CN107656053A - AIDS diagnosis comprising hydrophobic substrate multichannel micro-fluidic chip device - Google Patents

AIDS diagnosis comprising hydrophobic substrate multichannel micro-fluidic chip device Download PDF

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CN107656053A
CN107656053A CN201610626767.4A CN201610626767A CN107656053A CN 107656053 A CN107656053 A CN 107656053A CN 201610626767 A CN201610626767 A CN 201610626767A CN 107656053 A CN107656053 A CN 107656053A
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micro
fluidic chip
substrate
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aids
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宋岳
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    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/50Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
    • G01N33/53Immunoassay; Biospecific binding assay; Materials therefor
    • G01N33/569Immunoassay; Biospecific binding assay; Materials therefor for microorganisms, e.g. protozoa, bacteria, viruses
    • G01N33/56983Viruses
    • G01N33/56988HIV or HTLV
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/26Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
    • G01N27/416Systems
    • G01N27/48Systems using polarography, i.e. measuring changes in current under a slowly-varying voltage
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N2333/00Assays involving biological materials from specific organisms or of a specific nature
    • G01N2333/005Assays involving biological materials from specific organisms or of a specific nature from viruses
    • G01N2333/08RNA viruses
    • G01N2333/15Retroviridae, e.g. bovine leukaemia virus, feline leukaemia virus, feline leukaemia virus, human T-cell leukaemia-lymphoma virus
    • G01N2333/155Lentiviridae, e.g. visna-maedi virus, equine infectious virus, FIV, SIV

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  • Chemical Kinetics & Catalysis (AREA)
  • Automatic Analysis And Handling Materials Therefor (AREA)
  • Medicinal Chemistry (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Cell Biology (AREA)
  • Biotechnology (AREA)
  • Food Science & Technology (AREA)
  • Electrochemistry (AREA)
  • AIDS & HIV (AREA)

Abstract

The present invention relates to a kind of AIDS diagnosis multichannel micro-fluidic chip device comprising hydrophobic substrate, belong to analysis testing field.Technology barrier be present with dimethyl silicone polymer i.e. PDMS that is cheap and easily processing come the substrate for making AIDS diagnosis micro-fluidic chip;Its surface of the PDMS is strongly hydrophobic, and targetedly surface is modified or surface modification, its effect are difficult to persistently, and this case aims to solve the problem that the serial relevant issues.This case main points are, the selected PDMS with ecosystem surface of substrate, and fastening is positioned at the sample liquid stream terminal of the micro-fluidic chip its neighbor positions manually by the hinge-type fixture for being attached to miniature ultrasonic transducer units, interfacial tension is reduced with ultrasonic wave, strong absorbability using PDMS to ultrasonic wave simultaneously, reach ultrasonic intensity rapid decrement in short distance, so as to form interfacial tension difference at the both ends of the chip, sample liquid stream is thereby facilitated to be flowed along originally hydrophobic capillary channel to the terminal direction.

Description

AIDS diagnosis comprising hydrophobic substrate multichannel micro-fluidic chip device
Technical field
The present invention relates to a kind of AIDS diagnosis multichannel micro-fluidic chip device comprising hydrophobic substrate, belong to analysis Testing field.
Background technology
The micro-fluidic AIDS diagnosis technical background of associated multi-channel, it is special to may refer to the grade inventions of CN 200910151219.0 Sharp application case.
Only for the microflow control technique overall general picture of itself, famous micro-fluidic expert Mr. Lin Ping Cheng may refer to not The monograph " diagram Microfluid based Lab on a chip " gone out before long, the monograph is published via Science Press, and the monograph is for miniflow Past of control technology, now, and, vision of the future etc. etc., suffer from detail, be deep into long opinion of detail State.
So, the Important Problems of this case that to have a talk below concern.
The basic framework of micro-fluidic chip, including be etched with the substrate of small fluid course and fit together therewith Cover plate, the small fluid course on the substrate, before upper cover plate is assembled, it is apparent on see to be exactly some micro-channels, to wait until After covering cover plate thereon, just really closure forms the small fluid course, the conduit inner surface of the micro-channel together with The part cover plate that surround the micro-channel forms described small fluid course together;So, it is clear that after assembling completes The small fluid course, the major part of its inner surface area is the inner surface area of that micro-channel, in other words, should The state or property of micro-channel inner surface substantially determine the integrality or property of the small fluid course;Therefore say, this The inner surface state or inner surface property of micro-channel of the individual structure on substrate are key factors;In principle, it is any can The material of its solid forms is kept or kept substantially, can be used to make substrate and cover plate, such as, it can act as substrate and lid The material of piece can be monocrystalline silicon piece, quartz plate, sheet glass, high polymer for example dimethyl silicone polymer, polymethyl methacrylate, Makrolon etc.;Certainly, the selection of substrate and the selection of cover plate be able to can also be differed with identical;From material consumption, make From the point of view of difficulty and application popularization prospect etc. etc., not small difference, the especially choosing of that substrate between these materials be present Material, have a great influence.
In various substrate making materials, dimethyl silicone polymer, i.e. PDMS, comparatively very easily shaping, at this It is extremely simple that micro-channel is made on the substrate of sample, and the lower cost for material, base is made with the polydimethyl siloxane material Piece, micro-channel, and the cover plate phase made with the cheap material such as glass or polypropylene or other plastic sheets are being suppressed or etched thereon Coordinate, be a kind of more satisfactory selection seemingly;Certainly, patch material can also select to use cheap dimethyl silicone polymer Material:So, this substrate selection is the scheme of polydimethyl siloxane material, and material is extremely cheap, and making is extremely simple, seems It should be extremely easy to popularize, promote.
But thing is really not so simple.
First, this polydimethyl siloxane material, that is, the material that alphabetical PDMS is referred to of abridging, itself are a kind of strong Strong hydrophobic material, micro-channel is built on this material, if without being operated for the modified of the micro-channel surface, that , after overall assembling is completed, that is, after covering cover plate, because the micro-channel its inner surface in structure occupies most liquid The inner surface of circulation road, then, its strong hydrophobic property of the PDMS micro-channels inner surface, is deciding factor, it can cause Similar to the aqueous solution the fine liquid stream of polar liquid by becoming very difficult, its flow resistance is big, or even in general is micro- Pump is all difficult to promote, certainly, if cover plate also selects to use the PDMS material, then, problem is substantially identical, similar; Therefore, among prior art, modification is modified particular for the micro-channel inner surface on the PDMS material, is necessary behaviour Make;So, this is pretty troublesome for the modified operation of PDMS micro-channel inner surfacesThat falls nor this problem, is formed tight Weight technology puzzlement, be another problem:PDMS polymer molecules inside its body phase of this PDMS material substrate have automatic The characteristic diffuse to the surface, migrated, the spy that this substrate body phase inside PDMS polymer molecules are diffused to the surface, migrated automatically Property, the state after modification by its inner surface of that micro-channel of surface modifying and decorating will be caused can not to maintain long enough Time, the holding time for micro-channel its inner surface state after that is surface-modified be substantially only sufficient to complete laboratory internal The time of test experiments needs;In other words, by surface modification or the PDMS micro-channel inner surfaces of surface modification, it is modified The surface state that is formed can not be lasting afterwards or after saying modification, but soon automatically tends to or say and become surface modification again Surface state before, the strong hydrophobic surface state of that script is returned in the shorter time, then, just think, this The micro-fluidic chip of sample can largely make, mass storage, be widely popularized, and answer is it is obvious that is, impossible.This Micro-channel on PDMS material, if not doing surface modification, similar to the aqueous solution the fine liquid stream of polar solvent can not pump it is logical Cross, chip also cannot just use;And if having done surface modification, its state after modifying can not be persistently kept again, or together Sample can not popularization and application.
So, how to accomplish that substrate can either be made using cheap PDMS material, and the microflute can be released Road inner surface decorating state can not persistently, chip can not largely make, largely lay in and then be widely popularized and such a make ability The puzzlement that the numerous professionals in domain are entangled with for a long time, the highly difficult problem that exactly one its obvious technology barrier can not despise.
Be present many year in the highly difficult problem, so far, not yet properly settled.
Second, the PDMS material of non-surface modification, it is stated that, its surface is strongly hydrophobic above, this strong hydrophobic Material surface and also have another problem, that is, this strong hydrophobic PDMS surfaces can adsorb large biological molecule, and And these adsorbed large biological molecules can also further depression further on PDMS surfaces, gradually fall into it is gradually deep, until It is heavy to be trapped within the body phase of PDMS substrates, in fact, this process, partly it is also due to PDMS material body phase interior polymer Molecule, which has, to be diffused to the surface, caused by travel motion;Such case, it can also be explained from another angle, i.e. continue not Disconnectedly from inside PDMS body phases to those polymer molecules of its diffusion into the surface, migration, its result moved, be little by little by that It has been involved in a bit by the large biological molecule of adsorption within the body phase of PDMS substrates, briefly, these adsorbed biologies Macromolecular is exactly to be swallowed up by PDMS substrate body phases;So, this PDMS substrates body phase swallows up the phenomenon of large biological molecule, its institute Caused by influence, necessarily cause the severe deviations of all kinds of test data of experiment for being related to large biological molecule.
As described above, the problem of PDMS substrates, is, its not only adsorption large biological molecule, and swallow up biological big point Son, so, as the large biological molecule of experiment test object, its disappearance will not stop because surface saturation is adsorbed, and It is, it is constantly adsorbed, also constantly swallowed up.
On PDMS substrates, its body phase is constantly swallowed up and tests showing for associated biomolecule macromolecular in related experiment test process As, it is to say that another kind, which is explained, substantial amounts of Minute pores in PDMS body phases be present, associated biomolecule macromolecular by after adsorption, Depression enters these Minute pores, and then is swallowed up;However, inventor thinks, those can allow the sky of miniature scale Qi leel squeezes into the Minute pores therebetween, not equal to saying that they also can directly allow the large biological molecule of relative large scale to enter Enter, both difference on yardstick are huge, must not make sweeping generalizations.Explanation is bypassed, in any case, as dependence test analysis object Large biological molecule is adsorbed by PDMS substrate micro-channels inner surface, and then is constantly swallowed up by PDMS substrate body phases, and this is person in charge of reception at ceremonies Phenomenon existing for sight.
, can be from containment PDMS surfaces pair in order to prevent swallow up effect of this PDMS substrate bodies relative to large biological molecule The absorption of large biological molecule addresses, and method is chemically modified modification aiming at the PDMS material surface, for For PDMS is the situation of substrate material, modification exactly is chemically modified to the surface of described micro-channel part, by changing The micro-channel inner surface of modification is learned, its absorption to large biological molecule can be contained, and then avoid large biological molecule Swallowed up by PDMS substrate body phases;But or that old problem, that is, the chemical modification on PDMS material surface is modified Surface state afterwards can not persistently be kept, the polymer molecule inside the PDMS substrate body phases its diffuse to the surface, move automatically The process of shifting, it soon can become that micro-channel inner surface state being modified by surface chemical modification again script strong and dredge Water and the state of strong adsorption large biological molecule, in other words, no matter how professionals in the field turn from side to side, the PDMS bases Its micro-channel inner surface of piece is always rapidly to strong hydrophobic surface state evolution.
So, how can either obtain that PDMS material price is extremely cheap, substrate makes extremely easy benefit, and can is enough Reach and contain the absorption process of the PDMS substrate micro-channel inner surfaces to large biological molecule for a long time, and then prevent PDMS substrate body phases The effect of swallowing up to large biological molecule so that related chip manufactured goods be able to maintain that one it is prolonged enough, reasonably guarantee the quality Phase, it is exactly a very intractable problem.The problem equally makes this area numerous as another problem addressed above Professional is entangled with, perplexed for a long time, and the problem is equally the highly difficult problem that its obvious technology barrier can not despise. Also be present many year in the problem, so far, also not yet properly settled.
The content of the invention
The technical problem to be solved by the invention is to provide a package solution, solves totally above Two problems addressed, also, the solution is applied to AIDS diagnosis multichannel micro-fluidic chip field, form one The new AIDS diagnosis Multichannel device of kind.
The present invention solves the technical problem by following scheme, and the device that the program provides is that one kind includes hydrophobic substrate AIDS diagnosis multichannel micro-fluidic chip device, the structure of the device includes multichannel micro-fluidic chip, and this is micro-fluidic The structure of chip includes being bonded to each other the substrate and cover plate of installing together, and the substrate and cover plate are plate object or sheet The channel structure via mould pressing process or etching technics formation, the substrate are contained in thing, that face towards the cover plate of the substrate Also contain and be connected and pierce being formed via mould pressing process, etching technics or simple drilling technology for the substrate with the channel structure Window structure, be bonded to each other the substrate that is installed together and the cover plate and be built into jointly containing pipeline configuration and therewith The micro-fluidic chip of connected liquid pool structure, the locations of structures of the pipeline are located at the interface area that the substrate is bonded to each other with the cover plate Domain, its side of the window is blocked by the cover plate and opposite side opens, and the locations of structures of the window is exactly the structure bit of the liquid pool Put, the quantity of the liquid pool is three, and its locations of structures of two liquid pools therein is located at the sample introduction end of the micro-fluidic chip, remaining The liquid flowing in its chip when being located at the actual sample introduction test of the micro-fluidic chip of liquid pool its locations of structures terminal, the end End is located remotely from each other with the sample introduction end, and one end of the pipeline is via the manifold shape turnout for being similarly positioned in the interface zone being bonded to each other Respectively with the Liang Ge liquid pools UNICOM positioned at sample introduction end, the other end of the pipeline and the terminal positioned at the micro-fluidic chip A remaining liquid pool UNICOM, and, the working electrode that is sequentially respectively installed in the pipeline on diverse location and to electricity Pole and reference electrode, the working electrode is by conductive electrode and is attached on the conductive electrode and has embedded AIDS The gold size sensitive membrane of specific antigen is formed, and the construction of the pipeline is in parallel construction, and the pipeline in parallel construction is by four Lateral is in parallel to be formed, and the quantity of the working electrode is four, and the installation position of four working electrodes is located at institute respectively State in four laterals, and, the specific antigen in its top layer gold size sensitivity membrane structure of four working electrodes is respectively The four kinds of AIDS antigenic substances that can be specifically bound to aids antibody, four kinds of antigenic substances are AIDS disease-specific respectively Antigen p24, gp41, gp120 and gp36, its material of the working electrode be gold material or thermal decomposition conducting polymer material, Sheet or thread is presented in the working electrode its pattern, and emphasis is, its material of the substrate is dimethyl silicone polymer material, the base Its surface of piece is the surface of primary form, the surface of the primary form its be intended to refer to and do not pass through any surface chemical modification Or the surface of the primary form of the material of any surface chemical modification, the structure of the device also include hinge-type fixture, the conjunction Page fixture its appearance profile likeness in form hinge, the hinge-type fixture by two hinges being mutually hinged and through this two One fastening screw of individual hinge and one match with the fastening screw and are used for hand with what the fastening screw connected together The nut of dynamic fastening and hand break loose is formed, and two hinges of the hinge-type fixture are respectively mutually drawn close with its tip and to clamp this micro- Fluidic chip, the tip are positioned in the locations of structures of the neighbouring terminal of the micro-fluidic chip, and at least in one Fixation is attached in the individual hinge and is equiped with miniature ultrasonic transducer units, and, higher-order of oscillation electric signal transmission cable, the high frequency One end of vibration electric signal transmission cable links together with the miniature ultrasonic transducer units;The hinge-type fixture provides one The function of facilitating the device to disassemble;Its major function of the miniature ultrasonic transducer units is in the actual sample introduction test of micro-fluidic chip When, the ultrasonic wave launched using it reduces the interfacial tension between sample solution and the inwall of the pipeline, can It is compatible, also, utilize the sample introduction end and the distance between the terminal and the miniature ultrasonic transducer units installation position difference Difference on different and its ultrasonic intensity for being experienced, its interfacial tension of sample introduction end described in induced synthesis and the terminal its Difference between interfacial tension, interfacial tension difference between the micro-fluidic chip both ends can the micro-fluidic chip this two Pressure gap is formed between end, the pressure gap can drive sample solution to the end flow;The miniature ultrasonic transducer units Its function also include the ultrasonic wave launched with it check large biological molecule contained in sample its in the inner surface of pipeline On absorption, and then check swallow up effect of its body phase of the substrate of the dimethyl silicone polymer material to the large biological molecule;Institute Its function of the substrate of dimethyl silicone polymer material is stated including with cover plate and working electrode and to electrode and the isomorphism of reference electrode one Build the micro-fluidic chip, it is soft and have the substrate of the dimethyl silicone polymer material of elasticity its function and also include with it to ultrasound The property that ripple absorbs strongly, ultrasonic wave is absorbed strongly, and thereby micro-fluidic chip terminal to the sample introduction end it Between limited short distance within realize the rapid decrement of ultrasonic intensity, its locations of structures be located at the micro-fluidic chip it is actual enter A remaining liquid pool for the terminal of liquid flowing is also referred to as terminal liquid pool in its chip when sample is tested, and is filled out in the terminal liquid pool Filled with some high hydroscopic resin particles, its opening end of the terminal liquid pool is covered by breathable microporous film.
Described miniature ultrasonic transducer units can certainly be all installed in two hinges;But only install one Individual miniature ultrasonic transducer units are dealt with enough to be used.
The word of hinge one art-recognized meanings of itself are known.
The gold size sensitive membrane is to be sufficiently mixed chitosan gold size solution and AIDS specific antigen solution uniformly, is used Point sample instrument point sample is coated on specified structure position, and forms its drying and forming-film.AIDS in the gold size sensitive membrane is special Specific Antigen is the AIDS antigen of horseradish peroxidase or glucose oxidase mark, and the gold size sensitive membrane has been wrapped Containing complementary medium therein is introduced for the above-mentioned each AIDS specific antigen of fixation, the complementary medium such as shell gathers Sugar, cellulose acetate, gelatin be therein a kind of or their mixture.
The pipeline and the lateral and the manifold shape turnout in the microfluidic chip structure, in it Footpath size may each be arbitrarily selected size, still, for as far as possible less with prepare liquid sample and reduction reagent loss etc. Consideration, the pipeline and the lateral and the manifold shape turnout preferably select capillary level passage, institute The passage for stating capillary level implies that its internal diameter passage suitable with the internal diameter of the capillary on ordinary meaning.The capillary is in it The shape of cross section of portion's passage can be arbitrary shape, and the shape of cross section is for example circular, oval, square, rectangle, bar Shape, naturally it is also possible to it is the linear of bending arbitrarily be present, also, the interior shape of the capillary is with the extension of pipeline, The shape of cross section of different parts can also allow to be different shapes.Only for the word of capillary one, its art-recognized meanings is public Know.
What is be related in structure is the electrode of microsize to electrode and reference electrode, and its electrode shape, which may each be, appoints The selected shape of meaning, the arbitrarily selected shape such as square piece shape, rectangular patch, strip or round sheet etc..It is described Art-recognized meanings to electrode and the reference electrode vocabulary of itself are known.
It is related to several liquid pools in this case microfluidic chip structure, the liquid pool is the pond shape or capsule for transitional liquid storage Shape constructs, and its shape of the inner chamber of each liquid pool may each be arbitrarily selected shape, and the cavity shape is for example round Cylindrical cavity shape, square column type cavity-like, oblong cavity shape or spherical hollow space shape etc..The size of the liquid pool can be any Selected size, still, in order to as far as possible less with prepare liquid sample and reduce reagent loss, the liquid pool be preferably capable of with The liquid pool of the microminiature of capillary matching.
Only for professional of the word of ultrasonic transducer one art-recognized meanings of itself for ultrasonic technology field, It is known.
Various sizes, variously-shaped ultrasonic transducer are commercially available;Its size of commercially available miniature ultrasonic transducer units It may diminish to the magnitude only calculated with millimeter.
Only with regard to miniature ultrasonic transducer units its technique for fixing on general industry application solid body surface its It is known general technology for the professional in ultrasonic technology field for body.This case is not to this expansion superfluous words.
Only with regard to naked PDMS substrates itself micro-channel molding or lithographic technique for, be open-and-shut known skill Art;Similarly, the technology of hole-opening is even more known simple technique on naked PDMS substrates.This case is not also superfluous to this expansion Speech.
The industrial products market of involved its all size of higher-order of oscillation electric signal transmission cable is on sale.
The structure of the device can also include higher-order of oscillation electric signal generator;The higher-order of oscillation electric signal transmission cable Its other end can be connected with the higher-order of oscillation electric signal generator.
The involved higher-order of oscillation electric signal generator technology of itself, come for the professional in ultrasonic technology field Say, be simple and known;The higher-order of oscillation electric signal generator can customize to ultrasonic instrument specialized factory.
The preferred scope of its specified ultrasonic wave transmission power of the miniature ultrasonic transducer units is between 5 milliwatts and 9000 milliwatts Between;The preferred scope of the frequency of its ultrasonic wave operationally launched of the miniature ultrasonic transducer units be between 100KHz with Between 12MHz.
Only for the word of high hydroscopic resin one art-recognized meanings of itself, come for the professional of chemical field Say, be known.
The high hydroscopic resin is commercially available.
Only for the word of breathable microporous film one art-recognized meanings of itself, for the professional of technical field of membrane, It is known.
The breathable microporous film is commercially available.
This case device can further include some annexes certainly, and the annex is such as multiple tracks electrochemical workstation Deng the art-recognized meanings of the multiple tracks electrochemical workstation are known.The each work being related in this case microfluidic chip structure Electrode and to electrode and reference electrode etc., special it can get lines crossed and the multiple tracks electrochemical workstation via corresponding respectively The corresponding interface coupled.It is described that special to get lines crossed be for by each phase of each electrode and the multiple tracks electrochemical workstation Answer the private cable that interface is coupled to each other.The micro-fluidic chip in this case device, its structure can also include micro-valve, The quantity of the micro-valve is unlimited, and according to being actually needed, the micro-valve can be installed in any need in the microfluidic chip structure Position to be mounted;The word of micro-valve one is for the professional of micro fluidic chip technical field, the art-recognized meanings of itself It is known;The micro-valve itself manufacturing technology and the use of technology is also known;The component that the micro-valve is not required.
The diameter of the working electrode can allow to be that any setting is easily installed the suitable diameter used, still, It is recommending or say preferable its scope of the diameter between 0.1 micron to 2000 microns;The length of the working electrode can To allow to be that any setting is easily installed the length used, it is however recommended to or to say the preferable length its scope be 1 Micron is between 15000 microns.
It is installed in by spraying or point sample instrument point sample or the coating of other appropriate process described in the working electrode surface layer Gold size sensitive membrane, its thicknesses of layers can allow be any setting treat sample measuring liquid occur electrical signals response thickness, It is however recommended to thickness preferable thickness is between 10 nanometers and 200 nanometers in other words.
The cover plate in chip structure, its material can allow to be any electrical insulating property material, such as:Polypropylene, Glass, polymethyl methacrylate, dimethyl silicone polymer, etc., in order to make smaller size of micro-fluidic chip, for example do Into the micro-fluidic chip of only 2.0 centimetres to 3.0 centimetres of super-small of length, and realized in the extremely short distance to ultrasonic wave Extremely fast decay, can preferably dimethyl silicone polymer be used as cover plate.Certainly, selected on large-sized micro-fluidic chip Using dimethyl silicone polymer it is used as the cover plate, and this case technical scheme is allowed.
Positioned at the sample introduction end of the micro-fluidic chip two liquid pools its with positioned at the micro-fluidic chip terminal should Air line distance between a remaining liquid pool can be arbitrarily selected suitable distance, still, the distance as needed Preferred value is between 3 centimetres and 7 centimetres.
Described its thickness of cover plate and substrate can allow be any setting the thickness for being easy to assembling, the thickness of recommendation or say Preferable thickness is between 1.0 millimeters and 5.0 millimeters.Less thickness is advantageous to save material.
The application method of this case micro-fluidic chip:
Itd is proposed first based on this case and the first public new liquid stream driving principle, its application of this case micro-fluidic chip are transported Among work, the new liquid stream driving method is determined completely without involving any additional Micropump.
The interfacial tension difference that this case is formed between micro-fluidic chip both ends caused by the ultrasonic wave, Driving liquid stream flows in the capillary channel of the four-way micro-fluidic chip, right respectively using four-way electrochemical analytical instrument Four kinds of aids antibodies are detected.
Corresponding four kinds of aids antibodies are detected with four kinds of AIDS antigens, with detecting phase with four kinds of aids antibodies The four kinds of AIDS antigens answered, similarly, can diagnosis of aids;The principle of its foundation is, must in AIDS patient It is so antigen, antibody and deposits, and mutual Reversible binding, form reversible conjugate, therefore, antibody and thereby is detected with antigen Diagnosis of aids, with being gone to detect antigen and diagnosis of aids with antibody, diagnostic purpose can be reached.Certainly, different means Its corresponding electrode sensitive decorative layer technically and differs.
The specific detection of this case micro-fluidic chip is as follows using step:
1st, blood serum sample liquid is added in micro-pipe road, under ultrasonic wave driving, various aids antibody molecules are each The AIDS specific antigen for the corresponding horseradish peroxidase-labeled that gold size sensitive membrane embeds is caught on electrode surface in passage Obtain.
2nd, the AIDS specific antigen of horseradish peroxidase-labeled is formed with the aids antibody in blood serum sample and exempted from Epidemic disease compound.
3rd, using multi-channel electrochemical analyzer, the electron mediators such as catechol are added, it is above-mentioned using amperometric detection Curent change caused by reaction, it is derived from the species and content of various analytes.
4th, result is subjected to comprehensive analysis, comprehensive diagnos is carried out to aids antibody.
It is an advantage of the invention that its close position positions the hinge-type folder in the terminal of the micro-fluidic chip Tool, the miniature ultrasonic transducer units installed with institute's attaching in the hinge-type fixture its hinge, the low-power launched using it, height The ultrasonic wave of frequent section so that without in strong hydrophobic micro-fluidic chip of surface chemical modification or surface chemical modification Compatibility between its tube wall of portion's pipeline and the test object aqueous solution is significantly increased, and this is sample liquid stream by providing one Realistic possibility;Meanwhile using its strong absorbability to ultrasonic wave of dimethyl silicone polymer substrate, in shorter distance It is interior, it is, in from the terminal to the very short distance of only several centimeters yardsticks the sample introduction end, it is strong to reach ultrasonic wave The rapid decrement of degree, the difference of the interfacial tension is thereby caused at the both ends of the micro-fluidic chip, and then, using this two Pressure gap between its both ends for being formed of the difference of interfacial tension between end, driving sample liquid stream is in such a original Flowed in this strong hydrophobic capillary channel to the terminal direction.By this case liquid stream drive scheme, entirely without must be to this The substrate and its internal pipeline of dimethyl silicone polymer material carry out any surface chemical modification or chemical modification, altogether dispense with The laborious procedures of the surface chemical modification or chemical modification;And setting for traditional Micropump etc is altogether dispensed with It is standby;On the other hand, the ultrasonic wave of the low-power, high-frequency band, additionally it is possible to contain the large biological molecule in sample at this without modification Naked its inner surface of pipeline of dimethyl silicone polymer substrate on absorption, and then contain its body of the dimethyl silicone polymer substrate The effect of swallowing up of relatively described large biological molecule;The Reversible binding thing of the antigen, antibody and antigen and antibody is all certainly Belong to the type of described large biological molecule;Because described suction-operated and the described effect of swallowing up effectively are contained, Therefore, dependence test result will be better able to objectively reflect actual conditions;The effect of the low-power, high-frequency band ultrasonic wave, Certainly also include facilitating the Reversible binding between antigen, antibody react it is quick reach, this causes dependence test operates can be with Completed than faster speed.
Due to surface chemical modification or chemistry for its relevant surfaces of the dimethyl silicone polymer substrate need not be carried out Modified operation, therefore, this surface chemical modification layer or chemically modified layer not need to exist, then, the poly dimethyl Its body phase interior polymer molecule of siloxanes substrate constantly diffuses to the surface automatically, migrate caused by it to the surface chemistry The damaging influence of decorative layer or chemically modified layer is also just not present.
It is related that the technical scheme of this case has dissolved its application to dimethyl silicone polymer substrate addressed above totally A series of technical barriers.Based on this case scheme, the very cheap polydimethyl siloxane material of this kind is just possible to micro- at this It is prepared by fluidic chip, production, using etc. field play bigger effect.
The miniature ultrasonic transducer units have been installed in fixation in the hinge-type fixture its hinge in this case structure, the structure A function of facilitating the device to disassemble is provided, in this way, the hinge-type fixture is together with miniature ultrasonic appended in its hinge Transducer just easily can be mutually disengaged with the micro-fluidic chip, then, the component that the part can freely depart from just can be good Property is re-used cyclically many times;The architectural feature is advantageous to save the use cost of the device.
Brief description of the drawings
Fig. 1 is the schematic diagram of this case device embodiment chip part construction, it is shown that the vertical view of this structure The structural form of chip internal pipeline and each electrode and each related liquid pool under angle, the hinge-type is not depicted in the figure The miniature ultrasonic transducer units set up on fixture and its hinge and other annexes.
Fig. 2 is its rough outside side view of this case device.
In figure, 1,2,10 be the different liquid pool of three installation positions respectively, and 3 be manifold shape turnout, and 4,7,11,14 are respectively Installation position is different but four laterals parallel with one another for forming UNICOM's structure in parallel, and 5 be its that be installed in lateral 4 The working electrode that specific antigenic substance in the gold size sensitivity membrane structure of top layer is AIDS specific antigen p24,6 be to be installed in The work that the specific antigenic substance in its top layer gold size sensitivity membrane structure in lateral 7 is AIDS specific antigen gp41 Make electrode, 12 be that specific antigenic substance in its top layer gold size sensitivity membrane structure being installed in lateral 11 is AIDS Specific antigen gp120 working electrode, 13 be the spy in its top layer gold size sensitivity membrane structure being installed in lateral 14 Specific Antigen material is AIDS specific antigen gp36 working electrode, and 8 be to electrode, and 9 be reference electrode, and 15 be hinge-type Fixture, 16 sign linkwork positions, 17 be fastening screw, and 18 be higher-order of oscillation electric signal transmission cable, and 19 be miniature Ultrasonic transducer, 20,25 be two different hinges of locations of structures respectively, and 21 be cover plate, and 22 be substrate, and 23 be sample introduction end, 24 be terminal, and 26 be nut;The hinge-type clamp structure in legend is only the legend structure of signal, actually the hinge-type fixture Its structure is not limited to the legend hinge-type clamp structure;Arrow in legend indicate the micro-fluidic chip its in actual motion When, driven by pressure at two ends difference, the flow direction of its sample liquid stream.
Embodiment
In this case that Fig. 1 and Fig. 2 are shown embodiment, the structure of the device includes multichannel micro-fluidic chip, should The structure of micro-fluidic chip includes being bonded to each other the substrate 22 and cover plate 21 of installing together, and the substrate 22 and cover plate 21 are What is formed via mould pressing process or etching technics contained in plate object or tablet, that face towards the cover plate 21 of the substrate 22 Channel structure, the substrate 22 also containing be connected with the channel structure and pierce the substrate via mould pressing process, etching technics Or the window structure that simple drilling technology is formed, it is bonded to each other the substrate 22 being installed together and is built into jointly with the cover plate 21 Micro-fluidic chip containing pipeline configuration and the liquid pool structure being attached thereto, the liquid pool are liquid pool 1, liquid pool 2, liquid pool 10, the locations of structures of the pipeline is located at the interface zone that the substrate 22 is bonded to each other with the cover plate 21, and its side of the window is by this Cover plate 21 blocks and opposite side opens, and the locations of structures of the window is exactly the liquid pool 1, liquid pool 2, the locations of structures of liquid pool 10, The quantity of the liquid pool is three, and two liquid pools therein are that liquid pool 1 and liquid pool 2 its locations of structures are located at the micro-fluidic chip Sample introduction end 23, a remaining liquid pool are its chip when liquid pool 10 its locations of structures is located at the micro-fluidic chip actual sample introduction test The terminal 24 of interior liquid flowing, the terminal 24 are located remotely from each other with the sample introduction end 23, and one end of the pipeline is via being similarly positioned in the phase The manifold shape turnout 3 for the interface zone being mutually bonded respectively with the liquid pool 1 positioned at sample introduction end 23 and the UNICOM of liquid pool 2, the pipeline The other end and the remaining liquid pool of the terminal 24 positioned at the micro-fluidic chip be the UNICOM of liquid pool 10, and, according to Sequence is respectively installed in working electrode in the pipeline on diverse location and to electrode 8 and reference electrode 9, the working electrode It is made up of conductive electrode and the gold size sensitive membrane for having embedded AIDS specific antigen being attached on the conductive electrode, The construction of the pipeline is in parallel construction, and the pipeline in parallel construction is made up of four lateral parallel connections, the work electricity The quantity of pole is four, and respectively in four laterals, this four work the installation position of four working electrodes Electrode is working electrode 5, working electrode 6, working electrode 12, working electrode 13 respectively, and, four its top layers of working electrode Specific antigen in gold size sensitivity membrane structure is the four kinds of AIDS antigen things that can be specifically bound to aids antibody respectively Matter, four kinds of antigenic substances are AIDS specific antigen p24, gp41, gp120 and gp36 respectively, for specifically deploying, 5 It is that specific antigenic substance in its top layer gold size sensitivity membrane structure being installed in lateral 4 is AIDS specific antigen P24 working electrode, 6 be that specific antigenic substance in its top layer gold size sensitivity membrane structure being installed in lateral 7 is AIDS specific antigen gp41 working electrode, 12 be in its top layer gold size sensitivity membrane structure being installed in lateral 11 Specific antigenic substance be AIDS specific antigen gp120 working electrode, 13 be its that be installed in lateral 14 The working electrode that specific antigenic substance in the gold size sensitivity membrane structure of top layer is AIDS specific antigen gp36, the work Electrode 5, working electrode 6, working electrode 12, working electrode 13 its material are gold material or thermal decomposition conducting polymer material, The working electrode 5, working electrode 6, working electrode 12, its pattern presentation sheet or thread of working electrode 13, emphasis is the base Its material of piece 22 is dimethyl silicone polymer material, and its surface of substrate 22 is the surface of primary form, the table of the primary form Face its be intended to refer to the not no primary form of the material by any surface chemical modification or any surface chemical modification Surface, the structure of the device also include hinge-type fixture 15, its appearance profile likeness in form hinge of hinge-type fixture 15, the hinge-type Fixture 15 is by two hinges 20,25 being mutually hinged and a fastening screw 17 through two hinges 20,25 And one matched with the fastening screw 17 and with the fastening screw 17 connect together be used for manually fasten and hand break loose Nut 26 form, two hinges 20,25 of the hinge-type fixture 15 are respectively mutually drawn close with its tip and clamp the micro-fluidic core Piece, the tip are positioned in the locations of structures of the neighbouring terminal 24 of the micro-fluidic chip, an institute at least in State attached in hinge it is fixed be equiped with miniature ultrasonic transducer units, be installing to be attached in hinge 20 this is miniature super in this legend Acoustic wave transducer 19, it is of course also possible to allow all to install miniature ultrasonic transducer units, but, one in two hinges 20,25 As in fact, only in a hinge attach installing one miniature ultrasonic transducer units be just enough to deal with to be actually needed, and, Higher-order of oscillation electric signal transmission cable 18, one end and the miniature ultrasonic transducer units of the higher-order of oscillation electric signal transmission cable 18 19 link together;The hinge-type fixture 15 provides a function of facilitating the device to disassemble;The miniature ultrasonic transducer units 19 its major function be in the test of micro-fluidic chip actual sample introduction, the ultrasonic wave launched using it reduce sample solution with Interfacial tension between the inwall of the pipeline, can be compatible, also, utilizes the sample introduction end 23 and the terminal 24 Difference in the distance between the installation position of miniature ultrasonic transducer units 19 difference and its ultrasonic intensity experienced It is different, the difference between its interfacial tension of sample introduction end 23 described in induced synthesis and the terminal 24 its interfacial tension, the micro-fluidic core The piece both ends are that the interfacial tension difference between sample introduction end 23 and terminal 24 can be at the both ends of the micro-fluidic chip i.e. sample introduction end Pressure gap is formed between 23 and terminal 24, the pressure gap can drive sample solution to be flowed to the direction of terminal 24;This is micro- The ultrasonic wave that type ultrasonic transducer 19 its function also includes being launched with it check large biological molecule contained in sample its Absorption on the inner surface of pipeline, and then it is big to the biology to check its body phase of the substrate 22 of the dimethyl silicone polymer material The effect of swallowing up of molecule;Its function of the substrate 22 of the dimethyl silicone polymer material includes and cover plate 21 and working electrode 5, work Make electrode 6, working electrode 12, working electrode 13 and the micro-fluidic chip is together built to electrode 8 and reference electrode 9, softness is simultaneously Its function of the substrate 22 of the dimethyl silicone polymer material of tool elasticity also includes with its property to the strong absorption of ultrasonic wave, right Ultrasonic wave is absorbed strongly, and the thereby limited short distance between micro-fluidic chip terminal 24 to the sample introduction end 23 Within realize the rapid decrement of ultrasonic intensity, when its locations of structures is located at the micro-fluidic chip actual sample introduction test in its chip A remaining liquid pool for the terminal of liquid flowing is also referred to as terminal liquid pool, and some super absorbent resins are filled with the terminal liquid pool Fat particle, its opening end of the terminal liquid pool are covered by breathable microporous film.
Arrow in legend indicate the micro-fluidic chip its in actual motion, by pressure at two ends difference drive, its try The flow direction of sample liquid stream.
The miniature ultrasonic for being depicted without attaching installing in Fig. 1 in the hinge-type fixture 15 and one hinge changes Can device 19 and higher-order of oscillation electric signal transmission cable 18;Also, the higher-order of oscillation telecommunication is depicted without in Fig. 1 and Fig. 2 The associate member such as number generator and multiple tracks electrochemical workstation.
Involved hinge-type fixture 15 can be carried out simply cutting using commercially available hinge, changed a social system;The miniature ultrasonic Transducer 19 is commercially available;Commercially available miniature ultrasonic transducer units are various in style, can select to use as needed;This is miniature super Acoustic wave transducer 19 can also customize to ultrasonic transducer specialized factory.
Involved higher-order of oscillation electric signal transmission cable 18 is commercially available;Can also be special to ultrasonic transducer producer or cable Industry producer customizes.
Involved higher-order of oscillation electric signal generator in the market has the product close to needs commercially available;It can also determine to relevant manufacturers System.
Each working electrode in this example structure and can be respectively via each special electricity to electrode and reference electrode Cable or say is being got lines crossed respectively with the corresponding cable interface of the multiple tracks electrochemical workstation as annex or saying interface connection of getting lines crossed.
This case device is that a variety of corresponding aids antibodies are detected with a variety of AIDS antigens, thereby diagnoses AIDS Disease.

Claims (10)

1. including the AIDS diagnosis multichannel micro-fluidic chip device of hydrophobic substrate, the structure of the device is micro- including multichannel Fluidic chip, the structure of the micro-fluidic chip include being bonded to each other the substrate and cover plate of installing together, the substrate and cover plate It is plate object or tablet, what is formed via mould pressing process or etching technics contained in that face towards the cover plate of the substrate Channel structure, the substrate also containing be connected with the channel structure and pierce the substrate via mould pressing process, etching technics or The window structure that simple drilling technology is formed, is bonded to each other the substrate being installed together and has been built into jointly with the cover plate and contained The micro-fluidic chip of pipeline configuration and the liquid pool structure being attached thereto, the locations of structures of the pipeline are located at the substrate and the cover plate The interface zone being bonded to each other, its side of the window is blocked by the cover plate and opposite side opens, and the locations of structures of the window is exactly The locations of structures of the liquid pool, the quantity of the liquid pool is three, and it is micro-fluidic that its locations of structures of two liquid pools therein is located at this The sample introduction end of chip, liquid in its chip when its locations of structures of a remaining liquid pool is located at the test of the micro-fluidic chip actual sample introduction The terminal of body flowing, the terminal is located remotely from each other with the sample introduction end, and one end of the pipeline is via being similarly positioned in the boundary being bonded to each other The manifold shape turnout in face region is respectively with the Liang Ge liquid pools UNICOM positioned at sample introduction end, and the other end of the pipeline is with being located at the miniflow A remaining liquid pool UNICOM for the terminal of chip is controlled, and, sequentially it is respectively installed in the pipeline on diverse location Working electrode and to electrode and reference electrode, the working electrode is by conductive electrode and is attached to electric conductivity electricity The gold size sensitive membrane for having embedded AIDS specific antigen on extremely is formed, and the construction of the pipeline is in parallel construction, described in simultaneously The pipeline of connection construction is made up of four lateral parallel connections, and the quantity of the working electrode is four, four working electrodes Installation position is located in four laterals respectively, and, in its top layer gold size sensitivity membrane structure of four working electrodes Specific antigen be the four kinds of AIDS antigenic substances that can be specifically bound to aids antibody respectively, four kinds of antigenic substances It is AIDS specific antigen p24, gp41, gp120 and gp36 respectively, its material of the working electrode is gold material or heat point Conducting polymer material is solved, sheet or thread is presented in its pattern of the working electrode, it is characterised in that its material of the substrate is poly- Dimethyl siloxane material, its surface of the substrate are the surfaces of primary form, the surface of the primary form its be intended to refer to not There are the surface of the primary form by any surface chemical modification or the material of any surface chemical modification, the structure of the device Also include hinge-type fixture, hinge-type fixture its appearance profile likeness in form hinge, the hinge-type fixture is by being mutually hinged Two hinges and matched through a fastening screw of two hinges and one with the fastening screw and with the fastening What screw connected together is used for the nut of fastening and hand break loose composition manually, and two hinges of the hinge-type fixture are respectively with it Tip is mutually drawn close and clamps the micro-fluidic chip, and the tip is positioned at the structure of the neighbouring terminal of the micro-fluidic chip Fixation, which is attached, on position, in a hinge at least in is equiped with miniature ultrasonic transducer units, and, the higher-order of oscillation Electric signal transmission cable, one end and the miniature ultrasonic transducer units of the higher-order of oscillation electric signal transmission cable link together; The hinge-type fixture provides a function of facilitating the device to disassemble;Its major function of the miniature ultrasonic transducer units is micro- During the test of fluidic chip actual sample introduction, the ultrasonic wave launched using it is reduced between sample solution and the inwall of the pipeline Interfacial tension, can be compatible, also, filled using the sample introduction end and the terminal and the miniature ultrasonic transducer units If the difference on the distance between position difference and its ultrasonic intensity experienced, its boundary of sample introduction end described in induced synthesis Difference between face tension force and the terminal its interfacial tension, interfacial tension difference between the micro-fluidic chip both ends can be Pressure gap is formed between the both ends of the micro-fluidic chip, the pressure gap can drive sample solution to the end flow; The ultrasonic wave that its function of the miniature ultrasonic transducer units also includes being launched with it checks large biological molecule contained in sample Its absorption on the inner surface of pipeline, and then it is big to the biology to check its body phase of the substrate of the dimethyl silicone polymer material The effect of swallowing up of molecule;Its function of the substrate of the dimethyl silicone polymer material is included with cover plate and working electrode and to electrode It is soft and have the substrate of the dimethyl silicone polymer material of elasticity its function and reference electrode together builds the micro-fluidic chip Also include with its property to the strong absorption of ultrasonic wave, ultrasonic wave is absorbed strongly, and thereby should in the micro-fluidic chip Terminal is to the rapid decrement that ultrasonic intensity is realized within the limited short distance between the sample introduction end, and its locations of structures was positioned at should A remaining liquid pool for the terminal of liquid flowing is also referred to as terminal liquid in its chip when the actual sample introduction of micro-fluidic chip is tested Pond, some high hydroscopic resin particles are filled with the terminal liquid pool, its opening end of the terminal liquid pool is covered by breathable microporous film.
2. the AIDS diagnosis multichannel micro-fluidic chip device according to claim 1 comprising hydrophobic substrate, it is special Sign is that the pipeline and the lateral and the manifold shape turnout are capillary channel.
3. the AIDS diagnosis multichannel micro-fluidic chip device according to claim 1 comprising hydrophobic substrate, it is special Sign is that the thermal decomposition conducting polymer is the electric conductivity material formed by polyimides or polyacrylonitrile after anoxybiotic is heat-treated Material.
4. the AIDS diagnosis multichannel micro-fluidic chip device according to claim 1 comprising hydrophobic substrate, it is special Sign is, the width or diameter of the working electrode between 0.1 micron to 2000 microns, and, the working electrode Length is between 1 micron to 15000 microns.
5. the AIDS diagnosis multichannel micro-fluidic chip device according to claim 1 comprising hydrophobic substrate, it is special Sign is that the thickness of the gold size sensitive membrane is between 10 nanometers and 200 nanometers.
6. the AIDS diagnosis multichannel micro-fluidic chip device according to claim 1 comprising hydrophobic substrate, it is special Sign is, the cover plate its material in structure is dimethyl silicone polymer material.
7. the AIDS diagnosis multichannel micro-fluidic chip device according to claim 1 comprising hydrophobic substrate, it is special Sign is, positioned at the sample introduction end of the micro-fluidic chip two liquid pools its with positioned at the micro-fluidic chip terminal this is remaining Under a liquid pool between air line distance between 3 centimetres and 7 centimetres.
8. the AIDS diagnosis multichannel micro-fluidic chip device according to claim 1 comprising hydrophobic substrate, it is special Sign is that described its thickness of cover plate and substrate in structure is between 1.0 millimeters and 5.0 millimeters.
9. the AIDS diagnosis multichannel micro-fluidic chip device according to claim 1 comprising hydrophobic substrate, it is special Sign is, the structure of the device also includes higher-order of oscillation electric signal generator, and its is another for the higher-order of oscillation electric signal transmission cable One end is connected with the higher-order of oscillation electric signal generator.
10. the AIDS diagnosis multichannel micro-fluidic chip device according to claim 1 comprising hydrophobic substrate, it is special Sign is that for its specified ultrasonic wave transmission power of the miniature ultrasonic transducer units between 5 milliwatts and 9000 milliwatts, this is miniature super The frequency of its ultrasonic wave operationally launched of acoustic wave transducer is between 100KHz and 12MHz.
CN201610626767.4A 2016-07-26 2016-07-26 AIDS diagnosis comprising hydrophobic substrate multichannel micro-fluidic chip device Pending CN107656053A (en)

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Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN2747681Y (en) * 2004-12-09 2005-12-21 天津市科信新技术开发应用公司 Electric permanent magnet attraction actuator
CN101561444A (en) * 2008-04-18 2009-10-21 中国科学院大连化学物理研究所 Micro-fluidic chip with an integrated PDMS surface tension minipump and application thereof
CN101581725A (en) * 2009-06-19 2009-11-18 宁波大学 Multichannel micro-fluidic chip specially used for AIDS diagnosis and comprising quasi-one-dimensional sensitive electrodes
CN101620228A (en) * 2009-07-12 2010-01-06 宁波大学 Special AIDS diagnosis device combining and utilizing high polymer anoxybiotic pyrolysis product
CN102645429A (en) * 2012-04-23 2012-08-22 宁波大学 Self-cleaning and vibration wave energy digestion link containing electrogenerated chemiluminescence analyzing and detecting device
CN103331250A (en) * 2013-07-10 2013-10-02 任国祚 Ultrasonic energy converter

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN2747681Y (en) * 2004-12-09 2005-12-21 天津市科信新技术开发应用公司 Electric permanent magnet attraction actuator
CN101561444A (en) * 2008-04-18 2009-10-21 中国科学院大连化学物理研究所 Micro-fluidic chip with an integrated PDMS surface tension minipump and application thereof
CN101581725A (en) * 2009-06-19 2009-11-18 宁波大学 Multichannel micro-fluidic chip specially used for AIDS diagnosis and comprising quasi-one-dimensional sensitive electrodes
CN101620228A (en) * 2009-07-12 2010-01-06 宁波大学 Special AIDS diagnosis device combining and utilizing high polymer anoxybiotic pyrolysis product
CN102645429A (en) * 2012-04-23 2012-08-22 宁波大学 Self-cleaning and vibration wave energy digestion link containing electrogenerated chemiluminescence analyzing and detecting device
CN103331250A (en) * 2013-07-10 2013-10-02 任国祚 Ultrasonic energy converter

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
JAMES FRIEND ET AL.: "Microscale acoustofluidics: microfluidics driven via acoustics and ultrasonics", 《REVIEWS OF MODERN PHYSICS》 *
付其达: "高聚物PDMS超声改性的实验研究", 《中国优秀硕士学位论文全文数据库(信息科技辑)》 *

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