Non-invasive measurement of blood glucose using retinal imaging

• US 20050267343A1
• Filed: 07/07/2005
• Published: 12/01/2005
• 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:
  US11/176,986
• Publication Number:
  US 20050267343A1
• Time in Patent Office: Days
• US Class Current: 600/316
• 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 determining blood glucose concentration in an individual, the method comprising:

projecting time-varying light into retina of an eye of an individual; and

analyzing light reflected from the retina of the eye to determine the blood glucose concentration.

2. The method of claim 1, wherein analyzing the light reflected from the retina comprises calculating a rate related to the light reflected from the retina.

3. The method of claim 2, wherein the rate is a rate of bleaching of the retina.

4. The method of claim 2, wherein the rate is a rate of regeneration of visual pigment in the retina.

5. The method of claim 2, wherein the time-varying light consists of modulated light.

6. The method of claim 2, wherein the rate is determined by phase angles of reflected light relative to the time-varying light.

7. The method of claim 6, wherein the rate is determined by a change in reflectance from the retina during a single period of the modulated light.

8. The method of claim 6, wherein the rate is determined by a change in reflectance from the retina between multiple periods of the modulated light.

9. The method of claim 2, wherein the rate is determined by measuring retinal reflectance under a steady state light illumination level.

10. The method of claim 2, wherein the rate is determined by measuring retinal reflectance under at least two different steady-state light illumination levels.

11. The method of claim 2, wherein the rate is determined by measuring a steady state of retinal reflectance that corresponds to a glucose level.

12. The method of claim 2, wherein the rate is determined by a change in reflectance of the retina during a single pulse of light.

13. The method of claim 2, wherein the rate is determined by a change in reflectance of the retina during multiple pulses of light.

14. The method of claim 2, wherein the rate is determined by a change in reflectance of the retina between multiple pulses of light.

15. The method of claim 1, wherein the time-varying light consists of pulses of light.

16. The method of claim 15, wherein the pulses of light have varying amplitudes.

17. The method of claim 16, wherein the amplitudes of the pulses of light are adjusted to provide a constant level of reflectance of the retina.

18. The method of claim 15, wherein the pulses of light have constant amplitudes.

19. The method of claim 1, wherein the time-varying light has a wavelength that is absorbed by visual pigment in the retina of the eye.

20. The method of claim 1, wherein the time-varying light consists of a single pulse of light.

21. The method of claim 1, wherein the time-varying light consists of light modulated at a high frequency and light modulated at a low frequency.

22. The method of claim 21, wherein the rate is determined by a change in amplitude of the light modulated at the low frequency.

23. The method of claim 21, wherein the rate is determined by a change in amplitude of the light modulated at the high frequency.

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

25. The method of claim 1, further comprising projecting light through a confocal aperture.

26. A method for determining blood glucose level of an individual comprising:

illuminating retina of an eye of the individual with light;

performing a first measurement of reflectance of the retina of the individual; and

using the first measurement to determine the blood glucose level.

27. The method of claim 26, wherein the retina of the eye is illuminated using light at a first intensity level.

28. The method of claim 26 further comprising illuminating the retina using light at a second intensity level.

29. The method of claim 28, wherein the second intensity level is higher than the first intensity level.

30. The method of claim 28 further comprising performing a second measurement of reflectance of the retina.

31. The method of claim 30 further comprising using the second measurement in the blood glucose level determination.

32. A method for determining blood glucose level of an individual comprising:

sequentially illuminating retina of an eye of the individual with light, wherein the light has a plurality of light intensity levels;

measuring reflectance of the retina of the individual at each light intensity level of the plurality of light intensity levels; and

using the measured reflectance to determine the blood glucose level.

33. The method of claim 32, wherein the plurality of light intensity levels has a first intensity level and a second intensity level greater than the first intensity level.