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CN109300569A - Large-scale photothermal particle aggregation and migration method based on tapered optical fibers - Google Patents

Large-scale photothermal particle aggregation and migration method based on tapered optical fibers Download PDF

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Publication number
CN109300569A
CN109300569A CN201811093624.7A CN201811093624A CN109300569A CN 109300569 A CN109300569 A CN 109300569A CN 201811093624 A CN201811093624 A CN 201811093624A CN 109300569 A CN109300569 A CN 109300569A
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particle
fiber
conical fiber
aggregation
conical
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辛洪宝
李宝军
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Jinan University
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    • GPHYSICS
    • G21NUCLEAR PHYSICS; NUCLEAR ENGINEERING
    • G21KTECHNIQUES FOR HANDLING PARTICLES OR IONISING RADIATION NOT OTHERWISE PROVIDED FOR; IRRADIATION DEVICES; GAMMA RAY OR X-RAY MICROSCOPES
    • G21K1/00Arrangements for handling particles or ionising radiation, e.g. focusing or moderating
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B21/00Microscopes
    • G02B21/36Microscopes arranged for photographic purposes or projection purposes or digital imaging or video purposes including associated control and data processing arrangements
    • GPHYSICS
    • G02OPTICS
    • G02BOPTICAL ELEMENTS, SYSTEMS OR APPARATUS
    • G02B21/00Microscopes
    • G02B21/36Microscopes arranged for photographic purposes or projection purposes or digital imaging or video purposes including associated control and data processing arrangements
    • G02B21/365Control or image processing arrangements for digital or video microscopes

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  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
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  • Chemical & Material Sciences (AREA)
  • Analytical Chemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)
  • Computer Vision & Pattern Recognition (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • General Engineering & Computer Science (AREA)
  • High Energy & Nuclear Physics (AREA)
  • Lasers (AREA)

Abstract

本发明公开了一种基于锥形光纤的大规模光热颗粒聚集和迁移方法,具体包括以下步骤:锥形光纤的制作、悬浮液的配备、锥形光纤和实验装置的安装、颗粒或细胞的聚集以及高效迁移;本发明所使用的装置简单、试验过程方便、易操作,对于微纳颗粒或细胞的聚集与迁移效率高,对微纳颗粒或细胞无损伤,易用广泛。

The invention discloses a large-scale photothermal particle aggregation and migration method based on a tapered optical fiber, which specifically includes the following steps: the production of the tapered optical fiber, the preparation of the suspension, the installation of the tapered optical fiber and the experimental device, the preparation of the particles or cells Aggregation and efficient migration; the device used in the present invention is simple, the test process is convenient and easy to operate, the aggregation and migration efficiency of micro-nano particles or cells is high, no damage to micro-nano particles or cells, and it is widely used.

Description

Extensive photo-thermal particle aggregation and moving method based on conical fiber
Technical field
The invention belongs to bio-photons and field of biomedicine technology, more particularly to a kind of based on the big of conical fiber Scale photo-thermal particle aggregation and moving method.
Background technique
The progress such as micro-nano particle, biomolecule, biological cell are captured with aggregation and subsequent removal on a large scale, in biomedicine Suffer from important role with many fields such as physical chemistry, for example, micro-nano structure assembling, drug screening, drug targeting treat, Local Water warfare etc.;There are distinct methods to be used to that particle is assembled and assembled in the world at present, such as thermophoresis, electrophoresis, dielectric Swimming, sound field etc.;In order to realize the aggregation capture of extensive particle, these methods are typically necessary more complicated device, simultaneously Additional electrodes are also needed, in addition, these methods can not be directly realized by efficient particle targeting migration and remove.
In order to realize easy extensive particle aggregation and efficient migration, a kind of big rule based on conical fiber have been invented Mould photo-thermal particle aggregation and moving method.
Summary of the invention
The purpose of the present invention is to provide a kind of extensive photo-thermal particle aggregation and moving method based on conical fiber, with Realize extensive rapid aggregation, targeting migration micro-nano particle and biological cell, the equipment that this method uses is simple, easy to operate.
The technical scheme adopted by the invention is that extensive photo-thermal particle aggregation and moving method based on conical fiber, Specifically includes the following steps:
Step 1: the production of conical fiber
The buffer layer of business single-mode fiber jumper and plastic wrapper are removed using optical fiber wire stripper, removal position length 20~ 50cm protrudes into the optical fiber for removing housing in glass capillary, and after optical fiber passes through glass capillary, end is pulled out in alcolhol burner After flame envelope heats 100~150s, with the speed of 1~3mm/s by 20~30s of optical fiber melt-pulling of flame upper end, experiment is obtained Conical fiber;
Step 2: suspension is equipped with
By micro-nano particle or cellular invasion in deionization pure water, uniform suspension is formed, takes the suspension prepared It is added drop-wise on micro slide, and micro slide is put in spare on microscopical two-dimensional shift platform;
Step 3: installation conical fiber and experimental provision
The conical fiber made is fixed on fine adjustment frame, conical fiber tip is protruded into suspension, and the other end is logical It crosses erbium-doped fiber amplifier to be connected on laser, computer is connected on the microscope for being loaded with CCD, and experimentation can directly pass through Computer display screen is observed;
Step 4: large-scale aggregating particle
Laser is opened, the photo-thermal that incident laser, micro-nano particle or cell are passed through into conical fiber in incident laser is made Under, it is gathered in apart from the place at 100~500 μm of conical fiber tip;
Step 5: the particle of efficient migration aggregation
After particle is by large-scale aggregating, laser is kept to open, by adjusting the mobile conical fiber of fine adjustment frame to finger The migration to aggregated particle or cell is realized in fixed position.
Further, conical fiber end diameter is 1~10 μm in step 1.
Further, for the size of micro-nano particle or cell at 1~5 μm, particle or cell is molten in suspension in step 2 Degree is 1.0 × 107~1.0 × 108A/mL;For the size of particle or cell at 5~10 μm, solubility is 2.0 × 106~2.0 ×107A/mL.
Further, in step 4 incident power of incident laser be 100~170mW, wavelength 1550nm.
The beneficial effects of the present invention are: can quickly large-scale aggregating micro-nano particle and biological cell, and carried out Targeting migration;The equipment used during aggregation micro-nano particle and biological cell is simple, at low cost, the harm to sample itself The extremely low and process is simple and easy to operate, high to the transport efficiency of micro-nano particle or biological cell.
Detailed description of the invention
In order to more clearly explain the embodiment of the invention or the technical proposal in the existing technology, to embodiment or will show below There is attached drawing needed in technical description to be briefly described, it should be apparent that, the accompanying drawings in the following description is only this Some embodiments of invention for those of ordinary skill in the art without creative efforts, can be with It obtains other drawings based on these drawings.
Fig. 1 is the conical fiber figure of aggregation with migration.
Fig. 2 is the Experimental equipment for assembling and migrating.
Fig. 3 is the experimentation picture of aggregation with migration.
Fig. 4 be under different incident powers particle aggregation number and aggregation velocity with time variation diagram.
Fig. 5 is the experimental observation figure of extensive efficient migration particle.
In figure, 1. lasers, 2. erbium-doped fiber amplifiers, 3. fine adjustment framves, 4. conical fibers, 5. suspension, 6. is micro- Mirror, 7.CCD, 8. computers.
Specific embodiment
Following will be combined with the drawings in the embodiments of the present invention, and technical solution in the embodiment of the present invention carries out clear, complete Site preparation description, it is clear that described embodiments are only a part of the embodiments of the present invention, instead of all the embodiments.It is based on Embodiment in the present invention, it is obtained by those of ordinary skill in the art without making creative efforts every other Embodiment shall fall within the protection scope of the present invention.
Extensive photo-thermal particle aggregation and moving method based on conical fiber, specifically includes the following steps:
Step 1: the production of conical fiber 4
The buffer layer of business single-mode fiber jumper and plastic wrapper are removed using optical fiber wire stripper, removal position length 20~ 50cm protrudes into the optical fiber for removing housing in glass capillary, and after optical fiber protrudes into glass capillary, end is pulled out in alcolhol burner After flame envelope heats 100~150s, with the speed of 1~3mm/s by 20~30s of optical fiber melt-pulling of flame upper end, experiment is obtained Conical fiber 4;
The core diameter of single mode optical fiber is 9 μm, and covering is 125 μm;The length of glass capillary be 120mm, internal diameter 0.9mm, Thickness of pipe wall 0.1mm;4 end diameter of conical fiber is 1~10 μm;
4 structure of conical fiber is as shown in Figure 1;When 4 end diameter of conical fiber is greater than 10 μm, diameter is bigger, goes out accordingly It penetrates light field more to dissipate, the region that can generate photo-thermal effect is bigger, and the particle that can be applied to is also more, but the aggregation to particle Effect is deteriorated, and the particle of aggregation is compact, at compared with dispersed distribution, while migration effect is deteriorated;And fibre diameter is in 1~10 μm of model When enclosing interior, optical output field is concentrated, and the region for generating photo-thermal effect is small, but more preferable to the congregational rate of particle, and aggregation is compact, is moved It is also better to move effect;
Step 2: suspension 5 is equipped with
By micro-nano particle or cellular invasion in deionization pure water, uniform suspension 5 is formed, the suspension prepared is taken 5 are added drop-wise on micro slide, and micro slide are put in spare on the two-dimensional shift platform of microscope 6;
For the size of particle or cell at 1~5 μm, the solubility of particle and cell is 1.0 × 10 in suspension 57~1.0 × 108A/mL;For the size of particle or cell at 5~10 μm, solubility is 2.0 × 106~2.0 × 107A/mL;
5 middle particle concentration of suspension is bigger, and the particle that conical fiber 4 is collected is more, to realize the time collected completely It is longer, but since in transition process, particle or cell are easy to be deposited on sheet glass bottom, and migration effect can increase with concentration Add and reduces;When the diameter of micro-nano particle or cell becomes larger, micro-nano particle or cell are easy, to stay in sheet glass table Face is difficult to move, so that aggregation and migration effect can all be deteriorated;Micro-nano particle or cell size are too small, since Brownian movement is bright It is aobvious, it collects and the effect of migration can also reduce;
Step 3: installation conical fiber 4 and experimental provision
As shown in Fig. 2, the conical fiber 4 made is fixed on fine adjustment frame 3, suspension is protruded at 4 tip of conical fiber In liquid 5;4 other end of conical fiber is connected on laser 1 by erbium-doped fiber amplifier 2, and computer 8, which is connected to, is loaded with CCD7's On microscope 6, experimentation can be directly observed by 8 display screen of computer;
Step 4: large-scale aggregating particle
Laser 1 is opened, the laser that incident power is 100~170mW, wavelength is 1550nm is passed through into conical fiber 4, Deionized water is stronger to the absorption of laser, and micro-nano particle or biological cell are weaker to the absorption of laser, therefore micro-nano particle is in light Under heat effect, it is gathered on a large scale apart from the place at 100~500 μm of 4 tip of conical fiber;
Step 5: the particle of efficient migration aggregation
After particle is by large-scale aggregating, laser 1 is kept to open, is arrived by adjusting the mobile conical fiber 4 of fine adjustment frame 3 Specified position, the particle of aggregation also carry out collective's targeting migration accordingly.
Extensive photo-thermal particle aggregation and moving method based on conical fiber, to the particle of different sizes, different materials Or biological cell can realize large-scale aggregation and migration, aggregation and migration experiment behaviour to micro-nano particle and biological cell Make simple, high-efficient, the equipment price used is cheap, at low cost.
The present invention can be used for microorganism-collecting, local Water warfare etc.;For various sizes of particle and microbiological specimens, Due to its photo-thermal effect difference, can use the present invention can separating to particle and microorganism.
Embodiment 1
Extensive photo-thermal particle aggregation and moving method based on conical fiber, specifically includes the following steps:
Step 1: the production of conical fiber 4
The buffer layer of business single-mode fiber jumper and plastic wrapper are removed using optical fiber wire stripper, removal position length 20~ 50cm protrudes into the optical fiber for removing housing in glass capillary, after optical fiber protrudes into glass capillary, end is pulled out and is added Heat, with the speed of 1~3mm/s by 20~30s of optical fiber melt-pulling of flame upper end, is used after alcolhol burner flame envelope heats 100~150s Scissors cuts optical fiber waist, obtains experiment conical fiber 4, and the end diameter of conical fiber 4 is 3.1 μm, structure such as Fig. 1 institute Show;
Step 2: suspension 5 is equipped with
The silica dioxide granule that diameter is 2 μm is spread in deionized water, is spread under the auxiliary of Ultrasound Instrument uniformly, two Silicon oxide particle concentration is 1.0 × 107~1.0 × 108A/mL;The suspension 5 for taking 500 μ L to prepare is added drop-wise on micro slide, and Micro slide is put in spare on the two-dimensional shift platform of microscope 6;
Step 3: installation conical fiber 4 and experimental provision
As shown in Fig. 2, the conical fiber 4 made is fixed on fine adjustment frame 3, suspension is protruded at 4 tip of conical fiber In liquid 5;4 other end of conical fiber is connected on laser 1 by erbium-doped fiber amplifier 2, and computer 8, which is connected to, is loaded with CCD7's On microscope 6, experimentation can be observed directly by 8 display screen of computer in real time;
Step 4: large-scale aggregating particle
Open laser 1, the laser that incident power is 100mW, wavelength is 1550nm is passed through into conical fiber 4, go from Sub- water is stronger to the absorption of laser, and silica dioxide granule is weaker to the absorption of laser, and silica dioxide granule is under photothermy, quilt It is gathered on a large scale apart from the place at 100~500 μm of 4 tip of conical fiber;
Step 5: the particle of efficient migration aggregation
After particle is by large-scale aggregating, laser 1 is kept to open, is arrived by adjusting the mobile conical fiber 4 of fine adjustment frame 3 Specified position, the particle of aggregation also carry out collective's targeting migration accordingly.
Embodiment 2
150mW is set by the incident power of laser in 1 step 4 of embodiment, suspension 5 is observed by 8 display of computer The aggregation and migration situation of middle silica dioxide granule.
Embodiment 3
170mW is set by the incident power of laser in 1 step 4 of embodiment, suspension 5 is observed by 8 display of computer The aggregation and migration situation of middle silica dioxide granule.
The experimental result of 1~embodiment of embodiment 3 is as shown in figure 4, by Fig. 4 a it is found that silica dioxide granule in suspension 5 Aggregation number be presented growth trend at any time, increase early period more rapid, the later period increasess slowly, finally reach saturation state, When power is 100,150,170mW, the numbers of particles assembled under saturation state is respectively 2600,6550,10150;By scheming 4b it is found that the aggregation velocity increase presentation at any time of particle first increases and subtracts trend afterwards, power be 100,150, under 170mW, reach Time to maximum aggregation velocity is respectively 5.5,5.1 and 3.1min, and maximum aggregation velocity is respectively 7.4,14.8 and 22.1 A/second.
Particle in embodiment 3 in suspension 5 starts to assemble under photothermy;Result is observed by 8 display of computer As shown in figure 3, experiment is shown in Fig. 3 a starts rear 5s, particle starts to be assembled;After experiment starts 2min in Fig. 3 b, about There are 2100 particles to be assembled, forms a fusiform aggregation zone;As assemble index increases, the particle of aggregation is increasingly It is more, when 5 minutes, probably there are 5150 particles to be assembled, as shown in Figure 3c;As more and more particles are assembled, Spindle particle aggregation region is increasing, and the particle of outside is fewer and fewer, and aggregation velocity is also smaller and smaller, is 15 points when the time When clock, aggregation reaches a saturation state, and about 10150 particles are assembled, as shown in Figure 3d, at this point, particle is poly- Integrate 4 distance between two tips of centre distance conical fiber in region as d=380 μm.
After being continually fed into laser in embodiment 3, mobile conical fiber 4, the particle assembled is also moved, observed result As shown in Figure 5;Conical fiber 4 is shown to after 112 μm of the direction-y moving fiber in Fig. 5 a~Fig. 5 e, and the particle of aggregation is also therewith Mobile observation process, when mobile 65s, the particle of aggregation is nearly all moved to new position, only leave it is a small number of because It can not be migrated on the glass sheet for particle precipitating;After being moved to new position, to 172 μm of the direction+y moving fiber, of aggregation Grain is equally efficiently moved to new position, and for mobile observation process as shown in Fig. 5 f~Fig. 5 j, 95% or more particle is real Migration is showed.
Each embodiment in this specification is all made of relevant mode and describes, same and similar portion between each embodiment Dividing may refer to each other, and each embodiment focuses on the differences from other embodiments.Especially for system reality For applying example, since it is substantially similar to the method embodiment, so being described relatively simple, related place is referring to embodiment of the method Part explanation.
The foregoing is merely illustrative of the preferred embodiments of the present invention, is not intended to limit the scope of the present invention.It is all Any modification, equivalent replacement, improvement and so within the spirit and principles in the present invention, are all contained in protection scope of the present invention It is interior.

Claims (4)

1. extensive photo-thermal particle aggregation and moving method based on conical fiber, which is characterized in that specifically includes the following steps:
Step 1: the production of conical fiber (4)
The buffer layer of business single-mode fiber jumper and plastic wrapper are removed using optical fiber wire stripper, removal position length 20~ 50cm protrudes into the optical fiber for removing housing in glass capillary, and after optical fiber passes through glass capillary, end is pulled out in alcolhol burner After flame envelope heats 100~150s, with the speed of 1~3mm/s by 20~30s of optical fiber melt-pulling of flame upper end, experiment is obtained Conical fiber (4);
Step 2: suspension (5) is equipped with
By micro-nano particle or cellular invasion in deionization pure water, uniform suspension (5) are formed, the suspension prepared is taken (5) it is added drop-wise on micro slide, and micro slide is put in spare on the two-dimensional shift platform of microscope (6);
Step 3: installation conical fiber (4) and experimental provision
The conical fiber made (4) is fixed on fine adjustment frame (3), conical fiber (4) tip is protruded into suspension (5), The other end is connected on laser (1) by erbium-doped fiber amplifier (2), and computer (8) is connected to the microscope for being loaded with (7) CCD (6) on, experimentation can be directly observed by computer (8) display screen;
Step 4: large-scale aggregating particle
It opens laser (1), incident laser, micro-nano particle or cell is passed through into conical fiber (4) in the photo-thermal of incident laser Under effect, it is gathered in apart from the place at 100~500 μm of conical fiber (4) tip;
Step 5: the particle of efficient migration aggregation
After particle is by large-scale aggregating, laser (1) is kept to open, it is mobile conical fiber (4) by adjusting fine adjustment frame (3) To specified position, the migration to aggregated particle or cell is realized.
2. the extensive photo-thermal particle aggregation and moving method, feature according to claim 1 based on conical fiber exists In conical fiber (4) end diameter is 1~10 μm in the step 1.
3. the extensive photo-thermal particle aggregation and moving method, feature according to claim 1 based on conical fiber exists In for the size of micro-nano particle or cell at 1~5 μm, the solubility of particle or cell is 1.0 in suspension (5) in the step 2 ×107~1.0 × 108A/mL;For the size of particle or cell at 5~10 μm, solubility is 2.0 × 106~2.0 × 107A/ mL。
4. the extensive photo-thermal particle aggregation and moving method, feature according to claim 1 based on conical fiber exists In, in the step 4 incident power of incident laser be 100~170mW, wavelength 1550nm.
CN201811093624.7A 2018-09-19 2018-09-19 Large-scale photothermal particle aggregation and migration method based on tapered optical fibers Pending CN109300569A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114703141A (en) * 2022-03-23 2022-07-05 暨南大学 Photo-thermal induction reverse Marangoni flow-based method and drug cluster cell delivery method
CN115485544A (en) * 2020-05-08 2022-12-16 公立大学法人大阪 Micro object detection device, detection system and detection method

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080138772A1 (en) * 2003-05-08 2008-06-12 Eric Bornstein Instrument for Delivery of Optical Energy to the Dental Root Canal System for Hidden Bacterial and Live Biofilm Thermolysis
CN103990379A (en) * 2014-06-10 2014-08-20 中山大学 Optical separation method and device for micro-particles or biological cells
CN103993001A (en) * 2014-06-10 2014-08-20 中山大学 Microparticle or biological cell group trapping and migration method
CN103996423A (en) * 2014-03-21 2014-08-20 哈尔滨工程大学 Single-optical-fiber optical tweezers adjustable in transverse capture position
CN104678499A (en) * 2015-03-09 2015-06-03 哈尔滨工程大学 Small particle arrangement device and manufacturing method thereof
CN104698533A (en) * 2015-03-09 2015-06-10 哈尔滨工程大学 Optical fiber-based tiny particle moving device
CN106680985A (en) * 2017-03-23 2017-05-17 暨南大学 Optical capturing and detecting device and method based on quantum photon nano-jet array

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080138772A1 (en) * 2003-05-08 2008-06-12 Eric Bornstein Instrument for Delivery of Optical Energy to the Dental Root Canal System for Hidden Bacterial and Live Biofilm Thermolysis
CN103996423A (en) * 2014-03-21 2014-08-20 哈尔滨工程大学 Single-optical-fiber optical tweezers adjustable in transverse capture position
CN103990379A (en) * 2014-06-10 2014-08-20 中山大学 Optical separation method and device for micro-particles or biological cells
CN103993001A (en) * 2014-06-10 2014-08-20 中山大学 Microparticle or biological cell group trapping and migration method
CN104678499A (en) * 2015-03-09 2015-06-03 哈尔滨工程大学 Small particle arrangement device and manufacturing method thereof
CN104698533A (en) * 2015-03-09 2015-06-10 哈尔滨工程大学 Optical fiber-based tiny particle moving device
CN106680985A (en) * 2017-03-23 2017-05-17 暨南大学 Optical capturing and detecting device and method based on quantum photon nano-jet array

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
HONGBAO XIN ET AL: "Massive photothermal trapping and migration of particles by a tapered optical fiber", 《OPTICS EXPRESS》 *

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115485544A (en) * 2020-05-08 2022-12-16 公立大学法人大阪 Micro object detection device, detection system and detection method
US12345625B2 (en) 2020-05-08 2025-07-01 University Public Corporation Osaka Microscopic object detection device, detection system, and detection method
CN114703141A (en) * 2022-03-23 2022-07-05 暨南大学 Photo-thermal induction reverse Marangoni flow-based method and drug cluster cell delivery method
CN114703141B (en) * 2022-03-23 2023-07-07 暨南大学 A method based on photothermal induction of reverse Marangoni flow and a method for drug cluster cell delivery

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Application publication date: 20190201