CN108642141A - Nucleic acid detection reagent mixing adding set - Google Patents
Nucleic acid detection reagent mixing adding set Download PDFInfo
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- CN108642141A CN108642141A CN201810585901.XA CN201810585901A CN108642141A CN 108642141 A CN108642141 A CN 108642141A CN 201810585901 A CN201810585901 A CN 201810585901A CN 108642141 A CN108642141 A CN 108642141A
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- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6813—Hybridisation assays
- C12Q1/6834—Enzymatic or biochemical coupling of nucleic acids to a solid phase
- C12Q1/6837—Enzymatic or biochemical coupling of nucleic acids to a solid phase using probe arrays or probe chips
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Abstract
The present invention relates to a kind of nucleic acid detection reagent mixing adding sets, including：Sample chamber unit in centre position is set, stores the sample of nucleic acid being added, and by sample of nucleic acid decile under turning effort；It is connected to the sample chamber unit, and sample of nucleic acid is introduced to the first siphon valve of reaction chamber unit by siphonage；Chamber unit is reacted, is arranged in marginal position, sample of nucleic acid is mixed to reagent and carried out nucleic acid reaction, the reative cell for reacting chamber unit is also communicated with the second siphon valve；Import unit is stored with the reagent for reacting chamber unit connection, it is stored with reaction reagent, after importing sample of nucleic acid in reaction chamber unit, reaction reagent is imported into reaction chamber unit, can be detected for various blood diseases so that reaction reagent is reacted with sample of nucleic acid.The high degree of automation of present device, operating personnel only need single sampling that can realize that the detection of nucleic acid, control accuracy are high.
Description
Technical field
The present invention relates to field of nucleic acid detection more particularly to a kind of nucleic acid detection reagent mixing adding sets.
Background technology
In the prior art, with the fast development of gene sequencing technology, gene sequencing is sequenced from traditional genetic chip
High-throughput gene sequencing till now.Currently, gene sequencing system and device achieve considerable progress in all fields,
But it, which develops, is still within the starting stage, and various aspects are improved and innovated there is still a need for continuous.
Gene sequencing equipment in the prior art, the instrument for measuring gene order comprising data processing equipment and
Nucleic acid detection apparatus.The data processing equipment, connect with nucleic acid detection apparatus, for providing user interface and being referred to according to control
Enable the work of control nucleic acid detection apparatus, and the working condition of show nucleic acid detection device；The nucleic acid detection apparatus, for into
Row gene sequencing.Wherein, nucleic acid detection apparatus includes：Sequencing reaction small chamber, liquid transmission assembly, temperature control component, displacement component
With adopt figure component, the sequencing reaction small chamber is separately connected with liquid transmission assembly, temperature control component and displacement component, for into
Row sequencing reaction；The liquid transmission assembly, for transmitting liquid to sequencing reaction small chamber according to control instruction；The temperature control group
Part, the temperature for adjusting sequencing reaction small chamber；The displacement component, the position for adjusting sequencing reaction small chamber；It is described to adopt
Figure component, the sequencing image for acquiring sequencing reaction small chamber.In the technical solution, user can only be handled by operation data and be filled
The working condition of the various components to know nucleic acid detection apparatus is set, it is inconvenient for use.
However, nucleic acid detection apparatus in the prior art can only be mixed and detected to the nucleic acid of single kind, especially
It can not carry out automatically controlling different reagents for different reaction temperatures and time, so that different nucleic acid is according to reality
Reaction sequential and temperature reacted automatically.
Invention content
The purpose of the present invention is to provide a kind of nucleic acid detection reagent mixing adding sets, to overcome above-mentioned technology to lack
It falls into.
To achieve the above object, the present invention provides a kind of nucleic acid detection reagent mixing adding set, including：
Sample chamber unit in centre position is set, stores the sample of nucleic acid being added, and by nucleic acid under turning effort
Sample decile；It is connected to the sample chamber unit, and sample of nucleic acid is introduced to the first rainbow of reaction chamber unit by siphonage
Inhale valve；Chamber unit is reacted, is arranged in marginal position, sample of nucleic acid is mixed with reagent and carries out nucleic acid reaction, reative cell
The reative cell of unit is also communicated with the second siphon valve；Import unit is stored with the reagent for reacting chamber unit connection, is stored with
Reaction reagent after importing sample of nucleic acid in reaction chamber unit, imports reaction reagent, so that reaction reagent into reaction chamber unit
It is reacted with sample of nucleic acid；
Wherein, the sample chamber unit includes being arranged in the sample room in centre position, being connected to and be arranged in sample with sample room
Sample split channel that this outdoor is enclosed, several for being arranged on the outside of the sample split channel and being connected to sample split channel
The locellus such as sample, sample of nucleic acid under the first preset rotation speed from sample room by centrifugation force effect, be discharged to sample split channel
In, and flowed in sample split channel, continue outer layers movement under the influence of centrifugal force, respectively enters each sample decile
It is indoor.
Further, the sample room is eccentric structure, and sample of nucleic acid is in sample room's rotary course, to what is be relatively large in diameter
One side collects, and sample of nucleic acid collects to gap direction and flows to sample split channel from there；The lateral wall of the sample room is
The lateral wall of one arcwall, sample room gradually extends to center of circle side to form the inclined of sample room along clockwise direction since gap
Core structure is near the position in the sample room center of circle in arcwall end.
Further, sample of nucleic acid flows upward to the sample split channel by the gap, sample split channel with
Step surface is set between sample room, the height of sample split channel is higher than the height of sample room, meanwhile, the height of the locellus such as sample
Higher than the height of sample split channel.
Further, the first siphon valve has been connected in the end of the locellus such as each sample, to by sample etc.
Indoor sample of nucleic acid is divided to import the reative cell, when the first pre-set velocity rotates, sample of nucleic acid enters sample for the sample room
In this grade locellus, extra sample enters the first waste liquid chamber；The sample room stops operating, and sample in the locellus such as sample flows into the
In one siphon valve and it is full of the first siphon valve.
Further, first siphon valve includes the first siphon for being connected to locellus such as the samples and extending outward
Section is connected to the first siphon section and the second siphon section circumferentially and the second siphon section and the third rainbow that extends inwardly
The 4th siphon section for inhaling section, being set up in parallel and extend outward with third siphon section, third siphon section and the 4th siphon section it
Between be segmental arc, realize transition between tetra- siphon sections of third siphon Duan Yu, further include being connected to inclination with the 4th siphon section
The 5th siphon section extended outward is connected to the 6th siphon section that radially side extends, the 6th siphon with the 5th siphon section
The end of section is connected to the first reservoir of the reative cell.
Further, described device further includes the second siphon valve being connected to the reative cell, the second siphon valve packet
It includes and is connected to reative cell and the 7th siphon section that radially layer extends, is connected to the 7th siphon section the 8th siphon circumferentially
Section be connected to the 8th siphon section and the 9th siphon section of side extension, and arranged side by side, the edge with the 9th siphon section radially inward
The tenth siphon section that radially outward side extends, is additionally provided with the segmental arc of transition between nine siphon Duan Yu, ten siphon sections, the
The end of ten siphon sections is connected to the second waste liquid chamber.
Further, the reagent storage import unit includes the interior loading paraffin close to the paraffin wax room in centre,
Plugging action from when low temperature；One end of the paraffin wax room is also communicated with third exhaust passage, to arrange the indoor gas of paraffin wax
Go out the liquid smooth flow that can make in channel.
Further, the paraffin room, connect with two side-by-side branch, the first mineral oil is wherein set in the first branch
Room is inside mounted with mineral oil, and is connected to second siphon valve by the second connecting pipeline, is heated to paraffin
Afterwards, mineral oil flows to the second siphon valve along the second connecting pipeline, and full of the second siphon valve to block in one end of reative cell.
Further, the second branch upper edge chip radial direction set gradually from inside to outside the second mineral grease chamber, reagent chamber,
Primer room is connected between three by pipeline, inside stores mineral oil, LAMP reagents and primer respectively, logical in primer room one end
It crosses third pipeline to be connected to reative cell, melt after heating paraffin, centrifugation power drive dormant oil flowing, and then mineral oil pushes LAMP
Reagent, primer enter reative cell.
Further, the sample split channel is most annulus, and the end of most annulus is provided with the first catheter,
The end of first catheter is connected to the first waste liquid chamber, and the first waste liquid chamber is loading waste liquid.
The beneficial effects of the present invention are reaction chip of the present invention includes being arranged in centre position compared with prior art
Sample chamber unit stores the sample of nucleic acid being added, and by sample of nucleic acid decile under turning effort；With the sample chamber unit
Connection, and sample of nucleic acid is introduced to the first siphon valve for reacting chamber unit by siphonage, wherein the setting of the first siphon valve exists
On the downside in chip middle level；Chamber unit is reacted, the marginal position of layer in the chips is set, with the examination for reacting chamber unit connection
Agent stores import unit.The present invention chip can realize the function of detection of nucleic acids, can be examined for various blood diseases
It surveys, the high degree of automation of equipment, operating personnel only need single sampling that can realize the detection of nucleic acid；One single chip can be same
When detect a variety of viral nucleic acids, researcher according to the increase in demand of actual use or can reduce detection unit；Collect on chip
It is low to the skill set requirements of operating personnel at system for pretreating sample while low to the environmental requirement used, do not need dedicated core
Sour testing laboratory；It is designed with paraffin valve and capillary valve on chip, valve can be realized by controlling temperature and rotating speed
It opens and is closed, to control the order flowing of different samples；On detection device there is temperature control system can be directed to LAMP
Reaction and PCR reactions realize that temperature control, lamp reactions need temperature to be maintained at 65 degree, and PCR reactions need to realize the week of temperature
Phase property changes, and the alternating variation of temperature is realized in the collective effect of heating chip and refrigerating chip.
In particular, sample room's side wall makes sample room that there is eccentric structure, enhancing sample of nucleic acid to exist by the way that involute shape is arranged
Movement under centrifugal action makes the nucleic acid in flowing in particular, forming gap by the both ends of sample room's side wall of involute shape
Sample pours into rapidly sample split channel in superfine narrow passage, quickly to be shunted to sample of nucleic acid.Furthermore sample shunting is logical
The height in road is higher than the height of sample room, meanwhile, the height of the locellus such as sample is higher than the height of sample split channel, passes through setting
Primary raised structure avoids sample of nucleic acid from generating irregular flowing when not rotated, moreover, passing through gradually raised knot
Structure, it may be convenient to realize that specified and sample of nucleic acid flows by controlling the rotating speed of sample room, such as pass through first default turn
Sample of nucleic acid is discharged into sample split channel by speed from sample room, and sample split channel is discharged into sample etc. by the second preset rotation speed
Locellus facilitates control.
Further, the first siphon valve of the invention is extended past from locellus such as samples to the extension of chip radially inner side, core
Piece radial outside extends, until being connected to reative cell；Second siphon valve from reative cell extend past to chip radially inner side extend,
Outside extends, until being connected to the second waste liquid chamber.The present invention makes sample of nucleic acid enter the locellus such as sample by the first pre-set velocity,
By stopping, so that sample is entered the first siphon valve, so that the sample of the locellus such as sample is passed through the first siphon by the second pre-set velocity
Valve enters reative cell, prevents waste liquid from by the second siphon valve, by stopping, capillary force makes waste liquid fill in the second pre-set velocity
Full second siphon valve, makes waste liquid pass through the second siphon valve and is discharged into the second waste liquid chamber by third pre-set velocity, and therefore, the present invention is logical
The rotation and stopping for crossing interval, make sample of nucleic acid sequentially reach predeterminated position, also, sequentially complete required movement, and control is accurate
It is coherent.
Further, for the present invention by paraffin in low temperature and high temperature melt two states, storage respectively blocks reaction reagent
And primer, centrifugal force can make reaction reagent and primer enter reative cell reaction after thawing, meanwhile, pass through the mineral at reative cell both ends
Oil is blocked, it is ensured that reative cell normal reaction.Due to only need by heating can be completed state conversion, reacted automatically,
Meanwhile the second siphon valve is set on reaction chip middle level, the mineral oil of one of branch passes through the second siphon valve from one end
Reative cell is blocked, another branch by reaction reagent and primer push-in reative cell reaction, and passes through mine under the promotion of centrifugal force
Object oil sealing is stifled, realize automatic reaction, automatic-sealed effect.
Further, in the present invention, import the first siphon valve setting layer bottom surface in the chips of sample of nucleic acid, storage and
Layer top surface in the chips is arranged in the reagent storage import unit and the second siphon valve for importing reaction reagent, passes through layer in the chips
Liquid guiding structure is arranged in tow sides, has saved chip middle space, meanwhile, avoid the interference between liquid, reaction control
System is accurate.
Description of the drawings
Fig. 1 is the structural schematic diagram on the chip upper layer of the nucleic acid detection reagent mixing adding set of the present invention；
Fig. 2 is the structural schematic diagram of the chip lower layer of the nucleic acid detection reagent mixing adding set of the present invention；
Fig. 3 is the overall structure diagram of the chip of the present invention；
Fig. 4 is the first structure schematic diagram in the chip middle level of the nucleic acid detection reagent mixing adding set of the present invention；
Fig. 5 is the structure in the chip middle level with the first siphon valve of the nucleic acid detection reagent mixing adding set of the present invention
Schematic diagram；
Fig. 6 is second structural schematic diagram in the chip middle level of the nucleic acid detection reagent mixing adding set of the present invention；
Fig. 7 is the structural schematic diagram of the sample chamber unit of the present invention；
Fig. 8 is the first siphon valve structural schematic diagram of the present invention；
Fig. 9 is that the reagent in the chip middle level of the present invention stores the structural schematic diagram of import unit；
Figure 10 is the structural schematic diagram of reative cell of the present invention；
Figure 11 is the first schematic diagram of chip of the present invention reaction；
Figure 12 is the second schematic diagram of chip of the present invention reaction；
Figure 13 is the third schematic diagram of chip of the present invention reaction；
Figure 14 is the 4th schematic diagram of chip of the present invention reaction；
Figure 15 is the structural schematic diagram of the nucleic acid detection apparatus of the present invention；
Figure 16 is the half section structure diagram of the nucleic acid detection apparatus of the present invention；
Figure 17 is the structural schematic diagram of the temperature control modules of the nucleic acid detection apparatus of the present invention.
Specific implementation mode
Below in conjunction with attached drawing, the forgoing and additional technical features and advantages are described in more detail.
The preferred embodiment of the present invention described with reference to the accompanying drawings.It will be apparent to a skilled person that this
A little embodiments are used only for explaining the technical principle of the present invention, it is not intended that limit the scope of the invention.
It should be noted that in the description of the present invention, the instructions such as term "upper", "lower", "left", "right", "inner", "outside"
Direction or the term of position relationship be direction based on ... shown in the drawings or position relationship, this is intended merely to facilitate description, and
It is not instruction or implies that described device or element must have a particular orientation, with specific azimuth configuration and operation, therefore not
It can be interpreted as limitation of the present invention.In addition, term " first ", " second " are used for description purposes only, and should not be understood as indicating
Or imply relative importance.
In addition it is also necessary to explanation, in the description of the present invention unless specifically defined or limited otherwise, term " peace
Dress ", " connected ", " connection " shall be understood in a broad sense, for example, it may be being fixedly connected, may be a detachable connection, or integrally
Connection；It can be mechanical connection, can also be electrical connection；Can be directly connected, can also indirectly connected through an intermediary,
It can be the connection inside two elements.To those skilled in the art, it can understand that above-mentioned term exists as the case may be
Concrete meaning in the present invention.
It please refers to Fig.1, shown in 2,3, is respectively the chip for the nucleic acid detection reagent mixing adding set that Fig. 1 is the present invention
Upper layer, chip lower layer structural schematic diagram；And the overall structure diagram of chip.The overall structure packet of the chip of the present embodiment
Chip upper layer 1, chip lower layer 3 and chip middle level 2 are included, chip upper layer 1, chip middle level 2 and chip lower layer 3 are sequentially arranged, and
Setting FTA cards 4 and the dependency structure of loaded reagent, nucleic acid in layer 2 in the chips.It is arranged on chip upper layer 1
Three layers of chip are fixed as one by upper layer location hole 13, under the die setting lower layer location hole 13 on layer 3 by vacuum thermal bonding
Body.It is provided with upper layer gas vent 12 on chip upper layer 1, the gas in chip is discharged.On upper layer, the intermediate position of chip 1 is also
It is provided with well 11, sample of nucleic acid to be added into chip middle level 2, chip mixes nucleic acid and reagent to be added by rotating
It closes.
It is the first of the chip middle level of the nucleic acid detection reagent mixing adding set of the present invention shown in Fig. 4,5,6
Structural schematic diagram, the structural schematic diagram in chip middle level with the first siphon valve, chip middle level the second structural schematic diagram.This reality
The chip middle level 2 for applying example includes：Sample chamber unit 21 in centre position is set, stores the sample of nucleic acid being added, and revolving
It transfers to sample of nucleic acid decile with lower；It is connected to the sample chamber unit, and sample of nucleic acid is introduced by siphonage and is reacted
At least two first siphon valves 26 of chamber unit, wherein the setting of the first siphon valve 26 is in the chips on the downside of layer 2；Reaction
Chamber unit is arranged the marginal position of layer 2 in the chips, sample of nucleic acid is mixed with reagent and carries out nucleic acid reaction；With it is anti-
The reagent storage import unit 25 that chamber unit is connected to is answered, reaction reagent is stored with, nucleic acid sample is imported in reaction chamber unit
After this, reaction reagent is imported into reaction chamber unit, so that reaction reagent is reacted with sample of nucleic acid.
In conjunction with shown in Fig. 7, for the structural schematic diagram of the sample chamber unit of the present invention；Sample chamber unit includes being arranged in
Between position sample room 211, be connected to sample room and be arranged sample room periphery sample split channel 212, be arranged described
The locellus 213 such as several samples being connected on the outside of sample split channel and with sample split channel；The sample of nucleic acid of the present embodiment
It is discharged in sample split channel 212 by centrifugation force effect from sample room 211 under certain rotating speed, and is shunted in sample
Flowing in channel 212 continues outer layers movement, respectively enters in the locellus such as each sample 213 under the influence of centrifugal force.When
So, the setting of the locellus such as sample of the present embodiment 213 at least three, such as four, five, six, could realize the sample of the present embodiment
The effect of this decile can also realize that the present embodiment adds the priority of multiple nucleic acids sample respectively.
Shown in Fig. 7, in order to further enhance the movement of sample room 211 under the action of the centrifugal force, the present embodiment
Sample room 211 be eccentric structure, that is, the edge of the horizontal cross-section of sample room 211 be involute-type or radius it is increasing
Shaped form, to enhance centrifugal action.Sample of nucleic acid collects in 211 rotary course of sample room to the side being relatively large in diameter,
In the present embodiment, sample of nucleic acid collects to the direction of gap 215 and flows to sample split channel 212 from there.Sample room 211
Lateral wall 210 is an arcwall, the lateral wall of sample room since gap 215 ing along clockwise direction gradually to the extension of center of circle side with
The eccentric structure for forming sample room is near the position in the sample room center of circle in the end of arcwall 210 214.In conjunction with Fig. 6 institutes
Show, sample of nucleic acid flows upward to sample split channel 212 by gap 215, in the present embodiment, sample split channel 212 with
Step surface 216 is set between sample room 211, the height of sample split channel 212 is higher than the height of sample room 211, meanwhile, sample
The height of equal locellus 213 is higher than the height of sample split channel 212.In the present embodiment, the locellus such as sample 213 are with arc
The rectangular channel at end, it is of course also possible on the one hand elliptical slot or rectangular channel, terminally positioned arcuate structure can be made in centrifugation
Have certain buffering to sample of nucleic acid with lower, on the other hand, setting arcuate structure can not residual liquid, to meet actual demand.
In the present embodiment, sample split channel 212 is most annulus, and the end of most annulus is provided with the first drain
Pipe 217, in conjunction with shown in Fig. 4, the end of the first catheter 217 is connected to the first waste liquid chamber 202, and the first waste liquid chamber 202 is filling
Carry waste liquid.At the edge of the first waste liquid chamber 202, first exhaust passage 243 is set, it is close up and down since sample room is chip middle level
Envelope, therefore first exhaust passage is set, high pressure gas is discharged when sample of nucleic acid flows, it is ensured that sample of nucleic acid smooth flow.
Specifically, sample of the present invention room side wall makes sample room have eccentric structure, enhancing by the way that involute shape is arranged
The movement of sample of nucleic acid under the action of the centrifugal makes stream in particular, forming gap by the both ends of sample room's side wall of involute shape
Sample of nucleic acid in dynamic pours into rapidly sample split channel in superfine narrow passage, quickly to be shunted to sample of nucleic acid.Furthermore
The height of sample split channel is higher than the height of sample room, meanwhile, the height of the locellus such as sample is higher than the height of sample split channel
Degree avoids sample of nucleic acid from generating irregular flowing when not rotated, moreover, passing through by the way that primary raised structure is arranged
Gradually raised structure, it may be convenient to realize that specified and sample of nucleic acid flows by controlling the rotating speed of sample room, it is such as logical
It crosses the first preset rotation speed and sample of nucleic acid is discharged into sample split channel from sample room, sample is shunted by the second preset rotation speed and is led to
Road is discharged into the locellus such as sample, facilitates control.
Fig. 8 is the first siphon valve structural schematic diagram of the present invention；It has been connected in the end of the locellus such as each sample 213
First siphon valve, the sample of nucleic acid in the locellus such as sample 213 is imported reative cell 257, chip passes through the first pre-set velocity
After rotation, sample of nucleic acid enters in the locellus such as sample 213, and extra sample enters the first waste liquid chamber 202.Chip stops operating, sample
Sample in this grade locellus flows into the first siphon valve 276 and is full of the first siphon valve, and when chip is turned with the first pre-set velocity
When dynamic, sample can not be full of the first siphon valve due to the effect of centrifugal force.Chip of the present invention is prevented by sequentially rotating and stopping
Only sample movement disorder.In order to keep the amount of liquid storage of locellus 213 such as the sample of nucleic acid stored in the first siphon valve 26 and sample suitable,
Namely keeping 257 reaction requirement suitable with reaction, bending structure is arranged in first siphon valve 26 of the present embodiment, also can further increase
Strong siphon effect.First siphon valve 26 includes the first siphon section for being connected to the locellus such as sample 213 and extending to chip outside
261, be connected to the first siphon section 261 and along chip the second siphon section 262 circumferentially, with the second siphon section 262 and to core
The third siphon section 263 extended on the inside of piece, the 4th siphon section for being set up in parallel with third siphon section 263 and extending to chip outside
264, it is segmental arc between third siphon section and the 4th siphon section, was realized between tetra- siphon sections of third siphon Duan Yu
It crosses, further includes being connected to the 5th siphon section 265 for being tilted towards and extending on the outside of chip with the 4th siphon section 264, with the 5th siphon section 265
It is connected to along chip the 6th siphon section 266 that radially outward side extends, the end of the 6th siphon section 266 and the first of reative cell 257
Reservoir 2571 is connected to.End of first reservoir 2571 as the first siphon valve 26, revolves in chip according to the first preset rotation speed
Turn after stopping, sample of nucleic acid is full of entire first siphon valve 26 under siphon principle effect.Chip is revolved according to the second pre-set velocity
Turn, due to the effect of centrifugal force, the sample of nucleic acid in the first siphon valve 26 is subject to centrifugal forces through the first reservoir 2571
Into reative cell 257, FTA cards 4 extract and adsorb the sample of nucleic acid in sample.Chip stops operating, the sample in reative cell 257
It flows into the second siphon valve 27, chip is rotated with third pre-set velocity, and the liquid in reative cell 257 flows into the second waste liquid chamber 201.
Shown in Fig. 8, second siphon valve 27 of the present embodiment includes being connected to reative cell 257 and radially to core
7th siphon section 274 of piece outer layer extension is connected to the 8th siphon section 273 along chip circumferential direction and the 8th with the 7th siphon section 274
Siphon section 273 is connected to and along chip the 9th siphon section 272 that radially-inwardly side extends, and is arranged side by side with the 9th siphon section,
Along chip the tenth siphon section 271 that radially outward side extends, transition is additionally provided between nine siphon Duan Yu, ten siphon sections
Segmental arc, the end of the tenth siphon section 271 are connected to the second waste liquid chamber 201.In conjunction with shown in Fig. 4, due to the second of the present embodiment
Waste liquid chamber 201 is collected the waste liquid for extracting acid sample, and collection waste liquid amount is larger, and the second waste liquid chamber 201 is an annular groove,
It is additionally provided with second exhaust channel 242 in one end of annular groove 201, so that liquid can enter the second waste liquid chamber.In conjunction with Fig. 9 institutes
Show, the second waste liquid chamber 201 and the connectivity part in second exhaust channel 242 also set up interim reservoir 2421, so that it is smoothly vented.
The second pipe 254 being connected to reagent storage import unit is also set up in the tenth siphon section 271.
Specifically, first siphon valve of the present embodiment from the locellus such as sample extend past to chip radially inner side extend,
Chip radial outside extends, until being connected to reative cell；Second siphon valve, which is extended past from reative cell to chip radially inner side, to be prolonged
It stretches, outside extension, until being connected to the second waste liquid chamber.The present invention makes sample of nucleic acid enter sample decile by the first pre-set velocity
Room, chip material is hydrophilic material, and after chip stops operating, capillary force makes sample enter the first siphon valve, and the first siphon valve is opened
It opens, so that the sample of the first siphon valve is entered reative cell by the second pre-set velocity, so that waste liquid is entered the by the second pre-set velocity
Two siphon valves, by stopping, capillary force makes waste liquid be full of the second siphon valve, and the second siphon valve is opened, default by third later
Speed makes the second siphon valve sample be discharged into the second waste liquid chamber, and therefore, the present invention makes sample of nucleic acid by the rotation and stopping of interval
Sequentially reach predeterminated position, also, sequentially complete required movement, controls precisely coherent.Two siphon valves are to open up in the chips
2 groove upper and lower surfaces of of layer, avoid interfering.
As shown in fig.9, it stores the structural schematic diagram of import unit for the reagent in the chip middle level of the present invention；This implementation
The reagent storage import unit 25 of example can store LAMP or PCR reaction reagents and primer, be sealed by mineral oil, paraffin,
Not up to paraffin melting temperature when, LAMP or PCR reaction reagents and primer storage in a groove, heating paraffin thawing after, from
Mental and physical efforts drive LAMP or PCR reaction reagents and primer to enter in reative cell, and are blocked by mineral oil, keep it suitable in the reaction chamber
Profit reaction.Specifically, reagent storage import unit 25 includes close to the paraffin wax room 251 at chip center position, it is interior to load stone
Wax, in low temperature from plugging action；One end of paraffin wax room 251 is also communicated with third venting channels 241, can make paraffin wax room 251,
Reagent in first mineral grease chamber 252, the second mineral grease chamber 253, reagent chamber 255, primer room 256 is smoothly flowed into specified chamber
Room.Paraffin room 251 is connect with two side-by-side branch, and the first mineral grease chamber 252 is wherein arranged in the first branch, is inside mounted with
Mineral oil, and be connected to the second siphon valve 27 by the second connecting pipeline 254, after being heated to paraffin, mineral oil is along
Two connecting pipelines 254 flow to the second siphon valve 27, and full of the second siphon valve 27 to block in one end of reative cell 257, at this
In embodiment, the first mineral grease chamber 252 is arranged along direction of the opposite paraffin room 251 far from chip center, the second connecting pipeline 254
Arrange that, in this way, when chip rotates, mineral oil can be along chip diameter along direction of the first mineral grease chamber 252 far from chip center
To centrifugation force direction flowing.Wherein, the second branch upper edge chip radial direction sets gradually the second mineral grease chamber from inside to outside
253, reagent chamber 255, primer room 256 are connected between three by pipeline, inside store mineral oil, LAMP reagents respectively and draw
Object is connected to by third pipeline 258 with reative cell 257 in 256 one end of primer room, after heating paraffin, centrifugation power drive dormant oil,
LAMP reagents, primer enter reative cell, also, mineral oil blocks in reaction the piping outside the house, to ensure that reative cell is normally anti-
It answers.
Specifically, the present invention by paraffin in low temperature and high temperature melt two states, storage respectively blocks reaction reagent
And primer, centrifugal force makes reaction reagent and primer enter reative cell reaction after thawing, meanwhile, pass through the mineral oil at reative cell both ends
It is blocked, it is ensured that reative cell normal reaction.Due to only needing that state conversion can be completed by heating, reacted automatically, together
When, the second siphon valve is set on reaction chip middle level, and the mineral oil of one of branch passes through the second siphon jam pot cover from one end
Stifled reative cell, under the influence of centrifugal force, reaction reagent and primer flow into reative cell reaction to another branch, and pass through mineral oil
Block, realize automatic reaction, automatic-sealed effect.
As shown in fig.10, it is the structural schematic diagram of reative cell of the present invention；Reative cell 257 by respectively with introduce nucleic acid
First siphon valve 26 of sample, the reagent storage and import unit for introducing reaction reagent and primer, discharge waste liquid and plugging action
The second siphon valve 27 connection, various composition is sequentially introduced, realize reaction.
It participates in shown in Figure 11-14, for the schematic diagram of chip of the present invention reaction；The mistake of chips of embodiment of the present invention reaction
Cheng Wei：
Sample of nucleic acid is added to the sample room 211 in chip middle level 2 by step a, the well 11 on chip upper layer 1；
Sample of nucleic acid is discharged into sample shunting from sample room and led to by step b successively according to the first preset rotation speed rotary chip
The locellus such as road, sample, extra sample of nucleic acid enter the first waste liquid chamber；
Step c, chip stop operating, and the sample in the locellus such as sample flows into the first siphon valve, and the first siphon valve is opened；
Step d, chip is with the second default rotation, and due to the effect of centrifugal force, the liquid in the locellus such as sample is by centrifugal force
Effect enter reative cell by the first siphon valve, FTA cards extract and adsorb the nucleic acid in sample；
Step e, chip stop operating, and the sample of nucleic acid waste liquid in reative cell flows into the second siphon valve in the second siphon valve and opens
It opens, chip is rotated with third pre-set velocity, and the sample of nucleic acid waste liquid in reative cell is under the influence of centrifugal force through the second siphon valve
Flow into the second waste liquid chamber；
Step f, according to previous step a-e, layer adds the first cleaning solution and the second cleaning solution in the chips automatically, according to sample
The locellus such as this split channel, sample, the second siphon valve, which sequentially circulate, cleans FTA cards；
Step g, chip are rotated and are heated according to the 4th pre-set velocity, will be paraffin melting, centrifuge the first branch under force effect
Middle LAMP or PCR reaction reagents and primer flow into reative cell, and are sealed reative cell by mineral oil, the second branch mineral oil in fluid
Into in the second siphon valve, waste liquid chamber is sealed；
Step h, chip is heated to be suitble to the temperature of LAMP or PCR reactions, after the completion of reaction, with fluoroscopic examination, reads anti-
Answer result.
In the present invention, layer bottom surface in the chips, storage and importing reaction is arranged in the first siphon valve for importing sample of nucleic acid
Layer top surface in the chips is arranged in the reagent storage import unit of reagent and the second siphon valve, passes through layer tow sides in the chips
Liquid guiding structure is set, chip middle space has been saved, meanwhile, the interference between liquid is avoided, reaction controlling is accurate.
Refering to fig. 1 shown in 5, for the structural schematic diagram of the nucleic acid detection apparatus of the present invention；The present embodiment device includes：With
To load the chip room of chip, chip room includes ring 54 under chip room upper cover 51, chip room middle ring 52, chip room, above-mentioned three
It is sequentially connected with from top to bottom；Further include 57, two sample-adding pumps 56 of motor being arranged in chip room side, motor 57 drives sample-adding pump
56 actions are to add sample of nucleic acid into reaction chip；Further include the radiator 50 being arranged in chip room side, to reative cell
Cool down, to control reaction chamber temperature within a preset range；Further include controller 6, setting display screen 61, control button
62, controller to the control of the rotating speed of reaction chip, temperature and motor by completing reaction test.The chip of the present embodiment
Room is arranged on a pedestal 58, and support leg 59 is arranged in pedestal lower end, to support base.Meanwhile in chip room upper cover 51 also
It is provided with the video camera 531 and ultraviolet source 53 to be recorded to reaction chip.
Refering to fig. 1 shown in 6, for the half section structure diagram of the nucleic acid detection apparatus of the present invention；The present embodiment device is also
Include the cleaning solution 71 cleaned to reaction chip, cleaning solution is loaded or adds to reaction chip by being loaded pipe 561.This reality
Apply the output end setting first pulley 571 of the motor 57 of example, connect with the second belt wheel 573 by transmission belt 572, second lead the way and
One rotary shaft 576 connects, and rotary shaft 576 connect with chip tray 521 and chip tray 521 is driven to be rotated according to pre-set velocity,
The reaction chip of the present embodiment is fixed on chip tray.Alignment sensor 63 is set in 576 lower end of the rotary shaft, to rotation
Shaft position is detected, to ensure the Stability and veracity of its movement；Bearing 574 is set on the rotary shaft, to support rotation
Shaft is additionally provided with conducting slip ring 575 on the rotary shaft, is passed through with for conducting wire.It is real in order to be carried out to the temperature of reaction chip
When monitor, temperature sensor 64 is provided on chip tray, the temperature of reaction chip is detected in real time.
Refering to fig. 1 shown in 7, for the structural schematic diagram of the temperature control modules of the nucleic acid detection apparatus of the present invention；At this
In embodiment, reaction chip is arranged in chip room middle ring 52, and support is arranged between ring 54 under chip room middle ring 52 and chip room
Plate is provided with refrigeration module and heating module in support plate, is controlled to the temperature to the reaction chip on the upside of it.It is propping up
The first heat exchanging fin 82, the second heat exchanging fin 84 are provided on fagging, the setting heating piece 83 on two heat exchanging fins；It is supporting
The first refrigeration module 85 is provided on plate；First refrigeration module 85 is also connected to by connecting tube 80 with heat conductive circulation pump 86, heat conduction
Circulating pump 86 is connected to the second refrigeration module 88；Further include circulating fan 81, cross-ventilation is generated, to freeze or heat.
Specifically, two heating modules and refrigeration module are connect with controller, temperature sensor will detect knot in real time
Fruit is transmitted in controller, and is controlled reaction chip temperature by controlling heating module and refrigeration module, to realize stone
The operations such as wax thawing；Meanwhile the start and stop of controller control motor, the addition of sample and the rotation of reaction chip are controlled, in turn
Control reaction process.
The present embodiment is more preferably accurate in order to control temperature, and the present embodiment is provided with one group of three temperature on chip tray
Sensor, three temperature sensors are respectively detected the temperature of reaction chip and are transmitted in controller, the controller 6
Chosen module is set, and the chosen module judges that the first temperature sensor, second temperature sense according to following mean operation formula
First fiducial value P of device21：
In formula, P21Indicate the first temperature sensor, second temperature sensor position the first fiducial value, r1Indicate first
The real-time sampling value of temperature sensor, r2Indicate the real-time sampling value of second temperature sensor；r3Indicate third temperature sensor
Real-time sampling value；T indicates that mean square deviation operation, I indicate integral operation.
Wherein I indicates the arbitrary integral operation based on quadratic function, and above-mentioned formula is to obtain the ratio information of integral, following
Two formula are identical, are such as based on function y=ax2, it is in (a, b) in x values, a ＜ b are any number.
The rudimentary algorithm of above-mentioned mean operation is：By obtaining the positional value of all sampled points within some period,
Integral operation and mean square deviation operation are carried out to each value in some period, ratio is then taken, show that is compared is averaged
Value.
The chosen module judges that the first temperature sensor, third temperature sensor second compare according to the following equation
Value P31：
In formula, P31Indicate the first temperature sensor, second temperature sensor position the second fiducial value, r1Indicate first
The real-time sampling value of temperature sensor, r2Indicate the real-time sampling value of second temperature sensor；r3Indicate third temperature sensor
Real-time sampling value；T indicates that mean square deviation operation, I indicate integral operation.
The chosen module judges that second temperature sensor, the third of third temperature sensor compare according to the following equation
Value P23：
In formula, P23Indicate the third fiducial value of second temperature sensor, second temperature sensor, r1Indicate that the first temperature passes
The real-time sampling value of sensor, r2Indicate the real-time sampling value of second temperature sensor；r3Indicate adopting in real time for third temperature sensor
Sample value；T indicates that mean square deviation operation, I indicate integral operation.
The P obtained by aforesaid way21、P31、P23, the difference comparsion of three fiducial values is obtained, determines whether to be more than storage
In the threshold value P of chosen module, if being more than threshold value P there are one difference, there is deviation, needs to re-start reaction chip in temperature
Heating and adjusting, to prevent chip local heating from generating deviation, especially melting needs to candle, accurately temperature controls, so that wax
Candle can melt at a suitable temperature, so that candle is melted and push mineral oil to position appropriate, mineral oil driving a reaction is made to try
In agent and primer to reative cell, detection reaction is completed.
So far, it has been combined preferred embodiment shown in the drawings and describes technical scheme of the present invention, still, this field
Technical staff is it is easily understood that protection scope of the present invention is expressly not limited to these specific implementation modes.Without departing from this
Under the premise of the principle of invention, those skilled in the art can make the relevant technologies feature equivalent change or replacement, these
Technical solution after change or replacement is fallen within protection scope of the present invention.
Claims (10)
1. a kind of nucleic acid detection reagent mixing adding set, which is characterized in that including：
Sample chamber unit in centre position is set, stores the sample of nucleic acid being added, and by sample of nucleic acid under turning effort
Decile；
It is connected to the sample chamber unit, and sample of nucleic acid is introduced to the first siphon valve of reaction chamber unit by siphonage；
Chamber unit is reacted, is arranged in marginal position, sample of nucleic acid is mixed to reagent and carried out nucleic acid reaction, reative cell list
The reative cell of member is also communicated with the second siphon valve；
Import unit is stored with the reagent for reacting chamber unit connection, is stored with reaction reagent, is imported in reaction chamber unit
After sample of nucleic acid, reaction reagent is imported into reaction chamber unit, so that reaction reagent is reacted with sample of nucleic acid；
Wherein, the sample chamber unit includes being arranged in the sample room in centre position, being connected to and be arranged in sample room with sample room
The sample split channel of periphery, several samples for being arranged on the outside of the sample split channel and being connected to sample split channel
Equal locellus, sample of nucleic acid under the first preset rotation speed from sample room by centrifugation force effect, be discharged in sample split channel, and
It is flowed in sample split channel, continues outer layers movement under the influence of centrifugal force, respectively enter each sample etc. point interior.
2. nucleic acid detection reagent mixing adding set according to claim 1, which is characterized in that the sample room is bias
Structure, sample of nucleic acid collect, sample of nucleic acid collects simultaneously to gap direction in sample room's rotary course to the side being relatively large in diameter
Sample split channel is flowed to from there；
The lateral wall of the sample room is an arcwall, and the lateral wall of sample room is since gap along clockwise direction gradually to circle
Heart side extends to form the eccentric structure of sample room, is near the position in the sample room center of circle in arcwall end.
3. nucleic acid detection reagent mixing adding set according to claim 2, which is characterized in that described in sample of nucleic acid passes through
Gap flows upward to the sample split channel, and step surface, sample split channel are arranged between sample split channel and sample room
Height be higher than the height of sample room, meanwhile, the height of the locellus such as sample is higher than the height of sample split channel.
4. nucleic acid detection reagent mixing adding set according to claim 1, which is characterized in that in each described sample etc.
The end of locellus has connected the first siphon valve, the indoor sample of nucleic acid of sample decile is imported the reative cell, institute
Sample room is stated when the first pre-set velocity rotates, sample of nucleic acid enters in the locellus such as sample, and extra sample enters the first waste liquid chamber；
The sample room stops operating, and the sample in the locellus such as sample flows into the first siphon valve under the action of siphon power and full of the
One siphon valve.
5. nucleic acid detection reagent mixing adding set according to claim 4, which is characterized in that the first siphon valve packet
It the first siphon section for being connected to locellus such as the samples and extending outward is included, is connected to the first siphon section and circumferentially
Second siphon section is set up in parallel and outward with the second siphon section and the third siphon section extended inwardly and third siphon section
The 4th siphon section extended is segmental arc between third siphon section and the 4th siphon section, in tetra- rainbows of third siphon Duan Yu
Transition is realized between suction section, further includes being connected to be tilted towards the 5th siphon section that outside extends with the 4th siphon section, with the 5th siphon
Duan Liantong the 6th siphon sections that radially side extends, the end of the 6th siphon section connect with the first reservoir of the reative cell
It is logical.
6. nucleic acid detection reagent mixing adding set according to claim 1, which is characterized in that described device further include with
Second siphon valve of reative cell connection, second siphon valve include being connected to reative cell and radially layer extends
7th siphon section is connected to the 8th siphon section circumferentially with the 7th siphon section, is connected to the 8th siphon section and side radially inward
The 9th siphon section extended, and be arranged side by side with the 9th siphon section, the tenth siphon section that radially side extends, in nine rainbows
The segmental arc of transition is additionally provided between suction ten siphon sections of Duan Yu, the end of the tenth siphon section is connected to the second waste liquid chamber.
7. nucleic acid detection reagent mixing adding set according to claim 1, which is characterized in that the reagent storage imports
Unit includes the paraffin wax room close to centre, in load paraffin, in low temperature from plugging action；One end of the paraffin wax room
It is also communicated with third exhaust passage, makes the liquid smooth flow in channel.
8. nucleic acid detection reagent mixing adding set according to claim 7, which is characterized in that the paraffin room, with simultaneously
Two branches connection of row, is wherein arranged the first mineral grease chamber in the first branch, be inside mounted with mineral oil, and connect by second
Siphunculus road is connected to second siphon valve, and after being heated to paraffin, mineral oil flows to the second rainbow along the second connecting pipeline
Valve is inhaled, and full of the second siphon valve to block in one end of reative cell.
9. nucleic acid detection reagent mixing adding set according to claim 8, which is characterized in that the second branch upper edge chip
Radial direction sets gradually the second mineral grease chamber, reagent chamber, primer room from inside to outside, is connected to by pipeline between three, in
Mineral oil, LAMP reagents and primer are stored respectively, are connected to reative cell by third pipeline in primer room one end, in heating paraffin
Shi Ronghua, the flowing of centrifugal force pulls dormant oil, and then mineral oil pushes LAMP reagents, primer to enter reative cell.
10. nucleic acid detection reagent mixing adding set according to claim 3, which is characterized in that the sample shunting is logical
Road is most annulus, and the end of most annulus is provided with the first catheter, end and the first waste liquid of first catheter
Room is connected to, and the first waste liquid chamber is loading waste liquid.
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