CN202951486U - Micro-fluidic chip integrating functions of micro-cavity dynamic polymerase chain reactions (PCRs) and capillary electrophoresis (CE) - Google Patents
Micro-fluidic chip integrating functions of micro-cavity dynamic polymerase chain reactions (PCRs) and capillary electrophoresis (CE) Download PDFInfo
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Abstract
The utility mode relates to a micro-fluidic chip integrating functions of micro-cavity dynamic polymerase chain reactions (PCRs) and capillary electrophoresis (CE). The micro-fluidic chip is in a four-layer structure, a third layer is provided with a denaturation micro-cavity, an annealing micro-cavity, an extending micro-cavity, a formamide sample adding cell, a mixer, a sample cell, a buffer solution cell, a sample waste liquid cell, a waste liquid cell, a channel between the denaturation micro-cavity and the annealing micro-cavity, a channel between the annealing micro-cavity and the extending micro-cavity, a channel between the extending micro-cavity, the formamide sample adding cell and the mixer, a channel between the mixer and the sample cell and a cross channel. A first layer is provided with a heating electrode, a temperature sensing electrode, electrode points and high voltage electrodes, wherein the heating electrode and the temperature sensing electrode are opposite to the positions of the denaturation micro-cavity, the annealing micro-cavity and the extending micro-cavity, the electrode points are opposite to the positions of the sample cell, the buffer solution cell, the sample waste liquid cell and the waste liquid cell, and the high voltage electrodes are connected with the electrode points. A second layer is a bonding layer, the third layer is bonded on the first layer, a sample placing hole is arranged on the first layer, and a pneumatic micro-pump is arranged on a fourth layer. The micro-fluidic chip integrating functions of micro-cavity dynamic PCRs and the CE has the function of real-time and end point detection of one or a plurality of PCR sections.
Description
Technical field
The utility model relates to the dynamic PCR of a kind of micro chamber and Capillary Electrophoresis CE function integrated microfluidic chip, belongs to PCR and CE integrated technology field.
Background technology
Micro-fluidic chip (Microfludics) refers to chemistry or the biology laboratory that makes up at more than one square centimeters chip, can under microchannel, rely on the variety of ways such as electricity, magnetic, machinery, chemistry to carry out experimental implementation, to realize the function of its design.Target is with chemistry and the sample preparation, the reaction that relate to of biological field, separate, detection, cultivation, sorting etc. are integrated on the microchip, and can repeatedly use, and finally developing direction is micro-total analysis system.Its maximum characteristics of micro-fluidic chip are that biochemical environment depends on the microfluidic environment that the MEMS microfabrication is made, and run through whole system with reliable microfluid, and this also is the origin of its Chinese translation.The structure of micro-fluidic chip is generally the composite package of sandwich construction, the simplest micro-fluidic chip uses a plate substrate to be carved with fine channel with micro-processing technology exactly, then be laminated with together with an other flat substrates, formation has the chip of closed channel, also have therein the import and export of passage on a slice, to carry out the fluid communication inside and outside the chip.Micro-fluidic chip has following outstanding feature in application:
1) fluid is in micron order even the nano level microchannel environment, so fluid substantially all presents the characteristics of low reynolds number and Laminar Flow, so that its flow condition all shows different situation with macro-scale with the situation of mixing.By rational fluid channel design, the process of the complexity that the mixing of fluid, shunting, change flow to will be finished in the short time, the simultaneously processing of MEMS technology can so that microfluidic channel can control by the variety of way convection cell such as electricity, magnetic, machinery and internal fluid medium so that micro-fluidic chip has high operability;
2) micro-fluidic chip mesoscale is microcosmic, fluid all has high body surface area ratio with particle, can improve the speed of biochemical reaction, therefore the dosage of the reaction needed in the microchannel is little but to present high flux, reaction time very short, often be second even Millisecond, so that micro-fluidic chip has efficient characteristics;
3) thermal capacity of the microenvironment of chip is little, can carry out heating and cooling control at a high speed, and the temperature of the accurate Detection ﹠ Controling zones of different of energy; The temperature that is difficult to realize under the easier realization macro-scale in microfluidic channel accurately changes fast, and high-precision temperature control has outstanding contributions to studying special biochemical reaction;
4) micro-fluidic chip can adopt multiple detection means that the reagent in the microfluidic channel is carried out direct-detection, comprise the modes such as laser-Induced Fluorescence Detection (Laser induced fluorescence, LIF), real-time fluorescence detection, Electrochemical Detection, Mass Spectrometer Method etc.Therefore the result who carries out biochemical reaction in the micro-fluidic chip can obtain online, and is converted into the signal of telecommunication and directly outputs in the computer and process, and greatly reduces the complexity of experiment, has improved precision and adjustable to experimental result;
5) height degree of integration will be so that the course of reaction of different complexity can be integrated on the same reaction chip practical function integral automation, waste and the pollution of reagent when having prevented from shifting by rational chip design; Simultaneously because the MEMS process technology, the micro-fluidic chip that this height is integrated can also be produced by mass cheaply, is conducive to thisly have the integrated micro-system of sophisticated functions in the development of every field.
PCR (PCR) is a kind of Protocols in Molecular Biology, be used for amplifying specific dna fragmentation, the special dna replication dna that can regard in vitro as, round pcr principle are similar to the natural reproduction process of DNA, and its specificity depends on the Oligonucleolide primers with the complementation of target sequence two ends.PCR is made of sex change-annealing-extension three basic reactions steps: the 1. sex change of template DNA: template DNA is after being heated to 94 ℃ of left and right sides certain hours, template DNA double-stranded DNA double-stranded or that form through pcr amplification is dissociated, make it to become strand, in order to be combined with primer, for subsequent reactions is prepared; 2. the annealing (renaturation) of template DNA and primer: template DNA is after heat denatured becomes strand, and temperature is down to 50-65 ℃, the complementary series pairing combination of primer and template DNA strand; 3. the extension of primer: dna profiling-primer bond is under the effect of Taq archaeal dna polymerase, take dNTP as reaction raw materials, target sequence is template, press base complementrity pairing and semi-conservative replication principle, synthetic new and the semi-conservative replication chain complementation of template DNA chain, repetitive cycling sex change-annealing-extension three processes just can obtain more " semi-conservative replication chain ", and this new chain can become again the template of circulation next time.Round pcr has been important development direction in life science and the medical domain development, becomes a kind of detection means and technical method of extensive use, all has wide using value at aspects such as life science, engineering in medicine, genetics, forensic identifications.
The key of pcr amplification is to control fast and accurately temperature cycles, there is the shortest effective reaction time in each step in the pcr amplification circulation, temperature changing process is oversize not only loses time, and descend gradually along with the activity of the prolongation Taq archaeal dna polymerase of time, therefore long course of reaction is very disadvantageous to PCR.The thinking that therefore the PCR reaction efficiency directly is provided is exactly to reduce the volume of PCR mixed liquor, can shorten circulation timei, improves the content of amplified production.This is the outstanding feature of the micro-fluidic chip take micron as yardstick exactly.Therefore utilize the MEMS process technology to produce the important branch that efficient PCR micro-fluidic chip becomes the micro-fluidic chip development.The PCR micro-fluidic chip is round pcr and the efficient combination of MEMS technology under New Technological Environment.Along with the micro-fluidic chip technical development, the PCR micro-fluidic chip that processes on silicon, glass and polymeric material basis with the MEMS processing technology, the fluid control elements such as inner integrated little valve, Micropump and micro-heater, microsensor equitemperature control element, in micron dimension even lower enclosed environment, finish operation and the PCR reaction of sample, and can also finish the separation and detection of amplification in the detection part that subsequent set becomes.Therefore so that the PCR reaction has obtained larger integrated level and high reaction efficiency.The PCR micro-fluidic chip has following clear superiority:
1) the temperature circulatory system volume reduces, and thermal capacitance reduces, can reach very high lifting/lowering temperature speed (even can be up to 60-90 ℃/s), the reaction time shortens at double;
2) the reactant liquor volume reduces, and the consumption of reaction reagent reduces, and the uniformity of reacting liquid temperature improves, and the specificity of amplification strengthens, and has not only provided cost savings but also has improved efficient;
3) specific area of microchannel is larger, can select the high material of thermal conductivity factor, promotes heat transfer rate, greatly reduces time and required the expending time in of circulation of reacting liquid temperature balance, and temperature can be stablized and detect faster;
4) chip is easy to integrated and functionalization, can realize quickly and easily amplification, interpretation of result is integrated, the reducing of space scale can further improve heat transfer rate so that can utilize micro-processing technology that micro-heater and temperature sensor etc. directly is integrated on the chip; Also can with chip with Sample Purification on Single, mix, the operating process such as in real time detections of chip electrophoresis and fluorescence is integrated, raising automaticity and integrated process.
The PCR micro-fluidic chip mainly can be divided into static microcavity cell-type PCR and Continuous Flow PCR two large classes in development, both main difference are to carry out PCR circulation time reactant liquor and whether are in flow regime, generally be attributable to static chamber profile if remain static, then generally can be attributed to continuous flow pattern if be in continuous flow regime.
Traditional static micro chamber type pcr chip is relatively simple for structure, and the normal operation micro-processing technology processes the micro chamber (micro chamber has the fluid inlet and outlet that can seal) of reaction, is used for electrode and cooling and the heat abstractor of heating and TEMP.Its basic principle is close with the normal PCR instrument, is the PCR reactant mixture that injects in the reaction chamber is carried out direct heating and cooling control, realizes temperature cycles.Although simple in structure, because the micro-scale effect, thermal inertia is little, the PCR reactant liquor can carry out heating and cooling work soon in micro chamber, and heat sensor also can in time feed back and temperature be controlled.Because the micro chamber chip structure is simple, also means and at a plurality of reaction tanks of wafer processing, to carry out simultaneously a plurality of PCR reactions.Micro chamber by produced by micro processing also can control links to each other with other functional parts with fluid by the microchannel, and practical function is integrated, and these characteristics all have very large advantage in actual use.Static micro chamber type pcr chip has reduced the consumption of mixed liquor significantly, but the heating and cooling speed that temperature control system and structural design directly determine is still to temperature cycles and the stable decisive influence that plays, in general with desirable heating and cooling reaction speed old certain gap still.General heating needs integrated processing on chip with heat abstractor, and this is so that also to some extent rising of processing cost.And the reagent of traditional static chamber pcr chip is prepared, the rear reagent of reaction extracts still need to have outside transfer process, may cause the waste of reagent and the appearance of transferring the pollution.Therefore, all become the direction of static chamber pcr chip development towards the many warm area circulations of the independence that realizes similar Continuous Flow PCR and more function integrated development.
Capillary Electrophoresis (Capillary Electrophoresis CE) chip is the micro-fluidic chip starting point of development, also is the widest maximum direction of micro-fluidic chip development.It is the differential of a comparative maturity from the detection technique means, can realize the separation of various biomolecules, ion is detected.CE chip principle and operation are all very simple, and it relates generally to two kinds of electrical phenomenas in the microfluidic environment: electric osmose and electrophoresis.Electric osmose is a kind of method of using electrode voltage that the fluid in the microfluidic channel is driven, in micro-fluidic chip, if use high-field electrode to contact with microchannel internal reaction reagent, applies voltage; At PH〉under 3 conditions, can form one deck idol electricity layer at the solid-liquid interface place of inside microchannels, idol electricity layer meeting displacement under the effect of the electric field force at passage two ends, because the effect of viscosity can drive liquid in tens microns together flow (microchannel design size generally will so that electric osmose drives whole fluid) simultaneously, under the frictional force balance, form a kind of liquid stream directed movement of flat pattern, Here it is electroosmosis.Electric osmose is a kind of fluid control type of drive that is suitable for very much the micro-fluidic chip environment owing to can utilize voltage to control easily flowing of fluid, is widely used for a long time and studies.Within electric osmose causes the microchannel in the liquid flow, the voltage that applies at two ends, microchannel is also so that the charged particle in the liquid environment moves Here it is electrophoresis to opposite electrode direction under electric field action.Electrophoresis will form the corresponding bands of a spectrum that separate so that the particle of different charge-mass ratios separates under the micro-scale under the electric field force effect.If separate bands of a spectrum affix fluorescence and with the analysis of optics instrument record or use its absorption characteristic to spectrum to analyze, the quantitative result that just can obtain separating, thus realized the purpose of separation detection.
Under the condition that has positively charged, negative electricity and uncharged mixture to exist, can be easy to separately with the method for electric osmose, if but only have under the condition of electronegative DNA, suppress electric osmose, DNA is carried out electrophoresis, resolution ratio can be higher like this.In order to suppress electric osmose, general carry out dynamic embellishment or channel surface is carried out the alkylation modification with compounds such as polyvinyl alcohol, linear polyacrylamide, poly--N-ethoxy acrylamide, pyrrolidones, can suppress like this EOF and can prevent that again DNA is in the absorption of channel surface.
Various biologies and chemical process all are to be in the geometric scale of micron dimension in the micro-fluidic chip, and the narrow and small fast reaction with detecting reagent of detection space is so that the detection mode requirement of micro-fluidic chip is highly sensitive, and fast response time can be microminiaturized.Detector and micro-fluidic chip together develop, and therefore inherit in the development of micro-fluidic chip initial stage capillary electrophoresis chip, comprise that the optical detection of laser-Induced Fluorescence Detection, chemiluminescence and UV absorption etc. is the detection means of main flow always; The electrochemical detection method detection is cheap, device is simple, be highly susceptible to integration, is suitable for the less demanding field of some sensitivity; Mass Spectrometer Method possesses high-resolution, and susceptibility and structural analysis ability have outstanding advantages, but equipment is expensive.LIF (Laser Induced Fluorescence, LIF) detect be at present the sensitiveest also be one of the most frequently used detection method of microfluidic chip, its detectability is very low, generally can reach 10-9-10-13mol/L, even can reach Single Molecule Detection under some improvement technical supports.Use different detection methods according to different needs.
Summary of the invention
The purpose of this utility model is to overcome the deficiency that prior art exists, and the dynamic PCR of a kind of micro chamber and Capillary Electrophoresis CE function integrated microfluidic chip are provided, and realizes detecting simultaneously a function with a plurality of PCR fragments, even identical clip size is also distinguishable.
The purpose of this utility model is achieved through the following technical solutions:
The dynamic PCR of micro chamber and Capillary Electrophoresis CE function integrated microfluidic chip, characteristics are: described chip is four-layer structure, comprises successively ground floor, the second layer, the 3rd layer the 4th layer;
Described the 3rd layer lower surface is provided with the sex change microcavity, the annealing microcavity, extend microcavity, the formamide addition pool, blender, sample cell, buffer pool, the sample waste liquid pool, waste liquid pool, raceway groove between sex change microcavity and the annealing microcavity, raceway groove between annealing microcavity and the extension microcavity, extend the raceway groove between microcavity and the blender, raceway groove between formamide addition pool and the blender, raceway groove between blender and the sample cell and sample cell, buffer pool, the sample waste liquid pool, cross raceway groove between the waste liquid pool, the sex change microcavity, the annealing microcavity, extend the volume of microcavity all less than 1 microlitre, extend the sample outlet end of microcavity and the sample introduction end of sample cell and be equipped with little valve;
Described ground floor is substrate layer, the heating electrode that the upper surface of ground floor is provided with the heating electrode relative with the sex change microcavity position on the 3rd layer and TEMP electrode, the microcavity position of annealing is relative and TEMP electrode, relative heating electrode and the TEMP electrode in extension microcavity position, and the electrode points relative with the position of sample cell, buffer pool, sample waste liquid pool, waste liquid pool respectively, and the high-field electrode that directly is electrically connected with sample cell electrode points, buffer pool electrode points, sample waste liquid pool electrode points, waste liquid pool electrode points respectively;
The described second layer is bonded layer, be overlying on the ground floor, the 3rd layer is bonded on the ground floor, position relative with the position of sample cell, buffer pool, sample waste liquid pool, waste liquid pool on ground floor is respectively equipped with the setting-out hole, also be respectively equipped with through hole on the bonded layer relative with described setting-out hole, the setting-out aperture through hole pond corresponding with it connects;
Described the 4th layer is the Pneumatic Micropump layer, is provided with Pneumatic Micropump, and Pneumatic Micropump is positioned at the top of the sex change microcavity on the 3rd layer, and communicates with the sex change microcavity; Perhaps, sex change microcavity, annealing microcavity and the top of extending microcavity are equipped with a Pneumatic Micropump, communicate with corresponding microcavity respectively.
Further, the dynamic PCR of above-mentioned micro chamber and Capillary Electrophoresis CE function integrated microfluidic chip, the material of described ground floor is aluminium oxide, aluminium nitride, copper, silicon, glass, quartz or transparent high polymer material.Described transparent high polymer material is epoxy resin, polymethyl methacrylate, dimethyl silicone polymer, Merlon, cyclic olefine copolymer, Parylene, polyimides or poly-terephthalic acids second diester.The thickness of described ground floor is 100 μ m～2mm.
Further, the dynamic PCR of above-mentioned micro chamber and Capillary Electrophoresis CE function integrated microfluidic chip, described the 3rd layer material is silicon, glass, quartz or polymeric material.Described polymeric material is epoxy resin, polymethyl methacrylate, dimethyl silicone polymer, Merlon, cyclic olefine copolymer, Parylene, polyimides or poly-terephthalic acids second diester.Described the 3rd layer thickness is 100 μ m～10mm.
Again further, the dynamic PCR of above-mentioned micro chamber and Capillary Electrophoresis CE function integrated microfluidic chip, the described second layer is polymer film, its thickness is below the 100 μ m.Described polymer film is the PDMS film.
Again further, the dynamic PCR of above-mentioned micro chamber and Capillary Electrophoresis CE function integrated microfluidic chip, described the 4th layer material is the PDMS film, its thickness is 100 μ m～10mm.
The substantive distinguishing features of technical solutions of the utility model and progressive being mainly reflected in:
1) three flat-temperature zones are arranged, the temperature-fall period that do not heat up, liquid can reach rapidly corresponding temperature after arriving which warm area, greatly shorten the time of each temperature cycles, and cycle-index are unrestricted;
2) be of a size of microcosmic in the micro-fluidic chip, fluid all has high body surface area ratio with particle, can improve the speed of biochemical reaction, and PCR micro chamber volume is less than 1 microlitre (μ l), dwindling of volume can greatly reduce the PCR reaction time, is easy to mass and produces cheaply;
3) chip is sandwich construction, and sandwich construction can integrated several functions, and is above can being integrated in such as heating electrode, higher to temperature controlled accuracy;
4) thermal capacity of the microenvironment of chip is little, can carry out heating and cooling control at a high speed, and the temperature of the accurate Detection ﹠ Controling zones of different of energy; Can adopt multiple detection means that the reagent in the microfluidic channel is carried out in real time and end point determination; Realize the automation of PCR-CE function integration, waste and the pollution of reagent when having prevented from shifting;
5) the temperature circulatory system volume reduces, and thermal capacitance reduces, can reach very high lifting/lowering temperature speed (even can be up to 60-90 ℃/s), the reaction time shortens at double; The reactant liquor volume reduces, and the uniformity of reacting liquid temperature improves, and the specificity of amplification strengthens, and has not only provided cost savings but also has improved efficient; Chip is easy to integrated and functionalization, can realize quickly and easily amplification, interpretation of result is integrated; Has the function that detects simultaneously and a plurality of PCR fragments, even identical clip size is also distinguishable.
Description of drawings
Below in conjunction with accompanying drawing technical solutions of the utility model are described further:
Fig. 1: the aufbauprinciple schematic diagram of the utility model chip.
The specific embodiment
The utility model design is a kind of to have in real time and the dynamic PCR of micro chamber and the Capillary Electrophoresis CE function integrated microfluidic chip of the one or more PCR fragment of end point determination function, the equal and opposite in direction of fragment has the characteristic that detects multicolored fluorescence, even also can be differentiated.
As shown in Figure 1, the dynamic PCR of micro chamber and Capillary Electrophoresis CE function integrated microfluidic chip, chip is four-layer structure, comprises successively ground floor, the second layer, the 3rd layer the 4th layer; The 3rd layer lower surface is provided with sex change microcavity 2, annealing microcavity 5, extend microcavity 6, formamide addition pool 8, blender 9, sample cell 10, buffer pool 11, sample waste liquid pool 13, waste liquid pool 12, raceway groove between sex change microcavity 2 and the annealing microcavity 5, raceway groove between annealing microcavity 5 and the extension microcavity 6, extend the raceway groove between microcavity 6 and the blender 9, raceway groove between formamide addition pool 8 and the blender 9, raceway groove between blender 9 and the sample cell 10 and sample cell 10, buffer pool 11, sample waste liquid pool 13, cross raceway groove 14 between the waste liquid pool 12, sex change microcavity 2, annealing microcavity 5, extend the volume of microcavity 6 all less than 1 microlitre (μ l), extend the sample outlet end of microcavity 6 and the sample introduction end of sample cell 10 and be equipped with little valve 7;
Ground floor is substrate layer, the heating electrode that the upper surface of ground floor is provided with the heating electrode 3 relative with the sex change microcavity position on the 3rd layer and TEMP electrode 4, the microcavity position of annealing is relative and TEMP electrode, relative heating electrode and the TEMP electrode in extension microcavity position, and the electrode points relative with the position of sample cell, buffer pool, sample waste liquid pool, waste liquid pool respectively, and the high-field electrode 15 that directly is electrically connected with sample cell electrode points, buffer pool electrode points, sample waste liquid pool electrode points, waste liquid pool electrode points respectively;
The second layer is bonded layer, be overlying on the ground floor, the 3rd layer is bonded on the ground floor, position relative with the position of sample cell, buffer pool, sample waste liquid pool, waste liquid pool on ground floor is respectively equipped with the setting-out hole, also be respectively equipped with through hole on the bonded layer relative with described setting-out hole, the pond that setting-out aperture through hole is corresponding with it (sample cell, buffer pool, sample waste liquid pool, waste liquid pool) connects;
The 4th layer is the Pneumatic Micropump layer, is provided with Pneumatic Micropump 1, and Pneumatic Micropump 1 is positioned at the top of the sex change microcavity on the 3rd layer, and communicates with the sex change microcavity.Perhaps, sex change microcavity, annealing microcavity, extend microcavity, there is a Pneumatic Micropump top of each microcavity, communicates with corresponding microcavity respectively, makes liquid be in different microcavitys by regular extruding.
Wherein, the material of ground floor is aluminium oxide, aluminium nitride, copper, silicon, glass, quartz or transparent high polymer material, and the transparent high polymer material is epoxy resin, polymethyl methacrylate, dimethyl silicone polymer, Merlon, cyclic olefine copolymer, Parylene, polyimides or poly-terephthalic acids second diester; The thickness of ground floor is 100 μ m～2mm.
The 3rd layer material is silicon, glass, quartz or polymeric material, and polymeric material is epoxy resin, polymethyl methacrylate, dimethyl silicone polymer, Merlon, cyclic olefine copolymer, Parylene, polyimides or poly-terephthalic acids second diester; The 3rd layer thickness is 100 μ m～10mm.
The second layer is polymer film, and its thickness is below the 100 μ m, and polymer film is the PDMS film.
The 4th layer material is PDMS, and its thickness is 100 μ m～10mm.
The micro-fluidic chip that integrated PCR-CE chip is comprised of PCR reaction member and CE split tunnel, be four-layer structure, ground floor is substrate (glass or hard high polymer material), and this one deck needs heating electrode in the sputter, temperature sensor and high voltage source electrode.The second layer is that the PDMS layer is with electrode and the isolation of passage solution.The 3rd layer is the microchannel layer, and the above is carved with microchannel.The 4th layer is the Pneumatic Micropump layer, and Pneumatic Micropump one side is perhaps above microcavity.During work, make first the pump extruding microcavity of annealing microcavity and extension microcavity, make liquid be in the position of sex change microcavity, then make the sex change microcavity and extend microcavity to be in squeezed state, liquid is in the position of annealing microcavity; At last, sex change microcavity and annealing microcavity are in the state that is extruded, and liquid is in the position of extending microcavity, and such circulation is finished.
Integrated Micropump on micro-fluidic chip, form the PCR mixed liquor in the circulation of three reaction warm areas, sample at first enters 95 degrees centigrade sex change microcavity 2 from hand-hole and carries out sex change, then under Micropump drives, enter annealing microcavity 5 and anneal, under the secondary of Micropump drives, enter extension microcavity 6 at last and extend.In the Micropump reverse drive so that the PCR mixed liquor is got back to sex change microcavity 2 to annealing microcavity 5 more at last from extending microcavity 6.Move in circles like this.Because three flat-temperature zones are arranged, the temperature-fall period that do not heat up, liquid can reach rapidly corresponding temperature after arriving which warm area, greatly shorten the time of each temperature cycles, and cycle-index are unrestricted.To extend at last PCR reactant liquor in the microcavity is driven into electrophoretic cell and carries out electrophoresis.
In sum, the dynamic PCR of the utility model micro chamber and Capillary Electrophoresis CE function integrated microfluidic chip highlight following characteristics:
1) three flat-temperature zones are arranged, the temperature-fall period that do not heat up, liquid can reach rapidly corresponding temperature after arriving which warm area, greatly shorten the time of each temperature cycles, and cycle-index are unrestricted;
2) be of a size of microcosmic in the micro-fluidic chip, fluid all has high body surface area ratio with particle, can improve the speed of biochemical reaction, and PCR micro chamber volume is less than 1 microlitre (μ l), dwindling of volume can greatly reduce the PCR reaction time, is easy to mass and produces cheaply;
3) chip is sandwich construction, and sandwich construction can integrated several functions, and is above can being integrated in such as heating electrode, higher to temperature controlled accuracy;
4) thermal capacity of the microenvironment of chip is little, can carry out heating and cooling control at a high speed, and the temperature of the accurate Detection ﹠ Controling zones of different of energy; Can adopt multiple detection means that the reagent in the microfluidic channel is carried out in real time and end point determination; Realize the automation of PCR-CE function integration, waste and the pollution of reagent when having prevented from shifting;
5) the temperature circulatory system volume reduces, and thermal capacitance reduces, can reach very high lifting/lowering temperature speed (even can be up to 60-90 ℃/s), the reaction time shortens at double; The reactant liquor volume reduces, and the uniformity of reacting liquid temperature improves, and the specificity of amplification strengthens, and has not only provided cost savings but also has improved efficient; Chip is easy to integrated and functionalization, can realize quickly and easily amplification, interpretation of result is integrated; Has the function that detects simultaneously and a plurality of PCR fragments, even identical clip size is also distinguishable.
What need to understand is: the above only is preferred embodiment of the present utility model; for those skilled in the art; under the prerequisite that does not break away from the utility model principle; can also make some improvements and modifications, these improvements and modifications also should be considered as protection domain of the present utility model.
Claims (1)
1. the dynamic PCR of micro chamber and Capillary Electrophoresis CE function integrated microfluidic chip, it is characterized in that: described chip is four-layer structure, comprises successively ground floor, the second layer, the 3rd layer the 4th layer;
Described the 3rd layer lower surface is provided with the sex change microcavity, the annealing microcavity, extend microcavity, the formamide addition pool, blender, sample cell, buffer pool, the sample waste liquid pool, waste liquid pool, raceway groove between sex change microcavity and the annealing microcavity, raceway groove between annealing microcavity and the extension microcavity, extend the raceway groove between microcavity and the blender, raceway groove between formamide addition pool and the blender, raceway groove between blender and the sample cell and sample cell, buffer pool, the sample waste liquid pool, cross raceway groove between the waste liquid pool, the sex change microcavity, the annealing microcavity, extend the volume of microcavity all less than 1 microlitre, extend the sample outlet end of microcavity and the sample introduction end of sample cell and be equipped with little valve;
Described ground floor is substrate layer, the heating electrode that the upper surface of ground floor is provided with the heating electrode relative with the sex change microcavity position on the 3rd layer and TEMP electrode, the microcavity position of annealing is relative and TEMP electrode, relative heating electrode and the TEMP electrode in extension microcavity position, and the electrode points relative with the position of sample cell, buffer pool, sample waste liquid pool, waste liquid pool respectively, and the high-field electrode that directly is electrically connected with sample cell electrode points, buffer pool electrode points, sample waste liquid pool electrode points, waste liquid pool electrode points respectively;
The described second layer is bonded layer, be overlying on the ground floor, the 3rd layer is bonded on the ground floor, position relative with the position of sample cell, buffer pool, sample waste liquid pool, waste liquid pool on ground floor is respectively equipped with the setting-out hole, also be respectively equipped with through hole on the bonded layer relative with described setting-out hole, the setting-out aperture through hole pond corresponding with it connects;
Described the 4th layer is the Pneumatic Micropump layer, is provided with Pneumatic Micropump, and Pneumatic Micropump is positioned at the top of the sex change microcavity on the 3rd layer, and communicates with the sex change microcavity; Perhaps, sex change microcavity, annealing microcavity and the top of extending microcavity are equipped with a Pneumatic Micropump, communicate with corresponding microcavity respectively.
2. the dynamic PCR of micro chamber according to claim 1 and Capillary Electrophoresis CE function integrated microfluidic chip, it is characterized in that: the material of described ground floor is aluminium oxide, aluminium nitride, copper, silicon, glass, quartz or transparent high polymer material.
3. the dynamic PCR of micro chamber according to claim 2 and Capillary Electrophoresis CE function integrated microfluidic chip, it is characterized in that: described transparent high polymer material is epoxy resin, polymethyl methacrylate, dimethyl silicone polymer, Merlon, cyclic olefine copolymer, Parylene, polyimides or poly-terephthalic acids second diester.
4. the dynamic PCR of micro chamber according to claim 1 and Capillary Electrophoresis CE function integrated microfluidic chip, it is characterized in that: the thickness of described ground floor is 100 μ m～2mm.
5. the dynamic PCR of micro chamber according to claim 1 and Capillary Electrophoresis CE function integrated microfluidic chip, it is characterized in that: described the 3rd layer material is silicon, glass, quartz or polymeric material.
6. the dynamic PCR of micro chamber according to claim 5 and Capillary Electrophoresis CE function integrated microfluidic chip, it is characterized in that: described polymeric material is epoxy resin, polymethyl methacrylate, dimethyl silicone polymer, Merlon, cyclic olefine copolymer, Parylene, polyimides or poly-terephthalic acids second diester.
7. the dynamic PCR of micro chamber according to claim 1 and Capillary Electrophoresis CE function integrated microfluidic chip, it is characterized in that: described the 3rd layer thickness is 100 μ m～10mm.
8. the dynamic PCR of micro chamber according to claim 1 and Capillary Electrophoresis CE function integrated microfluidic chip, it is characterized in that: the described second layer is polymer film, its thickness is below the 100 μ m.
9. the dynamic PCR of micro chamber according to claim 8 and Capillary Electrophoresis CE function integrated microfluidic chip, it is characterized in that: described polymer film is the PDMS film.
10. the dynamic PCR of micro chamber according to claim 1 and Capillary Electrophoresis CE function integrated microfluidic chip, it is characterized in that: described the 4th layer material is the PDMS film, its thickness is 100 μ m～10mm.
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102899246A (en) * | 2012-10-10 | 2013-01-30 | 凯晶生物科技(苏州)有限公司 | Dynamic PCR (Polymerase Chain Reaction) and CE (capillary electrophoresis) functional integrated micro-fluidic chip of microcavity |
| CN103439241A (en) * | 2013-08-23 | 2013-12-11 | 东南大学 | Micro-fluidic chip detection system based on single-cell multi-parameter representation |
| CN109865543A (en) * | 2019-04-02 | 2019-06-11 | 武汉大学 | Micro-fluidic bulk wave sorting chip of a kind of high throughput and preparation method thereof |
| WO2023216361A1 (en) * | 2022-05-07 | 2023-11-16 | 合肥诺迈基生物科技有限公司 | Poct micro-fluidic chip, detection system, detection method, and application |
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102899246A (en) * | 2012-10-10 | 2013-01-30 | 凯晶生物科技(苏州)有限公司 | Dynamic PCR (Polymerase Chain Reaction) and CE (capillary electrophoresis) functional integrated micro-fluidic chip of microcavity |
| CN103439241A (en) * | 2013-08-23 | 2013-12-11 | 东南大学 | Micro-fluidic chip detection system based on single-cell multi-parameter representation |
| CN103439241B (en) * | 2013-08-23 | 2016-03-16 | 东南大学 | The fluidic chip detecting system that unicellular multiparameter characterizes |
| CN109865543A (en) * | 2019-04-02 | 2019-06-11 | 武汉大学 | Micro-fluidic bulk wave sorting chip of a kind of high throughput and preparation method thereof |
| CN109865543B (en) * | 2019-04-02 | 2020-06-23 | 武汉大学 | High-flux microfluidic bulk wave sorting chip and preparation method thereof |
| WO2023216361A1 (en) * | 2022-05-07 | 2023-11-16 | 合肥诺迈基生物科技有限公司 | Poct micro-fluidic chip, detection system, detection method, and application |
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