Method and apparatus for multi-spectral analysis in noninvasive nir spectroscopy

• US 5,747,806 A
• Filed: 02/02/1996
• Issued: 05/05/1998
• Est. Priority Date: 02/02/1996
• Status: Expired due to Fees

• Current Assignee: GLT Acquisition Corporation
• Original Assignee: Instrumentation Metrics Inc.
• Inventors: Malin, Stephen F., Khalil, Gamal
• Primary Examiner(s): Hannaher, Constantine
• Application Number:
  US08/596,409
• Time in Patent Office: 823 Days
• Field of Search: 250/339.12, 250/341.8, 250/339.11, 250/339.09
• US Class Current: 250/339.12
• CPC Class Codes: A61B 5/14532 for measuring glucose, e.g. by tissue impedance measurement
• CPC Class Codes: A61B 5/1455 using optical sensors, e.g. spectral photometrical oximeters
• CPC Class Codes: G01N 21/314 with comparison of measurements at specific and non-specific wavelengths dual wavelength spectrometry G01J3/427
• CPC Class Codes: G01N 21/3577 for analysing liquids, e.g. polluted water
• CPC Class Codes: G01N 21/359 using near infrared light

Abstract

The concentration of an analyte present in a sample is determined using multi-spectral analysis in the near infrared range. Incident radiation containing a plurality of distinct, nonoverlapping regions of wavelengths in the range of approximately 1100 to 3500 nm is used to scan the sample. Diffusively reflected radiation emerging from the sample is detected, and a value indicative of the concentration of the analyte is obtained using an application of chemometrics techniques. Information obtained from each nonoverlapping region of wavelengths can be cross-correlated to remove background interferences.

Claims

1. An apparatus for determining the concentration of an analyte in a sample, comprising:

(a) means for irradiating the sample with incident radiation containing a plurality of distinct, nonoverlapping regions of wavelengths in the range of approximately 1100 to 3500 nm;

(b) means for collecting reflected radiation emerging from the sample and directing said reflected radiation into first and second light paths, wherein the first light path comprises radiation from a first region of wavelengths;

(c) first filter means disposed in the first light path, wherein the first filter means is capable of selectively passing radiation having substantially no correlation with the concentration of the analyte;

(d) first detection means for receiving selectively passed radiation emerging from the first filter means, and means for converting the same into a signal representative of the intensity of said radiation;

(e) adjustable filter means disposed in the second light path, wherein the adjustable filter means attenuates the intensity of radiation in the second light path;

(f) principal analyte filter means capable of receiving attenuated radiation emerging from the adjustable filter means, and selectively passing one or more independent wavelengths therefrom, wherein the said one or more independent wavelengths are specifically correlated with the concentration of the analyte;

(g) second filter means capable of receiving the one or more independent wavelengths emerging from the principal analyte filter means and attenuating the intensity of each independent wavelength;

(h) second detection means for receiving the attenuated independent wavelengths emerging from the second filter means; and

(i) means for converting the detected wavelengths into a signal representative of the intensity of said wavelengths.

2. The apparatus of claim 1, wherein the first filter means comprises a narrow band-pass filter.

3. The apparatus of claim 2, wherein the adjustable filter means comprises a neutral density filter used in concert with correlation filters in a filter system.

4. The apparatus of claim 3, wherein the signal obtained from the first detection means is used to regulate attenuation provided by the adjustable filter means.

5. The apparatus of claim 1, wherein the second filter means comprises a neutral density filter used in concert with correlation filters in a filter system.

6. The apparatus of claim 5, wherein the attenuation provided by the second filter means is established using weighting factors.

7. The apparatus of claim 6, wherein the weighting factors are derived using chemometrics techniques.

8. The apparatus of claim 7, wherein the weighting factors are derived using rotated principal components analysis of an absorption spectrum of the analyte.

9. The apparatus of claim 1, wherein the sample comprises body tissue and the analyte comprises an organic blood analyte.

10. The apparatus of claim 9, wherein the blood analyte is selected from the group consisting of glucose, urea (BUN), lipids, bilirubin and ethyl alcohol.

11. The apparatus of claim 9, wherein the blood analyte is glucose.

12. An apparatus for determining the concentration of an analyte in a sample, comprising:

(a) a source capable of emitting near infrared radiation containing a plurality of distinct, nonoverlapping regions of wavelength in the range of approximately 1100 to 3500 nm;

(b) means for dividing radiation emerging from the source of part (a) into first and second beam paths;

(c) means for irradiating the sample with the radiation in the first beam path, thereby providing reflected radiation;

(d) means for collecting the reflected radiation emerging from the sample and directing said reflected radiation into a reflected light path;

(e) a first optical transfer cell disposed in the reflected light path, said first cell comprising first positive correlation filter means having absorption characteristics adapted to accept the reflected radiation and emphasize one or more wavelengths from the reflected radiation, wherein said one or more wavelengths have high correlation with the concentration of the analyte in the sample;

(f) means for receiving the one or more emphasized wavelengths from the first optical transfer cell and for converting the same into signals representative of the intensity of said emphasized wavelengths;

(g) a second optical transfer cell disposed in the second beam path, said second cell comprising neutral density filter means having absorption characteristics sufficient to attenuate the intensity of the radiation from the second beam path equally over a selected range of near infrared wavelengths;

(h) means for receiving attenuated radiation from the second optical transfer cell and for converting the same into signals representative of the intensity thereof; and

(i) means for calculating the concentration of the analyte in the sample using the signals generated by parts (f) and (h).

13. The apparatus of claim 12, wherein the means for calculating the concentration of the analyte in the sample converts the signals generated by parts (f) and (h) into a digital signal indicative of the ratio of the intensity of the radiation emerging from the source and corresponding radiation emerging from the sample.

14. The apparatus of claim 12, wherein the means for calculating the concentration of analyte in the sample comprises means for applying a chemometrics algorithm to the signals generated by parts (f) and (h).

15. The apparatus of claim 12, wherein the first positive correlation filter means comprises a plurality of layers, each layer having selected absorption characteristics such that said filter means emphasizes a population of wavelengths having high correlation with the analyte concentration.

16. The apparatus of claim 12, wherein the sample comprises body tissue and the analyte comprises an organic blood analyte.

17. The apparatus of claim 16, wherein the blood analyte is selected from the group consisting of glucose, urea (BUN), lipids, bilirubin and ethyl alcohol.

18. The apparatus of claim 16, wherein the blood analyte is glucose.

19. An apparatus for determining the concentration of an analyte in a sample, comprising:

(a) a source capable of emitting near infrared radiation containing a plurality of distinct, nonoverlapping regions of wavelength in the range of approximately 1100 to 3500 nm;

(b) means for dividing radiation emerging from the source of part (a) into first and second beam paths;

(c) means for irradiating the sample with the radiation in the first beam path, thereby providing reflected radiation;

(d) means for collecting the reflected radiation emerging from the sample and directing said reflected radiation into a reflected light path;

(e) a first optical transfer cell disposed in the reflected light path, said first cell comprising first positive correlation filter means having absorption characteristics adapted to accept the reflected radiation and emphasize one or more wavelengths from the reflected radiation, wherein said one or more wavelengths have high correlation with the concentration of the analyte in the sample;

(f) means for receiving the one or more emphasized wavelengths from the first optical transfer cell and for converting the same into signals representative of the intensity of said emphasized wavelengths;

(g) a second optical transfer cell disposed in the second beam path, said second cell comprising a second positive correlation filter means having absorption characteristics identical to those of the first positive correlation filter means;

(h) means for receiving attenuated radiation from the second optical transfer cell and for converting the same into signals representative of the intensity thereof; and

(i) means for calculating the concentration of the analyte in the sample using the signals generated by parts (f) and (h).

20. The apparatus of claim 19, wherein the first positive correlation filter means comprises a plurality of layers, each layer having selected absorption characteristics such that said filter means emphasizes a population of wavelengths having high correlation with the analyte concentration.

21. The apparatus of 20, wherein the absorption characteristics of at least one layer from the first and second positive correlation filter means are established using weighting factors.

22. The apparatus of claim 21, wherein the weighting factors are derived using chemometrics techniques.

23. The apparatus of claim 22, wherein the weighting factors are derived using rotated principal components analysis of an absorption spectrum of the analyte.