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Non-contact stationary type fluorescent molecular tomography method and device

A technology of fluorescent molecular tomography and imaging methods, which is applied in the directions of measuring devices, fluorescence/phosphorescence, and material analysis through optical means, and can solve the problems affecting the survival of experimental animals, limiting the application of fluorescent molecular tomography, and difficult to achieve high throughput. Experiments and other issues to achieve the effect of shortening the shooting distance, shortening the exposure time, and improving the quality

Inactive Publication Date: 2009-07-22
TSINGHUA UNIV
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  • Abstract
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  • Claims
  • Application Information

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Problems solved by technology

[0005] In the existing non-contact fluorescent molecular tomography, the CCD camera 114 and the excitation light source 113 must be rotated relative to the experimental animal body 111 to obtain a 360° full-angle fluorescent signal on the boundary of the experimental animal body 111. If the system imaging time is long, Not only does it affect the survival of the experimental animal body, it is not conducive to the construction of small animal models in the body for a long period of time, but also the experimental imaging efficiency is low, and it is difficult to achieve high-throughput experiments, which limits the application of fluorescence molecular tomography

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  • Non-contact stationary type fluorescent molecular tomography method and device
  • Non-contact stationary type fluorescent molecular tomography method and device
  • Non-contact stationary type fluorescent molecular tomography method and device

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Embodiment 1

[0028] Such as Figure 4 , Figure 5As shown, the device of this embodiment includes 24 light-transmitting optical fibers 31-324 and 4 optical lenses 41-44 arranged around the object 7 to be measured, and an imaging plane of each optical lens 41-44 is respectively arranged A detector 6 is arranged at the bifurcated end of the image-transmitting optical fiber 5 and the light outlet of the compound end of the image-transmitting optical fiber 51-54; A computer is used to receive instructions from the computer to switch the excitation light to any light-transmitting optical fiber 31-324. An excitation light source 1 is arranged on the light-incoming side of the light switching part 2, and an excitation light filter 10 is arranged on the front end of the light switching part 2, so that the excitation light that can excite the luminescence band of the fluorescent substance in the measured object 7 enters the light switching Part 2, while filtering out other stray light. At the sa...

Embodiment 2

[0032] Such as Figure 6 As shown, most of the device of this embodiment is the same as that of Embodiment 1, but the excitation light source 1 in this embodiment adopts a semiconductor laser with a wavelength of 671 nanometers and an output power of 200 milliwatts, so it is not necessary to set the front end of the optical switching component 2 Excitation light filter 10. There are 12 light transmission optical fibers 3 in this embodiment, and there may be more or less. In addition, the fluorescence filters 11 arranged at the front ends of the optical lenses 41 - 44 may not be provided, and only one fluorescence filter 11 is arranged at the front end of the detector 6 .

[0033] When this embodiment is used, firstly, the computer controls the light switching component 2, and the excitation light from the excitation light source 1 is irradiated on the object 7 through any light transmission optical fiber 31-312, and the measured object 7 is irradiated by each optical lens 41-...

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Abstract

The invention relates to a noncontact fixed fluorescence molecular tomography method and device, and is characterized in that an imaging device comprising an excitation light source, an optical switch part, a plurality of light transmitting optical fibers, a plurality of optical lenses, an image transmitting optical fiber and a detector is arranged; the plurality of the light transmitting optical fibers and the plurality of the optical lenses are respectively arranged around an object to be detected; the optical switch part is controlled by a computer; excitated light emitted by the excitation light source irradiates on the object to be detected through any light transmitting optical fiber; fluorescence excitated by the object to be detected is imaged on each forky end of the image transmitting optical fiber through each optical lens and then is transmitted to the detector arranged on the light outlet of the image transmitting optical fiber through the composite end of the image transmitting optical fiber; the excitated light is switched to the light transmitting optical fibers at different positions through the optical switch part in turn; the fluorescence signal acquisition process is repeated to realize 360-degree full-angle fluorescence signal on the boundary of the object to be detected. The noncontact fixed fluorescence molecular tomography method and device can realize 360-degree full-angle and noncontact fixed acquisition of the fluorescence signal of the object to be detected, and has high imaging efficiency and quality.

Description

technical field [0001] The invention relates to a fluorescent molecular imaging method and device, in particular to a non-contact fixed fluorescent molecular tomographic imaging method and device. Background technique [0002] Fluorescence molecular tomography (Fluorescence molecular tomography, also known as fluorescence molecular tomography or fluorescence diffusion optical tomography) uses specific fluorescent molecules that have been widely used in biological and medical research as probes for labeling Specific molecules or cells, which observe the changes of molecular levels in organisms in vivo, and provide information such as the distribution of targets through image reconstruction, thereby overcoming the limitations of planar imaging, and obtaining more information about biological and medical behaviors. information. Fluorescence molecular tomography has the advantages of high sensitivity, quick and easy, low cost, and relatively high throughput. It not only support...

Claims

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Application Information

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IPC IPC(8): A61B5/00G01N21/64
CPCG01N21/6456G01N21/4795
Inventor 白净陈延平董志华汪待发陈欣潇
Owner TSINGHUA UNIV
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