CN204731160U - A kind of autofluorescence life-span imaging and fluorescence spectrum combine the device being used for early diagnosis of cancer - Google Patents
A kind of autofluorescence life-span imaging and fluorescence spectrum combine the device being used for early diagnosis of cancer Download PDFInfo
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- CN204731160U CN204731160U CN201520366390.4U CN201520366390U CN204731160U CN 204731160 U CN204731160 U CN 204731160U CN 201520366390 U CN201520366390 U CN 201520366390U CN 204731160 U CN204731160 U CN 204731160U
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Abstract
The utility model belongs to technical field of medical equipment, is specially a kind of autofluorescence life-span imaging and fluorescence spectrum combines for early diagnosis of cancer device.Comprise laser scanning co-focusing microscope device and two-way fluorescence signal acquisition device; Specifically by LASER Light Source, two, XY direction galvanometer, the first catoptron, the second catoptron, dichroic mirror, the first convergent lens group, object lens, objective table, pin hole, the 3rd catoptron, removable slide block, the second convergent lens group, first color filter, photomultiplier, the 4th catoptron, the 3rd convergent lens group, second color filter, grating spectrograph, CCD detection instrument, principal computer, display screen, galvanometer control module, synchronizing signal forms.The utility model energy direct-detection goes out the various dimensions information such as fluoroscopic image, fluorescence lifetime, fluorescence spectrum of tested biological specimen, realizes carrying out early detection and diagnosis to kinds cancer, is with a wide range of applications in fields such as biomedicine, clinical diagnosises.
Description
Technical field
The utility model belongs to technical field of medical equipment, is specifically related to a kind of device for early diagnosis of cancer.
Background technology
Optical diagnostics is the important content of Biomedical Photonics, and it utilizes the method for optics to check and analysis of disease.The technology of optical diagnostics can be divided into two classes: spectral diagnosis of tissue and organism optical image-forming diagnose.Laser-induced autofluorescence spectral technique is a kind of effective optical diagnostic method.Human canceration's tissue is compared with normal structure, and set of biomolecules is divided and changed, and the fluorescence therefore sent there are differences, and utilizes laser-induced fluorescence spectroscopy to be suitable for collecting metabolic or structural-functional data, thus reaches the object of cancer diagnosis.Utilize fluorescence spectroscopy technique can provide experimental basis for the early diagnosis of cancer, and provide reference for the methods for the treatment of that tumour is follow-up, this technology is existing at present developed, and is little by little applied to the optical diagnostics of human lesion tissue.Fluorescence spectrum can provide very important information, but the result of the just equalization provided, the source of different fluorescent molecule substance in biological tissue or the environment variations of identical fluorescence molecule can not be embodied.And fluorescence lifetime is only relevant with the microenvironment residing for fluorescence molecule, the not impact of the factor such as stimulated luminescence Strength Changes, photobleaching.Therefore, the many physics in microenvironment residing for molecule, biology, chemical parameters such as ion concentration, oxygen content, pH value etc. are provided information by fluorescence lifetime imaging and durability analysis.Fluorescence lifetime analysis and fluorescence spectrum are combined, the more multi-layered secondary information such as metabolization, structure function difference about biological tissue can be obtained, be expected to high sensitivity diagnosis is realized for early-stage cancer.
Summary of the invention
The purpose of this utility model is the device for early diagnosis of cancer providing a kind of fluorescence lifetime imaging and fluorescence spectral measuring to combine, by carrying out the information such as the metabolism relevant to canceration with the measurement acquisition of fluorescence spectrum of autofluorescence life-span, structure function are abnormal to biological specimen, thus early diagnosis is carried out to cancer, improve accuracy, reduce misdiagnosis rate.
The autofluorescence life-span imaging that the utility model provides and fluorescence spectrum combine for early diagnosis of cancer device, that fluorescence lifetime imaging measurement and fluorescence spectral measuring are coupled with laser scanning co-focusing microscope, for observing the cytological appearance of biological specimen, realize the new device of early diagnosis of cancer in conjunction with autofluorescence life-span and spectral information.This device comprises laser scanning co-focusing microscope device and two-way fluorescence signal acquisition device, receive fluorescence lifetime information and fluorescence spectrum information by different detectors respectively, and utilize computer processing system to process autofluorescence life information and fluorescence spectrum information.Concrete structure as shown in Figure 1.This device is by two, LASER Light Source 1, XY direction galvanometer 2, first catoptron 3, second catoptron 4, dichroic mirror 5, the first convergent lens group 6, object lens 7, objective table 8, pin hole 9, the 3rd catoptron 10, removable slide block 11, second convergent lens group 12, first color filter 13, photomultiplier 14, the 4th catoptron the 15, three convergent lens group 16, second color filter 17, grating spectrograph 18, CCD detection instrument 19, principal computer 20, display screen 21, galvanometer control module 22, synchronizing signal 23 forms.Wherein:
LASER Light Source 1, for generation of exciting light;
Two, XY direction galvanometer 2, is connected with described LASER Light Source 1, for realizing the scanning of described LASER Light Source to tested biological specimen horizontal direction;
Galvanometer control module 22, is connected with described two, XY direction galvanometer, for scanning position and the sweep velocity of control XY galvanometer;
First catoptron 3, is connected with described two, XY direction galvanometer 2, for described exciting light is adjusted to the second catoptron 4;
Second catoptron 4, is connected with described first catoptron 3, for described exciting light is adjusted to dichroic mirror 5;
Dichroic mirror 5, is connected with described second catoptron 4; The autofluorescence of biological specimen is separated with exciting light by dichroic mirror 5; I.e. dichroic mirror 5 reflected excitation light, and the autofluorescence that the tested biological specimen of transmission produces, make it enter fluorescent collecting light path;
First convergent lens group 6, is connected with described dichroic mirror 5, for assembling described exciting light and autofluorescence;
Object lens 7, are connected with described first convergent lens group 6, for the exciting light after described convergence is focused on tested biological specimen, excite the fluorescence molecule emitting fluorescence in induction biological specimen;
Objective table 8, is connected with described object lens, for placing tested biological specimen;
Pin hole 9, is connected with described dichroic mirror 5, is positioned at the position of exciting light focus conjugation, for filtering the parasitic light outside focal plane;
3rd catoptron 10, is connected with described pin hole 9, for reflecting the autofluorescence that tested biological specimen is launched;
Removable slide block 11, is connected with described 3rd catoptron 10, for controlling the position of described 3rd catoptron;
Second convergent lens group 12, is connected with described 3rd catoptron 10, for assembling the autofluorescence that described tested biological specimen is launched;
First color filter 13, is connected with described second convergent lens group 12;
Photomultiplier 14, is connected with described first color filter 13, for detecting described autofluorescence signal;
4th catoptron 15, is connected with described pin hole 9, for reflecting the autofluorescence that tested biological specimen is launched;
3rd convergent lens group 16, is connected with described 4th catoptron 15, for assembling the autofluorescence that described biological specimen is launched;
Second color filter 17, is connected with described 3rd convergent lens group 16;
Grating spectrograph 18 is connected with described second color filter 17 with charge-coupled device CCD19, for gathering the spectral information of described fluorescence;
Synchronizing signal 23 exports from excitation source, and sends into principal computer 20, for triggered time correlated single photon counter.
In the utility model, described LASER Light Source 1 can adopt psec or the femtosecond pulse laser of high repetition frequency, wherein, picosecond pulse laser is used for the one-photon excitation to Auto-fluorescence substance in tested biological specimen, and femtosecond pulse laser is used for the multiphoton excitation to Auto-fluorescence substance in tested biological specimen.
In the utility model, described LASER Light Source 1 can adopt continuous light laser instrument, also can adopt quasi-continuous light laser, for the measurement to tested biological specimen fluorescence spectrum.
In the utility model, the spectral range of laser instrument used both can be fixed wave length, also can be wavelengthtunable, wavelength permission variation range can (as 320nm-1400nm near ultraviolet near infrared, for one-photon excitation or multiphoton excitation), select different wave length to detect according to the different fluorescent material of tested biological specimen.
In the utility model, adopting highly sensitive photomultiplier 14, for detecting the single photon signal of autofluorescence, realizing carrying out highly sensitive detection to weak signal.
In the utility model, Single Photon Counting device is adopted the signal that photomultiplier detects to be carried out to the time domain measurement of fluorescence lifetime.
In the utility model, isolated autofluorescence signal by input photomultiplier 14 after the first color filter (cut-off filter plate) 13, or ends filter plate by the first color filter 17() input grating spectrograph 18.
In the utility model, two, XY direction galvanometer 2 is added in the voltage on two panels galvanometer respectively by the control break of galvanometer control module 22, thus changes sweep velocity and the position of galvanometer, obtains the information of different microcell biological sample.
In the utility model, the 3rd catoptron 10 is movable mirror, for the selection of two-way fluorescence detection light path.The 3rd described catoptron 10 is arranged in the below of laser scanning co-focusing microscope device pin hole 9, and be connected with removable slide block 11, selection by simple push-and-pull control realization detection light path: when removable slide block 11 is in propelling position, fluorescence signal enters fluorescence lifetime measurement light path through the 3rd catoptron 10, carries out the collection of fluorescence lifetime information; When removable slide block 11 is in pull-out location, fluorescence signal enters fluorescence spectral measuring light path through the 4th catoptron 15 reflection, carries out the collection of fluorescence spectrum information.
In the utility model, in tested biological specimen autofluorescence life diagram picture, the fluorescence lifetime Information Pull Multiple-Index Model of each pixel carries out matching.
In the utility model, the object lens 7 in described laser scanning co-focusing microscope system can be low power lens, also can be high power lenses, as 10 times of-100 times of object lens, for the requirement that satisfied different enlargement ratio is observed.
In the utility model, described pin hole 9 size can change, and its scope is 60 μm-300 μm, obtains bright, that noise is low fluorescence lifetime imaging result according to the suitable aperture size of selection.
In the utility model, adopt high performance color filter to filtering by transmissible laser, and filter out other parasitic lights, only remaining autofluorescence signal enters harvester, reduces background influence, improves signal to noise ratio (S/N ratio).
In the utility model, when removable slide block 11 is in propelling position, 3rd catoptron 10 enters light path, thus the autofluorescence of pin hole 9 transmission is reflected, after the second convergent lens group 12 is assembled, transfer to the first color filter 13, filter the exciting light of biological specimen reflection, after photomultiplier 14 detects, analyze the fluorescence lifetime imaging data of tested biological specimen by the process of Single Photon Counting system acquisition.When removable slide block 11 is in pull-out location, 3rd catoptron 10 is away from light path, then the autofluorescence of pin hole 9 transmission transfers to the 4th catoptron 15, assemble through the 3rd convergent lens group 16 after reflection, after filtering the exciting light of reflection by the second color filter 17, gathered by grating spectrograph 18 and charge-coupled image sensor 19, finally analyze its fluorescence spectrum information by the principal computer 20 being configured with fluorescence spectrum process software.
In the utility model embodiment, the 3rd catoptron 10, removable slide block 11 and slide rail 24 form movable mirror device, and shown in Fig. 2, the 3rd catoptron 10 is connected with removable slide block 11 by connecting link, and removable slide block 11 is provided with handle 27.3rd catoptron 10 is placed with pin hole 9 angle at 45 °.Removable slide block 11 is in advanced state and is namely positioned at position 25, and removable slide block 11 is in pull-out state and is namely in position 26.
Adopt the utility model device, energy direct-detection goes out the various dimensions information such as fluoroscopic image, fluorescence lifetime, fluorescence spectrum of tested biological specimen, realizes carrying out early detection and diagnosis to kinds cancer.The advantage of the method and apparatus of this early diagnosis is: definite principle, and equipment is simple, simple operation, check that each section information obtained is many, detection speed is fast, and efficiency is high, can realize, to the highly sensitive detection of early carcinomatous change, being with a wide range of applications in fields such as biomedicine, clinical diagnosises.
Accompanying drawing explanation
Fig. 1 is the device schematic diagram that autofluorescence life-span of the present utility model and fluorescence spectrum combine for early diagnosis of cancer.
Fig. 2 is the device schematic diagram of movable mirror in the utility model.
Number in the figure: 1 is LASER Light Source, 2 is two, XY direction galvanometer, 3 is the first catoptron, 4 is the second catoptron, 5 is dichroic mirror, 6 is the first convergent lens group, 7 is object lens 8: objective table, 9 is pin hole, 10 is the 3rd catoptron, 11 is removable slide block, 12 is the second convergent lens group, 13 is the first color filter, 14 is photomultiplier, 15 is the 4th catoptron, 16 is the 3rd convergent lens group, 17 is the second color filter, 18 is grating spectrograph, 19 is CCD detection instrument, 20 is main frame, 21 is display screen, 22 is galvanometer control module, 23 is synchronizing signal, 24 is slide rail, and 25 is advanced state position, and 26 is pull-out state position, and 27 is can the handle of push-and-pull slide block 11.
Embodiment
The utility model is further described below in conjunction with drawings and Examples:
Embodiment 1:
Shown in Fig. 1 and Fig. 2, make the measurement mechanism of an autofluorescence life-span imaging of the present utility model and fluorescence spectrum combination.First the measurement of tested biological specimen autofluorescence life-span imaging is carried out: laser instrument 1 sends picosecond pulse laser or femtosecond pulse; The laser that laser instrument sends two through XY direction galvanometers 2 realize the Surface scan to XY plane; This exciting light is adjusted to dichroic mirror 5 through the reflection of the first catoptron 3 and the second catoptron 4; This dichroic mirror 5 pairs of exciting lights reflect completely; Object lens 7 are entered by the convergence of the first convergent lens group 6 by the exciting light reflected; Light after convergence focuses on tested biological specimen by object lens 7; The autofluorescence that tested biological specimen sends by object lens 7, then converges at dichroic mirror 5 through the first convergent lens group 6; This dichroic mirror 5 is for the complete transmission of autofluorescence; Advance removable slide block 11 to position 25, the autofluorescence through dichroic mirror 5 transmission is reflected by the 3rd catoptron 10; Autofluorescence after reflection is assembled through the second convergent lens group 12; Autofluorescence after convergence through the first color filter 13 filter may exist by the exciting light of dichroic mirror 5 transmission; Autofluorescence is detected by photomultiplier 14; Meanwhile the synchronizing signal 23 of exciting light is transferred in the data acquisition board of principal computer 20, the principal computer 20 of signal through being provided with Single Photon Counting device after photomultiplier 14 amplifies processes, and simulates fluorescence lifetime and obtain fluorescence lifetime image finally by fluorescence lifetime process software.
Tiny area characteristic on image is carried out again to the measurement of Autofluorescence: laser instrument 1 sends continuous laser or quasi-continuous lasing; The laser that laser instrument 1 sends two through XY direction galvanometers 2 realize the Surface scan to XY plane; This scan light is adjusted to dichroic mirror 5 through the reflection of the first catoptron 3 and the second catoptron 4; This dichroic mirror 5 pairs of exciting lights reflect completely; Object lens 7 are entered by the convergence of the first convergent lens group 6 by the exciting light reflected; Object lens 7 by assemble after Laser Focusing in tested tissue; The autofluorescence that tested tissue sends by object lens 7, then converges at dichroic mirror 5 through the first convergent lens group 6; This dichroic mirror 5 is for the complete transmission of autofluorescence; Pull out removable slide block 11 and be in position 26, the autofluorescence through dichroic mirror 5 transmission is reflected by the 4th catoptron 15; Autofluorescence after reflection is assembled through the 3rd convergent lens group 16; Fluorescence after convergence through the second color filter 17 filter may exist by the exciting light of dichroic mirror 5 transmission; Autofluorescence gathers through grating spectrograph 18 and charge coupled device ccd 19; Signal after collection is processed by the computer system 20 being provided with fluorescence spectrum process software, and shows its fluorescence spectrum information at display screen 21.
Embodiment 2:
Implement by embodiment 1: the measurement first the epithelium region of human body cervical tissue being carried out to fluorescence lifetime imaging.Tested cervical tissue section is placed on objective table 8, uses 60 times of object lens to observe cervical tissue epidermal cell form.Advance removable slide block 11 to position 25, the fluorescent material of picosecond pulse laser to tested cervical tissue of use 50MHz, 405 nm wavelength excites, and the first color filter 13 in fluorescent collecting light path and the second color filter 17 are the cut-off filter plate of 430 nm high passes.After signal after photomultiplier 14 amplifies is processed by the main frame 20 being provided with Single Photon Counting device, simulate fluorescence lifetime by fluorescence lifetime process software and obtain the result of fluorescence lifetime image.
By use the utility model device, human body cervical tissue is carried out to the result of fluorescence lifetime imaging measurement, the left and right two width figure in result are respectively normally, canceration cervical epithelial tissue fluorescence lifetime imaging figure.The measurement result using the utility model device to carry out fluorescence lifetime imaging can demonstrate normal cervical tissues epithelial cell and the difference of canceration cervical tissue epithelial cell on Morphology and structure clearly, cellular morphology in cancerous issue trends towards circle, and the ratio shared by core increases greatly.Image is clear, resolution is high, and each pixel of image all comprises the information of fluorescence lifetime.By contrasting the change of normal cervical epithelial tissue and canceration cervical epithelial tissue fluorescence lifetime, the situation that residing for normal and canceration cervical epithelial cells, microenvironment changes can be obtained further.The utility model device is used cervical epithelial tissue to be carried out to the measurement of fluorescence lifetime imaging, the change of cellular morphology and structure can be judged exactly, simultaneously by contrasting the fluorescence lifetime of normal and canceration cervical epithelial tissue, the early diagnosis for cancer provides foundation and information.
Based on the image of fluorescence lifetime imaging gained, respectively normal and canceration cervical tissue epithelium region are carried out to the measurement of fluorescence spectrum.Pull out removable slide block 11 to position 26, the fluorescent material of continuous light to tested cervical tissue using 405nm wavelength instead excites.
By use the utility model device, human body cervical tissue is carried out to the result of fluorescence spectral measuring.In result, dotted line is the fluorescent spectrum curve of normal cervical tissues, and solid line is the fluorescent spectrum curve of canceration cervical tissue.The fluorescence spectrum of normal cervical epithelial tissue comprises 440 ± 5 nm and 470 ± 4 nm, two peaks, and the fluorescence spectrum of canceration cervical epithelial tissue has three peaks at 440 ± 4 nm, 490 ± 5 nm and 540 ± 5 nm places.By use the utility model device, tested cervical tissue is carried out to the measurement of fluorescence spectrum, the structure of the curve of spectrum, difference that is normal and canceration cervical tissue can be judged rapidly and accurately, thus provide a fast approach accurately for the early diagnosis of cancer.
Claims (9)
1. an autofluorescence life-span imaging and fluorescence spectrum combine and are used for early diagnosis of cancer device, it is characterized in that comprising laser scanning co-focusing microscope device and two-way fluorescence signal acquisition device, receive fluorescence lifetime information and fluorescence spectrum information by different detectors respectively, and utilize computer processing system to process autofluorescence life information and fluorescence spectrum information; Specifically by LASER Light Source, two, XY direction galvanometer, the first catoptron, the second catoptron, dichroic mirror, the first convergent lens group, object lens, objective table, pin hole, the 3rd catoptron, removable slide block, the second convergent lens group, first color filter, photomultiplier, the 4th catoptron, the 3rd convergent lens group, second color filter, grating spectrograph, CCD detection instrument, principal computer, display screen, galvanometer control module, synchronizing signal forms; Wherein:
LASER Light Source, for generation of exciting light;
Two, XY direction galvanometer, is connected with described LASER Light Source, for realizing the scanning of described LASER Light Source to tested biological specimen horizontal direction;
Galvanometer control module, is connected with described two, XY direction galvanometer, for scanning position and the sweep velocity of control XY galvanometer;
First catoptron, is connected, for described exciting light is adjusted to the second catoptron with described two, XY direction galvanometer;
Second catoptron, is connected with described first catoptron, for described exciting light is adjusted to dichroic mirror;
Dichroic mirror, is connected with described second catoptron; The autofluorescence of biological specimen is separated with exciting light by dichroic mirror; I.e. dichroic mirror reflected excitation light, and the autofluorescence that the tested biological specimen of transmission produces, make it enter fluorescent collecting light path;
First convergent lens group, is connected with described dichroic mirror, for assembling described exciting light and autofluorescence;
Object lens, are connected with described first convergent lens group, for the exciting light after described convergence is focused on tested biological specimen, excite the fluorescence molecule emitting fluorescence in induction biological specimen;
Objective table, is connected with described object lens, for placing tested biological specimen;
Pin hole, is connected with described dichroic mirror, is positioned at the position of exciting light focus conjugation, for filtering the parasitic light outside focal plane;
3rd catoptron, is connected with described pin hole, for reflecting the autofluorescence that tested biological specimen is launched;
Removable slide block, is connected with described 3rd catoptron, for controlling the position of described 3rd catoptron;
Second convergent lens group, is connected with described 3rd catoptron, for assembling the autofluorescence that described tested biological specimen is launched;
First color filter, is connected with described second convergent lens group;
Photomultiplier, is connected with described first color filter, for detecting described autofluorescence signal;
4th catoptron, is connected with described pin hole, for reflecting the autofluorescence that tested biological specimen is launched;
3rd convergent lens, is connected with described 4th catoptron, for assembling the autofluorescence that described biological specimen is launched;
Second color filter, is connected with described 3rd convergent lens group;
Grating spectrograph is connected with described second color filter with charge-coupled device CCD, for gathering the spectral information of described fluorescence;
Synchronizing signal exports from excitation source, and sends into principal computer, for triggered time correlated single photon counter.
2. autofluorescence life-span imaging according to claim 1 and fluorescence spectrum combine and are used for early diagnosis of cancer device, it is characterized in that, described LASER Light Source adopts psec or the femtosecond pulse laser of high repetition frequency, wherein, picosecond pulse laser is used for the one-photon excitation to Auto-fluorescence substance in tested biological specimen, and femtosecond pulse laser is used for the multiphoton excitation to Auto-fluorescence substance in tested biological specimen.
3. autofluorescence life-span imaging according to claim 1 and 2 and fluorescence spectrum combine and are used for early diagnosis of cancer device, it is characterized in that, described LASER Light Source adopts continuous light laser instrument, or adopts quasi-continuous light laser, for the measurement to tested biological specimen fluorescence spectrum.
4. autofluorescence life-span imaging according to claim 3 and fluorescence spectrum combine and are used for early diagnosis of cancer device, it is characterized in that, the spectral range of laser instrument used is fixed wave length, or wavelengthtunable, wavelength allows variation range near ultraviolet near infrared, selects different wave length to detect according to the different fluorescent material of tested biological specimen.
5. the autofluorescence life-span imaging according to claim 1,2 or 4 and fluorescence spectrum combine and are used for early diagnosis of cancer device, it is characterized in that, adopt Single Photon Counting device the signal that photomultiplier detects to be carried out to the time domain measurement of fluorescence lifetime.
6. the autofluorescence life-span imaging according to claim 1,2 or 4 and fluorescence spectrum combine and are used for early diagnosis of cancer device, it is characterized in that, 3rd catoptron and removable slide block are connected to become movable mirror, for the selection of two-way fluorescence detection light path; When removable slide block is in propelling position, fluorescence signal enters fluorescence lifetime measurement light path through the 3rd catoptron, carries out the collection of fluorescence lifetime information; When removable slide block is in pull-out location, fluorescence signal enters fluorescence spectral measuring light path through the 4th catoptron reflection, carries out the collection of fluorescence spectrum information.
7. the autofluorescence life-span imaging according to claim 1,2 or 4 and fluorescence spectrum combine and are used for early diagnosis of cancer device, it is characterized in that, in tested biological specimen autofluorescence life diagram picture, the fluorescence lifetime Information Pull Multiple-Index Model of each pixel carries out matching.
8. the autofluorescence life-span imaging according to claim 1,2 or 4 and fluorescence spectrum combine and are used for early diagnosis of cancer device, and it is characterized in that, object lens are times object lens of 10 times-100, for the requirement that satisfied different enlargement ratio is observed.
9. autofluorescence life-span imaging according to claim 1 and 2 and fluorescence spectrum combine and are used for early diagnosis of cancer device, it is characterized in that, described aperture size can change, its scope is 60 μm-300 μm, selects suitable aperture size to obtain bright, that noise is low fluorescence lifetime imaging result.
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| CN104880445A (en) * | 2015-06-01 | 2015-09-02 | 复旦大学 | Early cancer diagnosis device based on combination of auto-fluorescence lifetime imaging and fluorescence spectroscopy |
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| CN104880445B (en) * | 2015-06-01 | 2017-12-01 | 复旦大学 | A kind of autofluorescence life-span imaging and fluorescence spectrum combine the device for early diagnosis of cancer |
| CN104880445A (en) * | 2015-06-01 | 2015-09-02 | 复旦大学 | Early cancer diagnosis device based on combination of auto-fluorescence lifetime imaging and fluorescence spectroscopy |
| CN105891171A (en) * | 2016-03-01 | 2016-08-24 | 中国科学院重庆绿色智能技术研究院 | Efficient high-precision low-temperature laser scanning double-focus microscope system |
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| CN106841165B (en) * | 2017-03-24 | 2023-11-21 | 钢研纳克检测技术股份有限公司 | Portable Raman spectrometer capable of turning optical path |
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| CN108333157A (en) * | 2018-01-23 | 2018-07-27 | 深圳大学 | biomolecule three-dimensional dynamic analysis method and system |
| CN108333157B (en) * | 2018-01-23 | 2021-08-03 | 深圳大学 | Method and system for three-dimensional dynamic analysis of biomolecules |
| CN108548803A (en) * | 2018-04-08 | 2018-09-18 | 薛笑杰 | Nondestructive detection system based on fluorescent material |
| CN108562565A (en) * | 2018-04-08 | 2018-09-21 | 薛笑杰 | Lossless detection method based on fluorescent material |
| CN108362675A (en) * | 2018-04-08 | 2018-08-03 | 薛笑杰 | Non-destructive detecting device based on fluorescent material |
| CN108844929A (en) * | 2018-05-14 | 2018-11-20 | 杨佳苗 | It is divided the discrete fluorescence spectrum of pupil differential confocal and fluorescence lifetime detection method and device |
| CN108844930A (en) * | 2018-05-14 | 2018-11-20 | 杨佳苗 | It is divided the confocal discrete fluorescence spectrum of pupil and fluorescence lifetime detection method and device |
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