Optical Probes for Non-Invasive Analyte Measurements

• US 20080319286A1
• Filed: 08/04/2008
• Published: 12/25/2008
• Est. Priority Date: 05/24/2004
• Status: Abandoned Application

• Current Assignee: TruTouch Technologies, Inc.
• Original Assignee: TruTouch Technologies, Inc.
• Inventors: ver Steeg, Ben, Ridder, Trent, Mills, Mike
• Application Number:
  US12/185,217
• Publication Number:
  US 20080319286A1
• Time in Patent Office: Days
• US Class Current: 600/310
• CPC Class Codes: A61B 2562/0233 Special features of optical sensors or probes classified in A61B5/00
• CPC Class Codes: A61B 2562/0238 Optical sensor arrangements for performing transmission measurements on body tissue
• CPC Class Codes: A61B 2562/046 in a matrix array
• CPC Class Codes: A61B 2562/12 Manufacturing methods specially adapted for producing sensors for in-vivo measurements
• 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 5/1455 using optical sensors, e.g. spectral photometrical oximeters
• CPC Class Codes: G01N 2021/4745 Fused bundle, i.e. for backscatter
• CPC Class Codes: G01N 21/474 Details of optical heads therefor, e.g. using optical fibres
• CPC Class Codes: G01N 21/4795 spatially resolved investigating of object in scattering medium in vivo A61B
• CPC Class Codes: G01N 21/49 within a body or fluid
• CPC Class Codes: G01N 2201/0846 Fibre interface with sample, e.g. for spatial resolution
• CPC Class Codes: Y10T 29/49764 with testing or indicating

Abstract

An optical probe for non-invasively measuring an analyte property in a biological sample of a subject, comprises a plurality of illumination fibers that deliver source light from an optical probe input to a sample interface, a plurality of collection fibers that deliver light returned from the sample interface to an optical probe output, and wherein the illumination and collection fibers are oriented substantially perpendicular to the sample interface and the illumination and collection fibers are stacked in a plurality of linear rows to provide a stack of fibers arranged in a rectangular pattern. The optical probe is amenable to manufacturing on a scale consistent with a commercial product.

Claims

1. An optical probe for non-invasively measuring an analyte property in a biological sample of a subject, comprising:

a plurality of illumination fibers that deliver source light from an optical probe input to a sample interface,

a plurality of collection fibers that deliver light returned from the sample interface to an optical probe output, and

wherein the illumination and collection fibers are oriented substantially perpendicular to the sample interface and the illumination and collection fibers are stacked in a plurality of linear rows to provide a stack of fibers.

2. The optical probe of claim 1, wherein the stack of fibers forms a rectangle.

3. The optical probe of claim 2, wherein the stack of fibers forms a square.

4. The optical probe of claim 1, wherein the illumination and collection fibers comprise separate rows in the stack of fibers.

5. The optical probe of claim 4, wherein the illumination and collection fibers comprise alternating separate rows in the stack of fibers thereby providing a linear stack of fibers.

6. The optical probe of claim 1, wherein every other row in the stack of fibers consists of illumination fibers and the intervening rows comprise both illumination and collection fibers.

7. The optical probe of claim 6, wherein the intervening rows comprise alternating illumination and collection fibers such that each collection fiber has eight adjacent illumination fibers thereby providing a linear stack 8:

1 of fibers.

8. The optical probe of claim 1, wherein each linear row comprises alternating illumination and collection fibers such that each collection fiber has four adjacent illumination fibers thereby providing an alternating linear stack of fibers.

9. The optical probe of claim 1, further comprising an optical homogenizer at the optical probe input to homogenize the source light at the input of the illumination fibers.

10. The optical probe of claim 1, further comprising an optical homogenizer at the optical probe output to homogenize the return light at the output of the collection fibers.

11. The optical probe of claim 10, further comprising an aperture at the output of the optical homogenizer to reduce the size of the optical probe output.

12. The optical probe of claim 1, wherein the numerical aperture of the illumination fibers is different than the numerical aperture of the collection fibers.

13. The optical probe of claim 1, wherein the illumination and collection fibers comprise a silica core and a cladding comprises fused silica, doped silica, Teflon, or a fluoropolymer.

14. The optical probe of claim 1, wherein the relative spacing, angle, numerical aperture, and placement of the illumination and collection fibers are arranged to achieve depth targeting.

15. The optical probe of claim 1, further comprising means to control the temperature of the sample interface.

16. The optical probe of claim 1, further comprising an index matching fluid at the optical interface between the sample and the sample interface to match the optical index of the illumination and collection fibers to the sample.

17. The optical probe of claim 1, wherein the plurality of illumination fibers comprises at least two different illumination channels, each illumination channel comprising a plurality of illumination fibers that illuminate the sample with source light from a different perspective than each of the other illumination channels.

18. The optical probe of claim 1, wherein the plurality of collection fibers comprises at least two different collection channels, each collection channel comprising a plurality of collection fibers that collect returned light the sample from a different perspective than each of the other collection channels.

19. The optical probe of claim 18, wherein the at least two different collection channels comprises a first collection channel comprising rows of collection fibers spaced proximate a row of illumination fibers and a second collection channel comprising rows of collection fibers spaced distal the row of illumination fibers.

20. A method for non-invasively measuring an analyte property in a biological sample of a subject, comprising:

providing an optical probe as in claim 1;

disposing the optical probe in an operative relationship with the biological sample;

illuminating the biological sample with source light delivered by the plurality of illumination fibers from the optical probe input to the sample interface;

collecting light returned from the biological sample to the sample interface and delivering the collected light to the optical probe output; and

analyzing the returned light from the optical probe output to measure the analyte property.

21. The method of claim 20, wherein the analyte comprises an alcohol, alcohol byproduct, alcohol biomarker, substance of abuse, or biometric, or a combination thereof.

22. The method of claim 20, wherein the biological sample of a subject comprises a forearm of a person and wherein the stack of fibers forms a rectangle such that the long axis of the rectangle is oriented with the forearm at the sample interface that is contacted with the forearm.

23. The method of claim 20, wherein the biological sample of a subject comprises a finger of a person and wherein the stack of fibers forms a square at the sample interface that is contacted with the finger.

24. The method of claim 20, wherein the relative spacing, angle, numerical aperture, and placement of the illumination and collection fibers are arranged to achieve depth targeting in the biological sample.

25. The method of claim 20, further comprising controlling the temperature of the sample interface.

26. The method of claim 20, further comprising providing an index matching fluid at the optical interface between the sample and the sample interface to match the optical index of the illumination and collection fibers to the sample.

27. The method of claim 20, wherein the plurality of illumination fibers comprises at least two different illumination channels, each illumination channel comprising a plurality of illumination fibers that illuminate the sample with source light from a different perspective than each of the other illumination channels.

28. The method of claim 20, wherein the plurality of collection fibers comprises at least two different collection channels, each collection channel comprising a plurality of collection fibers that collect returned light the sample from a different perspective than each of the other collection channels.

29. The method of claim 28, wherein the at least two different collection channels comprises a first collection channel comprising rows of collection fibers spaced proximate a row of illumination fibers and a second collection channel comprising rows of collection fibers spaced distal the row of illumination fibers.

30. An analyte measurement system, comprising:

a. an optical probe as in claim 1;

b. an illumination system adapted to supply light to the optical probe input;

c. a detection system adapted to detect light from the optical probe output;

d. an analysis system adapted to determine an analyte property from the detected light.