of claim 1, wherein the second light is directed into the retina over a selected period of time such that visual pigment is not significantly bleached.

4. The method of claim 1, wherein the first light contains light of a visual wavelength.

5. The method of claim 1, wherein the second light projected into the retina is in the form of pulses of light.

6. The method of claim 1, wherein the second light projected into the retina is in the form of steady-state light.

7. The method of claim 1, wherein the second light projected into the retina is in the form of a time-varying or modulated light.

8. The method of claim 1, wherein the second light has a variable intensity level.

9. The method of claim 1 wherein the first light has a first intensity level selected to bleach visual pigment in the retina of the eye.

10. The method of claim 1, wherein the step of measuring the visual pigment regeneration rate is performed with a photodetector.

11. The method of claim 1 further comprising forming an image of at least a selected area of the retina.

12. The method of claim 1, wherein the first light and second light are of different wavelengths.

13. The method of claim 1, further comprising maintaining a consistent area of measurement in the retina of the eye using retinal feature identification.

14. The method of claim 1, wherein measuring visual pigment regeneration rate comprises measuring light reflected from foveal region of the retina.

15. The method of claim 14, further comprising obtaining images of the foveal region using a photodetector array.

16. The method of claim 14, wherein measuring the light reflected from the foveal region is performed utilizing a photodiode.

17. The method of claim 16, wherein measuring the light reflected from the foveal region comprises measuring light reflected from a central area of the foveal region to account for movement of the retina and the foveal region.

18. The method of claim 1, wherein measuring the visual pigment regeneration rate is performed using cone receptors regeneration rate.

19. The method of claim 18, further comprising illuminating the retina with blue light while measuring the visual pigmentation regeneration rate.

20. The method of claim 1, further comprising using a near-infrared light source for observing retinal features while measuring the visual pigment regeneration rate.

21. The method of claim 20, wherein the near-infrared light source is directed to a region of the retina spatially distinct from the foveal region.

22. The method of claim 20, wherein the near-infrared light source uses a wavelength that does not bleach visual pigment.

23. The method of claim 1 further comprising measuring a temperature of the individual during the measurement of the visual pigmentation regeneration rate.

24. The method of claim 23, wherein measuring the temperature comprises optically measuring the eye.

25. The method of claim 23, wherein measuring the temperature of the individual is used to correct variations in the visual pigment regeneration rate.

26. The method of claim 1, further comprising projecting light through a pinhole aperture.

27. The method of claim 1, further comprising projecting light through a confocal aperture to foveal region of the retina.

28. The method of claim 27, wherein the light has a circular extent, and wherein the light comprises a single spot.

29. The method of claim 27, wherein the light comprises a plurality of spots on the retina, and wherein each spot of the plurality of spots has a different intensity level.

30. The method of claim 29, wherein the plurality of spots are deployed in a radially symmetrical pattern.

31. The method of claim 29, wherein the plurality of spots are deployed in a grid pattern.

32. The method of claim 1, wherein visual pigment regeneration rate is measured by a rate at which the light reflected from the retina decreases.

33. The method of claim 1 further comprising correcting a refractive error in the retina of the individual.

34. An apparatus for determining blood glucose concentration in an individual, the apparatus comprising:

a first light adapted to project a first light into retina of an eye of the individual;

a second light adapted to project a second light into the retina of the eye;

a light detector adapted to detect light reflected from the retina from projecting the second light; and

a processor with programmed instructions adapted to calculate the blood glucose concentration using the light reflected from the retina.

35. The apparatus of claim 34, wherein the first light has a wavelength that is absorbed by visual pigment in the retina of the eye.

36. The apparatus of claim 35, wherein the first light has an intensity level sufficient to bleach the visual pigment in the retina.

37. The apparatus of claim 34, wherein the second light has a wavelength that is absorbed by visual pigment in the retina of the eye.

38. The apparatus of claim 34, wherein the processor analyzes the light reflected from the retina to determine visual pigment regeneration rate in the retina.

39. The apparatus of claim 38, wherein the processor measures the visual pigment regeneration rate using a rate at which the light reflected from the retina decreases.

40. The apparatus of claim 38, wherein the processor calculates the blood glucose concentration using the visual pigment regeneration rate.

41. The apparatus of claim 34 further comprising a pinhole aperture through which the second light passes.

42. The apparatus of claim 34 further comprising a confocal aperture to focus the second light to foveal region of the retina.

43. The apparatus of claim 34, wherein the second light comprises a single light pulse.

44. The apparatus of claim 34, wherein the second light comprises a plurality of light pulses on the retina.

45. The apparatus of claim 44, wherein each light pulse of the plurality of pulses has a different intensity level.

46. The apparatus of claim 34 further comprising means for correction of refractive error in the eye of the individual.

47. The apparatus of claim 34, wherein the first light and the second light have different wavelengths.

48. The apparatus of claim 34, wherein the first light, the second light, the light detector, and the processor form an integrated unit configured to be worn by the individual.

49. The apparatus of claim 48, wherein the integrated unit comprises a form of glasses or goggles.

50. The apparatus of claim 48, wherein the integrated unit weighs less than ten ounces.

51. The apparatus of claim 48, wherein the integrated unit weighs less than sixteen ounces.

52. The apparatus of claim 48, wherein the integrated unit occupies a volume of less than twelve cubic inches.

53. The apparatus of claim 48, wherein the integrated unit occupies a volume of less than forty cubic inches.

54. The apparatus of claim 48, wherein the integrated unit has a form of a hand-held monocular device.

55. The apparatus of claim 48, wherein the integrated unit has a form of a hand-held binocular device.

56. The apparatus of claim 48, wherein the integrated unit comprises a form of a head-mounted apparatus.

57. A device for optical measurement of blood glucose concentration in an individual in a noninvasive manner, the device comprising:

a light projector adapted to project light into retina of the eye of an individual, the light having a wavelength that is absorbed by visual pigment in the retina of the eye;

a light detector adapted to detect light reflected from the retina of the eye; and

a processor with programmed instructions adapted to calculate the blood glucose concentration utilizing a measurement of the rate of regeneration of visual pigment in the retina.

58. The device of claim 57, wherein the light projector, the light detector, and the processor form a head mounted device.

59. The device of claim 57, wherein the light projector, the light detector, and the processor are contained within an integrated unit.

60. The device of claim 59, wherein the integrated unit weighs less than ten ounces.

61. The device of claim 59, wherein the integrated unit weighs less than sixteen ounces.

62. The device of claim 59, wherein the integrated unit occupies a volume of less is than twelve cubic inches.

63. The device of claim 59, wherein the integrated unit occupies a volume of less than forty cubic inches.

64. The device of claim 59, wherein the integrated unit has the form of a pair of glasses or goggles.

65. The device of claim 59, wherein the integrated unit having the form of a hand-held monocular device.

66. The device of claim 59, wherein the integrated unit having the form of a hand-held binocular device.

67. The device of claim 57, wherein the light projector projects steady state light.

68. The device of claim 67, wherein the processor determines the rate of regeneration of the visual pigment by measuring retinal reflectance.

69. The device of claim 57, wherein the processor determines the rate of regeneration of the visual pigments using an electroretinogram.

70. The device of claim 57, wherein the processor measures the rate of regeneration of the visual pigments using an electroencephalogram.

71. The device of claim 57, wherein the light has a visual wavelength.