MONITORING BLOOD CONSTITUENT LEVELS IN BIOLOGICAL TISSUE

• US 20120209094A1
• Filed: 04/25/2012
• Published: 08/16/2012
• Est. Priority Date: 08/11/2004
• Status: Active Grant

• Current Assignee: Masimo Corporation
• Original Assignee: GLT Acquisition Corporation
• Inventors: Schurman, Matthew J., Shakespeare, Walter J.
• Granted Patent: US 8,788,003 B2
• Time in Patent Office: Days
• US Class Current: 600/316
• CPC Class Codes: A61B 5/0064 Body surface scanning
• CPC Class Codes: A61B 5/0066 Optical coherence imaging
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/441 Skin evaluation, e.g. for skin disorder diagnosis

Abstract

In accordance with the invention, a low coherence interferometer is used to non-invasively monitor the concentration of glucose in blood by shining a light over a surface area of human or animal tissue, continuously scanning the light over a two dimensional area of the surface, collecting the reflected light from within the tissue and constructively interfering this reflected light with light reflected along a reference path to scan the tissue in depth. Since the reflection spectrum is sensitive to glucose concentration at particular wavelengths, measurement and analysis of the reflected light provides a measure of the level of glucose in the blood. The measurement of glucose is taken from multiple depths within blood-profused tissue, and sensitivity is preferably enhanced by the use of multiple wavelengths. Noise or speckle associated with this technique is minimized by continuously scanning the illuminated tissue in area and depth.

Claims

1. An apparatus for non-invasively measuring blood constituent levels within biological tissue, the apparatus comprising:

at least one light source for providing a sample beam and a reference beam, the at least one light source providing at least one wavelength of light, the at least one light source configured to direct the sample beam to the biological tissue;

a phase shifter configured to adjust phase path of the reference beam;

a scanner configured to scan the sample beam over an area of the subject'"'"'s tissue;

an interferometer that allows comparison of a reflected sample beam from the subject tissue with the reference beam;

at least one photodetector configured to generate non-image measurements from the reference beam and the reflected sample beam, the non-image measurements including at least scatter measurements of the light; and

a data output configured to communicate the non-image measurements to a blood constituent monitor, the blood constituent monitor configured to calculate a level of a first blood constituent based at least partly on the non-image measurements.

2. The apparatus of claim 1 further comprising:

a beam splitter to split light from the at least one light source into the sample beam and the reference beam;

wherein the phase shifter is configured to direct the reference beam to interfere with the reflected sample beam.

3. The apparatus of claim 1, wherein the scanner is configured to continuously scan a two-dimensional area of the biological tissue.

4. The apparatus of claim 1 wherein the scanner comprises a rapidly movable lens array or a rapidly movable diffractive optical element.

5. A system for non-invasively monitoring blood constituent level within biological tissue, the system comprising:

one or more processors configured to;

initiate scanning by an interferometric sensor of an area of biological tissue with light having scattering properties sensitive to a first blood constituent;

receive non-image measurements from the interferometric sensor for at least one tissue depth, the non-image measurements including at least scatter measurements of the light; and

determine a level of the first blood constituent within the biological tissue based at least partly on the scatter measurements of the light.

6. The system of claim 5, wherein the one or more processors are configured to cause the interferometric sensor to provide the light from one or more light sources, wherein the light is split into a sample beam and a reference beam.

7. The system of claim 5, wherein the one or more processors are configured to cause the interferometric sensor to continuously scan the light over a two-dimensional area of the biological tissue.

8. The system of claim 5, further comprising the interferometer sensor.

9. The system of claim 8, wherein the interferometric sensor is an optical coherence tomography (OCT) sensor.

10. The system of claim 8, wherein the interferometric sensor includes a first wavelength and a second wavelength source, the first wavelength source configured to produce a first wavelength having measurably different scattering properties for hemoglobin-containing tissue or indicators of such tissue relative to a second wavelength produced by the second wavelength source.

11. The system of claim 5, wherein the interferometric sensor includes multiple wavelength sources, including wavelength sources for at least infrared light and near infrared light.

12. The system of claim 5, wherein the first blood constituent comprises hemoglobin.

13. The system of claim 5, wherein the first blood constituent comprises glucose.

14. A method for non-invasively monitoring blood constituent level within biological tissue, the method comprising:

initiating scanning by an interferometric sensor of an area of biological tissue with light having scattering properties sensitive to a first blood constituent;

receiving light measurements from the interferometric sensor for at least one tissue depth, the light measurements including at least scatter measurements of the light; and

without generating an image from the light measurements, determining a level of the first blood constituent within the biological tissue based at least partly on the scatter measurements of the light.

15. The method of claim 14, wherein said initiating scanning by the interferometric sensor comprises causing the interferometric sensor to provide the light from one or more light sources, wherein the light is split into a sample beam and a reference beam.

16. The method of claim 15, further comprising varying phase of the reference beam and causing a reflected portion of the sample beam to interfere with the reference beam.

17. The method of claim 15, further comprising adjusting the reference beam to constructively interfere with reflected light from a selected depth within the biological tissue.

18. The method of claim 14, wherein said initiating scanning by the interferometric sensor comprises causing the interferometric sensor to continuously scan the sample beam over a two-dimensional area of the biological tissue.

19. The method of claim 14, wherein the interferometric sensor includes a first wavelength and a second wavelength source, the first wavelength source configured to produce a first wavelength having measurably different scattering properties for hemoglobin-containing tissue or indicators of such tissue relative to a second wavelength produced by the second wavelength source.

20. The method of claim 19, wherein the first wavelength source and second wavelength source produce wavelengths at about 1310 nm and at about 1450 nm, respectively.

21. The method of claim 19, wherein at least one of the first and second wavelength sources produce wavelengths within a range from 820 nm to 960 nm.

22. The method of claim 14, wherein the first blood constituent comprises hemoglobin.