CN1033557A - A kind of medical laser fluoresence diagnostic apparatus that is used for diagnosing tumour - Google Patents
A kind of medical laser fluoresence diagnostic apparatus that is used for diagnosing tumour Download PDFInfo
- Publication number
- CN1033557A CN1033557A CN 87105948 CN87105948A CN1033557A CN 1033557 A CN1033557 A CN 1033557A CN 87105948 CN87105948 CN 87105948 CN 87105948 A CN87105948 A CN 87105948A CN 1033557 A CN1033557 A CN 1033557A
- Authority
- CN
- China
- Prior art keywords
- optical fiber
- fluoresence
- mentioned
- laser
- diagnostic apparatus
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Landscapes
- Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
- Endoscopes (AREA)
Abstract
Existing malignant tumor fluoresence diagnostic apparatus is owing to utilize the opto-electronic conversion treatment technology of serial, so speed is slower, when as the diagnosis of in-vivo tissue, because in-vivo tissue is at continuous wriggling, thereby makes spectral signal distortion greatly, even the phenomenon of omission takes place.
The present invention adopts multiple tracks parallel optoelectronic conversion processor, and adopts advanced y-type structure optical fiber and computer processing system, makes this instrument have quick, accurate, easy to operate advantage.Through clinical trial, the accuracy rate of diagnosis of Patients with Gastric Cancer is reached more than 90%.
Description
The invention belongs to Medical Instruments.
Utilize laser irradiation human tumor position, receive the autofluorescence of tumor, thereby make a definite diagnosis the character of human tumor, admitted by medical circle, and entered clinical practice from the experimental stage according to the spectral characteristic of human body autofluorescence.As the Shanghai City medical device research as described in the patent " malignant tumor fluoresence diagnostic apparatus " of on April 1st, 1985 application.
It is that the black light of 3000~4000 A is by the surface of fiber optic transmission to tested biological tissue that this instrument penetrates wavelength by light-source system, activate the characteristic spectrum of biological tissue (comprising normal structure and malignant tumor) and present autofluorescence, excited fluorescent is given beam splitting system (spectrogrph) by fiber optic transmission, after converting optical signal to the signal of telecommunication through 0.5 second automatic scanning system, can show the intrinsic fluorescence spectra that excites after handling by Circuits System, and can numeral show and report to the police.
But this instrument has a main shortcoming, promptly because this instrument adopts 0.5 second automatic scanning system for this process of opto-electronic conversion, this is actually the photoelectric conversion process of a serial, be about to satisfy a space narrow slit optical filter by some by the polychromatic spectra of beam splitting system (spectrogrph) output, give for example photomultiplier tube of a photoelectric sensor, carry out record to satisfy a signal of telecommunication that obtains various spectrum compositions.Because the result of above-mentioned such serial process makes that the processing speed of instrument is quite slow, serious is, when the tumor of human body in-vivo tissue is diagnosed, lasing light emitter is deep into the in-vivo tissue surface by endoscope, because in-vivo tissue is constantly being wriggled, if therefore tissue receiving is worked for the autofluorescence that the some position excites soon, the fluorescence signal that then receives becomes the superposition of the fluorescence signal of organizing multi-point shooting in fact, the signal of the feasible autofluorescence that receives has bigger distortion, even the omission phenomenon takes place, thereby greatly reduce the reliability and the accuracy of instrument diagnoses malignant tumor.
The present invention is intended to solve this subject matter in the prior art, develops fast, correctly to be used for the fluoresence diagnostic apparatus that the human clinical diagnoses various tumors.
Fig. 1 is a theory diagram of the present invention.
Fig. 2 is the opto-electronic conversion processor sketch map of multiple tracks parallel organization.
Fig. 3 is the y-type optical fiber structural representation that uses among the present invention.
Principle of the present invention is that embodiment can be illustrated by Fig. 1.
Laser beam by light-source system 1 ejaculation, the present invention can adopt the frequency tripling 3650A near ultraviolet pulse laser of xenon ion laser instrument output 3650A near ultraviolet pulse laser or the output of YAG laser instrument, also available other similar lasing light emitter, scioptics 13 focus on and enter Laser Transmission silica fibre 12, shine testee by endoscope and activate biological tissue.Produce autofluorescence as testee, then being accepted optical fiber 11 by the fluorescence in Laser Transmission and the fluorescence acquisition system 2 receives, be transferred to colour splitting system (spectrogrph) 3 and be launched into the polychromatic spectra signal, handle to convert the signal of telecommunication after 4 the processing to and deliver to electronic processing system 23 and carry out data acquisition and processing by opto-electronic conversion, make diagnosis.
The present invention is characterized in:
1) this instrument also comprises one by cold light source 5, the light source isochronous controller that electronic shutter 6 and control circuit 22 are formed.When the laser fiber endoscopically is deep into in-vivo tissue, must open cold light source this moment, seek structural Suspected Area by operator by the surveillance of forming by low-light gamma camera 7 and monitor 8, this moment, electronic shutter 6 must cut out, in case stronger cold light source damages highly sensitive opto-electronic conversion processor 4, when in case operator find the Suspected Area of tissue to diagnose, switching cold light source and electronic shutter by operator synchronously by control circuit 22 makes cold light source close, electronic shutter is opened, thereby carries out the collection and the processing of fluorescence.
2) the opto-electronic conversion processor of above-mentioned opto-electronic conversion processor 4 employing parallel organizations, as shown in Figure 2.This transducer by few to 256 road as many as, 1024 roads an opto-electronic conversion pop one's head in and form an array, 24 are wherein one among the figure, polychromatic spectra signal by spectrogrph 3 outputs is received by the opto-electronic conversion probe simultaneously, form a multiple tracks parallel optoelectronic conversion processor, this transducer can will convert the signal of telecommunication to by the optical signal of spectrogrph 3 outputs in smaller or equal to the time of 40ms, and be converted into digital signal, store and handle by electronic processing system 23.
This opto-electronic conversion processor can adopt secondary to resemble enhancement mode silicon target camera tube structure, glue together by dielectric material between secondary casting image intensifier and the silicon target camera tube, and at the peripheral embedding silica gel of secondary casting image intensifier, thereby the sensitivity that improves optical-electrical converter greatly improves signal to noise ratio.
As a kind of conversion, above-mentioned opto-electronic conversion processor also can adopt fixedly camera device of advanced CCD.
3) above-mentioned Laser Transmission and fluorescence acquisition system 2 adopt the y-type structure laser fiber, as shown in Figure 3.Wherein laser transmission fiber adopts silica fibre 12, fluorescence receives optical fiber when adopting glass fibre 11, two road optical fiber to begin respectively for independently one, merging into one later on becomes coaxial optical fiber.The core diameter of silica fibre 12 is 300u~400u, and glass optical fiber 11 is made up of smaller or equal to the multiply glass fiber bundle of 30u diameter.Silica fibre 12 on the end face 25 of the y-type structure optical fiber 2 of insertion endoscope is positioned at central authorities, is glass fibre 11 all around, and the contact lens 28 of a lens type is arranged on end face; Glass fiber bundle on the y-type structure fiber end face 26 is arranged in the slit structure, and its width is 0.5mm~1.0mm, and its length is 5mm~8mm; Y-type structure fiber end face 27 can be fixed on the optical fiber five times regualting frame and finely tune; Whole y-type optical fiber outermost layer can be by having certain rigidity but the flexible jacket pipe is protected.
4) above-mentioned beam splitting system (spectrogrph) 3 adopts the grating type spectrogrph of large apertures input, and general at present spectrogrph commonly used has two kinds of prism-type and grating types, though the low dispersion non-linearity of the big resolution of prism-type spectrogrph transmitance; The grating type spectrogrph then has the resolution height, and the advantage of chromatic dispersion linearity is generally about 1/5 but the aperture is less, and is so transmitance is little, therefore, all not very good.The present invention adopts the grating type spectrogrph of large aperture input, and its aperture reaches between 1/2~1/3, collects above-mentioned two types advantage, under the prerequisite that keeps high-resolution, chromatic dispersion linearity, has improved transmitance and has obtained good effect.
5) above-mentioned electronic processing system adopts computer to carry out control treatment.It comprises A/D converter 15, master computer 16, D/A interpreter 17, display 18, drawing apparatus 19, printer 20, data file 21.Under the programme-control of establishment in advance, master computer is finished LASER Light Source startup, spectrum data gathering, data-storing, data superposition, is sought a series of functions such as malignant characteristic peak, spectrogram shape, spectra re-recorded figure, printing spectroscopic data.
The present invention makes this instrument have fast owing to made full use of modern various advanced persons' science and technology, accurately, and easy to operate advantage.Through clinical trial, effect is remarkable, and the rate of accuracy reached of diagnosing gastric cancer is more than 90%, and process is to the patient's of the non-bent type hypertrophy of part gastric tissue serious (belonging to precancer) inspection, also find to have characteristic peak, promptly wide prospect has been showed in gastric cancer patient's in early stage diagnosis near cancer.This instrument also can be diagnosed in other various bodies and the cancer of body surface simultaneously, so the present invention will be subjected to more and more widely attention and application on cancer diagnosis.
Claims (7)
1, a kind of medical laser fluoresence diagnostic apparatus that is used for diagnosing tumour, it comprises light-source system 1, Laser Transmission and fluorescence acquisition system 2, beam splitting system (spectrogrph) 3, opto-electronic conversion processor 4, electronic processing system is characterized in that: it also comprises a light source isochronous controller; Above-mentioned opto-electronic conversion processor 4 is a multiple tracks parallel optoelectronic conversion processor of being made up of 256~1024 road opto-electronic conversion probe, can will convert the signal of telecommunication simultaneously to by the polychromatic spectra signal that spectrogrph is exported in smaller or equal to the time of 40ms; Above-mentioned Laser Transmission and fluorescence acquisition system 2 adopt the y-type structure laser fiber, wherein laser transmission fiber adopts silica fibre 12, fluorescence receives optical fiber and adopts glass fibre 11, when two road optical fiber begin respectively for independently one, merge into one later on and become coaxial optical fiber, silica fibre 12 on the end face 25 of the y-type optical fiber in insertion speculum forceps hole is positioned at central authorities, be glass fibre 11 all around, the contact lens 28 that one lens type is arranged on end face, the reception optical fiber on the end face 26 of y-type optical fiber is arranged in the slit structure; Above-mentioned electronic processing system adopts computer to carry out control treatment.
2, fluoresence diagnostic apparatus according to claim 1, it is characterized in that above-mentioned multiple tracks is parallel, opto-electronic conversion processor 4 is that secondary resembles enhancement mode silicon target camera tube structure, glues together by dielectric material between secondary casting image intensifier and the silicon target camera tube, and at the peripheral embedding silica gel of secondary casting image intensifier.
3, according to claim 1,2 described fluoresence diagnostic apparatuses is characterized in that above-mentioned multiple tracks parallel optoelectronic conversion processor 4 can adopt the CCD solid camera device.
4, y-type structure laser fiber according to claim 1, the core diameter that it is characterized in that above-mentioned silica fibre 12 is 300~400u, glass fibre 11 is made up of smaller or equal to the multiply glass fiber bundle of 30u diameter, receiving the width that optical fiber is arranged in slit on the end face 26 is 0.5mm~1.0mm, length is 5mm~8mm, and end face 27 can be fixed on the optical fiber five times regualting frame and finely tune; Whole y-type optical fiber outermost layer has certain rigidity but the flexible jacket pipe is protected.
5, large aperture input grating type spectrogrph according to claim 1, the relative aperture that it is characterized in that this spectrogrph is between 1/2~1/3.
6, fluoresence diagnostic apparatus according to claim 1 is characterized in that above-mentioned light source isochronous controller is made up of cold light source 5, electronic shutter 6, control circuit 22; Low-light gamma camera 7, TV monitor 8 are formed a surveillance, estimate cold light source 5 and electronic shutter 6 are finished in the back by control circuit synchronous switching by operator.
7, fluoresence diagnostic apparatus according to claim 1, it is characterized in that the computer-controlled electronic processing system of above-mentioned employing by A/D converter 15, master computer 16, D/A converter 17, display 18, drawing apparatus 19, printer 20, data file 21 are formed.Under the programme-control of establishment in advance, master computer is finished a series of functions such as LASER Light Source startup, spectrum data gathering, data-storing, superposition, searching malignant characteristic peak, spectrogram shape, spectra re-recorded figure, printing spectroscopic data.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 87105948 CN1024112C (en) | 1987-12-24 | 1987-12-24 | Laser fluorescent diagnostic unit for malignant tumour |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 87105948 CN1024112C (en) | 1987-12-24 | 1987-12-24 | Laser fluorescent diagnostic unit for malignant tumour |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1033557A true CN1033557A (en) | 1989-07-05 |
CN1024112C CN1024112C (en) | 1994-04-06 |
Family
ID=4815523
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN 87105948 Expired - Fee Related CN1024112C (en) | 1987-12-24 | 1987-12-24 | Laser fluorescent diagnostic unit for malignant tumour |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1024112C (en) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1310617C (en) * | 2001-01-22 | 2007-04-18 | V-目标技术有限公司 | Ingestible pill |
CN101975769A (en) * | 2010-09-17 | 2011-02-16 | 福建师范大学 | Human tissue autofluorescence detection system based on excitation of light sources with different wavelength |
CN102599884A (en) * | 2011-01-19 | 2012-07-25 | 中国科学院安徽光学精密机械研究所 | Laser early cancer diagnosis instrument |
CN106706585A (en) * | 2016-12-31 | 2017-05-24 | 中国科学院昆明动物研究所 | Device and method for recording living body fluorescence signals |
CN108742490A (en) * | 2018-05-30 | 2018-11-06 | 广州众健医疗科技有限公司 | A kind of spectral detection system of diagnosing gastric cancer gastroscope |
CN108937828A (en) * | 2018-05-29 | 2018-12-07 | 广州众健医疗科技有限公司 | A kind of Multifunctional gastroscope endoscope for diagnosing gastric cancer |
CN110082322A (en) * | 2018-12-25 | 2019-08-02 | 华中科技大学 | A kind of preparation method of optical fiber probe Fluorescence Spectrometer and optical fiber probe |
CN111166281A (en) * | 2020-01-24 | 2020-05-19 | 复旦大学 | Near-infrared fluorescence imaging detection system for ovaries assisted by colposcope |
-
1987
- 1987-12-24 CN CN 87105948 patent/CN1024112C/en not_active Expired - Fee Related
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1310617C (en) * | 2001-01-22 | 2007-04-18 | V-目标技术有限公司 | Ingestible pill |
CN101975769A (en) * | 2010-09-17 | 2011-02-16 | 福建师范大学 | Human tissue autofluorescence detection system based on excitation of light sources with different wavelength |
CN102599884A (en) * | 2011-01-19 | 2012-07-25 | 中国科学院安徽光学精密机械研究所 | Laser early cancer diagnosis instrument |
CN106706585A (en) * | 2016-12-31 | 2017-05-24 | 中国科学院昆明动物研究所 | Device and method for recording living body fluorescence signals |
CN108937828A (en) * | 2018-05-29 | 2018-12-07 | 广州众健医疗科技有限公司 | A kind of Multifunctional gastroscope endoscope for diagnosing gastric cancer |
CN108742490A (en) * | 2018-05-30 | 2018-11-06 | 广州众健医疗科技有限公司 | A kind of spectral detection system of diagnosing gastric cancer gastroscope |
CN110082322A (en) * | 2018-12-25 | 2019-08-02 | 华中科技大学 | A kind of preparation method of optical fiber probe Fluorescence Spectrometer and optical fiber probe |
CN111166281A (en) * | 2020-01-24 | 2020-05-19 | 复旦大学 | Near-infrared fluorescence imaging detection system for ovaries assisted by colposcope |
Also Published As
Publication number | Publication date |
---|---|
CN1024112C (en) | 1994-04-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4957114A (en) | Diagnostic apparatus for intrinsic fluorescence of malignant tumor | |
CN100512760C (en) | Method and apparatus for forming an image that shows information about a subject | |
US5408996A (en) | System and method for localization of malignant tissue | |
US6741884B1 (en) | Infrared endoscopic balloon probes | |
CN101485558B (en) | Single-optical fiber multiphoton fluorescence scanning endoscope | |
DE60219824T2 (en) | FIGURE APPARATUS AND ASSOCIATED METHOD | |
US20160066772A1 (en) | Infrared endoscopic balloon probes | |
US20040186382A1 (en) | Spectral volume microprobe arrays | |
JP3467131B2 (en) | Electronic endoscope device for fluorescence diagnosis | |
CN102389288B (en) | Confocal laser micro-endoscope | |
GB2203831A (en) | Diagnosis of malignant tumours by fluorescence | |
WO2000041615A1 (en) | Spectral volume microprobe arrays | |
WO2013066107A1 (en) | Probe for diagnosing otitis media using terahertz waves and otitis media diagnosis system and method | |
CA2428074A1 (en) | A method for the detection of viable microorganisms | |
US20220133273A1 (en) | Transparent ultrasound transducers for photoacoustic imaging | |
CN1024112C (en) | Laser fluorescent diagnostic unit for malignant tumour | |
CN105167736A (en) | Novel multi-modal gastroendoscope system | |
JPH02200237A (en) | Fluorescent observing method | |
JP4451509B2 (en) | Fluorescence measuring device and apparatus using such a device | |
CN202191264U (en) | Endoscope | |
DE102007047093B4 (en) | Device for measuring fluorescence radiation on biological substances with a semiconductor sensor arrangement | |
JP3255373B2 (en) | In vivo measuring device | |
CA2358558A1 (en) | An image guide and method for sub-micron imaging and picosecond timing | |
DE29613103U1 (en) | Endoscope head | |
WO2000013578A1 (en) | Infrared endoscopic balloon probes |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C06 | Publication | ||
PB01 | Publication | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
C20 | Patent right or utility model deemed to be abandoned or is abandoned | ||
CF01 | Termination of patent right due to non-payment of annual fee |