SCANNING FIBER-OPTIC NONLINEAR OPTICAL IMAGING AND SPECTROSCOPY ENDOSCOPE

• US 20070213618A1
• Filed: 01/17/2007
• Published: 09/13/2007
• Est. Priority Date: 01/17/2006
• Status: Abandoned Application

• Current Assignee: University of Washington
• Original Assignee: University of Washington
• Inventors: Li, Xingde, MacDonald, Daniel, Myaing, Mon
• Application Number:
  US11/623,974
• Publication Number:
  US 20070213618A1
• Time in Patent Office: Days
• US Class Current: 600/476
• CPC Class Codes: A61B 1/00096 Optical elements
• CPC Class Codes: A61B 1/00172 with means for scanning
• CPC Class Codes: A61B 1/00183 for variable viewing angles
• CPC Class Codes: A61B 1/043 for fluorescence imaging
• CPC Class Codes: A61B 5/0068 Confocal scanning
• 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 5/0084 for introduction into the body, e.g. by catheters A61B5/1459 takes precedence
• CPC Class Codes: A61B 5/6852 Catheters
• CPC Class Codes: G01J 3/02 Details
• CPC Class Codes: G01J 3/0218 using optical fibers
• CPC Class Codes: G01J 3/0291 Housings; Spectrometer accessories; Spatial arrangement of elements, e.g. folded path arrangements
• CPC Class Codes: G01J 3/06 Scanning arrangements arrangements for order-selection
• CPC Class Codes: G01J 3/42 Absorption spectrometry; Double beam spectrometry; Flicker spectrometry; Reflection spectrometry beam switching arrangements G01J3/08
• CPC Class Codes: G01J 3/4406 Fluorescence spectrometry
• CPC Class Codes: G01N 2021/6421 Measuring at two or more wavelengths
• CPC Class Codes: G01N 2021/6423 Spectral mapping, video display
• CPC Class Codes: G01N 21/6428 Measuring fluorescence of fluorescent products of reactions or of fluorochrome labelled reactive substances, e.g. measuring quenching effects, using measuring "optrodes" in vivo A61B5/00; immunoassay G01N33/53
• CPC Class Codes: G01N 21/6456 Spatial resolved fluorescence measurements; Imaging
• CPC Class Codes: G01N 2201/0697 Pulsed lasers

Abstract

A miniature, flexible, fiber-optic scanning endoscope for nonlinear optical imaging and spectroscopy. The endoscope uses a tubular piezoelectric actuator for activating a cantilevered optical fiber from which pulsed light produced by a laser source exits and is directed to a target region through a micro-lens. The actuator is activated by two modulated signals that achieve two-dimensional beam scanning in a desired scan pattern. A double-clad optical fiber is employed for delivery of the excitation pulsed light and collection of emitted light received from the target region. The pulsed light travels through a core of the double-clad optical fiber, and the emitted light from the target region is directed into the core and inner cladding of the optical fiber and conveyed to a proximal end, for detection and processing. The emitted light can include multiphoton fluorescence, second harmonic generation light, and spectroscopic information, for use in imaging.

Claims

1. A system for capturing light emissions from a target region within a patient'"'"'s body, comprising:

(a) a light source that produces a pulsed light;

(b) an optical fiber having a core covered by a plurality of claddings, a proximal end, and a distal end, the core being configured to couple at the proximal end of the optical fiber to the light source producing the pulsed light, for conveying the pulsed light to the distal end of the optical fiber through the core;

(c) a cantilevered optical fiber that includes a core within a plurality of claddings, the cantilevered optical fiber being coupled to the distal end of the optical fiber to receive the pulsed light that is conveyed through the optical fiber, so that the pulsed light is conveyed through the core of the cantilevered optical fiber and exits from a free end of the cantilevered optical fiber;

(d) an actuator for driving the cantilevered optical fiber to move, so that the pulsed light exiting from the free end scans in a desired scanning pattern;

(e) a lens to focus the pulsed light traveling from the free end of the cantilevered optical fiber toward a target region within a patient'"'"'s body, so that the pulsed light excites molecules at the target region to emit light in response to the pulsed light, and to focus emitted light received from the target region back into the core and an inner cladding of the cantilevered optical fiber, the emitted light being conveyed through the cantilevered optical fiber and through the core and an inner cladding of the optical fiber that is coupled thereto toward the proximal end of the optical fiber;

(f) a splitter that separates the emitted light conveyed back through the optical fiber from the pulsed light that is produced by the light source, so that the emitted light exiting the proximal end of the optical fiber is conveyed along a detection path, while the pulsed light is introduced into the proximal end of the optical fiber and conveyed thereby to the target region;

(g) a photodetector disposed in the detection path, for responding to the emitted light and producing a corresponding electrical output signal; and

(h) a processor for processing the electrical output signal, for use in determining a characteristic of the target region based upon the emitted light.

2. The system of claim 1, wherein the photodetector comprises an imaging photodetector and wherein the output signal comprises an image signal that is processed to produce an image of the target region in response to the emitted light.

3. The system of claim 2, wherein the emitted light comprises multiphoton fluorescence (MPF) that is emitted by molecules at the target region that have each absorbed multiple photons of the pulsed light, the electrical output signal being used to produce an MPF image of the target region.

4. The system of claim 1, wherein the photodetector comprises a spectrometer disposed in front of an imaging device that produces the output signal, so that the output signal is responsive to a spectral content of the emitted light from the target region.

5. The system of claim 4, wherein the emitted light comprises multiphoton fluorescence (MPF), and wherein the electrical output signal produced by the photodetector comprising the spectrometer and CCD is processed to produce MPF images at a desired specific wavelength within a spectrum range of the MPF.

6. The system of claim 4, wherein the emitted light comprises multiphoton fluorescence (MPF), and wherein the spectrometer is an imaging spectrometer and the electrical output signal is processed to produce spectroscopic information indicative of an intensity of different wavelengths of an MPF emission spectrum.

7. The system of claim 1, wherein the emitted light is generated as a second harmonic of the pulsed light, due to the absorption of two photons of the pulsed light by molecules at the target region, which then produce emitted light that is at twice an energy level of each of two photons comprising the pulsed light absorbed by non-centrosymmetric molecules at the target region, the emitted light thus comprising second harmonic generation (SHG) light.

8. The system of claim 7, further comprising a polarization controller for adjusting a polarization of the emitted light, in order to substantially maximize the SHG light produced in the target region.

9. The system of claim 1, wherein the splitter comprises a dichroic mirror that transmits light of a first waveband, while reflecting light of a second waveband that is substantially different than the first waveband, the pulsed light having a waveband that is substantially equal to one of the first and the second wavebands, and the emitted light having a waveband that is substantially equal to the other of the first and second wavebands.

10. The system of claim 1, wherein the actuator drives the cantilevered optical fiber to move in the desired scanning pattern defined relative to two generally orthogonal axes.

11. The system of claim 10, wherein the actuator is energized by a drive signal modulated with a voltage waveform selected from a group consisting of a triangular waveform;

a sinusoidal waveform; and

modified versions of the triangular and sinusoidal waveforms.

12. The system of claim 1, wherein the desired scanning pattern comprises a pattern selected from the group consisting of:

(a) a linear scan pattern;

(b) a raster scan pattern;

(c) a spiral scan pattern;

(d) a propeller scan pattern;

(e) a Lissajous scan pattern; and

(f) a circular scan pattern.

13. The system of claim 1, further comprising a pulse dispersion manager disposed in a path between the light source and the proximal end of the optical fiber, the pulse dispersion manager negatively pre-chirping pulses of the pulsed light to compensate for a pulse broadening caused by a positive dispersion of the pulsed light within the core of the optical fiber having the plurality of claddings.

14. The system of claim 13, wherein the pulse dispersion manager comprises a pulse stretcher that includes a grating, a lens, and a plurality of reflective surfaces.

15. The system of claim 13, wherein the pulse dispersion manager comprises a photonic bandgap filter selected to have a desired negative dispersion to compensate for the pulse broadening in the core of the optical fiber having the plurality of claddings.

16. The system of claim 1, further comprising a coupling lens for coupling the pulsed light into the core at the proximal end of the optical fiber.

17. The system of claim 1, wherein the lens that focuses pulsed light exiting from the free end of the cantilevered optical fiber comprises a micro-lens selected from the group consisting of:

(a) a gradient index (GRIN) lens;

(b) a micro achromatic compound lens;

(c) a micro-spherical lens; and

(d) an aspherical lens.

18. The system of claim 1, wherein the light source that produces the pulsed light comprises a laser that produces the pulsed light with a pulse width on the order of from several femtoseconds to several tens of picoseconds.

19. The system of claim 1, wherein the actuator comprises a tubular piezoelectric actuator.

20. A scope for use in producing and collecting light emissions from a target region within a patient'"'"'s body, comprising:

(a) an optical fiber having a core covered by a plurality of claddings, a proximal end, and a distal end, the core being configured to couple at the proximal end of the optical fiber to a light source producing a pulsed light, for conveying the pulsed light to the distal end of the optical fiber through the core;

(b) an elongate housing, which is disposed at the distal end of the optical fiber;

(c) a scanning device that is disposed within the housing and is coupled to the distal end of the optical fiber to receive the pulsed light conveyed through the core of the optical fiber, the scanning device having a free end that is actuated to scan in a desired scanning pattern, so that the pulsed light exiting from the free end scans a target region within a patient'"'"'s body; and

(d) a lens disposed within the housing and configured for focusing the pulsed light exiting from the free end of the scanning device onto a target region and for focusing emitted light from the target region back into the scanning device, the emitted light being conveyed through the core and an inner cladding of the optical fiber to the proximal end of the optical fiber, which is configured to couple the emitted light onto a photodetector.

21. The scope of claim 20, wherein the scanning device includes an actuator, and a cantilevered optical fiber, the cantilevered optical fiber having a proximal end coupled to the optical cable and driven to move by the actuator, and a distal free end through which the pulsed light exits and through which the emitted light is received, the actuator being configured to connect via electrical leads that extend proximally from the actuator to an external power source that can energize the actuator to drive the cantilevered optical fiber to move in the desired scanning pattern.

22. The scope of claim 21, wherein the actuator comprises a piezoelectric actuator that is able to drive the cantilevered optical fiber to move relative to at least one axis that is transverse to a longitudinal axis of the actuator.

23. The scope of claim 21, wherein the cantilevered optical fiber includes a core around which is disposed a plurality of cladding layers, the pulsed light being conveyed through the core of the cantilevered optical fiber, and the emitted light being received at the free end of the cantilevered optical fiber and conveyed through the core and an inner cladding of the cantilevered optical fiber and into the core and the internal cladding of the optical fiber.

24. The scope of claim 20, wherein the lens comprises a micro-lens selected from the group consisting of:

(a) a gradient index (GRIN) lens;

(b) a micro achromatic compound lens;

(c) a micro-spherical lens; and

(d) an aspherical lens.

25. A method for producing light emissions from a target region in a patient'"'"'s body, comprising the steps of:

(a) introducing pulsed light into a proximal end of an optical fiber having a core and a plurality of cladding layers, the pulsed light being conveyed by the core to a distal end of the optical fiber that is configured to be advanced to a position proximate to the target region;

(b) actuating a scanning device disposed at the distal end of the optical fiber where the scanning device receives the pulsed light, movement of the scanning device causing the pulsed light to scan the target region in a desired scanning pattern;

(c) focusing the pulsed light from the scanning device onto the target region;

(d) focusing emitted light received from the target region into the scanning device, the emitted light being produced in response to excitation of molecules at the target region by the pulsed light;

(e) conveying the emitted light received from the target region back through the core and an inner cladding layer of the optical fiber, to the proximal end of the optical fiber;

(f) directing the emitted light exiting the optical fiber so that the emitted light is incident on a photodetector, the photodetector producing a signal indicative of a characteristic of the target region; and

(g) producing an image responsive to the signal output by the photodetector for evaluating a condition of the target region.

26. The method of claim 25, wherein the scanning device moves a cantilevered optical fiber relative to two axes, to scan the target region in the desired scanning pattern, the step of actuating the scanning device comprising the step of energizing the scanning device with modulated signals to move the cantilevered optical fiber relative to the two axes.

27. The method of claim 25, wherein the desired scanning pattern comprises a space-filling pattern.

28. The method of claim 25, further comprising the step of negatively pre-chirping pulses of the pulsed light before the step of introducing the pulsed light into the optical fiber, to compensate for a pulse broadening caused by a dispersion of the pulsed light within the core of the optical fiber.

29. The method of claim 25, wherein the steps of focusing the pulsed light exiting from the scanning device onto the target region comprises the steps of passing the pulsed light through a micro-lens.

30. The method of claim 29, wherein the steps of focusing the emitted light received from the target region into the scanning device comprises the step of passing the multiphoton light through the micro-lens.

31. The method of claim 25, wherein the emitted light comprises multiphoton fluorescence (MPF) light that is emitted by molecules that have each absorbed multiple photons of the pulsed light, and wherein the step of producing the image comprises the step of producing an MPF image of the target region in response to the MPF light emitted by the molecules at the target region.

32. The method of claim 31, wherein the step of producing the image further comprises the step of detecting the MPF light at a desired specific wavelength within an MPF spectrum range.

33. The method of claim 31, wherein the step of producing the image further comprises the step of producing MPF spectroscopic images by detecting an intensity of the MPF light at different wavelengths of an MPF emission spectrum.

34. The method of claim 25, wherein the emitted light is generated as a second harmonic of the pulsed light, due to the absorption of two photons of the pulsed light by molecules at the target region, which then produce emitted light that is at twice an energy level of each of two photons comprising the pulsed light that is absorbed by non-centrosymmetric molecules at the target region, the emitted light thus comprising second harmonic generation (SHG) light, wherein the step of producing the images comprises the step of producing SHG images of the target region in response to the SHG light.

35. The method of claim 34, further comprising the step of adjusting a polarization of the pulsed light, to substantially maximize the SHG light produced in the target region.