TW201907858A - Rapid tissue molecule spectral imaging device - Google Patents

Abstract

The invention provides a rapid tissue molecule spectral imaging device. The device comprises a light emitting unit, a steering unit, a scanning unit and a detection unit, wherein the light emitting unit is used for emitting linear light beams; the steering unit is used for steering the linear light beams and fluorescence passing through samples; the scanning unit is used for adjusting the direction of the steered linear light beams to scan the samples line by line; the detection unit is used for collecting the fluorescence and forming spatial images and spectral information of the samples. The spatial images and spectral information of tissue molecules are obtained by combining the linear light beams with the spectral detection unit so that the imaging speed of the tissue molecules can be greatly increased, and real-time imaging can be achieved; the spectral information can assist in analyzing tissue conditions (such as used for tumor analysis). The scanning unit only performs one-dimensional scanning, so that the stability of a system can be effectively improved.

Description

Rapid tissue molecular imaging imaging device

The present invention relates to the field of medical devices, and more particularly to a rapid tissue molecular spectral imaging device.

Tumors are major diseases that pose a serious threat to human health. Numerous studies have shown that more than 90% of tumors are derived from epithelial cell lesions, and molecular and cellular levels of variation occur during cancer development. Fiber-optic beam-based high-resolution optical endoscopic imaging technology that achieves micron or sub-micron resolution, enabling endoscopic magnification up to 1000 times, and is lossless compared to other medical imaging techniques (such as CT, MRI, PET, etc.) The technical advantages of immediate and in vivo detection of microscopic tumor lesions can better improve the early diagnosis rate of tumors. The probe end of the endoscopic imaging can penetrate deep into the living body to complete the micro-scale in-vivo non-destructive testing, and realize the “in-vivo biopsy” without sampling, which brings new technical means for early detection of molecular molecular lesions.

The present invention has been made in consideration of the above problems. The present invention provides a rapid tissue molecular spectroscopic imaging apparatus comprising a light emitting unit, a steering unit, a scanning unit and a spectral detecting unit, wherein the light emitting unit is for emitting a line beam; the steering unit is for steering the line beam And transmitting fluorescence through the sample; the scanning unit is configured to adjust a direction of the turned line beam to scan the sample line by line; and the spectral detecting unit is configured to collect the fluorescence and form a spatial image and spectrum of the sample News.

Illustratively, the light emitting unit includes: a light source for emitting a collimated beam; and a beam expander focus concentrator disposed at an exit of the light source for expanding and collimating the collimated beam For the line beam.

Illustratively, the steering unit is a dichroic mirror.

Illustratively, the scanning unit is a single scanning galvanometer, or a spatial light modulator.

Illustratively, the apparatus further includes a relay unit and an internal view unit disposed downstream of the scanning unit, wherein the relay unit is configured to focus a line beam scanned by the scanning unit to the internal view unit The inner view unit is configured to conduct and focus the focused line beam onto the sample and receive fluorescence emitted by the sample; the fluorescent light passing through the relay unit, the scanning unit, and the steering unit It is then collected by the spectral detection unit.

Illustratively, the inner view unit includes a coupling objective lens and an imaging fiber bundle, wherein the coupling objective lens is disposed at one end of the imaging fiber bundle for coupling the focused line beam into a proximal end of the fiber bundle And the imaging fiber bundle is used to conduct incoming line beams.

Illustratively, the interior view unit further includes a miniature objective lens disposed at the other end of the imaging fiber bundle for focusing a beam of light conducted by the bundle of fibers onto the sample.

Illustratively, the detecting unit comprises a line array detecting unit, a spectrum detecting unit and a switching control unit, wherein: the line array detecting unit is configured to collect fluorescence and form a spatial image of the sample; the spectrum detecting unit, Generating information for collecting fluorescence and forming a sample; the switching control unit is configured to perform switching selection between the line array detecting unit and the spectrum detecting unit.

Illustratively, the detecting unit further includes a first focusing lens disposed between the line array detecting unit and the switching control unit for focusing the fluorescent light emitted by the sample to The line array detecting unit.

Illustratively, the spectral detection unit is a spectral camera.

Illustratively, the detecting unit further includes a second focusing lens disposed between the spectrum detecting unit and the switching control unit for focusing the fluorescent light emitted by the sample to the The spectral detection unit.

Exemplarily, the spectral detecting unit comprises a prism-grating-prism, a converging lens and an area array detector arranged in sequence, wherein the prism-grating-prism is used for dispersively splitting the fluorescence transmitted by the steering unit; The converging lens is configured to focus the dispersively split fluorescent light onto a photosensitive surface of the area array camera; the area array detector is configured to form the spectral information.

Illustratively, the detecting unit further includes a first focusing lens and/or a second focusing lens for focusing the fluorescence emitted by the sample, wherein: the first focusing lens is disposed at the line array detecting unit Between the switching control unit and the switching control unit; the second focusing lens is disposed between the spectral detecting unit and the switching control unit.

The detecting unit further includes a second focusing lens and a collimating lens sequentially disposed between the switching control unit and the spectrum detecting unit, wherein: the second focusing lens is used to emit fluorescence of the sample Focusing; and the collimating lens is used to collimate the focused fluorescent light.

Illustratively, the detecting unit further includes a slit and/or a filter disposed downstream of the second focusing lens, wherein: the slit is for allowing only fluorescent light of a focusing plane to pass; and the filtering The light is used to filter out stray light.

The fast tissue molecular spectroscopic imaging device uses a line source to excite the sample, scans the line beam with a one-dimensional scanning unit (such as a single scanning galvanometer), and uses the spectral detection unit to detect the sample excitation light, achieving a total of one-dimensional directions. Focus. The combination of a line beam and a spectral detection unit to obtain spatial image and spectral information of tissue molecules can not only greatly improve the imaging speed of tissue molecules, but also enable instant imaging, and can also assist tissue analysis by spectral information (for example, for Tumor analysis). Since the scanning unit performs only one-dimensional scanning, the stability of the system can be effectively improved.

In order to make the objects, the technical solutions and the advantages of the present invention more apparent, the exemplary embodiments according to the present invention will be described in detail below with reference to the accompanying drawings. It is apparent that the described embodiments are only a part of the embodiments of the present invention, and are not to be construed as limiting the embodiments of the invention. All other embodiments obtained by those skilled in the art based on the embodiments of the present invention described herein without departing from the scope of the invention are intended to fall within the scope of the invention.

FIG. 1 schematically illustrates a block diagram of a rapid tissue molecular spectral imaging apparatus 100 in accordance with one embodiment of the present invention. The fast tissue molecular spectral imaging apparatus 100 includes a light emitting unit 110, a steering unit 120, a scanning unit 130, and a detecting unit 160. The rapid tissue molecular spectroscopic imaging apparatus 100 can be widely applied to tissue molecular imaging of various parts such as the digestive tract and the respiratory tract to realize early diagnosis of the tumor.

The light emitting unit 110 is for emitting a line beam. In one embodiment, as shown in FIGS. 2-3, the light emitting unit 110 can include a light source 112 and a beam expander focus concentrator 114. Light source 112 is used to emit a collimated beam of light. Light source 112 can be a collimator that emits a collimated laser of a particular wavelength. The specific wavelength range may be from 20 nm to 2000 nm. Lasers in this wavelength range can excite a wide range of phosphors. Light source 112 can be a quantum well laser, a solid state laser, a gas laser (such as an argon ion laser), or a laser diode. A beam expander focus concentrator 114 is disposed at the exit of the light source 112 for expanding the collimated beam of light from the source 112 and focusing it in one dimension into a line beam. The beam expander focus concentrator 114 can include a beam expander lens and a cylindrical lens. The beam expander lens may include two L1, L2, and the two beam expanders L1, L2 cooperate to expand the collimated beam emitted by the light source 112 to change the diameter of the collimated beam. The cylindrical lens includes L3 that focuses the expanded beam into a line beam and conducts it to the steering unit 120.

The steering unit 120 is located downstream of the light emitting unit 110 for turning to the line beam emitted by the light emitting unit 110 and capable of transmitting the fluorescent light of the sample. In Figures 1-3, the solid line is used to indicate the line beam emitted by the light emitting unit 110, and the dashed line is used to indicate that the sample is excited by the fluorescent light. The steering unit 120 is for separating the light emitted by the light emitting unit 110 and the fluorescent light generated by the sample excitation. The transmittance of the diverting unit 120 to the fluorescent light can reach 90% or more, and substantially all of the light of the other wavelengths is reflected. Then, the line beam emitted from the light emitting unit 110 is reflected to the scanning unit 130 through the steering unit 120. The fluorescent light returned along the same optical path as the line beam is transmitted almost entirely through the steering unit 120 and conducted to the detecting unit 160. The steering unit 120 that satisfies the above conditions may be a dichroic mirror. Preferably, the dichroic mirror may have a wavelength in the wavelength range of 40 nm to 2200 nm.

The scanning unit 130 is located downstream of the steering unit 120 and performs a one-dimensional sweep of the steered line beam for adjusting the direction of the steered line beam to scan the sample line by line. Specifically, the line beam may be, for example, a line beam extending in the X direction, and the scanning unit 130 diverts the line beam to a downstream optical component (for example, the relay unit 140) while performing Y-direction scanning. The Y direction is at an angle to the X direction, for example at a right angle of 90 degrees. The scanning unit 130 mainly performs one-dimensional scanning in the Y direction. Thus, the entire image can be formed by performing a one-dimensional scanning with the line beam in the X direction. It can be seen that the line beam combining detection unit 160 can image line by line, so the imaging speed is greatly improved compared to the existing point-by-point imaging. Since only the sweep in the one-dimensional direction is performed, the scanning unit 130 may be a single scanning galvanometer. The frequency of the scanning galvanometer can be in the frequency range of 10-2000 kHz. The use of a single scanning galvanometer can greatly reduce noise, and the complexity of the composition and control of the device improves the stability of the whole machine while reducing manufacturing costs and maintenance costs. Further, the scanning unit 130 can also be a spatial light modulator. Spatial light modulators are relatively expensive compared to scanning galvanometers.

The fast tissue molecular spectral imaging apparatus 100 further includes a relay unit 140 and an internal view unit 150 disposed downstream of the scanning unit 130. 2-3 illustrate optical path diagrams and block diagrams of a fast tissue molecular spectral imaging apparatus 200 in accordance with an embodiment of the present invention. The same or similar components in Fig. 2-3 as in Fig. 1 are given the same reference numerals. A specific implementation of the relay unit 140, the inner view unit 150, and the probe unit 160 in accordance with a specific embodiment of the present invention will be described in detail below with reference to FIGS. 2-3.

The relay unit 140 is configured to focus the line beam scanned by the scanning unit 130 to the inner view unit 150. The relay unit 140 is typically a lens group, such as lenses L4, L5.

The inner view unit 150 is for conducting and focusing the line beam focused by the relay unit 140 onto the sample, and receiving the fluorescence emitted by the sample. The fluorescent light is collected by the detecting unit 160 after being relayed by the relay unit 140 and the steering unit 120. The interior view unit 150 can include a coupling objective 152, a miniature objective 156, and an imaging fiber bundle 154 coupled between the coupling objective 152 and the micro objective 156. The relay unit 140 may include two relay lenses L4, L5 that cooperate to relay the scanned line beam to the rear pupil of the coupling objective 152 in the inner view unit 150. The coupling objective 152 is used to couple (e.g., focus) the line beam into the proximal end of the imaging fiber bundle 154 (near the operator's end). The imaging fiber bundle 154 is used to conduct a line beam to the distal end of the imaging fiber bundle 154 (away from the end of the operator). The miniature objective lens 156 is used to focus the laser guided by the imaging fiber bundle 154 onto the detection surface of the sample. The detection surface can be located at a desired depth below the surface of the sample. The fluorophore at the detection surface of the sample is excited to emit fluorescence. The fluorescent signal is collected by the miniature objective lens 156, transmitted through the imaging fiber bundle 154, the coupling objective lens 152, and the relay unit 140, and the scanning unit 130 reflects and passes through the steering unit 120 to enter the detecting unit 160. The number of fiber bundles included in the imaging fiber bundle 154 can be greater than ten. The miniature objective lens 156 is not required. In the case where the definition is not high, the micro objective lens 156 may alternatively be omitted. The micro objective lens 156 can be designed to extend into the digestive tract, the respiratory tract, and the like, and is in contact with the surface of the digestive tract, the respiratory tract, and the like.

The detecting unit 160 collects the fluorescence returned through the inner view unit 150, the relay unit 140, the scanning unit 130, and the steering unit 120 in sequence, and forms a spatial image and spectral information of the sample. The spatial image of the sample includes a two-dimensional image of the detection surface of the sample. The spectral information includes the energy distribution of the fluorescence generated by the sample stimulated at different wavelengths to illustrate the acquisition of tissue information (eg, for analysis of tumors). In a specific embodiment, the detection unit 160 can include a line array detection unit 162, a spectral detection unit 164, and a switching control unit 166, as shown in FIGS. 2-3.

Line array detection unit 162 is used to collect fluorescence and form a spatial image of the sample. The line array detecting unit 162 can be various types of line array cameras, such as a Charge Coupled Device (CCD) line array camera or a Complementary Metal Oxide Semiconductor (CMOS) line array camera. The imaging speed of the line array detecting unit 162 is in the range of several tens of frames to tens of millions of frames. Preferably, the detecting unit 160 further includes a first focusing lens L6, and the first focusing lens L6 is disposed between the line array detecting unit 162 and the switching control unit 166, as shown in FIG. 3, for focusing the fluorescent light emitted from the sample to The line array detecting unit 162 is in a clear image.

The spectral detection unit 164 is used to collect fluorescence and form spectral information of the sample, which will be described in detail later.

The switching control unit 166 is configured to perform switching selection between the line array detecting unit 162 and the spectrum detecting unit 164 to selectively acquire spatial images or spectral information. The switching control unit 166 selectively switches the transmission path of the fluorescent light, for example, to cause the fluorescent light to enter the line array detecting unit 162 or the spectrum detecting unit 164. Illustratively, the switching control unit 166 may be a mirror, a Digital Micromirror Device (DMD) or a spatial light modulator. Among them, the digital micro-mirror device can realize the projection or reflection of the optical path by controlling the on-off. An embodiment using a digital micromirror device as the switching control unit 166 is schematically illustrated in FIG. In use, first, the switching control unit 166 is turned on to transmit the fluorescent light, and the linear array detecting unit 162 performs spatial imaging to find a destination area (for example, a tumor); then, when it is desired to perform specific analysis on the destination area, the switching is controlled. The control unit 166 blocks, reflects the fluorescence to the spectrum detecting unit 164, and acquires the spectral information of the destination area by the spectrum detecting unit 164. For the case where the switching control unit 166 employs a mirror or a spatial light modulator, those skilled in the art can modify the optical path in accordance with the principles disclosed herein.

In a preferred embodiment (such as the embodiment shown in Figures 2-3), spectral detection unit 164 is a spectroscopic camera. Spectral cameras can be any type of spectroscopic camera that may or may not be present in the future, such as the Pika L-type spectroscopic camera from RESONON, USA, and the FX10 spectroscopic camera from Specim, Finland. As long as the spectral information of the sample can be formed according to the collected fluorescence. Preferably, the detecting unit 160 further includes a second focusing lens L7 disposed between the spectrum detecting unit 164 and the switching control unit 166, as shown in FIG. 3, for focusing the fluorescent light emitted from the sample to Spectral detection unit 164 to obtain more reliable spectral information.

4-5 illustrate optical path diagrams and block diagrams of a fast tissue molecular spectral imaging apparatus 300 in accordance with another embodiment of the present invention. The spectral detection unit 164 may include prism-grating-prisms arranged in sequence (Prisim-Grating- Prism) , abbreviated as PGP) 164a, a converging lens 164b, and an area array detector 164c. When switching to the spectral function by the switching control unit 166, the PGP prism 164a is used to perform dispersion splitting of the fluorescent light transmitted by the steering unit 120. The condenser lens 164b is for focusing the dispersion-separated fluorescent light onto the photosensitive surface of the area lens camera 166. The number of converging lenses 164b is related to the number of channels of the obtained spectrum, that is, more spectral images of more channels are desired, and more converging lenses are used. The area array detector 164c is used to form spectral information of the sample. The area array detector 166 can be various types of area array cameras, such as a CCD area array camera or a CMOS area array camera.

Further preferably, as shown in FIG. 5, the detecting optical path 160 preferably further includes a second focusing lens L7 and a collimating lens L8 between the switching control unit 166 and the spectrum detecting unit 164 along the optical path direction. Set them in sequence, as shown in Figure 4-5. The second focus lens L7 is used to focus the fluorescence emitted by the sample. The focused line beam illuminates the fluorescence emitted by the sample to be received. Through the steering and scanning of the scanning unit 130, the fluorescence emitted by all the rows of the sample is finally received by the detecting unit 160, and arranged into spectral cube data according to the scanning trajectory. In order to quickly obtain the spectral information of the organization. The collimating lens L8 is used to collimate the focused fluorescent light. Alternatively, a slit (not shown) may be provided between the second focus lens L7 and the collimator lens L8 for allowing only the fluorescence of the focus plane to pass. The size of the slit may range from several tens of nanometers to several tens of millimeters. The presence of the slits causes stray light outside the focus plane to be blocked. Optionally, the detecting unit 160 may further include a filter. A filter (not shown) is disposed downstream of the second focus lens L7, that is, between the second focus lens L7 and the collimator lens L8 for filtering out stray light. In the embodiment having a slit, a filter may be disposed between the second focus lens L7 and the slit.

In summary, the collimated beam emitted by the light source 112 is expanded by the beam expander concentrator 114 and concentrated into a line beam in one dimension, the steering unit 120 folds the line beam, and the scanning unit 130 couples the line beam through the relay unit 140. Entering the interior view unit 150 and performing a one-dimensional scan, the interior view unit 150 conducts the laser beam to the sample, excites the fluorescence and passes it back to the detection unit 160 to form a spatial image and spectral information.

Illustratively, the data collected by the detection unit can be sent to a computer for reception and processing by the computer. In addition, the computer can also control the scanning unit (such as the frequency of the galvanometer, etc.), the exposure and gain of the detecting unit, and the transmitting power of the light emitting unit.

The fast tissue molecular spectroscopic imaging apparatus 100 uses a line source to excite the sample, scans the line beam with a one-dimensional scanning unit 130 (for example, a single scanning galvanometer), and uses the detecting unit 160 to detect the sample excitation light in a one-dimensional direction. Achieve confocal. Since the linear beam and the detecting unit 160 are combined to obtain the spatial image and spectral information of the tissue molecules, the imaging speed of the tissue molecules can be greatly improved, real-time imaging can be realized, and the tissue condition can be assisted by spectral information (for example, for Tumor analysis). Since the scanning unit 130 performs only one-dimensional scanning, the stability of the system can be effectively improved.

Although the example embodiments have been described herein with reference to the drawings, it is understood that the foregoing exemplary embodiments are only illustrative, and are not intended to limit the scope of the invention. A person skilled in the art can make various changes and modifications without departing from the scope and spirit of the invention. All such changes and modifications are intended to be included within the scope of the present invention as claimed.

In the several embodiments provided by the present application, it should be understood that the disclosed apparatus and method may be implemented in other manners. For example, the device embodiments described above are merely illustrative. For example, the division of the unit is only a logical function division. In actual implementation, there may be another division manner, for example, multiple units or components may be combined or may be Integrate into another device, or some features can be ignored or not executed.

In the description provided herein, numerous specific details are set forth. However, it is understood that the embodiments of the invention may be practiced without these specific details. In some instances, well-known methods, structures, and techniques are not shown in detail so as not to obscure the understanding of the description.

Similarly, the various features of the invention are sometimes grouped together into a single embodiment, in the description of the exemplary embodiments of the invention, Figure, or a description of it. However, the method of the present invention should not be construed as reflecting the intention that the claimed invention requires more features than those specifically recited in the appended claims. Rather, as the invention is reflected by the appended claims, it is claimed that the technical problems can be solved with fewer features than all of the features of a single disclosed embodiment. Therefore, the claims following the specific embodiments are hereby explicitly incorporated into the embodiments, and each of the claims as a separate embodiment of the invention.

It will be understood by those skilled in the art that all features disclosed in the specification, including the accompanying claims, the abstract and the drawings, and all methods or devices so disclosed, may be employed in any combination, unless the features are mutually exclusive. Process or unit combination. Each feature disclosed in this specification (including the accompanying claims, the abstract and the drawings) may be replaced by alternative features that provide the same, equivalent or similar purpose.

In addition, those skilled in the art will appreciate that, although some embodiments described herein include certain features that are included in other embodiments and not in other features, combinations of features of different embodiments are intended to be within the scope of the present invention. Different embodiments are formed and formed. For example, in the claims, any one of the claimed embodiments can be used in any combination.

It is to be noted that the above-described embodiments are illustrative of the invention and are not intended to be limiting, and that the invention may be devised without departing from the scope of the appended claims. In the claims, any reference signs placed between parentheses shall not be construed as a limitation. The word "comprising" does not exclude the presence of the elements or steps that are not recited in the claims. The word "a" or "an" The invention can be implemented by means of a hardware comprising several distinct elements and by means of a suitably programmed computer. In the unit claims enumerating several means, several of these means can be embodied by the same hardware item. The use of the words first, second, and third does not indicate any order. These words can be interpreted as names.

The above is only the specific embodiment of the present invention or the description of the specific embodiments, and the scope of the present invention is not limited thereto, and any person skilled in the art can easily within the technical scope disclosed by the present invention. Any changes or substitutions are contemplated as being within the scope of the invention. The scope of the invention should be determined by the scope of the claims.

100, 200, 300‧‧‧fast tissue molecular imaging imaging device

110‧‧‧Light emitting unit

112‧‧‧Light source

114‧‧‧beam expander focus

120‧‧‧steering unit

130‧‧‧Scan unit

140‧‧‧Relay unit

150‧‧‧Vision unit

160‧‧‧Detection unit

L1, L2‧‧‧ beam expander lens

L3‧‧‧ cylindrical lens

L4, L5‧‧‧ relay lens, lens

L6‧‧‧First Focusing Lens

L7‧‧‧second focusing lens

L8‧‧‧ collimating lens

152‧‧‧coupled objective

154‧‧‧ imaging fiber bundle

156‧‧‧ miniature objective

162‧‧‧Line array detection unit

164‧‧‧Spectrum detection unit

166‧‧‧Switch control unit

164a‧‧ ‧ Prism-Grating-Prism, PGP Prism

164b‧‧‧ Converging lens

164c‧‧ ‧ area array detector

The above as well as other objects, features and advantages of the present invention will become more apparent from the embodiments of the invention. The drawings are intended to provide a further understanding of the embodiments of the invention, In the figures, the same reference numerals generally refer to the same or similar parts or steps. 1 shows a schematic block diagram of a rapid tissue molecular spectral imaging apparatus in accordance with one embodiment of the present invention; FIG. 2 shows a schematic block of a fast tissue molecular spectral imaging apparatus in accordance with a first set of embodiments of the present invention. Figure 3 shows a schematic diagram of the optical path of a fast tissue molecular spectral imaging apparatus according to a first set of embodiments of the present invention; Figure 4 shows a fast tissue molecular spectral imaging apparatus according to a second specific embodiment of the present invention. Schematic block diagram; and Figure 5 shows a schematic diagram of the optical path of a fast tissue molecular spectral imaging apparatus in accordance with a second set of embodiments of the present invention.

Claims (14)

A rapid tissue molecular spectroscopic imaging apparatus includes a light emitting unit, a steering unit, a scanning unit and a detecting unit, wherein: the light emitting unit is configured to emit a line beam; and the steering unit is configured to turn the line beam And transmitting fluorescence through a sample; the scanning unit is configured to adjust a direction of the steered line beam to scan the sample line by line; and the detecting unit is configured to collect the fluorescent light and form one of the samples Spatial image and a spectral information. The apparatus of claim 1, wherein the light emitting unit comprises: a light source for emitting a collimated light beam; and a beam expander focus concentrator disposed at an exit of the light source, For expanding the collimated beam and focusing one-dimensionally into the line beam. The device of claim 1, wherein the steering unit is a dichroic mirror. The device of claim 1, wherein the scanning unit is a single scanning galvanometer or a spatial light modulator. The device of claim 1, wherein the device further comprises a relay unit and an internal view unit disposed downstream of the scanning unit, wherein: the relay unit is configured to scan the a line beam after unit scanning is focused to the inner view unit; the inner view unit is configured to conduct and focus the focused line beam onto the sample and receive fluorescence emitted by the sample; Light is collected by the spectrum detecting unit after passing through the relay unit, the scanning unit, and the steering unit. The device of claim 5, wherein the inner view unit comprises a coupling objective lens and an imaging fiber bundle, wherein the coupling objective lens is disposed at one end of the imaging fiber bundle for focusing the A line beam is coupled into the proximal end of the imaging fiber bundle; and the imaging fiber bundle is used to conduct the incoming line beam. The device of claim 6, wherein the inner view unit further comprises a micro objective lens disposed at the other end of the imaging fiber bundle for conducting the imaging fiber bundle A line beam is focused onto the sample. The apparatus of claim 1, wherein the detecting unit comprises a line array detecting unit, a spectrum detecting unit and a switching control unit, wherein: the line array detecting unit is configured to collect and form a fluorescent light. a spatial image of the sample; the spectral detection unit is configured to collect fluorescence and form a spectral information of the sample; the switching control unit is configured to detect the line array and the spectral detection The unit makes a switch selection. The apparatus of claim 8, wherein the detecting unit further comprises a first focusing lens disposed between the line array detecting unit and the switching control unit, Fluorescent light emitted from the sample is focused to the line array detecting unit. The device of claim 8, wherein the spectral detection unit is a spectroscopic camera. The apparatus of claim 10, wherein the detecting unit further comprises a second focusing lens disposed between the spectrum detecting unit and the switching control unit for Fluorescence emitted by the sample is focused to the spectral detection unit. The apparatus of claim 8, wherein the spectral detecting unit comprises a prism-grating-prism, a converging lens and a side array detector arranged in sequence, wherein the prism-grating-prism is used for The fluorescent light transmitted by the steering unit performs dispersion splitting; the converging lens is configured to focus the dispersion-divided fluorescent light onto a photosensitive surface of the area array detector; the area array detector is used to form the spectrum News. The apparatus of claim 12, wherein the detecting unit further comprises a second focusing lens and a collimating lens sequentially disposed between the switching control unit and the spectrum detecting unit, wherein: The second focusing lens is for focusing the fluorescent light emitted by the sample; and the collimating lens is for collimating the focused fluorescent light. The apparatus of claim 11 or claim 13, wherein the detecting unit further comprises a slit and/or a filter disposed downstream of the second focusing lens, wherein: the narrow The slit is used to allow only the fluorescence of the focal plane to pass; and the filter is used to filter out stray light.