TIME-RESOLVED NON-INVASIVE OPTOMETRIC DEVICE FOR DETECTING DIABETES

• US 20070156036A1
• Filed: 12/13/2006
• Published: 07/05/2007
• Est. Priority Date: 06/17/2004
• Status: Abandoned Application

• Current Assignee: Regents of the University of California (University of California)
• Original Assignee: Regents of the University of California (University of California)
• Inventors: Katika, Kamal, Pilon, Laurent
• Application Number:
  US11/610,423
• Publication Number:
  US 20070156036A1
• Time in Patent Office: Days
• 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 5/1455 using optical sensors, e.g. spectral photometrical oximeters
• CPC Class Codes: A61B 5/441 Skin evaluation, e.g. for skin disorder diagnosis
• CPC Class Codes: A61B 5/6816 Ear lobe
• CPC Class Codes: A61B 5/6824 Arm or wrist
• CPC Class Codes: A61B 5/6825 Hand
• CPC Class Codes: A61B 5/6829 Foot or ankle
• CPC Class Codes: G01N 2021/6493 by alternating fluorescence/transmission or fluorescence/reflection
• CPC Class Codes: G01N 21/6408 with measurement of decay time, time resolved fluorescence
• CPC Class Codes: G01N 21/6486 Measuring fluorescence of biological material, e.g. DNA, RNA, cells G01N21/6428 takes precedence
• CPC Class Codes: G01N 2800/042 Disorders of carbohydrate metabolism, e.g. diabetes, glucose metabolism
• CPC Class Codes: G01N 33/582 with fluorescent label
• CPC Class Codes: G01N 33/6893 related to diseases not provided for elsewhere

Abstract

A time-resolved fluorescence device is described for the detection and diagnosis of diabetes in a noninvasive manner. The device uses an ultra-short excitation pulse of light in the UV, infrared or visible range that comprises of a repetition of nanosecond pulses. The excitation pulse is directed incident onto a strategically selected area of the patient body such as the forearm, the feet, and the palm. This light interacts with the different layers of the skin. The absorbed light excites the AGEs in the skin, which in turn generate a fluorescence signal, which is collected by a detector. A processor is coupled to the detector to measure the transient fluorescence intensity decay of the skin in terms of lifetimes, and the contribution of individual fluorophores to the overall fluorescence signal. The nature and location of the fluorophores may be identified and a medical diagnostics may be performed.

Claims

1. A method for non-invasively detecting diabetes in a patient;

comprising;

directing a pulse of excitation light at a region of the patient'"'"'s skin;

exciting one or more AGE products in the skin;

wherein excitation of said one or more AGE products generates a fluorescence signal;

detecting the fluorescence signal generated by the one or more AGE products; and

measuring the fluorescence signal as a function of time.

2. A method as recited in claim 1, wherein directing a pulse of excitation light comprises repeatedly directing a plurality of excitation pulses in succession at the region of the patient'"'"'s skin.

3. A method as recited in claim 2, wherein the excitation pulses are subjected on the patient'"'"'s skin at a rate of at least 1 MHz.

4. A method as recited in claim 3, wherein the successive pulses are added to increase the signal-to noise ratio of the signal.

5. A method as recited in claim 1, further comprising measuring the reflectance of the excitation pulse of light at the sensing region.

6. A method as recited in claim 5, further comprising measuring the transmittance of the excitation pulse.

7. A method as recited in claim 6, wherein the transmittance, reflectance, and time-resolved fluorescence measurements are performed simultaneously.

8. A method as recited in claim 1, further comprising:

storing measured fluorescence signal values acquired from a plurality of reference patients in a database.

9. A method as recited in claim 8, further comprising:

comparing the measured fluorescence signal values to key fluorophore values indicative of diabetes.

10. A method as recited in claim 9, wherein the compared fluorescence signal is used to assess the long term glycemic control in the patient.

11. A method as recited in claim 9, wherein the compared fluorescence signal is used to assess the impaired glucose tolerance in the patient.

12. A method as recited in claim 1, further comprising identifying one or more fluorophores from the measured in-vivo fluorescence signal.

13. A method as recited in claim 12, further comprising locating one or more fluorophores within the region of skin.

14. A method as recited in claim 12, wherein the fluorescence signal is deconvoluted to isolate the contribution of individual fluorophores to a cumulative signal.

15. An apparatus for detecting diabetes in a patient;

comprising;

an excitation source configured to direct electromagnetic excitation energy at a region of the patient'"'"'s skin;

a detector directed at the region of skin;

the detector configured to receive a fluorescence signal resulting from the excitation energy at the patient'"'"'s skin; and

a processor configured to measure intensity decay of the fluorescence signal as a function of time to diagnose the diabetic condition of the patient.

16. An apparatus as recited in claim 15, wherein the excitation source comprises one or more LEDs.

17. An apparatus as recited in claim 16, further comprising one or more light guides for directing the excitation energy at the region of the patient'"'"'s skin.

18. An apparatus as recited in claim 17, further comprising one or more light guides for directing the fluorescence signal emanating from the region to the detector.

19. An apparatus as recited in claim 15, wherein the excitation source is configured to repeatedly direct a plurality of excitation pulses in succession at the region of the patient'"'"'s skin.

20. An apparatus as recited in claim 19, wherein the processor is further configured to measure the time resolved transmittance of the excitation pulses at the patient'"'"'s skin.

21. An apparatus as recited in claim 20, wherein the processor is further configured to measure the reflectance of the excitation pulse at the patient'"'"'s skin.

22. An apparatus as recited in claim 18, wherein the one or more light guides for directing the excitation energy are configured to be positioned on an opposing side of the region of skin opposite said one or more light guides for directing the fluorescence signal.

23. An apparatus as recited in claim 22, wherein the processor is further configured to perform transmittance, reflectance, and time-resolved fluorescence measurements simultaneously.

24. An apparatus as recited in claim 15, further comprising one or more optical filters displaced in the field of view of the detector.

25. An apparatus as recited in claim 15, wherein the excitation source is coupled with a sphygmomanometer cuff of a blood pressure monitoring device such that excitation energy may be directed while pressure is being applied to the region of the patient'"'"'s skin.

26. A method for performing time-resolved fluorescence measurements to diagnose the diabetic condition of a patient;

comprising;

directing an excitation pulse at a region of the patient'"'"'s skin;

exciting a portion of the patient'"'"'s skin as a result of the excitation pulse at the region to generate a fluorescence signal indicative of the composition of the patient'"'"'s skin;

detecting the fluorescence signal generated by the excitation pulse; and

measuring a transient intensity decay of the fluorescence signal to determine the diabetic condition of the patient.

27. A method as recited in claim 26, wherein exciting a portion of the patient'"'"'s skin comprises exciting one or more AGE products in the skin;

the one or more AGE products each generating a fluorescence signal.

28. A method as recited in claim 27, wherein directing an excitation pulse comprises repeatedly directing a plurality of ultra short pulses in succession at the region of the patient'"'"'s skin.

29. A method as recited in claim 27, wherein directing an excitation pulse comprises repeatedly directing a frequency modulated light at the region of the patient'"'"'s skin.

30. A method as recited in claim 28, wherein signals from the successive pulses are added to increase the signal-to noise ratio of the signal.

31. A method as recited in claim 28, further comprising measuring the reflectance of the excitation pulse.

32. A method as recited in claim 28, further comprising:

distinguishing between the one or more AGE products by measuring their emission wavelengths.

33. A method as recited in claim 32, further comprising:

distinguishing the one or more AGE products having similar wavelengths by measuring their fluorescence lifetimes.

34. A method as recited in claim 28, further comprising:

identifying the location of the one or more AGE products by identifying their emission wavelengths.

35. A method as recited in claim 28, wherein the fluorescence signal is deconvoluted to isolate the contribution of individual fluorophores to a cumulative signal.

36. A method as recited in claim 31, further comprising measuring the transmittance of the excitation pulse.

37. A method as recited in claim 26, further comprising:

storing measured intensity decay values acquired from a plurality of reference patients in a database.

38. A method as recited in claim 37, further comprising:

comparing the measured intensity decay to key fluorophore values corresponding to diabetes.

39. A method as recited in claim 38, wherein the compared intensity decay is used to assess the long term glycemic control in the patient.

40. A method as recited in claim 38, wherein the compared intensity decay is used to assess the patient'"'"'s risk of developing diabetes.

41. A method of non-invasively pre-screening a patient for diabetes, comprising:

directing an excitation pulse at a region of the patient'"'"'s skin to generate a fluorescence signal indicative of the composition of the patient'"'"'s skin;

measuring a transient intensity decay of the fluorescence signal; and

comparing the measured transient intensity decay to a reference transient intensity decay value to diagnose the diabetic condition of the patient.

42. A method as recited in claim 41, wherein the measured transient intensity decay is compared against a reference value according to the patient'"'"'s age group.

43. A method as recited in claim 42, wherein directing an excitation pulse comprises exciting one or more AGE products in the skin;

the one or more AGE products each generating a fluorescence signal having an identifiable wavelength and fluorescence lifetime.

44. A method as recited in claim 43, further comprising:

measuring the fluorescence wavelength and lifetime;

wherein comparing the measured transient intensity decay comprises identifying a particular AGE product of interest via the fluorescence wavelength and lifetime; and

comparing the AGE product of interest with a reference value for the AGE product of interest.

45. A method as recited in claim 41, further comprising:

controlling the excitation pulse to vary wavelength, pulse width, repetition rate, peak and average power of the excitation pulse.

46. A method as recited in claim 41, wherein the measured transient intensity decay is compared to a reference transient intensity decay value to diagnose the impaired glucose tolerance of the patient.