Systems and methods for multi-view nonlinear optical imaging for improved signal-to-noise ratio and resolution in point scanning multi-photon microscopy

Patent metadata

Field	Value
Publication number	US-11041807-B2
Application number	US-201615754948-A
Country	US
Kind code	B2
Filing date	Aug 22, 2016
Priority date	Aug 26, 2015
Publication date	Jun 22, 2021
Grant date	Jun 22, 2021

Abstract

Various embodiments of a multi-photon microscopy system that uses sequential excitation of a sample through three or more objective lenses oriented at different axes intersecting the sample are disclosed. Each objective lens is capable of focused sequential excitation of the sample that elicits fluorescence emissions from the excited sample, which is then simultaneously detected by each respective objective lens along a respective longitudinal axis every time the sample is illuminated through only a single objective lens.

First claim

What is claimed is:

1. A multi-photon microscopy system comprising:
a first objective lens oriented along a first longitudinal axis that intersects a sample at a first angle;
a second objective lens oriented along a second longitudinal axis that intersects the sample at a second angle;
a third objective lens oriented along a third longitudinal axis that intersects the sample at a third angle; and
at least one laser source for generating a laser beam and a scanner for sequentially transmitting the laser beam through the first objective lens at a first illumination point focused in the sample, the second objective lens at a second illumination point focused in the sample, or the third objective lens at a third illumination point focused in the sample when sequentially illuminating the sample, and wherein fluorescence emissions emitted from the sample are simultaneously detected through the first objective lens, the second objective lens, and the third objective lens from a detection volume within a working distance of at least one of the first, second and third objective lenses.

2. The multi-photon microscopy system of claim 1 , further comprising:
first, second, and third optical arrangements operatively associated with the first, second and third objective lenses, respectively, wherein the first, second, and third optical arrangements each comprise a mirror for transmitting the fluorescence emissions to a detector for detection of fluorescence emissions through each of the first, second, and third objective lenses, respectively.

3. The multi-photon microscopy system of claim 2 , wherein the mirror comprises a dichroic mirror.

4. The multi-photon microscopy system of claim 1 , wherein the detector comprises a point detector.

5. The multi-photon microscopy system of claim 2 , further comprising:
a processor in operative communication with the detector for each of the first, second and third optical arrangements for processing image data derived from the fluorescence emissions emitted by the sample when only one of the first, second and third objective lenses illuminates the sample such that a first image is generated by the processor based on the fluorescence emissions detected through the first objective lens, a second image is generated by the processor based on the fluorescence emissions detected through the second objective lens, and a third image is generated by the processor based on the fluorescence emissions detected through the third objective lens.

6. The multi-photon microscopy system of claim 5 , wherein the processor combines the first image, the second image and the third image combined and then registered relative to each other.

7. The multi-photon microscopy system of claim 1 , further comprising:
one or more additional objective lenses in operative association with the laser source and the scanner for sequentially illuminating the sample and detecting the fluorescence emissions emitted by the sample.

8. The multi-photon microscopy system of claim 2 , further comprising:
a processor in operative communication with the detector for obtaining image data derived from the detected fluorescence emissions and applying a deconvolution algorithm to the image data.

9. The multi-photon microscopy system of claim 1 , wherein the first, second, and third longitudinal axes of the first, second and third objective lenses, respectively, are oriented at a 120 degree angle relative to each other.

10. The multi-photon microscopy system of claim 1 , wherein the first, second and third longitudinal axes intersect different portions of the sample.

11. The multi-photon microscopy system of claim 1 , wherein the scanner comprises a two-dimensional mirror.

12. A multi-photon microscopy system comprising:
at least three objective lenses oriented along a first longitudinal axis, a second longitudinal axis, and a third longitudinal axis, respectively, that intersect a sample at different angles; and
at least one laser source for generating a laser beam and a scanner for sequentially transmitting the laser beam through each of the at least three objective lenses at a respective illumination point in the sample when illuminating the sample to generate fluorescence emissions, and wherein the fluorescence emissions emitted from the sample are simultaneously detected through the at least three objective lenses from a detection volume within a working distance of at least three objective lenses.

13. The multi-photon microscopy system of claim 12 , further comprising:
at least three optical arrangements operatively associated with the at least three objective lenses, respectively, wherein the at least three optical arrangements each comprise a mirror for transmitting the fluorescence emissions to a detector for detection of fluorescence emissions through each of the at least three objective lenses, respectively.

14. A method for multi-view nonlinear imaging comprising:
positioning three or more objective lenses oriented along first, second and third longitudinal axes, respectively, that intersect a sample to be illuminated;
operatively associate at least one laser source with a respective one of the three or more objective lenses for illuminating the sample with a laser beam at a respective illumination point focused in the sample;
sequentially illuminate the sample with the laser beam through one of the at least three objective lenses in a first sequence; and
simultaneously detect the fluorescence emissions generated by the illumination of the sample through each of the at least three objective lenses from a detection volume within a working distance of at least one of the three or more objective lenses.

15. The method of claim 14 , further comprising:
sequentially illuminate the sample again with the laser beam through another one of the at least three objective lenses in a second sequence; and
simultaneously detect the fluorescence emissions generated by the illumination of the sample through each of the at least three objective lenses.

16. The method of claim 15 , further comprising:
sequentially illuminate the sample again with the laser beam through yet another one of the at least three objective lenses in a third sequence; and
simultaneously detect the fluorescence emissions generated by the illumination of the sample through each of the at least three objective lenses.

17. The method of claim 15 further comprising:
operatively associate three or more optical arrangements with the three or more objective lenses, respectively, wherein the three or more optical arrangements each comprise a mirror for transmitting the fluorescence emissions to a detector for detection of fluorescence emissions through each of the three or more objective lenses.

Assignees

• The Us Secretary Depart Of Health And Human Services
• Us Health

Inventors

• Shroff Hari
• Wu Yicong

Classifications

• G02B2207/114

  Two photon or multiphoton effect · CPC title

• G01N21/636

  using an arrangement of pump beam and probe beam; using the measurement of optical non-linear properties; (non-linear optics per se G02F1/35) · CPC title

• G02B21/16 Primary

  adapted for ultraviolet illumination {; Fluorescence microscopes (G02B21/0076 takes precedence)} · CPC title

• G02B21/002

  Scanning microscopes (scanning near field optical microscopes G01Q60/18) · CPC title

• G02B21/0076

  arrangements using fluorescence or luminescence · CPC title