Analyzer
By using independently designed sample needle and reagent needle assemblies and optimizing the reagent tray layout and movement trajectory, the problems of limited test speed and difficult maintenance of the analyzer have been solved, enabling efficient and reliable biochemical analysis.
Patent Information
- Application Number
- CN202520174748.7
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2025-01-26
- Publication Date
- 2026-01-27
- Estimated Expiration
- 2035-01-26
AI Technical Summary
Existing analyzers have limited testing speed, complex equipment structure, difficult maintenance, inconvenient reagent management, and the problem of having to stop operation when reagents are exhausted.
The sample needle assembly and reagent needle assembly are independently designed and located on both sides of the reaction plate. They achieve high-precision movement through linear guide rails and rotating rocker arms, optimizing the layout and movement trajectory of the reagent plate assembly and avoiding cross-contamination.
It improves the testing efficiency and reliability of the analyzer, reduces equipment downtime, optimizes space utilization, reduces energy consumption, and ensures the accuracy and reliability of analysis results.
Smart Images

Figure CN223841921U_ABST
Abstract
Description
Technical Field
[0001] This utility model relates to the field of biomedical technology, and in particular to an analyzer. Background Technology
[0002] Analyzers are indispensable equipment in modern medicine and chemical testing, primarily used to detect the concentration and activity of substances by observing changes in their optical properties during chemical reactions. These devices are widely used in clinical laboratories and research institutions, providing rapid and accurate results to support doctors' diagnostic and treatment decisions.
[0003] With the continuous advancement of medical technology and increasing emphasis on health management, the demand for analytical instruments is growing. Most existing analyzers in the industry employ a dual-measurement system design, increasing testing speed by setting up two independent measurement systems on the same device. However, the single-unit testing speed of mainstream high-speed analyzers on the market is generally only around 2000 results / hour, and its improvement is difficult due to limitations in design and control technology.
[0004] While traditional dual-measurement system designs improve testing efficiency to some extent, they also have several drawbacks. First, the dual-system approach requires two reagent management and dispensing subsystems, leading to increased structural complexity and maintenance difficulties. If one dispensing subsystem malfunctions or requires maintenance, the efficiency of the other will be affected, thus reducing overall system efficiency. Furthermore, when placing similar components in the reagent management subsystem, if one system runs out of reagents, the entire system must be paused for replenishment, further impacting testing continuity and efficiency. Additionally, the layout of existing products often results in overcrowding between reagent tray and reagent needle assemblies, limiting tray capacity and overall device size, increasing energy consumption and maintenance complexity. Therefore, a novel analyzer design is urgently needed to optimize the layout of the reagent management and dispensing subsystems, improve testing speed and operational efficiency, and address the shortcomings and deficiencies of existing technologies.
[0005] The above information disclosed in the background art of this utility model is only used to understand the background of the concept of this utility model, and may include information that does not constitute prior art. Utility Model Content
[0006] Therefore, it is necessary to provide an analyzer to address the above problems.
[0007] This application provides an analyzer comprising:
[0008] frame;
[0009] A track, which is disposed on the frame;
[0010] A reaction disk, which is disposed on the frame and includes an inner ring and an outer ring of the reaction disk on which a reaction cup is loaded;
[0011] A sample needle assembly, which is disposed on the rack and used to pick up samples from the track and transfer them into a reaction cup on the reaction plate;
[0012] A first reagent tray assembly is disposed on the rack and loaded with reagent bottles;
[0013] The second reagent tray assembly is disposed on the frame and loaded with reagent bottles. The first reagent tray assembly and the second reagent tray assembly are arranged at intervals and are respectively located on both sides of the reaction tray.
[0014] The first reagent needle assembly is disposed on the frame and is movable relative to the frame, and is used to draw reagent from the reagent bottle on the first reagent tray assembly and transfer it to the reaction cup in the inner ring of the reaction tray;
[0015] The second reagent needle assembly is disposed on the frame and is movable relative to the frame, and is used to draw the reagent from the reagent bottle on the second reagent tray assembly and transfer it to the reaction cup on the outer ring of the reaction tray;
[0016] The movement trajectory of the first reagent needle assembly does not intersect with the movement trajectory of the second reagent needle assembly.
[0017] The aforementioned analyzer achieves at least the following beneficial effects: The independent design of the sample needle assembly and reagent needle assembly allows for flexible scheduling during sample transfer and reagent addition, adapting to different experimental needs and improving the applicability of the equipment. By placing the first and second reagent tray assemblies on opposite sides of the reaction tray and equipping each with an independent reagent needle assembly, reagent aspiration and transfer can be performed simultaneously, effectively shortening the testing cycle and improving overall testing efficiency. Since the movement trajectories of the first and second reagent needle assemblies do not intersect, even if one reagent needle assembly malfunctions or requires maintenance, the other assembly can still operate independently, thereby reducing equipment downtime and improving equipment reliability and availability. The spaced arrangement of the reagent tray assemblies avoids reagent bottle congestion, optimizes the spatial layout, improves the internal space utilization of the equipment, and facilitates maintenance and operation. Simultaneously, this design also helps reduce equipment energy consumption and improve overall performance. Through a reasonable layout design, the sample and reagent transfer paths are optimized, reducing the risk of cross-contamination, ensuring the accuracy and reliability of the reaction, and thus improving the quality of the analytical results. In summary, the design of this analyzer not only improves testing efficiency and reliability, but also optimizes the operation process and spatial layout, providing users with a more efficient and convenient biochemical analysis solution.
[0018] In some embodiments, the first reagent tray assembly includes an inner ring and an outer ring containing reagent bottles. The outer ring is fitted over the inner ring, and both the inner and outer rings are rotatable independently. The first reagent needle assembly includes an inner and an outer needle. The inner needle is mounted on the frame and movable relative to it, and is used to draw reagents from the bottles in the inner ring of the reagent tray and transfer them to the reaction cup in the inner ring of the reaction tray. The outer needle is mounted on the frame and movable relative to it, and is used to draw reagents from the bottles in the outer ring of the reagent tray and transfer them to the reaction cup in the inner ring of the reaction tray. The movement trajectories of the inner and outer needles do not intersect. The independent rotation of the inner and outer rings makes reagent acquisition and transfer more efficient. The rotation of the reagent tray can be flexibly adjusted as needed to quickly locate the required reagent bottle, reducing waiting time and improving overall work efficiency. Due to the independent rotation design of the inner and outer rings, the rotation speed and direction can be better controlled during operation, reducing vibration and instability caused by improper rotation, thereby improving the overall stability and reliability of the equipment. The first reagent needle assembly includes a first inner reagent needle and a first outer reagent needle, used to aspirate reagents from the inner and outer rings of the first reagent tray, respectively. This dual-needle design not only improves the reagent transfer speed but also allows for the extraction of reagents from different locations simultaneously, further enhancing the equipment's processing capacity. The movement trajectories of the first inner and outer reagent needles do not intersect, avoiding interference and collisions during movement that could lead to damage or jamming. It also ensures that cross-contamination does not occur during reagent transfer, a design particularly important for the analyzer, as cross-contamination can cause errors in analytical results and affect experimental accuracy. This design also allows for the simultaneous use of multiple reagents in the same experiment, adapting to different experimental needs. This flexibility enables the analyzer to be widely used in various biochemical detection scenarios, meeting diverse experimental requirements. In summary, this implementation method, by optimizing the structural design of the first reagent tray assembly, further improves the efficiency, accuracy, and ease of operation of the analyzer, providing users with a superior analytical experience.
[0019] In some embodiments, the second reagent tray assembly includes an inner ring and an outer ring containing reagent bottles. The outer ring is fitted over the inner ring, and both rings can rotate independently. The second reagent needle assembly includes an inner and an outer needle. The inner needle is mounted on the frame and can move relative to it, and is used to draw reagents from the bottles in the inner ring and transfer them to the reaction cup in the outer ring. The outer needle is also mounted on the frame and can move relative to it, and is used to draw reagents from the bottles in the outer ring and transfer them to the reaction cup in the outer ring. The movement trajectories of the inner and outer needles do not intersect. The independent rotation of the inner and outer rings makes reagent acquisition and transfer more efficient. The rotation of the reagent tray can be flexibly adjusted as needed to quickly locate the required reagent bottle, reducing waiting time and improving overall work efficiency. Due to the independent rotation design of the inner and outer rings, the rotation speed and direction can be better controlled during operation, reducing vibration and instability caused by improper rotation, thereby improving the overall stability and reliability of the equipment. The second reagent needle assembly includes a second inner reagent needle and a second outer reagent needle, used to aspirate reagents from the inner and outer rings of the second reagent tray, respectively. This dual-needle design not only improves the reagent transfer speed but also allows for the extraction of reagents from different locations simultaneously, further enhancing the equipment's processing capacity. The non-intersecting motion trajectories of the second inner and outer reagent needles prevent interference and collisions during movement, thus avoiding damage or jamming. It also ensures no cross-contamination occurs during reagent transfer, a crucial design feature for the analyzer, as cross-contamination can lead to errors in analytical results and affect experimental accuracy. This design also allows for the simultaneous use of multiple reagents in the same experiment, adapting to different experimental needs. This flexibility enables the analyzer to be widely applied in various biochemical detection scenarios, meeting diverse experimental requirements. In summary, this implementation method, by optimizing the structural design of the second reagent tray assembly, further improves the efficiency, accuracy, and ease of operation of the analyzer, providing users with a superior analytical experience.
[0020] In some embodiments, the first and second reagent needle assemblies can be mounted to the frame via linear guides and / or a rotating rocker arm to enable movement of the first and second reagent needle assemblies relative to the frame. The use of linear guides and rotating rocker arms allows for high-precision movement of the reagent needle assemblies. This precise control is crucial for reagent extraction and transfer processes, ensuring accurate positioning and effective extraction, thereby improving experimental reliability. This design not only supports linear movement of the reagent needles but also enables multi-dimensional movement, expanding the device's functionality. For example, the linear guides allow the reagent needle assemblies to move smoothly along a set track, while the rotating rocker arm allows operation at different angles. This flexibility allows the device to adapt to different types of reagent bottle and reaction cup layouts, meeting diverse experimental needs. Furthermore, the rotating rocker arm allows the reagent needles to operate at different angles, adapting to more complex experimental requirements.
[0021] In some embodiments, the rotating rocker arm includes a first rocker arm assembly and a second rocker arm assembly mounted on the frame with independent motion trajectories. The first rocker arm assembly includes a first inner rocker arm and a first outer rocker arm mounted on the frame with independent motion trajectories. The first inner rocker arm is connected to the first inner reagent needle and drives the first inner reagent needle to move. The first outer rocker arm is connected to the first outer reagent needle and drives the first outer reagent needle to move. The second rocker arm assembly includes a second inner rocker arm and a second outer rocker arm mounted on the frame with independent motion trajectories. The second inner rocker arm is connected to the second inner reagent needle and drives the second inner reagent needle to move. The second outer rocker arm is connected to the second outer reagent needle and drives the second outer reagent needle to move. The independent design of the first and second rocker arm assemblies ensures that the movements of the two reagent needles do not interfere with each other during operation. This independence allows the device to process different reagents simultaneously, improving experimental efficiency and flexibility. The first inner and first outer rocker arms are respectively connected to their corresponding reagent needles, enabling precise control of the reagent needle's motion trajectory. This precise control is crucial for ensuring accurate reagent extraction and transfer, reducing operational errors. By configuring the first inner rocker arm, the first outer rocker arm, the second inner rocker arm, and the second outer rocker arm separately, the design can more effectively utilize rack space, making the equipment more compact in structure and adaptable to the needs of different laboratory environments. At the same time, this design can also reduce the overall size of the equipment, facilitating operation and maintenance.
[0022] In some embodiments, the first rocker arm assembly is disposed between the reaction tray and the first reagent tray assembly, and the second rocker arm assembly is disposed between the reaction tray and the second reagent tray assembly. Positioning the rocker arm assembly between the reaction tray and the reagent tray assembly effectively utilizes the internal space of the equipment, reducing the floor space required. This compact design helps improve the space utilization rate of the laboratory, making the equipment more suitable for use in space-constrained environments.
[0023] In some embodiments, the sample needle assembly can be mounted to the frame via linear guides and / or a rotating rocker arm to enable movement of the sample needle assembly relative to the frame. The use of linear guides allows for smooth linear movement of the sample needle assembly, ensuring accuracy during sample extraction and transfer. This high-precision motion control is crucial for the reliability of experimental results. The rotating rocker arm design allows the sample needle assembly to move at multiple angles, enabling the device to adapt to different experimental needs. For example, the sample needle can operate at different heights and angles, increasing the flexibility of the device. The linear guides and rotating rocker arms can be used individually or in combination, making the sample needle assembly more stable during movement and reducing errors caused by vibration or imbalance. This stability is particularly important for high-precision experiments, ensuring accurate sample extraction and transfer. In summary, the design of mounting the sample needle assembly to the frame via linear guides and / or a rotating rocker arm not only improves the accuracy and flexibility of movement but also simplifies installation and maintenance processes, providing users with an efficient, stable, and intelligent experimental solution.
[0024] In some embodiments, the sample needle assembly is positioned between the track and the reaction disk. The sample needle assembly includes a first sample needle and a second sample needle mounted on the frame with non-interfering motion trajectories. The first sample needle is used to aspirate samples from the track and transfer them to a reaction cup on the inner ring of the reaction disk, while the second sample needle is used to aspirate samples from the track and transfer them to a reaction cup on the outer ring of the reaction disk. Positioning the sample needle assembly between the track and the reaction disk helps optimize the spatial layout of the equipment and reduce its footprint. This compact design is suitable for space-constrained laboratory environments, improving the overall space utilization of the equipment. The first and second sample needles are responsible for sample transfer in the inner and outer rings, respectively, allowing the equipment to flexibly manage multiple samples. This flexibility enables the equipment to adapt to different experimental needs, meet the requirements of multi-sample processing, significantly improve sample transfer efficiency, reduce processing time, and is suitable for high-throughput experiments. By designing sample needles with non-interfering motion trajectories, interference and collisions between sample needles are prevented, reducing the risk of damage, and cross-interference during sample extraction and transfer is also ensured. This design improves operational safety and accuracy and reduces the risk of sample contamination.
[0025] In some embodiments, from a top-down view, the track is located above the reaction disk, the sample needle assembly is positioned between the reaction disk and the track, and the first reagent needle assembly and the second reagent needle assembly are located on either side of the reaction disk, further away from the track than the reaction disk. Positioning the track above the reaction disk and placing the sample needle assembly between the reaction disk and the track effectively utilizes experimental space, reduces the equipment's footprint, and is suitable for environments with limited space. Separating the sample needle assembly and reagent needle assembly makes sample and reagent transfer more convenient for operators, simplifying equipment maintenance and cleaning procedures. Operators can more easily access each component, ensuring long-term stable operation of the equipment.
[0026] In some embodiments, from a top-down view, the track is located above the reaction disk, the sample needle assembly is disposed between the reaction disk and the track, and the first reagent needle assembly and the second reagent needle assembly are located on both sides of the reaction disk, closer to the track than the reaction disk itself. Positioning the track above the reaction disk and placing the sample needle assembly between the reaction disk and the track, with the reagent needle assemblies located on both sides of the reaction disk and closer to the track, results in a more compact layout, effectively utilizing space, reducing the equipment's footprint, and making it suitable for spaces with limited space.
[0027] In some embodiments, from a top-down view, the track is located to the left or right of the reaction disk, the sample needle assembly is disposed between the reaction disk and the track, and the first reagent needle assembly and the second reagent needle assembly are located on both sides of the reaction disk and are further away from the track than the reaction disk. Attached Figure Description
[0028] To more clearly illustrate the technical solutions in the embodiments of this utility model or the conventional technology, the drawings used in the description of the embodiments or the conventional technology will be briefly introduced below. Obviously, the drawings described below are only some embodiments of this utility model. For those skilled in the art, other drawings can be obtained based on these drawings without creative effort.
[0029] Figure 1 This is a schematic diagram of an analyzer provided in one embodiment of the present invention.
[0030] Figure 2 This is another schematic diagram of the analyzer provided in one embodiment of the present invention, wherein the dashed lines show the movement trajectories of the reagent needle and the sample needle.
[0031] Figure 3This is another schematic diagram of the analyzer provided in one embodiment of the present invention, wherein the dashed lines show the movement trajectories of the reagent needle and the sample needle.
[0032] Figure 4 This is another schematic diagram of the analyzer provided in one embodiment of the present invention, wherein the dashed lines show the movement trajectories of the reagent needle and the sample needle.
[0033] Figure 5 This is another schematic diagram of the analyzer provided in one embodiment of the present invention, wherein the dashed lines show the movement trajectories of the reagent needle and the sample needle.
[0034] Figure label:
[0035] 10. Analyzer; 100. Frame; 200. Track; 300. Reaction plate; 310. Inner ring of reaction plate; 320. Outer ring of reaction plate; 400. Sample needle assembly; 410. First sample needle; 420. Second sample needle; 510. First reagent plate assembly; 511. Inner ring of first reagent plate; 512. Outer ring of first reagent plate; 520. Second reagent plate assembly; 521. Inner ring of second reagent plate; 522. Outer ring of second reagent plate; 610. First reagent needle assembly; 611. First inner reagent needle; 612. First outer reagent needle; 620. Second reagent needle assembly; 621. Second inner reagent needle; 622. Second outer reagent needle; 710. First rocker arm assembly; 711. First inner rocker arm; 712. First outer rocker arm; 720. Second rocker arm assembly; 721. Second inner rocker arm; 722. Second outer rocker arm. Detailed Implementation
[0036] To make the above-mentioned objects, features, and advantages of this utility model more apparent and understandable, the specific embodiments of this utility model will be described in detail below with reference to the accompanying drawings. Many specific details are set forth in the following description to provide a full understanding of this utility model. However, this utility model can be implemented in many other ways different from those described herein, and those skilled in the art can make similar modifications without departing from the spirit of this utility model. Therefore, this utility model is not limited to the specific embodiments disclosed below.
[0037] Please see Figures 1 to 5In some embodiments, the present invention provides an analyzer 10, which includes a frame 100, a track 200, a reaction disk 300, a sample needle assembly 400, a first reagent disk assembly 510, a second reagent disk assembly 520, a first reagent needle assembly 610, and a second reagent needle assembly 620. The track 200 is disposed on the frame 100; the reaction disk 300 is disposed on the frame 100 and includes an inner ring 310 and an outer ring 320 containing a reaction cup; the sample needle assembly 400 is disposed on the frame 100 and is used to aspirate samples from the track 200 and transfer them to a reaction cup on the reaction disk 300; the first reagent disk assembly 510 is disposed on the frame 100 and contains a reagent bottle; the second reagent disk assembly 520 is disposed on the frame 100 and contains a reagent bottle, the first reagent disk assembly 510 and the second reagent disk assembly 520 being spaced apart from each other and respectively located on the reaction disk 300. On both sides of 00; the first reagent needle assembly 610 is disposed on the frame 100 and can move relative to the frame 100, and is used to draw the reagent in the reagent bottle on the first reagent tray assembly 510 and transfer it to the reaction cup in the inner ring 310 of the reaction tray; the second reagent needle assembly 620 is disposed on the frame 100 and can move relative to the frame 100, and is used to draw the reagent in the reagent bottle on the second reagent tray assembly 520 and transfer it to the reaction cup in the outer ring 320 of the reaction tray; wherein, the movement trajectory of the first reagent needle assembly 610 and the movement trajectory of the second reagent needle assembly 620 do not intersect.
[0038] The analyzer 10 described above achieves at least the following beneficial effects: The independent design of the sample needle assembly 400 and the reagent needle assembly allows for flexible scheduling during sample transfer and reagent addition, adapting to different experimental needs and improving the applicability of the equipment. By placing the first reagent tray assembly 510 and the second reagent tray assembly 520 on opposite sides of the reaction tray 300 and equipping them with independent reagent needle assemblies, reagent aspiration and transfer can be performed simultaneously, effectively shortening the testing cycle and improving overall testing efficiency. Since the movement trajectories of the first reagent needle assembly 610 and the second reagent needle assembly 620 do not intersect, even if one reagent needle assembly malfunctions or requires maintenance, the other assembly can still work independently, thereby reducing equipment downtime and improving equipment reliability and availability. The spaced arrangement of the reagent tray assemblies avoids reagent bottle congestion, optimizes the spatial layout, improves the internal space utilization of the equipment, and facilitates maintenance and operation. At the same time, this design also helps to reduce equipment energy consumption and improve overall performance. Through a reasonable layout design, the sample and reagent transfer paths are optimized, reducing the risk of cross-contamination, ensuring the accuracy and reliability of the reaction, and thus improving the quality of the analytical results. In summary, the design of this analyzer 10 not only improves testing efficiency and reliability, but also optimizes the operation process and spatial layout, providing users with a more efficient and convenient biochemical analysis solution.
[0039] In some embodiments, the first reagent tray assembly 510 includes an inner reagent tray 511 and an outer reagent tray 512 containing reagent bottles. The outer reagent tray 512 is fitted onto the inner reagent tray 511, and the inner and outer reagent trays are rotatable independently. The first reagent needle assembly 610 includes an inner reagent needle 611 and an outer reagent needle 612. The inner reagent needle 611 is mounted on the frame 100 and is movable relative to the frame 100, and is used to draw reagents from the reagent bottles in the inner reagent tray 511 and transfer them to the reaction cup in the inner reaction tray 310. The outer reagent needle 612 is mounted on the frame 100 and is movable relative to the frame 100, and is used to draw reagents from the reagent bottles in the outer reagent tray and transfer them to the reaction cup in the inner reaction tray 310. The movement trajectories of the inner and outer reagent needles do not intersect. The inner ring 511 and outer ring 512 of the first reagent tray can rotate independently. This design makes reagent acquisition and transfer more efficient. The rotation of the reagent tray can be flexibly adjusted as needed to quickly locate the required reagent bottle, reducing waiting time and improving overall work efficiency. Due to the independent rotation design of the inner and outer rings, the rotation speed and direction can be better controlled during operation, reducing vibration and instability caused by improper rotation, thereby improving the overall stability and reliability of the equipment. The first reagent needle assembly 610 includes a first inner reagent needle 611 and a first outer reagent needle 612, which are used to draw reagents from the inner ring 511 and outer ring of the first reagent tray, respectively. This dual-needle design not only improves the reagent transfer speed but also allows for the extraction of reagents from different locations simultaneously, further enhancing the processing capacity of the equipment. The movement trajectories of the first inner reagent needle 611 and the first outer reagent needle 612 do not intersect, avoiding interference and collisions during movement that could lead to damage or jamming. This design also ensures no cross-contamination occurs during reagent transfer, a crucial feature for the analyzer 10 as cross-contamination can cause errors in analytical results and affect experimental accuracy. This design also allows for the simultaneous use of multiple reagents in the same experiment, adapting to diverse experimental needs. This flexibility enables the analyzer 10 to be widely applied in various biochemical detection scenarios, meeting diverse experimental requirements. In summary, this implementation, through optimizing the structural design of the first reagent tray assembly 510, further improves the efficiency, accuracy, and ease of operation of the analyzer 10, providing users with a superior analytical experience.
[0040] In some embodiments, the second reagent tray assembly 520 includes a second reagent tray inner ring 521 and a second reagent tray outer ring 522 containing reagent bottles. The second reagent tray outer ring 522 is fitted onto the second reagent tray inner ring 521, and the second reagent tray inner ring 521 and the second reagent tray outer ring 522 can rotate independently of each other. The second reagent needle assembly 620 includes a second inner reagent needle 621 and a second outer reagent needle 622. The second inner reagent needle 621 is disposed on the frame 100 and can move relative to the frame 100, and is used to draw reagents from the reagent bottles in the second reagent tray inner ring 521 and transfer them to the reaction cup in the reaction tray outer ring 320. The second outer reagent needle 622 is disposed on the frame 100 and can move relative to the frame 100, and is used to draw reagents from the reagent bottles in the second reagent tray outer ring 522 and transfer them to the reaction cup in the reaction tray outer ring 320. The movement trajectories of the second inner reagent needle 621 and the second outer reagent needle 622 do not intersect. The inner ring 521 and outer ring 522 of the second reagent tray can rotate independently. This design makes reagent acquisition and transfer more efficient. The rotation of the reagent tray can be flexibly adjusted as needed to quickly locate the required reagent bottle, reducing waiting time and improving overall work efficiency. Due to the independent rotation design of the inner and outer rings, the rotation speed and direction can be better controlled during operation, reducing vibration and instability caused by improper rotation, thereby improving the overall stability and reliability of the equipment. The second reagent needle assembly 620 includes a second inner reagent needle 621 and a second outer reagent needle 622, which are used to draw reagents from the inner ring 521 and outer ring of the second reagent tray, respectively. This dual-needle design not only improves the reagent transfer speed but also allows for the extraction of reagents from different locations simultaneously, further enhancing the processing capacity of the equipment. The movement trajectories of the second inner reagent needle 621 and the second outer reagent needle 622 do not intersect, avoiding interference and collisions during movement that could cause damage or jamming. This design also ensures no cross-contamination occurs during reagent transfer, a crucial feature for the analyzer 10 as cross-contamination can lead to errors in analytical results and affect experimental accuracy. Furthermore, this design allows for the simultaneous use of multiple reagents in the same experiment, adapting to diverse experimental needs. This flexibility enables the analyzer 10 to be widely applied in various biochemical detection scenarios, meeting diverse experimental requirements. In summary, this implementation, through optimized structural design of the second reagent tray assembly 520, further improves the efficiency, accuracy, and ease of operation of the analyzer 10, providing users with a superior analytical experience.
[0041] In some embodiments, the first reagent needle assembly 610 and the second reagent needle assembly 620 can be mounted to the frame 100 via linear guides and / or a rotating rocker arm to enable movement of the first reagent needle assembly 610 and the second reagent needle assembly 620 relative to the frame 100. The use of linear guides and rotating rocker arms allows for high-precision movement of the reagent needle assemblies. This precise control is crucial for reagent extraction and transfer processes, ensuring accurate positioning and effective extraction of reagents, thereby improving experimental reliability. This design not only supports linear movement of the reagent needles but also enables multi-dimensional movement, expanding the functionality of the device. For example, the linear guides allow the reagent needle assemblies to move smoothly along a set track 200, while the rotating rocker arm allows the reagent needle assemblies to operate at different angles. This flexibility allows the device to adapt to different types of reagent bottle and reaction cup layouts, meeting diverse experimental needs. Furthermore, the rotating rocker arm allows the reagent needles to operate at different angles, thus adapting to more complex experimental requirements.
[0042] In some embodiments, the rotating rocker arm includes a first rocker arm assembly 710 and a second rocker arm assembly 720 disposed on the frame 100 and whose motion trajectories do not interfere with each other. The first rocker arm assembly 710 includes a first inner rocker arm 711 and a first outer rocker arm 712 disposed on the frame 100 and whose motion trajectories do not interfere with each other. The first inner rocker arm 711 is connected to the first inner reagent needle 611 and is used to drive the first inner reagent needle 611 to move. The first outer rocker arm 712 is connected to the first outer reagent needle 612 and is used to drive the first outer reagent needle 612 to move. The second rocker arm assembly 720 includes a second inner rocker arm 721 and a second outer rocker arm 722 disposed on the frame 100 and whose motion trajectories do not interfere with each other. The second inner rocker arm 721 is connected to the second inner reagent needle 621 and is used to drive the second inner reagent needle 621 to move. The second outer rocker arm 722 is connected to the second outer reagent needle 622 and is used to drive the second outer reagent needle 622 to move. The independent design of the first rocker arm assembly 710 and the second rocker arm assembly 720 ensures that the movements of the two reagent needles do not interfere with each other during operation. This independence allows the device to process different reagents simultaneously, improving experimental efficiency and flexibility. The first inner rocker arm 711 and the first outer rocker arm 712 are connected to their respective reagent needles, enabling precise control of the needle's movement trajectory. This precise control is crucial for ensuring accurate reagent extraction and transfer, reducing operational errors. By separately configuring the first inner rocker arm 711, the first outer rocker arm 712, the second inner rocker arm 721, and the second outer rocker arm 722, the design more effectively utilizes the rack space 100, making the device more compact and adaptable to different laboratory environments. Simultaneously, this design reduces the overall size of the device, facilitating operation and maintenance.
[0043] In some embodiments, the first rocker arm assembly 710 is disposed between the reaction tray 300 and the first reagent tray assembly 510, and the second rocker arm assembly 720 is disposed between the reaction tray 300 and the second reagent tray assembly 520. Positioning the rocker arm assemblies between the reaction tray 300 and the reagent tray assemblies effectively utilizes the internal space of the equipment, reducing its footprint. This compact design helps improve the space utilization rate of the laboratory, making the equipment more suitable for use in space-constrained environments.
[0044] In some embodiments, the sample needle assembly 400 can be mounted to the frame 100 via a linear guide and / or a rotating rocker arm to enable movement of the sample needle assembly 400 relative to the frame 100. The use of a linear guide enables smooth linear movement of the sample needle assembly 400, ensuring accuracy during sample extraction and transfer. This high-precision motion control is crucial for the reliability of experimental results. The rotating rocker arm design allows the sample needle assembly 400 to move at multiple angles, enabling the device to adapt to different experimental needs. For example, the sample needle can operate at different heights and angles, increasing the flexibility of the device. The linear guide and rotating rocker arm can be used individually or in combination, making the sample needle assembly 400 more stable during movement and reducing errors caused by vibration or imbalance. This stability is particularly important for high-precision experiments, ensuring accurate sample extraction and transfer. In summary, the design of mounting the sample needle assembly 400 to the frame 100 via linear guides and / or a rotating rocker arm not only improves the accuracy and flexibility of movement but also simplifies the installation and maintenance process, providing users with an efficient, stable, and intelligent experimental solution.
[0045] In some embodiments, the sample needle assembly 400 is disposed between the track 200 and the reaction disk 300. The sample needle assembly 400 includes a first sample needle 410 and a second sample needle 420 disposed on the frame 100 with independent movement trajectories. The first sample needle 410 is used to aspirate samples from the track 200 and transfer them to a reaction cup on the inner ring 310 of the reaction disk. The second sample needle 420 is used to aspirate samples from the track 200 and transfer them to a reaction cup on the outer ring 320 of the reaction disk. Distributing the sample needle assembly 400 between the track 200 and the reaction disk 300 helps optimize the spatial layout of the equipment and reduce its footprint. This compact design is suitable for space-constrained laboratory environments, improving the overall space utilization of the equipment. The first sample needle 410 and the second sample needle 420 are responsible for sample transfer in the inner and outer rings, respectively, enabling the equipment to flexibly manage multiple samples. This flexibility allows the equipment to adapt to different experimental needs, meet the requirements of multi-sample processing, significantly improve sample transfer efficiency, reduce processing time, and is suitable for high-throughput experimental needs. By designing sample needles whose motion trajectories do not interfere with each other, it is possible to prevent interference and collisions between sample needles, reducing the risk of damage, and also ensuring that no cross-interference occurs during sample extraction and transfer. This design improves the safety and accuracy of the operation and reduces the risk of sample contamination.
[0046] like Figure 2 As shown, in some embodiments, from a top-down view, the track 200 is located above the reaction disk 300, the sample needle assembly 400 is disposed between the reaction disk 300 and the track 200, and the first reagent needle assembly 610 and the second reagent needle assembly 620 are located on both sides of the reaction disk 300, further away from the track 200 than the reaction disk 300. Positioning the track 200 above the reaction disk 300 and placing the sample needle assembly 400 between the reaction disk 300 and the track 200 effectively utilizes experimental space, reduces the equipment's footprint, and is suitable for environments with limited space. Separating the sample needle assembly 400 and the reagent needle assembly makes sample and reagent transfer more convenient for operators, simplifying equipment maintenance and cleaning procedures. Operators can more easily access each component, ensuring long-term stable operation of the equipment.
[0047] like Figure 3As shown, in some embodiments, from a top-down view, the track 200 is located above the reaction disk 300, the sample needle assembly 400 is disposed between the reaction disk 300 and the track 200, and the first reagent needle assembly 610 and the second reagent needle assembly 620 are respectively located on both sides of the reaction disk 300, and are closer to the track 200 than the reaction disk 300. Positioning the track 200 above the reaction disk 300 and placing the sample needle assembly 400 between the reaction disk 300 and the track 200, with the reagent needle assemblies located on both sides of the reaction disk 300 and closer to the track 200, results in a more compact layout, effectively utilizing space, reducing the equipment's footprint, and making it suitable for spaces with limited space.
[0048] like Figure 4 and Figure 5 As shown, in some embodiments, from a top view, the track 200 is located to the left or right of the reaction disk 300, the sample needle assembly 400 is disposed between the reaction disk 300 and the track 200, and the first reagent needle assembly 610 and the second reagent needle assembly 620 are respectively located on both sides of the reaction disk 300 and are further away from the track 200 than the reaction disk 300.
[0049] The technical features of the above embodiments can be combined in any way. For the sake of brevity, not all possible combinations of the technical features in the above embodiments are described. However, as long as there is no contradiction in the combination of these technical features, they should be considered to be within the scope of this specification.
[0050] The embodiments described above are merely illustrative of several implementations of this utility model, and while the descriptions are relatively specific and detailed, they should not be construed as limiting the scope of the patent application. It should be noted that those skilled in the art can make various modifications and improvements without departing from the concept of this utility model, and these all fall within the protection scope of this utility model. Therefore, the protection scope of this utility model patent should be determined by the appended claims.
[0051] In the description of this utility model, it should be understood that if terms such as "center", "longitudinal", "transverse", "length", "width", "thickness", "upper", "lower", "front", "rear", "left", "right", "vertical", "horizontal", "top", "bottom", "inner", "outer", "clockwise", "counterclockwise", "axial", "radial", "circumferential", etc. appear, these terms indicate the orientation or positional relationship based on the orientation or positional relationship shown in the accompanying drawings. They are only for the convenience of describing this utility model and simplifying the description, and do not indicate or imply that the device or element referred to must have a specific orientation, or be constructed and operated in a specific orientation. Therefore, they should not be construed as limitations on this utility model.
[0052] Furthermore, where the terms "first" and "second" appear, these terms are for descriptive purposes only and should not be construed as indicating or implying relative importance or implicitly specifying the number of technical features indicated. Thus, a feature defined with "first" or "second" may explicitly or implicitly include at least one of that feature. In the description of this utility model, where the term "multiple" appears, "multiple" means at least two, such as two, three, etc., unless otherwise explicitly specified.
[0053] In this utility model, unless otherwise explicitly specified and limited, the terms "installation," "connection," "joining," and "fixing," etc., should be interpreted broadly. For example, they can refer to a fixed connection, a detachable connection, or an integral part; they can refer to a mechanical connection or an electrical connection; they can refer to a direct connection or an indirect connection through an intermediate medium; they can refer to the internal communication of two components or the interaction between two components, unless otherwise explicitly limited. Those skilled in the art can understand the specific meaning of the above terms in this utility model according to the specific circumstances.
[0054] In this utility model, unless otherwise explicitly specified and limited, the use of descriptions such as "above" or "below" the second feature indicates that the first and second features are in direct contact, or indirect contact via an intermediate medium. Furthermore, "above," "on top of," and "over" the second feature can mean that the first feature is directly above or diagonally above the second feature, or simply that the first feature is at a higher horizontal level than the second feature. Similarly, "below," "below," and "under" the second feature can mean that the first feature is directly below or diagonally below the second feature, or simply that the first feature is at a lower horizontal level than the second feature.
[0055] It should be noted that if an element is referred to as being "fixed to" or "set on" another element, it can be directly on the other element or there may be an intervening element. If an element is considered to be "connected to" another element, it can be directly connected to the other element or there may be an intervening element. If so, the terms "vertical," "horizontal," "upper," "lower," "left," "right," and similar expressions used in this invention are for illustrative purposes only and do not represent the only possible implementation.
[0056] In this specification, the use of terms such as "an embodiment," "another implementation," etc., refers to a specific feature, structure, material, or characteristic described in connection with that embodiment or example that is included in at least one embodiment or example of the present invention. In this specification, the illustrative descriptions of the above terms do not necessarily refer to the same embodiment or example. Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention pertains. The terminology used herein is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention.
Claims
1. An analyzer, characterized in that, include: frame; A track, which is disposed on the frame; A reaction disk, which is disposed on the frame and includes an inner ring and an outer ring of the reaction disk on which a reaction cup is loaded; A sample needle assembly, which is disposed on the rack and used to pick up samples from the track and transfer them into a reaction cup on the reaction plate; A first reagent tray assembly is disposed on the rack and loaded with reagent bottles; The second reagent tray assembly is disposed on the frame and loaded with reagent bottles. The first reagent tray assembly and the second reagent tray assembly are arranged at intervals and are respectively located on both sides of the reaction tray. The first reagent needle assembly is disposed on the frame and is movable relative to the frame, and is used to draw reagent from the reagent bottle on the first reagent tray assembly and transfer it to the reaction cup in the inner ring of the reaction tray; The second reagent needle assembly is disposed on the frame and is movable relative to the frame, and is used to draw the reagent from the reagent bottle on the second reagent tray assembly and transfer it to the reaction cup on the outer ring of the reaction tray; The movement trajectory of the first reagent needle assembly does not intersect with the movement trajectory of the second reagent needle assembly.
2. The analyzer according to claim 1, characterized in that, The first reagent tray assembly includes an inner ring and an outer ring containing reagent bottles. The outer ring is fitted over the inner ring, and the inner and outer rings can rotate independently. The first reagent needle assembly includes an inner and an outer needle. The inner needle is mounted on the frame and can move relative to the frame. It is used to draw reagents from the reagent bottles in the inner ring of the first reagent tray and transfer them to the reaction cup in the inner ring of the reaction tray. The outer needle is mounted on the frame and can move relative to the frame. It is used to draw reagents from the reagent bottles in the outer ring of the first reagent tray and transfer them to the reaction cup in the inner ring of the reaction tray. The movement trajectories of the inner and outer needles do not intersect.
3. The analyzer according to claim 2, characterized in that, The second reagent tray assembly includes an inner ring and an outer ring containing reagent bottles. The outer ring is fitted onto the inner ring, and the inner and outer rings can rotate independently. The second reagent needle assembly includes an inner and an outer reagent needle. The inner needle is mounted on the frame and can move relative to the frame. It is used to draw reagents from the reagent bottles in the inner ring of the second reagent tray and transfer them to the reaction cup in the outer ring of the reaction tray. The outer needle is mounted on the frame and can move relative to the frame. It is used to draw reagents from the reagent bottles in the outer ring of the second reagent tray and transfer them to the reaction cup in the outer ring of the reaction tray. The movement trajectories of the inner and outer reagent needles do not intersect.
4. The analyzer according to claim 3, characterized in that, The first reagent needle assembly and the second reagent needle assembly can be mounted to the frame via linear guide rails and / or rotating rocker arms to enable movement of the first reagent needle assembly and the second reagent needle assembly relative to the frame.
5. The analyzer according to claim 4, characterized in that, The rotating rocker arm includes a first rocker arm assembly and a second rocker arm assembly mounted on the frame with independent motion trajectories. The first rocker arm assembly includes a first inner rocker arm and a first outer rocker arm mounted on the frame with independent motion trajectories. The first inner rocker arm is connected to the first inner reagent needle and is used to drive the first inner reagent needle to move. The first outer rocker arm is connected to the first outer reagent needle and is used to drive the first outer reagent needle to move. The second rocker arm assembly includes a second inner rocker arm and a second outer rocker arm mounted on the frame with independent motion trajectories. The second inner rocker arm is connected to the second inner reagent needle and is used to drive the second inner reagent needle to move. The second outer rocker arm is connected to the second outer reagent needle and is used to drive the second outer reagent needle to move.
6. The analyzer according to claim 5, characterized in that, The first rocker arm assembly is disposed between the reaction disk and the first reagent disk assembly, and the second rocker arm assembly is disposed between the reaction disk and the second reagent disk assembly.
7. The analyzer according to any one of claims 1 to 6, characterized in that, The sample needle assembly can be mounted to the frame via a linear guide rail and / or a rotating rocker arm to enable movement of the sample needle assembly relative to the frame; And / or, the sample needle assembly is disposed between the track and the reaction disk, the sample needle assembly includes a first sample needle and a second sample needle disposed on the frame and whose movement trajectories do not interfere with each other, the first sample needle is used to pick up the sample on the track and transfer it to the reaction cup on the inner ring of the reaction disk, and the second sample needle is used to pick up the sample on the track and transfer it to the reaction cup on the outer ring of the reaction disk.
8. The analyzer according to any one of claims 1 to 6, characterized in that, From a top-down view, the track is located above the reaction disk, the sample needle assembly is located between the reaction disk and the track, and the first reagent needle assembly and the second reagent needle assembly are located on both sides of the reaction disk and are further away from the track than the reaction disk.
9. The analyzer according to any one of claims 1 to 6, characterized in that, From a top-down view, the track is located above the reaction disk, the sample needle assembly is located between the reaction disk and the track, and the first reagent needle assembly and the second reagent needle assembly are located on both sides of the reaction disk and are closer to the track than the reaction disk.
10. The analyzer according to any one of claims 1 to 6, characterized in that, From a top-down view, the track is located to the left or right of the reaction disk, the sample needle assembly is located between the reaction disk and the track, and the first reagent needle assembly and the second reagent needle assembly are located on both sides of the reaction disk and are further away from the track than the reaction disk.