Tissue and cellular imaging

Patent metadata

Field	Value
Publication number	US-10022042-B2
Application number	US-201214354690-A
Country	US
Kind code	B2
Filing date	Oct 29, 2012
Priority date	Oct 28, 2011
Publication date	Jul 17, 2018
Grant date	Jul 17, 2018

Abstract

Systems and methods for imaging ear tissue include: directing illumination radiation to pass through an intact biological structure and be incident on ear tissue that does not include an exogenous fluorophore, at a plurality of locations, the illumination radiation including a plurality of light pulses each having a temporal duration of 500 femtoseconds or less; for each one of the plurality of locations, using a detector to detect radiation emitted from the location that passes through the intact biological structure; and forming an image of the tissue based on the detected radiation at each of the plurality of locations, where the emitted radiation corresponds to endogenous two-photon fluorescence of the tissue.

First claim

What is claimed is:

1. A method for imaging ear tissue, the method comprising:
without contacting a round window membrane of a cochlea comprising the ear tissue, directing illumination radiation to pass through the round window membrane and be incident on ear tissue that does not comprise an exogenous fluorophore at a plurality of locations, the illumination radiation comprising a plurality of light pulses each having a temporal duration of 500 femtoseconds or less;
for each one of the plurality of locations, using a detector to detect radiation emitted from the location that passes through the round window membrane; and
forming an image showing at least one of inner ear neurons and inner ear hair cells of the tissue based on the detected radiation at each of the plurality of locations,
wherein the emitted radiation corresponds to endogenous two-photon fluorescence of the tissue.

2. The method of claim 1 , wherein the radiation emitted by the tissue comprises radiation produced by harmonic conversion of the incident radiation.

3. The method of claim 2 , further comprising, prior to illuminating the tissue, selecting a central wavelength of the illumination radiation to increase an efficiency of the harmonic conversion of the incident radiation, relative to an efficiency of harmonic conversion of the incident radiation induced by uniform exposure to a band of wavelengths from 400 nm to 800 nm.

4. The method of claim 1 , further comprising, prior to illuminating the tissue, selecting a central wavelength of the illumination radiation to increase an efficiency of the endogenous two-photon fluorescence of the tissue, relative to an efficiency of two-photon fluorescence emission induced by uniform exposure to a band of wavelengths from 400 nm to 800 nm.

5. The method of claim 1 , further comprising:
positioning an endoscope proximal to the round window membrane;
using the endoscope to deliver the illumination radiation to the round window membrane; and
using the endoscope to collect the emitted radiation emerging through the round window membrane, and to transport the emitted radiation to the detector.

6. The method of claim 1 , further comprising:
identifying hair cells in the image; and
determining whether acoustically-induced damage has occurred in the tissue based on the identified hair cells.

7. The method of claim 1 , further comprising:
identifying a cell in the image;
measuring a spectrum of a portion of the emitted radiation corresponding to the cell to generate a measured emission spectrum for the cell;
comparing the measured emission spectrum to a reference two-photon fluorescence emission spectrum for an undamaged cell; and
determining whether the cell is damaged based on the comparison between the spectra.

8. The method of claim 7 , wherein the comparing comprises determining a bandwidth of the measured emission spectrum, and comparing the determined bandwidth to a bandwidth for the reference emission spectrum.

9. The method of claim 1 , further comprising:
repeating the steps of the method of claim 1 to form a plurality of successive images of the tissue;
after forming each one of the successive images, directing the illumination radiation to a different plurality of locations so that a next one of the successive images comprises contributions from a different region of the tissue; and
combining the plurality of successive images to form a three-dimensional image of the tissue.

10. The method of claim 1 , further comprising:
identifying a plurality of cells of the tissue in the image; and
determining whether each one of the cells is a neuron or a hair cell based on a central wavelength of a portion of the emitted radiation corresponding to the cell.

11. The method of claim 8 , further comprising determining that the cell is damaged if a difference between the bandwidths of the measured and reference emission spectra is 5% or more.

Assignees

• Massachusetts Eye & Ear Infirmary
• Ecole Polytechnique Fed Lausanne Epfl

Inventors

• Stankovic Konstantina
• Psaltis Demetri
• Yang Xin
• Pu Ye
• Hsieh Chia-Lung

Classifications

• A61B5/0084

  for introduction into the body, e.g. by catheters (A61B5/1459 takes precedence) · CPC title

• A61B5/0066

  Optical coherence imaging · CPC title

• A61B1/043

  for fluorescence imaging · CPC title

• A61B5/0071

  by measuring fluorescence emission · CPC title

• A61B5/0068

  Confocal scanning · CPC title