Method and apparatus to compensate for melanin and hemoglobin variation in determination of a measure of a glycation end-product or disease state using tissue fluorescence

• US 8,676,283 B2
• Filed: 12/26/2007
• Issued: 03/18/2014
• Est. Priority Date: 04/04/2002
• Status: Expired due to Fees

• Current Assignee: Veralight, Inc. (Britannia Life Sciences, Inc.)
• Original Assignee: Veralight, Inc. (Britannia Life Sciences, Inc.)
• Inventors: Matter, Nathaniel, Ediger, Marwood Neal, Maynard, John D
• Primary Examiner(s): WINAKUR, ERIC FRANK
• Application Number:
  US11/964,665
• Publication Number:
  US 20080103373A1
• Time in Patent Office: 2,274 Days
• Field of Search: 600/310, 600/316, 600/317, 600/322, 600/473, 600/476
• US Class Current: 600/310
• CPC Class Codes: A61B 5/0059 using light, e.g. diagnosis by transillumination, diascopy, fluorescence A61B5/0093, A61B5/1455, A61B5/02416 and A61B5/0261 take precedence
• CPC Class Codes: A61B 5/0071 by measuring fluorescence emission
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/443 Evaluating skin constituents, e.g. elastin, melanin, water
• CPC Class Codes: A61B 5/4875 Hydration status, fluid retention of the body

Abstract

A method of determining a measure of a tissue state (e.g., glycation end-product or disease state) in an individual is disclosed. A portion of the skin of the individual is illuminated with excitation light, then light emitted by the tissue due to fluorescence of a chemical with the tissue responsive to the excitation light is detected. The detected light can be combined with a model relating fluorescence with a measure of tissue state to determine a tissue state. The invention can illuminate the skin and detect responsive light over a time that spans a plurality of cardiac cycles of the individual, which can, as an example, help mitigate the effects of time-varying signals such as those due to hemoglobin. The invention can also determine the amount of light to be directed to the skin, for example by controlling the time that a light source is energized. The amount of illumination light can be determined from a skin reflectance characteristic such as pigmentation or melanin in the skin. Controlling the amount of light directed to the tissue can reduce the dynamic range required of a corresponding optical system, for example by allowing a single system to accurately measure individuals with very light skin and individuals with very dark skin.

Claims

1. A method of determining a tissue state of the tissue of an individual, comprising:

(a) illuminating a portion of the skin of the individual with excitation light in two or more illumination events which together span, in time, a plurality of heart beats of the individual, and determining the duration of each illumination event, the number of illumination events, or a combination thereof, responsive to a characteristic of the skin;

(b) detecting light emitted from the tissue by fluorescence of a chemical within the tissue responsive to the illumination events;

(c) determining the tissue state from the detected light and a model relating fluorescence and a tissue state.

2. A method as in claim 1, wherein the illumination events span, in time, at least four heart beats of the individual.

3. A method as in claim 1, further comprising collecting light reflected from the skin in response to the excitation light, and wherein determining the tissue state comprises determining the tissue state from the detected light, the reflected light, and a model relating fluorescence and a tissue state.

4. A method as in claim 1, wherein the total light energy directed to the skin during an illumination event is determined from a characteristic of the skin.

5. A method as in claim 4, wherein the characteristic of the skin comprises the pigmentation of the skin.

6. A method as in claim 5, further comprising determining the pigmentation of the skin by determining the magnitude of light returned from the skin in response to illumination of the skin.

7. A method as in claim 5, further comprising determining the optical density of the skin by determining the magnitude of light returned from the skin in response to illumination of the skin.

8. A method as in claim 4, wherein the characteristic of the skin comprises the measured reflectance of the skin in response to excitation by a white light.

9. A method as in claim 8, wherein the characteristic of the skin comprises the measured reflectance of the skin in response to excitation by a white light.

10. A method as in claim 4, wherein a light source is energized for a determined amount of time in an illumination event, and wherein the determined amount of time is determined from a characteristic of the skin.

11. A method as in claim 10, wherein the characteristic of the skin comprises the pigmentation of the skin.

12. A method as in claim 8, further comprising determining the pigmentation of the skin by determining the magnitude of light returned from the skin in response to illumination of the skin.

13. A method as in claim 12, wherein the determined amount of illumination time is a first time for a first skin pigmentation, and a second time, longer then the first time, for a second skin pigmentation darker than the first skin pigmentation.

14. A method as in claim 12, wherein the determined amount of illumination time is a first time for a first skin optical density, and a second time, longer the first time, for a second skin optical density greater than the first skin optical density.

15. A method as in claim 12, wherein detecting light comprises using a detector having a desirable performance over a range of incident energy values, and wherein the amount of time in an illumination event is determined, from the skin pigmentation, to be an amount of time such that the detected light will be within the detector range.

16. A method as in claim 12, wherein detecting light comprises using a detector having a desirable performance over a range of incident energy values, and wherein the amount of time in an illumination event is determined, from the skin optical density, to be an amount of time such that the detected light will be within the detector range.

17. A method as in claim 11, further comprising determining the optical density of the skin by determining the magnitude of light returned from the skin in response to illumination of the skin.

18. A method as in claim 10, further comprising determining the characteristic of the skin before the first illumination event.

19. A method as in claim 4, further comprising determining the characteristic of the skin before the first illumination event.

20. A method as in claim 4, wherein detecting light comprises using a detector to detect light, and wherein the total energy directed to the skin during an illumination event is determined to be less than the total energy that would lead to a total incident energy on the detector that would be greater than the total incident energy consistent with desirable performance of the detector.

21. A method of determining a tissue state of the tissue of an individual, comprising:

(a) determining a skin reflectance characteristic;

(b) illuminating a portion of the skin of the individual with excitation light in two or more illumination events wherein the total excitation light energy is determined from the skin reflectance characteristic, and wherein the illumination events span a plurality of heart beats of the individual regardless of the skin reflectance characteristics;

(c) detecting light emitted from the tissue by fluorescence of a chemical within the tissue responsive to the excitation light;

(d) determining the tissue state from the detected light, either the skin reflectance characteristic or the excitation light, and a model relating fluorescence and a tissue state.

22. A method as in claim 21, wherein the skin reflectance characteristic comprises the pigmentation of the skin, and wherein illuminating a portion of the skin comprises energizing a light source for an amount of time determined responsive to the skin pigmentation.

23. A method as in claim 21, wherein the skin reflectance characteristic comprises the optical density of the skin, and wherein illuminating a portion of the skin comprises energizing a light source for an amount of time determined responsive to the skin optical density.

24. A method as in claim 21, wherein detecting light comprises using a detector, having desirable performance over a range of incident energy values, and wherein the total excitation light energy is determined from the skin reflectance characteristic to be a total that will result in incident light on the detector within the range.

25. A method as in claim 21, wherein illuminating a portion of the skin comprises energizing a light source for a plurality of pulses, wherein the time span of a pulse is determined from the skin reflectance characteristic and a light output characteristic of the light source;

and wherein detecting light comprises detecting light emitted from the tissue responsive to each pulse.