IP Library Granted Patent US 8,380,270
Granted Patent B2
US 8,380,270 · App. 12/694,208 · Granted Feb 19, 2013

Non-invasive ocular monitoring

Inventor: Naresh Menon (Pasadena, CA)
Assignee: Chromologic LLC
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Quick Facts
Patent No.
US 8,380,270
App. No.
12/694,208
Granted
Feb 19, 2013
Kind
B2
Abstract

A device for measuring an analyte concentration level in a subject. The device includes: a light source configured for illuminating at least a portion of an anterior region of an eye of the subject with incident light having a substantially broad illumination spectrum at an angle substantially tangential to the surface of the eye; an optical collector configured for detecting reflected light from the at least a portion of the anterior region of the eye; an analyzer configured for analyzing the detected reflected light; and a processor configured to determine the analyte concentration level in the subject based on the analyzed reflected light.

Claims (38)

1. A device for measuring an analyte concentration level in a subject, the device comprising:

a light source configured for illuminating at least a portion of an anterior region of an eye of the subject with incident light having a substantially broad illumination spectrum at an angle substantially tangential to the surface of the eye;

an optical collector configured for detecting at least one of scattered or reflected light from the at least a portion of the anterior region of the eye;

an analyzer configured for analyzing the detected at least one of scattered or reflected light; and

a processor configured to determine the analyte concentration level in the subject based on the analyzed at least one of scattered or reflected light.

2. The device of claim 1 , wherein the processor determines a health condition of the subject based on the analyte concentration level and reference data, and wherein the reference data corresponds to an analyte concentration level in an anterior region of a healthy eye.

3. The device of claim 1 , wherein the illumination spectrum comprises wavelengths ranging from about 200 nm to about 900 nm.

4. The device of claim 1 , wherein the angle at which the eye is illuminated ranges from about 70 degrees to about 90 degrees.

5. The device of claim 1 , further comprising a modulator configured for modulating the incident light to reduce extraneous effects.

6. The device of claim 1 , wherein the analyzer comprises an optical spectrometer.

7. The device of claim 1 , wherein the analyzer comprises an interferometer.

8. The device of claim 1 , wherein the light source comprises an incoherent light source.

9. The device of claim 1 , wherein the analyte concentration level measured is of an analyte comprising at least one of metabolic compounds selected from the group consisting of: carbohydrates, sodium, sodium based salts, sugars, glucose, proteins, peptides, amino acids, fats, fatty acids, triglycerides, polysaccharides, alcohols, ethanol, toxins, hormones, vitamins, bacteria-related substances, fungus-related substances, virus-related substances, parasite-related substances, pharmaceutical compounds, non-pharmaceutical compounds, pro-drugs, drugs, precursors, metabolites, degradation products, biomarkers, and surrogate markers.

10. A method for measuring an analyte concentration level in a subject, the method comprising:

irradiating at least a portion of an anterior region of an eye with incident light having a substantially broad illumination spectrum at an angle substantially tangential to the surface of the eye;

detecting at least one of scattered or reflected light from the at least a portion of the anterior region;

analyzing the at least one of scattered or reflected light; and

determining the analyte concentration level based on the analyzed at least one of scattered or reflected light.

11. The method of claim 10 , further comprising determining a health condition of the subject based the analyte concentration level and reference data, wherein the reference data corresponds to an analyte concentration level in the anterior region of a healthy eye.

12. The method of claim 10 , wherein the illumination spectrum comprises wavelengths ranging from about 200 nm to about 900 nm.

13. The method of claim 10 , further comprising modulating the incident light to reduce extraneous effects.

14. The method of claim 10 , wherein the analyte concentration level measured is of an analyte comprising at least metabolic compound selected from the group consisting of: carbohydrates, sodium, sodium based salts, sugars, glucose, proteins, peptides, amino acids, fats, fatty acids, triglycerides, polysaccharides, alcohols, ethanol, toxins, hormones, vitamins, bacteria-related substances, fungus-related substances, virus-related substances, parasite-related substances, pharmaceutical compounds, non-pharmaceutical compounds, pro-drugs, drugs, precursors, metabolites, degradation products, biomarkers, and surrogate markers.

15. A device for measuring an analyte concentration level in a subject, the device comprising:

a light source configured for illuminating at least a portion of an anterior region of an eye of the subject with incident light having a substantially broad illumination spectrum at an angle substantially tangential to the surface of the eye;

an optical splitter configured for splitting the incident light into first polarized rays and second polarized rays, wherein a polarization of the first polarized rays is substantially perpendicular to a polarization of the second polarized rays;

a first polarization rotation element configured for rotating the polarization of the first polarized rays to be substantially parallel to the polarization of the second polarized rays;

a first variable rotator configured for rotating the polarization of the first polarized rays and the polarization of the second polarized rays;

a second variable rotator configured for rotating a polarization of first reflected rays and a polarization of second reflected rays, wherein the first reflected rays and the second reflected rays comprise at least one of scattered or reflected light reflected from the at least a portion of the anterior region of the eye;

a second polarization rotation element configured for rotating the polarization of the second reflected rays to be substantially perpendicular to the polarization of the first reflected rays;

an optical combiner configured for combining the first and second reflected rays into combined reflected rays;

an optical collector configured for detecting the combined reflected rays;

an analyzer configured for analyzing the combined reflected rays; and

a processor configured to determine the analyte concentration level in the subject based on the analyzed combined reflected rays.

16. The device of claim 15 , wherein the processor determines a health condition of the subject based on the analyte concentration level and reference data, and wherein the reference data corresponds to an analyte concentration level in an anterior chamber of a healthy eye.

17. The device of claim 15 , wherein the illumination spectrum comprises wavelengths ranging from about 200 nm to about 900 nm.

18. The device of claim 15 , wherein the angle at which the eye is illuminated ranges from about 70 degrees to about 90 degrees.

19. The device of claim 15 , wherein a path length of the second polarized rays and a path length of the second reflected rays in the aqueous humor is greater than a path length of the first polarized rays and a path length of the first reflected rays, respectively, in the aqueous humor.

20. The device of claim 15 , wherein the analyte concentration level measured is of an analyte comprising at least one of metabolic compounds selected from the group consisting of: carbohydrates, sodium, sodium based salts, sugars, glucose, proteins, peptides, amino acids, fats, fatty acids, triglycerides, polysaccharides, alcohols, ethanol, toxins, hormones, vitamins, bacteria-related substances, fungus-related substances, virus-related substances, parasite-related substances, pharmaceutical compounds, non-pharmaceutical compounds, pro-drugs, drugs, precursors, metabolites, degradation products, biomarkers, and surrogate markers.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 27, 2010
From: MENON, NARESH
To: CHROMOLOGIC LLC
Reel/Frame 023858/0104 →
Continuity (1)
Related Publication 20110184262A1 · Jul 28, 2011