Fiber-optic methods and devices enabling multiphoton imaging with improved signal-to-noise ratio

Patent metadata

Field	Value
Publication number	US-2016357008-A1
Application number	US-201615169917-A
Country	US
Kind code	A1
Filing date	Jun 1, 2016
Priority date	Jun 2, 2015
Publication date	Dec 8, 2016
Grant date	—

Abstract

The present invention is directed to a fiber optic device that enables multiphoton imaging with improved signal-to-noise ratio having a single piece of double-clad fiber (DCF). The device also includes all components for focusing, scanning and signal collection within an endomicroscope probe of 2.1 mm outer diameter (OD). The unprecedented imaging capability of this miniature endomicroscope is demonstrated herein via both ex vivo and in vivo experiments.

First claim

1 . A device comprising:
a housing; a single light guide configured for delivery of excitation light and collection of emission light disposed within the housing; a piezoelectric tube (PZT) configured to function as an actuator disposed at a first end of the housing; an achromatic objective lens disposed at a second end of the housing.

2 . The device of claim 1 wherein the single light guide comprises an optical fiber.

3 . The device of claim 1 wherein the single light guide comprises a single or multiple single-mode cores and multiple claddings, with the core(s) for delivery of excitation light to the sample, and at least one cladding (and the core(s)) for collection of emission light from the sample.

4 . The device of claim 1 wherein the single light guide comprises one selected from a group consisting of a pure silica core, a potassium doped silica sore, and a hollow core.

5 . The device of claim 1 wherein the single light guide comprises an optical fiber having at least one single-mode core and one cladding also including a low refractive index coating.

6 . The device of claim 1 wherein the objective lens comprises low or no chromatic aberration and configured to have a wavelength range of interest to improve the efficiency of coupling the emission light back into the fiber.

7 . The device of claim 1 wherein the achromatic objective lens is configured for collecting the emission light with a short wavelength (e.g. 350-600 nm) mainly generated from the focal volume of the excitation light of a long wavelength (e.g. 750-1060 nm).

8 . The device of claim 1 wherein the achromatic objective lens comprises a miniature compound lens further comprising multi-elements of different refractive index profiles (including GRIN lenses/glasses) and/or curvatures to correct chromatic aberration and field flatness for a scanning input imaging beam.

9 . The device of claim 1 wherein the achromatic objective lens comprises a miniature compound lens with a diffraction element/mask to compensate the chromatic aberration and thus reduce the longitudinal focal shift, while maintaining a high numerical aperture (and thus resolution) and small size.

10 . The device of claim 1 further comprising a built-in mechanism to perform 2D and 3D beam scanning.

11 . The device of claim 10 wherein the built-in mechanism to perform 2D and 3D beam scanning comprises one selected from a group consisting of a PZT actuated 2D fiber scanner, an MEMS actuated 2D or 3D fiber scanner, a built-in depth scanner, and a mechanical scanner consisting of a compressed spring and shape-memory alloy wires to translate parts of the focusing optics relative to the rest of the probe.

12 . The device of claim 10 wherein the built-in mechanism is equipped with corresponding drive and control electronics.

13 . The device of claim 1 further comprising a short pulsed light source as the excitation light source.

14 . The device of claim 1 further comprising a dispersion management unit configured to compensate the dispersion of the fiber and other optics in the system to achieve short pulses and good emission signal production.

15 . The device of claim 14 wherein the dispersion management unit comprises one selected from a group consisting of a photonic bandgap fiber, a pair of gratings, a pair of prisms, and a grating-lens pair.

16 . The device of claim 1 further comprising a mechanism to separate the emission light from the excitation light.

17 . The device of claim 16 wherein the mechanism to separate the emission light from the excitation light comprises a dichroic mirror.

18 . The device of claim 1 further comprising a light detector configured to detect the emission light, electronics to condition and acquire the signal, and electronics to digitize and store the signal in digital form.

19 . The device of claim 18 wherein the light detector comprises a photomultiplier tube.

20 . The device of claim 1 further comprising a control device, imaging beam scanner drive, data acquisition, display and storage unit to control and synchronize the drive signals and data acquisition, digitize the data, process the data, and store data.

21 . The device of claim 1 further comprising optics configured to couple the light between free space and optical fiber.

Assignees

• Univ Johns Hopkins

Inventors

• Li Xingde
• Wu Yicong
• Liang Wenxuan

Classifications

• A61B10/04 Primary

  Endoscopic instruments, e.g. catheter-type instruments · CPC title

• G01N2201/0866

  Use of GRIN elements · CPC title

• G01N2201/10

  Scanning · CPC title

• G01N33/4833

  of solid biological material, e.g. tissue samples, cell cultures (tissue in vivo A61B5/00; cell suspensions G01N33/48735) · CPC title

• G02B23/2469

  using optical fibres · CPC title