CN208795661U - A kind of chemiluminescence micro-fluidic chip and the analysis instrument containing it - Google Patents
A kind of chemiluminescence micro-fluidic chip and the analysis instrument containing it Download PDFInfo
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- CN208795661U CN208795661U CN201820619104.4U CN201820619104U CN208795661U CN 208795661 U CN208795661 U CN 208795661U CN 201820619104 U CN201820619104 U CN 201820619104U CN 208795661 U CN208795661 U CN 208795661U
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Abstract
The utility model discloses a kind of chemiluminescence micro-fluidic chips comprising chip body and the injection port being arranged in the chip body, liquid driven power entrance, substrate luminescent solution entrance, filter washing water inlet, substrate luminescent solution subchannel, cleaning solution subchannel, main fluid passageway and multiple functional areas；The main fluid passageway is connected to the multiple functional areas.The invention also discloses the analysis instruments with chemiluminescence micro-fluidic chip.The chemiluminescence micro-fluidic chip of the utility model realizes that the identification of fluid sample positions and quantitatively, reduces the manufacture craft difficulty of chip, improve the accuracy of detection by specific liquid quantitative area.
Description
Technical field
The utility model relates to microelectronics technology more particularly to a kind of chemiluminescence micro-fluidic chip and containing its point
Analyzer device.
Background technique
In-vitro diagnosis (In Vitro Diagnosis, IVD) refers to taking-up sample (blood, body fluid, the tissue from human body
Deng) test and analyze to being diagnosed to disease, need corresponding instrument and reagent in detection process, and these instruments and
Reagent just constitutes extracorporeal diagnostic system.The system of in-vitro diagnosis is roughly divided into two kinds；One is be with inspection center laboratory
Represent, it have system modular, automation, the carry out Sample of pipeline system, thus also have high throughput, high efficiency,
The advantage of high sensitive, but whole system also has somewhat expensive, shared volume is big, the defect for needing professional to operate, it
It is mainly used in large hospital.Another be with detect immediately (point-of-care testing, POCT) be representative, it
System have it is integrated, miniaturization, carry out Sample whenever and wherever possible, thus also have price material benefit, it is easy to operate, as a result
Report timely advantage, but its test result compares that there is also sensitivity, the not high disadvantages of stability with central laboratory.
For POCT, has both at home and abroad and microflow control technique is applied in the product of in-vitro diagnosis.It is micro-fluidic
It (microfluidics) is a cross discipline for carrying out control operation to microfluid on one piece of chip with microchannel,
It is related to the fields such as biology, chemistry, fluid physics, electronics, optics, mechanical engineering.Micro fluidic device is commonly known as micro-fluidic
Chip, also referred to as chip lab (Lab on a Chip).Usually biology, chemical, medical analysis process sample system
The basic operations such as standby, reaction, separation, detection are concentrated on one chip, and a system function is completed.Existing micro-fluidic chip
Mainly based on qualitative detection, the micro-fluidic chip of quantitative detection is less, and existing quantitative micro-fluidic chip preparation is complicated, raw
Low efficiency is produced, " a kind of magnetic microparticle chemiluminescence is micro-fluidic as the Chinese patent application of Publication No. " CN105214744 " discloses
Chip ", the micro-fluidic chip include top plate and bottom plate, wherein the top plate includes air pump, adding mouth, sample fill area, mark
Remember ligand storage pool and sample mixed zone；The bottom plate includes filtering area, magnetic particle coating area, cleaning area, detection zone, cleaning solution
Storage pool, luminous substrate liquid storage pool and liquid release channel；The top plate and bottom plate all include liquid sensing device, are used to true
Determine the flow regime of liquid in micro-fluidic chip and whether be mixed into bubble etc., the chip in this patent uses multilayered structure, and
It uses the bag container of specific volume to realize quantifying for liquid, although such D-M (Determiner-Measure) construction is simple, bag container surface is easily
Liquid hanging bag phenomenon occur, (when extruding liquid from bag container, partially liq extension is stayed in bag, not can guarantee liquid is complete
Portion extrudes), and the deflection that bag container is squeezed every time is all different, so each amount of liquid remained in bag container is not
Unanimously, and then the amount of liquid that is extruded of liquid is different, and when in particular for gobbet, the error of bag container is more
Greatly, relative to micro-fluidic chip, what is needed is all tens microlitres of amount, so the quantitative accurate degree of bag container is unable to reach and wants
It asks, dosing accuracy is poor, to influence testing result, while bag container needs to be built into chip, increases the life of chip
Produce difficulty.
Utility model content
To solve the above problems, one side the utility model provides a kind of chemiluminescence micro-fluidic chip, it can be real
Now accurate quantitative detection, and structure is simple, reduces the manufacture craft difficulty of chip.
A kind of the technical solution adopted in the utility model are as follows: chemiluminescence micro-fluidic chip comprising chip body and
Injection port, liquid driven power entrance, substrate luminescent solution entrance, filter washing water inlet, substrate hair in the chip body are set
Light liquid subchannel, cleaning solution subchannel, main fluid passageway and multiple functional areas；The main fluid passageway is connected to the multiple function
Area；
The multiple functional areas include the embedding of enzyme mark the primary antibody area, magnetic mark secondary antibody being sequentially communicated by the main fluid passageway
Embed area and chemiluminescence detection area；Wherein, enzyme mark primary antibody embedding area is embedded with enzyme mark primary antibody；The magnetic mark secondary antibody embedding
Area is embedded with magnetic mark secondary antibody；Meanwhile magnetic mark secondary antibody embedding area is liquid quantitative area；
The injection port is connected to the main fluid passageway respectively with the liquid driven power entrance, the driving force entrance
For connecting liquid driving device to drive liquid to flow in or out the functional areas；One end of substrate luminescent solution subchannel
It is connected to the substrate luminescent solution entrance, the other end is connected to the inlet in magnetic mark secondary antibody embedding area, substrate luminescent solution
Enter magnetic mark secondary antibody embedding area through the substrate luminescent solution entrance, substrate luminescent solution subchannel to be quantified；The cleaning
One end of liquid subchannel is connected to the filter washing water inlet, and the other end is connected to the inlet in magnetic mark secondary antibody embedding area,
Cleaning solution enters magnetic mark secondary antibody embedding area through the filter washing water inlet, cleaning solution subchannel and carries out magnetic bead cleaning.
The liquid driving device is plunger pump in one of the embodiments,.
Enzyme mark primary antibody embedding area is also liquid quantitative area in one of the embodiments,；It is additionally provided in chip body
Dilution entrance and dilution subchannel；One end of the dilution subchannel is connected to the dilution entrance, the other end
It is connected to the inlet in enzyme mark primary antibody embedding area, sample diluting liquid enters through the dilution entrance, dilution subchannel
Enzyme mark primary antibody embedding area is quantified.
The functional areas further include sample amounts area in one of the embodiments, and the sample amounts area is also liquid
Quantification area, fluid sample flow into the sample amounts area through injection port and are quantified；The sample amounts area is located at the enzyme mark
The upstream in primary antibody embedding area；
The air subchannel for being additionally provided with air intake on the chemiluminescence micro-fluidic chip and communicating therewith, the air
One end of subchannel is connected to the air intake, the mainstream between the other end and the sample amounts area and the injection port
The connection of body channel, the other end of air subchannel and the connectivity part of main fluid passageway are adjacent to sample amounts area.
The liquid quantitative area has scheduled volume in one of the embodiments, and goes out liquid in liquid quantitative area
It is provided with Liquid identification site at mouthful, the liquid that need to be quantified flows into the liquid quantitative from the inlet in the liquid quantitative area
Area, full of reaching the liquid outlet behind the liquid quantitative area.
Liquid identification site is also equipped at the inlet in liquid quantitative area in one of the embodiments,.
The chemiluminescence detection area has scheduled volume in one of the embodiments, and in the chemiluminescence
Liquid identification site, inlet stream of the liquid to be detected through the chemiluminescence detection area are provided at the liquid outlet of detection zone
Enter the chemiluminescence detection area, full of reaching liquid outlet behind the chemiluminescence detection area, the chemiluminescence detection area
Volume is less than or equal to the volume in magnetic mark secondary antibody embedding area.
Liquid identification site is also equipped at the inlet in the chemiluminescence detection area in one of the embodiments,；
The volume in the chemiluminescence detection area is equal to the volume in magnetic mark secondary antibody embedding area.
The Liquid identification site is set to the chemiluminescence micro-fluidic chip for positioning in one of the embodiments,
External Liquid identification device；The Liquid identification device includes light source generation module and photoelectric sensor；
The Liquid identification site includes upper site for positioning the light source generation module and for positioning the light
The lower site of electric inductor, the upper site and the lower site are respectively arranged on the outside of the chip body, the upper site
It is corresponding with the position in the lower site and corresponding liquid outlet or inlet so that positioning after the light source generation module,
Corresponding liquid outlet or inlet, the perpendicular line of the photoelectric sensor are successively laid.
The liquid quantitative area is hexagonal structure in one of the embodiments,.
The width of the inlet in the liquid quantitative area is 0.3-3mm in one of the embodiments, is highly 0.3-
3mm；The width of the liquid outlet in the liquid quantitative area is 0.3-3mm, is highly 0.3-3mm；Or
The surface in the liquid quantitative area is the surface formed after hydrophilic surface is modified；The liquid quantitative area
The width of inlet is 0.3-5mm, is highly 0.3-3mm；The width of the liquid outlet in the liquid quantitative area is 0.3-5mm, high
Degree is 0.3-3mm；Or
The surface in the liquid quantitative area is the surface formed after hydrophobic surface is modified, the liquid quantitative area
The width of inlet is 0.3-2mm, is highly 0.3-3mm；The width of the liquid outlet in the liquid quantitative area is 0.3-2mm, high
Degree is 0.3-3mm.
The chip body includes top plate and bottom plate in one of the embodiments,；The top plate and the bottom plate are laminated
Connection；The bottom plate is smooth plate, is provided with micropore, microchannel or microcavity body on the top plate to be formed with the bottom plate
The injection port, liquid driven power entrance, substrate luminescent solution entrance, filter washing water inlet, substrate luminescent solution subchannel, cleaning solution branch
Channel, main fluid passageway or functional areas.
Whole Blood Filtration area is equipped between the injection port and the sample amounts area in one of the embodiments, it is described
Whole blood filter membrane is equipped in Whole Blood Filtration area.
One is respectively laid for positioning magnetic above and below magnetic mark secondary antibody embedding area in one of the embodiments,
The fixed site of the magnet of iron, the diagonally opposing corner that the fixed site of two magnet corresponds to magnetic mark secondary antibody embedding area are laid.
First is equipped between the enzyme mark primary antibody embedding area and magnetic mark secondary antibody embedding area in one of the embodiments,
Mix channel；Second, which is equipped with, between the magnetic mark secondary antibody embedding area and the chemiluminescence detection area mixes channel.
The injection port and the liquid driven power entrance are separately positioned on the main fluid in one of the embodiments,
The both ends in channel.
The other end of substrate luminescent solution subchannel and the magnetic mark secondary antibody embed area in one of the embodiments,
The connectivity part of inlet is located in the main fluid passageway neighbouring with the inlet.
The cleaning solution enters the magnetic through the filter washing water inlet, cleaning solution subchannel in one of the embodiments,
Mark secondary antibody embedding area is quantified；The company of the other end of the cleaning solution subchannel and the inlet in magnetic mark secondary antibody embedding area
Logical place is located in the main fluid passageway neighbouring with the inlet.
The volume of the injection port is 10ul-300ul in one of the embodiments,；Enzyme mark primary antibody embedding area
Volume is 5-50ul；The volume in magnetic mark secondary antibody embedding area is 10-200ul；The volume in the chemiluminescence detection area is 10-
200ul。
On the other hand, the utility model additionally provides a kind of analysis instrument with chemiluminescence micro-fluidic chip, packet
Include apparatus frame, substrate luminescent solution storage pool, cleaning solution storage pool, liquid driving device, magnet, Liquid identification device, detection
Device and above-described chemiluminescence micro-fluidic chip；Wherein, the chemiluminescence micro-fluidic chip is mounted on the instrument
In frame；The liquid driving device is connected with the liquid driven power entrance of the chemiluminescence micro-fluidic chip, the substrate
Luminescent solution storage pool can be connected to on-off with the substrate luminescent solution entrance, the cleaning solution storage pool and the filter washing water inlet
It can be connected to on-off；The detection device is for receiving the chemiluminescence signal for handling the chemiluminescence detection area；The liquid
Body identification device is located at the Liquid identification site, and the position of the magnet is corresponding with magnetic mark secondary antibody embedding area.
The liquid driving device is plunger pump in one of the embodiments,；The substrate luminescent solution storage pool, cleaning
The opening being connected to outside air is respectively equipped on liquid storage pool.
Compared with the existing technology, the utility model has the following beneficial effects:
The chemiluminescence microfluidic chip structure of the utility model is compact, such as magnetic mark secondary antibody embedding area is applied not only to embed
Magnetic mark secondary antibody can also be used in quantifying substances luminescent solution as liquid quantitative area, and liquid quantitative area need not separately be arranged again, institute
It states magnetic mark secondary antibody embedding Qu Haike and is further used as the region cleaned for magnetic bead, and magnetic bead cleaning area need not be separately set again,
The volume of chip is greatly saved；Meanwhile reagent storage pool (such as substrate luminescent solution storage pool, cleaning solution storage pool) can be external
In chip, reagent is plated in chip compared with the existing technology, is reduced the manufacture craft difficulty of chip, is improved detection
Accuracy.
The chip body of the chemiluminescence micro-fluidic chip of the utility model may include the top plate and bottom plate being stacked, and need
On the settable top plate of the structure to be completed the process, bottom plate is only smooth plate, can further decrease the system of chip in this way
Make technology difficulty, improves production efficiency.
Detailed description of the invention
Fig. 1 is a kind of structural schematic diagram of embodiment of chemiluminescence micro-fluidic chip provided by the utility model；
Fig. 2 is the schematic cross-section of Liquid identification device provided by the utility model；
Fig. 3 is a kind of arrangement structure for sensor of embodiment of chemiluminescence micro-fluidic chip provided by the utility model
Figure；
Fig. 4 is that the section of magnet setting position when chemiluminescence micro-fluidic chip provided by the utility model uses is illustrated
Figure；
Fig. 5 is a kind of structural schematic diagram of embodiment of liquid driving device provided by the utility model；
Wherein, 1, top plate；2, injection port, 3, Whole Blood Filtration area；4, sample amounts area；5, enzyme mark primary antibody embeds area；6,
One mixes channel；7, magnetic mark secondary antibody embeds area；8, second channel is mixed；9, chemiluminescence detection area；10, dilution entrance；11,
Substrate luminescent solution entrance；12, filter washing water inlet；13, liquid driven power entrance；14, air intake；15, gasket；16, it dilutes
Liquid subchannel；17, substrate luminescent solution subchannel；18, cleaning solution subchannel；19, plunger pump；20, bottom plate；21, dilution stores
Pond；22, substrate luminescent solution storage pool；23, cleaning solution storage pool；24, waste liquid pool；25a/25b, magnet；26, magnetic bead；27, air
Subchannel；28, light source generation module；29, photoelectric sensor；191, the inlet of plunger pump；192, the liquid outlet of plunger pump；
193, plunger；194, pump chamber.
Specific embodiment
The following will be combined with the drawings in the embodiments of the present invention, carries out the technical scheme in the embodiment of the utility model
Clearly and completely describe, it is clear that the described embodiments are only a part of the embodiments of the utility model, rather than whole
Embodiment.Based on the embodiments of the present invention, those of ordinary skill in the art are without creative efforts
Every other embodiment obtained, fall within the protection scope of the utility model.
Embodiment 1
Please refer to FIG. 1 to FIG. 5, present embodiments provide a kind of chemiluminescence micro-fluidic chip comprising chip body, with
And injection port 2, liquid driven power entrance 13, substrate luminescent solution entrance 11, filter washing water inlet 12, bottom in chip body are set
Object luminescent solution subchannel 17, cleaning solution subchannel 18, main fluid passageway and multiple functional areas；It is specifically described below.
In the present embodiment, main fluid passageway is connected to multiple functional areas, to guide flowing of the fluid between functional areas.
Functional areas include the enzyme mark primary antibody embedding area 5 being sequentially communicated by main fluid passageway, magnetic mark secondary antibody embedding area 7 and change
Learn the detection zone 9 that shines.
Wherein, enzyme mark primary antibody embedding area 5 is embedded with enzyme mark primary antibody；Magnetic mark secondary antibody embedding area 7 is embedded with magnetic mark secondary antibody；Magnetic mark
It is liquid quantitative area that secondary antibody, which embeds area 7,；Liquid quantitative area be used for quantitative liquid, to quantitative liquid (such as substrate luminescent solution) into
After entering liquid quantitative area, quantitative (obtaining desired amount of liquid) can be realized in liquid quantitative area, with quantitative liquid
Sample or the reaction of other reaction reagents, to realize quantitative detection.
Chemiluminescence detection area 9 is for accommodating chemiluminescence reaction product, to complete detection in conjunction with external detection device
Process.
In the present embodiment, injection port 2 is connected to main fluid passageway respectively with liquid driven power entrance 13, driving force entrance
13 are used to connect liquid driving device to drive liquid inflow or downstream area；Injection port 2 is used to introduce fluid sample and lead
In fluid channel, fluid sample enters each functional areas through main fluid passageway.
In the present embodiment, one end of substrate luminescent solution subchannel 17 is connected to substrate luminescent solution entrance 11, the other end
It is connected to the inlet in magnetic mark secondary antibody embedding area 7, substrate luminescent solution is through substrate luminescent solution entrance 11, substrate luminescent solution subchannel 17
It is quantified into magnetic mark secondary antibody embedding area 7.
One end of cleaning solution subchannel 18 is connected to filter washing water inlet 12, the other end and magnetic mark secondary antibody embedding area 7 into
The connection of liquid mouth, the cleaned liquid entrance 12 of cleaning solution, cleaning solution subchannel 18 enter magnetic mark secondary antibody embedding area 7 and carry out magnetic bead cleaning.
The micro-fluidic chip of the present embodiment is in use, substrate luminescent solution entrance 11, filter washing water inlet 12 are sent out with substrate respectively
Light liquid storage pool 22, cleaning solution storage pool 23 can be connected to on-off by valve V2, V3, substrate luminescent solution storage pool 22, cleaning
The opening being connected to outside air is respectively equipped on liquid storage pool 23；Liquid driving device is mounted on liquid driven power entrance 13
Place, flows to liquid in driving chip；The outside in magnetic mark secondary antibody embedding area 7 is fixed with magnet (such as magnet 25a, 25b), with
Just magnetic bead 26 is fixed.It is liquid quantitative area that magnetic mark secondary antibody, which embeds area, can be used for quantifying substances luminescent solution, optionally, can also be into
One step is used for quantitative cleaning solution.
One working method of the micro-fluidic chip of the present embodiment is as follows: the fluid sample of predetermined amount is (such as through diluted
Serum or blood plasma afterwards) under the action of liquid driving device at injection port 2 through main fluid passageway flow to enzyme mark primary antibody embedding
Area 5, with the enzyme mark primary antibody hybrid reaction wherein embedded, reaction solution reaches magnetic mark secondary antibody and embeds area 7 thereafter, with the magnetic wherein embedded
Mark secondary antibody continuess to mix reaction, and the reactant of double antibodies sandwich structure is formed on magnetic bead, and magnetic bead is adsorbed by magnet, and reactant is in magnetic
Under the action of pearl stablize magnetic mark secondary antibody embedding area 7 in, and remaining reaction solution under the action of liquid driving device through liquid
Chip is discharged in driving force entrance 13；Then, the air inflow end mouth (such as sample inlet) on chip is closed, cleaning solution storage is opened
Valve V3 between pond 23 and filter washing water inlet 12, cleaning solution under the action of liquid driving device cleaned liquid subchannel 18 into
Enter magnetic mark secondary antibody embedding area 7 to clean to magnetic bead therein, when magnetic mark secondary antibody embedding area 7 completes to quantify cleaning solution
When, the valve V3 between cleaning solution storage pool 23 and filter washing water inlet 12 can be closed, air inflow end mouth is opened, after cleaning
Chip is discharged through liquid driven power entrance 13 under the action of liquid driving device in liquid can be repeatedly in order to guarantee cleaning effect
(magnetic bead cleaning way is not limited to mode described herein, can also be for example, by the moving magnet in cleaning solution for several times for cleaning
Mode realizes the cleaning of magnetic bead)；The air inflow end mouth (such as sample inlet) being then switched off on chip opens the storage of substrate luminescent solution
The valve V2 between pond 22 and substrate luminescent solution entrance 11 is deposited, substrate luminescent solution is sent out under the action of liquid driving device through substrate
Light liquid subchannel 19 enter magnetic mark secondary antibody embed area 7, when magnetic mark secondary antibody embedding area 7 complete to substrate luminescent solution it is quantitative when, close
The valve V2 between substrate luminescent solution storage pool 22 and substrate luminescent solution entrance 11 is closed, liquid driving device stops driving effect,
Substrate luminescent solution is no longer flow into magnetic mark secondary antibody embedding area 7, the air inflow end mouth (such as sample inlet) on chip is opened, after quantitative
Substrate luminescent solution and the reactant of magnetic capture carry out luminescence-producing reaction, remove magnet later, magnetic mark secondary antibody embeds anti-in area 7
It answers liquid to flow into chemiluminescence detection area 9 under the action of liquid driving device to be detected.
Above-mentioned chemiluminescence microfluidic chip structure is compact, such as magnetic mark secondary antibody embedding area is applied not only to embedding magnetic mark two
It is anti-, it can also be used in quantifying substances luminescent solution as liquid quantitative area, and liquid quantitative area need not be separately set again, magnetic mark secondary antibody
Embedding Qu Haike is further used as the area cleaned for magnetic bead, and magnetic bead cleaning area need not separately be arranged again, and core is greatly saved
The volume of piece；Meanwhile reagent storage pool (such as substrate luminescent solution storage pool, cleaning solution storage pool) is external to chip, relatively
It is plated in chip in prior art reagent, reduces the manufacture craft difficulty of chip, improve the accuracy of detection.
It should be noted that main fluid passageway and multiple functional areas can be more by laser processing, model injection molding etc.
Kind of mode shapes inside chip body, can also be processed on top plate or bottom plate by being set as the top plate and bottom plate of separate type
Then specific shape out is mutually packaged together；Since former processing method is relatively complicated, in a preferred embodiment
In, chip body includes top plate 1 and bottom plate 20；Top plate 1 and the stacking of bottom plate 20 connect；The junction of top plate 1 and bottom plate 20 is arranged
There are main fluid passageway and multiple functional areas；It is highly preferred that bottom plate 20 be smooth plate, top plate 20 be arranged micropore, microchannel or
Microcavity body with bottom plate cooperatively form injection port 2, liquid driven power entrance 13, substrate luminescent solution entrance 11, filter washing water inlet 12,
Substrate luminescent solution subchannel 17, cleaning solution subchannel 18, main fluid passageway or multiple functional areas, such micro-fluidic chip preparation
Get up more convenient, further reduced producting process difficulty, only required specific structure need to be processed on top plate, into one
Step improves production efficiency.In one embodiment, bottom plate 20 be smooth plate, top plate 1 be equipped with multiple microchannels with
Bottom plate 20, which combines, forms main fluid passageway, and top plate 1 is equipped with multiple microcavitys to be combined to form multiple functional areas, top plate with bottom plate 20
1, which is equipped with multiple Kong Yiyu bottom plates 20, combines and forms injection port 2, liquid driven power entrance 13, substrate luminescent solution entrance 11 and clear
Wash liquor inlet 12；For the ease of sample introduction, the size of injection port 2 is typically larger than the size of other entrances.
Therefore, the chip body of above-mentioned chemiluminescence micro-fluidic chip may include the top plate and bottom plate being stacked, and need
On the settable top plate of the structure completed the process, bottom plate is only smooth plate, can further decrease the production of chip in this way
Technology difficulty improves production efficiency.
Preferably, liquid quantitative area has scheduled volume, and liquid knowledge is provided at the liquid outlet in liquid quantitative area
Other site, the liquid that need to be quantified reach out behind the inlet influent quantification area in liquid quantitative area, hydraulically full quantification area
Liquid mouth；Liquid identification site is for positioning or fixing liquid identification device, Liquid identification device liquid for identification.When liquid arrives
When at up to liquid outlet, Liquid identification device can provide liquid arriving signal, and liquid quantitative area is full of by indicating liquid, this time control
Liquid driving device processed stops driving liquid, and liquid quantifying in liquid quantitative area can be realized.The micro-fluidic core of chemiluminescence
Piece realizes quantifying for liquid in conjunction with liquid driving device by specific liquid quantitative area, and quantitative accuracy can be improved.
Optionally, Liquid identification site is also equipped at the inlet in liquid quantitative area.The setting in this Liquid identification site
Two kinds of quantitative liquids can be can also be achieved convenient for being monitored, controlling to the flowing of liquid in chip and bubble that may be present
Between mixing, such as the mixing between fluid sample and reagent (such as reaction reagent, sample processing reagent).In the chip
Portion needs the contact of two kinds of liquid to realize the mixing of two kinds of liquid, and centre is not present gap, and the miniflow of the utility model
Control chip to realize the contact of quantitative and two kinds of liquid of liquid simultaneously, this requires it is one of it is quantitative after liquid stop
Pre-position is stayed in, another liquid preferably begins to flow into liquid quantitative area from this predetermined position, real in liquid quantitative area
It is now quantitative, and at the optimal selection in this predetermined position, that is, liquid quantitative area inlet；Liquid identification position is set at inlet
For point to position Liquid identification device, this Liquid identification device is the stop indication signal and another kind that can provide one of liquid
Determining for liquid can be realized under the cooperation of the Liquid identification device at the liquid outlet in liquid quantitative area in the feed liquor signal of liquid
The contact of amount and two kinds of liquid.
Further, enzyme mark primary antibody embedding area 5 is also liquid quantitative area, is additionally provided with 10 He of dilution entrance in chip body
Dilution subchannel 16；One end of dilution subchannel 16 is connected to dilution entrance 10, and the other end and enzyme mark primary antibody embed area 5
Inlet connection, sample diluting liquid through dilution entrance, dilution subchannel enter enzyme mark primary antibody embedding area 5 quantified.
Further, it is respectively arranged with Liquid identification site at the inlet and liquid outlet in enzyme mark primary antibody embedding area 5, the liquid that need to be quantified
Body flows into enzyme mark primary antibody from its inlet and embeds area 5, reaches liquid outlet after embedding area 5 full of enzyme mark primary antibody.Sample diluting liquid is not
Only can diluent liquid sample (such as serum, blood plasma), its concentration and viscosity are reduced, wherein the substance contained can also reduce liquid
The background values of body sample, so that detection is more accurate, while sample diluting liquid can preferably redissolve enzyme mark primary antibody；In this technology
In scheme, enzyme mark primary antibody embedding area can be used for quantifying sample diluting liquid, without realizing determining for sample diluting liquid in chip exterior
Amount, quantitative sample diluting liquid can embed area in enzyme mark primary antibody and be mixed with quantitative fluid sample, can save manpower, operate
It is more convenient.In use, dilution entrance 10 can be connect to on-off with dilution storage pool 21 by valve V1, dilution storage
It deposits pond 21 and is equipped with the opening being connected to outside air；Fluid sample (serum or blood such as after diluted of predetermined amount
Slurry) it flow to the inlet in enzyme mark primary antibody embedding area 5 through main fluid passageway at injection port 2 under the action of liquid driving device
Place closes the air intake (such as sample inlet) on chip, opens the valve between dilution storage pool 21 and dilution entrance 10
Door V1, sample diluting liquid enters enzyme mark primary antibody through dilution subchannel 16 under the action of liquid driving device and embeds area 5, when it
Area 5 is embedded full of enzyme mark primary antibody, when reaching at the liquid outlet in enzyme mark primary antibody embedding area 5, closes dilution storage pool 21 and dilution
Valve V1 between liquid entrance 10 is opened air inflow end mouth (such as sample inlet), and fluid sample and sample diluting liquid can be
Continue to flow under the suction function of liquid driving device, and can be in the positive pressure of liquid driving device, negative pressure alternating action in mainstream
Body channel, the embedding of enzyme mark primary antibody realize mixing in area 5, can also realize preferably mixing by the hybrid channel of setting certainly.
Optionally, chemiluminescence detection area 9 has scheduled volume, and sets at the liquid outlet in chemiluminescence detection area 9
It is equipped with Liquid identification site, liquid to be detected flows into chemiluminescence detection area 9 through the inlet in chemiluminescence detection area 9, fills
Liquid outlet is reached behind full chemiluminescence detection area 9, the volume in chemiluminescence detection area 9 is less than or equal to magnetic mark secondary antibody embedding area 7
Volume.The Liquid identification site being arranged at the liquid outlet in chemiluminescence detection area 9 can be used for positioning or fixing liquid identification device,
Reaction solution after substrate luminescent solution is reacted with the reactant of magnetic capture reaches at the liquid outlet in chemiluminescence detection area
When, Liquid identification device issues signal, and liquid driving device controls reaction solution and stops flowing, can be detected at this time.Into one
Step, Liquid identification site also is provided at the inlet in chemiluminescence detection area 9, the volume in chemiluminescence detection area 9 is equal to magnetic
Mark the volume in secondary antibody embedding area 7.
Optionally, for the ease of the mixing between fluid sample, reagent (sample diluting liquid, substrate luminescent solution etc.), mainstream
Body channel includes that the first mixing channel 6 and second mix channel 8；First, which mixes channel 6, is set to enzyme mark primary antibody embedding area 5 and magnetic mark
Secondary antibody embeds between area 7；Second, which mixes channel 8, is set between magnetic mark secondary antibody embedding area 7 and chemiluminescence detection area 9.
Optionally, injection port 2 and liquid driven power entrance 13 are separately positioned on the both ends of main fluid passageway.
As shown in figure 4, optionally, for the ease of fixed magnetic bead, chip body position corresponding with magnetic mark secondary antibody embedding area 7
Place is provided with the fixed site of magnet；Further, it is carried out since the cleaning of magnetic bead can embed area 7 in magnetic mark secondary antibody, in order to more preferable
Realize that magnetic bead cleaning, the embedding of magnetic mark secondary antibody respectively lay one for phase magnet 25a, the magnet of 25b above and below area 7 in ground
Fixed site, two magnet 25a, the diagonally opposing corner that 25b corresponds to magnetic mark secondary antibody embedding area 7 are laid.
Optionally, liquid driving device is plunger pump 19, and the description as described in plunger pump is suitable for this implementation in embodiment 2
Example.
Optionally, functional areas further include sample amounts area 4, and sample amounts area 4 is also liquid quantitative area, fluid sample pass through into
Sample mouth flows into sample amounts area 4 and is quantified；Sample amounts area 4 is located at the upstream in enzyme mark primary antibody embedding area 5；On micro-fluidic chip
One end of the air subchannel 27 for being additionally provided with air intake 14 and communicating therewith, air subchannel 27 is connected to air intake 14,
Main fluid passageway between the other end and sample amounts area 4 and injection port 2 is connected to, the other end and main fluid of air subchannel 27
The connectivity part in channel is adjacent to sample amounts area 4.In one embodiment, " neighbouring " usually can be regarded as " determining apart from sample herein
Measure the 0.5~10mm of inlet (preferably 0.5~2mm) in area 4 ".It, can be convenient for fluid sample by being provided with sample amounts area
It is quantitative, without separately quantitative outside chip so that chip use it is more convenient.Further, the liquid outlet in sample amounts area 4
Place is provided with Liquid identification site, and the liquid that need to be quantified flows into sample amounts area 4 from its inlet, full of behind sample amounts area 4
Reach liquid outlet.Further, Liquid identification site is also equipped at the inlet in sample amounts area 4.
Micro-fluidic chip in use, air intake and the air pipeline of chip exterior can be connected to on-off by valve,
Enter chip interior to control air.Fluid sample under the action of liquid driving device through injection port from sample amounts areas into
Liquid mouth flows into sample amounts area, when at the liquid outlet that fluid sample flow to sample amounts area, that is, is full of sample amounts area, this
When the Liquid identification device that is positioned on the Liquid identification site of liquid outlet issue indication signal, control air intake is opened,
The driving force as needed for the flowing of air in air subchannel is small, and driving force needed for the flowing of fluid sample is bigger, therefore liquid
Body sample rests on air subchannel and the connectivity part of main fluid passageway does not continue to flow into sample amounts area, and liquid can be completed
Sample quantifying in sample amounts area.Fluid sample after quantitative can continue to flow to enzyme mark under the action of liquid driving device
Primary antibody embeds area.
Optionally, fluid sample is whole blood, and Whole Blood Filtration area 3, whole blood mistake are equipped between injection port 7 and sample amounts area 4
It filters and is equipped with whole blood filter membrane in area 3；When micro-fluidic chip is used for clinical diagnosis, whole blood is common test sample, and when detection is logical
Often need to carry out whole blood separation with by whole blood serum or blood plasma separate, then reacted with reagent；It is arranged in chip
Whole Blood Filtration area uses convenient for detection, while compared to whole blood is first quantified, then carrying out the mode of whole blood separation, injection port with
It is equipped with Whole Blood Filtration area between sample amounts area, knot can be measured by the dosage of sample amounts area direct quantitative serum or blood plasma
Fruit is more accurate.The material of whole blood filter membrane can be glass fibre, cotton linter fiber, polyester fiber, fiber or blend fibre；It is optional
Ground, Whole Blood Filtration filter bed with a thickness of 0.2-2.5mm；The adsorption rate of Whole Blood Filtration filter bed is 4-150s/4cm, and water imbibition is
30-250mg/cm2。
The description as described in liquid quantitative area is applicable in liquid quantitative area (including magnetic mark two in this present embodiment in embodiment 3
It is anti-embedding area 7, enzyme mark primary antibody embedding area 5 and sample amounts area 4) description, details are not described herein.
Description is applicable in Liquid identification in this present embodiment as described in Liquid identification site and Liquid identification device in embodiment 4
The description of site and Liquid identification device, details are not described herein.
Optionally, the connectivity part position of the other end of substrate luminescent solution subchannel 17 and the inlet in magnetic mark secondary antibody embedding area 7
In in the main fluid passageway of the inlet in magnetic mark secondary antibody embedding area 7；In one embodiment, " neighbouring " usually can be regarded as herein
" 0.5~10mm of inlet (preferably 0.5~2mm) apart from magnetic mark secondary antibody embedding area 7 ".
Optionally, the cleaned liquid entrance 12 of cleaning solution, cleaning solution subchannel 18 enter magnetic mark secondary antibody embedding area 7 and are determined
Amount；The connectivity part of the inlet in the other end and magnetic mark secondary antibody the embedding area 7 of cleaning solution subchannel 18 is located at neighbouring with inlet
In main fluid passageway；In one embodiment, herein " neighbouring " be interpreted as " apart from magnetic mark secondary antibody embedding area 7 inlet 0.5~
10mm (preferably 0.5~2mm) ".Preferably, the inlet of the other end of cleaning solution subchannel 18 and magnetic mark secondary antibody embedding area 7
Connectivity part substrate luminescent solution subchannel 17 the other end and magnetic mark secondary antibody embedding area 7 inlet connectivity part downstream,
It can avoid substrate luminescent solution in this way and be cleaned liquid dilution.
Optionally, the other end of dilution subchannel 16 and enzyme mark primary antibody embedding area 5 inlet connectivity part be located at
In the neighbouring main fluid passageway of the inlet in enzyme mark primary antibody embedding area 5；In one embodiment, herein " neighbouring " be interpreted as " away from
0.5~10mm of inlet (preferably 0.5~2mm) from enzyme mark primary antibody embedding area 5 ".
Optionally, the volume of injection port 2 is 10ul-300ul.
Optionally, the liquid outlet in Whole Blood Filtration area 3 is triangle liquid outlet；3 area of Whole Blood Filtration area is 30-300mm2,
Width is 2-20mm, a length of 5-25mm, depth 0.3-3mm, and the angle of front end triangle is 15-160 DEG C.
Optionally, the volume in sample amounts area 4 is 1-50ul.
Optionally, the volume in enzyme mark primary antibody embedding area 5 is 5-50ul.
Optionally, first mix pipeline 6 and second mix pipeline 8 width be 200-2000um, a length of 5mm-40mm, depth is
0.2-3mm。
Optionally, the volume in magnetic mark secondary antibody embedding area 7 is 10-200ul.
Optionally, the volume in chemiluminescence detection area 9 is 10-200ul.
Next, describing a kind of inspection of the micro-fluidic chip of embodiment according to the present utility model in conjunction with FIG. 1 to FIG. 5
Survey method.The method comprising the steps of 101 to step 110, and each step is specific as follows:
Step 101: whole blood sample being added to injection port 2, will be stored respectively with dilution storage pool 21, substrate luminescent solution
Pond 22, cleaning solution storage pool 23, plunger pump 19, air communication steel needle insertion chip in closed pad 15, wherein steel needle distinguish
It is connect with dilution entrance 10, substrate luminescent solution entrance 11, filter washing water inlet 12, liquid driven power entrance 13, air intake 14；
It opens solenoid valve V4 and negative-pressure sucking is generated by plunger pump 19, whole blood sample is sucked into Whole Blood Filtration area 3.
Step 102: whole blood sample completes filtered serum and is inhaled into sample amounts area 4, and by sample amounts area 4 into
The photoelectric sensor (a1, a2) being arranged on liquid mouth and liquid outlet completes the quantitative measurment of serum.
When whole blood sample is by being that inductor output voltage value changes above photoelectric sensor a1, to system one
Identification signal judges the flow locations of liquid in the chips.When sample passes through photoelectric sensor a2, judgement sample determines sample
Amount area 4 is full of, and the intrinsic volume in the region is the quantitative values of sample.
Step 103: blocking injection port 2 and open solenoid valve V5, so that serum is inhaled into enzyme mark primary antibody embedding area 5.
Step 104: when the photoelectric sensor (b1) being arranged on the inlet in enzyme mark primary antibody embedding area 5 detects serum,
Solenoid valve V5 is closed, solenoid valve V1 is opened, so that external sample dilution enters enzyme mark primary antibody embedding area 5 from solenoid valve V1.
Step 105: when the photoelectric sensor (b2) being arranged on enzyme mark primary antibody embedding 5 liquid outlet of area detects that external sample is dilute
When releasing liquid, solenoid valve V1 is closed, solenoid valve V5 is opened, and positive pressure and negative-pressure sucking are sequentially generated by plunger pump 19, so that blood
Clearly, external dilution liquid, the enzyme mark primary antibody embedded in advance are embedded in enzyme mark primary antibody and are flowed back and forth between area 5 and the first mixing pipeline 6
It redissolves, obtains the first mixed liquor.
Step 106: the first mixed liquor is inhaled into magnetic mark secondary antibody embedding area 7, and makes first to mix by the second mixing pipeline 8
Liquid is closed in conjunction with antigen-antibody, the reactant of formation is captured by magnetic bead, and magnetic bead is adsorbed by the magnet in 7 outside of magnetic mark secondary antibody embedding area
And stablize in magnetic mark secondary antibody embedding area 7, remaining reaction solution is under the negative-pressure sucking of plunger pump 19 through liquid driven power entrance
Chip is discharged, then carries out next cleaning step.
Step 107: closing solenoid valve V5, and open solenoid valve V3, exterior washings liquid is made to enter magnetic mark secondary antibody embedding area
7, and the note that the photoelectric sensor (c1, c2) being arranged on 7 inlet of area and liquid outlet controls cleaning solution is embedded by magnetic mark secondary antibody
Enter amount.
Step 108: after external cleaning solution and magnetic bead clean repeatedly, magnet 25a, 25b adsorb magnetic bead, are produced by plunger pump
Liquid suction after cleaning is discharged in external waste liquid pool 24 by raw negative-pressure sucking.
Step 109: closing solenoid valve V3, open solenoid valve V2, external substrate luminescent solution is made to enter the embedding of magnetic mark secondary antibody
Area 7, and pass through the injection rate of photoelectric sensor (c1, c2) control substrate luminescent solution.
Step 110: after substrate luminescent solution is sufficiently reacted with the antigen-antibody on magnetic bead, obtaining reaction solution, reaction solution quilt
Chemiluminescence detection area 9 is transported, to complete chemiluminescence detection；Wherein, on 9 inlet of chemiluminescence detection area and liquid outlet
The photoelectric sensor (d1, d2) of setting is used to detect capacity and the position of reaction solution.
Reaction principle in the chemiluminescence micro-fluidic chip of the present embodiment between substance is the same as magnetic particle immunochemiluminescence
Reaction principle, i.e. antigen in sample by and enzyme mark primary antibody (primary antibody is marked with the catalytic groups such as HRP, AP) combine, then with
Magnetic mark secondary antibody (secondary antibody is fixed on magnetic bead), which combines, forms double antibodies sandwich compound, and magnet adsorbs magnetic bead, washes unbonded
Antigen and enzyme mark primary antibody, substrate reactions liquid is added, the enzymes group catalysis substrate reaction solution such as HRP, AP marked on primary antibody shines.
Luminous intensity and the amount of antigen are directly proportional.
Embodiment 2
Referring to FIG. 5, the utility model provides the liquid driving device of function described in achievable embodiment 1.At this
In embodiment, liquid driving device is plunger pump 19.
For structure, liquid driving device may be configured as a variety of, such as existing syringe pump, diaphragm pump, peristaltic pump, all
It is that by and liquid is driven to the presumptive area to chip under pressure, the protection model of the utility model should all be fallen into
It encloses.Although syringe pump, diaphragm pump, peristaltic pump can drive liquid to flow, they cannot control liquid in certain bits well
Stop is set, and plunger pump can preferably solve this problem.Plunger pump suitable for the utility model can be art technology
Plunger pump known to personnel, generally includes pump chamber 194 and plunger 193, and pump chamber 194 is equipped with inlet 191 and liquid outlet
192, the top of plunger 193 is inserted into pump chamber, and plunger 193 is reciprocating in its axial direction along the inner wall of pump chamber 194；Feed liquor
Valve V4, V6 are respectively equipped at mouth 191, liquid outlet 192.Since plunger pump is applied to imbibition, drain by more, set on pump chamber
Two mouths set are commonly known as " inlet and liquid outlet ", but it should be recognized that " inlet and liquid outlet " herein is simultaneously
It is not limited to use in feed liquor and out liquid, in the present embodiment, when plunger pump work, after the valve V4 at inlet 191 is opened, plunger
It moving downward, the pressure that liquid closes on one end of plunger pump inlet 191 at this time becomes smaller, and cause liquid both ends to generate pressure difference,
Liquid moves under the action of pressure difference to 191 direction of inlet, when liquid reaches pre-position, opens at liquid outlet
Valve V6, so that chip interior is connected to outside atmosphere, in two sides air, (wherein the air of side is through going out liquid respectively for liquid two sides
Mouthful, inlet enter chip interior, the air of the other side can be from air inflow end mouth (such as injection port or separately the air branch that is arranged
Channel) enter chip interior) under the action of, pressure keeps balance, and liquid can rest on pre-position.
Embodiment 3
Fig. 1 and Fig. 3 are please referred to, the utility model provides the liquid quantitative area of function described in achievable embodiment 1.
It should be noted that the liquid quantitative area of the utility model can be realized " need to liquid quantitatively from liquid quantitative area
Inlet influent quantification area, reach liquid outlet behind hydraulically full quantification area ", shape and structure can as needed into
Row selection, the utility model impose any restrictions not to this, such as it can be pipe shape, polygonal shape etc..
In the present embodiment, liquid quantitative area is hexagonal structure.Specifically, the inlet and liquid outlet in liquid quantitative area
Respectively two of hexagonal structure diagonal；Two diagonal angles are less than 120 °.
Optionally, the width of the inlet in liquid quantitative area is 0.3-3mm (preferably 0.8-1.5mm), is highly 0.3-
3mm；The width of the liquid outlet in liquid quantitative area is 0.3-3mm (preferably 0.8-1.5mm), is highly 0.3-3mm.Feed liquor mouth width
Spend wide or narrow, excessive height or it is too low be unfavorable for quantitative progress, when inlet width is wide or excessive height, hold
Easily cause liquid can not hydraulically full quantification area flow to its liquid outlet, cannot achieve accurate liquid quantitative in this way, and when into
When liquid mouth width spends narrow or highly too low, then needs to increase accordingly requirement of the length to meet volume, may result in core in this way
The increase of leaf length and the increase of chip volume.
Optionally, the surface in liquid quantitative area is the surface formed after hydrophilic surface is modified；Liquid quantitative area
The width of inlet is 0.3-5mm, is highly 0.3-3mm；The width of the liquid outlet in liquid quantitative area is 0.3-5mm, is highly
0.3-3mm.Hydrophilic surface modification includes but is not limited to plasma, hydroxylating, carboxylated modification.The surface in liquid quantitative area into
After row Hydrophilic modification, be more advantageous to the filling of liquid in the cavity, at this time can larger fluid quantification area appropriate inlet,
The width of liquid outlet, so as to reduce the length in liquid quantitative area and chip.
Optionally, the surface in liquid quantitative area is the surface formed after hydrophobic surface is modified, liquid quantitative area
The width of inlet is 0.3-2mm, is highly 0.3-3mm；The width of the liquid outlet in liquid quantitative area is 0.3-2mm, is highly
0.3-3mm.Hydrophobically modified includes but is not limited to hydrophobicity physical modification, (such as nanoparticle coating adds for hydrophobic chemical modification
The alkyl etc. of long-chain).The surface in liquid quantitative area can prevent liquid wall built-up after hydrophobic surface is modified, and can guarantee liquid
Body reaches liquid outlet after being full of in liquid quantitative area.
Above with respect to three liquid quantitative areas of the description suitable for embodiment 1 of the structure in liquid quantitative area, i.e. magnetic mark
Secondary antibody embeds area, enzyme mark primary antibody embedding area and sample amounts area sample.
Embodiment 4
Fig. 2 is referred to, the utility model provides Liquid identification site and the liquid of function described in achievable embodiment 1
Identification device.
It should be noted that Liquid identification site is for positioning or fixing liquid identification device, the utility model is for liquid
The structure of body identification device with no restriction, as long as being able to achieve the identification of liquid.It is special such as Publication No. " 105214744A "
Liquid sensing device disclosed in benefit application can be used as the Liquid identification device of the utility model, but such liquid sensing dress
It is complex to set structure, conductive pin needs to be built into chip interior, and conductive pin is contacted with reaction liquid, in any case
It will affect experimental result, and chip preparation difficulty is larger, provides a kind of preferred Liquid identification device in the present embodiment.
In the present embodiment, Liquid identification site includes that light source is raw for positioning Liquid identification device, Liquid identification device
At module 28 and photoelectric sensor 29；Liquid identification site includes for the upper site of positioned light source generation module 28 and for fixed
The lower site of position photoelectric sensor 29, upper site and lower site are respectively arranged on the outside of chip body, upper site, corresponding feed liquor
Mouth or liquid outlet, the lower perpendicular line in site area are successively laid.Correspondingly, light source generation module 28, corresponding inlet or liquid out
Mouth, the perpendicular line of photoelectric sensor 29 are successively laid.Since Liquid identification device can be set to liquid quantitative area or chemiluminescence inspection
It surveys at the inlet or liquid outlet in area, therefore " corresponding inlet or liquid outlet " herein corresponds to liquid quantitative area or chemistry
The inlet or liquid outlet of luminous detection zone；For example, when Liquid identification device is arranged in the liquid outlet in magnetic mark secondary antibody embedding area, light
The perpendicular line of liquid outlet, photoelectric sensor that source generation module, magnetic mark secondary antibody embed area is successively laid；When magnetic mark secondary antibody embeds area
Inlet when Liquid identification device is set, light source generation module, the magnetic mark secondary antibody embedding inlet in area, photoelectric sensor are in hanging down
Straight line is successively laid；When Liquid identification device is arranged in the liquid outlet in sample amounts area, light source generation module, sample amounts areas
The perpendicular line of liquid outlet, photoelectric sensor is successively laid.
Using optical sensing come to Liquid identification, quantitative and control, relative to the way of contact of conducting type, the method is reduced
Intervention of the metal to reaction system in chip can be improved detection efficiency, and then improve quantitative accuracy, while such liquid
Body identification device can be set to outside micro-fluidic chip, convenient for being fixed in instrument, without being arranged on chip, reduce chip
Difficulty of processing.In use, only light source generation module and photoelectric sensor alignment liquid recognition site need to be placed.Specifically
Ground, chip body include top plate 1 and bottom plate 20；Top plate 1 and the stacking of bottom plate 20 connect；The junction of top plate 1 and bottom plate 20 is arranged
There are main fluid passageway and multiple functional areas；The inlet or liquid outlet being located in liquid quantitative area is arranged in light source generation module 28
The surface of the corresponding position of corresponding top plate 1, photoelectric sensor 29 are located in inlet or liquid outlet with liquid quantitative area
The underface of the corresponding position of corresponding bottom plate 20.
Light source generation module can provide the module of light source, can be LED, halogen lamp, laser lamp etc..In the photograph of light source
It penetrates down, since gas, liquid are to the transmissivity and refractive index difference of light, the light intensity for being irradiated to photoelectric sensor is different, photoelectricity
Inductor can identify gas and liquid, to distinguish whether liquid arrives the point of induction., when liquid flow to inlet or goes out
When liquid mouth, Liquid identification device can be identified quickly, to control liquid driving device.
Embodiment 5
The embodiments of the present invention additionally provide a kind of analysis instrument with micro-fluidic chip comprising instrument frame
Frame, substrate luminescent solution storage pool, cleaning solution storage pool, liquid driving device, magnet, Liquid identification device, detection device and with
The chemiluminescence micro-fluidic chip of upper any embodiment；Wherein, chemiluminescence micro-fluidic chip is mounted in apparatus frame；Liquid
Driving device is connected with the liquid driven power entrance of chemiluminescence micro-fluidic chip, substrate luminescent solution storage pool and substrate luminescent solution
Entrance can be connected to on-off, and cleaning solution storage pool can be connected to on-off with filter washing water inlet；Detection device is physical and chemical for receiving area
Learn the chemiluminescence signal for the detection zone that shines；Liquid identification device is located at Liquid identification site, the position of magnet and magnetic mark
It is corresponding that secondary antibody embeds area.
Optionally, liquid driving device is plunger pump；Be respectively equipped on substrate luminescent solution storage pool, cleaning solution storage pool with
The opening of outside air connection.
The above is preferred embodiments of the present invention, it is noted that for the ordinary skill of the art
For personnel, without departing from the principle of this utility model, several improvements and modifications can also be made, these are improved and profit
Decorations are also considered as the protection scope of the utility model.
Claims (22)
1. a kind of chemiluminescence micro-fluidic chip, which is characterized in that including chip body and be arranged in the chip body
Injection port, liquid driven power entrance, substrate luminescent solution entrance, filter washing water inlet, substrate luminescent solution subchannel, cleaning solution branch it is logical
Road, main fluid passageway and multiple functional areas；The main fluid passageway is connected to the multiple functional areas；
The multiple functional areas include the enzyme mark primary antibody embedding area being sequentially communicated by the main fluid passageway, the embedding of magnetic mark secondary antibody
Area and chemiluminescence detection area；Wherein, enzyme mark primary antibody embedding area is embedded with enzyme mark primary antibody；Magnetic mark secondary antibody embedding area packet
It is embedded with magnetic mark secondary antibody；Meanwhile magnetic mark secondary antibody embedding area is liquid quantitative area；
The injection port is connected to the main fluid passageway respectively with the liquid driven power entrance, and the driving force entrance is used for
Liquid driving device is connected to drive liquid to flow in or out the functional areas；One end of substrate luminescent solution subchannel and institute
The connection of substrate luminescent solution entrance is stated, the other end is connected to the inlet in magnetic mark secondary antibody embedding area, and substrate luminescent solution is through institute
State substrate luminescent solution entrance, substrate luminescent solution subchannel enters magnetic mark secondary antibody embedding area and quantified；The cleaning solution branch
The one end in channel is connected to the filter washing water inlet, and the other end is connected to the inlet in magnetic mark secondary antibody embedding area, is cleaned
Liquid enters magnetic mark secondary antibody embedding area through the filter washing water inlet, cleaning solution subchannel and carries out magnetic bead cleaning.
2. chemiluminescence micro-fluidic chip according to claim 1, which is characterized in that the liquid driving device is plunger
Pump.
3. chemiluminescence micro-fluidic chip according to claim 1, which is characterized in that the enzyme mark primary antibody embeds Qu Yewei
Liquid quantitative area；Dilution entrance and dilution subchannel are additionally provided in the chip body；The one of the dilution subchannel
End is connected to the dilution entrance, and the other end is connected to the inlet in enzyme mark primary antibody embedding area, sample diluting liquid warp
The dilution entrance, dilution subchannel enter enzyme mark primary antibody embedding area and are quantified.
4. chemiluminescence micro-fluidic chip according to claim 1, which is characterized in that the functional areas further include that sample is fixed
Area is measured, the sample amounts area is also liquid quantitative area, and fluid sample flows into the sample amounts area through injection port and quantified；
The sample amounts area is located at the upstream in enzyme mark primary antibody embedding area；
The air subchannel for being additionally provided with air intake on the chemiluminescence micro-fluidic chip and communicating therewith, the air branch are logical
The one end in road is connected to the air intake, and the main fluid between the other end and the sample amounts area and the injection port is logical
Road connection, the other end of air subchannel and the connectivity part of main fluid passageway are adjacent to sample amounts area.
5. chemiluminescence micro-fluidic chip according to any one of claims 1 to 4, which is characterized in that the liquid is fixed
Measuring area has scheduled volume, and Liquid identification site is provided at the liquid outlet in liquid quantitative area, need to liquid quantitatively from
The inlet in the liquid quantitative area flows into the liquid quantitative area, full of reaching the liquid outlet behind the liquid quantitative area.
6. chemiluminescence micro-fluidic chip according to claim 5, which is characterized in that at the inlet in liquid quantitative area
It is provided with Liquid identification site.
7. chemiluminescence micro-fluidic chip according to claim 1, which is characterized in that the chemiluminescence detection area has
Scheduled volume, and Liquid identification site is provided at the liquid outlet in the chemiluminescence detection area, liquid warp to be detected
The inlet in the chemiluminescence detection area flows into the chemiluminescence detection area, full of reaching behind the chemiluminescence detection area
Liquid outlet, the volume in the chemiluminescence detection area are less than or equal to the volume in magnetic mark secondary antibody embedding area.
8. chemiluminescence micro-fluidic chip according to claim 7, which is characterized in that the chemiluminescence detection area into
Liquid identification site is also equipped at liquid mouth；The volume in the chemiluminescence detection area is equal to the appearance in magnetic mark secondary antibody embedding area
Product.
9. chemiluminescence micro-fluidic chip according to claim 5, which is characterized in that the Liquid identification site is for fixed
Position is set to the Liquid identification device outside the chemiluminescence micro-fluidic chip；The Liquid identification device includes that light source generates mould
Block and photoelectric sensor；
The Liquid identification site includes upper site for positioning the light source generation module and for positioning the light inductance
The lower site of device is answered, the upper site and the lower site are respectively arranged on the outside of the chip body, the upper site and institute
Position and the corresponding liquid outlet or inlet for stating lower site are corresponding, so that the light source generation module after positioning, corresponding
Liquid outlet or inlet, the perpendicular line of the photoelectric sensor successively lay.
10. chemiluminescence micro-fluidic chip according to claim 1, which is characterized in that the side the liquid quantitative Qu Weiliu
Shape structure.
11. chemiluminescence micro-fluidic chip according to claim 1, which is characterized in that the feed liquor in the liquid quantitative area
The width of mouth is 0.3-3mm, and the height of inlet is 0.3-3mm；The width of the liquid outlet in the liquid quantitative area is 0.3-
3mm, the height of liquid outlet are 0.3-3mm；Or
The surface in the liquid quantitative area is the surface formed after hydrophilic surface is modified；The feed liquor in the liquid quantitative area
The width of mouth is 0.3-5mm, and the height of inlet is 0.3-3mm；The width of the liquid outlet in the liquid quantitative area is 0.3-
5mm, the height of liquid outlet are 0.3-3mm；Or
The surface in the liquid quantitative area is the surface formed after hydrophobic surface is modified, the feed liquor in the liquid quantitative area
The width of mouth is 0.3-2mm, and the height of inlet is 0.3-3mm；The width of the liquid outlet in the liquid quantitative area is 0.3-
2mm, the height of liquid outlet are 0.3-3mm.
12. chemiluminescence micro-fluidic chip according to claim 1, which is characterized in that the chip body includes top plate
And bottom plate；The top plate and bottom plate stacking connect；The bottom plate is smooth plate, be provided on the top plate micropore,
Microchannel or microcavity body are to form the injection port, liquid driven power entrance, substrate luminescent solution entrance, cleaning solution with the bottom plate
Entrance, substrate luminescent solution subchannel, cleaning solution subchannel, main fluid passageway or functional areas.
13. chemiluminescence micro-fluidic chip according to claim 4, which is characterized in that the injection port and the sample
It is equipped with Whole Blood Filtration area between quantification area, is equipped with whole blood filter membrane in the Whole Blood Filtration area.
14. chemiluminescence micro-fluidic chip according to claim 1, which is characterized in that magnetic mark secondary antibody embedding area
Above and below respectively lay the fixed site of the magnet for phase magnet, the fixed sites of two magnet correspond to the magnetic mark
The diagonally opposing corner that secondary antibody embeds area is laid.
15. chemiluminescence micro-fluidic chip according to claim 1, which is characterized in that enzyme mark primary antibody embedding area and
First, which is equipped with, between magnetic mark secondary antibody embedding area mixes channel；The magnetic mark secondary antibody embedding area and the chemiluminescence detection area
Between be equipped with second mix channel.
16. chemiluminescence micro-fluidic chip according to claim 1, which is characterized in that the injection port and the liquid
Driving force entrance is separately positioned on the both ends of the main fluid passageway.
17. chemiluminescence micro-fluidic chip according to claim 1, which is characterized in that substrate luminescent solution subchannel
The other end and the connectivity part of inlet in magnetic mark secondary antibody embedding area be located at the main fluid passageway neighbouring with the inlet
On.
18. chemiluminescence micro-fluidic chip according to claim 1, which is characterized in that the cleaning solution is through the cleaning
Liquid entrance, cleaning solution subchannel enter magnetic mark secondary antibody embedding area and are quantified；The other end of the cleaning solution subchannel with
The connectivity part of the inlet in magnetic mark secondary antibody embedding area is located in the main fluid passageway neighbouring with the inlet.
19. the chemiluminescence micro-fluidic chip according to any one of claim 6~8, which is characterized in that the liquid is known
Other site is used to position the Liquid identification device being set to outside the chemiluminescence micro-fluidic chip；The Liquid identification device packet
Include light source generation module and photoelectric sensor；
The Liquid identification site includes upper site for positioning the light source generation module and for positioning the light inductance
The lower site of device is answered, the upper site and the lower site are respectively arranged on the outside of the chip body, the upper site and institute
Position and the corresponding liquid outlet or inlet for stating lower site are corresponding, so that the light source generation module after positioning, corresponding
Liquid outlet or inlet, the perpendicular line of the photoelectric sensor successively lay.
20. chemiluminescence micro-fluidic chip according to claim 1, which is characterized in that the volume of the injection port is
10ul-300ul；The volume in enzyme mark primary antibody embedding area is 5-50ul；The volume in magnetic mark secondary antibody embedding area is 10-
200ul；The volume in the chemiluminescence detection area is 10-200ul.
21. a kind of analysis instrument with chemiluminescence micro-fluidic chip, which is characterized in that shine including apparatus frame, substrate
Described in liquid storage pool, cleaning solution storage pool, liquid driving device, magnet, Liquid identification device, detection device and claim 1
Chemiluminescence micro-fluidic chip；Wherein, the chemiluminescence micro-fluidic chip is mounted in the apparatus frame；The liquid
Driving device is connected with the liquid driven power entrance of the chemiluminescence micro-fluidic chip, the substrate luminescent solution storage pool and institute
Stating substrate luminescent solution entrance can be connected to on-off, and the cleaning solution storage pool can be connected to on-off with the filter washing water inlet；Institute
Detection device is stated for receiving the chemiluminescence signal for handling the chemiluminescence detection area；The Liquid identification device is located in
At the Liquid identification site, the position of the magnet is corresponding with magnetic mark secondary antibody embedding area.
22. the analysis instrument according to claim 21 with chemiluminescence micro-fluidic chip, which is characterized in that the liquid
Body drive is plunger pump；It is respectively equipped on the substrate luminescent solution storage pool, cleaning solution storage pool and is connected to outside air
Opening.
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| CN108519373A (en) * | 2018-04-27 | 2018-09-11 | 广州万孚生物技术股份有限公司 | A kind of chemiluminescence micro-fluidic chip and the analytical instrument containing it |
| CN108704677A (en) * | 2018-04-27 | 2018-10-26 | 广州万孚生物技术股份有限公司 | A kind of micro-fluidic chip and the analytical instrument containing it |
| CN110346585A (en) * | 2019-07-10 | 2019-10-18 | 深圳金迈隆电子技术有限公司 | A kind of on piece laboratory testing method and system |
| CN111693515A (en) * | 2020-05-07 | 2020-09-22 | 四川轻化工大学 | Flow type electrochemical luminescence real-time detection device and detection method |
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