Illumination device and method for spectroscopic analysis

• US 6,862,091 B2
• Filed: 04/11/2001
• Issued: 03/01/2005
• Est. Priority Date: 04/11/2001
• Status: Expired due to Fees

• Current Assignee: Rio Grande Medical Technologies Incorporated
• Original Assignee: Inlight Solutions, Inc.
• Inventors: Johnson, Robert D.
• Primary Examiner(s): Lee, Diane I.
• Assistant Examiner(s): Lee, Seung H
• Application Number:
  US09/832,586
• Publication Number:
  US 20030007147A1
• Time in Patent Office: 1,420 Days
• Field of Search: 356319-323, 356325-326, 356/328
• US Class Current: 356/326
• CPC Class Codes: G01J 3/02 Details
• CPC Class Codes: G01J 3/0216 using light concentrators or collectors or condensers
• CPC Class Codes: G01J 3/0218 using optical fibers
• CPC Class Codes: G01J 3/10 Arrangements of light sources specially adapted for spectrometry or colorimetry
• CPC Class Codes: G02B 27/0927 Systems for changing the beam intensity distribution, e.g. Gaussian to top-hat
• CPC Class Codes: G02B 27/0994 Fibers, light pipes optical fibers per se G02B6/02
• CPC Class Codes: G02B 6/4206 Optical features G02B6/4207, G02B6/421 take precedence
• CPC Class Codes: G02B 6/4298 coupling with non-coherent light sources and/or radiation detectors, e.g. lamps, incandescent bulbs, scintillation chambers

Abstract

An illumination subsystem for use in optical analysis which provides spatially and angularly homogenized radiation to the sample being analyzed. The system eliminates the illumination system as an interferent in the overall optical analysis. Thus, modest translations or rotations of the illumination source or changing the illumination source does not require recalibration of the instrument or prior modeling of illumination variability due to such changes. Illumination stability is achieved by incorporating a light pipe which both angularly and spatially homogenizes the light. Further, a series of filters and/or lenses are incorporated to provide bandpass filtering which eliminates unwanted wavelengths or bands of wavelengths from contacting the tissue and allows for a higher signal-to-noise ratio when the sample is tissue, while preventing thermal damage.

Claims

1. A spectroscopic system for measuring analyte concentration in a sample, the system comprising:

a radiation source emitter, the emitter emitting radiation;

a radiation homogenizer disposed to receive at least a portion of said emitted radiation, wherein the homogenizer angularly and spatially homogenizes at least a portion of said emitted radiation, wherein said homogenized radiation illuminates said sample; and

a sample source, the sample source having an analyte; and

a detector for receiving at least a portion of the radiation subsequent to interacting with said sample.

2. The spectroscopic system of claim 1, wherein the radiation source emitter is a tungsten-halogen lamp.

3. The spectroscopic system of claim 1, wherein the emitted radiation possesses a band of wavelengths within the infrared regions of the electromagnetic spectrum.

4. The spectroscopic system of claim 1, wherein the spectroscopic system includes a means for concentrating the radiation emitted by the radiation source emitter.

5. The spectroscopic system of claim 1, wherein the spectroscopic system includes a means for channeling the emitted radiation to the sample source.

6. The spectroscopic system of claim 5, wherein the channeling means is at least one fiber optic wire.

7. The spectroscopic system of claim 5, wherein the channeling means is at least one mirror.

8. The spectroscopic system of claim 5, wherein the channeling means is at least one optic lens.

9. The spectroscopic system of claim 1, wherein the radiation homogenizer is a light pipe, wherein the light pipe has a proximal end, a distal end, and a length of material therebetween, the light pipe further having a cross-sectional area.

10. The spectroscopic system of claim 9, wherein the light pipe includes a plurality of bends.

11. The spectroscopic system of claim 10, wherein the plurality of bends form an S-shaped bend.

12. The spectroscopic system of claim 9, wherein the cross-sectional area of the light pipe is polygonal in shape.

13. The spectroscopic system of claim 1, wherein the sample is biological tissue.

14. The spectroscopic system of claim 1, wherein the sample is a human appendage, or a portion thereof.

15. The spectroscopic system of claim 1, wherein the analyte measured is glucose.

16. The spectroscopic system of claim 1, wherein the analyte measured is alcohol.

17. The spectroscopic system of claim 1, wherein the spectroscopic system includes at least one bandpass filter.

18. A method for homogenizing radiation for spectroscopic analysis, the method comprising the steps of:

providing a spectroscopic system, wherein the system comprises a radiation source emitter, a radiation homogenizer, a sample having an analyte concentration, and a radiation detector;

emitting radiation by means of the radiation source emitter;

angularly homogenizing the emitted radiation;

spatially homogenizing the emitted radiation;

illuminating the sample source with the homogenized radiation; and

detecting the analyte concentration within the sample source.

19. The method for homogenizing radiation for spectroscopic analysis of claim 18, wherein the radiation homogenizer is a light pipe.

20. An optical measurement system used to measure an analyte or attribute in a biological system, the system comprising:

a spectrometer including a source and a collection system;

a sampling system for performing reflectance measurements on tissue;

a measurement system for measuring multiple wavelengths in the range for 4000 cm<sup>−

1</sup> to 7500 cm<sup>−

1</sup>;

a prediction process that uses multiple variables obtained from the measurement system; and

an illumination system that does not introduce prediction errors of clinical significance when used in a standard manner.

21. The illumination system of claim 20, wherein the illumination system uses both angular and spatial homogenization of the source output.

22. The system of claim 21, wherein standard operation would include bulb aging and replacement of the bulb.

23. The system of claim 21, wherein the analyte of interest is glucose and a prediction error of clinical significance is 10 mg/dl.