Interferometric sensor for characterizing materials

• US 7,307,734 B2
• Filed: 08/16/2004
• Issued: 12/11/2007
• Est. Priority Date: 08/14/2003
• Status: Active Grant

• Current Assignee: University of Central Florida (State University System of Florida)
• Original Assignee: University of Central Florida (State University System of Florida)
• Inventors: Dogariu, Aristide
• Primary Examiner(s): LEE, HWA S
• Application Number:
  US10/919,223
• Publication Number:
  US 20050190372A1
• Time in Patent Office: 1,212 Days
• Field of Search: 356/479, 356/497, 356/335, 356/336
• US Class Current: 356/497
• CPC Class Codes: A61B 2562/0242 for varying or adjusting the optical path length in the tissue
• CPC Class Codes: A61B 5/0066 Optical coherence imaging
• 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: G01N 21/474 Details of optical heads therefor, e.g. using optical fibres
• CPC Class Codes: G01N 21/49 within a body or fluid

Abstract

An integrated optical sensor, using low coherence interferometry, is capable of determining analyte concentration in a material sample based on absorption, scattering and polarization. The sensor includes one or more light collectors, with each collector having a separation distance from the region where the sample is illuminated by the source. The light backscattered from the sample is combined with reference arm light at the same optical path length for each light collector. The intensity of interference may be correlated with the concentration of an analyte in the material, for example the glucose concentration in a turbid medium like skin. The sensor operation can be based on fiber optics technology, integrated optics, or a combination of these. The operation is such that the spectrally resolved scattering and absorption coefficients can be measured simultaneously. In addition, the operation of the sensor can be synchronized with other sensors, for example temperature, pressure, or heartrate.

Claims

1. An interferometer based sensor comprising:

a low coherence light source;

a light splitter positioned to direct light from said low coherence light source to at least one sample and to at least one reference arm;

at least one sample light collector for collecting light from the sample disposed apart from a site of light injection into the sample by a separation distance;

an optical coupler for combining light from the sample and light from the reference arm;

a detector for detecting interference between the sample light and the light from the reference arm; and

a processor for determining absorption and scattering of light from the sample based on the interference between the sample light and the light from the reference arm.

2. The sensor of claim 1, further comprising a housing.

3. The sensor of claim 1, wherein the separation distance is less than about 1 centimeter.

4. The sensor of claim 1, comprising at least a first sample light collector and at least one second sample light collector disposed apart from a site of light injection into the sample.

5. The sensor of claim 2, wherein said housing comprises a portion of an endoscope.

6. The sensor of claim 1, wherein the at least one sample light collector samples light having a trajectory dominated by sample absorption.

7. The sensor of claim 1, wherein light is propagated through optical fibers.

8. The sensor of claim 1, wherein the reference light has an optical delay that is fixed, adjustable, or a combination thereof.

9. The sensor of claim 1, further comprising a plurality of light sources, wherein each light source has a different wavelength.

10. The sensor of claim 1, further comprising a plurality of light collectors, each light collector having a different separation distance from the site of light injection into the sample.

11. The sensor of claim 1, further comprising one or more polarizers.

12. A method for characterizing a sample with an interferometer comprising:

propagating low coherence light from a source into a light splitter, said light splitter directing a portion of said low coherence light to one or more sites of light injection on the sample and directing a portion of said low coherence light to a reference arm;

collecting backscattered light from one or more regions of the sample disposed apart from the one or more sites of light injection by a separation distance;

determining the intensity of interference between the low coherence light in said reference arm and the backscattered light from the one or more regions of the sample;

calculating absorption and scattering of the sample from said interference intensities; and

characterizing said sample based on said absorption and scattering.

13. The method of claim 12, wherein the low coherence light is directed onto the sample and backscattered light is collected using one or more transceivers.

14. The method of claim 12, wherein the reference arm is scanned through a plurality of optical path lengths.

15. The method of claim 12, wherein the backscattered light from one or more regions of said sample have different trajectories in the sample.

16. The method of claim 12, further comprising correlating the absorption coefficient and a scattering coefficient to the concentration of an analyte in the sample.

17. The method of claim 12, wherein the sample is heterogeneous.

18. The method of claim 12, further comprising detecting interference between the reference arm light and light backscattered from one or more regions using one or more detectors and measuring the intensity of interference between reference arm light and light backscattered from one or more regions at a distance from the region where said light is directed on said sample.

19. The method of claim 16, wherein said analyte is glucose and said sample is skin.

20. An integrated optical sensor for glucose monitoring in biological tissue, comprising:

means for generating low coherence light;

means for controlling an optical path length of said low coherence light;

means for discriminating between scattering and absorption;

means for recording spectral measurements over a limited range; and

means for determining glucose concentrations based on the spectral measurements.

21. The integrated optical sensor of claim 20, wherein the biological tissue is human skin.

22. The integrated optical sensor of claim 20, wherein the low coherence light source includes a super luminescent diode.

23. The integrated optical sensor of claim 20, wherein the length of the optical path is controlled by an optical delay line.

24. The integrated optical sensor of claim 20, further comprising a plurality of light sources, each light source having a different wavelength.

25. The integrated optical sensor of claim 20, wherein the sensor is designed to limit the interference between light scattering and absorption.

26. The integrated optical sensor of claim 20, wherein the means for generating low coherence light includes an optical fiber based transmission medium.

27. A system for monitoring glucose concentration in biological specimen using the integrated optical sensor of claim 20.

28. The system for monitoring glucose concentration of claim 27, wherein the monitoring is non-invasive.

29. The system for monitoring glucose concentration of claim 27, wherein the monitoring can be synchronized with the heartbeat of the biological specimen.

30. The system for monitoring glucose concentration of claim 27, wherein the biological specimen is a human being.

31. A method for determining glucose concentration using an integrated optical sensor, comprising:

generating low coherence light;

directing said low coherence light into a sample and a reference arm;

controlling a length of the optical path of said low coherence light in said reference arm;

collecting backscattered light from one or more points of said sample disposed apart from a site of light injection into the sample by a separation distance and collecting light from said reference arm;

recording spectral measurements from the backscattered light from one or more points of said sample disposed apart from a site of light injection of low coherence light into the sample by a separation distance and backscattered light from said reference arm over a limited range;

determining the intensity of interference between the backscattered light from reference arm and the backscattered light from the one or more points of said sample disposed apart from a site of light injection of low coherence light into the sample by a separation distance;

calculating an absorption coefficient and a scattering coefficient from the intensity of interference; and

determining glucose concentration based on the absorption coefficient and scattering coefficient.

32. The method of claim 31, wherein the glucose concentration is determined in biological tissue.

33. The method of claim 32, wherein the biological tissue is human skin.

34. The method of claim 31, wherein the low coherence light is generated from a source including a super luminescent diode.

35. The method of claim 31, wherein the length of the optical path is controlled by an optical delay line.

36. An interferometer based sensor comprising:

a low coherence light source;

a reference arm having an optical delay;

a first light splitter positioned to propagate a portion of said source light from said light source to a first site of light injection into said sample and a portion of said light to the reference arm;

a first light collector for collecting backscattered light from a first region of said sample at or near the first site of light injection;

a second light splitter positioned to propagate a portion of said source light from said light source to a second site of light injection into said sample and a portion of said light to the reference arm;

a second light collector for collecting backscattered light from a second region of said sample disposed apart from the second site of light injection;

said second region separated from said first region on said sample;

a first detector that measures the intensity of interference between backscattered light from said first region of said sample and light from said reference arm at the optical delay, said first detector generating a first signal proportional to said interference intensity of said first region;

a second detector that measures the intensity of interference between backscattered light from said second region of said sample and light from said reference arm at the optical delay, said second detector generating a second signal proportional to the interference intensity of said second region; and

a processor to determine absorption, scattering, or both of the sample from said first signal and said second signal.

37. The sensor of claim 36, wherein said sensor comprises a portion of an endoscope or a catheter.

38. The sensor of claim 36, wherein the position of said second light collector samples light having a trajectory dominated by sample absorption.

39. The sensor of claim 36, wherein light is propagated through single mode optical fibers, polarization maintaining optical fibers or a combinations thereof.

40. The sensor of claim 36, further comprising one or more polarizer.

41. The sensor of claim 36, wherein the optical delay of the reference arm is adjustable.

42. The sensor of claim 36, wherein the separation distance between the second site of light injection and second region is adjustable.

43. The sensor of claim 36, wherein the separation of the first site of light injection and the first region and second site of light injection and the second region results in two different light trajectories in said sample.