Bioequivalence pre-test detection kit

Abstract

The utility model relates to the technical field of biological detection, in particular to a bioequivalence pre-test detection kit which comprises a main kit body and a limiting assembly, a kit cover is arranged at the upper end of the main kit body, and the limiting assembly is arranged at the upper end in the main kit body. The limiting assembly comprises a limiting block, mounting seats, reset springs, a clamping ring, a clamping groove, a clamping block and a reagent rack, the mounting seats are mounted on the two sides of the interior of the limiting block, the reset springs are arranged outside the mounting seats, the clamping ring is mounted at the front ends of the reset springs, the clamping groove is formed in the middle end of the interior of the limiting block, and the clamping block is connected to the interior of the clamping groove; the detection kit has the beneficial effects that through the arrangement of the limiting assembly, the problem that the subsequent detection effect is affected due to the fact that most detection kits do not have the use performance of limiting the reagent racks and the reagent racks are likely to collide in the kits is solved, and the overall practicability of the detection kits is conveniently improved.

Description

Technical Field

[0001] The utility model relates to the technical field of biological detection, in particular to a bioequivalence pre-test detection kit. Background Art

[0002] A test kit is a packaging box that holds test reagents. The kit contains a variety of test reagents and testing instruments. The test kit can protect these test reagents and testing instruments to prevent them from being damaged during carrying and transportation. Preliminary testing refers to the process of preliminarily exploring the direction of testing by directly observing the appearance, odor and other properties of the test materials, or conducting some simple chemical reactions such as pH testing and color change reactions, or conducting animal toxicity tests, etc., when conducting unknown substance testing, to provide a basis for the design of the test plan. In order to improve the efficiency of unknown substance detection, a test kit is needed.

[0003] In the prior art, a patent document with application number 202222472551.0 discloses a detection kit. The utility model realizes a sealed connection between the reaction tube and the detection box, which can ensure a tight fit between the reaction tube and the detection box, and ensure that the reaction tube will not leak air or liquid, thereby improving the detection accuracy and detection stability of the detection kit.

[0004] However, when the existing detection kits are used, since most of the detection kits do not have the function of limiting the position of the reagent rack, several reagent racks are prone to collision inside the kit, thereby damaging the equipment and affecting the subsequent detection results, resulting in reduced practicality of the detection kit and reduced use efficiency. Utility Model Content

[0005] The purpose of the utility model is to provide a bioequivalence pre-test detection kit to solve the problems raised in the above background technology.

[0006] To achieve the above-mentioned purpose, the utility model provides the following technical solutions: comprising a main box body and a limit assembly, wherein a box cover is arranged at the upper end of the main box body, a limit assembly is arranged at the upper end inside the main box body, and the limit assembly comprises a limit block, a mounting seat, a reset spring, a clamping ring, a clamping groove, a clamping block and a reagent rack, mounting seats are installed on both sides inside the limit block, a reset spring is arranged outside the mounting seat, and a clamping ring is installed at the front end of the reset spring, a clamping groove is opened at the middle end inside the limit block, and a clamping block is connected inside the clamping groove, and a reagent rack is installed outside the clamping block, and a storage assembly is arranged at the lower end inside the main box body.

[0007] Preferably, the return spring is embedded in the limit block, and the return spring is threadedly connected to the limit block via a mounting seat.

[0008] Preferably, the clamping ring is symmetrically arranged on both sides of the middle end of the limit block, and the clamping ring is elastically connected to the limit block via a reset spring.

[0009] Preferably, the outer dimensions of the clamping block match the inner dimensions of the clamping slot, and the clamping block is connected to the limiting block via the clamping slot.

[0010] Preferably, the storage assembly comprises a storage cavity, a magnetic block, a storage drawer and a magnetic baffle, a magnetic block is additionally provided on the outside of the storage cavity, and the storage drawer is connected to the inside of the storage cavity, and a magnetic baffle is installed on the outside of the storage drawer.

[0011] Preferably, the storage assembly further comprises a limiting slide groove, a fixed block and a movable baffle, and a limiting slide groove is provided inside the storage drawer, the limiting slide groove is internally connected to a fixed block, and a movable baffle is installed outside the fixed block.

[0012] Preferably, the inner dimensions of the limiting slide groove match the outer dimensions of the fixed block, and the movable baffle is slidably connected to the limiting slide groove via the fixed block.

[0013] Compared with the prior art, the beneficial effects of the utility model are:

[0014] The bioequivalence pre-test detection kit proposed by the utility model avoids the problem that most detection kits do not have the use performance of limiting the reagent rack through the setting of the limit component, which makes it easy for several reagent racks to collide inside the kit, thereby damaging the instrument and affecting the subsequent detection effect, causing the problem of reduced practicality of the detection kit. The limit blocks are fixedly installed on both sides of the inside of the main box body through fasteners, and the reset spring is fixedly installed inside the limit blocks by using the mounting seat and the fastening bolts, and the use of the reset spring is limited by the movable rod installed in the middle of the reset spring, and the clamping ring is installed at the front end of the reset spring so that the clamping ring is elastically connected to the limit block through the reset spring. The internal size of the clamping groove opened at the middle end of the limit block matches the external size of the clamping blocks added on both sides of the outside of the reagent rack, and then the clamping block is limited at the middle end of the limit block through the clamping groove, and the clamping block is limited for the second time in cooperation with the clamping ring, so as to further avoid the position deviation of the reagent rack and protect the instrument, thereby improving the use efficiency of the detection kit.

[0015] The bioequivalence pre-test detection kit proposed by the utility model avoids the situation that most detection kits do not have storage space for auxiliary supplies through the setting of storage components, so that the auxiliary supplies need to be carried separately and are inconvenient to operate, resulting in reduced use efficiency of the detection kit. A storage cavity is opened at the lower end of the main box body, and the internal size of the storage cavity matches the external size of the storage drawer, and then the storage drawer is slidably installed into the main box body through the storage cavity, and the magnetic block added outside the storage cavity and the magnetic baffle installed outside the storage drawer are magnetically attracted to each other, so that the storage drawer is limited inside the main box body, and at the same time, the internal size of the limiting slide grooves opened on both sides of the storage drawer matches the external size of the fixed blocks added on both sides of the movable baffle, and then the movable baffle is installed inside the storage drawer through the limiting slide groove and the fixed block, and the limiting slide groove is cooperated with the fixed block to make the movable baffle slide inside the storage drawer, and the storage space inside the storage drawer is adjusted by the activity of the movable baffle, so that auxiliary supplies such as disposable gloves and disinfectant can be limited and stored inside the storage drawer, thereby improving the activity during the use of the detection kit. BRIEF DESCRIPTION OF THE DRAWINGS

[0016] Figure 1 It is a schematic diagram of the overall three-dimensional structure of the utility model;

[0017] Figure 2 This is a schematic diagram of the three-dimensional structure of the limit assembly of the utility model;

[0018] Figure 3 It is a schematic diagram of the three-dimensional structure of the storage component of the utility model.

[0019] In the figure: 1. main box body; 2. box cover; 3. limit assembly; 301. limit block; 302. mounting seat; 303. reset spring; 304. clamping ring; 305. snap-in groove; 306. snap-in block; 307. reagent rack; 4. storage assembly; 401. storage cavity; 402. magnetic block; 403. storage drawer; 404. magnetic baffle; 405. limit slide groove; 406. fixed block; 407. movable baffle. DETAILED DESCRIPTION

[0020] In order to make the purpose and technical solution of the utility model clearly and completely described, and the advantages more clearly understood, the embodiments of the utility model are further described in detail in conjunction with the accompanying drawings. It should be understood that the specific embodiments described here are part of the embodiments of the utility model, not all of the embodiments, and are only used to explain the embodiments of the utility model, and are not used to limit the embodiments of the utility model. All other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the utility model. Embodiment 1

[0021] See also Figure 1 and Figure 2 The utility model provides a technical solution: comprising a main box body 1 and a limiting assembly 3, wherein the upper end of the main box body 1 is provided with a box cover 2, the limiting assembly 3 is provided at the upper end of the main box body 1, and the limiting assembly 3 comprises a limiting block 301, a mounting seat 302, a reset spring 303, a clamping ring 304, a clamping groove 305, a clamping block 306 and a reagent rack 307, the mounting seats 302 are installed on both sides of the limiting block 301, and the reset spring 303 is provided outside the mounting seat 302, and the front end of the reset spring 303 is installed There is a clamping ring 304, a clamping groove 305 is opened at the middle end of the limit block 301, and the clamping groove 305 is connected to the clamping block 306, and a reagent rack 307 is installed on the outside of the clamping block 306, the reset spring 303 is embedded with the limit block 301, and the reset spring 303 is threadedly connected to the limit block 301 through the mounting seat 302, the clamping ring 304 is symmetrically arranged on both sides of the middle end of the limit block 301, and the clamping ring 304 is elastically connected to the limit block 301 through the reset spring 303, and the clamping block 3 The outer dimensions of 06 match the inner dimensions of the clamping groove 305, and the clamping block 306 is connected to the limit block 301 through the clamping groove 305, and the limit block 301 is fixedly installed on both sides of the inside of the main box body 1 through fasteners, and the reset spring 303 is fixedly installed inside the limit block 301 by using the mounting seat 302 in conjunction with the fastening bolts, and the use of the reset spring 303 is limited by the movable rod installed in the middle of the reset spring 303, and the clamping ring 304 is installed at the front end of the reset spring 303 so that the clamping ring 304 is elastically connected to the limit block 301 through the return spring 303. The internal size of the clamping groove 305 opened in the middle end of the limit block 301 matches the external size of the clamping blocks 306 added on both sides of the outside of the reagent rack 307. Then, the clamping block 306 is limited in the middle end of the limit block 301 through the clamping groove 305, and the clamping block 306 is limited for the second time in cooperation with the clamping ring 304, so as to further avoid the position deviation of the reagent rack 307 and protect the instrument, thereby improving the use efficiency of the detection kit. Embodiment 2

[0022] See also Figure 1 and Figure 3, a storage component 4 is provided at the lower end of the main box body 1, the storage component 4 includes a storage cavity 401, a magnetic block 402, a storage drawer 403 and a magnetic baffle 404, a magnetic block 402 is added to the outside of the storage cavity 401, and the storage cavity 401 is connected to the storage drawer 403, and the storage drawer 403 is installed with a magnetic baffle 404, the storage component 4 also includes a limiting slide 405, a fixed block 406 and a movable baffle 407, and at the same time, a limiting slide 405 is provided inside the storage drawer 403, the limiting slide 405 is connected to the fixed block 406, and the fixed block 406 is installed with a movable baffle 407, the internal size of the limiting slide 405 matches the external size of the fixed block 406, and the movable baffle 407 is slidably connected to the limiting slide 405 through the fixed block 406, a storage cavity 401 is provided at the lower end of the main box body 1, and the internal size of the storage cavity 401 matches the external size of the storage drawer 403 The storage drawer 403 is matched, and then the storage drawer 403 is slidably installed into the main box body 1 through the storage cavity 401, and the magnetic block 402 added outside the storage cavity 401 is magnetically attracted to the magnetic baffle 404 installed outside the storage drawer 403, so that the storage drawer 403 is limited inside the main box body 1, and at the same time, the internal dimensions of the limiting slide grooves 405 opened on both sides of the storage drawer 403 match the external dimensions of the fixed blocks 406 added on both sides of the movable baffle 407, and then the movable baffle 407 is installed in the storage drawer 403 through the limiting slide grooves 405 and the fixed blocks 406, and the limiting slide grooves 405 are used to make the movable baffle 407 slide inside the storage drawer 403, and the storage space inside the storage drawer 403 is adjusted by the activity of the movable baffle 407, so that auxiliary supplies such as disposable gloves and disinfectants can be limited and stored inside the storage drawer 403, thereby improving the mobility during the use of the detection kit.

[0023] In actual use, the main box body 1 is first sealed by the box cover 2 installed on the upper end of the main box body 1, so as to facilitate the taking and transportation of the detection kit, and the limit blocks 301 are fixedly installed on both sides of the inside of the main box body 1 through fasteners, and the reset spring 303 is fixedly installed inside the limit blocks 301 by using the mounting seat 302 and the fastening bolts, and the use of the reset spring 303 is limited by the movable rod installed in the middle of the reset spring 303, and the clamping ring 304 is installed in front of the reset spring 303. The clamping ring 304 is elastically connected to the limit block 301 through the return spring 303, and the inner size of the clamping groove 305 opened in the middle end of the limit block 301 matches the outer size of the clamping blocks 306 added on both sides of the outside of the reagent rack 307, and then the clamping block 306 is limited in the middle end of the limit block 301 through the clamping groove 305, and the clamping ring 304 is used to limit the clamping block 306 for the second time, so as to further avoid the position deviation of the reagent rack 307. Then, at the lower end of the main box body 1, A storage cavity 401 is provided, and the internal dimensions of the storage cavity 401 match the external dimensions of the storage drawer 403, and then the storage drawer 403 is slidably installed into the main box body 1 through the storage cavity 401, and the magnetic block 402 added on the outside of the storage cavity 401 and the magnetic baffle 404 installed on the outside of the storage drawer 403 are magnetically attracted to each other, so that the storage drawer 403 is limited inside the main box body 1, and at the same time, the internal dimensions of the limiting slide grooves 405 opened on both sides of the storage drawer 403 match the internal dimensions of the limiting slide grooves 405 added on both sides of the outside of the movable baffle 407. The outer dimensions of the fixed block 406 are matched, and the movable baffle 407 is installed inside the storage drawer 403 through the limiting slide groove 405 in cooperation with the fixed block 406, and the movable baffle 407 slides inside the storage drawer 403 in cooperation with the limiting slide groove 405, and the storage space inside the storage drawer 403 is adjusted by the movement of the movable baffle 407, so that auxiliary supplies such as disposable gloves and disinfectants can be stored in the storage drawer 403 in a limited manner, thereby improving the mobility of the detection kit during use.

[0024] Although embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that various changes, modifications, substitutions and variations may be made to the embodiments without departing from the principles and spirit of the present invention, and that the scope of the present invention is defined by the appended claims and their equivalents.

Claims

1. A bioequivalence pre-test detection kit, comprising a main box body (1) and a limiter assembly (3), characterized in that: The upper end of the main box body (1) is provided with a box cover (2); a limit assembly (3) is provided at the upper end of the main box body (1), and the limit assembly (3) comprises a limit block (301), a mounting seat (302), a return spring (303), a clamping ring (304), a clamping groove (305), a clamping block (306) and a reagent rack (307); the mounting seats (302) are installed on both sides of the limit block (301), the mounting seat (302) is provided on the outside of the mounting seat (302), and the clamping ring (304) is installed at the front end of the reset spring (303); a clamping groove (305) is provided at the middle end of the limit block (301), the clamping groove (305) is connected to the inside of the clamping block (306), and the reagent rack (307) is installed on the outside of the clamping block (306); and a storage assembly (4) is provided at the lower end of the main box body (1).

2. A bioequivalence pre-test detection kit according to claim 1, characterized in that: The return spring (303) is embeddedly connected to the limit block (301), and the return spring (303) is threadedly connected to the limit block (301) via the mounting seat (302).

3. A bioequivalence pre-test detection kit according to claim 2, characterized in that: The clamping ring (304) is symmetrically arranged on both sides of the middle end of the limit block (301), and the clamping ring (304) is elastically connected to the limit block (301) via a return spring (303).

4. A bioequivalence pre-test detection kit according to claim 1, characterized in that: The external dimensions of the clamping block (306) match the internal dimensions of the clamping slot (305), and the clamping block (306) is connected to the limiting block (301) via the clamping slot (305).

5. A bioequivalence pre-test detection kit according to claim 1, characterized in that: The storage assembly (4) comprises a storage cavity (401), a magnetic block (402), a storage drawer (403) and a magnetic baffle (404); the storage cavity (401) is provided with a magnetic block (402) on the outside, the storage cavity (401) is connected to the storage drawer (403) on the inside, and the storage drawer (403) is installed with a magnetic baffle (404) on the outside.

6. A bioequivalence pre-test detection kit according to claim 5, characterized in that: The storage assembly (4) further comprises a limiting slide groove (405), a fixed block (406) and a movable baffle (407); the limiting slide groove (405) is provided inside the storage drawer (403); the fixing block (406) is connected inside the limiting slide groove (405), and the movable baffle (407) is installed outside the fixing block (406).

7. A bioequivalence pre-test detection kit according to claim 6, characterized in that: The inner dimensions of the limiting slide groove (405) match the outer dimensions of the fixed block (406), and the movable baffle (407) is slidably connected to the limiting slide groove (405) via the fixed block (406).

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