Method and apparatus for noninvasive targeting

• US 20060217602A1
• Filed: 03/03/2006
• Published: 09/28/2006
• Est. Priority Date: 03/04/2005
• Status: Abandoned Application

• Current Assignee: Sensys Medical, Inc. (Sensys Medical Limited)
• Original Assignee: Sensys Medical, Inc. (Sensys Medical Limited)
• Inventors: Hope, Josh, Abul-Haj, Alan, Hazen, Kevin H., Blank, Thomas B., Henderson, James Ryan, Ruchti, Timothy
• Application Number:
  US11/367,884
• Publication Number:
  US 20060217602A1
• Time in Patent Office: Days
• US Class Current: 600/316
• CPC Class Codes: A61B 2562/0242 for varying or adjusting the optical path length in the tissue
• CPC Class Codes: A61B 2562/146 for optical coupling
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/1495 Calibrating or testing of in-vivo probes
• CPC Class Codes: A61B 5/7264 Classification of physiological signals or data, e.g. using neural networks, statistical classifiers, expert systems or fuzzy systems neural networks per se G06N3/00; expert systems per se G06N5/00

Abstract

The invention relates to noninvasive sampling. In one embodiment, the invention relates to a sample probe interface method and apparatus for targeting a tissue depth and/or pathlength that is used in conjunction with a noninvasive analyzer to control spectral variation. In a second embodiment, a signal from a sample or target probe of a tissue feature or volume is used in positioning a portion of a measuring system relative to the sample. The system is optionally used in conjunction with a targeting system used to control the sampling location of the measuring system.

Claims

1. A method for noninvasively determining an analyte property of a tissue sample, comprising the steps of:

collecting a feedback targeting signal with a targeting system;

adjusting an optical measuring system to enhance sampling of at least a tissue layer, said tissue layer having an analyte concentration exceeding an average concentration of said analyte in all of said tissue sample, wherein said step of adjusting uses said feedback targeting signal;

noninvasively collecting at least one spectrum of said tissue sample using said adjusted optical measuring system; and

chemometrically determining said analyte property from said at least one spectrum.

2. The method of claim 1, wherein said targeting signal comprises a signal representative of at least one of:

a target below a surface of said tissue sample;

a subcutaneous feature; and

a dermis thickness within a specification.

3. The method of claim 1, wherein said targeting system comprises at least one capacitance sensor.

4. The method of claim 1, wherein said targeting system comprises use of any of:

an imaging system;

a multiple detector system;

an impedence reading;

an acoustic signature;

an ultrasound system;

a pulsed laser; and

an electromagnetic field.

5. The method of claim 4, wherein said targeting signal comprises a signal representative of any of:

a manmade target;

a natural tissue component;

a chemical feature;

a physical feature;

an abstract feature of a skin parameter;

a fluorescent marker;

a marking feature added to the skin;

a skin surface feature;

a tissue morphology; and

a measurement of tissue strain.

6. The method of claim 1, wherein said step of adjusting positions said measuring system in terms of any of:

an x-axis position;

a y-axis position;

a z-axis position; and

tilt of a sample probe of said measuring system relative to a surface of said tissue sample.

7. The method of claim 1, wherein said step of adjusting changes at least one of orientation, shape, and position of an internal optical component of said measuring system resulting in change of direction of photons projecting from said analyzer.

8. The method of claim 1, wherein said step of adjusting controls an average depth of penetration into said tissue sample for detected photons.

9. The method of claim 1, wherein said step of adjusting targets an average optical pathlength for detected photons.

10. The method of claim 1, wherein said tissue layer comprises an aqueous based layer when said analyte is hydrophilic.

11. The method of claim 1, wherein said tissue layer comprises an adipose rich layer.

12. The method of claim 1, wherein said analyte comprises a blood borne constituent.

13. The method of claim 1, wherein said step of determining said analyte property through use of chemometrics comprises use of at least one of:

multivariate analysis; and

a derivative.

14. An apparatus for noninvasively determining glucose concentration, comprising:

a spectroscopic analyzer comprising a targeting system and a measuring system;

means for collecting a feedback signal of a skin tissue with said targeting system;

means for adjusting said measurement system to enhance targeting of an internal tissue layer;

means for collecting a second signal representative of at least said tissue layer using said adjusted measurement system; and

a chemometrics module for deriving said glucose concentration from said second signal.

15. The apparatus of claim 14, wherein said feedback signal comprises a signal representative of at least one of:

a target below a surface of said skin tissue;

a subcutaneous feature; and

a dermis thickness within a specification.

16. The apparatus of claim 14, wherein said targeting system comprises at least one capacitance sensor.

17. The apparatus of claim 14, wherein said means for adjusting repositions said measuring system in terms of any of:

an x-axis position;

a y-axis position;

a z-axis position; and

tilt of a sample probe of said measurement system relative to a surface of said skin tissue.

18. The apparatus of claim 14, wherein said step of adjusting changes at least one of orientation, shape, or position of an internal optical component of said analyzer resulting in change of direction of incident photons projecting from said analyzer.

19. The apparatus of claim 14, wherein said step of adjusting controls an average depth of penetration into said tissue sample for detected photons.

20. The apparatus of claim 14, wherein said step of adjusting targets an average optical pathlength for detected photons.