Method and device for glucose concentration measurement with special attention to blood glucose determinations

• US 6,999,808 B2
• Filed: 06/08/2001
• Issued: 02/14/2006
• Est. Priority Date: 06/12/1997
• Status: Expired due to Term

• Current Assignee: Alan J. Leszinske
• Original Assignee: Alan J. Leszinske
• Inventors: Gobeli, Garth W., Leszinske, Alan J.
• Primary Examiner(s): WINAKUR, ERIC FRANK
• Application Number:
  US09/878,307
• Publication Number:
  US 20010031914A1
• Time in Patent Office: 1,712 Days
• Field of Search: 600/310, 600/316, 600/318, 600/319, 600/322
• US Class Current: 600/319
• CPC Class Codes: A61B 3/10 Objective types, i.e. instruments for examining the eyes independent of the patients' perceptions or reactions
• CPC Class Codes: A61B 5/14507 specially adapted for measuring characteristics of body fluids other than blood devices for taking samples of body liquids A61B10/0045
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/14558 by polarisation

Abstract

The concentration of glucose in the anterior chamber of an eye is non-invasively measured by guiding a beam through a polarizer (4), a quarter wave plate (6), a polarization modulator (20), and an analyzer (7). After initializing the polarizer and the analyzer to extinguish the beam, it is guided parallel to the iris (56) of the eye (50) and introduced into the anterior chamber (57), wherein it is refracted, impinges on and is reflected from the iris, and exits the anterior chamber approximately collinear with the portion (55A) of the beam incident on the anterior chamber. The beam then is guided onto a detector (10), and a sufficient signal is applied to the polarization modulator to extinguish the beam. The signal represents the glucose concentration in the patient'"'"'s blood.

Claims

1. A method of measuring concentration of an optically active substance in the anterior chamber of an eye, comprising the steps of:

(a) guiding a polarized beam so it is generally parallel to a reflective interior surface of the eye;

(b) introducing the beam into the anterior chamber such that it is refracted within the anterior chamber, impinges on the reflective interior surface, is reflected therefrom, and then exits the anterior chamber approximately collinear with the beam immediately before the point at which it is introduced into the anterior chamber;

(c) guiding the beam exiting from the anterior chamber through an analyzer and onto a detector; and

(d) applying a signal to a polarization modulator to extinguish light passing from the analyzer to the detector, the signal representing the concentration of the optically active ingredient in the anterior chamber.

2. The method of claim 1 including the step of adjusting the orientation of a portion of the beam incident on a cornea of the eye until a stable, substantially increased output signal level is produced by the detector.

3. The method of claim 1 wherein the optically active substance includes glucose.

4. The method of claim 1 including calibrating the analyzer to extinguish light passing from the analyzer to the detector before performing step (a).

5. The method of claim 4 wherein step (d) includes simultaneously applying a DC signal and an AC signal to the polarization modulator to extinguish light of the beam to prevent it from passing from the analyzer to the detector by shifting the DC signal to a value that produces a null in the AC component of a corresponding output signal produced by the detector, the value of the shifted DC signal then representing the glucose concentration in the anterior chamber.

6. A method of measuring concentration of an optically active substance in the anterior chamber of an eye, comprising the steps of:

(a) guiding a beam through a polarizer oriented in a first direction to polarize the light in a first direction, and then through a polarization modulator and an analyzer oriented in the second direction to polarize the light in a second direction, and then guiding the beam from the analyzer to a detector;

(b) adjusting at least one of the polarizer and the analyzer to extinguish light of the beam to prevent it from passing from the analyzer to the detector;

(c) guiding the beam, after it passes through the polarizer, so it is generally parallel to a reflective interior surface of the eye and then introducing the beam into the anterior chamber such that it is refracted within the anterior chamber and impinges on the reflective interior surface, is reflected therefrom, and then exits the anterior chamber approximately collinear with the beam immediately before the point at which it is introduced into the anterior chamber;

(d) guiding the beam exiting from the anterior chamber onto the detector; and

(e) modifying a signal applied to the polarization modulator to extinguish light passing from the analyzer to the detector, the amount of modification of the signal representing the concentration of the optically active ingredient in the anterior chamber.

7. The method of claim 6 including the step of adjusting the orientation of a portion of the beam incident on a cornea of the eye until a stable, substantially increased output signal level is produced by the detector.

8. The method of claim 6 wherein the optically active substance includes glucose.

9. The method of claim 6 wherein step (e) includes simultaneously applying a DC signal and an AC signal to the polarization modulator to extinguish light of the beam to prevent it from passing from the analyzer to the detector by shifting the DC signal to a value that produces a null in the AC component of a corresponding output signal produced by the detector, the value of the shifted DC signal then representing the glucose concentration in the anterior chamber.

10. The method of claim 6 wherein step (b) is performed before step (e).

11. A system for measuring concentration of an optically active substance in an anterior chamber of the eye, comprising in combination:

(a) a light source producing a beam;

(b) a polarizer oriented in a first direction to polarize light of the beam in a first direction;

(c) a polarization modulator transmitting the beam after is has passed through the polarizer;

(d) an analyzer polarizing light from the polarization modulator in a second direction;

(e) a detector receiving light from the analyzer;

(f) a first optical structure introducing the beam, after it passes through the polarizer, into the anterior chamber generally parallel to a reflective interior surface of the eye so that the beam is refracted within the anterior chamber and impinges onto the reflective interior surface, is reflected from the reflective interior surface, and then exits the anterior chamber approximately collinear with the introduced beam;

(g) a second optical structure receiving the beam after it exits the anterior chamber and guiding it to the detector; and

(h) a polarization modulator control device coupled to a control terminal of the polarization modulator and operative to shift a DC bias signal applied to the polarization modulator to extinguish light of the beam to prevent it from passing from the analyzer to the detector.

12. The system of claim 11 wherein the polarization modulator control device is operative to simultaneously apply a DC signal and an AC signal to the polarization modulator to extinguish any light passing through the analyzer to the detector by shifting the DC signal to a value that extinguishes any AC component of an output signal produced by the detector, the value of the shifted DC signal then representing the concentration of the optically active ingredient in the anterior chamber.

13. The system of claim 12 wherein the polarization modulator includes a Kerr cell.

14. The system of claim 12 wherein the polarization modulator includes a Pockels cell.

15. The system of claim 11 wherein the optically active substance includes glucose.

16. A method of measuring glucose concentration in a sample, comprising the steps of:

(a) passing a beam of collimated light through a polarizer oriented in a first direction to polarize the light in the first direction, a polarization modulator, an analyzer oriented in a second direction to polarize the light in a second direction, and a focusing lens, and then to a detector;

(b) adjusting at least one of the polarizer and the analyzer to extinguish any light passing from the analyzer to the detector;

(c) locating the sample between the polarizer and the analyzer; and

(d) simultaneously applying a DC signal and an AC signal to the polarization modulator to extinguish any light passing from the analyzer to the detector, by shifting the DC signal to a value that produces a null in the AC component of an output signal produced by the detector, the value of the shifted DC signal then representing the glucose concentration in the sample,

the method including passing the beam through the aqueous humor of a human eye so that a portion of the beam passing through the aqueous humor is approximately parallel to a reflective interior surface of the eye.

17. A method of measuring glucose concentration in a sample, comprising the steps of:

(a) passing a beam of collimated light through a polarizer oriented in a first direction to polarize the light in the first direction, a polarization modulator, an analyzer oriented in a second direction to polarize the light in a second direction, and a focusing lens, and then to a detector;

(b) adjusting at least one of the polarizer and the analyzer to extinguish any light passing from the analyzer to the detector;

(c) locating a sample, namely a portion of a person'"'"'s skin in vivo, between the polarizer and the analyzer; and

(d) simultaneously applying a DC signal and an AC signal to the polarization modulator to extinguish any light passing from the analyzer to the detector, by shifting the DC signal to a value that produces a null in the AC component of an output signal produced by the detector, the value of the shifted DC signal then representing the glucose concentration in the sample.

18. The method of claim 17 wherein the ratio of the magnitude of the AC signal to the magnitude of the DC signal is in the range from about 10,000 to about 1,000,000.