Methods and Apparatuses for Noninvasive Determinations of Analytes

• US 20110184260A1
• Filed: 02/28/2011
• Published: 07/28/2011
• Est. Priority Date: 02/09/2005
• Status: Abandoned Application

• Current Assignee: Robert D. Johnson, Robinson M. Ries, Russell E. Abbink
• Original Assignee: Robert D. Johnson, Robinson M. Ries, Russell E. Abbink
• Inventors: Johnson, Robert D., Abbink, Russell E., Robinson, M. Ries
• Application Number:
  US13/036,012
• Publication Number:
  US 20110184260A1
• Time in Patent Office: Days
• US Class Current: 600/316
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/14546 for measuring analytes not otherwise provided for, e.g. ions, cytochromes
• CPC Class Codes: A61B 5/14558 by polarisation
• CPC Class Codes: A61B 5/7257 using Fourier transforms
• CPC Class Codes: G01J 3/02 Details
• CPC Class Codes: G01J 3/0208 using focussing or collimating elements, e.g. lenses or mirrors; performing aberration correction
• CPC Class Codes: G01J 3/021 using plane or convex mirrors, parallel phase plates, or particular reflectors
• CPC Class Codes: G01J 3/0218 using optical fibers
• CPC Class Codes: G01J 3/0262 Constructional arrangements for removing stray light
• CPC Class Codes: G01N 2021/4792 Polarisation of scatter light
• CPC Class Codes: G01N 21/21 Polarisation-affecting properties G01N21/19 takes precedence
• CPC Class Codes: G01N 21/49 within a body or fluid

Abstract

The present invention provides methods and apparatuses for accurate noninvasive determination of tissue properties. Some embodiments of the present invention comprise an optical sampler having an illumination subsystem, adapted to communicate light having a first polarization to a tissue surface; a collection subsystem, adapted to collect light having a second polarization communicated from the tissue after interaction with the tissue; wherein the first polarization is different from the second polarization. The difference in the polarizations can discourage collection of light specularly reflected from the tissue surface, and can encourage preferential collection of light that has interacted with a desired depth of penetration or path length distribution in the tissue. The different polarizations can, as examples, be linear polarizations with an angle between, or elliptical polarizations of different handedness.

Claims

1. An apparatus for determining the presence, concentration, or both, of an analyte based upon a response of tissue to incident light, comprising:

(a) an illumination subsystem configured to communicate light having a first polarization to a surface of the tissue;

(b) a collection subsystem configured to collect light having a second polarization communicated from the tissue after interaction with the tissue;

wherein the first polarization is different from the second polarization;

(c) a multiplexing spectrometer to measure the collected light at a plurality of wavelengths;

(d) an analysis subsystem configured to determine the presence, concentration, or both, of an analyte from the measured light.

2. An apparatus as in claim 1, wherein the first polarization is different from the second polarization such that the collection system preferentially collects light returned from deeper than the tissue surface and the superficial layer.

3. An apparatus as in claim 1, wherein the first polarization is different from the second polarization such that the collection system preferentially collects light that has interacted with a selected depth of the tissue deeper than the superficial layer.

4. An apparatus as in claim 1, wherein the first and second polarizations are linear, with a nonzero relative angle between the first and second polarizations.

5. An apparatus as in claim 1, wherein the first and second polarizations are elliptical, and wherein the first and second polarizations are different handed.

6. An apparatus as in claim 1, wherein the multiplex spectrometer comprises a Fourier Transform spectrometer.

7. An apparatus as in claim 1, wherein the plurality of wavelengths comprises 10 or more wavelengths.

8. An apparatus as in claim 7, wherein the collection system collects light in a non-imaging manner.

9. An apparatus as in claim 1, wherein the illumination system is configured to communicate light having any of a first plurality of polarization states to a tissue surface.

10. An apparatus as in claim 9, wherein the collection system is configured to collect light having any of a second plurality of polarization states communicated from the tissue after interaction with the tissue.

11. An apparatus as in claim 1, wherein the illumination system is configured to communicate light having any of a first plurality of polarization states to a tissue surface;

or the collection system is configured to collect light having any of a second plurality of polarization states communicated from the tissue after interaction with the tissue;

or both.

12. An apparatus as in claim 1, wherein at least one of the illumination system or the collection system comprises optics having a variable focus.

13. An apparatus as in claim 12, further comprising an interface quality detector, and wherein the focus of the illumination system, the focus of the collection system, or both, are varied responsive to the interface quality detector.

14. An apparatus as in claim 1, further comprising a tissue location system.

15. An apparatus as in claim 14, wherein the tissue location system comprises a system that images a component of the vascular system of a human subject whose tissue is being sampled.

16. An apparatus as in claim 14, further comprising a feedback system to communicate to a user the location of the tissue surface relative to the sampler.

17. An apparatus as in claim 14, wherein the physical relationship, relative to the tissue surface, of at least one of (a) the illumination system and (b) the collection system, can be varied responsive to the tissue location system.

18. A method of determining the presence, concentration, or both, of an analyte from examination of the response of tissue to incident light, comprising:

(a) applying a smoothing agent to a portion of the tissue surface;

(b) using an apparatus as in claim 1, illuminating the portion of the tissue surface such that illumination light impinges on the smoothing agent before impinging on the tissue surface, and collecting light communicated from the tissue surface without physically contacting the smoothing agent with the optical sampler, and determining the presence, concentration, or both, of the analyte from the measured light.

19. A method as in claim 18, further comprising analyzing the light measurements from the multiplexing spectrometer to determine the presence of the smoothing agent.

20. A method as in claim 19, wherein the smoothing agent has a characteristic absorption, and wherein analyzing the light measurements comprises determining whether the collected light has interacted with a material having the characteristic absorption.

21. A method as in claim 20, further comprising determining a thickness of smoothing agent that has interacted with the light from the light measurements.

22. A method of determining the direction of change, rate of change, or both, of an analyte in tissue, comprising sampling the tissue with an apparatus as in claim 1, and analyzing the light measurements to determine the direction of change, rate of change, or both, of the analyte.

23. An analyte measurement system, comprising an illumination system, collection system, and optical instrumentation utilizing Fellgett'"'"'s advantage, wherein the illumination system and the collection system are configured to collect spectroscopic information in a non-imaging manner at a first polarization state and at a second polarization state, where the first and second polarization states are distinct, and where the analyte measurement system is configured to use at least a portion of the information obtained at each of the two polarization states.

24. An analyte measurement system as in claim 23 where the analyte measurement system is configured to use the information from the two polarization states to characterize tissue differences.

25. An analyte measurement system as in claim 24, where the information obtained from the two polarization states is used to calculate the degree of polarization.

26. An analyte measurement system as in claim 24 where the analyte measurement system is configured to select a measurement method responsive at least in part to the tissue differences.

27. A method of determining the response of portions of a tissue sample deeper than the superficial layer to light, comprising:

(a) illuminating the tissue sample with light having a first polarization;

(b) collecting light, in a non-imaging manner, having a second polarization;

(c) collecting light, in a non-imaging manner, having a third polarization to preferentially select photons from tissue deeper than the superficial layer;

(d) wherein the second polarization, and the third polarization are each different from one another; and

(e) measuring the collected light at a plurality of wavelengths using a multiplexing spectrometer.

28. A method as in claim 27, wherein the first, second, and third polarizations are linear.

29. A method as in claim 27, wherein the first, second, and third polarizations are elliptical, and wherein the second and third polarizations are different handed.

30. A method as in claim 27, wherein the tissue is illuminated and light collected from substantially the same tissue portion at each of the first, second, and third polarizations.

31. A method for determining the presence or concentration of an analyte in tissue deeper than the superficial layer, comprising:

(f) determining the spectroscopic response of the tissue to light according to the method of claim 27; and

(g) determining the presence or concentration of the analyte from the spectroscopic response of the tissue determined in step (f).

32. A noninvasive glucose measurement system comprising:

(a) a multiplexing spectrometer configured to determine spectral information of near infrared light;

(b) a noncontact sampling system configured to use polarization to preferentially exclude superficially reflected photons;

(c) an illumination system configured to emit multiple wavelengths of light;

(d) a detection system configured to simultaneously record multiple wavelengths of light;

(e) an analysis system configured to determine a glucose concentration from multivariate analysis of at least 10 wavelengths of light.