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Laser scanning super-resolution microscopic imaging device, method and equipment based on multiple signal classification algorithm and storage medium

A technology of multiple signal classification and laser scanning, applied in the field of laser scanning super-resolution microscopy imaging devices, can solve the problems of difficulty in improving the lateral resolution of confocal microscopy technology, and achieve the effect of improving lateral resolution

Active Publication Date: 2022-03-01
HARBIN INST OF TECH
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Problems solved by technology

[0004] In order to overcome the defects in the above-mentioned prior art, the present invention provides a laser scanning super-resolution microscopic imaging device, method, equipment and storage medium based on a multiple signal classification algorithm, which can solve the problem that the horizontal resolution of confocal microscopy technology is difficult to improve

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  • Laser scanning super-resolution microscopic imaging device, method and equipment based on multiple signal classification algorithm and storage medium
  • Laser scanning super-resolution microscopic imaging device, method and equipment based on multiple signal classification algorithm and storage medium
  • Laser scanning super-resolution microscopic imaging device, method and equipment based on multiple signal classification algorithm and storage medium

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specific Embodiment approach

[0058] After the light emitted by the laser light source 15 is collimated by the collimating objective lens 7, it passes through the scanning galvanometer 8, the telecentric scanning lens 9 and the tube mirror 10 to realize dynamic beam scanning, passes through the dichroic mirror 11, and focuses on the surface of the sample through the objective lens 12 to generate fluorescence Sample 3, utilize dichroic mirror 11 and optical filter 13 to separate the fluorescent sample 3 collected by objective lens 12 and the reflected illumination light, the fluorescence emitted by fluorescent sample 3 passes through objective lens 12, dichroic mirror 11, optical filter 13 and collecting lens 14 to focus on the image plane of CCD camera 6 .

[0059] With the angular deflection of the scanning galvanometer 8, the focused light spot moves on the surface of the fluorescent sample 3, and after passing through the objective lens 12, dichroic mirror 11, filter 13 and collecting lens 14, the intens...

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Abstract

The invention discloses a laser scanning super-resolution microscopic imaging device, method and equipment based on a multi-signal classification algorithm, and a storage medium, belongs to the technical field of optical precision measurement, and aims to solve the problem that the transverse resolution of a confocal microscopic technology is difficult to improve. Comprising a laser light source, and a collimator objective, a scanning galvanometer, a telecentric scanning lens, a tube lens, a dichroscope, an objective lens, a fluorescence sample, an optical filter, a collection lens and a CCD camera are sequentially arranged in the light propagation direction of the laser light source. A CCD camera is used for collecting low-resolution image sequences generated in the random flickering process of a sample in different scanning focusing light spot illumination areas, a multi-signal classification algorithm is used for reconstructing the low-resolution image sequence of each scanning position, reconstruction results corresponding to all the scanning positions are spliced, and a high-resolution image is obtained. And the transverse resolution of the confocal microscopy technology can be effectively improved.

Description

technical field [0001] The invention relates to the technical field of optical precision measurement, in particular to a laser scanning super-resolution microscopic imaging device, method, equipment and storage medium based on a multiple signal classification algorithm. Background technique [0002] In the field of live cell imaging, optical microscopy stands out among many methods due to its non-destructive and non-contact imaging properties, but the existence of the optical diffraction limit limits its imaging resolution. In order to realize the observation of smaller-sized cells and subcellular biological samples, it is of great significance to improve the imaging resolution of optical microscopy techniques. [0003] Confocal microscopy has unique advantages in axial tomography capability, but its lateral resolution is limited to 1.4 times that of ordinary wide-field microscopy, and its imaging results are greatly affected by the diameter of the pinhole, while existing im...

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Application Information

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IPC IPC(8): G01N21/64
CPCG01N21/6486
Inventor 邹丽敏肖彩妮张甦丁雪梅
Owner HARBIN INST OF TECH
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