Method and apparatus for the non-invasive sensing of glucose in a human subject

• US 20060281982A1
• Filed: 06/13/2006
• Published: 12/14/2006
• Est. Priority Date: 06/14/2005
• Status: Abandoned Application

• Current Assignee: Dominion Assets LLC
• Original Assignee: Diasense Inc.
• Inventors: Pitsakis, Michael N., Grata, Jeremy
• Application Number:
  US11/451,864
• Publication Number:
  US 20060281982A1
• Time in Patent Office: Days
• US Class Current: 600/316
• CPC Class Codes: A61B 2562/0233 Special features of optical sensors or probes classified in A61B5/00
• CPC Class Codes: A61B 5/1112 Global tracking of patients, e.g. by using GPS
• 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: G01J 1/46 using a capacitor
• CPC Class Codes: G01J 3/02 Details
• CPC Class Codes: G01J 3/027 Control of working procedures of a spectrometer; Failure detection; Bandwidth calculation
• CPC Class Codes: G01J 3/42 Absorption spectrometry; Double beam spectrometry; Flicker spectrometry; Reflection spectrometry beam switching arrangements G01J3/08
• CPC Class Codes: G01N 21/359 using near infrared light

Abstract

An apparatus for a non-invasive sensing of biological analytes in a sample includes an optics system having at least one radiation source and at least one radiation detector; a measurement system operatively coupled to the optics system; a control/processing system operatively coupled to the measurement system and having an embedded software system; a user interface/peripheral system operatively coupled to the control/processing system for providing user interaction with the control/processing system; and a power supply system operatively coupled to the measurement system, the control/processing system and the user interface system for providing power to each of the systems. The embedded software system of the control/processing system processes signals obtained from the measurement system to determine a concentration of the biological analytes in the sample.

Claims

1. An apparatus for a non-invasive sensing of biological analytes in a sample comprising:

a) an optics system comprising at least one radiation source and at least one radiation detector;

b) a measurement system operatively coupled to the optics system;

c) a control/processing system operatively coupled to the measurement system and having an embedded software system;

d) a user interface/peripheral system operatively coupled to the control/processing system for providing user interaction with the control/processing system; and

e) a power supply system operatively coupled to the measurement system, the control/processing system, the user interface/peripheral system or any combination thereof for providing power thereto,

wherein the embedded software system of the control/processing system processes signals obtained from the measurement system to determine a concentration of the biological analytes in the sample.

2. The apparatus of claim 1, wherein an absorbance spectrum obtained from the optics system is used, together with a previously stored calibration vector, by the embedded software system of the control/processing system to determine the concentration of the biological analytes in the sample.

3. The apparatus of claim 1, wherein the sample is interstitial fluid of living tissue, the capillary bed of living tissue, a blood sample or any combination thereof.

4. The apparatus of claim 1, wherein the radiation source is one of a selectable emission wavelength and selectable emission intensity TPCOPO device or a selectable emission wavelength and selectable emission intensity laser diode array.

5. The apparatus of claim 1, wherein the radiation detector is fabricated from InGaAs, Ge or any combination thereof.

6. The apparatus of claim 1, wherein the biological analyte of glucose, lipids, alcohol or any combination thereof.

7. The apparatus of claim 6, wherein an emission spectrum of the radiation source covers a range of about 1,200 nm to about 1,900 nm.

8. The apparatus of claim 6, wherein a responsivity of the radiation detector covers a range of about 1,200 nm to about 1,900 nm.

9. The apparatus of claim 1, wherein the biological analyte is alcohol, and an emission spectrum of the radiation source covers a range of about 800 nm to about 1,300 nm.

10. The apparatus of claim 9, wherein the biological analyte is alcohol, and a responsivity of the radiation detector covers a range of about 800 nm to about 1,300 nm.

11. The apparatus of claim 1, wherein the user interface/peripheral system is configured to:

a) alert a user, in case of pending hypoglycemia or hyperglycemia, by an audible tone and/or display of a text message;

b) alert other individuals equipped with an alarm, in case of pending hypoglycemia, using an alarm module;

c) determine the user'"'"'s location using a Global Positioning System module and, in case of hypoglycemia, transmits an emergency text message to a telephone number or relay biological analyte concentration data to a centralized server;

d) relay coded glucose concentration readings when they are taken to an insulin pump programmed to recognize the code and connected to the user, via the alarm module for the purpose of automatic release of insulin, or any combination thereof.

12. The apparatus of claim 1, wherein the at least one radiation source is fabricated from optical crystals, semiconductor material monolayer structures or any combination thereof.

13. The apparatus of claim 12, wherein a semiconductor pump source is integrated with a beam steering structure and a TPCOPO layer to achieve emission wavelength selection and intensity.

14. The apparatus of claim 13, wherein the at least one radiation source is comprised of a pair of GaAs Bragg reflectors with a GaAs TPCOPO active layer, a GaAs narrowband coherent source pump and GaAs Electro-Optical beam deflecting layer therebetween.

15. The apparatus of claim 14, wherein the pump source and beam steering structure are one of parallel to the TPCOPO layer along the entire length of a Bragg cavity or reside at one end of the Bragg cavity to allow for beam steering before launching the pump source into the Bragg cavity containing the TPCOPO layer.

16. The apparatus of claim 14, wherein separate electrical connection means are made to the pump layer and the GaAs Electro-Optical beam deflecting layer.

17. The apparatus of claim 14, wherein an applied electric current to the pump layer determines an intensity of emitted radiation.

18. The apparatus of claim 14, wherein an applied voltage to the GaAs Electro-Optical beam deflecting layer determines a wavelength of emitted radiation.

19. A method for a non-invasive sensing of biological analytes in a sample through spectrophotometric referencing utilizing two beams, each close in space, applicable to measuring interstitial fluid diffuse reflectance and comprising the steps of:

a) providing an optics system utilizing a first radiation source, a second radiation source, a first radiation detector and a second radiation detector, thereby establishing four optical beam paths close in space through the system;

b) modulating the sources with different time functions;

c) configuring the optics system in a manner in which all optical elements of the optics system transmit and/or reflect the beams;

d) separating a first pair of the beams and a second pair of the beams at one point in the system, focusing the first pair of beams on a user'"'"'s skin and focusing the second pair of beams into a reference sample;

e) demodulating signals produced by the first detector and the second detector and separating signals produced by the detectors from the beams; and

f) computing a spectrophotometric transmittance as a ratio of a first ratio to a second ratio.

20. The method of claim 19, wherein the first ratio is the ratio of a skin diffuse reflectance signal incident on the second radiation detector due to radiation from the first radiation source to a reference diffuse reflectance signal incident on the second radiation detector due to radiation of the second radiation source, and the second ratio is an instrument signal incident on the first radiation detector due to radiation of first radiation source to an instrument signal incident on the first radiation detector due to radiation of the second radiation source.

21. The method of claim 19, wherein the spectrophotometric transmittance is used to determine a concentration of biological analytes in the sample.

22. The method of claim 19, wherein the optics system has an area of separation between a sample beam and a reference beam that is restricted to an interior portion of an optical glass element.

23. The method of claim 22, wherein the area of separation between the sample beam and the reference beam is protected by an enclosure.

24. A method of spectrophotometric referencing that utilizes pulse differential spectroscopy applicable to capillary blood diffuse reflectance by:

a) providing an optics system with at least one optical path;

b) sampling one path that changes minutely close in time as the minimum and maximum photon path changes during a heart pulse;

c) synchronously detecting a time signal at each wavelength;

d) computing a spectrophotometric transmittance as a ratio of a maxima to a minima of a diffuse reflectance signal; and

e) determining a concentration of biological analytes in a sample using the spectrophotometric transmittance.