Reduction of spectral site to site variation

• US 20020058864A1
• Filed: 11/13/2001
• Published: 05/16/2002
• Est. Priority Date: 11/13/2000
• Status: Abandoned Application

• Current Assignee: Argose, Inc.
• Original Assignee: Argose, Inc.
• Inventors: Marini, Solomon, Trepagnier, Pierre, Messerschmidt, Robert G., Mansfield, James R.
• Application Number:
  US09/987,192
• Publication Number:
  US 20020058864A1
• Time in Patent Office: Days
• US Class Current: 600/316
• 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 5/444 Evaluating skin marks, e.g. mole, nevi, tumour, scar
• CPC Class Codes: A61B 5/6833 Adhesive patches
• CPC Class Codes: A61B 5/6834 using vacuum
• CPC Class Codes: A61B 5/6842 by marking the skin

Abstract

The invention relates to devices and methods that improve the quality of optic measurements from surfaces such as skin and biological materials. Three methods for reducing spectral site to site variation in fluorescence and/or reflectance signals obtained from a sample surface are: repeated measurements taken at identifiable location(s) determined by fiducial marks, repeat of measurements at different locations on the sample, and tensioning the sample surface during measurement to alleviate surface heterogeneity. Combinations of these methodologies provide best results, and are expected to improve the ability to measure blood glucose non-invasively.

Claims

1. A method of minimizing error in optic spectra from a sample comprising the steps of:

applying one or more fixed fiducial points to the sample surface; and

referencing an optical probe to said one or more fiducial points, so that the spectra are taken in the same place.

2. The method of claim 1, wherein at least 1 fiducial point is applied to the sample surface.

3. The method of claim 1, wherein at least 2 fiducial points are applied to the sample surface.

4. The method of claim 1, wherein at least 3 fiducial points are applied to the sample surface.

5. The method of claim 1, wherein the sample surface is skin of a living body.

6. The method of claim 4, wherein the fluorescence spectra information is used to determine the level of an analyte in the body.

7. The method of claim 5 in which the analyte is glucose.

8. The method of claim 1, wherein the optical probe comprises a fiber optic bundle.

9. The method of claim 8, wherein the optic bundle is bifurcated and contains at least 16 light conducting fibers.

10. The method of claim 1, wherein a plurality of spectra are combined to form a representative spectrum by the further steps:

comparing a spectra measurement with a combined spectra to generate a compared spectra;

discarding the compared spectra if substantially different from a reference; and

combining the remaining spectra to form a representative spectrum.

11. A method of minimizing the variation of optic spectra from a sample comprising the steps of:

gathering a plurality of spectra at nearby points on the sample; and

combining the spectra so as to form a representative measurement.

12. The method of claim 11, wherein the sample surface is skin of a living body.

13. The method of claim 12, wherein the fluorescence spectra information is used to determine the level of an analyte in the body.

14. The method of claim 13 in which the analyte is glucose.

15. The method of claim 11, wherein the optical probe comprises a fiber optic bundle.

16. The method of claim 15, wherein the optic bundle is bifurcated and contains at least 16 light conducting fibers.

17. The method of claim 15, wherein the optic bundle contains at least 64 light conducting fibers.

18. The method of claim 11, wherein the probe contains at least two apertures, each of which acquires a fluorescence measurement at a different location on the sample.

19. The method of claim 18, wherein a plurality of spectra are combined to form a representative spectrum by the further steps:

a) comparing a spectra measurement with a combined spectra to generate a compared spectra;

b) discarding the compared spectra if substantially different from a reference; and

c) combining the remaining spectra to form a representative spectrum.

20. A method of minimizing the variation of measured optic spectra from a flexible sample surface comprising tensioning the sample surface prior to or at the time of making a spectral measurement with an optical probe.

21. The method of claim 20, wherein tensioning is carried out by:

adhering one or more fiduciary marks on the skin to provide a friction fitting

a) contact with the probe;

b) inserting the probe into the friction fitting contact;

c) making a spectral measurement from the probe; and

d) repeating steps b) and c) for successive measurements.

22. The method of claim 20, wherein the sample surface is skin of a living body.

23. The method of claim 21, wherein the fluorescence spectra information is used to determine the level of an analyte in the body.

24. The method of claim 22 in which the analyte is glucose.

25. The method of claim 20, wherein the optical probe comprises a fiber optic bundle.

26. The method of claim 25, wherein the optic bundle is bifurcated and contains at least 16 light conducting fibers.

27. The method of claim 26, wherein the optic bundle contains at least 64 light conducting fibers.

28. The method of claim 20, wherein the probe contains at least two apertures, each of which acquires a fluorescence measurement at a different location on the sample.

29. The method of claim 28, wherein a plurality of spectra are combined to form a representative spectrum by the further steps:

c) comparing a spectra measurement with a combined spectra to generate a compared spectra;

d) discarding the compared spectra if substantially different from a reference; and

e) combining the remaining spectra to form a representative spectrum.