Raman spectral analysis of sub-surface tissues and fluids

• US 8,243,269 B2
• Filed: 11/25/2005
• Issued: 08/14/2012
• Est. Priority Date: 12/09/2004
• Status: Active Grant

• Current Assignee: UK Research and Innovation
• Original Assignee: Science and Technology Facilities Council
• Inventors: Matousek, Pavel, Parker, Anthony William
• Primary Examiner(s): ROZANSKI, MICHAEL T
• Application Number:
  US11/792,701
• Publication Number:
  US 20080076985A1
• Time in Patent Office: 2,454 Days
• Field of Search: 600/310, 600473-477, 250/358.1, 356/301, 356/318, 356/337, 356/342
• US Class Current: 356/301
• 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 5/0071 by measuring fluorescence emission
• 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 5/441 Skin evaluation, e.g. for skin disorder diagnosis
• CPC Class Codes: A61B 5/4504 Bones A61B5/4547 takes precedence
• CPC Class Codes: G01N 2021/656 Raman microprobe
• CPC Class Codes: G01N 21/65 Raman scattering

Abstract

Apparatus and methods for determining, in-vivo, characteristics of sub-surface tissues or fluids in the human or animal body are disclosed. Incident radiation is supplied at one or more entry regions on a surface, and light is collected from one or more collection regions spaced from the entry regions. Raman features are detected in the collected light and depth related information derived therefrom.

Claims

1. A method of determining, in vivo, one or more characteristics of a sub-surface tissue or fluid, through a diffusely scattering overlying tissue, comprising steps of:

(a) supplying incident light as a continuous wave laser beam at one or more entry regions on a surface of the overlying tissue;

(b) collecting, from one or more collection regions on the surface of the overlying tissue, light produced by scattering of said incident light within the overlying tissue, wherein the one or more collection regions on the surface are located at a plurality of spacings from the one or more entry regions on the surface;

(c) detecting using a detector, in the collected light, a plurality of Raman features for said plurality of spacings, wherein one or more of the Raman features corresponds to each different spacing, said Raman features being spectrally related to the incident light and originating from the sub-surface tissue; and

(d) determining said characteristics of the sub-surface tissue or fluid from said Raman features.

2. The method of claim 1, wherein the sub-surface tissue or fluid comprises one of bone, cartilage, breast tissue and blood.

3. The method of claim 1, wherein the overlying tissue comprises one of skin and nail.

4. The method of claim 1, wherein the step of detecting comprises spectrally dispersing the collected light to form a Raman spectrum.

5. The method of claim 1, wherein the step of detecting comprises filtering the collected light to isolate one or more of said Raman spectral features.

6. The method of claim 1, wherein determining said characteristic comprises associating the Raman features from different spacings with different depths or distributions of depth within the overlying tissue and sub-surface tissue or fluid.

7. The method of claim 1, wherein determining said characteristic comprises combining the Raman features from different spacings to select for a depth or distribution of depth.

8. The method of claim 1 wherein the step of collecting comprises collecting light from a plurality of collection regions spaced by different distances from a common entry region.

9. The method of claim 1 wherein one or more collection regions surround an entry region.

10. The method of claim 9, wherein each collection region is an annulus, and the scattered light is collected by a plurality of collection optical fibres distributed around one or more illumination optical fibres used to supply the incident radiation to the entry region.

11. The method of claim 1, wherein one or more entry regions surround a common collection region.

12. The method of claim 1 further comprising adjusting collection optics disposed in the path of the collected light to adjust the distance between a collection region and an entry region.

13. The method of claim 1 further comprising disposing one or more mirror elements adjacent to the surface of the overlying tissue, outside the collection region, to reflect light back into the tissue.

14. A method of determining whether a patient has a cancer condition in a target tissue, comprising:

carrying out the steps of claim 1 to measure, in the target tissue, one or more Raman spectral features characteristic of a cancer condition; and

determining, based on the Raman spectral features, whether the patient has a cancer condition in the target tissue.

15. A method of determining whether a patient has a medical condition related to bone tissues of the patient, comprising:

carrying out the steps of claim 1 to measure one or more Raman spectral features characteristic of the bone tissue; and

determining, based on the Raman spectral features, whether the patient has a bone tissue condition.

16. A method of diagnosis comprising collecting from a sample, consisting of a surface region of an overlying tissue and a sub-layer region of a deep tissue which is different to the overlying tissue, one or more Raman spectra using the method of claim 1.

17. A method of diagnosis as claimed in claim 16, further comprising identifying one or more features specific to the Raman spectrum of the sub-layer region of the sample in the one or more collected Raman spectra and comparing the one or more identified features with those obtained from a healthy control specimen.

18. The method of claim 1, wherein at one of the plurality of spacings the entry and collection regions are at the same place or substantially overlapping.

19. The method of claim 1, wherein the plurality of entry and collection regions are non-overlapping.

20. The method of claim 1, wherein said characteristics are determined from changes in intensities of the one or more Raman features between the different spacings.

32. A method as claimed in claim 18, wherein the light probe comprises two or more separate wavelengths and is generated by one or more lasers.

33. A method as claimed in claim 32, wherein the light probe is generated by a single tunable laser.

34. A method as claimed in claim 32, wherein the two or more separate wavelengths of the light probe are generated by two or more respective lasers.

21. A method of measuring, in-vivo, a sub-surface Raman spectrum of a diffusely-scattering tissue, comprising:

a) irradiating the tissue with a continuous wave laser beam light probe of incident radiation at a point of irradiation on the surface of the tissue;

b) collecting light scattered by the tissue; and

c) spectrally separating at least a portion of the collected light to detect one or more Raman spectral features, wherein light produced by scattering of said incident radiation by the tissue is collected from a plurality of spatial locations on the surface of the tissue, each spatial location being at a different distance from the point of irradiation, at least a portion of the light collected at each spatial location being separately spectrally dispersed to form a plurality of Raman spectra corresponding to said plurality of spatial locations such that a separate Raman spectrum corresponds to each spatial location; and

d) analysing the plurality of Raman spectra to extract information on the Raman spectrum of a sub-surface region of the tissue.

22. A method as claimed in claim 21, wherein at least two Raman spectra are collected and are analysed using a scaled subtraction, the Raman spectrum collected at a distance closest to the point of irradiation being subtracted from the Raman spectrum collected further from the point of irradiation, whereby features of the Raman spectrum for a sub-layer of the tissue are identified.

23. A method as claimed in claim 21, wherein the Raman spectrum for the chemical composition of the surface of the tissue is known and the Raman spectra are analysed by scaled subtraction of the known Raman spectrum from the Raman spectra of the collected light.

24. A method as claimed in claim 21, wherein the plurality of Raman spectra are analysed using multivariate data analysis.

25. A method as claimed in claim 24, wherein the plurality of Raman spectra are analysed using principal component analysis.

26. A method as claimed in claim 24, wherein at least twenty Raman spectra are collected at different distances from the point of irradiation.

27. A method as claimed in claim 21, wherein the tissue is irradiated at two or more different wavelengths and the collected light is a combination of a Raman spectrum and fluorescence and wherein the method comprises the further step of extracting the Raman spectrum from the collected light.

28. A method as claimed in claim 21, wherein at least one of the tissue, the collection optics and the point or region of irradiation is moved relative to the others to enable the collection of Raman spectra at different distances from the point of irradiation.

29. A method as claimed in claim 28, wherein a movable stage is provided on which the tissue is mounted and the probe beam is arranged to track the movement of the tissue whereby the tissue is moved relative to fixed collection optics for the collection of scattered light at different distances from the point of irradiation.

30. A method as claimed in claim 29, wherein the scattered light is collected from point regions at different distances from the point of irradiation.

31. A method as claimed in claim 29, wherein the scattered light is collected from a plurality of substantially parallel lines substantially transverse to the distance as measured from the point of irradiation.

35. A method as claimed in claim 21, wherein the probe beam is supplied using optical fibres and the scattered light is collected using optical fibres arranged in a plurality of concentric circles around the probe beam optical fibres whereby the scattered light is collected in concentric rings at differing radii from the point of irradiation.

36. A method as claimed in claim 21, wherein the collected light is spectrally dispersed using a spectrometer in combination with a CCD camera.

37. The method of claim 21, wherein the incident radiation has a wavelength greater than 600 nm.

38. The method of claim 21, wherein the incident radiation has a wavelength greater than 800 nm.

39. A method of carrying out an in-vivo sub-cutaneous inspection of a sub-surface tissue or fluid without surgical intervention, comprising:

irradiating a surface tissue with a continuous wave laser beam;

collecting light scattered beneath the surface, from one or more collection regions on the surface, said one or more collection regions being located at a plurality of spacings from an incidence location of the laser beam on the surface tissue; and

detecting, using a detector, one or more Raman spectral features from the collected light for each spacing,

wherein the sub-surface tissue or fluid is one of bone, cartilage and blood.

40. The method of claim 39, wherein the collection regions do not overlap the laser beam.

41. Apparatus for determining, in-vivo, one or more characteristics of a sub-surface tissue or fluid, through a diffusively scattering overlying tissue, comprising:

a light source arranged to supply incident light as a continuous wave laser beam at one or more entry regions on a surface of the overlying tissue;

a collector arranged to collect light scattered within the overlying tissue, from one or more collection regions on the surface of the overlying tissue, wherein the one or more collection regions on the surface are located at a plurality of spacings from the one or more entry regions on the surface;

a detector arranged to detect, in the collected light, a plurality of Raman features for said plurality of spacings, wherein at least one Raman feature corresponds to each spacing, said Raman features being spectrally related to the incident light, which originate from the sub-surface tissue or fluid; and

an analyzer adapted to derive, from the Raman features, one or more characteristics of the sub-surface tissue or fluid.

42. The apparatus of claim 41 , adapted to collect light from multiple spacings between the entry and collection region, said analyzer being adapted to combine the Raman features from said multiple spacings to select for a depth or distribution of depth.

43. The apparatus of claim 41, wherein the sub-surface tissue comprises at least one of bone, cartilage, breast tissue and blood.

44. The apparatus of claim 41, wherein the overlying tissue comprises at least one of skin and nail.

45. The apparatus of claim 41, wherein the detector comprises a spectrometer arranged to spectrally disperse the collected light to separate out said Raman features.

46. The apparatus of claim 41, wherein the detector comprises one or more filters arranged to select said Raman features.

47. The apparatus of claim 41, wherein either the entry region or the collection region is an annular region surrounding the other of the two regions.

48. The apparatus of claim 47 further comprising an optics arrangement adapted to controllably adjust the diameter of the annular region.

49. The apparatus of claim 41, further comprising a masking device arranged to controllably adjust the spacing between the entry region and the collection region.

50. The apparatus of claim 41 further comprising one or more mirror elements disposed adjacent to the overlying tissue surface outside the one or more collection and entry regions, so as to reflect light back into the tissue.

51. The apparatus of claim 41, wherein the incident radiation has a wavelength greater than 600 nm.

52. The apparatus of claim 41, wherein the incident radiation has a wavelength greater than 800 nm.

53. The apparatus of claim 41 implemented as an endoscope for inspection within the body by access through a natural or surgically formed orifice.

54. The apparatus of claim 41, wherein at one of the plurality of spacings the entry and collection regions are at the same place or substantially overlapping.

55. The apparatus of claim 41, wherein the plurality of entry and collection regions are non-overlapping.

56. The apparatus of claim 41, wherein the analyzer is adapted to derive the characteristics from changes in intensities of the one or more Raman features between the different spacings.

57. Apparatus for in-vivo selective measurement of Raman spectra generated at different depths within a diffusely-scattering tissue, the apparatus comprising:

a light source for irradiating the tissue with a continuous wave laser probe beam of incident radiation;

collection optics for collecting light scattered by the tissue and passing it to a spectrometer;

detection means for detecting light dispersed by the spectrometer,

wherein the apparatus is adapted for scattered light to be collected at a plurality of spatial locations on the surface of the tissue, each spatial location being at a different distance from a point of irradiation on the tissue and at least a portion of the light collected at each spatial location being separately spectrally dispersed by the spectrometer to form a plurality of Raman spectra corresponding to said plurality of spatial locations, and wherein the apparatus further includes an analyser for identifying features specific to the Raman spectrum of a sub-layer of the tissue from the plurality of Raman spectra.

58. Apparatus as claimed in claim 57, wherein the analyser is adapted to perform a scaled subtraction between Raman spectra.

59. Apparatus as claimed in claim 57, wherein the analyser is adapted to perform multivariate data analysis on the Raman spectra.

60. Apparatus as claimed in claim 59, wherein the analyser is adapted to perform principal component analysis on the Raman spectra.

61. Apparatus as claimed in claim 57, further comprising a movable stage for relative movement of at least one of the tissue, the collection optics and the point of irradiation to enable the collection of Raman spectra at different distances from the point of irradiation.

62. Apparatus as claimed in claim 61, wherein the movable stage is a movable sample stage and wherein means are provided for tracking the probe beam with respect to movement of the tissue whereby the sample may be moved relative to the fixed collection optics to enable scattered light to be collected at a plurality of distances from the point of irradiation.

63. Apparatus as claimed in claim 57, wherein the collection optics comprises optical fibres arranged in a plurality of concentric circles around the probe beam.

64. Apparatus as claimed in claim 57, wherein the detection means comprises a CCD camera.

65. Medical sub-cutaneous inspection apparatus for carrying out an in-vivo inspection of a sub-surface tissue without surgical intervention, comprising:

a probe light beam source arranged to irradiate a surface tissue with a continuous wave laser beam;

a collector arranged to collect light scattered beneath the surface, from one or more collection regions on the surface, said one or more collection regions being located at a plurality of spacings from an incidence location of the laser beam on the surface tissue;

a detector arranged to detect one or more Raman spectral features from the collected light for each spacing; and

an analyzer arranged to derive one or more characteristics of the sub-surface tissue from intensities of the Raman spectral features.

66. The apparatus of claim 65, wherein the collection regions do not overlap with the laser beam.