ENDOSCOPE

• US 20080004495A1
• Filed: 05/24/2007
• Published: 01/03/2008
• Est. Priority Date: 11/25/2004
• Status: Abandoned Application

• Current Assignee: Optiscan Pty Ltd.
• Original Assignee: Optiscan Pty Ltd.
• Inventors: Allen, John, Delaney, Peter
• Application Number:
  US11/753,506
• Publication Number:
  US 20080004495A1
• Time in Patent Office: Days
• US Class Current: 600/160
• CPC Class Codes: A61B 1/043 for fluorescence imaging
• CPC Class Codes: A61B 1/05 characterised by the image sensor, e.g. camera, being in the distal end portion
• CPC Class Codes: A61B 1/0638 providing two or more wavelengths
• CPC Class Codes: A61B 1/0646 with illumination filters
• CPC Class Codes: A61B 5/0068 Confocal scanning
• CPC Class Codes: A61B 5/0071 by measuring fluorescence emission
• CPC Class Codes: A61B 5/0084 for introduction into the body, e.g. by catheters A61B5/1459 takes precedence

Abstract

An endoscope comprising a first light source for illuminating biological tissue with light, a first detector for detecting macroscopic images and fluorescent images from the tissue by reflected light and fluorescent light induced in the tissue, a second light source for illuminating the tissue with light, a confocal microscopic waveguide for supplying light from the second light source to the tissue and for supplying microscopic fluorescent images of the tissue, and a second detector for detecting the microscopic fluorescent images from the confocal microscopic waveguide.

Claims

1. An endoscope comprising:

a first light source configured to illuminate biological tissue with light;

a first detector configured to detect macroscopic images and fluorescent images from the tissue by reflected light and fluorescent light induced in said tissue;

a second light source configured to illuminate the tissue with light;

a confocal microscopic waveguide configured to supply light from said second light source to said tissue and to supply microscopic fluorescent images of said tissue; and

a second detector configured to detect the microscopic fluorescent images from said confocal microscopic waveguide;

wherein light from said first light source and light from said second light source are transmitted to said tissue along different optical paths.

2. The endoscope as claimed in claim 1, wherein said first light source comprises a white light source and a filter for changing effective illumination of said tissue through the visible spectrum, such that different tissue structures being illuminated by the changing wavelengths of the illumination light reflect varying amounts of light to said first detector.

3. The endoscope as claimed in claim 2, wherein said detector comprises a monochrome detector.

4. The endoscope as claimed in claim 1, wherein said first light source comprises a continuous white light source and said first detector is a color detector configured to detect various amounts of the different wavelengths of reflected light.

5. The endoscope as claimed in claim 1, further comprising a waveguide for supplying light from said first light source to said tissue.

6. The endoscope as claimed in claim 5, wherein said further waveguide comprises a single fiber or a fiber bundle for conducting light from said first light source to said tissue and the first detector is at a free end of the endoscope.

7. The endoscope as claimed in claim 5, wherein said further waveguide comprises a first waveguide configured to conduct light to a free end of the endoscope and a second waveguide configured to receive reflected light and convey the reflected light to said first detector.

8. The endoscope as claimed in claim 7, further comprising a filter configured to filter light received by said second waveguide, located either at said free end of said endoscope or between said first detector and said second waveguide.

9. An endoscope as claimed in claim 1, wherein said endoscope has a variable focal plane.

10. The endoscope as claimed in claim 7, wherein said first and second waveguides comprise single fibers or fiber bundles.

11. The endoscope as claimed in claim 1, wherein said confocal microscopic waveguide is a single fiber or fiber bundle.

12. The endoscope as claimed in claim 11, wherein said confocal microscopic waveguide includes a fiber coupler configured to receive fluorescent light and direct said fluorescent light to said second detector.

13. The endoscope as claimed in claim 1, including a monitor configured to provide a display that comprises an overlap of the macroscopic and fluorescent images to produce a single image.

14. The endoscope as claimed in claim 1, wherein said second light source produces light at a predetermined monochrome wavelength for passage through said confocal microscopic waveguide.

15. The endoscope as claimed in claim 1, wherein said second light source comprises a laser light source.

16. The endoscope as claimed in claim 1, wherein said first detector is connectable to a processor and said first detector includes a plurality of different color chips so that the intensity gains for said different color chips in said first detector are adjustable to maximize detection of returning fluorescent light and reduce detection of any background reflected light.

17. The endoscope as claimed in claim 16, wherein said second detector is connectable to said processor so that said processor can process said images and display on a monitor the light image, the macroscopic fluorescent image and the microscopic fluorescent image.

18. The endoscope as claimed in claim 1, wherein said fluorescent light is induced in said tissue by administering an exogenous fluorescent contrast agent to a patient.

19. A method of inspecting a patient'"'"'s tissue by use of an endoscope, comprising:

applying an exogenous contrast agent to the patient;

illuminating said tissue with said endoscope;

detecting with said endoscope a light image of said tissue;

detecting with said endoscope a macroscopic fluorescent image; and

detecting with said endoscope a microscopic confocal fluorescent image of said tissue.

20. The method as claimed in claim 19, wherein the method further comprises controlling filter parameters and gain of a color detector of said endoscope to be at the maximum excitation and emission peaks respectively for said contrast agent.

21. The method as claimed in claim 19, further comprising inspecting the macroscopic fluorescent image to identify regions of interest and further inspecting microscopic confocal fluorescent images of those regions.

22. The method as claimed in claim 19, wherein applying said exogenous contrast agent to the patient comprises applying acriflavine.

23. An endoscope comprising:

a selector mechanism configured to select between a plurality of modes of operation, the modes of operation comprising;

a white light color mode of operation in which a color image of a patient'"'"'s tissue is obtained;

a macroscopic fluorescent mode in which a macroscopic fluorescent image of the tissue is obtained; and

a microscopic confocal fluorescent mode in which a microscopic fluorescent image of said tissue is obtained.

24. The endoscope as claimed in claim 23, wherein said endoscope has a variable focal plane.

25. The endoscope as claimed in claim 23, wherein the selector mechanism comprises a filter configured to produce light of two or more selectable wavelengths based on the selected mode of operation.

26. The endoscope as claimed in claim 23, wherein the selector mechanism comprises a charge coupled device (CCD) configured to detect light of two or more selectable wavelengths based on the selected mode of operation.

27. A method of obtaining images of a patient with a single endoscope, the method comprising:

administering an exogenous contrast agent to the patient; and

obtaining one or more of a white light color image, a macroscopic fluorescent image and a microscopic confocal fluorescent image of tissue of said patient.