CN212364334U

CN212364334U - Liquid phase chip detection equipment

Info

Publication number: CN212364334U
Application number: CN202021254948.7U
Authority: CN
Inventors: 张健; 王东风
Original assignee: Shenzhen Yexin Technology Co ltd
Current assignee: Shenzhen Yexin Technology Co ltd
Priority date: 2020-06-30
Filing date: 2020-06-30
Publication date: 2021-01-15
Anticipated expiration: 2030-06-30

Abstract

The application discloses liquid phase chip check out test set relates to biochip and detects technical field, including loading mechanism, move liquid mechanism, acquisition mechanism, detection area and detection device. The loading mechanism is used for detachably loading the reagent card, and the pipetting mechanism is used for transferring the sample from the sample position for accommodating the sample to the reaction position for providing the reaction site, transferring the reagent from the reagent position to the reaction position, and/or removing the solution after the reaction from the reaction position. The sample and the reagent react at the reaction site to obtain particles to be analyzed, and the collecting mechanism is used for collecting the particles to be analyzed. The detection zone comprises a microfluidic detection zone or a fixed detection zone, the light source is used for irradiating the particles in the detection zone, and the detection device is used for detecting the optical signal emitted by each particle. Because the liquid transfer mechanism and the collecting mechanism are added, the manual operation steps of the liquid-phase chip detection equipment are reduced, the labor intensity of operators is favorably reduced, and errors caused by manual operation are reduced.

Description

Liquid phase chip detection equipment

Technical Field

The application relates to the technical field of biochip detection, in particular to liquid-phase chip detection equipment.

Background

The liquid phase suspension chip technology is a tip molecule detection technology integrating a current collector technology, a particle synthesis technology, a molecule hybridization technology and a high-efficiency digital signal processing technology, and the principle of the technology is that known molecules (DNA, RNA, polypeptide, protein, small molecules and the like) are integrated on the surface of one or more particles to form a probe array, one or more objects to be detected in a sample are captured, one or more luminescent objects (fluorescent dye, fluorescent group or fluorescent particle, Raman spectrum characteristic molecule and the like) are coupled to the objects to be detected to be marked, and then the detection is carried out by an optical method. The liquid phase suspension chip technology is used for biomolecule detection, has the obvious advantages of high precision, high flux, high speed, low cost and the like, and is a novel biomolecule detection technology.

The liquid phase suspension chip detector used in the current market mainly realizes detection based on the principles of flow cytometry and fluorescence imaging. However, except that basic control such as detection is completed by a machine, other processes such as sample adding, reagent adding, incubation and the like can be completed only by manual participation, so that the labor cost of manpower is increased, errors are easily caused by manual operation, and the accuracy of a detection result is influenced.

Disclosure of Invention

The application provides a liquid phase chip check out test set for solve the more problem of manual operation step of current liquid phase chip check out test set.

The application provides a liquid phase chip check out test set includes:

a loading mechanism for removably loading a reagent card, the reagent card including a reagent site for containing a reaction reagent;

a pipetting mechanism for transferring a sample from a sample site for accommodating the sample to a reaction site for providing a reaction site, transferring a reagent from a reagent site to the reaction site, and/or removing a reacted solution from the reaction site;

the collection mechanism is used for collecting the particles to be analyzed;

the particle detection device comprises a detection area, a detection mechanism and a detection mechanism, wherein the detection area comprises a micro-flow detection area or a fixed detection area, the acquisition mechanism can drive particles to be analyzed to move to the detection area, the particles are restricted to a single layer or a single row to pass through the micro-flow detection area, or the particles are arranged in the fixed detection area in a single layer;

and the detection device is used for detecting the optical signal emitted by each particle and converting the optical signal into optical signal data, wherein the optical signal data is the data of the analyte and/or the content of the analyte which can be referred by the optical signal after being processed.

As a further improvement of the liquid phase chip detection device, the liquid transferring mechanism is provided with a sampling structure, at least one of the liquid transferring mechanism and the loading mechanism is provided with a driving component, and the driving component can drive the liquid transferring mechanism and/or the loading mechanism to move, so that the sampling structure can extend into the accommodating cavity of the reagent position, the sample position and/or the reaction position.

As a liquid phase chip check out test set's further improvement, move liquid mechanism and include first sampling needle, first sampling drive assembly, first pipeline and first fluid driving piece, first sampling drive assembly can drive first sampling needle along first route motion to make first sampling needle stretch into with first sampling needle position relative reagent position, sample position and/or reaction position hold in the cavity, the one end and the first sampling needle intercommunication of first pipeline, the other end and the first fluid driving piece of first pipeline are connected.

As a further improvement of the liquid phase chip detection device, the loading mechanism comprises a loading plate and a loading driving assembly, the loading plate is detachably connected with the reagent card, and the loading driving assembly can drive the loading plate to move along the second path so as to drive the reagent position, the sample position and/or the reaction position to move to a position opposite to the first sampling needle.

As a further improvement of the liquid phase chip detection device, the liquid transfer mechanism further comprises a first needle frame and a first slide rail, the first sampling needle is arranged on the first needle frame, and the first slide rail extends along a first direction;

first sampling drive assembly includes first motor, first lead screw and first slider, first lead screw rotates the setting, and is parallel with first slide rail, first slider movable sleeve is established on first lead screw, first slider and first slide rail sliding connection, first slider and first needle frame are connected, the output and the first lead screw of first motor are connected, first motor is used for driving first lead screw to rotate to drive first slider and first needle frame along the first direction motion.

As a further improvement of liquid phase chip check out test set, loading mechanism still includes the second slide rail, load board and second slide rail sliding connection, the second slide rail extends along the second direction, load drive assembly includes second motor, second lead screw and second slider, the second lead screw rotates the setting, and is parallel with the second slide rail, second slider activity cover is established on the second lead screw, the second slider is connected with the load board, the output and the second lead screw of second motor are connected, the second motor is used for driving the second lead screw and rotates to drive second slider and load board and move along the second direction.

As a further improvement of the liquid phase chip detection equipment, the acquisition mechanism comprises a second sampling needle, a second sampling driving component, a second pipeline and a second fluid driving component, the second sampling driving component can drive the sampling needle to move along a third path, so that the second sampling needle extends into a containing cavity of a reaction position opposite to the second sampling needle in position, one end of the second pipeline is communicated with the second sampling needle, the other end of the second pipeline is communicated with an inlet of the detection area, and the second fluid driving component can drive particles to be detected to flow to the detection area through the second sampling needle and the second pipeline.

As a further improvement of the liquid-phase chip detection device, a plurality of reaction sites are arranged along a third direction, the acquisition mechanism further comprises a third slide rail, a fourth slide rail, a first bearing plate and a second needle frame, and the second sampling needle is arranged on the second needle frame;

the second sampling driving assembly comprises a third motor, a fourth motor, a third screw rod, a fourth screw rod, a third slider and a fourth slider, the third slide rail extends along a third direction, the third screw rod is parallel to the third slide rail, the third slider is connected with the third slide rail in a sliding manner, the third slider is movably sleeved on the third screw rod, the first bearing plate is connected with the third slider, the output end of the third motor is connected with the third screw rod, the third motor is used for driving the third screw rod to rotate so as to drive the third slider and the first bearing plate to move along the third direction and drive the second sampling needle to move to a position opposite to the reaction position;

the fourth slide rail sets up on first loading board, and extends along the first direction, the fourth lead screw is parallel with the fourth slide rail, fourth slider and fourth slide rail sliding connection, fourth slider movable sleeve establishes on the fourth lead screw, the second needle frame is connected with the fourth slider, the output and the fourth lead screw of fourth motor are connected, the fourth motor is used for driving the fourth lead screw to rotate to drive fourth slider and second needle frame along the first direction motion, and drive the second sampling needle and stretch into rather than the cavity that holds of relative reaction position.

As a further improvement of the liquid phase chip detection apparatus, the apparatus further comprises a cleaning mechanism, wherein the cleaning mechanism comprises a third pipeline, a cleaning liquid container and a gating device, the second fluid driving member is communicated with an outlet of the detection area through the gating device, the gating device is communicated with the cleaning liquid container through the third pipeline, the gating device can be switched between a first state and a second state, in the first state, a liquid path between the second fluid driving member and the detection area is communicated, and in the second state, a liquid path between the second fluid driving member and the cleaning liquid container is communicated.

As the liquid phase chip check out test set's further improvement, still include the first position of tip, the first position of tip is used for bearing the tip head, the first position of tip sets up on the reagent card and/or sets up on loading mechanism, move the liquid mechanism and include first sampling needle, collection mechanism includes the second sampling needle, first sampling needle and/or second sampling needle have connecting portion, connecting portion are used for with the first detachable connection of tip.

Conduct liquid phase chip check out test set's further improvement still includes tip head isolating construction, tip head isolating construction includes separator and separation drive assembly, the activity of separator sets up, separation drive assembly is used for driving the separator and moves between primary importance and second place, when separator moves to primary importance, be used for promoting the separation of tip head and the connecting portion of sampling needle, when separator moves to the second place, do not hinder tip head and the detachable connection of connecting portion.

As a further improvement of the liquid phase chip detection device, the liquid phase chip detection device further comprises a sample position and/or a reaction position, and the sample position and/or the reaction position are/is arranged on the reagent card and/or the loading mechanism.

As a further improvement of the liquid phase chip detection device, the loading mechanism further comprises a heating plate, the heating plate is in contact with the loading plate, and the heating plate is used for providing a heating environment for the reaction sites.

As a further improvement of the liquid phase chip detection equipment, the loading mechanism further comprises a magnetic attraction device, the magnetic attraction device is arranged towards the reaction position, the particles comprise magnetic particles, and the magnetic attraction device is used for generating a magnetic field so as to adsorb the magnetic particles on the side part or the bottom of the reaction position.

As a further improvement of the liquid phase chip detection device, the sample position is arranged on the reagent card or on the loading mechanism, and the reaction position is arranged on the reagent card or on the loading mechanism.

As a further improvement of the liquid phase chip detection device, the liquid phase chip detection device further comprises a light source, wherein the light source is used for irradiating the particles in the detection area, so that the particles emit light signals related to the characteristics of the particles after being irradiated.

The beneficial effect of this application:

the application provides a liquid phase chip check out test set, including loading mechanism, move liquid mechanism, collection mechanism, detection area and detection device. Because increased and moved liquid mechanism and collection mechanism, reduced liquid phase chip check out test set's manual operation step, be favorable to reducing operating personnel's intensity of labour, reduce the error that manual operation caused, promote the accuracy that detects the structure.

Drawings

FIG. 1 is a schematic diagram illustrating an external structure of a liquid chip detection apparatus according to an embodiment of the present disclosure;

FIG. 2 is a schematic diagram of an internal structure of an embodiment of an LC chip inspection apparatus at a viewing angle;

FIG. 3 is a schematic diagram of an internal structure of an LC chip inspection apparatus at another viewing angle according to an embodiment of the present disclosure;

FIG. 4 is a schematic view of the pipetting mechanism according to an embodiment of the present application;

FIG. 5 is a schematic view of a collection mechanism and a cleaning mechanism in one embodiment of the present disclosure;

FIG. 6 is a schematic view of an alternate view of the collection mechanism and the cleaning mechanism in an embodiment of the present application;

FIG. 7 is a schematic view of the fluid paths of the collection mechanism and the cleaning mechanism in one embodiment of the present application;

FIG. 8 is a schematic view of the fluid paths of the acquisition mechanism and the cleaning mechanism in a more particular embodiment of the present application;

FIG. 9 is a schematic view of the fluid paths of the collection mechanism and the cleaning mechanism in another more particular embodiment of the present application;

FIG. 10 is a schematic view of a loading mechanism according to an embodiment of the present application;

FIG. 11 is a schematic view of another perspective of a loading mechanism according to an embodiment of the present application;

FIG. 12 is a schematic view of a reagent card from a first perspective in one embodiment of the present application;

FIG. 13 is a schematic view of a reagent card from a second perspective in one embodiment of the present application;

FIG. 14 is a schematic view of a reagent card from a third perspective in one embodiment of the present application;

FIG. 15 is a schematic representation of a tip-tagged reagent card according to one embodiment of the present application.

Reference numerals:

100. a loading mechanism; 110. a loading plate; 120. a loading drive assembly; 121. a second motor; 122. a second lead screw; 123. a second slider; 130. a second slide rail; 140. a magnetic member; 150. a sixth slide rail; 160. a magnetic attraction drive assembly; 161. a sixth motor; 162. a sixth lead screw; 163. a sixth slider; 170. a reagent rack; 171. a hand-held portion;

200. a pipetting mechanism; 210. a first sampling needle; 220. a first sampling drive assembly; 221. a first motor; 222. a first lead screw; 223. a first slider; 230. a first fluid driver; 240. a first needle frame; 250. a first slide rail;

300. a collection mechanism; 310. a second sampling needle; 320. a second sampling drive assembly; 321. a third motor; 322. a fourth motor; 323. a third screw rod; 324. a fourth screw rod; 325. a third slider; 326. a fourth slider; 330. a second conduit; 340. a second fluid drive; 350. a third slide rail; 360. a fourth slide rail; 370. a second needle frame; 380. a first bearing plate;

400. a reagent card; 10. a carrier; 11. a clamping part; 20. an accommodating cavity; 21. a sample chamber; 22. a reagent chamber; 23. a cleaning liquid cavity; 24. a reaction chamber; 30. tip head position; 40. a hand-held portion; 50. a positioning structure; 51. a first positioning block; 52. a second positioning block; 60. supporting ribs; 70. tip head;

500. a cleaning mechanism; 510. a third pipeline; 520. a cleaning solution container; 530. a gating means; 531. a three-way valve; 501. a first joint; 502. a second joint; 503. a third joint; 532. a fourth conduit; 533. a first valve; 534. a fifth pipeline; 540. a third sampling needle; 550. a third sampling drive assembly; 551. a seventh motor; 552. a seventh lead screw; 553. a seventh slider; 560. a third needle frame; 570. a second carrier plate; 580. a seventh slide rail;

600. detecting a region;

700. tip head separation structures; 710. a separating member; 720. separating the drive assembly; 721. a fifth motor, 722, a fifth screw; 723. a fifth slider; 730. a fifth slide rail;

800. a detection chamber;

900. a housing; 910. an access opening.

Detailed Description

The present application is described in further detail in the following detailed description of the preferred embodiments with reference to the figures, in which like elements in different embodiments are numbered with like associated element numbers. In the following description, numerous details are set forth in order to provide a better understanding of the present application. However, those skilled in the art will readily recognize that some of the features may be omitted or replaced with other elements, materials, methods in different instances. In some instances, certain operations related to the present application have not been shown or described in detail in order to avoid obscuring the core of the present application from excessive description, and it is not necessary for those skilled in the art to describe these operations in detail, so that they may be fully understood from the description in the specification and the general knowledge in the art.

Furthermore, the features, operations, or characteristics described in the specification may be combined in any suitable manner to form various embodiments. Also, the various steps or actions in the method descriptions may be transposed or transposed in order, as will be apparent to one of ordinary skill in the art. Thus, the various sequences in the specification and drawings are for the purpose of describing certain embodiments only and are not intended to imply a required sequence unless otherwise indicated where such sequence must be followed.

The numbering of the components as such, e.g., "first", "second", etc., is used herein only to distinguish the objects as described, and does not have any sequential or technical meaning. The term "connected" and "coupled" when used in this application, unless otherwise indicated, includes both direct and indirect connections (couplings).

The embodiment provides a liquid phase chip detection device.

Referring to fig. 1 to 11, the liquid phase chip detection apparatus includes a loading mechanism 100, a pipetting mechanism 200, a collecting mechanism 300, a detection area 600, a light source and a detection device.

Referring to fig. 1-3 and 10, 11, the loading mechanism 100 is for removably loading a reagent card 400, the reagent card 400 including reagent sites for containing reaction reagents. Multiple reagent cards 400 may be mounted on the loading mechanism 100 for simultaneously performing multiple sets of reactions of the sample with the reagent. The reagent amount contained in the reagent card 400 may be an amount for a single test or an amount for a plurality of tests, the number of reagent sites in the reagent card 400 is at least one, and the kind of reagent contained in the reagent card 400 is at least one.

Specifically, the reagents stored in the reagent card 400 include a particle-coated reagent and/or a luminescent labeling reagent. The state in which the particles stored in the reagent card 400 coat the reagent may be a dry state, a gel state, and/or a liquid state. The state of the luminescence labeling reagent stored in the reagent card 400 may be a dry state, a gel state, and/or a liquid state.

The reagent may also include an antibody reagent, a buffer reagent (e.g., a reagent for adjusting pH or ion concentration), and the like, and the present invention is not limited thereto.

In some tests, a diluent is required, so the diluent can be stored in the reagent card, and the diluent can be stored in other positions of the equipment instead of the reagent card.

The sample site is provided on the reagent card 400 or on the loading mechanism 100, and the reaction site is provided on the reagent card 400 or on the loading mechanism 100. The reagent position, the sample position and the reaction position can be three independent accommodating cavities, or the reagent position and the reaction position can be the same accommodating cavity, or the sample position and the reaction position can be the same accommodating cavity, namely, the reaction can be carried out in the accommodating cavity of the reagent position or the sample position.

Referring to fig. 4, the pipetting mechanism 200 is used to transfer a sample from a sample site for accommodating the sample to a reaction site, transfer a reagent from a reagent site to a reaction site for providing a reaction site, and/or remove a solution after reaction from the reaction site. The sample and the reagent react at the reaction site and obtain particles to be analyzed, and the collecting mechanism 300 is used for collecting the particles to be analyzed.

Specifically, when the sample site, the reaction site, and the reagent site are three separate accommodating chambers, the pipetting mechanism 200 needs to transfer the sample from the sample site to the reaction site, and transfer the reagent from the reagent site to the reaction site. When the sample site and the reaction site are the same housing chamber, the pipetting mechanism 200 needs to transfer a reagent from the reagent site to the sample site. When the reagent site and the reaction site are the same accommodating chamber, the pipetting mechanism 200 needs to transfer the sample from the sample site to the reagent site. The sample position, the reaction position and the reagent position can be the same accommodating cavity, for example, when the reagent position and the reaction position are the same accommodating cavity and manual sample adding is performed to the reaction position, the sample and the reagent do not need to be transferred through the liquid transferring mechanism 200, the liquid transferring mechanism 200 plays a role in transferring out the reacted solution from the reaction position, and specifically, the reacted solution can be transferred to the detection area, the waste liquid level or other positions.

Specifically, the liquid-transferring mechanism 200 and the collecting mechanism 300 both pump liquid through the sampling needles to realize liquid transferring or collecting, so that liquid transferring and collecting can be realized simultaneously by arranging one type of sampling needle, and two types of sampling needles can be arranged, wherein one type of sampling needle is specially used for realizing liquid transferring, and the other type of sampling needle is specially used for realizing collecting. That is, the pipetting mechanism 200 and the collecting mechanism 300 may be the same mechanism or may be two mechanisms provided separately.

With reference to fig. 7-9, the detection zone 600 includes a microfluidic detection zone or a fixed detection zone, and the collection mechanism 300 is capable of driving particles to be analyzed to move to the detection zone 600, where the particles are constrained to pass through the microfluidic detection zone in a single layer or column, or where the particles are arranged in a single layer at the fixed detection zone.

The light source is used to illuminate the particles in the detection region 600 so that the particles emit light signals related to the characteristics of the particles themselves after illumination. In particular, the particles and/or the vicinity of the particles may be provided with a luminescent substance, which is capable of emitting a characteristic spectrum upon excitation by light. The luminescent material may be a fluorescent dye, a fluorescent gene, a fluorescent particle, a quantum dot, a time-resolved luminescent material, a light-activated chemiluminescent material, a raman spectrum characteristic molecule, etc., and the present invention is not limited thereto.

In other embodiments, the liquid-phase chip detection device may not include a light source, but may employ a method that does not require a light source in chemiluminescence and/or electrochemiluminescence.

In one embodiment, the particle to be analyzed is contacted with a substrate containing a reagent associated with a chemiluminescent reaction, such that the particle and/or the substrate contacted with the particle undergoes a chemiluminescent reaction to produce an optical signal associated with a characteristic of the particle itself.

In another embodiment, the liquid phase chip detection device further comprises electrodes for applying an electric field to the particles to be analyzed in the detection region, so that the particles to be analyzed and/or the buffer solution in contact with the particles generate an electrochemiluminescence reaction, and an optical signal related to the characteristics of the particles to be analyzed are emitted. In certain aspects of methods using electrochemiluminescence, the detection zone can also be used to contain a buffer, which is used to effect and/or facilitate the electrochemiluminescence reaction.

The detection device is used for detecting the optical signal emitted by each particle and converting the optical signal into optical signal data, wherein the optical signal data is processed to obtain the data of the analyte and/or the content of the analyte which are indicated by the optical signal.

Referring to FIGS. 2, 7-9, in one embodiment, the liquid phase chip detection apparatus includes a detection chamber 800, and the detection region 600, the light source and the detection device are disposed in the detection chamber 800.

Referring to fig. 1, in an embodiment, the liquid phase chip detection apparatus further includes a housing 900, the housing 900 has an access opening 910, and the loading plate 110 of the loading mechanism 100 can move to an area corresponding to the access opening 910.

Referring to fig. 2 and 3, the liquid transfer mechanism 200 and the collection mechanism 300 are added, so that the manual operation steps of the liquid-phase chip detection equipment are reduced, the labor intensity of operators is reduced, errors caused by manual operation are reduced, and the accuracy of the detection structure is improved.

It should be noted that, although the structure of the reagent card 400 is described in the present embodiment, this is for the purpose of facilitating description and understanding of the structure of the liquid-phase chip detection apparatus, and the liquid-phase chip detection apparatus may not include the reagent card 400. That is, in one embodiment, the liquid-phase chip testing apparatus includes a reagent card 400, and the reagent card 400 is an integral part of the liquid-phase chip testing apparatus. In another embodiment, the liquid-phase chip detection apparatus does not include the reagent card 400, and the reagent card 400 is a subject of use of the liquid-phase chip detection apparatus, and is not a component of the liquid-phase chip detection apparatus.

Referring to fig. 2-4, in one embodiment, the pipetting mechanism 200 has a sampling structure and at least one of the pipetting mechanism 200 and the loading mechanism 100 has a drive assembly capable of driving movement of the pipetting mechanism 200 and/or the loading mechanism 100 to enable the sampling structure to extend into the receiving cavity of the reagent site, the sample site, and/or the reaction site.

When it is desired to transfer liquid in a reagent site, sample site and/or reaction site, pipetting mechanism 200 and/or loading mechanism 100 is driven by the drive assembly to move so that the sampling structure is aligned with and extends into the receiving cavity of the reagent site, sample site and/or reaction site to aspirate and/or expel liquid through the sampling structure. The sampling structure may be a sampling needle, a sampling tube, or other suitable structure.

Specifically, in some embodiments, only the loading mechanism 100 may have a driving component, and the driving component of the loading mechanism 100 drives the loading plate 110 to move, so as to drive the reagent site, the sample site and/or the reaction site to move, so that the sampling structure extends into the accommodating cavity of the reagent site, the sample site and/or the reaction site.

In other embodiments, it may be that only the pipetting mechanism 200 has a drive assembly that drives the movement of the sampling structure such that the sampling structure protrudes into the receiving cavity of the reagent site, the sample site, and/or the reaction site.

In other embodiments, the pipetting mechanism 200 and the loading mechanism 100 may both have a driving component, the driving component of the loading mechanism 100 drives the loading plate 110 to move to drive the reagent site, the sample site and/or the reaction site, and the driving component of the pipetting mechanism 200 drives the sampling structure to move, so that the sampling structure extends into the accommodating cavity of the reagent site, the sample site and/or the reaction site through the movement of the loading plate 110 and the sampling structure.

Referring to fig. 2-4, in one embodiment, the pipetting mechanism 200 includes a first sampling needle 210, a first sampling driving assembly 220, a first conduit and a first fluid driving member 230, wherein the first sampling driving assembly 220 can drive the first sampling needle 210 to move along a first path so that the first sampling needle 210 extends into a receiving cavity of a reagent site, a sample site and/or a reaction site opposite to the first sampling needle 210, one end of the first conduit is connected to the first sampling needle 210, and the other end of the first conduit is connected to the first fluid driving member 230.

On one hand, when liquid in the accommodating cavity needs to be transferred, the first sampling needle 210 is driven to move along the first path by the first sampling driving component 220, so that the first sampling needle 210 extends into the accommodating cavity of the reagent position, the sample position and/or the reaction position opposite to the first sampling needle 210, and then the first sampling needle 210 sucks or discharges the liquid, thereby realizing the transfer of the liquid. On the other hand, when the liquid in the accommodating cavity needs to be mixed uniformly, the liquid in the accommodating cavity can be repeatedly sucked and discharged through the first sampling needle 210, so that the liquid in the accommodating cavity is mixed uniformly.

Specifically, the sampling needle (including the first sampling needle 210) in this embodiment may be a sampling needle having a needle body directly contacting with the liquid, or a sampling needle capable of mounting a tip head. Referring to fig. 4, in the present embodiment, a plurality of first sampling needles 210 may be arranged along a third direction. In other embodiments, only one first sampling needle 210 may be provided. The fluid driver (including the first fluid driver 230) in this embodiment may be a fluid pump.

It should be noted that, in an embodiment, referring to fig. 4, the "first path" refers to a moving path of the first sampling needle 210 along a vertical direction. In other embodiments, the "first path" may also be a movement path in which a horizontal direction or a plurality of directions are combined in sequence, and the "first path" is not limited to a straight path, and may also be a circular path, a circular arc path, or another suitable path.

Specifically, the power source of the first sampling driving assembly 220 may be a motor, an air cylinder, a hydraulic pump and/or other suitable driving members, and the transmission structure of the first sampling driving assembly 220 may be a screw slider, a chain transmission structure, a belt transmission structure, a gear transmission structure and/or other suitable transmission structures.

Referring to fig. 10 and 11, in an embodiment, the loading mechanism 100 includes a loading plate 110 and a loading driving assembly 120, the loading plate 110 is configured to be detachably connected to the reagent card 400, and the loading driving assembly 120 is configured to drive the loading plate 110 to move along a second path to move the reagent site, the sample site and/or the reaction site to a position opposite to the first sampling needle 210.

When it is desired to transfer the liquid in the receiving cavity, the loading plate 110 is driven to move along the second path by the loading driving assembly 120, so as to achieve the alignment of the first sampling needle 210 with the reagent site, the sample site and/or the reaction site.

It should be noted that, in one embodiment, referring to fig. 10 and 11, the "second path" refers to a moving path of the loading plate 110 in the horizontal direction. In other embodiments, the "second path" may also be a moving path in which a vertical direction or a plurality of directions are combined in sequence, and the "second path" is not limited to a straight path, and may also be a circular path, a circular arc path, or another suitable path.

Specifically, the power source of the loading driving assembly 120 may be a motor, an air cylinder, a hydraulic pump and/or other suitable driving members, and the transmission structure of the loading driving assembly 120 may be a screw slider, a chain transmission structure, a belt transmission structure, a gear transmission structure and/or other suitable transmission structures.

Referring to fig. 10 and 11, in one embodiment, the loading mechanism 100 further includes a reagent rack 170, the reagent rack 170 being configured to carry reagent cards 400. Specifically, the reagent card 400 has a clamping portion, the reagent rack 170 has a clamping slot, and the clamping portion of the reagent card 400 is embedded into the clamping slot of the reagent rack 170, so that the reagent card 400 is detachably connected with the reagent rack 170. Multiple card slots may be provided on the reagent rack 170 to simultaneously carry multiple reagent cards 400.

The loading plate 110 is provided with a first mounting structure for mounting the reagent card 400 and a second mounting structure for mounting the reagent rack 170. When the reagent card 400 is mounted, the reagent card 400 may be mounted on the reagent rack 170 and then the reagent rack 170 may be mounted on the loading plate 110, or the reagent card 400 may be directly mounted on the loading plate 110. The first and second mounting structures may be recesses and/or projections.

Referring to fig. 2-4, in one embodiment, the pipetting mechanism 200 further includes a first needle rack 240 and a first sliding rail 250, the first sampling needle 210 is disposed on the first needle rack 240, and the first sliding rail 250 extends along a first direction. The first sampling driving assembly 220 comprises a first motor 221, a first screw rod 222 and a first sliding block 223, the first screw rod 222 is rotatably arranged and parallel to the first sliding rail 250, the first sliding block 223 is movably sleeved on the first screw rod 222, the first sliding block 223 is slidably connected with the first sliding rail 250, the first sliding block 223 is connected with the first needle frame 240, the output end of the first motor 221 is connected with the first screw rod 222, and the first motor 221 is used for driving the first screw rod 222 to rotate so as to drive the first sliding block 223 and the first needle frame 240 to move along a first direction.

When the first sampling needle 210 needs to be driven to move, the first lead screw 222 is driven to rotate by the first motor 221, so that the first sliding block 223 and the first needle frame 240 are driven to move along the first direction, and the first sampling needle 210 is further driven.

It should be noted that, referring to fig. 2, in an embodiment, the "first direction" refers to a vertical direction, and the "second direction" and the "third direction" are two directions perpendicular to each other in a horizontal plane, that is, the "first direction" is a direction shown by an arrow a, the "second direction" is a direction shown by an arrow b, and the "third direction" is a direction shown by an arrow c. In other embodiments, "the first direction", "the second direction", and "the third direction" may be defined as other directions (for example, "the first direction" may not be a vertical direction, but an inclined direction having an acute angle with a horizontal plane), as long as the "first direction", "the second direction", and "the third direction" are perpendicular to each other.

Referring to fig. 10 and 11, in an embodiment, the loading mechanism 100 further includes a second slide rail 130, the second slide rail 130 extends along a second direction, the loading plate 110 is slidably connected to the second slide rail 130, the loading driving assembly 120 includes a second motor 121, a second screw 122 and a second slider 123, the second screw 122 is rotatably disposed and parallel to the second slide rail 130, the second slider 123 is movably sleeved on the second screw 122, the second slider 123 is connected to the loading plate 110, an output end of the second motor 121 is connected to the second screw 122, and the second motor 121 is configured to drive the second screw 122 to rotate, so as to drive the second slider 123 and the loading plate 110 to move along the second direction.

When the loading plate 110 needs to be driven to move, the second lead screw 122 is driven to rotate by the second motor 121, and the second slider 123 and the loading plate 110 are driven to move along the second direction.

Referring to fig. 5-9, in an embodiment, the collecting mechanism 300 includes a second sampling needle 310, a second sampling driving assembly 320, a second tube 330 and a second fluid driving member 340, the second sampling driving assembly 320 can drive the sampling needle to move along a third path, so that the second sampling needle 310 extends into a receiving cavity of the reaction site opposite to the second sampling needle 310, one end of the second tube 330 is communicated with the second sampling needle 310, the other end is communicated with an inlet of the detection area 600, and the second fluid driving member 340 can drive the particles to be detected to flow to the detection area 600 through the second sampling needle 310 and the second tube 330.

It should be noted that, in an embodiment, referring to fig. 2 and 5-9, the "third path" refers to a moving path of the second sampling needle 310 moving along the third direction and the first direction in sequence. In other embodiments, the "third path" may also be a motion path in which a horizontal direction, a vertical direction, or a combination of multiple directions are combined in sequence, and the "third path" is not limited to a straight path, and may also be a circular path, a circular arc path, or another suitable path.

Specifically, the power source of the second sampling driving assembly 320 may be a motor, an air cylinder, a hydraulic pump and/or other suitable driving members, and the transmission structure of the second sampling driving assembly 320 may be a screw slider, a chain transmission structure, a belt transmission structure, a gear transmission structure and/or other suitable transmission structures.

Referring to fig. 2 and 5-9, in an embodiment, a plurality of reaction sites are disposed along a third direction, the collecting mechanism 300 further includes a third slide rail 350, a fourth slide rail 360, a first bearing plate 380 and a second needle frame 370, and the second sampling needle 310 is disposed on the second needle frame 370. The second sampling driving assembly 320 includes a third motor 321, a fourth motor 322, a third lead screw 323, a fourth lead screw 324, a third slider 325 and a fourth slider 326, the third slide rail 350 extends along a third direction, the third lead screw 323 is parallel to the third slide rail 350, the third slider 325 is slidably connected to the third slide rail 350, the third slider 325 is movably sleeved on the third lead screw 323, the first bearing plate 380 is connected to the third slider 325, an output end of the third motor 321 is connected to the third lead screw 323, the third motor 321 is configured to drive the third lead screw 323 to rotate, so as to drive the third slider 325 and the first bearing plate 380 to move along the third direction, and drive the second sampling needle 310 to move to a position opposite to the reaction site. The fourth slide rail 360 is disposed on the first bearing plate 380 and extends along the first direction, the fourth lead screw 324 is parallel to the fourth slide rail 360, the fourth slider 326 is slidably connected to the fourth slide rail 360, the fourth slider 326 is movably sleeved on the fourth lead screw 324, the second needle holder 370 is connected to the fourth slider 326, the output end of the fourth motor 322 is connected to the fourth lead screw 324, the fourth motor 322 is configured to drive the fourth lead screw 324 to rotate, so as to drive the fourth slider 326 and the second needle holder 370 to move along the first direction and drive the second sampling needle 310 to extend into the accommodating cavity of the reaction site opposite thereto.

When the particles to be analyzed need to be collected, the third screw 323 is driven to rotate by the third motor 321 to drive the third slider 325 and the first bearing plate 380 to move along the third direction, so as to achieve the alignment of the second sampling needle 310 and the reaction site, and then the fourth screw 324 is driven to rotate by the fourth motor 322 to drive the fourth slider 326 and the second needle holder 370 to move along the first direction and drive the second sampling needle 310 to extend into the accommodating cavity of the reaction site opposite to the second sampling needle 310, so as to suck the particles to be analyzed through the second sampling needle 310.

Referring to fig. 5-9, in an embodiment, the cleaning mechanism 500 further includes a third pipeline 510, a cleaning solution container 520, and a gating device 530, the second fluid driver 340 is communicated with an outlet of the detection area 600 through the gating device 530, the gating device 530 is communicated with the cleaning solution container 520 through the third pipeline 510, and the gating device 530 can be switched between a first state in which a fluid path between the second fluid driver 340 and the detection area 600 is conducted and a second state in which the fluid path between the second fluid driver 340 and the cleaning solution container 520 is conducted.

When the cleaning operation is required, the gating device 530 is switched to the second state, the cleaning solution in the cleaning solution container 520 is sucked by the second fluid driving member 340, and then the gating device 530 is switched to the first state, and the cleaning solution is driven by the second fluid driving member 340 to be discharged from the inlet of the detection area 600 and the second sampling needle 310, so that the detection area 600 and the second sampling needle 310 are cleaned.

Specifically, the cleaning solution container 520 may be disposed at the reagent card 400, the loading plate 110, or other suitable location. The end of the third pipe 510 for communicating with the cleaning solution container 520 may be provided with a third sampling needle 540. The cleaning solution container 520 and the third pipe 510 may be both fixedly disposed, or at least one of the cleaning solution container 520 and the third pipe 510 may be movable, as long as the third pipe 510 can communicate with the cleaning solution container 520 when the cleaning solution is pumped.

Referring to fig. 5 and 6, in an embodiment, the cleaning mechanism 500 further includes a third sampling driving assembly 550, a third needle frame 560, a second supporting plate 570 and a seventh sliding rail 580, the second supporting plate 570 is connected to the third slider 325, the seventh sliding rail 580 is disposed on the second supporting plate 570 and extends along the first direction, and the third sampling needle 540 is disposed on the third needle frame 560. The third sampling driving assembly 550 includes a seventh motor 551, a seventh lead screw 552 and a seventh slider 553, the seventh lead screw 552 is rotatably disposed and parallel to the seventh lead screw 552, the seventh slider 553 is slidably connected to the seventh slide rail 580, the seventh slider 553 is movably sleeved on the seventh lead screw 552, the third needle holder 560 is connected to the seventh slider 553, an output end of the seventh motor 551 is connected to the seventh lead screw 552, and the seventh motor 551 is configured to drive the seventh lead screw 552 to rotate, so as to drive the seventh slider 553 and the third needle holder 560 to move along the first direction.

When cleaning is needed, the third slider 325 drives the second bearing plate 570 and the third needle holder 560 to move along the third direction, so as to align the third sampling needle 540 with the cleaning solution container 520, and then the seventh motor 551 drives the seventh lead screw 552 to rotate, so as to drive the seventh slider 553 and the third needle holder 560 to move along the first direction, so that the third sampling needle 540 extends into the cleaning solution container 520.

In other embodiments, the power source of the third sampling driving assembly 550 may be a motor, a cylinder, a hydraulic pump and/or other suitable driving members, and the transmission structure of the third sampling driving assembly 550 may be a screw slider, a chain transmission structure, a belt transmission structure, a gear transmission structure and/or other suitable transmission structures.

In one embodiment, the liquid chip detection apparatus further comprises a waste liquid level for containing waste liquid generated by the reaction or washing, and the waste liquid level is disposed on the reagent card 400, the loading plate 110, or other suitable position. The waste liquid level can be a separately arranged accommodating cavity, and can also be the same accommodating cavity with the sample level, the reagent level and/or the reaction level, namely, the waste liquid level can be reused after the sample level, the reagent level and/or the reaction level are used.

Referring to fig. 8, in one embodiment, the gating device 530 includes a three-way valve 531 and a fourth pipe 532, and the three-way valve 531 has a first connector 501, a second connector 502 and a third connector 503 for liquid inflow and outflow. The first connector 501 is connected to the second fluid driver 340 via a fourth conduit 532, the second connector 502 is in communication with the wash solution reservoir 520 via a third conduit 510, and the third connector 503 is in communication with an outlet of the detection zone 600. The gate 530 is switched to the first state when the fluid paths between the first junction 501 and the third junction 503 of the three-way valve 531 are communicated, and the gate 530 is switched to the second state when the fluid paths between the first junction 501 and the second junction 502 of the three-way valve 531 are communicated. Specifically, the liquid path switching of the three-way valve 531 may be realized by an electronic valve or a manual valve.

Referring to fig. 9, in another embodiment, the second fluid driving member 340 is a fluid pump having a first port and a second port, the gating device 530 includes a first valve 533, a second valve (not shown), and a fifth pipe 534, the first port of the fluid pump communicates with the outlet of the detection area 600 through the fifth pipe 534, the second port of the fluid pump communicates with the cleaning solution container 520 through the third pipe 510, the first valve 533 is disposed on the third pipe 510 for controlling the opening and closing of the third pipe 510, the second valve is disposed on the fifth pipe 534, or the second valve is disposed on the second pipe 330. The gating device 530 switches to the second state when the first valve 533 is open and the second valve is closed, and the gating device 530 switches to the first state when the first valve 533 is closed and the second valve is open.

In other embodiments, the gating device 530 may also be implemented by other types of pipes or valves, as long as the state of fluid communication between the second fluid driver 340 and the detection region 600 and the state of fluid communication between the second fluid driver 340 and the cleaning solution container 520 can be switched.

Referring to fig. 2-6, in an embodiment, the kit further includes a tip head for carrying a tip head, the tip head is disposed on the reagent card 400 and/or on the loading mechanism 100, the pipetting mechanism 200 includes a first sampling needle 210, the collecting mechanism 300 includes a second sampling needle 310, and the first sampling needle 210 and/or the second sampling needle 310 have a connecting portion for detachably connecting with the tip head.

When liquid needs to be sucked, the first sampling needle 210 and/or the second sampling needle 310 are/is moved to be detachably connected with the tip head at the tip position, and then the liquid is sucked through the tip head. Specifically, the tip head and the sampling needle may be detachably connected.

Referring to fig. 2-6, in an embodiment, the liquid phase chip detection apparatus further includes a tip head separation structure 700, where the tip head separation structure 700 includes a separation member 710 and a separation driving assembly 720, the separation member 710 is movably disposed, the separation driving assembly 720 is configured to drive the separation member 710 to move between a first position and a second position, when the separation member 710 moves to the first position, the separation member is configured to push the tip head to separate from the connection portion of the sampling needle, and when the separation member 710 moves to the second position, the removable connection between the tip head and the connection portion is not hindered.

When the tip head after being used needs to be separated from the connecting part of the sampling needle, the separating piece 710 is driven to move to the first position by the separation driving component 720, the separating piece 710 pushes the tip head to be separated from the connecting part of the sampling needle, and then the separating piece 710 is driven to move to the second position by the separation driving component 720, so that the separating piece 710 does not obstruct the detachable connection of the connecting part and a new tip head.

Specifically, the power source of the separation driving assembly 720 may be a motor, a cylinder, a hydraulic pump and/or other suitable driving members, and the transmission structure of the separation driving assembly 720 may be a screw slider, a chain transmission structure, a belt transmission structure, a gear transmission structure and/or other suitable transmission structures.

Referring to fig. 2-6, in an embodiment, the tip head separation structure 700 further includes a fifth slide rail 730, the separation driving assembly 720 includes a fifth motor 721, a fifth lead screw 722 and a fifth slider 723, the fifth slide rail 730 extends along the first direction, the fifth lead screw 722 is rotatably disposed and parallel to the fifth slide rail 730, the fifth slider 723 is movably sleeved on the fifth lead screw 722, the separation member 710 is connected with the fifth slider 723, an output end of the fifth motor 721 is connected with the fifth lead screw 722, and the fifth motor 721 is configured to drive the fifth lead screw 722 to rotate, so as to drive the fifth slider 723 and the separation member 710 to move along the first direction. The separating piece 710 is provided with a separating through hole, the first sampling needle 210 and/or the second sampling needle 310 penetrate through the separating through hole, the tip cap is sleeved on the connecting portion of the sampling needle and clamped with the connecting portion, and the diameter of the separating through hole is smaller than the maximum diameter of the outer wall of the tip head, so that when the separating piece 710 moves to the first position, the tip head can be pushed to be separated from the connecting portion of the sampling needle.

Referring to fig. 10 and 11, in one embodiment, the loading mechanism 100 further includes a heating plate in contact with the loading plate 110, the heating plate being used to provide a heated environment for the reaction sites. Specifically, the heating plate may be disposed at the bottom of the loading plate 110, and provide a heating environment for the reaction between the reagent and the sample through the heating plate, so as to achieve incubation of the reaction solution.

Referring to fig. 10 and 11, in an embodiment, the loading mechanism 100 further includes a magnetic attraction device disposed toward the reaction site, the particles include magnetic particles, and the magnetic attraction device is configured to generate a magnetic field to attract the magnetic particles to a side or a bottom of the reaction site. Specifically, the magnetic attraction device can be arranged on the side of the reaction site.

Referring to fig. 10 and 11, in an embodiment, the magnetic attraction device includes a magnetic attraction member 140 and a magnetic attraction driving assembly 160, and the magnetic attraction driving assembly 160 is used for driving the magnetic attraction member 140 to move toward or away from the reaction site. Specifically, the power source of the magnetic attraction driving assembly 160 may be a motor, an air cylinder, a hydraulic pump and/or other suitable driving members, the transmission structure of the magnetic attraction driving assembly 160 may be a screw slider, a chain transmission structure, a belt transmission structure, a gear transmission structure and/or other suitable transmission structures, and the magnetic attraction member 140 may be a magnet, an electromagnet, etc.

Referring to fig. 10 and 11, in an embodiment, the magnetic attraction device further includes a sixth sliding rail 150, the sixth sliding rail 150 extends along the second direction, the magnetic attraction driving assembly 160 includes a sixth motor 161, a sixth screw 162 and a sixth sliding block 163, the sixth screw 162 is rotatably disposed and parallel to the sixth sliding rail 150, the sixth sliding block 163 is movably sleeved on the sixth screw 162, the magnetic attraction element 140 is connected to the sixth sliding block 163, an output end of the sixth motor 161 is connected to the sixth screw 162, and the sixth motor 161 is configured to drive the sixth screw 162 to rotate, so as to drive the sixth sliding block 163 and the magnetic attraction element 140 to move along the second direction.

On the other hand, the present embodiment provides a loading mechanism 100, and the loading mechanism 100 is applied to the liquid-phase chip detection apparatus.

Referring to fig. 10 and 11, the loading mechanism 100 includes a loading plate 110, a magnetic attraction device, and a driving assembly.

Referring to fig. 10 and 11, the loading plate 110 is used for detachably loading the reagent card 400, the reagent card 400 includes a reagent site for containing a reaction reagent, and the loading plate 110 and/or the reagent card 400 is provided with a containing cavity for containing magnetic particles to be analyzed obtained after the reaction of the reagent and the sample. The magnetic device includes a magnetic member 140, and the magnetic member 140 is used for generating a magnetic field. The driving component can drive the loading plate 110 and/or the magnetic attracting device to move, so that the magnetic particles are in a magnetic field of the magnetic attracting device, and the magnetic particles are attracted to the side portion or the bottom portion of the accommodating cavity where the magnetic particles are located through the magnetic attracting device.

Because the movement path of the loading plate and/or the magnetic attraction device is set to be that the magnetic attraction device can be matched with the accommodating cavity for loading the magnetic particles on the loading plate 110 and/or the reagent card 400, when the operations such as transferring liquid and/or cleaning the magnetic particles are carried out, the magnetic particles can be fixed on the side part or the bottom of the accommodating cavity through the magnetic attraction device, so that the length specially used for being matched with the magnetic attraction device does not need to be specially arranged on the tip, and the universality of the liquid-phase chip detection equipment on the tip is enhanced. And the cost of tip head used by liquid-phase chip detection equipment is reduced. Specifically, the magnetic device may include a magnet, an electromagnetic coil, and a magnet or an iron block sleeved with the electromagnetic coil.

Referring to fig. 10 and 11, in one embodiment, the driving assembly includes a loading driving assembly 120, and the loading driving assembly 120 is capable of driving the loading plate 110 to move toward and away from the magnetic attraction device.

Referring to fig. 10 and 11, in an embodiment, the loading mechanism 100 further includes a second slide rail 130, the loading plate 110 is slidably connected to the second slide rail 130, the second slide rail 130 extends along a second direction, the loading driving assembly 120 includes a second motor 121, a second screw 122 and a second slider 123, the second screw 122 is rotatably disposed and parallel to the second slide rail 130, the second slider 123 is movably sleeved on the second screw 122, the second slider 123 is connected to the loading plate 110, an output end of the second motor 121 is connected to the second screw 122, and the second motor 121 is configured to drive the second screw 122 to rotate, so as to drive the second slider 123 and the loading plate 110 to move along the second direction.

Referring to fig. 10 and 11, in one embodiment, the magnetic attraction device includes a magnetic attraction member 140, the driving assembly includes a magnetic attraction driving assembly 160, and the magnetic attraction driving assembly 160 can drive the magnetic attraction member 140 to move toward and away from the loading plate 110.

Specifically, the power source of the magnetic attraction driving assembly 160 may be a motor, an air cylinder, a hydraulic pump and/or other suitable driving members, and the transmission structure of the magnetic attraction driving assembly 160 may be a screw slider, a chain transmission structure, a belt transmission structure, a gear transmission structure and/or other suitable transmission structures.

Referring to fig. 10 and 11, in an embodiment, the loading mechanism 100 further includes a sixth slide rail 150, the magnetic attraction driving assembly 160 includes a sixth motor 161, a sixth screw 162 and a sixth sliding block 163, the sixth screw 162 is rotatably disposed and parallel to the sixth slide rail 150, the sixth sliding block 163 is movably sleeved on the sixth screw 162, the magnetic attraction member 140 is connected to the sixth sliding block 163, an output end of the sixth motor 161 is connected to the sixth screw 162, and the sixth motor 161 is configured to drive the sixth screw 162 to rotate so as to drive the sixth sliding block 163 and the magnetic attraction member 140 to move along the second direction.

When the magnetic attraction piece 140 needs to be driven to move, the sixth screw 162 is driven to rotate by the sixth motor 161, so as to drive the sixth slider 163 and the magnetic attraction piece 140 to move along the second direction.

When magnetic particles need to be fixed by the magnetic attraction element 140, only the loading plate 110 may be driven to move close to the magnetic attraction element 140, only the magnetic attraction element 140 may be driven to move close to the loading plate 110, and the loading plate 110 and the magnetic attraction element 140 may be driven to move toward each other at the same time. In this embodiment, the advantage of driving the loading plate 110 and the magnetic member 140 to move simultaneously is that, on one hand, the time for the loading plate 110 and the magnetic member 140 to move to the engaging position (i.e. the position where the magnetic particles are located in the magnetic field) can be shortened, and on the other hand, the engaging position of the loading plate 110 and the magnetic member 140 can be arbitrarily adjusted, for example, the engaging position of the two can be below the first sampling needle 210, below the second sampling needle 310, or in other suitable positions.

Referring to fig. 10 and 11, in one embodiment, the loading plate 110 has a placing area having a placing slot shaped to fit the reagent card 400, the placing slot being used to place the reagent card 400. The reagent card 400 is fitted to the placement groove, whereby the reagent card 400 is placed and positioned on the loading plate 110.

Referring to fig. 10 and 11, in an embodiment, the loading mechanism 100 further includes a reagent rack 170, the reagent rack 170 has a first mounting portion, the loading plate 110 has a second mounting portion, the first mounting portion is detachably connected to the second mounting portion, and the reagent rack 170 has a slot for detachably engaging with an edge of the reagent card 400.

The detachable connection of the reagent card 400 and the reagent rack 170 is realized through the matching of the edge of the reagent card 400 and the clamping groove. Specifically, a plurality of card slots may be disposed in the third direction on the reagent rack 170 so as to simultaneously carry a plurality of reagent cards 400.

In one embodiment, the first mounting portion includes a plug plate protruding from the bottom of the reagent rack 170, and the second mounting portion includes a plug hole corresponding to the plug plate.

Referring to fig. 10 and 11, in an embodiment, a hand-held portion 171 is disposed at a middle portion of the reagent rack 170, so that a worker can conveniently take and place the reagent rack 170.

Referring to fig. 10 and 11, in one embodiment, the reagent rack 170 has a first carrying surface for carrying the reagent cards 400, the loading plate 110 has a second carrying surface for carrying the reagent cards 400, and the first carrying surface and the second carrying surface are flush in the first direction.

When the reagent card 400 is mounted, the reagent card 400 may be mounted on the reagent rack 170 and then the reagent rack 170 may be mounted on the loading plate 110, or the reagent card 400 may be directly mounted on the loading plate 110. Because the first bearing surface and the second bearing surface are flush in the first direction, when the reagent card 400 is installed by adopting the two installation methods, the position of the reagent card 400 in the first direction is unchanged. Therefore, when the first sampling needle 210 and the second sampling needle 310 are used for pipetting, the distance of movement in the first direction is not changed, and the operation parameters of the first sampling needle 210 and the second sampling needle 310 do not need to be adjusted according to different reagent card 400 installation modes.

Referring to fig. 10 and 11, in an embodiment, the loading plate 110 has an extended portion extending outward from an edge of the loading plate, the extended portion is used for covering the accommodating cavity for loading the magnetic particles, a matching slot is formed in a region of the extended portion opposite to the magnetic attraction member 140, and the magnetic attraction member 140 can be driven to a position where the magnetic attraction member is inserted into the matching slot.

When the heating reaction is performed, the accommodating cavity for loading the magnetic particles is close to the edge of the loading plate 110, and the edge of the loading plate 110 can radiate heat outwards, so that the temperature of the accommodating cavity for loading the magnetic particles has an error with the preset reaction temperature. Due to the fact that the matching groove is formed in the extending portion, when the magnetic attraction piece 140 extends into the matching groove, the distance between the magnetic attraction piece 140 and the magnetic particles can be shortened, and the magnetic attraction piece 140 can better adsorb and fix the magnetic particles on the side portion or the bottom portion of the accommodating cavity.

Referring to fig. 10 and 11, in one embodiment, the loading mechanism 100 further includes a heating plate in contact with the loading plate 110 for providing a heated reaction environment.

Specifically, the heating plate may be disposed at the bottom of the loading plate 110, and provide a heating environment for the reaction between the reagent and the sample through the heating plate, so as to achieve incubation of the reaction solution.

In another aspect, the present embodiments provide a reagent card.

The present embodiment provides a reagent card.

Referring to fig. 12 and 13, the reagent card comprises a carrier 10, a receiving cavity 20 and at least one tip head site 30.

Referring to fig. 12 and 15, the supporting member 10 is used for supporting, the supporting member 10 has a plurality of cavity openings, the cavity wall of the accommodating cavity 20 extends outwards from the periphery of the cavity opening and encloses to form the accommodating cavity 20, and the cavity opening connects the accommodating cavity 20 with the outside. The receiving chamber 20 is used for receiving substances required for the reaction and providing a reaction site for the reaction. tip head bits 30 are provided on the carrier 10, the tip head bits 30 being used to carry tip heads 70.

Referring to fig. 12 and 15, since the tip header 30 is added to the reagent card, the tip header 70 can be placed at the tip header 30 of the reagent card, when the biological detection device needs to use the tip header 70, the tip header 70 is extracted from the tip header 30, after the detection is completed, the biological detection device replaces the waste tip header 70 to the tip header 30, and when the worker discards the used reagent card, the worker discards the waste tip header 70 at the same time. On the one hand, need not to set up the refuse collection container who is used for holding abandonment tip head 70 in biological detection equipment, reduced the space that refuse collection container occupy, be favorable to dwindling biological detection equipment's volume, on the other hand, the staff need not to do the operation of abandoning the interior abandonment tip head 70 of refuse collection container again, has simplified staff's operation.

The reagent card with tip head 30 of the present embodiment can be used in liquid-phase chip testing equipment and other biological testing equipment, as long as the shape of the reagent card and the number, specification, shape and layout of the accommodating cavities 20 are adaptively adjusted according to the requirements of various biological testing equipment.

Referring to fig. 12 and 13, in one embodiment, at least two tip header bits 30 are provided on the carrier 10.

Referring to fig. 12 and 15, in actual testing, it is often necessary to place a plurality of reagent cards side by side in a biological testing apparatus, which simultaneously performs operations such as pipetting on the plurality of reagent cards through a plurality of sampling structures arranged side by side, and when the operation steps of the plurality of reagent cards are different, the biological testing apparatus may place tip heads 70 corresponding to reagent cards having different operation steps on tip head positions 30 in different rows so as to perform reactions and tests on reagent cards having different operation steps.

Referring to fig. 12 and 13, in an embodiment, the carrier 10 has a carrying opening, and the tip head 30 includes a carrying cavity, and the cavity wall of the carrying cavity extends outward from the periphery of the carrying opening and encloses to form the carrying cavity.

In this embodiment, the tip head 70 is supported by the supporting cavity. In other embodiments, the tip head 30 may be a through opening without a surrounding cavity wall, and the tip head 70 is engaged with the through opening. the tip header bits 30 may also be other structures capable of carrying the tip header 70.

Referring to fig. 12 and 15, in one embodiment, the reagent card further includes a tip header 70, the tip header 70 being positioned at the tip header location 30.

The reagent card includes a preloaded tip head 70, so that the worker does not need to install the tip head 70 before using the reagent card, further simplifying the operation steps of the worker. In other embodiments, the reagent card may not include a tip head 70, but rather the tip head 70 may be mounted to the reagent card by a worker prior to use of the reagent card.

Referring to fig. 12 and 13, in one embodiment, the receiving cavities 20 and tip header locations 30 are aligned on the carrier 10. The sampling structure of the biological detection device can align each accommodating cavity 20 and tip head position 30 only by moving on a straight line, which is beneficial to simplifying the movement path of the sampling structure.

In other embodiments, the accommodating cavities and tip headers may be arranged in multiple rows, in a circular arrangement, in a radial arrangement, or in other forms according to actual requirements.

Referring to fig. 12 and 13, in one embodiment, the accommodating cavity 20 has a constricted portion, and the inner diameter of the constricted portion is gradually reduced in a direction away from the cavity opening.

When tip head 70 is used for absorbing liquid in accommodating cavity 20, a gap needs to be left between tip head 70 and the bottom of accommodating cavity 20, and the tip head 70 cannot absorb the liquid at the bottom of accommodating cavity 20, so that the space at the bottom of accommodating cavity 20 belongs to a dead volume, the contraction part can reduce the dead volume of accommodating cavity 20, the contraction part is favorable for saving liquid such as reagent, sample, diluent and cleaning liquid, the residual quantity of waste liquid in cleaning is reduced, and the cleaning effect is improved.

Referring to fig. 12 and 13, in an embodiment, the edges of two opposite sides of the supporting member 10 have clamping portions 11, and the clamping portions 11 are used for movably clamping with the clamping grooves of the reagent rack. The detachable connection of the reagent card and the reagent frame is realized through the matching of the clamping part 11 and the clamping groove.

Referring to fig. 12 and 13, in an embodiment, a hand-held portion 40 is disposed on one side of the carrier 10, and a surface of the hand-held portion 40 has a friction structure.

The staff can pinch handheld portion 40 and operate the reagent card, and the friction structure on handheld portion 40 surface makes the staff be difficult for the slippage when pinching handheld portion 40. In particular, the friction structure may be a raised structure, a recessed structure or a coating of a high coefficient of friction material.

Referring to fig. 13 and 14, in an embodiment, the supporting member 10 is provided with a positioning structure 50, and the positioning structure 50 is used for positioning the supporting member 10 and the clamping groove of the reagent rack. Specifically, the positioning structure 50 includes a positioning protrusion and/or a positioning groove. The positioning of the carrier 10 on the snap-in groove is achieved by the positioning structure 50.

Referring to fig. 13 and 14, in a more specific embodiment, the holding portion 40 has first positioning blocks 51 extending to two opposite sides, and the first positioning blocks 51 are used for contacting with one end of the clamping groove on the reagent rack.

Referring to fig. 13 and 14, in a more specific embodiment, the lower surface of the carrier 10 is provided with a second positioning block 52, the second positioning block 52 is hemispherical, and the second positioning block 52 is configured to be matched with a positioning recess of an inner wall of the clamping groove.

Referring to fig. 12 and 13, in an embodiment, the accommodating cavity 20 includes a first-type cavity and a second-type cavity, the first-type cavity has a circular opening and the first-type cavity has a circular cross section, the first-type cavity is used for accommodating a sample, a reagent, a diluent and/or providing a reaction site for a reaction, the second-type cavity has a rectangular opening and the second-type cavity has a rectangular cross section, and the second-type cavity is used for accommodating a cleaning solution. Because the quantity of the cleaning liquid is larger, the second-class cavity is arranged to be rectangular, and more cleaning liquid can be contained conveniently.

Referring to fig. 12 and 13, in an embodiment, the inner wall of the second-type cavity is provided with opposite support ribs 60, the upper portions of the support ribs 60 are flush with the upper surface of the carrier 10, the upper surfaces of the support ribs 60 are used for supporting the sealing film, and a gap is formed between the opposite support ribs 60.

The structural strength of two types of cavitys can be strengthened on the one hand to the brace rod 60, on the other hand, after the liquid is adorned, need use the seal membrane will hold the cavity opening at cavity 20 top sealed, two types of cavitys are great in the span that holds 10 extending direction, prick when the tip head 70 covers the seal membrane at two types of cavitys's top, the seal membrane can be sunken to the middle part, lead to the seal membrane difficult be pricked, after supporting the seal membrane through brace rod 60, the seal membrane has been reduced to the sunken space in middle part, make the tip head 70 easily prick the seal membrane.

Referring to fig. 12 and 13, in an embodiment, the carrier 10 has a first end and a second end opposite to each other, the accommodating cavity 20 includes a sample cavity 21 and a reaction cavity 24, the sample cavity 21 is used for accommodating a sample, the sample cavity 21 is located at the first end of the carrier 10 and is adjacent to the tip head 30, the reaction cavity 24 is used for providing a reaction site for a reaction between a reagent and the sample, and the sample cavity 21 is located at the second end of the carrier 10.

The sample and tip head 70 is typically packaged by a worker before testing, and the sample chamber 21 is disposed at the first end of the carrier 10 and adjacent to the tip head 30, which facilitates the worker to package the sample and tip head 70. The reaction cavity 24 is located at the second end of the bearing member 10, which facilitates the matching of the reaction cavity 24 and the magnetic attraction device of the biological detection apparatus.

Referring to fig. 12 and 13, the accommodating chamber 20 further includes a reagent chamber 22 and a cleaning solution chamber 23, the reagent chamber 22 is used for accommodating a reagent and a diluent, and the cleaning solution chamber 23 is used for accommodating a cleaning solution.

Specifically, referring to fig. 12 and 13, in the present embodiment, a sample chamber 21, two carrying chambers, four reagent chambers 22, two cleaning solution chambers 23, and a reaction chamber 24 are sequentially disposed from a first end to a second end of the carrying member 10. In other embodiments, the number and position of the accommodating cavities 20 can be set arbitrarily according to requirements.

In this embodiment, the sample chamber 21, the reagent chamber 22, and the reaction chamber 24 are of one type, and the cleaning liquid chamber 23 is of a second type. In other embodiments, the shape and capacity of various cavities can be flexibly set according to requirements.

It should be noted that the various chambers in this embodiment can be used more flexibly, for example, the reaction chamber 24 can be pre-filled with reagents (which may be magnetic bead reagents) or directly added to the sample, i.e., the reaction chamber 24 has both the function of providing reaction sites and the function of containing reagents or samples. Various cavities in this embodiment, after being used, all can be used for holding the waste liquid that detects the production, realize the reutilization. In some reagent cards that require manual sample application, the receiving cavity of the reagent card may not include a sample cavity.

The foregoing is a more detailed description of the present application in connection with specific embodiments thereof, and it is not intended that the present application be limited to the specific embodiments thereof. It will be apparent to those skilled in the art from this disclosure that many more simple derivations or substitutions can be made without departing from the inventive concepts herein.

Claims

1. A liquid phase chip detection apparatus, comprising:

the collection mechanism is used for collecting the particles to be analyzed;

2. The liquid phase chip detection apparatus of claim 1, wherein the pipetting mechanism has a sampling structure, and at least one of the pipetting mechanism and the loading mechanism has a driving assembly capable of driving the pipetting mechanism and/or the loading mechanism to move so that the sampling structure can protrude into the accommodating cavity of the reagent site, the sample site and/or the reaction site.

3. The apparatus for liquid phase chip detection according to claim 2, wherein the pipetting mechanism comprises a first sampling needle, a first sampling driving assembly, a first conduit and a first fluid driving member, wherein the first sampling driving assembly can drive the first sampling needle to move along a first path so that the first sampling needle extends into the accommodating cavity of the reagent site, the sample site and/or the reaction site opposite to the first sampling needle, one end of the first conduit is communicated with the first sampling needle, and the other end of the first conduit is connected with the first fluid driving member.

4. The apparatus for liquid phase chip detection according to claim 3, wherein the loading mechanism comprises a loading plate for detachably connecting with the reagent card and a loading driving assembly capable of driving the loading plate to move along the second path to move the reagent site, the sample site and/or the reaction site to a position opposite to the first sampling needle.

5. The liquid phase chip detection apparatus according to claim 4, wherein the pipetting mechanism further comprises a first needle holder on which the first sampling needle is disposed and a first slide rail extending in a first direction;

6. The apparatus for detecting liquid phase chip as claimed in claim 4, wherein the loading mechanism further comprises a second slide rail, the loading plate is slidably connected to the second slide rail, the second slide rail extends along a second direction, the loading driving assembly comprises a second motor, a second lead screw and a second slider, the second lead screw is rotatably disposed and parallel to the second slide rail, the second slider is movably sleeved on the second lead screw, the second slider is connected to the loading plate, an output end of the second motor is connected to the second lead screw, and the second motor is configured to drive the second lead screw to rotate so as to drive the second slider and the loading plate to move along the second direction.

7. The LC chip detection apparatus of claim 1, wherein the collection mechanism comprises a second sampling needle, a second sampling driving assembly, a second conduit and a second fluid driving member, the second sampling driving assembly is capable of driving the sampling needle to move along a third path so that the second sampling needle extends into the accommodating cavity of the reaction site opposite to the second sampling needle, one end of the second conduit is communicated with the second sampling needle, the other end of the second conduit is communicated with the inlet of the detection region, and the second fluid driving member is capable of driving the particles to be detected to flow to the detection region through the second sampling needle and the second conduit.

8. The liquid phase chip detection apparatus according to claim 7, wherein a plurality of reaction sites are arranged along a third direction, the collection mechanism further comprises a third slide rail, a fourth slide rail, a first bearing plate and a second needle frame, and the second sampling needle is arranged on the second needle frame;

9. The liquid phase chip detection apparatus of claim 7, further comprising a cleaning mechanism, the cleaning mechanism comprising a third conduit, a cleaning liquid container, and a gating device, the second fluid driving member being in communication with an outlet of the detection region through the gating device, the gating device being in communication with the cleaning liquid container through the third conduit, the gating device being switchable between a first state in which the second fluid driving member is in communication with a liquid path between the detection region and a second state in which the second fluid driving member is in communication with a liquid path between the cleaning liquid container.

10. The liquid phase chip detection apparatus according to any one of claims 1 to 9, further comprising a tip head position for carrying a tip head, wherein the tip head position is disposed on the reagent card and/or on the loading mechanism, wherein the pipetting mechanism comprises a first sampling needle, wherein the collecting mechanism comprises a second sampling needle, and wherein the first sampling needle and/or the second sampling needle has a connecting portion for detachably connecting with the tip head.

11. The liquid phase chip detection device according to claim 10, further comprising a tip head separation structure, wherein the tip head separation structure comprises a separation member and a separation driving assembly, the separation member is movably disposed, the separation driving assembly is configured to drive the separation member to move between a first position and a second position, the separation member is configured to push the tip head to separate from the connection portion of the sampling needle when moving to the first position, and the separation member does not prevent the tip head from being detachably connected to the connection portion when moving to the second position.

12. The liquid phase chip detection apparatus according to any one of claims 1 to 9, further comprising a sample site and/or a reaction site, wherein the sample site and/or the reaction site is provided on a reagent card and/or a loading mechanism.

13. The apparatus for liquid phase chip detection according to any of claims 1 to 9, wherein the loading mechanism further comprises a heating plate in contact with the loading plate, the heating plate being configured to provide a heated environment for the reaction site.

14. The apparatus for detecting liquid phase chip of any one of claims 1 to 9, wherein the loading mechanism further comprises a magnetic attraction device disposed toward the reaction site, the particles comprise magnetic particles, and the magnetic attraction device is configured to generate a magnetic field to attract the magnetic particles to a side or a bottom of the reaction site.

15. The liquid phase chip detection apparatus according to any one of claims 1 to 9, wherein the sample site is provided on a reagent card or on a loading mechanism, and the reaction site is provided on a reagent card or on a loading mechanism.

16. The liquid phase chip detection apparatus according to any one of claims 1 to 9, further comprising a light source for irradiating the particles in the detection region so that the particles emit light signals related to the characteristics of the particles themselves after being irradiated.