Side-firing linear optic array for interstitial optical therapy and monitoring using compact helical geometry

• US 20070282404A1
• Filed: 04/06/2007
• Published: 12/06/2007
• Est. Priority Date: 04/10/2006
• Status: Abandoned Application

• Current Assignee: University of Rochester
• Original Assignee: University of Rochester
• Inventors: Foster, Thomas, Cottrell, William
• Application Number:
  US11/783,199
• Publication Number:
  US 20070282404A1
• Time in Patent Office: Days
• US Class Current: 607/89
• CPC Class Codes: A61B 18/22 the beam being directed along or through a flexible conduit, e.g. an optical fibre; Couplings or hand-pieces therefor
• CPC Class Codes: A61B 18/24 with a catheter A61B18/26, A61B18/28 take precedence
• CPC Class Codes: A61B 2018/1807 using light other than laser radiation
• CPC Class Codes: A61B 2018/2216 Braided or helically wound
• 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: A61N 2005/0662 Visible light
• CPC Class Codes: A61N 5/0601 Apparatus for use inside the body
• CPC Class Codes: A61N 5/062 Photodynamic therapy, i.e. excitation of an agent
• CPC Class Codes: A61N 5/067 using laser light
• CPC Class Codes: G02B 6/06 the relative position of the fibres being the same at both ends, e.g. for transporting images

Abstract

An optical probe has multiple side-firing optical fibers which terminate in a linearly staggered fashion. A central fiber can be used as well. In diagnostic techniques, one fiber can be used as an emitter, while the others are used as receivers, or various fibers can be used as emitters and receivers at different times to form a map of the area. In therapeutic techniques, the treatment light can be emitted from the fibers in parallel or in sequence, and the fluence can be independently adjusted for each of the fibers. Therapy is readily combined with diagnosis and monitoring by directing the therapeutic light through the central fiber and using the side-firing fibers for reflectance and/or fluorescence spectroscopy before, during, and after therapy.

Claims

1. An optical fiber probe comprising:

a plurality of helically wound side-firing optical fibers; and

a plurality of fiber ends, one on each of the fibers, the fiber ends being arranged in a linear side-firing array.

2. The optical fiber probe of claim 1, further comprising a central optical fiber around which the plurality of fibers are wound.

3. The optical fiber probe of claim 2, further comprising a cylindrical diffuser on an end of the central optical fiber.

4. The optical fiber probe of claim 2, wherein the central optical fiber comprises a material which is opaque to an imaging modality.

5. The optical fiber probe of claim 4, wherein the material comprises gold.

6. The optical fiber probe of claim 1, further comprising a catheter in which the fibers are disposed.

7. The optical fiber probe of claim 1, further comprising a needle in which the fibers are disposed.

8. The optical fiber probe of claim 7, wherein the needle has optical ports corresponding to the fiber ends.

9. The optical fiber probe of claim 8, further comprising a central optical fiber around which the plurality of fibers are wound and a cylindrical diffuser on an end of the central optical fiber, and wherein the needle comprises a transparent cone at an end of the needle.

10. The optical fiber probe of claim 1, wherein the plurality of fibers are wound in a same direction.

11. The optical fiber probe of claim 1, wherein the plurality of fibers comprise pairs of fibers which are wound in opposite directions.

12. An optical fiber probe system comprising:

a plurality of helically wound side-firing optical fibers;

a plurality of fiber ends, one on each of the fibers, the fiber ends being arranged in a linear side-firing array;

at least one light source for outputting light from at least one of the fiber ends through at least one of the fibers; and

a spectrometer for receiving light from at least one of the fiber ends through at least one of the fibers and for analyzing the received light.

13. The system of claim 12, wherein the at least one light source comprises a source of white light.

14. The system of claim 12, wherein the at least one light source comprises a treatment laser.

15. The system of claim 12, wherein the fibers are connected to the at least one light source and the spectrometer such that the fibers can be selectively connected either to the at least one light source or to the spectrometer.

16. A method for treating or diagnosing tissue, the method comprising:

(a) inserting an optical fiber probe into the tissue, the optical fiber probe comprising a plurality of helically wound side-firing optical fibers and a plurality of fiber ends, one on each of the fibers, the fiber ends being arranged in a linear side-firing array; and

(b) applying light to the tissue through at least one of the fibers.

17. The method of claim 16, wherein the light is light from a treatment laser.

18. The method of claim 17, wherein the light is emitted from the plurality of fibers in parallel.

19. The method of claim 17, wherein the light is emitted from the plurality of fibers in sequence.

20. The method of claim 17, wherein the light is emitted from the plurality of fibers, and wherein a fluence of the light is independently adjusted for each of the fibers.

21. The method of claim 16, wherein the light is diagnostic light, and further comprising:

(c) receiving light from the tissue through at least one other one of the fibers; and

(d) spectroscopically analyzing the received light for diagnosis.

22. The method of claim 21, wherein the light received in step (c) is reflected light.

23. The method of claim 21, wherein the light received in step (c) is fluorescently emitted light.

24. The method of claim 21, wherein step (b) is performed through one of the fibers, and wherein step (c) is performed through other ones of the fibers.

25. The method of claim 21, wherein steps (b) and (c) are performed at different times using different ones of the fibers, and wherein step (d) is performed for different regions in the tissue.