Electromagnetic method and apparatus to measure constituents of human or animal tissue

Claims

We claim:

1. A non-invasive method for measuring the concentration of analytes in living tissue containing fluids, comprising the steps of:

a) illuminating the tissue with an electromagnetic beam comprised of alternate periods of monochromatic wavelengths, one of the alternate periods having a wavelength that is absorbed by the analyte, and the other alternate period having a wavelength selected so as to have an extinction coefficient in the tissue identical with that of the first wavelength;

b) detecting the electromagnetic beam after reaction with the tissue to produce a first electrical signal;

c) adjusting the intensity relation between wavelength periods of the illuminating beam so as to produce a substantially zero alternating component in the first electrical signal;

d) varying the balance of analyte present in the tissue; and

e) detecting an alternating component of the beam that has interacted with the tissue to generate a second electrical signal proportional to the concentration of analyte in the tissue; and

f) calculating the concentration of the analyte in the tissue.

2. The method according to claim 1 where the residual amplitude of the alternating component, if there is any remaining after step (c), is recorded and used to calculate the concentration of the analyte.

3. The method according to claim 1 wherein varying the balance of analyte includes changing tissue thickness.

4. The method according to claim 3 wherein the tissue thickness change is substantially equal to the inverse of the extinction coefficient of the tissue at the wavelengths used.

5. The method according to claim 4 wherein the tissue thickness change is repeated cyclically, and the second electrical signal variation over the cycle is used as a measure of the concentration of the analyte in blood.

6. The method according to claim 1 wherein varying the balance of analyte is accomplished by the normal pulsatile cycle produced by the heart beat.

7. The method according to claim 1, whereby, before illuminating the sample with the electromagnetic beam, the tissue is illuminated by a radiation transmitting means with a pulsed beam containing only one of the two alternating wavelengths, and the radiation that has interacted with the sample is detected with a radiation detecting means to produce a third electrical signal.

8. The method according to claim 7 whereby at the beginning of the measurement, the thickness of the tissue between the radiation transmitting means and the radiation detecting means is decreased gradually until the amplitude of the transmitted radiation pulse train attains a predetermined value.

9. The method according to claim 7 whereby the third electrical signal is recorded and the second electrical signal obtained in step e) of claim 1 is normalized by dividing it by the third electrical signal.

10. The method according to claim 1 wherein the electromagnetic beam traverses the tissue.

11. The method according to claim 1 wherein the electromagnetic beam is reflected from the tissue.

12. The method according to claim 1 wherein the analyte is a heterologous material.

13. The method according to claim 1 wherein the analyte is a homologous material.

14. The method of claim 1 wherein the analyte is glucose and the alternate wavelengths are 2155 nm and 2272 nm.

15. A non-invasive apparatus for measuring the concentration of analytes in a living tissue, comprising:

a) a source of electromagnetic radiation for illuminating the tissue with an electromagnetic beam comprised of alternate periods of different wavelengths, one of the alternate periods having a first wavelength that is absorbed by the analyte, and the other alternate period having a wavelength selected so as to have an extinction coefficient in the tissue identical with that of said first wavelength;

b) a detector means for detecting the electromagnetic beam after reaction with the tissue to produce a first electrical signal proportional to the intensity of said electromagnetic beam; and

c) intensity control means for adjusting the intensity relation between wavelength periods of the illuminating beam so as to produce, a reference level component in the first electrical signal when a minimum level of analyte is present in the tissue;

d) whereby the first electrical signal when analyte is present is proportional to the concentration of analyte in the tissue.

16. The apparatus according to claim 15 wherein the radiation source comprises a master source and a slave source, each generating a beam of light which beams are combined to form said alternating periods of different wavelengths.

17. The apparatus according to claim 16 wherein the master source and slave source comprise incandescent lamps with filters for passing monochromatic light of different wavelengths .lambda..sub.1 and .lambda..sub.2.

18. The apparatus of claim 17 wherein .lambda..sub.1 is 2155 nm and .lambda..sub.2 is 2272 nm and the analyte is glucose.

19. The apparatus of claim 15 including means for changing tissue thickness to produce the minimal level of analyte in the tissue.

20. The apparatus according to claim 19 wherein the tissue thickness change is substantially equal to the inverse of the extinction coefficient of the tissue at the wavelengths used.

21. A non-invasive apparatus for measuring the concentration of analytes in a living tissue, comprising:

a) a source of electromagnetic radiation for illuminating the tissue with an electromagnetic beam comprised of alternate periods of different wavelengths, one of the alternate periods having a first wavelength that is absorbed by the analyte, and the other alternate period having a wavelength selected so as to have an extinction coefficient in the tissue identical with that of said first wavelength;

b) a detector means for detecting the electromagnetic beam after reaction with the tissue to produce a first electrical signal proportional to the intensity of said electromagnetic beam; and

c) analyte level changing means for changing the level of analyte in the tissue;

d) intensity control means for adjusting the intensity relation between wavelength periods of the illuminating beam so as to produce, a reference level component in the first electrical signal when a minimum level of analyte is present in the tissue whereby the first electrical signal when analyte is present is proportional to the concentration of analyte in the tissue;

e) temperature control means for maintaining the temperature of the tissue substantially constant during measurement.

22. The apparatus according to claim 21 wherein the radiation source comprises a master source and a slave source, each generating a beam of light which beams are combined to form said alternating periods of different wavelengths and fiber optic means for transmitting the combined beam to the tissue.

23. The apparatus according to claim 22 wherein the master source and slave source comprise incandescent lamps with filters for passing monochromatic light of different wavelengths .lambda..sub.1 and .lambda..sub.2.

24. The apparatus of claim 23 wherein .lambda..sub.1 is 2155 nm and .lambda..sub.2 is 2272 nm and the analyte is glucose.

25. The apparatus of claim 21 wherein the analyte level changing means includes means for changing tissue thickness to produce the change in level of analyte in the tissue.

26. The apparatus of claim 21 wherein the temperature control means includes a pair of oppositely disposed thermally conductive bodies disposed opposite each other with a variable gap between them, into which gap the tissue is adapted to be placed and wherein the temperature of the bodies is sensed and controlled.

27. The apparatus of claim 26 including an opening through said bodies for passing the radiation beam through the tissue for detection.

28. The apparatus of claim 27 wherein the analyte level changing means comprises actuator means for moving one body relative to the other to squeeze said tissue.