Optical analysis of biomedical specimens

• US 4,017,192 A
• Filed: 02/06/1975
• Issued: 04/12/1977
• Est. Priority Date: 02/06/1975
• Status: Expired due to Term

• Current Assignee: NIR Instruments Company
• Original Assignee: Neotec, Inc.
• Inventors: Rosenthal, Robert D.
• Primary Examiner(s): Corbin, John K.
• Assistant Examiner(s): Rosenberger, Richard A.
• Application Number:
  US05/547,658
• Time in Patent Office: 796 Days
• Field of Search: 356/39, 356/188, 356/51, 356/201
• US Class Current: 356/432
• CPC Class Codes: A61B 5/0059 using light, e.g. diagnosis by transillumination, diascopy, fluorescence A61B5/0093, A61B5/1455, A61B5/02416 and A61B5/0261 take precedence
• CPC Class Codes: G01J 2001/182 with SH sample and hold circuits
• CPC Class Codes: G01J 2003/1243 Pivoting IF or other position variation
• 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 21/35 using infrared light G01N21/39 takes precedence
• CPC Class Codes: G01N 21/59 Transmissivity G01N21/25 takes precedence

Abstract

A technique for automatic detection of abnormalities, particularly pathology, in biomedical specimens. Light transmittance or reflectance data over a large number of wavelengths for numerous samples are correlated mathematically with conventional clinical results to select test wavelengths and constants for a correlation equation. Optical instrumentation with an analog or digital computer applies the resulting correlation equation to the spectral data on a given specimen at the test wavelengths to determine quantitatively the presence of the abnormality.

Claims

1. A method of detecting pathological abnormality in a multicellular bulk biomedical specimen comprising the steps of recording and analyzing light absorption spectrum data of the multicellular bulk specimen in accordance with a mathematical expression which correlates the spectrum data of a multiplicity of corresponding biomedical samples with the results of typing of said samples by clinical pathology.

2. A method of detecting the presence of a pathological abnormality in a multicellular bulk biomedical specimen, comprising the steps of illuminating the multicellular bulk specimen sequentially with a plurality of difference light wavelengths, recording selected light absorption dependent values within the sample'"'"'s light output spectrum, computing the value of a mathematical function of said selected absorption-dependent values, said mathematical function being selected to produce a computed value which correlates with the presence or absence of said pathological abnormality, and comparing the level of the computed value to a predetermined screening level.

3. The method of claim 2, wherein said absorption-dependent values are light transmittance-dependent values.

4. The method of claim 3, wherein said transmittance-dependent values are optical density values at selected wavelengths.

5. The method of claim 3, wherein each said transmittance-dependent value is the ratio of a derivative of the transmittivity of the specimen and absolute transmissivity at a selected wavelength.

6. The method of claim 2, wherein said pathological abnormality is malignancy and said specimen is animal tissue.

7. The method of claim 6, werein each said absorption-dependent value is the ratio of a derivative of the transmissivity of the specimen and absolute transmissivity at a selected wavelength.

8. The method of claim 6, wherein said animal tissue is human cervical tissue.

9. The method of claim 6, wherein said animal tissue is rat liver tissue.

10. The method of claim 6, wherein said animal tissue is mouse bladder tissue.

11. The method of claim 6, wherein said animal tissue is human female reproductive organ tissue.

12. The method of claim 2, wherein said specimen is serum and said pathological abnormality therein is bacterial contamination.

13. The method of claim 2, wherein said wavelengths are all greater than 5,000 A.