CN202102170U - System employing concentric double conical surface mirror for realizing total internal reflection fluorescence microscopy - Google Patents
System employing concentric double conical surface mirror for realizing total internal reflection fluorescence microscopy Download PDFInfo
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- CN202102170U CN202102170U CN2010205686876U CN201020568687U CN202102170U CN 202102170 U CN202102170 U CN 202102170U CN 2010205686876 U CN2010205686876 U CN 2010205686876U CN 201020568687 U CN201020568687 U CN 201020568687U CN 202102170 U CN202102170 U CN 202102170U
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Abstract
The utility model relates to a system employing concentric double conical surface mirror for realizing total internal reflection fluorescence microscopy, comprising a parallel light generating device as well as a ring light beam generating apparatus, a fluorescence excitation apparatus, and an imaging apparatus which are sequentially arranged upon the optical path, wherein the parallel light generating device generates parallel light; the ring light beam generating apparatus is arranged upon the optical path of the parallel light; and the right light beam generating apparatus comprises a hollow reflector arranged at a position forming an angle of 45 degrees with the incident direction of the parallel light, a recessed surface axicon lens sharing same axis with the parallel light, and a convex surface axicon lens arranged at the center of recessed surface axicon lens. The system of the utility model solves the problem of low transmittance of the conventional object lens type total internal reflection fluorescence microscopy method, with the luminous energy utilization rate closing to 100%. Moreover, the switch between the total internal reflection fluorescence microscopy and the common wide field fluorescence microscopy can be conveniently realized. The system allows the imaging over a single cell, even over a single organelle, thereby being capable of meeting the requirement of most living body bio-experiments.
Description
Technical field
The utility model relates to a kind of micro-system of concentric bipyramid face mirror realization total internal reflection fluorescent that uses, can be adaptable across biology, medical science, the research in fields such as biophysics and materials chemistry.
Background technology
Fluorescence probe is meant after absorbing the light of specific wavelength, can convert absorbing light into the general designation of one type of material that the light of different wave length emits.Use the different fluorescence probes can the different position of mark sample interior, thereby can be used for surveying the micromechanism of sample, can also fluorescently-labeled gene of Real Time Observation and the movable and reaction of cell in the living animal body.Fluorescence microscopy has become the strong instrument of chemistry and biological sample imaging.
A subject matter of puzzlement fluorescence microscopy is the background interference that the fluorescence signal of sample out of focus part brings.How to eliminate ground unrest, the signal to noise ratio (S/N ratio) and the resolution that improve micro-image are the fluorescence microscopy hot research fields.Laser co-focusing fluorescence microscopy and TOTAL INTERNAL REFLECTION FLUORESCENCE MICROSCOPY are present two kinds of the most frequently used technical schemes.
The laser co-focusing fluorescence microscopy utilizes the laser beam of high order focusing to sample point by point scanning imaging, is surveyed collection by photomultiplier after the filtering of fluorescence signal process detecting pinhole, can reconfigure through computer software and generate a 3-D view.The laser co-focusing fluorescence microscopy has the three-dimensional imaging ability but also has good spatial resolution, but because it adopts the spot scan imaging mode, so its image taking speed is also unhappy and easily sample is produced optical damage.
Total internal reflection (claiming total reflection again) is meant when light and enters into optically thinner medium from optically denser medium, and incident angle is during greater than critical angle, all is reflection because refraction not, so be referred to as total internal reflection.From the angle of geometrical optics, when total reflection took place, light can reflect fully on glass interface and not get in the liquid solution.In fact, because fluctuation effect, the energy of some light can pass contacting permeation in solution, and this part light field is exactly so-called evanescent wave.Evanescent wave is parallel to the interface to be propagated, perpendicular to the boundary strength exponential damping.The field strength E that dies declines
zCan be expressed as:
Wherein
The penetration depth that being defined as declines dies.
E
0Be electric field intensity at the interface, λ is the optical wavelength in the vacuum, n
1Be the refractive index of optically denser medium, n
2It is the refractive index of optically thinner medium.
The penetration depth that dies of declining is very little, has only about 200nm usually.
Intracellular a lot of important vital movement process all is present in cell surface.The micro-evanescent wave excited sample of utilizing total internal reflection to produce of total internal reflection fluorescent; Excitation area is limited at the skim scope interior (200nm) of sample surfaces; Do not receive interference from deep regions signal in the sample; Therefore have high signal to noise ratio (S/N ratio) and contrast, be widely used in the monomolecular fluorescence imaging by biophysicists in recent years.In addition; Total internal reflection fluorescent micro-imaging method no longer adopts scanning imagery and uses the CCD camera; Obtain a complete two dimensional image at a time point; Improve image taking speed greatly, reduced the sample optical damage, thereby become research cell surface science such as biological chemistry dynamics, unimolecule the most promising dynamic (dynamical) optical image technology.
The total internal reflection fluorescent micro-imaging can be divided into two kinds on prism-type and object lens type according to the difference of its imaging system.The prism-type system is fairly simple in realization; Also be not easy to receive the interference of incident optical signal; Laser (is equipped with the immersion oil of refractive index match) at the interface through what prism-coupled was radiated at sample and microslide between prism and the microslide; Accurately the adjustment incident angle makes the generation total reflection, and fluorescence signal is surveyed by the another side entering microcobjective of sample and by CCD.The shortcoming of prism-type system is the restriction that the position of sample receives prism, and the fluorescence that inspires will just can be detected through whole sample, has reduced the contrast of imaging.
The placement of sample is then very convenient in the object lens type system, and microscopical object lens are both as the receiver of collecting the fluorescent signal, simultaneously again as the optical device of experiences total internal reflection.And can combine with multiple other technology, Laser Micro-Machining for example, therefore optical tweezer technologies etc. show more tempting application prospect.Because the typical index of cell is about 1.35; According to the snell law; Want to realize total internal reflection; Therefore the numerical aperture NA of microcobjective must when we are used for the object lens of NA=1.4, have only very little a part of objective aperture scope (1.4-1.35=0.05) to be utilized greater than 1.35.In experiment, in order to guarantee uniform illumination, laser beam is modulated into usually and is pupil behind the very thin ring of light entering microcobjective.As shown in Figure 1, use a circular light barrier to block the center section of parallel beam usually, obviously, light barrier has blocked most of illumination light, so the transmitance of total system very low (less than 5%) causes brightness of illumination not enough.
To the low shortcoming of existing object lens type total internal reflection fluorescent microtechnic transmitance, the utility model proposes a kind of micro-technology and device of concentric bipyramid face mirror realization total internal reflection fluorescent that use.This device has the advantage of efficiency of light energy utilization height (near 100%), and can realize the switching of the micro-and common wide field of total internal reflection fluorescent fluorescence microscopy easily.
Summary of the invention
In order to solve the low problem of existing object lens type total internal reflection fluorescent microscopic method transmitance, the utility model provides a kind of and uses concentric bipyramid face mirror to realize the micro-system of total internal reflection fluorescent.
The technical solution of the utility model is:
A kind of micro-system of concentric bipyramid face mirror realization total internal reflection fluorescent that uses comprises the directional light generating means and is successively set on annular beam generation device, fluorescence excitation device and the imaging device on the light path,
Said directional light generating means produces directional light, and said annular beam generation device is arranged on the light path of directional light;
Said fluorescence excitation device comprises the dichroic mirror 11 that is arranged on the annular beam generation device light path, the objective table 13 that is arranged on the microcobjective 12 on dichroic mirror 11 reflected light paths and is arranged on the microcobjective top;
Said imaging device comprises second catoptron 15, is successively set on tube mirror 16, optical filter 17 and CCD camera 18 on second catoptron, 15 reflected light paths; Said second catoptron 15 be arranged on objective table 13 under;
Its special character is: said annular beam generation device comprises the hollow catoptron 6 that becomes 45 degree to place with the directional light incident direction, with the concave surface axicon lens 7 of the coaxial setting of directional light, be arranged on the convex surface axicon lens 8 at concave surface axicon lens center; The axis of said convex surface axicon lens 8 is over against the center of hollow catoptron 6;
Said dichroic mirror 11 is arranged on the reflected light path of annular beam of hollow catoptron 6 and with the reflected light direction and becomes miter angle.
Above-mentioned annular beam generation device also comprises telescopic system, and said telescopic system comprises second lens 9 and the 3rd lens 10 that are arranged between hollow catoptron 6 and the dichroic mirror 11.
A kind of micro-method of concentric bipyramid face mirror realization total internal reflection fluorescent of using, its special character is: may further comprise the steps:
1] produces parallel beam;
2] produce annular beam:
Directional light is passed the hollow catoptron 6 that 45 degree are provided with; Impinge perpendicularly on the convex surface axicon lens 8; Reflexed on the concave surface axicon lens 7 of convex surface axicon lens 8 outer circumferential sides by convex surface axicon lens 8 again, reflexed to hollow catoptron 6 by concave surface axicon lens 7 again, reflected to form annular beam by hollow catoptron 6 again;
3] annular beam carries out fluorescence excitation to sample behind the fluorescence excitation device;
4] with the fluorescence signal imaging that inspires.
Above-mentioned steps 3] also comprise the micro-switching with the wide field fluorescence microscopy of total internal reflection fluorescent:
Convex surface axicon lens 8 is come and gone along the axis direction of concave surface axicon lens 7 moves, the regulating ring shaped light beam objective table and sample at the interface converge the angle, when annular beam objective table and sample at the interface converge the angle less than critical angle the time be the wide field fluorescence microscopy; When annular beam objective table and sample at the interface converge the angle more than or equal to critical angle the time, then be that total internal reflection fluorescent is micro-.
Above-mentioned steps 2] also comprise the adjusting of the annular beam angle of divergence:
Annular beam through the telescopic system of forming by second lens 9 and the 3rd lens 10 after the incident dichroic mirror.
Above-mentioned steps 4] also comprise the adjusting of image definition:
Regulate gain coefficient, CCD cryogenic temperature and the time shutter of CCD camera 18, obtain micro-image clearly.
Above-mentioned steps 3] concrete steps following: annular beam converges to objective table through dichroic mirror incident microcobjective through microcobjective, shines sample through the evanescent wave that produces at the interface at objective table and sample; Send fluorescence signal after microcobjective is collected at sample under the exciting of evanescent wave, pass dichroic mirror 11 again and be incident to second catoptron 15.
Above-mentioned steps 4] concrete steps following:
The fluorescence signal that is incident to second catoptron 15 gets into 18 imagings of CCD camera through tube mirror 16 and optical filter 17.
The advantage that the utlity model has:
1, the utility model uses concentric bipyramid face mirror generation annular beam and is used for total internal reflection fluorescent micro-; Compare with common total internal reflection fluorescent microtechnic; The almost nil waste of the utility model luminous energy; The efficiency of light energy utilization high (near 100%), thereby be applicable to that miniature low-power semiconductor laser as lighting source, is convenient to the integrated of total internal reflection fluorescent microscopic system.
2, the utility model is through move the relative position in convex surface axicon lens and the concave surface axicon lens vertically; Change the dutycycle of parallel ring of light light field; Just change annular beam objective table and sample at the interface converge the angle, thereby can realize the micro-switching with the wide field fluorescence microscopy of total internal reflection fluorescent easily.Total internal reflection fluorescent is micro-can only observe the fluorescence that extremely thin at the interface one deck sample sends, and signal to noise ratio (S/N ratio) is very high; Though and the micro-signal to noise ratio (S/N ratio) in wide field is lower, it can be deep into sample interior and observe, and is more convenient.Usually when carrying out the total internal reflection fluorescent microscope experiment, all need carry out the contrast of same position wide field micro-image.Like Fig. 4 and shown in Figure 5.
3, the employed laser power density of the utility model is very low, and is very little to the destruction and the laser bleaching effect of biological tissue.At first, with the laser co-focusing compared with techniques of spot scan, total internal reflection fluorescent is micro-to be a kind of wide field microtechnic, and wide field microtechnic itself just has weak photobleaching and optical damage effect; In addition, the utility model uses concentric bipyramid face mirror to produce annular beam, and therefore transmitance can use lower powered laser instrument near 100%, has further reduced the possibility of optical damage.
Description of drawings
Fig. 1 is the structural representation that existing use light barrier produces annular beam;
Fig. 2 is that the utility model uses concentric bipyramid face mirror to produce the annular beam synoptic diagram;
Fig. 3 is that the utility model uses concentric bipyramid face mirror to realize the micro-system light path figure of total internal reflection fluorescent;
Reference numeral is: 1-laser instrument, 2-fiber coupler, 3-multimode optical fiber, 4-first lens, 5-first catoptron; 6-hollow catoptron, 7-concave surface axicon lens, 8-convex surface axicon lens, 9-second lens, 10-the 3rd lens 3; The 11-dichroic mirror, 12-microcobjective, 13-objective table, 14-sample; 15-second catoptron, 16-tube mirror, 17-optical filter, 18-CCD camera.
Embodiment
As shown in Figure 2, the utility model uses the conical reflector (8, one concave mirrors 7 of a convex mirror) of two drift angles, 90 degree to place with one heart, and concave surface axicon lens 7 centers are porose, and convex surface axicon lens 8 can move axially in concave surface axicon lens 7 center pits.Parallel beam pass one become the hollow catoptron 7 that 45 degree place with the incident light direction after; Normal incidence convex surface axicon lens 8, light are behind convex surface awl 8 reflections 90 degree, again by concave surface awl 7 reflections 90 degree; Again via behind hollow catoptron 6 reflections 90 degree, can produce a parallel annular light beam at last.The relative position that moves convex surface axicon lens 8 and concave surface axicon lens 7 can change the dutycycle of annular beam.The method that produces the hollow ring of light with the round light barrier of the use of Fig. 1 is compared, and the technical scheme of the utility model obviously has the very high efficiency of light energy utilization, and can change the dutycycle of the ring of light easily.
Use concentric bipyramid face mirror to realize that the micro-system light path of total internal reflection fluorescent is as shown in Figure 3.The light beam that laser instrument 1 sends is coupled into multimode optical fiber 3 through fiber coupler 2.After removing spatial coherence through multimode optical fiber 3 again, be parallel beam by first lens, 4 collimations.Regulating first catoptron 5 makes parallel beam pass hollow catoptron 6 back normal incidence convex surface awls 8; Light is behind convex surface axicon lens 8 reflections 90 degree; By concave surface axicon lens 7 reflections 90 degree, again via behind hollow catoptron 6 reflections 90 degree, can produce a parallel annular light beam at last again.The relative position that moves convex surface axicon lens 8 and concave surface axicon lens 7 can change the dutycycle of annular beam.The telescopic system that second lens 9 and the 3rd lens 10 are formed is used for adjusting the angle of divergence of ring of light light field, thus an area that can corrective action on sample, declines and die.Annular beam gets into microcobjective 12 by dichroic mirror 11 reflections, is converged in the evanescent wave of generation at the interface of microslide by microcobjective 12.Fine tuning objective table 13 makes sample 14 be arranged in the field that dies of declining.The fluorescence signal that evanescent wave inspires passes dichroic mirror 11 again after microcobjective 12 is collected, change direction through second catoptron 15, gets into CCD camera 18 through tube mirror 16 and optical filter 17 at last.Gain coefficient, CCD cryogenic temperature and the time shutter of control CCD camera 18, thus total internal reflection fluorescent micro-image clearly obtained.Translation convex surface axicon lens 8 changes the relative position in convex surface axicon lens 8 and the concave surface axicon lens 7; Can change the dutycycle of parallel ring of light light field; When annular beam microslide and solution interface place converge the angle less than critical angle the time; Total reflection condition will be destroyed, and a part of refracted ray will get into solution and sample interior, thereby can realize the micro-switching with the wide field fluorescence microscopy of total internal reflection fluorescent.
Embodiment 1: diameter 1 μ m fluorescence bead is carried out the wide field fluorescence microscopy to the utility model device and the micro-imaging experiment of total internal reflection fluorescent compares.Scale 10 μ m, microcobjective is 63X in the experiment, NA=1.4 microcobjective, laser instrument are selected frequency multiplication YAG laser instrument, wavelength 532nm for use.Regulate the relative position of convex surface axicon lens 8 concave surface axicon lens 7 in during experiment, can realize the switching of the micro-and wide field fluorescence microscopy of total internal reflection fluorescent.The wide field fluorescence microscope images can be seen the ground unrest that the fluorescence bead of out of focus position brings.The total internal reflection fluorescent micro-image can only see the fluorescence bead that the focal plane is located, and contrast is very high.
Embodiment 2: the wide field fluorescence microscopy is carried out in lily of the valley section to the utility model device and the micro-imaging experiment of total internal reflection fluorescent compares.Scale 10 μ m, microcobjective is 100X in the experiment, NA=1.45 microcobjective, laser instrument are selected frequency multiplication YAG laser instrument, wavelength 532nm for use.Regulate the relative position of convex surface axicon lens 8 concave surface axicon lens 7 in during experiment, can realize that the micro-and switching wide field fluorescence microscopy of total internal reflection fluorescent is the wide field fluorescence microscope images, can see the sample autofluorescence of out of focus position.The total internal reflection fluorescent micro-image can only be seen fluorescence signal at the interface, and picture contrast is very high.
Claims (3)
1. one kind is used concentric bipyramid face mirror to realize the micro-system of total internal reflection fluorescent, and comprise the directional light generating means and be successively set on annular beam generation device, fluorescence excitation device and the imaging device on the light path,
Said directional light generating means produces directional light, and said annular beam generation device is arranged on the light path of directional light;
Said fluorescence excitation device comprises the dichroic mirror (11) that is arranged on the annular beam generation device light path, the objective table (13) that is arranged on the microcobjective (12) on dichroic mirror (11) reflected light path and is arranged on the microcobjective top;
Said imaging device comprises second catoptron (15), is successively set on tube mirror (16), optical filter (17) and CCD camera (18) on second catoptron (15) reflected light path; Said second catoptron (15) be arranged on objective table (13) under;
It is characterized in that: said annular beam generation device comprises the hollow catoptron (6) that becomes 45 degree to place with the directional light incident direction, with the concave surface axicon lens (7) of the coaxial setting of directional light, be arranged on the convex surface axicon lens (8) at concave surface axicon lens center; The axis of said convex surface axicon lens 8 is over against the center of hollow catoptron (6);
Said dichroic mirror (11) is arranged on the reflected light path of annular beam of hollow catoptron (6) and with the reflected light direction and becomes miter angle.
2. the concentric bipyramid face of use according to claim 1 mirror is realized the micro-system of total internal reflection fluorescent; It is characterized in that: said annular beam generation device also comprises telescopic system, and said telescopic system comprises second lens (9) and the 3rd lens (10) that are arranged between hollow catoptron (6) and the dichroic mirror (11).
3. the concentric bipyramid face of use according to claim 1 and 2 mirror is realized the micro-system of total internal reflection fluorescent; It is characterized in that: first catoptron (5) after said directional light generating means comprises laser instrument (1), fiber coupler (2), multimode optical fiber (3), first lens (4) and is arranged on first lens (4), said hollow catoptron (6) is arranged on the reflected light path of first catoptron (5).
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
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| CN102004307A (en) * | 2010-10-20 | 2011-04-06 | 中国科学院西安光学精密机械研究所 | System and method for realizing total internal reflection fluorescence microscopy by using concentric double conical surface lens |
| CN102860845A (en) * | 2012-08-30 | 2013-01-09 | 中国科学技术大学 | Method and corresponding device for capturing and controlling in-vivo cells of living body animal |
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| CN106896241A (en) * | 2015-12-17 | 2017-06-27 | 北京爱普益生物科技有限公司 | One kind can be with utilizing total internal reflection fluorescence microscope associated with AFM |
| CN108873285A (en) * | 2013-08-15 | 2018-11-23 | 卡尔蔡司显微镜有限责任公司 | High resolution scanning microscopy |
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- 2010-10-20 CN CN2010205686876U patent/CN202102170U/en not_active Expired - Fee Related
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| CN102004307A (en) * | 2010-10-20 | 2011-04-06 | 中国科学院西安光学精密机械研究所 | System and method for realizing total internal reflection fluorescence microscopy by using concentric double conical surface lens |
| CN102860845A (en) * | 2012-08-30 | 2013-01-09 | 中国科学技术大学 | Method and corresponding device for capturing and controlling in-vivo cells of living body animal |
| CN108873285A (en) * | 2013-08-15 | 2018-11-23 | 卡尔蔡司显微镜有限责任公司 | High resolution scanning microscopy |
| CN108873285B (en) * | 2013-08-15 | 2020-11-24 | 卡尔蔡司显微镜有限责任公司 | High resolution scanning microscopy |
| CN105043948A (en) * | 2015-08-26 | 2015-11-11 | 清华大学 | Measurement system and method for grain diameter of single nano particle |
| CN105043948B (en) * | 2015-08-26 | 2017-09-22 | 清华大学 | The measuring system and measuring method of single nanoparticle particle diameter |
| CN106896241A (en) * | 2015-12-17 | 2017-06-27 | 北京爱普益生物科技有限公司 | One kind can be with utilizing total internal reflection fluorescence microscope associated with AFM |
| CN106896241B (en) * | 2015-12-17 | 2019-05-14 | 北京爱普益生物科技有限公司 | One kind can be with utilizing total internal reflection fluorescence microscope associated with atomic force microscope |
| CN106841136A (en) * | 2017-01-10 | 2017-06-13 | 浙江大学 | A kind of high accuracy axially position to ultra-thin cell and imaging method and device |
| CN106841136B (en) * | 2017-01-10 | 2019-06-18 | 浙江大学 | A kind of high-precision axially position to ultra-thin cell and imaging method and device |
| JP2021036239A (en) * | 2020-10-30 | 2021-03-04 | ナノフォーム フィンランド オサケユイチアユルキネン | Apparatus and method for determining characteristics of surface structure and subsurface structure |
| JP7159260B2 (en) | 2020-10-30 | 2022-10-24 | ナノフォーム フィンランド オサケユイチアユルキネン | Apparatus and method for characterizing surface and subsurface structures |
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Granted publication date: 20120104 Termination date: 20121020 |