CN217628391U - Equipment that adaptation card box used - Google Patents

Abstract

The embodiment of the disclosure provides equipment adaptive to a card box, wherein a plurality of chambers of the card box are sealed by built-in moving parts after sample solution and reagents are placed in the chambers in advance, each chamber is independently controlled by a switch valve to realize the connection and disconnection with at least one liquid path, and the liquid path is used for transferring and guiding out liquid; the movable piece is a push-pull piston rod; the apparatus comprises: the liquid path on-off module is used for controlling the on-off valve to be opened or closed; and the liquid driving module is used for matching with the movable part to realize the transfer of liquid in the cassette when the switch valve is in an opening state. According to the technical scheme, the clamping box is configured into a sealing system, the processes of transferring, mixing, sample extracting, detecting and the like of the sample solution and the reagent in the clamping box are performed, the whole process is not in contact with the external environment, and the pollution of the external environment is avoided, so that the method is particularly suitable for the application scenes of extracting nucleic acid or extracting and detecting other samples which are easily polluted by the external environment, and the automation of the whole process is realized.

Description

Equipment for adapting to card box

Technical Field

The utility model relates to a biomedical instrument technical field, concretely relates to equipment that adaptation card box used.

Background

At present, a single liquid transfer device is mainly used in a biochemical laboratory, and the liquid transfer operation is completed through manual operation. However, aiming at the transfer and detection of pathogens of diseases such as avian influenza, novel coronavirus and the like which appear in recent years, due to the characteristics of high pathogenicity, easy infection and the like, the transfer and detection processes of the pathogens must be safe, quick and accurate, and if the existing single pipettor is continued, due to small detection flux, cross contamination is easy to occur in the extraction or detection process of a sample, so that the problems of false positive and the like are caused; the manual operation process is complex, and the probability of virus infection is easily increased by detection personnel in an open environment, so that the operation of the detection personnel in a PCR laboratory is required, and the large-scale detection requirement is not convenient to meet.

SUMMERY OF THE UTILITY MODEL

To solve the problems in the related art, embodiments of the present disclosure provide an apparatus that adapts to the use of a cartridge.

The disclosed embodiments provide an apparatus that adapts to the use of cartridges.

Specifically, a plurality of chambers of the cartridge are sealed by built-in movable parts after sample solution and reagents are placed in the chambers in advance, each chamber is independently controlled by a switch valve to realize the connection and disconnection with at least one liquid path, and the liquid paths are used for transferring and guiding out liquid; the movable piece is a push-pull piston rod;

the apparatus comprises:

the liquid path on-off module is used for controlling the on-off valve to be opened or closed;

and the liquid driving module is used for realizing the transfer of liquid in the cassette by matching with the movable part when the switch valve is in an opening state.

Optionally, the switch valve is a rotating member, and a plurality of switch valves are arranged linearly and arranged at the bottom of the cartridge.

Optionally, the liquid path switching module includes: the number and the arrangement mode of the rotary shaft array units are the same as those of the on-off valves arranged on the card box; wherein each rotating shaft included in the rotating shaft array unit is used for driving one switching valve to rotate.

Optionally, the fluid path on-off module further includes: and each driving unit independently controls one rotating shaft array unit.

Optionally, the drive unit comprises: a transmission mechanism and a sliding mechanism; the transmission mechanism is connected with the rotating shaft array unit and is fixed on the sliding mechanism.

Optionally, the transmission mechanism comprises: the driving device comprises a gear sleeved on each rotating shaft in the rotating shaft array unit, a rack in meshing transmission with the gear, and a third driving source in transmission connection with the rack.

Optionally, the liquid drive module comprises: each push rod array unit is used for being matched with a movable piece arranged in one cavity; the number and the arrangement mode of the push rod array units are the same as those of the chambers arranged on the card box.

Optionally, the liquid drive module comprises: the push rod array unit, the fourth driving source, the fifth driving source, the slide rail and the base; the base with slide rail sliding connection, the fourth drive source sets up on the base for at vertical direction drive the movable part cooperation in push rod array unit and a cavity, the fifth drive source sets up on the base, be used for at the horizontal direction drive the base slides, will push rod array unit removes to each the top of cavity.

Optionally, the apparatus further comprises: and the upper and lower machine modules are used for accommodating at least one clamping box and moving the clamping box to a position between the liquid path on-off module and the liquid driving module.

Optionally, the loader-unloader module includes: the card box holds carrier, the card box holds carrier and is rectangular frame, and the lateral wall is provided with the spacing groove, the spacing groove with the tip adaptation of card box.

Optionally, a support plate is provided on the cartridge carrier.

Optionally, the apparatus further comprises:

and the first driving source is used for controlling the upper machine module and the lower machine module to move relative to the liquid path on-off module.

Optionally, the chamber comprises two mixing chambers, the two mixing chambers being conducted by a first passageway; a sample extraction chamber is arranged in the first passage; the two mixing chambers are arranged at intervals of a preset distance, and a permanent magnet movement cavity is arranged below the sample extraction chamber.

Optionally, the apparatus further comprises:

the magnetic suction module comprises a permanent magnet and a permanent magnet driving source, and the permanent magnet driving source is used for driving the permanent magnet to enter the permanent magnet movement cavity.

Optionally, the permanent magnet drive source includes a seventh drive source and a link mechanism.

Optionally, the permanent magnet drive source is a lead screw motor.

Optionally, the apparatus further comprises:

the heating module comprises a sixth driving source and a heating external member connected with the sixth driving source, and is sleeved between the two mixing chambers.

Optionally, the liquid drive module comprises: the push rod driving device comprises a slide rail, two push rod array units, a fourth driving source, a fifth driving source and a base, wherein the fourth driving source, the fifth driving source and the base are matched with each push rod array unit; the two bases are located on two sides of the heating module and are in sliding connection with the sliding rails, the fourth driving source is arranged on each base and used for driving one push rod array unit to be matched with the moving part in the cavity on one side of the heating module in the vertical direction, and the fifth driving source is arranged on each base and used for driving the bases to slide in the horizontal direction and moving the push rod array units to the position above the cavity on one side of the heating module.

Optionally, the apparatus further comprises:

a PCR amplification instrument;

and the pressing module is matched with the card box and is used for limiting the collecting pipe in the hole groove of the PCR amplification instrument.

According to the technical scheme provided by the embodiment of the disclosure, the technical scheme of the disclosure can obtain the following beneficial effects:

this equipment of adaptation card box that openly provides, the card box is configured to sealed system, sample solution, reagent shift in the card box, mix, sample extraction, processes such as detection, whole process does not contact with external environment, avoids receiving external environment's pollution, consequently especially adapted nucleic acid extraction or other sample extraction, the application scene of detection that receive external pollution easily, the liquid way break-make module through the adaptation card box, liquid drive module have realized the automation of above-mentioned overall process.

The device for adapting the card box provided by the disclosure has the advantages of high automation degree, no dependence on a biological laboratory, no dependence on manual operation, convenience in carrying, simplicity in operation, quickness in detection and no cross contamination.

It is to be understood that both the foregoing general description and the following detailed description are exemplary and explanatory only and are not restrictive of the disclosure.

Drawings

Other features, objects, and advantages of the present disclosure will become more apparent from the following detailed description of non-limiting embodiments when taken in conjunction with the accompanying drawings. The following is a description of the drawings.

Figure 1 shows a front view of the cartridge of the present disclosure.

Figure 2 shows a schematic view of a cartridge fluid path of the present disclosure.

Figure 3 shows an exploded view of the cartridge of the present disclosure.

Fig. 4 shows a schematic structural view of the on-off valve of the present disclosure.

Fig. 5 shows a schematic structural view of the rubber stopper of the present disclosure.

Figure 6 illustrates a front view of the apparatus of the present disclosure adapted for use with a cartridge.

Figure 7 shows an exploded view of the equipment shown in figure 6 with a portion of the support frame removed.

Fig. 8 shows a schematic view of the loader module of the present disclosure.

Fig. 9 shows a schematic structural view of a cartridge carrier of the present disclosure.

Figure 10 shows a front view of the 8-gang cassette of the present disclosure.

Figure 11 illustrates a bottom view of the 8-gang cassette of the present disclosure.

Fig. 12 shows a top view of the fluid passage switching module of the present disclosure.

Fig. 13 shows a schematic structural diagram of the drive unit of the present disclosure.

Fig. 14 shows a schematic structural view of a liquid drive module of the present disclosure.

Fig. 15 shows a schematic diagram of the positional relationship of the liquid drive module of the present disclosure and the 8-gang cartridge.

Fig. 16 shows a schematic structural view of a heating module of the present disclosure.

Fig. 17 shows a schematic structural diagram of a magnetic module of the present disclosure.

Fig. 18 shows a schematic structural view of another magnetic module of the present disclosure.

Fig. 19 shows a schematic structural view of a push-down module of the present disclosure.

FIG. 20 is a schematic diagram showing the position relationship between the liquid path connection/disconnection module, the magnetic attraction module, the PCR amplification instrument and the cartridge.

It should be understood that the structural dimensions of the various components shown in the figures are not drawn to scale. Further, the same or similar reference numerals denote the same or similar components.

Detailed Description

Hereinafter, exemplary embodiments of the present disclosure will be described in detail with reference to the accompanying drawings so that those skilled in the art can easily implement them. Also, for the sake of clarity, parts not relevant to the description of the exemplary embodiments are omitted in the drawings.

In the present disclosure, it is to be understood that terms such as "including" or "having," etc., are intended to indicate the presence of the disclosed features, numbers, steps, behaviors, components, parts, or combinations thereof, and are not intended to preclude the possibility that one or more other features, numbers, steps, behaviors, components, parts, or combinations thereof may be present or added.

The same or similar reference numerals in the drawings of the present disclosure correspond to the same or similar components; in the description of the present disclosure, it is to be understood that, if there are terms such as "center", "upper", "lower", "left", "right", "horizontal", "inner", "outer", etc., indicating orientations or positional relationships based on the orientations or positional relationships shown in the drawings, the description is merely for convenience in describing the present disclosure and simplifying the description, but not for indicating or implying that the referred device or element must have a specific orientation, be constructed and operated in a specific orientation, and thus the positional relationships described in the drawings are for illustrative purposes only and are not to be construed as limitations of the present disclosure, and specific meanings of the terms may be understood by those skilled in the art according to specific circumstances. Furthermore, the terms "first," "second," "third," and the like are used merely to distinguish one element from another, and are not to be construed as indicating or implying relative importance.

Throughout the description of the present disclosure, it should also be noted that, unless expressly stated or limited otherwise, the terms "disposed," "mounted," "connected," and "coupled" are to be construed broadly, e.g., as meaning either a fixed connection, a removable connection, or an integral connection; can be mechanically or electrically connected; either directly or indirectly through intervening media, or may be interconnected between two elements. The specific meaning of the above terms in the present disclosure can be understood in specific instances by those of ordinary skill in the art.

It should be further noted that the embodiments and features of the embodiments in the present disclosure may be combined with each other without conflict. The present disclosure will be described in detail below with reference to the accompanying drawings in conjunction with embodiments.

Example 1

The present disclosure provides an apparatus adapted to be used with a cartridge, the cartridge is configured as a sealed system, for example, a plurality of chambers of the cartridge are sealed by a built-in movable member after a sample solution and a reagent are placed in the chambers in advance, each chamber is controlled by a switch valve independently to realize on/off with at least one liquid path, the liquid path is used for transferring and guiding out the liquid, when the switch valve is connected with the liquid path, the sample solution and the reagent are transferred, mixed, sample extracted and detected in the cartridge, and the whole process is not in contact with the external environment, so as to avoid being polluted by the external environment, and therefore, the apparatus is particularly suitable for nucleic acid extraction or other application scenarios of sample extraction and detection which are easily polluted by the external environment. The device comprises a liquid path on-off module of the adaptive card box, a liquid driving module of the adaptive card box and a liquid path on-off module, wherein the liquid path on-off module is used for controlling the opening or closing of the switch valve, the liquid driving module of the adaptive card box is used for realizing the transfer of liquid in the card box by matching with the moving part when the switch valve is in an opening state, and the automation of the whole process is realized by matching the liquid path on-off module, the liquid driving module and the card box.

The following examples are schematically illustrated by taking an application scenario of nucleic acid extraction as an example.

The method comprises the steps of firstly explaining the principle of extracting nucleic acid by a magnetic bead method, releasing the nucleic acid after a sample is added into a lysis solution, then carrying out specific binding on the nucleic acid by using treated magnetic beads (such as silica-based and amino-coated treatment) to form a nucleic acid-magnetic bead compound, separating the compound under the action of an external magnetic field, washing out impurities which are not specifically adsorbed by eluent, desalting, and purifying to obtain a nucleic acid substance to be extracted.

Next, a cartridge structure for extracting nucleic acid by the magnetic bead method will be described.

As shown in fig. 1 to 5, the cartridge 1 of the present disclosure includes: the device comprises a base 10 and a plurality of chambers arranged on the base 10, namely a primary sample adding pipe S11, a lysis solution chamber S12, an empty chamber S13, a first washing solution chamber S14, a second washing solution chamber S15, a first mixing chamber S21, a second mixing chamber S22, a mineral oil chamber S16, an elution solution chamber S17, a cleaning chamber S18 and a secondary sample adding pipe S19.

The base 10 comprises a base body 11 and outer shields 12 (only the outer shield on the A side is shown in FIG. 3) on the B side of the base body 11; the surface a and the surface B of the base body 11 are respectively provided with at least one groove, the outer guard 12 covers the surface a and the surface B of the base body 11, and forms at least one liquid path with the at least one groove, that is, a first path L1, a first channel L21, a second channel L22, a third channel L23, a liquid outlet channel L3, a sample quantitative channel L4, an exhaust channel L5, and a secondary sample adding channel L6. In the following description, the surface a is also referred to as the front surface of the base 10, and the surface B is also referred to as the back surface of the base 10.

The first passage L1 communicates the first mixing chamber S21 and the second mixing chamber S22, and the sample extraction chamber R1 is provided in the first passage L1; the first mixing chamber S21 and the second mixing chamber S22 are arranged at intervals of a preset distance and used for hitching and heating the module, and a permanent magnet movement cavity R2 is arranged below the sample extraction chamber R1; the first passage L21 is controlled by the on-off valve 20 to communicate the first washing chamber S14, the second washing chamber S15, and the first mixing chamber S21, respectively; the second channel L22 is controlled by the on-off valve 20 to communicate with the eluent chamber S17 and the second mixing chamber S22; the third channel L23 is respectively controlled by the switch valve 20 to be communicated with the sample suction pipe S11, the lysis liquid chamber S12, the empty chamber S13 and the first mixing chamber S21; a collecting pipe 50 is arranged at the liquid outlet of the liquid outlet channel L3 and is used for collecting the extracted nucleic acid; the sample quantitative channel L4 is respectively communicated with the second mixing chamber S22, the mineral oil chamber S16, the cleaning chamber S18 and the liquid outlet channel L3 under the control of the switch valve 20, a quantitative chamber R3 is arranged in the sample quantitative channel L4, and the quantitative pool R3 is positioned at the channel part of the mineral oil chamber S16 and the cleaning chamber S18 which are communicated under the control of the switch valve 20; the exhaust passage L5 is controlled by the on-off valve 20 to communicate the eluent chamber S17 with the collection tube 50.

A branch tube is provided on the side wall of the primary addition tube S11, a nucleic acid sample is added into the primary addition tube S11 through the branch tube, a secondary addition tube S19 is further provided at the other end of the base 10, a secondary reagent is added from the branch tube provided on the secondary addition tube S19 and introduced into the collection tube 50 through the secondary addition flow path L6, and the secondary reagent is usually a reagent that is not suitable for direct transfer in the cartridge 1, for example, a reagent that needs to be stored at a low temperature, so that the secondary reagent can be directly added into the collection tube 50 and then a sample detection is performed.

In this disclosure mode, ooff valve 20 is the rotation piece, come the break-make of each cavity and corresponding liquid way of independent control through rotating ooff valve 20, and a plurality of ooff valve 20 is linear arrangement, arrange in the bottom of card box 1, like this when parallelly connected a plurality of card boxes, form the parallelly connected ooff valve array of multichannel, through controlling one way ooff valve array, come the ooff valve of a plurality of card boxes of simultaneous control and open, realize the synchronization of the nucleic acid extraction process of a plurality of card boxes, thereby can once only detect a plurality of samples, the efficiency of nucleic acid detection has been promoted.

Referring to fig. 4, the switching valve 20 includes a valve handle 21 and a valve shaft 22. The top center of the valve shaft 22 may be provided with a first opening 221, and a valve hole 222, which may be a round or a kidney-shaped blind hole, may be formed on the sidewall near the top end of the valve shaft 22, for example, and the first opening 221 and the valve hole 222 form a through passage. It will be appreciated that the number of first openings 222 is one and forms a two-way valve or a three-way valve with the sealing plug 40.

Further, the valve stem 21 and the valve shaft 22 may be an integral structure or a split structure, for example, the valve stem 21 and the valve shaft 22 may be formed in an integral molding manner, or may also be formed in a split manner, and then the two are connected and fixed by a threaded connection or the like, which is not limited in this disclosure. The end face of the valve handle 21 may be machined to form a straight-line-shaped slot, or a slot with other shapes, which will not be described in detail in this disclosure.

The base 10 is provided at the bottom thereof with a plurality of cavities R4, and a switching valve 20 is disposed in each cavity R4. When the switch valve 20 is placed in the cavity R4, one end of the switching channel is connected to the chamber, and the other end is connected to the liquid path under the action of external force.

Referring to fig. 3 and 5, the cartridge 1 further includes: the bore seal 40 has a transfer passage received in the bore seal 40. The sealing plug 40 may be a rubber plug or a polyurethane plug, and the shape of the sealing plug 40 is adapted to the cavity R4, for example, the sealing plug has a cylindrical structure, so that the sealing plug cannot rotate relative to the cavity R4, and the blocking of the passage between the cavity and the liquid path is avoided. Of course, other suitable shapes may be used, and the present disclosure is not limited thereto. Through setting up sealing plug 40 and making the rotation of ooff valve 20 take place in sealing plug 40, can prevent that liquid from taking place to reveal from the chamber to the liquid path transfer in-process, reduced the pollution that probably receives, further promoted nucleic acid detection's accuracy.

The sealing plug 40 is of cylindrical configuration with a through hole 41 in the centre and at least one second opening 42 in the side wall. The through holes 41 are communicated with the chamber, the number of the second holes 42 is matched with the liquid paths arranged on the front surface and the back surface of the base 10, and when the liquid paths are arranged on the front surface and the back surface of the base 10 corresponding to the same chamber, the number of the second holes 42 is 2 and is respectively communicated with the liquid paths.

Referring to fig. 3, during assembly, the rubber plug 40 is first placed into the cavity R4, the valve shaft 22 is then placed into the through hole 41, the valve stem 21 is limited by the valve shaft pressing plate 13, and then the valve shaft pressing plate 13 is fixed to the bottom of the base body 11. The valve handle 21 can rotate relative to the valve shaft pressing plate 13, when the number of the first openings 42 is two, the valve 20 and the sealing plug 40 form a three-way valve, under the action of mechanical drive, the relative position of the valve hole 222 and the first openings 42 can be adjusted to be selectively communicated with one of the first openings 42, the communication between the cavity S and the second passage L2 is realized, and the blockage between the cavity S and the second passage L2 is realized when the positions of the cavity S and the second passage L2 are staggered.

In the disclosed embodiment, the steps of extracting nucleic acid using the cartridge are as follows:

s101, a preprocessing step: before the detection starts, keeping each switch valve at an initialization position, and blocking a passage with a liquid path; reagents, magnetic beads and the like required by nucleic acid extraction are pre-packaged in corresponding chambers, and moving pieces 30 such as push-pull piston rods are placed in the chambers for sealing;

for example, 750ul of lysis solution is prepackaged in the lysis solution chamber S12, 700ul of washing solution is prepackaged in each of the first washing solution chamber S14 and the second washing solution chamber S15, 50ul of mineral oil is prepackaged in the mineral oil chamber S16, 100ul of eluent is prepackaged in the eluent solution chamber S17, 600ul of magnetic bead solution is prepackaged in the first mixing chamber S21, and 600ul of ultrapure water or pure air is prepackaged in the washing chamber S18;

s102, sample adding step: the cap of the primary addition tube S11 is opened, and the collected nucleic acid sample is put into the primary addition tube by using a pipette, and the cap is closed.

S103, nucleic acid cleavage step: driving the push-pull piston rods in the first mixing chamber S21 and the second mixing chamber S22 to move, enabling the magnetic bead solution to flow back and forth between the two mixing chambers, adsorbing the magnetic beads in the sample extraction chamber R1 by using a magnet, and discharging the waste liquid into the empty chamber S13; then opening the switch valves corresponding to the primary sample adding pipe S11 and the first mixing chamber S21, transferring the sample to the first mixing chamber S21, closing the switch valve of the primary sample adding pipe S11, opening the switch valve corresponding to the lysate chamber S12, and transferring the lysate to the first mixing chamber S21; then, the push-pull piston rods in the first mixing chamber S21 and the second mixing chamber S22 are driven to move, so that the mixed liquid of the sample and the lysate is mixed, heated and cracked in the sample extraction chamber R1; the nucleic acid molecules after cracking can be adsorbed in the sample extraction chamber R1 by magnetic beads; the waste liquid is then discharged back into the lysate compartment S12;

s104, nucleic acid washing step: and (3) respectively conducting the switch valves of the first washing liquid chamber S14, the second washing liquid chamber S15 and the elution liquid chamber S17 by adopting a method similar to the step S103, so that the liquid reagents in the chambers respectively enter the first mixing chamber S21 and the second mixing chamber S22, mixing, adsorbing, cleaning and eluting are carried out, and the waste liquid after cleaning or after elution is respectively discharged into the original chambers for storage.

S105, a quantitative step: opening the corresponding switch valves at the two ends of the quantitative chamber R3 (the switch valves corresponding to the second mixing chamber S22 and the cleaning chamber S18 respectively), keeping the other switch valves in a closed state, and pushing the samples in the first mixing chamber S21 and the second mixing chamber S22 into the quantitative chamber R3 (the quantitative volume can be 5 ul) in a diamond-shaped area for example; in order to ensure that the dosing chamber R4 is filled with liquid and dosing accuracy is ensured, the present disclosure may over-push a portion of the liquid into the cleaning chamber S18.

S106, a nucleic acid transfer step: the switch valves of the second mixing chamber S22 and the cleaning chamber S18 are closed, the switch valve corresponding to the mineral oil chamber S16 and the switch valve communicated with the liquid outlet channel L3 are opened, the push-pull piston rod in the mineral oil chamber S16 is controlled to move downwards, and the sample is quantitatively discharged into the collecting pipe 50 by using mineral oil, wherein the mineral oil can also be used as a finally required reagent for covering.

S107, a secondary sample adding step: and (3) opening the tube cover of the secondary sample adding tube S19, putting a secondary reagent into the secondary sample adding tube S19 by using a liquid transfer device, and covering the tube cover. Then, the on-off valve communicated with the liquid outlet channel L3 is opened, the push-pull piston rod in the secondary sample adding pipe S19 is controlled to move downwards, and the secondary reagent is added into the collecting pipe 50.

S108, a nucleic acid detection step: the collection tube 50 is not separated from the cartridge 1, and is directly placed into a hole groove of a PCR amplification instrument for on-line detection.

The steps can also include a pipeline cleaning step, for example, before the same pipeline transfers different liquids, the pipeline can be cleaned by using ultrapure water or pure air pre-packaged in the cleaning chamber S18, and then the pipeline is transferred after cleaning, so that the cross effect of reagents can be avoided. However, this step is not essential and can be flexibly selected as required. It should be noted that, similar to the cleaning step, the quantifying step of step S105 is also an optional step, and those skilled in the art can flexibly select, for example, omit or reserve the corresponding passages and chambers, which is not limited by the present disclosure.

Example 2

As shown in fig. 6 and 7, the apparatus 100 for adapting the cartridge includes: the device comprises a support frame 110, a loading and unloading module 120, a liquid path on-off module 130, a liquid driving module 140, a heating module 150, a magnetic suction module 160 and a PCR amplification instrument 170.

It can be understood by those skilled in the art that fig. 6 and 7 exemplarily show the structure of the apparatus adapted to be used by the cartridge, wherein the support frame, the loading and unloading module, the heating module, the magnetic attraction module and the PCR amplification apparatus are all selectable modules, and any combination can be performed according to the needs, which is not limited in this disclosure.

The supporting frame 110 includes a top supporting frame 111, a bottom supporting frame 112, a supporting frame side plate 113 and a bottom plate 114, the top supporting frame 111 is fixed on a first driving source a, the first driving source a is fixed on the supporting frame side plate 113, and is used for driving the top supporting frame 111 to move towards the bottom supporting frame 112, and the bottom supporting frame 112 is located on the bottom plate 114.

The liquid driving module 140 and the heating module 150 are arranged on the top of the top plate 111a of the top support frame 111, the loading and unloading module 120 is arranged on the bottom of the top plate 111a, the liquid path on-off module 130 is arranged below the loading and unloading module 120, the liquid path on-off module 130 is fixed on the bottom support frame 112, and under the action of the first driving source a, the loading and unloading module 120, the liquid driving module 140 and the heating module 150 move towards the liquid path on-off module 130. The magnetic module 160 is disposed inside the bottom supporting frame 112, and the magnetic module 160 is located below the liquid path on-off module 130. The PCR amplifier 170 is located on one side of the bottom support 112.

In this disclosure mode, through the structural design of support frame, can combine each module for example on-off module, liquid way break-make module, liquid drive module, heating module, magnetism module, PCR amplification appearance organically, equipment compact structure on the whole is convenient for remove, can conveniently develop nucleic acid detection work at each community, check point, has greatly improved detection efficiency.

As shown in fig. 8 and 9, the boarding/alighting module 120 includes: the cartridge carrier 121 is used for accommodating at least one cartridge 1, the cartridge 1 is the cartridge shown in fig. 1, and the second driving source B is fixed on the frame 111B of the top supporting frame 111 and used for moving the cartridge carrier 121 between the liquid path opening/closing module 130 and the liquid driving module 140.

The cartridge bearing member 121 is a rectangular frame, the side wall of the cartridge bearing member 121 is provided with a limit groove 1211, the limit groove 1211 is matched with the end part of the cartridge 1, the two end parts of the cartridge 1 are aligned with the position of the limit groove 1211, so that the cartridge 1 is placed in the cartridge bearing member 121, and then the cartridge 1 moves towards the direction of the liquid path on-off module 130 under the action of the first driving source a, so that the on-off valve 20 at the bottom of the cartridge 1 is butted with a rotating shaft 1311 (see fig. 19) on the liquid path on-off module 130, which will be described later.

With continued reference to fig. 9, the cartridge carrier 121 is further provided with a support plate 1212 located near the collection tube 50 to better secure the cartridge 1.

In the present disclosure, one cartridge 1 is used for detecting one sample, and a plurality of identical cartridges 1 may be connected in parallel to form a multi-cartridge to increase the sample detection throughput, and fig. 10 shows a front view of an 8-cartridge, it is understood that the number of cartridges 1 connected in parallel is not limited to 8, and may be arbitrarily selected within the range of the number of cartridges that can be accommodated in the cartridge carrier 121 at one time.

The apparatus adapted to a multi-gang cartridge is further described below.

As shown in fig. 12, the liquid passage switching block 130 includes: a plurality of rotary shaft array units 131 fixed on the top plate 112a of the bottom support frame 112, the number and arrangement of the rotary shaft array units 131 are the same as those of the on-off valves 20 arranged on the cartridge 1; here, each of the rotary shafts 1311 included in the rotary shaft array unit 131 is used to drive one of the switching valves 20 to rotate.

Fig. 11 shows an arrangement of the on-off valves at the bottom of 8-up cartridges, wherein 8-up cartridges are arranged in the Y direction, the on-off valves 20 of each cartridge 1 are arranged in the X direction, each cartridge 1 includes 11 on-off valves 20, and fig. 12 shows an arrangement of rotary shaft array units, wherein 11 rotary shaft array units 131 are arranged in the X direction, and each rotary shaft array unit 131 includes 8 rotary shafts 1311. The 8-up cassette shown in fig. 11 is docked with the liquid passage opening/closing module 130 shown in fig. 12 in the XY direction (see fig. 19), the hole of the valve stem 21 is inserted into the rotary shaft 1311, and the rotary shaft array unit 131 is driven to rotate, thereby controlling the opening or closing of the one-way opening/closing valve array in the Y direction of the 8-up cassette.

With continued reference to fig. 13, the fluid make-and-break module 130 further includes: a plurality of driving units, each of which independently controls one of the rotation axis array units 131. The drive unit includes: a transmission mechanism connected to the rotation axis array unit 131 and fixed to the sliding mechanism. Specifically, the transmission mechanism includes: a gear (not shown) sleeved on each rotation shaft 1311 in the rotation shaft array unit 131, a rack 1312 engaged with the gear for transmission, and a third driving source C in transmission connection with the rack 1312. The slide mechanism includes: a first block 1313 and a first slide 1314, wherein the first block 1313 is slidably connected to the first slide 1314, a rack 1312 is fixed on the first block 1313, and a third driving source C drives the rack 1312 to move in the first slide 1314, thereby driving the rotating shafts in the rotating shaft array unit 131 to rotate synchronously.

Referring to fig. 14 and 15, the liquid driving module 140 includes: a slide rail 141, two push rod array units 142, fourth driving sources D1, D2 adapted to each push rod array unit 142, fifth driving sources E1, E2, a base 143. The slide rail 141 is disposed on the top supporting frame 111, and an opening for the push rod array unit 142 to move is formed on the top supporting frame 111. The two bases 143 are slidably connected with the slide rail 141, the fourth driving source D1 is disposed on each base 143, and is configured to drive one push rod array unit 142 to be matched with the movable element 30 in the primary sample adding tube S11, the lysis liquid chamber S12, the empty chamber S13, the first wash liquid chamber S14, the second wash liquid chamber S15, and the first mixing chamber S21 in the vertical direction, the fourth driving source D2 is configured to drive the other push rod array unit 142 to be matched with the movable element 30 in the second mixing chamber S22, the mineral oil chamber S16, the elution liquid chamber S17, the cleaning chamber S18, and the secondary sample adding tube S19, and the fifth driving sources E1 and E2 are disposed on each base 143, and are configured to drive the bases 143 to slide in the horizontal direction, so as to move the push rod array unit 142 above the chambers.

In this disclosure, two push rod array units 142 are adopted to adapt to the heating module 150, in some cases, the heating module 150 may be omitted and other heating methods may be adopted, and only one push rod array unit 142 may be provided, which is not described herein again.

In another embodiment, the liquid driving module 140 includes: a plurality of pushrod array units 142, each pushrod array unit 142 being adapted to cooperate with the movable element 30 housed in one of the chambers; the number and arrangement of the push rod array units 142 are the same as those of the chambers provided in the cartridge 1.

As shown in fig. 16, the heating module 150 includes: a heating kit holder 151, a heating kit 152, and a sixth driving source F. The heating kit 152 and the sixth driving source F are fixed to the heating kit holder 151, the heating kit holder 151 is fixed to the top support 111 and positioned between the two bases 143, and the heating kit 152 is fitted between the two mixing chambers, i.e., the first mixing chamber S21 and the second mixing chamber S22, and heats the mixing solution during nucleic acid extraction.

As shown in fig. 17, the magnetic module 160 includes: a permanent magnet 161 and a permanent magnet drive source 162. An opening for the permanent magnet 161 to pass through is formed in the bottom support frame 112, the permanent magnet 161 is a plurality of magnetic columns, and the permanent magnet driving source 162 is used for driving each magnetic column of the permanent magnet 161 to enter the permanent magnet movement cavity R2 of one cartridge 1. The permanent magnet driving source 162 may be a lead screw motor, or may be composed of a seventh driving source 1621 such as a pusher motor and a link mechanism 1622, as shown in fig. 18. In order to ensure the permanent magnet 161 to be tightly attached to the cartridge 1, a spring 163 is further disposed on the magnetic module 160.

Specifically, the permanent magnet 161 is fixed on the base 1611, a first upright column 1612 is arranged at the bottom of the base 1611, a sliding piece 1621 is arranged on the first upright column 1612 in a sliding manner, the lead screw motor is fixed on the permanent magnet support 1622, one end of the lead screw penetrates through the permanent magnet support 1622 and is fixed on the sliding piece 1621, a second upright column 1623 is arranged on the permanent magnet support 1622, and the base 1611 is sleeved on the second upright column 1623, and a spring 163 is arranged between the two. When the lead screw motor drives the lead screw to rotate, the slider 1621 is acted by the lead screw to drive the base 1611 to move on the second upright 1623, and at the moment, the permanent magnet 161 is far away from the permanent magnet movement cavity R2, and the spring 163 deforms. When the screw motor drives the screw to rotate in the opposite direction, the spring 163 restores to deform, the base 1611 can slide on the first upright column 1612 under the action of the spring 163, and the permanent magnet 161 enters the permanent magnet movement cavity R2 and is tightly attached to the card box 1.

Referring to fig. 7, fig. 19, and fig. 20, the apparatus further includes: the module 180 is pressed down. The pressing module 180 includes a stopper driving source 181, a stopper 182, and a link 183. The pressing module 180 is fixed to the bottom of the top plate 111a through a connector 183, and moves toward the liquid path switching module 130 together with the loader module 120, the liquid driving module 140, and the heating module 150 under the action of the first driving source a, the limiting block 182 is connected to the limiting block driving source 181, and the collecting tube 50 is tightly attached to the hole groove of the PCR amplification instrument 170 under the action of the limiting block driving source 181, so that the collecting tube 50 is uniformly heated in the hole groove. In order to ensure that the collection tube 50 is tightly attached to the hole groove of the PCR amplification apparatus 170, a spring may be further disposed on the pressing module 180, which is not limited by the present disclosure. In addition, black foam cotton can be attached to the bottom of the pressing module 180, so that the effect of shading light is achieved, and the phenomenon that light interferes with the work of the PCR amplification instrument 170 is avoided.

In the present disclosure, the first driving source a, the second driving source B, the third driving source C, the fourth driving sources D1 and D2, the fifth driving sources E1 and E2, the sixth driving source F, the permanent magnet driving source 162, and the stopper driving source 181 may be motor-driven, hydraulic-driven, or air-source-driven, and the present disclosure does not limit this.

According to an embodiment of the disclosure, the apparatus for adapting the use of a cartridge comprises: the liquid path on-off module is used for controlling the on-off valve to be opened or closed; and the liquid driving module is used for realizing the transfer of liquid in the card box by matching with the movable part when the switch valve is in an opening state, so that the automation of the processes of liquid transfer, mixing, sample extraction, detection and the like by using the card box is realized.

According to the embodiment of the disclosure, the switch valve is a rotating part, and the switch valves are linearly arranged and arranged at the bottom of the card box, when the card boxes are connected in parallel, a multi-path parallel switch valve array is formed, and the switch valves of the card boxes are simultaneously controlled to be opened by controlling the one-path switch valve array, so that the synchronization of the nucleic acid extraction process of the card boxes is realized, a plurality of samples can be detected at one time, and the efficiency of nucleic acid detection is improved.

According to an embodiment of the present disclosure, the liquid path on-off module includes: the number and the arrangement mode of the rotary shaft array units are the same as those of the on-off valves arranged on the card box; wherein, each rotating shaft included in the rotating shaft array unit is used for driving one switch valve to rotate.

For example, the 8-up cassette shown in fig. 11 is docked with the liquid passage opening/closing module 130 shown in fig. 12 in the XY direction (see fig. 19), the hole of the valve stem 21 is inserted into the rotary shaft 1311, and the rotary shaft array unit 131 is driven to rotate, thereby controlling the opening or closing of the one-way opening/closing valve array in the Y direction of the 8-up cassette.

In this disclosure, the liquid path connection/disconnection module further includes: and each driving unit independently controls one rotating shaft array unit.

Specifically, the driving unit includes: a transmission mechanism and a sliding mechanism; the transmission mechanism is connected with the rotating shaft array unit and is fixed on the sliding mechanism. The transmission mechanism includes: the gear, with the rack of gear engagement transmission and the third driving source that is connected with the rack transmission of every rotation axis in the rotation axis array unit of cover locating. The third driving source drives the rack to move in the sliding mechanism, thereby driving the rotary shafts in the rotary shaft array unit to rotate synchronously to open or close the switching valve.

According to an embodiment of the present disclosure, the liquid driving module includes: each push rod array unit is used for being matched with a movable piece arranged in one cavity; the number and the arrangement mode of the push rod array units are the same as those of the chambers arranged on the card box. Under the condition that the switch valves matched with the two chambers are opened, the push rod array unit in one chamber is controlled to apply acting force to the movable piece, and the liquid in the chamber is transferred into the other chamber by utilizing the positive pressure in the chamber. Similarly, the liquid in the other chamber is transferred into the chamber by controlling the push rod array unit in the other chamber to apply acting force on the movable piece.

According to an embodiment of the present disclosure, the liquid driving module includes: the push rod array unit, the fourth driving source, the fifth driving source, the slide rail and the base; the base with slide rail sliding connection, the fourth drive source sets up on the base for at vertical direction drive the movable part cooperation in push rod array unit and a cavity, the fifth drive source sets up on the base, be used for at the horizontal direction drive the base slides, will push rod array unit removes to each the top of cavity. Through setting up fourth drive source, fifth drive source, slide rail and base, can reduce the quantity of push rod array unit, when two chambeies need shift the liquid-transfering, can move push rod array unit to a chamber top, then exert the moving part of effort in this chamber, under the state that switch valve is opened, realize the transfer of liquid.

According to an embodiment of the present disclosure, the apparatus further comprises: and the upper and lower machine modules are used for accommodating at least one card box and moving the card box to a position between the liquid path on-off module and the liquid driving module, so that the card box is conveniently butted with the liquid path on-off module and the liquid driving module.

In an aspect of the present disclosure, the loading and unloading module includes: the card box holds carrier, the card box holds carrier is rectangular frame, and the lateral wall is provided with the spacing groove, the spacing groove with the tip adaptation of card box, the position of spacing groove is aimed at with two tip of card box to put into the card box and hold carrier with the card box, and then under the effect of first driving source, to the direction motion of liquid way break-make module, realize the butt joint of the ooff valve of card box bottom and the rotation axis (see fig. 19) on the liquid way break-make module.

According to an embodiment of the present disclosure, a support plate is provided on the cartridge carrier at a position close to the collection tube to better stabilize the cartridge.

According to an embodiment of the present disclosure, the apparatus further comprises: and the first driving source is used for controlling the upper and lower machine modules to move relative to the liquid path on-off module.

According to an embodiment of the present disclosure, the chamber comprises two mixing chambers, which are conducted by a first passage; a sample extraction chamber is arranged in the first passage; the two mixing chambers are arranged at intervals of a preset distance, and a permanent magnet movement cavity is arranged below the sample extraction chamber.

According to an embodiment of the present disclosure, the apparatus further comprises: the magnetic attraction module comprises a permanent magnet and a permanent magnet driving source, and the permanent magnet driving source is used for driving the permanent magnet to enter the permanent magnet movement cavity.

In the present disclosure, the permanent magnet drive source is a lead screw motor, for example, as shown in fig. 17.

In the present disclosure, the permanent magnet drive source includes a seventh drive source and a link mechanism, for example, as shown in fig. 18.

According to an embodiment of the present disclosure, the apparatus further comprises: and the heating module comprises a sixth driving source and a heating kit connected with the sixth driving source, is sleeved between the two mixing chambers and is used for heating the mixed solution during nucleic acid extraction.

In an aspect of the present disclosure, in order to adapt a heating module, the liquid driving module includes: the push rod driving device comprises a slide rail, two push rod array units, a fourth driving source, a fifth driving source and a base, wherein the fourth driving source, the fifth driving source and the base are matched with each push rod array unit; the two bases are located on two sides of the heating module and are in sliding connection with the sliding rail, the fourth driving source is arranged on each base and used for driving one push rod array unit to be matched with the moving piece in the cavity on one side of the heating module in the vertical direction, and the fifth driving source is arranged on each base and used for driving the bases to slide in the horizontal direction and moving the push rod array units to the position above the cavity on one side of the heating module.

According to an embodiment of the present disclosure, the apparatus further comprises: a PCR amplification instrument; and the pressing module is matched with the card box and is used for limiting the collecting pipe in a hole groove of the PCR amplification instrument.

The cartridge adapting device of the present disclosure is used for nucleic acid detection, and comprises the following specific steps:

s201, loading the cartridge into a machine: at least one cartridge 1 is placed in the cartridge carrier 121, and the cartridge 1 is moved between the liquid path opening/closing module 130 and the liquid driving module 140 by a second driving source B such as a screw motor.

S202, aligning the card box into the position and pressing down: under the action of a first driving source a, such as a lead screw motor, the up-down module 120 fixed on the top support frame 111 is driven to move together with the liquid driving module 140 and the heating module 150 in the direction of the liquid passage opening/closing module 130, so that the hole grooves of the valve shaft 22 at the bottom of the cartridge 1 are butted against the rotating shaft 1311. Meanwhile, the collection tube 50 is butted in the hole groove of the PCR amplification instrument 170 under the action of the pressing module 180.

S203, a nucleic acid extraction step in cooperation with the cartridge, the nucleic acid extraction step referring to step S101 to step S108 in example 1, comprising:

a liquid path switching step: under the action of a third driving source C, such as a linear push rod motor, at least two rotary shaft array units 131 are driven to rotate integrally with the corresponding switch valves 20 on the cartridge 1, and a liquid path between the two chambers is conducted.

A liquid driving step: under the action of fifth driving sources E1 and E2 such as a screw motor, the driving base 143 slides on the slide rail 141, the push rod array unit 142 is moved to the upper part of one of the chambers, then under the action of fourth driving sources D1 and D2 such as a linear push rod motor, one push rod array unit 142 is placed into the chamber to be matched with the movable member 30 in the chamber, the movable member 30 moves downwards after being stressed, the liquid in the chamber is transferred to the other chamber through a liquid path, and correspondingly, the movable member 30 in the other chamber moves upwards.

And repeating the liquid path switching step and the liquid driving step to realize the transfer of the liquid among different chambers.

A heating step: under the action of a sixth driving source F such as a screw motor, the heating kit 152 is sleeved between the first mixing chamber S21 and the second mixing chamber S22 to heat the mixed solution during extraction of nucleic acid.

Magnetic attraction movement step: under the action of a permanent magnet driving source 162 of a lead screw motor, for example, the driving permanent magnet 161 is controlled to pass through an opening formed on the bottom support frame 112 and enter the permanent magnet movement cavity R2 of the cartridge 1, so that the magnetic attraction and desorption of magnetic beads are realized.

A nucleic acid detection step: the extracted nucleic acid is led out into the collection tube 50, and then on-line detection is performed by using a PCR amplification instrument.

The equipment that adaptation card box that this disclosure provided used through the cooperation between each module to combine PCR amplification appearance to carry out automatic result interpretation, present the detection report at last, really realized that the sample advances-the result is gone out, have degree of automation height, need not to rely on biological laboratory, need not to rely on manual operation, convenient to carry, easy operation, detection are quick, no cross contamination's advantage.

The foregoing description is only exemplary of the preferred embodiments of the disclosure and is illustrative of the principles of the technology employed. It will be understood by those skilled in the art that the scope of the present invention is not limited to the specific combination of the above-mentioned features, but also covers other embodiments formed by any combination of the above-mentioned features or their equivalents without departing from the spirit of the present invention. For example, the above features and (but not limited to) the features disclosed in this disclosure having similar functions are replaced with each other to form the technical solution.

Claims (19)

1. The device matched with the cartridge is characterized in that a plurality of chambers of the cartridge are sealed by built-in movable parts after sample solution and reagents are placed in the chambers in advance, each chamber is independently controlled by a switch valve to realize the connection and disconnection with at least one liquid path, and the liquid path is used for transferring and guiding out liquid; the movable piece is a push-pull piston rod;

the apparatus comprises:

the liquid path on-off module is used for controlling the on-off valve to be opened or closed;

and the liquid driving module is used for matching with the movable part to realize the transfer of liquid in the cassette when the switch valve is in an opening state.

2. The apparatus of claim 1, wherein the on-off valve is a rotary member, and a plurality of on-off valves are arranged in a linear array at the bottom of the cartridge.

3. The apparatus of claim 2, wherein the fluid path switching module comprises: the number and the arrangement mode of the rotary shaft array units are the same as those of the on-off valves arranged on the card box; wherein, each rotating shaft included in the rotating shaft array unit is used for driving one switch valve to rotate.

4. The apparatus of claim 3, wherein the fluidic circuit switching module further comprises: and each driving unit independently controls one rotating shaft array unit.

5. The apparatus of claim 4, wherein the drive unit comprises: a transmission mechanism and a sliding mechanism; the transmission mechanism is connected with the rotating shaft array unit and is fixed on the sliding mechanism.

6. The apparatus of claim 5, wherein the transmission mechanism comprises: the gear, with the rack of gear engagement transmission and the third driving source that is connected with the rack transmission of every rotation axis in the rotation axis array unit of cover locating.

7. The apparatus of any of claims 1-6, wherein the liquid drive module comprises: each push rod array unit is used for being matched with a movable piece arranged in one cavity; the number and the arrangement mode of the push rod array units are the same as those of the chambers arranged on the card box.

8. The apparatus of any of claims 1-6, wherein the liquid drive module comprises: the push rod array unit, the fourth driving source, the fifth driving source, the slide rail and the base; the base with slide rail sliding connection, the fourth drive source sets up on the base for at vertical direction drive the movable part cooperation in push rod array unit and a cavity, the fifth drive source sets up on the base, be used for at the horizontal direction drive the base slides, will push rod array unit removes to each the top of cavity.

9. The apparatus of claim 1, further comprising: and the upper and lower machine modules are used for accommodating at least one clamping box and moving the clamping box to a position between the liquid path on-off module and the liquid driving module.

10. The apparatus of claim 9, wherein the loader module comprises: the card box holds carrier, the card box holds carrier and is rectangular frame, and the lateral wall is provided with the spacing groove, the spacing groove with the tip adaptation of card box.

11. The apparatus of claim 10, wherein a support plate is disposed on the cartridge carrier.

12. The apparatus of claim 9, further comprising:

and the first driving source is used for controlling the upper and lower machine modules to move relative to the liquid path on-off module.

13. The apparatus of any of claims 1-6, wherein the chamber comprises two mixing chambers, the two mixing chambers being in communication by a first passageway; a sample extraction chamber is arranged in the first passage; the two mixing chambers are arranged at intervals of a preset distance, and a permanent magnet movement cavity is arranged below the sample extraction chamber.

14. The apparatus of claim 13, further comprising:

the magnetic suction module comprises a permanent magnet and a permanent magnet driving source, and the permanent magnet driving source is used for driving the permanent magnet to enter the permanent magnet movement cavity.

15. The apparatus of claim 14, wherein the permanent magnet drive source comprises a seventh drive source and a linkage mechanism.

16. The apparatus of claim 14, wherein the permanent magnet drive source is a lead screw motor.

17. The apparatus of claim 13, further comprising:

the heating module comprises a sixth driving source and a heating external member connected with the sixth driving source, and is sleeved between the two mixing chambers.

18. The apparatus of claim 17, wherein the liquid drive module comprises: the push rod driving device comprises a slide rail, two push rod array units, a fourth driving source, a fifth driving source and a base, wherein the fourth driving source, the fifth driving source and the base are matched with each push rod array unit; the two bases are located on two sides of the heating module and are in sliding connection with the sliding rails, the fourth driving source is arranged on each base and used for driving one push rod array unit to be matched with the moving part in the cavity on one side of the heating module in the vertical direction, and the fifth driving source is arranged on each base and used for driving the bases to slide in the horizontal direction and moving the push rod array units to the position above the cavity on one side of the heating module.

19. The apparatus of claim 1, further comprising:

a PCR amplification instrument;

and the pressing module is matched with the card box and is used for limiting the collecting pipe in a hole groove of the PCR amplification instrument.

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