Microscope having three-dimensional imaging capability and three-dimensional microscopic imaging method

Patent metadata

Field	Value
Publication number	US-11194142-B2
Application number	US-201916394491-A
Country	US
Kind code	B2
Filing date	Apr 25, 2019
Priority date	Oct 26, 2016
Publication date	Dec 7, 2021
Grant date	Dec 7, 2021

Abstract

A microscope having three-dimensional imaging capability and a three-dimensional microscopic imaging method are provided, the microscope including: at least one excitation device configured to generate a detectable contrast in a detection target region of a sample which is to be detected, in an excitation principal axis direction; at least one detection device, configured to detect the contrast as generated from the detection target region of the sample in a detection principal axis; and at least one movement mechanism, configured to generate a relative movement of the sample relative to the excitation device and the detection device; the relative movement is in a direction neither parallel to nor perpendicular to the excitation principal axis direction or the detection principal axis direction.

First claim

What is claimed is:

1. A microscope having three-dimensional imaging capability, comprising:
at least one excitation device, which is configured to generate a detectable contrast in a detection target region of a sample which is to be detected, in an excitation principal axis direction;
at least one detection device, which is configured to detect the contrast as generated from the detection target region of the sample in a detection principal axis; and
at least one movement mechanism, which is configured to generate a relative movement of the sample relative to the at least one excitation device and the at least one detection device;
wherein the relative movement is implemented in a direction which is neither parallel to nor perpendicular to the excitation principal axis direction and also is neither parallel to nor perpendicular to the detection principal axis direction;
wherein in an overall process of imaging a three-dimensional region of the sample to be detected, neither the imaging process nor the relative movement has pause or stop therein, and the relative movement during the imaging is at a constant speed;
wherein in the detection target region to be detected by the at least one detection device, each of sample units is excited by the at least one excitation device for no longer than a time period in which a displacement of each of sample units due to the relative movement is no more than a requirement in resolution of the microscope, each sample unit in the detection target region of the sample being corresponding to a respective one of voxels which are imaged;
wherein the at least one excitation device and the at least one detection device are configured to operate synchronously with each other; and
wherein blurring incurred by the relative movement is suppressed with a continuum light source which is configured to implement an excitation of a point of the sample in an excitation time, by providing illumination for imaging by a switch modulation or by scanning, said excitation time being restricted such that a product of the excitation time for the sample multiplied by the movement speed of the relative movement is smaller than a minimal scale which is resolvable for the requirement in resolution of the microscope.

2. The microscope having three-dimensional imaging capability according to claim 1 , wherein an environment where the sample is located is filled with a transparent material having its refractive index equal to a refractive index of the sample.

3. The microscope having three-dimensional imaging capability according to claim 1 , wherein the at least one excitation device comprises an excitation light source selected from a group comprising: one or more light-emitting diodes, one or more continuous lasers, one or more pulsed lasers, or any combination thereof.

4. The microscope having three-dimensional imaging capability according to claim 1 , wherein the detectable contrast is a signal selected from a group comprising one of the following: fluorescent light, elastic scattering light, Raman scattering, SHG, THG, stimulated Raman scattering, or a combination thereof.

5. The microscope having three-dimensional imaging capability according to claim 1 , wherein the at least one excitation device generates at least one excitation light beam which is perpendicular to a detection direction of the at least one detection device.

6. A microscope having three-dimensional imaging capability according to claim 5 , wherein the at least one excitation device comprises at least one scanning mechanism which is configured to perform scanning by moving the excitation light beam.

7. The microscope having three-dimensional imaging capability according to claim 6 , wherein the excitation light beam is shaped to have a beam radius which has a varying rate of not more than 3 times within the detection target region in a direction of the light beam.

8. The microscope having three-dimensional imaging capability according to claim 6 , wherein the at least one scanning mechanism comprises one or more galvanometer scanners, one or more resonant scanning mirrors, one or more rotating polygonal mirrors, one or more acousto-optic modulators, or any combination thereof.

9. The microscope having three-dimensional imaging capability according to claim 6 , wherein the at least one detection device uses a matrix photosensitive device to function as an imaging device configured to operate synchronously with the scanning mechanism.

10. The microscope having three-dimensional imaging capability according to claim 9 , wherein the at least one detection device comprises a de-scanning mechanism which is configured to operate synchronously with the scanning mechanism, and is provided with an array photosensitive device or a matrix photosensitive device to function as the imaging device.

11. The microscope having three-dimensional imaging capability according to claim 1 , wherein the at least one excitation device comprises a beam splitter which is configured to split the excitation light beam into a plurality of excitation sub-beams.

12. The microscope having three-dimensional imaging capability according to claim 11 , wherein the beam splitter comprises a combination of one or more lens arrays, one or more mirror arrays, one or more semi-transparent mirrors or a combination thereof, or comprises a fixed or adjustable phase filter or a digital micro mirror device (abbreviated as DMD) array.

13. The microscope having three-dimensional imaging capability according to claim 1 , wherein the at least one excitation device and the at least one detection device are configured to form collectively a structure for confocal scanning microscopy.

14. The microscope having three-dimensional imaging capability according to claim 1 , wherein the at least one excitation device comprises an excitation light source selected from the group consisting of one or more light-emitting diodes, one or more continuous lasers, and one or more pulsed lasers.

15. The microscope having three-dimensional imaging capability according to claim 1 , wherein the at least one detection device comprises a photosensitive device selected from the group consisting of dot, array and matrix devices.

16. The microscope having three-dimensional imaging capability according to claim 15 , wherein each of the dot, array and matrix devices is selected from the group consisting of CCD photosensitive elements, CMOS photosensitive elements, photodiodes, and photomultipliers.

17. The microscope having three-dimensional imaging capability according to claim 1 , wherein the at least one movement mechanism comprises a sample table which moves horizontally to generate a relative movement of the sample relative to the at least one excitation device and the at least one detection device.

18. The microscope having three-dimensional imaging capability according to claim 1 , wherein the microscope is in a condition that the continuum light source is configured to implement an excitation of a point of the sample in an excitation time by scanning, the excitation light which is continuum light produced by the scanning of the continuum light source is set such that a time during which the excitation light sweeps across a field of view of the microscope is divided by a width of the field of view of the microscope and then multiplied by a width of the excitation light so as to obtain a result value which is smaller than the excitation time, thereby facilitating a condition that blurring incurred by the relative movement is not observable within the excitation

Assignees

• Univ Science & Technology China

Inventors

• Zhu Qingyuan
• Bi Guoqiang
• Wang Hao
• Lau Pak-Ming
• Ding Lufeng
• Yang Chaoyu
• Yang Qianru
• Bi Dasheng
• Xin Qi

Classifications

• G02B21/006

  focusing arrangements; selection of the plane to be imaged · CPC title

• G02B21/0032 Primary

  Optical details of illumination, e.g. light-sources, pinholes, beam splitters, slits, fibers (G02B21/0036 - G02B21/008; means for illumination of specimens in general G02B21/06) · CPC title

• G02B2207/114

  Two photon or multiphoton effect · CPC title

• G02B21/008

  Details of detection or image processing, including general computer control · 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