Method of and apparatus for investigating tissue histology

• US 7,647,085 B2
• Filed: 06/13/2005
• Issued: 01/12/2010
• Est. Priority Date: 11/19/1996
• Status: Expired due to Fees

• Current Assignee: MedX Health Corporation
• Original Assignee: Astron Clinica Ltd. (Boston Scientific Corporation)
• Inventors: Cane, Michael Roger, Beadman, Michael Andrew, Cotton, Symon D'Oyly
• Primary Examiner(s): Casler; Brian
• Assistant Examiner(s): Shahrestani; Nasir
• Application Number:
  US11/151,389
• Publication Number:
  US 20050251049A1
• Time in Patent Office: 1,674 Days
• Field of Search: 600/407, 600/473, 600475-478, 600/410, 382/128
• US Class Current: 600/410
• 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: A61B 5/0075 by spectroscopy, i.e. measuring spectra, e.g. Raman spectroscopy, infrared absorption spectroscopy A61B5/0071 takes precedence
• CPC Class Codes: A61B 5/1072 measuring distances on the body, e.g. measuring length, height or thickness A61B5/1076 takes precedence
• CPC Class Codes: A61B 5/1075 for measuring dimensions by non-invasive methods, e.g. for determining thickness of tissue layer A61B8/0858 takes precedence
• CPC Class Codes: A61B 5/443 Evaluating skin constituents, e.g. elastin, melanin, water
• CPC Class Codes: A61B 5/444 Evaluating skin marks, e.g. mole, nevi, tumour, scar
• CPC Class Codes: A61B 5/445 Evaluating skin irritation or skin trauma, e.g. rash, eczema, wound, bed sore
• 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 21/359 using near infrared light

Abstract

Apparatus for monitoring the presence of one or more chromophores in a tissue sample, comprises a light source for projecting light to illuminate an area of such tissue sample, a photo-receptor for receiving light remitted by the illuminated area of tissue, and spectroscopic analyzer means for monitoring the remitted light, a comparator having means for comparing variations in the intensity and spectral characteristics of the remitted light with respect to the intensity and spectral characteristics of the projected light at different wavelengths and with a record of the intensity and spectral characteristics of light remitted by a reference sample of such tissue and means for emitting a control signal in response to any such variations. Methods of analyzing tissue histology, especially skin histology, are discussed, and a mathematical model is proposed for the analysis and comparison of the remitted light with a reference sample.

Claims

1. Apparatus for monitoring the presence of individual chromophores in a tissue sample, said apparatus comprising:

a light source configured to illuminate an area of a tissue sample with different wavelengths of light;

a photo-receptor configured to receive light re-emitted by an area of a tissue sample illuminated by said light source; and

a spectroscopic analyzer configured to utilize the spectral characteristics of re-emitted light received by said photo-receptor and the spectral characteristics of light projected by said light source to identify the presence of said one or more chromophores within the area of the illuminated tissue sample from which re-emitted light is received by said photo-receptor, wherein said spectroscopic analyzer comprises;

records of the spectral characteristics of light re-emitted by reference samples of known structure containing identified chromophores;

said spectroscopic analyzer being configured to compare the spectral characteristics of re-emitted light received by said photo-receptor with said records to identify the record including spectral characteristics most closely matching the characteristics of said re-emitted light received by said photo-receptor and to output as an identification of individual chromophores present in the area of the illuminated tissue sample from which re-emitted light is received by said photo-receptor an identification of the chromophores associated with said spectral characteristics by said record.

2. Apparatus in accordance with claim 1, wherein said records comprise records of the spectral characteristics of light remitted by reference samples of epithelial or epithelial and sub-epithelial tissue.

3. Apparatus in accordance with claim 2, wherein said records comprise records of the spectral characteristics of light remitted by reference samples of skin.

4. Apparatus in accordance with claim 1, wherein said records comprise records of the spectral characteristics of light remitted by reference samples of normal healthy tissue.

5. Apparatus in accordance with claim 1, wherein said records comprise records of calculated estimated spectral characteristics of light re-emitted by samples of tissue of known structure containing identified chromophores.

6. Apparatus in accordance with claim 1 wherein said light source is operable to selectively illuminate an area of a tissue sample with different wavelengths of light.

7. Apparatus in accordance with claim 6, wherein said light source further comprises a set of filters for selective substitution into the tissue-incident light path in order to selectively illuminate an area of tissue with different wavelengths of light.

8. Apparatus in accordance with claim 1, wherein said light source further comprises a polarizing filter arranged to polarize the light which illuminates said area of tissue.

9. Apparatus in accordance with claim 8, further comprising a cross-polarizing filter arranged to cross-polarize light remitted from said area of tissue before it is received by said photo-receptor.

10. Apparatus in accordance with claim 1, wherein said light source is operable to illuminate said area of tissue with light having a wavelength in excess of 600 nm.

11. Apparatus in accordance with claim 1, wherein said photo-receptor is operable to detect re-emitted light having wavelengths in the 800 to 1000 nm band and the 600 to 800 nm band.

12. Apparatus in accordance with claim 1, wherein said photo-receptor is operable to receive light remitted from an array of points and said spectroscopic analyzer is operable to identify the presence of one or more individual chromophores at each of said points in said array.

13. Apparatus in accordance with claim 12, wherein said photo-receptor is operable to receive light remitted from points with a resolution of at least 20 lines or dots per mm.

14. Apparatus in accordance with claim 1 wherein said spectroscopic analyzer is operable to determine on the basis of the spectral characteristics of said received re-emitted light the depth of papillary dermis of a tissue sample being monitored and to identify the presence of said one or more individual chromophores within the area of the illuminated issue sample from which re-emitted light is received by said photo-receptor utilizing the spectral characteristics of said received re-emitted light and said determined depth of papillary dermis.

15. Apparatus in accordance with claim 1 wherein said light source, photo-receptor and spectroscopic analyzer are together adapted to generate a signal indicative of the presence of chromophores which is substantially independent to the variation of spectral characteristics of re-emitted light arising due to the presence of a predetermined chromophore.

16. Apparatus in accordance with claim 15 wherein said light source and photo-receptor are arranged to project and detect light at wavelengths which are substantially unaffected by the presence of a predetermined chromophore.

17. Apparatus in accordance with claim 15 wherein said spectroscopic analyzer is arranged to process data indicative of the spectral characteristics of re-emitted light received by said photo-receptor to generate signals which are indicative of the presence of chromophores which are substantially independent of the variation in spectral characteristics arising due to the presence of a predetermined chromophore.

18. Apparatus in accordance with claim 15, wherein said light source and photo-receptor are arranged to project and detect light at wavelengths which are substantially unaffected by the presence of a predetermined chromophore, and wherein said predetermined chromophore comprises a chromophore selected from the group consisting of melanin, blood and tattoo pigments.

19. Apparatus according to claim 1, further comprising a light guide of which a least part is flexible provided for conducting light between said light source, said tissue sample and said photo-receptor.

20. Apparatus according to claim 19, wherein said light guide comprises an endoscope.

21. Apparatus according to claim 19, wherein said light guide terminates in a head adapted for placing against an area of skin.

22. Apparatus according to claim 1, wherein said light source is operable to vary the size of the area of tissue from which re-emitted light is received.

23. Apparatus in accordance with claim 1, wherein said light source is operable to project light which either has a wavelength sufficiently far into the infra-red that its absorption by melanin and blood is negligible, or which has at least two wavelengths of which at least one is in excess of 600 nm, wherein said spectroscopic analyzer is operable to process data indicative of the spectral characteristics of re-emitted light received by said photo receiver to determine variations in spectral characteristics arising independently of variations due to the presence of melanin and blood and to utilize said determined independent variations in spectral characteristics to generate a signal indicative of the concentration of collagen within the papillary dermis of a tissue sample being monitored.

24. Apparatus in accordance with claim 1 further comprising a signal generator operable to generate control signals on the basis of the determination of the presence of one or more chromophores in a tissue sample by said spectroscopic analyzer, wherein said control signals are operable to control an apparatus selected from a display monitor, a printer, a medical laser and a treatment device.

25. A method of monitoring the presence of individual chromophores in a tissue sample, comprising:

illuminating an area of a tissue sample with different wavelengths of light using a light source;

receiving light re-emitted by an area of a tissue sample illuminated by said light source with a photo-receptor; and

operating a spectroscopic analyzer to utilize the spectral characteristics of re-emitted light received by said photo-receptor and the spectral characteristics of light projected by said light source to identify the presence of said chromophores within the area of the illuminated tissue sample from which re-emitted light is received by said photo-receptor, the operating of said spectroscopic analyzer including;

recording the spectral characteristics of light re-emitted by reference samples of tissue of known structure containing identified chromophores, and

arranging said spectroscopic analyzer to compare the spectral characteristics of re-emitted light received by said photo-receptor with said records to identify the record including spectral characteristics most closely matching the characteristics of said re-emitted light received by said photo-receptor and to output as an identification of individual chromophores present in the area of the illuminated tissue sample from which re-emitted light is received by said photo-receptor an identification of the chromophores associated with said spectral characteristics by said record; and

deriving data relating to the presence, depth, and concentration of chromophores and creating and displaying a map thereof.

26. The method according to claim 25, further comprising

deriving data relating to the presence, depth, and concentration of any chromophore selected from the group consisting of:

melanin, blood, hemoglobin, oxy-hemoglobin, bilirubin, tattoo pigments or dyestuffs, keratin, collagen and hair.

27. The method according to claim 25, further comprising mapping the extent of a basal cell carcinoma.

28. A method of monitoring the presence of individual chromophores in a sample of tissue, comprising:

storing records of the spectral characteristics of light re-emitted by reference samples of tissue of known structure containing identified chromophores;

illuminating an area of a tissue sample with different wavelengths of light using a light source;

receiving light re-emitted by the illuminated area of tissue at a photo-receptor;

comparing the spectral characteristics of re-emitted light received by said photo-receptor with said records to identify the record including spectral characteristics most closely matching the characteristics of said re-emitted light received by said photo-receptor; and

outputting as an identification of the individual chromophores present in the area of the illuminated tissue sample from which re-emitted light is received by said photo-receptor an identification of the chromophores associated with said spectral characteristics by said record.

29. A method according to claim 28, wherein the storing of the records includes storing records of the spectral characteristics of light remitted by reference samples of epithelial or epithelial and sub-epithelial tissue.

30. A method according to claim 29, wherein the storing of the records includes storing records of the spectral characteristics of light remitted by reference samples of skin.

31. A method according to claim 28, wherein the storing of the records includes storing records of the spectral characteristics of light remitted by reference samples of normal healthy tissue.

32. A method according to claim 28, wherein the storing of the records includes storing records of calculated estimated spectral characteristics of light re-emitted by samples of tissue containing identified chromophores.

33. A method according to claim 28, further comprising the steps of:

deriving data relating to the presence, depth, and concentration of chromophores; and

creating and displaying a map thereof.

34. A method according to claim 28, comprising:

deriving data relating to the presence, depth, and concentration of any chromophore selected from the group consisting of;

melanin, blood, hemoglobin, oxy-hemoglobin, bilirubin, tattoo pigments or dyestuffs, keratin, collagen and hair.

35. A method according to claim 28 which further comprising:

passing projected light and/or the remitted light through one or more filters and spectroscopically analyzing the remitted light such that the result of the analysis is independent of the presence of a predetermined chromophore in the tissue.

36. A method according to claim 35 wherein said light source and photo-receptor are arranged to project and detect light at wavelengths which are substantially unaffected by the presence of said predetermined chromophore.

37. A method according to claim 35 further comprising:

processing data indicative of the spectral characteristics of re-emitted light received by said photo-receptor to generate signals which are indicative of the presence of chromophores which are substantially independent of the variation in spectral characteristics arising due to the presence of said predetermined chromophores; and

comparing said processed data with said records to identify the record having the most closely corresponding spectral data.

38. A method according to claim 35 wherein said predetermined chromophore comprises a chromophore selected from the group consisting of melanin, blood and tattoo pigments.

39. A method according to claim 28, further comprising:

determining the depth of papillary dermis of a tissue sample being monitored on the basis of the spectral characteristics of said received re-emitted light; and

identifying the presence of individual chromophores within the area of the illuminated issue sample from which re-emitted light is received utilizing the spectral characteristics of said received re-emitted light and said determined depth of papillary dermis.