CN107213926A - The micro flow control chip device of ten Five-channel joint-detection Diagnostic Value of Several Serum Tumor Markers - Google Patents

The micro flow control chip device of ten Five-channel joint-detection Diagnostic Value of Several Serum Tumor Markers Download PDF

Info

Publication number
CN107213926A
CN107213926A CN201610205552.5A CN201610205552A CN107213926A CN 107213926 A CN107213926 A CN 107213926A CN 201610205552 A CN201610205552 A CN 201610205552A CN 107213926 A CN107213926 A CN 107213926A
Authority
CN
China
Prior art keywords
micro
sample introduction
tumor markers
fluidic chip
terminal
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
CN201610205552.5A
Other languages
Chinese (zh)
Inventor
李榕生
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to CN201610205552.5A priority Critical patent/CN107213926A/en
Publication of CN107213926A publication Critical patent/CN107213926A/en
Withdrawn legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5027Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
    • B01L3/50273Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by the means or forces applied to move the fluids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5027Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
    • B01L3/502761Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip specially adapted for handling suspended solids or molecules independently from the bulk fluid flow, e.g. for trapping or sorting beads, for physically stretching molecules
    • 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
    • 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
    • G01N33/574Immunoassay; Biospecific binding assay; Materials therefor for cancer
    • G01N33/57484Immunoassay; Biospecific binding assay; Materials therefor for cancer involving compounds serving as markers for tumor, cancer, neoplasia, e.g. cellular determinants, receptors, heat shock/stress proteins, A-protein, oligosaccharides, metabolites
    • G01N33/57488Immunoassay; Biospecific binding assay; Materials therefor for cancer involving compounds serving as markers for tumor, cancer, neoplasia, e.g. cellular determinants, receptors, heat shock/stress proteins, A-protein, oligosaccharides, metabolites involving compounds identifable in body fluids
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/12Specific details about materials
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/16Surface properties and coatings
    • B01L2300/161Control and use of surface tension forces, e.g. hydrophobic, hydrophilic
    • B01L2300/163Biocompatibility
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2400/00Moving or stopping fluids
    • B01L2400/04Moving fluids with specific forces or mechanical means
    • B01L2400/0403Moving fluids with specific forces or mechanical means specific forces
    • B01L2400/0415Moving fluids with specific forces or mechanical means specific forces electrical forces, e.g. electrokinetic
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2400/00Moving or stopping fluids
    • B01L2400/04Moving fluids with specific forces or mechanical means
    • B01L2400/0403Moving fluids with specific forces or mechanical means specific forces
    • B01L2400/0433Moving fluids with specific forces or mechanical means specific forces vibrational forces
    • B01L2400/0439Moving fluids with specific forces or mechanical means specific forces vibrational forces ultrasonic vibrations, vibrating piezo elements

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Immunology (AREA)
  • Analytical Chemistry (AREA)
  • Hematology (AREA)
  • Molecular Biology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Cell Biology (AREA)
  • Urology & Nephrology (AREA)
  • Clinical Laboratory Science (AREA)
  • Dispersion Chemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Biomedical Technology (AREA)
  • Biochemistry (AREA)
  • Oncology (AREA)
  • Biotechnology (AREA)
  • Hospice & Palliative Care (AREA)
  • Medicinal Chemistry (AREA)
  • Food Science & Technology (AREA)
  • Microbiology (AREA)
  • Electrochemistry (AREA)
  • Fluid Mechanics (AREA)
  • Investigating Or Analysing Biological Materials (AREA)

Abstract

The present invention relates to a kind of micro flow control chip device of ten Five-channels joint-detection Diagnostic Value of Several Serum Tumor Markers, belong to analysis testing field.PDMS is substrate of the dimethyl silicone polymer as being used for making the kind tumor markers joint-detection micro-fluidic chip of general type more than ten, is had a clear superiority, but there is also some problems for needing to overcome;This case is directed to the problem.This case main points are, the selected PDMS with ecosystem surface of substrate, and the elastic clip of miniature ultrasonic transducer units will be attached on its clamping limb with elastic force snap-in location in its neighbor positions of the test liquid stream terminal of the micro-fluidic chip, simultaneously, ultrasonic wave damper is installed at the sample introduction end of the micro-fluidic chip, reach ultrasonic intensity rapid decrement in short distance, so as to form interfacial tension difference at the two ends of the chip, test liquid stream is thereby facilitated to be flowed along originally hydrophobic capillary channel to terminal direction.The device is without using Micropump.

Description

The micro flow control chip device of ten Five-channel joint-detection Diagnostic Value of Several Serum Tumor Markers
Technical field
The present invention relates to a kind of micro flow control chip device of ten Five-channels joint-detection Diagnostic Value of Several Serum Tumor Markers, belong to analysis test neck Domain.
Background technology
Tumor markers (tumor marker, TM) refers in the generation and breeding of tumour, is produced in itself by tumour cell Raw either reacted by body tumour cell and produce, reflection tumour exist and growth a class material, including protein, Hormone, enzyme (isodynamic enzyme) and oncoprotein etc..The tumor markers in blood samples of patients or body fluid is chemically examined, can be in cancer screening Early detection tumour, and observe the curative effect of oncotherapy and judge patient's prognosis.The tumor markers clinically commonly used at present has: (1) alpha-fetoprotein (AFP) is the mark of the tumours such as primary carcinoma of liver, carcinoma of testis, oophoroma;(2) carcinomebryonic antigen (CEA) is digestion The mark of the tumours such as system tumor, lung cancer, breast cancer;(3) CA125 (CA125) is the mark of the tumours such as oophoroma; (4) CA153 (CA153) is the mark of the tumours such as breast cancer;(5) CA19-9 (CA19-9) is digestive system tumor Mark;(6) CA724 (CA724) is the mark of the tumours such as stomach cancer, oophoroma;(7) carbohydrate antigen 242 (CA242) For the mark of digestive system tumor;(8) CA50 (CA50) is the mark of the tumours such as digestive system tumor, breast cancer, lung cancer Thing;(9) CYFRA21-1 (Cy211) is the mark of the tumours such as non-small cell lung cancer;(10) neuronspecific enolase (NSE) For the mark of the tumours such as ED-SCLC, neuroendocrine tumor;(11) PSA (PSA) is prostate cancer Tumor markers;(12) human chorionic gonadotrophin (HCG) is that embryonic cell carcinoma, trophoblastic tumor (suede cancer, vesicular mole) etc. are swollen The mark of knurl;(13) thyroglobulin (TG) is the mark of thyroid cancer;(14) ferritin (SF) is digestive system tumor, liver The mark of the tumours such as cancer, breast cancer, lung cancer;(15) B2M (β 2-MG) is in chronic lymphocytic leukemia, lymph Raised in the patient body fluids such as knurl, myeloma, lung cancer, thyroid cancer, nasopharyngeal carcinoma;(16) squamous cell antigen (SCC) be cervical carcinoma, The tumor markerses such as lung squamous cancer, the cancer of the esophagus.The tumor markers overwhelming majority clinically detected at present is not only present in malignant tumour In, exist in benign tumour, embryonic tissue, even in normal structure.Therefore, tumor markers has dynamic chek and multinomial Joint inspection is more valuable.So for numerous tumor markerses, clinically how to selectDifferent tumours understands some phases To special tumor markers, such as CA153 often appears in breast cancer;CEA often appears in intestinal cancer, stomach cancer;CA19-9 is often appeared in Intestinal cancer, cancer of pancreas;CA125 often appears in oophoroma etc..Clinician can be according to the different mark of different tumor examinations. Same tumour or different types of tumour can have one or more of tumor markerses abnormal;Same tumor markers can be in difference Tumour in occur.To improve the additive diagnostic value of tumor markers and determining which kind of mark can be supervised as the follow-up after treatment Index is surveyed, tumor markers joint-detection, the complementary tumor markers group of several sensitivity of reasonable selection, specific performance can be carried out Into best of breed, joint-detection is carried out.In general the joint-detection of tumor markers can improve the accuracy to diagnosing tumor.
Only with regard to Diagnostic Value of Several Serum Tumor Markers its joint-detection background of related itself general picture or overview for, may refer to Lower Chinese invention patent application case:CN200410041175.3、CN200510026780.8、CN200610040051.2、 CN200910064647.X。
Only for the microfluidic chip technology overall general picture of itself, famous micro-fluidic expert Mr. Lin Ping Cheng may refer to soon Before the monograph " diagram Microfluid based Lab on a chip " that goes out, the monograph is published via Science Press, and the monograph is for micro-fluidic Past of technology, now, and, in terms of vision of the future etc., suffer from detail, be deep into long discussion of detail.
So, the focal issue that this case that to have a talk below is paid special attention to.
The basic framework of micro-fluidic chip, including it is etched with the substrate of small fluid course and the cover plate fit together therewith, Small fluid course on the substrate, assembling upper cover plate before, it is apparent on see to be exactly some micro-channels, wait until thereon After covering cover plate, just real closure forms the small fluid course, and the conduit inner surface of the micro-channel is together with surround this The part cover plate of micro-channel constitutes described small fluid course together;So, it is clear that this after assembling is completed is small Fluid course, the major part of its inner surface area is the inner surface area of that micro-channel, in other words, in the micro-channel The state or property on surface substantially determine the integrality or property of the small fluid course;Therefore say, this is built in base The inner surface state or inner surface property of micro-channel on piece are key factors;In principle, it is any to keep or protecting substantially The material of its solid forms is held, can be used to make substrate and cover plate, such as, the material that can act as substrate and cover plate can be with It is monocrystalline silicon piece, quartz plate, sheet glass, high polymer such as dimethyl silicone polymer, polymethyl methacrylate, makrolon etc. Deng;Certainly, the selection of substrate and the selection of cover plate be able to can also be differed with identical;From material consumption, manufacture difficulty and From the point of view of in terms of application popularization prospect etc., between these materials exist not small difference, the especially selection of that substrate, influence compared with Greatly.
In various substrate making materials, dimethyl silicone polymer, i.e. PDMS, comparatively very easily shaping, so Substrate on make that micro-channel is extremely simple, and the lower cost for material makes substrate with the polydimethyl siloxane material, Micro-channel is being suppressed or etched thereon, and is being engaged with the cover plate that the cheap material such as glass or polypropylene or other plastic sheets makes, It is a kind of more satisfactory selection seemingly;Certainly, patch material can also select to use cheap polydimethyl siloxane material: So, this substrate selection is the scheme of polydimethyl siloxane material, and material is extremely cheap, makes extremely simple, seems and should also be as It is extremely easy to popularize, promotes.
But, thing is really not so simple.
First, this polydimethyl siloxane material, that is, the material that the letter PDMS that abridges is referred to, itself are a kind of strong Hydrophobic material, micro-channel is built on this material, if without being operated for the modified of the micro-channel surface, then, After overall assembling is completed, that is, cover after cover plate, because the micro-channel its inner surface in structure occupies most liquid circulation The inner surface in road, then, its strong hydrophobic property of the PDMS micro-channels inner surface, is deciding factor, it can cause class Be similar to the aqueous solution the fine liquid stream of polar liquid by becoming very difficult, its flow resistance is big, or even general Micropump is all It is 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 Operation;So, this is pretty troublesome for the modified operation of PDMS micro-channel inner surfacesThat falls nor this problem, structure Perplex into serious technical, be another problem:PDMS polymer molecules tool inside its body phase of this PDMS material substrate There are PDMS polymer molecules inside the characteristic for diffusing to the surface, migrating automatically, this substrate body phase to diffuse to the surface, move automatically The characteristic of shifting, will cause the state after modification by its inner surface of that micro-channel of surface modifying and decorating can not maintain foot Enough long time, the holding time for micro-channel its inner surface state after that is surface-modified is substantially only sufficient to complete in laboratory The time of portion's test experiments needs;In other words, by surface modification or the PDMS micro-channel inner surfaces of surface modification, its The surface state that is formed can not be lasting after modification or after saying modification, but soon automatically tend to or say and become surface again and change Surface state before property, returns to the strong hydrophobic surface state of that script in the shorter time, then, just think, Such micro-fluidic chip can largely make, mass storage, be widely popularized, and answer is it is obvious that is, impossible. Micro-channel on this PDMS material, can not pump similar to the fine liquid stream of polar solvent of the aqueous solution if not doing surface modification Send and pass through, chip also cannot just be used;And if having done surface modification, the state after its modification can not be persistently kept again, also Being equally can not popularization and application.
So, how to accomplish that substrate can either be made using cheap PDMS material, and table in the micro-channel can be released Face decorating state can not persistently, chip can not largely make, largely lay in so that be widely popularized it is such a make this area it is numerous specially The puzzlement that industry personnel 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, above it is stated that, its surface is strongly hydrophobic, this strong hydrophobic Material surface and also 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 gradually deep, directly It is trapped in heavy within the body phase of PDMS substrates, in fact, this process is partly also due to inside PDMS material body phase Polymer molecule, which has, to be diffused to the surface, caused by travel motion;Such case, can also be explained from another angle, i.e. Continuously from inside PDMS body phases to its diffusion into the surface, migration those polymer molecules, its result moved, be by Gradually those are involved within the body phase of PDMS substrates by the large biological molecule of adsorption, briefly, these are inhaled Attached large biological molecule is exactly to be swallowed up by PDMS substrate body phases;So, this PDMS substrates body phase swallows up large biological molecule Phenomenon, the influence caused by it necessarily causes the severe deviations of all kinds of test data of experiment for being related to large biological molecule.
As described above, be the problem of PDMS substrates, its not only adsorption large biological molecule, and swallow up large biological molecule, So, as the large biological molecule of experiment test object, its disappearance will not stop because the absorption of surface saturation, but, no It is disconnected adsorbed, also constantly swallowed up.
On PDMS substrates in related experiment test process its body phase constantly swallow up test associated biomolecule macromolecular phenomenon, separately It is to say that one kind, which is explained, there are substantial amounts of Minute pores in PDMS body phases, and associated biomolecule macromolecular is by after adsorption, depression Into these Minute pores, and then swallowed up;However, inventor thinks, those can allow the air point of miniature scale Son squeezes into the Minute pores therebetween, and being not equal to them also can directly allow that the large biological molecule of relative large scale enters, and two Person's difference on yardstick is huge, must not make sweeping generalizations.Explanation is bypassed, in any case, the biology of object is analyzed as dependence test Macromolecular is adsorbed by PDMS substrate micro-channels inner surface, and then is constantly swallowed up by PDMS substrate body phases, and this is known objective The phenomenon of presence.
, can be from containment PDMS surfaces to life in order to prevent this PDMS substrate bodies relative to the effect of swallowing up of large biological molecule The absorption of thing macromolecular is addressed, 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 quilt PDMS substrate body phases are swallowed up;But, or that old problem, that is, the chemical modification on PDMS material surface changes Surface state after property can not persistently be kept, the polymer molecule inside the PDMS substrate body phases its diffuse to the surface automatically, The process of migration, 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 Its micro-channel inner surface of substrate 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, can reach again Growth stage contains absorption process of the PDMS substrate micro-channel inner surfaces to large biological molecule, and then prevents PDMS substrate body phases The effect of swallowing up to large biological molecule so that related chip manufactured goods are able to maintain that a prolonged enough, rational shelf-life, It is exactly a very intractable problem.The problem makes the numerous specialties in this area as another problem addressed above, equally Personnel are entangled with, perplexed for a long time, and the problem is equally the highly difficult problem that its obvious technology barrier can not despise.The hardly possible Also be present many year in topic, so far, also not yet properly settled.
The content of the invention
The technical problems to be solved by the invention are to provide a package solution, solve what is addressed above totally Two problems, also, by the solution, applied to building, a kind of new crowd's physical examination is blanket to be compared for ten kinds More typical primary tumor mark carries out examination simultaneously, while the micro flow control chip device of detection.
The present invention solves the technical problem by following scheme, and the device that the program is provided is a kind of ten Five-channels joint-detection The micro flow control chip device of Diagnostic Value of Several Serum Tumor Markers, program main points are that the structure of the device includes multichannel micro-fluidic chip, The structure of the micro-fluidic chip includes installing substrate and cover plate together bonded to each other, the substrate and cover plate be plate object or Contain the channel structure via mould pressing process or etching technics formation, the base in tablet, that face towards the cover plate of the substrate Piece also contains and is connected and pierces being formed via mould pressing process, etching technics or simple drilling technology for the substrate with the channel structure Window structure, substrate bonded to each other being installed together and the cover plate have been built into containing pipeline configuration and phase therewith jointly The micro-fluidic chip of liquid pool structure even, the locations of structures of the pipeline is located at the substrate and cover plate interface zone bonded to each other, Its side of the window is blocked by the cover plate and opposite side is opened, and the locations of structures of the window is exactly the locations of structures of the liquid pool, institute Stating liquid pool has two kinds, and two kinds of liquid pools are the sample introduction end liquid pool and terminal liquid pool positioned at different structure position respectively, and this is micro-fluidic The sample introduction end position of chip has one or more sample introduction end liquid pool, and the sample introduction end refers to that the micro-fluidic chip is real The injection end position of detected solution during the sample introduction of border, then has a terminal liquid pool in the terminal location of the micro-fluidic chip, described Terminal refers to the terminal location of liquid flowing in its chip when the actual sample introduction of the micro-fluidic chip is tested, the terminal and the sample introduction end It is located remotely from each other, one end of the pipeline and the sample introduction end liquid pool UNICOM positioned at sample introduction end, the other end of the pipeline are micro- with being located at this The terminal liquid pool UNICOM of the terminal of fluidic chip, and, sequentially or backward be respectively installed in the pipeline it is different Working electrode on position and to electrode and reference electrode, the order refers to that its locations of structures of the reference electrode is more leaned on The nearly terminal location, the backward refers to the reference electrode locations of structures closer to the sample introduction end position, the work Electrode is made up of conductive electrode and the gold size sensitive membrane for having embedded tumor markers antibody being attached on the conductive electrode, Parallel construction is presented in the construction of the pipeline, and the pipeline in parallel construction is made up of 15 lateral parallel connections, described to present Its appearance profile of the pipeline of parallel construction is similar to the profile of parallel circuit, and the quantity of the working electrode is 15, should The installation position of 15 working electrodes is located in 15 laterals respectively, and, 15 working electrode its tables Tumor markers antibody in the sensitive membrane structure of layer gold size is that can be specifically bound to tumor markers antigen 15 kinds swell respectively Tumor markers antibody materials, 15 kinds of antibody materials be respectively tumor markers antibody A FP, CEA, CA242, CA125, CA199, CA153, CA724, CA50, NSE, CYFRA21-1, FPSA, TPSA, β-hCG, SCCA and β 2-MG, The antigen is the antigen of broad sense, and the antibody is the antibody of broad sense, and its material of the working electrode is argent material, gold Column, sheet or thread is presented in material, carbon material or thermal decomposition conducting polymer material, its pattern of the working electrode, should Its material of substrate is dimethyl silicone polymer material, and its surface of the substrate is the surface of primary form, the surface of the primary form its It is intended to refer to not by any surface chemical modification or the surface of the primary form of the material of any surface chemical modification, should The structure of device also includes elastic clip, the neighbouring institute of two opposite clamping limb snap-in locations of the elastic clip in the micro-fluidic chip The position of terminal is stated, fixation is attached on a clamping limb at least in and is equiped with miniature ultrasonic transducer units, and, 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 are connected to Together;The elastic clip facilitates the function that the device is disassembled there is provided one;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, is installed using the sample introduction end and the terminal with the miniature ultrasonic transducer units Difference in the distance between position difference and its ultrasonic intensity experienced, its interface of sample introduction end described in induced synthesis Interfacial tension difference between difference between power and the terminal its interfacial tension, the micro-fluidic chip two ends can be in the miniflow Pressure gap is formed between the two ends for controlling chip, the pressure gap can drive sample solution to the end flow;This is miniature super Acoustic wave transducer its function also include with its ultrasonic wave launched check large biological molecule contained in sample its in the pipe Absorption on road inner surface, and then check swallow up work of its body phase of the substrate of the dimethyl silicone polymer material to the large biological molecule With;The substrate of the dimethyl silicone polymer material its function include with cover plate and working electrode and to electrode and reference electrode together 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, is absorbed strongly to ultrasonic wave, and thereby in the micro-fluidic chip terminal between the sample introduction end Limited short distance within realize the rapid decrement of ultrasonic intensity;And, ultrasonic wave damper, the ultrasonic wave damper its Profile is in block, tabular or bar-shaped;Its material of the ultrasonic wave damper is microcellular rubber, sponge rubber or microporous polyurethane elasticity Body;And, another elastic clip, another elastic clip is with its gripping strength by the sample introduction end of the micro-fluidic chip and the ultrasound Ripple damper is clipped together bonded to each otherly, the strong abatement to ultrasonic energy that the ultrasonic wave damper is brought with its material Effect, further supports to realize that ultrasonic wave is strong within micro-fluidic chip terminal to the limited short distance between the sample introduction end The rapid decrement of degree, and thereby further expand the difference between described its interfacial tension of sample introduction end and the terminal its interfacial tension It is different.
The tumor markers antibody is the antibody of broad sense, and the antibody of the broad sense refers to possessing antibody function or functionally similar Can occur to combine and formed immune complex or immune compound with the various involved tumor markerses of corresponding clinic in antibody The material of the analog of thing;The tumor markers antigen is the antigen of broad sense, and the antigen of the broad sense is referred to can be using accordingly Antibody or be functionally similar to antibody material carry out enzyme mark detection it is various it is clinical involved the need for differentiate, the tumor-marker of detection Thing.
Described miniature ultrasonic transducer units can certainly be all installed on two clamping limbs;But, only installing one is miniature Ultrasonic transducer is dealt with and used enough.
The word of elastic clip one art-recognized meanings of itself are known.
The gold size sensitive membrane is to be sufficiently mixed chitosan gold size solution and tumor markers antibody-solutions uniformly, uses point sample instrument Point sample is coated on specified structure position, and forms its drying and forming-film.Tumor markers antibody in the gold size sensitive membrane is equal The tumor markers antibody marked for horseradish peroxidase or glucose oxidase, the gold size sensitive membrane has been included as fixing Above-mentioned each tumor markers antibody and introduce complementary medium therein, the complementary medium for example chitosan, cellulose acetate, Gelatin is therein a kind of or their mixture.
The pipeline in the microfluidic chip structure includes the lateral, and its internal diameter size may each be arbitrarily selected Size, still, for less with the consideration in terms of prepare liquid sample and reduction reagent loss, the pipeline includes described as far as possible The passage of the preferred capillary level of lateral, the passage of the capillary level implies that the interior of its internal diameter and the capillary on ordinary meaning The suitable passage in footpath.The shape of cross section of its inner passage of capillary can be arbitrary shape, the shape of cross section example Such as circular, oval, square, rectangle, bar shaped, naturally it is also possible to be arbitrarily the presence of the linear of bending, also, the hair The interior shape of tubule is with the extension of pipeline, and the shape of cross section of different parts can also allow to be different shapes.Only with regard to hair For the word of tubule one, its art-recognized meanings is known.
What is be related in structure is the electrode of microsize to electrode and reference electrode, and its electrode shape may each be any choosing Fixed shape, the arbitrarily selected shape such as column, sheet, strip or thread etc..It is described to electrode and the ginseng Art-recognized meanings than the 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 scrotiform structure for transitional liquid storage Make, its shape of the inner chamber of each liquid pool may each be arbitrarily selected shape, the cavity shape such as cylindrical empty Cavity-like, square column type cavity-like, oblong cavity shape or spherical hollow space shape etc..
It is public only for professional of the word of ultrasonic transducer one art-recognized meanings of itself for ultrasonic technology field Know.
Various sizes, variously-shaped ultrasonic transducer are commercially available;Commercially available miniature ultrasonic transducer units its sizes can be with It is small 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 itself and Speech, is known general technology for the professional in ultrasonic technology field.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 technology;Together Sample, the technology of hole-opening is even more known simple technique on naked PDMS substrates.This case is not also to this expansion superfluous words.
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;Its is another for the higher-order of oscillation electric signal transmission cable One 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, for the professional in ultrasonic technology field, be It is simple and known;The higher-order of oscillation electric signal generator can be customized to ultrasonic instrument specialized factory.
The preferred scope of its specified ultrasonic wave transmission power of the miniature ultrasonic transducer units be between 5 milliwatts and 5000 milliwatts it 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.
This case device can further include some annexes, the annex such as multiple tracks electrochemical workstation etc., institute certainly The art-recognized meanings for stating multiple tracks electrochemical workstation are known.Each working electrode for being related in this case microfluidic chip structure and , can be respectively via corresponding special the corresponding interface got lines crossed with the multiple tracks electrochemical workstation to electrode and reference electrode etc. Coupled.It is described that special to get lines crossed be for each the corresponding interface of each electrode and the multiple tracks electrochemical workstation is carried out into phase The private cable being mutually coupled with.The micro-fluidic chip in this case device, its structure can also include micro-valve, the number of the micro-valve Amount is not limited, according to actual needs, and the micro-valve can be installed in any required position installed in the microfluidic chip structure; The word of micro-valve one is for the professional of micro fluidic chip technical field, and the art-recognized meanings of itself are known;The micro-valve The manufacturing technology of itself 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, it is however recommended to Or say preferred its scope of the diameter between 0.1 micron to 2000 microns;The length of the working electrode can permit Permitted to be that any setting is easily installed the length used, it is however recommended to or to say preferred its scope of the length be at 1 micron To between 15000 microns.
The gold size for being installed in the working electrode surface layer by spraying or point sample instrument point sample or the coating of other appropriate process is quick Feel film, its thicknesses of layers can allow be any setting treat sample measuring liquid occur electrical signals response thickness, still, push away Preferred thickness is between 10 nanometers and 200 nanometers in other words for the thickness recommended.
The cover plate in chip structure, its material can allow to be any electrical insulating property material, for example:Polypropylene, glass Glass, polymethyl methacrylate, dimethyl silicone polymer, etc., in order to make smaller size of micro-fluidic chip, such as do Realized into the micro-fluidic chip of only 2.0 centimetres to 3.0 centimetres of super-small of length, and 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 It is used as the cover plate using dimethyl silicone polymer, is also that this case technical scheme is allowed.
The preferred scope of the distance between the terminal and the sample introduction end is between 3 centimetres and 10 centimetres.
Described its thickness of cover plate and substrate can allow be any setting be easy to assembling thickness, the thickness of recommendation or say preferably Thickness be between 1.0 millimeters and 5.0 millimeters.Less thickness is conducive to saving material.
Described its size of ultrasonic wave damper is not limited, and described its length of ultrasonic wave damper, width, thickness may each be basis Need the arbitrary size of setting.
It is known in field of rubber technology only for the word of microcellular rubber one art-recognized meanings of itself.
The microcellular rubber is commercially available.
It is known in field of rubber technology only for the word of sponge rubber one art-recognized meanings of itself.
The sponge rubber is commercially available.
It is known in technical field of macromolecules only for the word of microporous polyurethane elastomer one art-recognized meanings of itself.
The polyurethane micropore elastomer material is commercially available.
The microcellular rubber preferred microporous silicon rubber or micropore fluorubber.
It is known in field of rubber technology only for the word of micropore silicon rubber one art-recognized meanings of itself.
The microporous silicon Rubber market is on sale.
It is known in field of rubber technology only for the word of micropore fluorubber one art-recognized meanings of itself.
The micropore fluorubber is commercially available.
Another described elastic clip, naturally also elastic clip;The word of elastic clip one art-recognized meanings of itself are known.
Various elastic clip market is all on sale.
The application method of this case micro-fluidic chip:
Proposed first based on this case and the first public New stream driving principle, its application running of this case micro-fluidic chip In, the New stream driving method is determined completely without involving any additional Micropump.
The interfacial tension difference of this case to be formed between micro-fluidic chip two ends caused by the ultrasonic wave, drives liquid Stream flows in the capillary channel of the ten Five-channels micro-fluidic chip, using multi-channel electrochemical analyzer device respectively to 15 kinds Tumor markers carries out joint-detection.
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 tumor markers antigen molecules are each In passage on electrode surface gold size sensitive membrane embed corresponding horseradish peroxidase-labeled tumor markers specific antibody Capture.
2nd, the tumor markers antigen in the tumor markers specific antibody and blood serum sample of horseradish peroxidase-labeled is formed Immune complex.
3rd, using multi-channel electrochemical analyzer, the electron mediators such as catechol are added, using the above-mentioned reaction of amperometric detection Caused curent change, is derived from the species and content of various analytes.
4th, result is subjected to comprehensive analysis, comprehensive diagnos is carried out to tumor markers antigen.
It is an advantage of the invention that in elastic clip described in the terminal of the micro-fluidic chip its close position snap-in location, with The miniature ultrasonic transducer units installed, the low-power launched using it, high-frequency band are attached on the clamping limb of the elastic clip Ultrasonic wave so that without its pipe of strong hydrophobic micro-fluidic chip internal pipeline of surface chemical modification or surface chemical modification Compatibility between wall and the test object aqueous solution is significantly increased, and this is test liquid stream by there is provided a realistic possibility; Meanwhile, using its strong absorbability to ultrasonic wave of dimethyl silicone polymer substrate, in shorter distance, it is, In from the terminal to the very short distance of only several centimeters yardsticks the sample introduction end, reach the fast express delivery of ultrasonic intensity Subtract, the difference of the interfacial tension is thereby caused at the two ends of the micro-fluidic chip, and then, utilize the boundary between the two ends Pressure gap between its two ends for being formed of the difference of face tension force, driving test liquid stream is strong hydrophobic in such a script Flowed in capillary channel to the terminal direction.By this case liquid stream drive scheme, entirely without must be to the dimethyl silicone polymer The substrate and its internal pipeline of material carry out any surface chemical modification or chemical modification, have altogether dispensed with the surface chemical modification Or the laborious procedures of chemical modification;And altogether dispense with the equipment of traditional Micropump etc;On the other hand, the low work( The ultrasonic wave of rate, high-frequency band, additionally it is possible to contain the large biological molecule in sample in the literalness naked dimethyl silicone polymer Absorption on its inner surface of pipeline of substrate, and then contain that its body phase of the dimethyl silicone polymer substrate is gulped down to the large biological molecule Do not act on;The Reversible binding thing of the antigen, antibody and antigen and antibody is all the class for belonging to described large biological molecule certainly Type;Because described suction-operated and the described effect of swallowing up effectively are contained that therefore, dependence test result more will can It is enough objectively to reflect actual conditions;The effect of the low-power, high-frequency band ultrasonic wave, certainly also include facilitate antigen, antibody it Between Reversible binding reaction quick reaching, this causes dependence test operation can be to be completed than faster speed.
Due to the surface chemical modification for the dimethyl silicone polymer substrate its relevant surfaces or chemical modification behaviour need not be carried out Make, therefore, this surface chemical modification layer or chemically modified layer not need to exist, then, the dimethyl silicone polymer Its body phase interior polymer molecule of substrate constantly diffuses to the surface automatically, migrate caused by it to surface chemical modification layer or The damaging influence of chemically modified layer is also just not present.
This case its installation position is located at the ultrasonic wave damper at the sample introduction end, from its terminal of this case micro-fluidic chip to Said on the sport technique segment that ultrasonic intensity rapid decrement is realized in the such short distance in sample introduction end, its effect of the ultrasonic wave damper is suitable In the size expansion device of micro-fluidic chip, in other words, the ultrasonic wave damper its function as and significantly extend miniflow Its terminal of chip is controlled the distance between to sample introduction end, is the equal of from several centimetres of extension of script to more than ten centimetres of length Or twenties centimetres of length or longer length, so so that described terminal to the ultrasonic wave between sample introduction end in short distance The sport technique segment of intensity rapid decrement can relatively easily be reached, also, the size expansion device namely the ultrasonic wave damper Demolition, installation are convenient, it is important that it can also be reused.
The technical scheme of this case has dissolved its application related one to dimethyl silicone polymer substrate addressed above totally Row technical barrier.Based on this case scheme, this kind very cheap polydimethyl siloxane material is just possible in the micro-fluidic chip Prepare, production, using etc. field play bigger effect.
The miniature ultrasonic transducer units have been installed in fixation on the elastic clip its clamping limb in this case structure, this architecture provides One facilitates the function that the device is disassembled, in this way, the elastic clip just can facilitate together with miniature ultrasonic transducer units appended thereon Ground is mutually disengaged with the micro-fluidic chip, then, the component that the part can freely depart from is reused in which just can circulate benignly to be permitted Repeatedly;The architectural feature is conducive to saving the use cost of the device.
The framework of its large-scale integrated of this case micro-fluidic chip, determines it among actual test application, to Serum samples The need for measure smaller, this helps to reduce the body and mind damage of related subject.
Brief description of the drawings
Fig. 1 is its rough outside side view of this case device.
In figure, 1 is elastic clip, and 2,7 be two clamping limbs of elastic clip respectively, and 3 be the terminal of the micro-fluidic chip, 4 be the sample introduction end of the micro-fluidic chip, and 5 be the substrate of dimethyl silicone polymer material, and 6 be cover plate, and 8 be miniature super Acoustic wave transducer, 9 be higher-order of oscillation electric signal transmission cable, and 10 be tension spring;The spring clamp structure in legend only shows The legend structure of meaning, actual spring clamp structure is not limited to the legend spring clamp structure;It is micro-fluidic that arrow in legend indicates this Chip its in actual motion, by pressure at two ends difference drive, the flow direction of its test liquid stream.
It is depicted without in the ultrasonic wave damper, legend being also depicted without another elastic clip in legend.
Embodiment
In this case that Fig. 1 is shown embodiment, its main points of the example are that the structure of the device includes multichannel micro-fluidic core Piece, the structure of the micro-fluidic chip includes the substrate 5 and cover plate 6 of installing bonded to each other together, the substrate 5 and cover plate 6 It is plate object or tablet, that face towards the cover plate 6 of the substrate 5 is contained to be formed via mould pressing process or etching technics Channel structure, the substrate 5 also containing be connected with the channel structure and pierce the substrate 5 via mould pressing process, etch work Skill or the window structure of simple drilling technology formation, substrate 5 bonded to each other being installed together are built into jointly with the cover plate 6 Micro-fluidic chip containing pipeline configuration and the liquid pool structure being attached thereto, the locations of structures of the pipeline be located at the substrate 5 with The cover plate 6 interface zone bonded to each other, its side of the window is blocked by the cover plate 6 and opposite side is opened, the structure of the window Position is exactly the locations of structures of the liquid pool, and the liquid pool has two kinds, and two kinds of liquid pools are entering positioned at different structure position respectively There is the one or more sample introduction end liquid sample end liquid pool and terminal liquid pool, the position of sample introduction end 4 of the micro-fluidic chip Pond, the sample introduction end 4 refers to the injection end position of detected solution during the micro-fluidic chip actual sample introduction, in the micro-fluidic chip The position of terminal 3 then have a terminal liquid pool, the terminal 3 refers to its core during the actual sample introduction test of the micro-fluidic chip The terminal location that liquid flows in piece, the terminal 3 is located remotely from each other with the sample introduction end 4, and one end of the pipeline is with being located at sample introduction end 4 The sample introduction end liquid pool UNICOM, the other end of the pipeline with positioned at the micro-fluidic chip the terminal 3 the terminal liquid pool UNICOM, and, sequentially or backward be respectively installed in working electrode in the pipeline on diverse location and to electrode and ginseng Than electrode, the order refers to its locations of structures of the reference electrode closer to the position of terminal 3, and the backward is referred to The reference electrode locations of structures is closer to the position of sample introduction end 4, and the working electrode is by conductive electrode and is attached to this The gold size sensitive membrane for having embedded tumor markers antibody on conductive electrode is constituted, and parallel construction, institute is presented in the construction of the pipeline State and be made up of in the pipeline of parallel construction 15 lateral parallel connections, its appearance profile of the pipeline of the presentation parallel construction It is similar to the profile of parallel circuit, the quantity of the working electrode is 15, the installation position difference of 15 working electrodes In 15 laterals, and, the tumor-marker in the sensitive membrane structure of its top layer gold size of 15 working electrodes Thing antibody is the 15 kinds of tumor markers antibody materials that can be specifically bound to tumor markers antigen, 15 kinds of antibody respectively Material be respectively tumor markers antibody A FP, CEA, CA242, CA125, CA199, CA153, CA724, CA50, NSE, CYFRA21-1, FPSA, TPSA, β-hCG, SCCA and β 2-MG, the antigen is the antigen of broad sense, and the antibody is The antibody of broad sense, its material of the working electrode is argent material, gold material, carbon material or thermal decomposition conducting polymer Column, sheet or thread is presented in material, the working electrode its pattern, and its material of the substrate 5 is dimethyl silicone polymer material, Its surface of substrate 5 is the surface of primary form, the surface of the primary form its be intended to refer to not pass through any surface chemistry The surface of the primary form of the material of modification or any surface chemical modification, the structure of the device also includes elastic clip 1, the bullet Two opposite clamping limbs 2 of power folder 1,7 snap-in locations are in the position of the neighbouring terminal 3 of the micro-fluidic chip, at least Clamping limb described in one of which for example attaches fixation on clamping limb 7 and is equiped with miniature ultrasonic transducer units 8, and, high frequency Electric signal transmission cable 9 is vibrated, one end of the higher-order of oscillation electric signal transmission cable 9 is connected with the miniature ultrasonic transducer units 8 Together;The elastic clip 1 facilitates the function that the device is disassembled there is provided one;Its major function of the miniature ultrasonic transducer units 8 It is that in the test of micro-fluidic chip actual sample introduction, the ultrasonic wave launched using it reduces the inwall of sample solution and the pipeline Between interfacial tension, can be compatible, also, utilize the sample introduction end 4 and the terminal 3 and the miniature ultrasonic Difference in the distance between the installation position of transducer 8 difference and its ultrasonic intensity experienced, enters described in induced synthesis Between difference between its interfacial tension of sample end 4 and the terminal 3 its interfacial tension, the micro-fluidic chip two ends 3,4 Interfacial tension difference can form pressure gap between the two ends 3,4 of the micro-fluidic chip, and the pressure gap can drive sample Solution flows to the terminal 3;Its function of the miniature ultrasonic transducer units 8 also includes checking sample with its ultrasonic wave launched In contained large biological molecule its absorption on the inner surface of pipeline, and then check the base of the dimethyl silicone polymer material Swallow up effect of its body phase of piece 5 to the large biological molecule;Its function of the substrate 5 of the dimethyl silicone polymer material includes and lid Piece 6 and working electrode and the micro-fluidic chip is together built to electrode and reference electrode, soft poly dimethyl silicon for simultaneously having elasticity The substrate 5 of oxygen alkane material its function also includes, with its property to the strong absorption of ultrasonic wave, ultrasonic wave being absorbed strongly, and Thereby the quick of ultrasonic intensity is realized within micro-fluidic chip terminal 3 to the limited short distance between the sample introduction end 4 Successively decrease;And, ultrasonic wave damper, its profile of ultrasonic wave damper is in block, tabular or bar-shaped;The ultrasonic wave damper Its material is microcellular rubber, sponge rubber or microporous polyurethane elastomer;And, another elastic clip, another elastic clip With its gripping strength by the sample introduction end 4 of the micro-fluidic chip and the ultrasonic wave damper it is bonded to each other clip together, the ultrasonic wave The strong consumption to ultrasonic energy that damper is brought with its material, is further supported in the micro-fluidic chip terminal 3 to the rapid decrement that ultrasonic intensity is realized within the limited short distance between the sample introduction end 4, and thereby further expands institute State the difference between its interfacial tension of sample introduction end 4 and the terminal 3 its interfacial tension.
It is depicted without in the ultrasonic wave damper, legend being also depicted without another elastic clip in legend.
Arrow in legend indicate the micro-fluidic chip its in actual motion, by pressure at two ends difference drive, its test liquid The flow direction of stream.
The associate members such as the higher-order of oscillation electric signal generator and multiple tracks electrochemical workstation are depicted without in Fig. 1.
Itself is commercially available for involved elastic clip.It is available for commercially available alternative spring clamp structure and make that this case structure is used Type and size etc., quality are various, and specific elastic clip pattern can be selected as needed.
Involved miniature ultrasonic transducer units 8 are commercially available;It can also be customized to ultrasonic transducer producer.
Involved higher-order of oscillation electric signal transmission cable 9 is commercially available;Can also be to ultrasonic transducer producer or cable special manufacturer Family's customization.
Involved higher-order of oscillation electric signal generator market has the product close to needs commercially available;It can also be customized to relevant manufacturers.
Each working electrode in this example structure and electrode and reference electrode via each special cable or can be said respectively Get lines crossed respectively with the corresponding cable interface of the multiple tracks electrochemical workstation as annex or saying interface connection of getting lines crossed.
The multiple tracks electrochemical workstation is commercially available;The multiple tracks electrochemical workstation can also be according to specific needs to related special Industry producer customizes.
In view of this case pipeline of the presentation parallel construction its form that related text expresses that it is described above is clear enough It is clear, the concrete form of the pipeline in this kind of micro-fluidic chip of this case is no longer specifically illustrating in this case embodiment.
Antibody described in this case refers to the antibody of broad sense;Antigen described in this case refers to the antigen of broad sense;It is immunized described in this case multiple Compound refers to the immune complex of broad sense.

Claims (10)

1. the micro flow control chip device of ten Five-channel joint-detection Diagnostic Value of Several Serum Tumor Markers, it is characterised in that the structure bag of the device Multichannel micro-fluidic chip is included, the structure of the micro-fluidic chip includes the substrate and cover plate of installing bonded to each other together, the base Piece and cover plate are plate object or tablet, and that face towards the cover plate of the substrate is contained via mould pressing process or etching technics The channel structure of formation, the substrate also containing be connected with the channel structure and pierce the substrate via mould pressing process, etch work Skill or the window structure of simple drilling technology formation, substrate bonded to each other being installed together has been built into jointly with the cover plate to be contained The micro-fluidic chip of liquid pool structure for having pipeline configuration and being attached thereto, the locations of structures of the pipeline is located at the substrate and the cover plate Interface zone bonded to each other, its side of the window is blocked by the cover plate and opposite side is opened, and the locations of structures of the window is exactly institute State the locations of structures of liquid pool, the liquid pool has two kinds, two kinds of liquid pools respectively be positioned at different structure position sample introduction end liquid pool with And terminal liquid pool, the sample introduction end position of the micro-fluidic chip has one or more sample introduction end liquid pool, the sample introduction end The injection end position of detected solution during the micro-fluidic chip actual sample introduction is referred to, then has one in the terminal location of the micro-fluidic chip The individual terminal liquid pool, the terminal refers to the terminal position of liquid flowing in its chip when the actual sample introduction of the micro-fluidic chip is tested Put, the terminal is located remotely from each other with the sample introduction end, one end of the pipeline and the sample introduction end liquid pool UNICOM positioned at sample introduction end, the pipe The other end in road with positioned at the micro-fluidic chip the terminal the terminal liquid pool UNICOM, and, sequentially or backward point The working electrode that is not installed in the pipeline on diverse location and to electrode and reference electrode, the order refers to the ginseng Than its locations of structures of electrode closer to the terminal location, the backward refers to the reference electrode locations of structures closer to described Sample introduction end position, the working electrode is resisted by conductive electrode and the tumor markers that embedded being attached on the conductive electrode The gold size sensitive membrane of body is constituted, and parallel construction is presented in the construction of the pipeline, and the pipeline in parallel construction is by 15 branched pipes Road parallel connection is constituted, and its appearance profile of the pipeline of the presentation parallel construction is similar to the profile of parallel circuit, the work electricity The quantity of pole is 15, and the installation position of 15 working electrodes is located in 15 laterals respectively, and, Tumor markers antibody in the sensitive membrane structure of its top layer gold size of 15 working electrodes is to tumor markers antigen energy respectively Specific binding 15 kinds of tumor markers antibody materials, 15 kinds of antibody materials be respectively tumor markers antibody A FP, CEA、CA242、CA125、CA199、CA153、CA724、CA50、NSE、CYFRA21-1、FPSA、TPSA、β-hCG、 SCCA and β 2-MG, the antigen is the antigen of broad sense, and the antibody is the antibody of broad sense, its material of the working electrode It is argent material, gold material, carbon material or thermal decomposition conducting polymer material, post is presented in its pattern of the working electrode Shape, sheet or thread, its material of the substrate are dimethyl silicone polymer materials, and its surface of the substrate is the surface of primary form, The surface of the primary form its be intended to refer to the material not no by any surface chemical modification or any surface chemical modification Primary form surface, the structure of the device also includes elastic clip, and two opposite clamping limb snap-in locations of the elastic clip exist Attaching fixation is equiped with miniature on the position of the neighbouring terminal of the micro-fluidic chip, a clamping limb at least in Ultrasonic transducer, and, higher-order of oscillation electric signal transmission cable, one end of the higher-order of oscillation electric signal transmission cable is micro- with this Type ultrasonic transducer links together;The elastic clip facilitates the function that the device is disassembled there is provided one;The miniature ultrasonic is changed Can device its major function be in the actual sample introduction test of micro-fluidic chip, the ultrasonic wave launched using it reduce sample solution and Interfacial tension between the inwall of the pipeline, can be compatible, also, using the sample introduction end and the terminal with being somebody's turn to do Difference in the distance between miniature ultrasonic transducer units installation position difference and its ultrasonic intensity experienced, induces shape Boundary between difference between described its interfacial tension of sample introduction end and the terminal its interfacial tension, the micro-fluidic chip two ends Face tension difference can form pressure gap between the two ends of the micro-fluidic chip, and the pressure gap can drive sample solution to institute State end flow;Its function of the miniature ultrasonic transducer units also includes checking life contained in sample with its ultrasonic wave launched Its absorption on the inner surface of pipeline of thing macromolecular, and then check the substrate of the dimethyl silicone polymer material its body phase to this The effect of swallowing up of large biological molecule;The substrate of the dimethyl silicone polymer material its function includes and cover plate and working electrode and right Electrode and reference electrode together build the micro-fluidic chip, soft and have the substrate of the dimethyl silicone polymer material of elasticity its work( Can also include, with its property to the strong absorption of ultrasonic wave, ultrasonic wave being absorbed strongly, and thereby the micro-fluidic chip this Terminal is to the rapid decrement that ultrasonic intensity is realized within the limited short distance between the sample introduction end;And, ultrasonic wave damper, Its profile of ultrasonic wave damper is in block, tabular or bar-shaped;Its material of the ultrasonic wave damper is microcellular rubber, sponge rubber Or microporous polyurethane elastomer;And, another elastic clip, another elastic clip is with its gripping strength by the micro-fluidic chip Sample introduction end and the ultrasonic wave damper clip together bonded to each otherly, the ultrasonic wave damper with its material brought to ultrasound The strong consumption of wave energy, is further supported in micro-fluidic chip terminal to the limited short distance between the sample introduction end Within realize the rapid decrement of ultrasonic intensity, and thereby further expand described its interfacial tension of sample introduction end and its boundary of the terminal Difference between the tension force of face.
2. the micro flow control chip device of ten Five-channels joint-detection Diagnostic Value of Several Serum Tumor Markers according to claim 1, its feature It is, it is capillary channel that the pipeline, which includes the lateral,.
3. the micro flow control chip device of ten Five-channels joint-detection Diagnostic Value of Several Serum Tumor Markers according to claim 1, its feature Be, the thermal decomposition conducting polymer be by polyimides or polyacrylonitrile be heat-treated through anoxybiotic after the conductive material that is formed.
4. the micro flow control chip device of ten Five-channels joint-detection Diagnostic Value of Several Serum Tumor Markers according to claim 1, its feature Be, 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 micro flow control chip device of ten Five-channels joint-detection Diagnostic Value of Several Serum Tumor Markers according to claim 1, its feature It is, the thickness of the gold size sensitive membrane is between 10 nanometers and 200 nanometers.
6. the micro flow control chip device of ten Five-channels joint-detection Diagnostic Value of Several Serum Tumor Markers according to claim 1, its feature It is, its material of the cover plate in structure is dimethyl silicone polymer material.
7. the micro flow control chip device of ten Five-channels joint-detection Diagnostic Value of Several Serum Tumor Markers according to claim 1, its feature It is, the distance between the terminal and the sample introduction end are between 3 centimetres and 10 centimetres, its thickness of the cover plate and substrate Degree is between 1.0 millimeters and 5.0 millimeters.
8. the micro flow control chip device of ten Five-channels joint-detection Diagnostic Value of Several Serum Tumor Markers according to claim 1, its feature It is, the microcellular rubber is micropore silicon rubber or micropore fluorubber.
9. the micro flow control chip device of ten Five-channels joint-detection Diagnostic Value of Several Serum Tumor Markers according to claim 1, its feature Be, the structure of the micro fluidic device also includes higher-order of oscillation electric signal generator, the higher-order of oscillation electric signal transmission cable its The other end is connected with the higher-order of oscillation electric signal generator.
10. the micro flow control chip device of ten Five-channels joint-detection Diagnostic Value of Several Serum Tumor Markers according to claim 1, its feature It is, its specified ultrasonic wave transmission power of the miniature ultrasonic transducer units is between 5 milliwatts and 5000 milliwatts, and this is miniature super The frequency of its ultrasonic wave operationally launched of acoustic wave transducer is between 100KHz and 12MHz.
CN201610205552.5A 2016-03-22 2016-03-22 The micro flow control chip device of ten Five-channel joint-detection Diagnostic Value of Several Serum Tumor Markers Withdrawn CN107213926A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610205552.5A CN107213926A (en) 2016-03-22 2016-03-22 The micro flow control chip device of ten Five-channel joint-detection Diagnostic Value of Several Serum Tumor Markers

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610205552.5A CN107213926A (en) 2016-03-22 2016-03-22 The micro flow control chip device of ten Five-channel joint-detection Diagnostic Value of Several Serum Tumor Markers

Publications (1)

Publication Number Publication Date
CN107213926A true CN107213926A (en) 2017-09-29

Family

ID=59927447

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610205552.5A Withdrawn CN107213926A (en) 2016-03-22 2016-03-22 The micro flow control chip device of ten Five-channel joint-detection Diagnostic Value of Several Serum Tumor Markers

Country Status (1)

Country Link
CN (1) CN107213926A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107238705A (en) * 2016-03-29 2017-10-10 李榕生 Tumor markers is generally investigated with ten Five-channel micro flow control chip devices

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101587123A (en) * 2009-06-19 2009-11-25 宁波大学 Special micro-fluidic chip for cholera diagnosis with one-dimensional self-assembly magnetic bead chain electrodes
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
CN107199058A (en) * 2016-03-18 2017-09-26 葛宇杰 The general type Diagnostic Value of Several Serum Tumor Markers joint inspection chip apparatus conveniently disassembled

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101587123A (en) * 2009-06-19 2009-11-25 宁波大学 Special micro-fluidic chip for cholera diagnosis with one-dimensional self-assembly magnetic bead chain electrodes
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
CN107199058A (en) * 2016-03-18 2017-09-26 葛宇杰 The general type Diagnostic Value of Several Serum Tumor Markers joint inspection chip apparatus conveniently disassembled

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
JAMES FRIEND: "Microscale acoustofluidics: microfluidics driven via acoustics and ultrasonics", 《REVIEWS OF MODERN PHYSICS》 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107238705A (en) * 2016-03-29 2017-10-10 李榕生 Tumor markers is generally investigated with ten Five-channel micro flow control chip devices

Similar Documents

Publication Publication Date Title
CN107199057A (en) Dismounting brief classifiable tumor mark joint inspection chip apparatus convenient to both
CN107199059A (en) For the classifiable tumor mark joint inspection chip apparatus of women physical examination examination
CN107199056A (en) Easily-disassembled male's classifiable tumor markers in detecting chip apparatus
CN107213926A (en) The micro flow control chip device of ten Five-channel joint-detection Diagnostic Value of Several Serum Tumor Markers
CN107213925A (en) Joint-detection male's classifiable tumor mark micro flow control chip device
CN107199058A (en) The general type Diagnostic Value of Several Serum Tumor Markers joint inspection chip apparatus conveniently disassembled
CN107225005A (en) Six kinds of classifiable tumor mark multichannels are while detection micro flow control chip device
CN107225003A (en) The classifiable tumor markers in detecting micro flow control chip device that male is applicable
CN107225002A (en) The classifiable tumor markers in detecting micro flow control chip device that women is applicable
CN107694632A (en) Easily-disassembled male's classifiable tumor markers in detecting chip apparatus
CN106568952A (en) Micro-fluidic chip device for simultaneously detecting women's various typical tumor markers
CN107282151A (en) Ten Five-channel micro flow control chip devices of common tumor markers examination
CN107694635A (en) Six kinds of classifiable tumor mark multichannels while detection micro flow control chip device
CN107694647A (en) Dismount brief classifiable tumor mark joint inspection chip apparatus convenient to both
CN107213924A (en) The micro flow control chip device of a variety of classifiable tumor marks of women is detected simultaneously
CN107213923A (en) Typical six kinds of tumor markers joint-detection micro flow control chip devices
CN107225004A (en) General type is used for the micro flow control chip device for detecting Diagnostic Value of Several Serum Tumor Markers simultaneously
CN107233938A (en) The tumor markers joint-detection six-channel microfluidic chip device simplified
CN107238705A (en) Tumor markers is generally investigated with ten Five-channel micro flow control chip devices
CN106568953A (en) Microfluidic chip device for detecting multiple tumor markers based on 15-channel joint detection
CN106563513A (en) Microfluidic chip device for combined detection of six typical tumor markers
CN107233940A (en) A variety of everywoman's co-detections of tumor markers in benign micro flow control chip devices
CN107233939A (en) Physical examination examination male's classifiable tumor mark micro flow control chip device
CN106563514A (en) Microfluidic chip apparatus for combined detection of male typical tumor markers
CN106706913A (en) Pervasive micro-fluidic chip device for simultaneously detecting multiple tumour markers

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
WW01 Invention patent application withdrawn after publication
WW01 Invention patent application withdrawn after publication

Application publication date: 20170929