CN216595015U

CN216595015U - Rapid drug detection kit

Info

Publication number: CN216595015U
Application number: CN202122980493.8U
Authority: CN
Inventors: 辛毅娟; 韩雅君; 孙继红; 张静; 安西宁; 刘岩; 贾燕妮; 薛文英; 王迎; 邓克廷; 王瑶; 井发红; 高娟; 马梦影
Original assignee: Xi'an Liangsheng Biology Technology Co ltd
Current assignee: Xi'an Liangsheng Biology Technology Co ltd
Priority date: 2021-11-30
Filing date: 2021-11-30
Publication date: 2022-05-24
Anticipated expiration: 2031-11-30

Abstract

The utility model relates to the technical field of kits, and discloses a rapid drug detection kit, which solves the problem that the drug detection speed is reduced due to the complicated drug halving process and comprises a kit, wherein a halving mechanism is arranged at the top end of the kit, a fixing mechanism is arranged at the top end of the halving mechanism, limiting grooves are symmetrically arranged on two sides of the kit, limiting blocks are arranged on two sides of the halving mechanism, a rotary disc is arranged at the bottom end inside the kit, a fixing block is arranged at the top end of the rotary disc, and test tubes are arranged in the fixing block at equal angles; in the work, the downward movement distance is different along with different amounts of the entered drugs through the arranged stocker, and then the size of the feed port of the feed rod is changed, so that the drugs are equally divided more accurately in the process that the fixed block rotates for a circle and the drugs in the stocker all enter the test tube to be equally divided, and the drug detection precision is improved.

Description

Rapid drug detection kit

Technical Field

The utility model belongs to the technical field of kits, and particularly relates to a rapid drug detection kit.

Background

Drug abuse has become one of the most serious public hazards in the world today, which not only harms human health, but also damages peace and economic development of society, and has become a serious international public nuisance.

In the detection process, the drugs need to be averagely divided into a plurality of samples for detection, so that a relatively accurate conclusion can be obtained, and the drug halving process is relatively complicated, so that the drug detection speed is reduced.

SUMMERY OF THE UTILITY MODEL

Aiming at the situation, in order to overcome the defects of the prior art, the utility model provides the rapid drug detection kit, which effectively solves the problem of low drug detection speed caused by complicated drug halving process.

In order to achieve the purpose, the utility model provides the following technical scheme: the utility model provides a drug rapid detection kit, includes the kit, the partition mechanism is installed on the top of kit, and fixed establishment is installed on the top of partition mechanism, and the spacing groove is installed to the bilateral symmetry of kit, and the stopper is all installed to the both sides of partition mechanism, and the carousel is installed to the inside bottom of kit, and the fixed block is installed on the top of carousel, and the test tube is installed to the inside equal angle of fixed block.

Preferably, the halving mechanism is including installing in the top cap on kit top, and the feed chute is installed on the top of top cap, and the baffle that is located the feed chute inside is installed on the top of top cap, and the feed rod that is located the baffle inside is installed on the top of fixed block, and the feed inlet has been seted up to the bilateral symmetry of feed rod, and the discharging pipe is installed to the bottom of feed inlet, and the stocker is installed in the outside of feed rod, and the spout has been seted up to the bilateral symmetry of baffle, and the slide is installed to the both sides of stocker, and the slide runs through to the baffle outside through the spout, and feeding spring is installed to the bottom of slide.

Preferably, the top of test tube and the top parallel and level of fixed block, the bottom of discharging pipe and the top of fixed block closely laminate.

Preferably, the bottom end of the stocker is tightly attached to the outer wall of the feeding rod, and the bottom end of the stocker is provided with a baffle ring attached to the outer side of the feeding rod.

Preferably, the fixed establishment is including installing in the roof on feed chute top, and the movable groove has been seted up to roof top symmetry, and the clamping bar is installed to the inside symmetry in movable groove, and the clamp splice is installed to the bottom of clamping bar, and the extrusion groove has been seted up to angles such as the outside of clamp splice, and the internally mounted in extrusion groove has the extrusion piece, and the front of clamp splice is seted up flutedly, and the internally mounted of recess has the kicking block, and the back mounted of kicking block has the kicking block spring, and the draw-in groove has been seted up to the inside of spout.

Preferably, a spring is arranged between the clamping rod and the movable groove, and the clamping rod is clamped with the movable groove.

Preferably, one end of the ejector block, which is positioned inside the clamping block, is hemispherical and matched with the extrusion groove.

Compared with the prior art, the utility model has the beneficial effects that:

1) in the work, the downward movement distances of the stocker are different along with the different amounts of the entered drugs, and then the size of the feed port of the feed rod is changed, so that the drugs are equally divided more accurately in the process that the fixed block rotates for a circle and the drugs in the stocker all enter the test tube to be equally divided, and the drug detection precision is improved;

2) the utility model discloses a test tube, in operation, through the test tube equal partition entering drugs that sets up, to adding detect reagent in the test tube after, drive the test tube rotation in the fixed block through the carousel for drugs and detect reagent can the rapid mixing reaction, thereby improve detection speed.

Drawings

The accompanying drawings, which are included to provide a further understanding of the utility model and are incorporated in and constitute a part of this specification, illustrate embodiments of the utility model and together with the description serve to explain the principles of the utility model and not to limit the utility model.

In the drawings:

FIG. 1 is a schematic structural view of the present invention;

FIG. 2 is a schematic view of the internal structure of the kit according to the present invention;

FIG. 3 is a schematic view of the aliquoting mechanism of the present invention;

FIG. 4 is a schematic structural view of a fixing mechanism of the present invention;

fig. 5 is a schematic view of the structure of the clamping block of the present invention.

In the figure: 1. a kit; 2. an equal division mechanism; 201. a top cover; 202. a feed chute; 203. a baffle plate; 204. a feed rod; 205. a feed inlet; 206. a discharge pipe; 207. a stocker; 208. a chute; 209. a slide plate; 210. a feed spring; 3. a fixing mechanism; 301. a top plate; 302. a movable groove; 303. a clamping bar; 304. a clamping block; 305. extruding a groove; 306. extruding the block; 307. a groove; 308. a top block; 309. a top block spring; 310. a card slot; 4. a limiting groove; 5. a limiting block; 6. a turntable; 7. a fixed block; 8. test tubes.

Detailed Description

The technical solutions in the embodiments of the present invention will be clearly and completely described below with reference to the drawings in the embodiments of the present invention, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, and not all of the embodiments; all other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.

In the first embodiment, as shown in fig. 1 to 5, the kit comprises a kit 1, wherein an equal division mechanism 2 is installed at the top end of the kit 1, a fixing mechanism 3 is installed at the top end of the equal division mechanism 2, limiting grooves 4 are symmetrically installed on two sides of the kit 1, limiting blocks 5 are installed on two sides of the equal division mechanism 2, a rotating disc 6 is installed at the bottom end inside the kit 1, a fixing block 7 is installed at the top end of the rotating disc 6, and test tubes 8 are installed inside the fixing block 7 at equal angles.

In the second embodiment, on the basis of the first embodiment, the equally dividing mechanism 2 includes a top cover 201 installed on the top end of the reagent kit 1, a feeding chute 202 is installed on the top end of the top cover 201, a baffle 203 located inside the feeding chute 202 is installed on the top end of the top cover 201, a feeding rod 204 located inside the baffle 203 is installed on the top end of the fixed block 7, feeding ports 205 are symmetrically opened on two sides of the feeding rod 204, a discharging pipe 206 is installed on the bottom end of the feeding port 205, a material storage device 207 is installed on the outer side of the feeding rod 204, sliding grooves 208 are symmetrically opened on two sides of the baffle 203, sliding plates 209 penetrate through the baffle 203, a feeding spring 210 is installed on the bottom end of the sliding plate 209, the top end of the test tube 8 is flush with the top end of the fixed block 7, the bottom end of the discharging pipe 206 is tightly attached to the top end of the fixed block 7, the bottom end of the material storage device 207 is tightly attached to the outer wall of the feeding rod 204, a stop ring attached to the outer side of the feeding rod 204 is installed at the bottom end of the material storage device 207, the top cover 201 is installed at the top end of the reagent kit 1, drugs are put into the material storage device 207, at the moment, the material storage device 207 moves downwards under the pressure of the drugs to enable the feeding spring 210 to contract, after the material storage device 207 is fixed, the rotating disc 6 is opened to enable the rotating disc 6 to drive the fixed block 7 and the test tubes 8 inside the fixed block 7 to rotate, the drugs are conveyed downwards from the feeding hole 205 and are output from the discharging pipe 206, when the bottom end of the discharging pipe 206 is in contact with the test tubes 8, the drugs enter the test tubes 8, when the discharging pipe 206 is in contact with the top end of the fixed block 7, the discharging pipe 206 is closed, when the rotating disc 6 drives the fixed block 7 to rotate for one circle, the output of the drugs in the material storage device 207 is finished, and because the discharging pipe 206 is in contact with each test tube 8 for the same time, the amount of the drugs in each test tube 8 is the same, the turntable 6 is closed.

Third embodiment, on the basis of the second embodiment, the fixing mechanism 3 includes a top plate 301 installed at the top end of the feeding chute 202, a movable groove 302 is symmetrically formed at the top end of the top plate 301, clamping rods 303 are symmetrically installed inside the movable groove 302, clamping blocks 304 are installed at the bottom ends of the clamping rods 303, extrusion grooves 305 are formed at equal angles outside the clamping blocks 304, extrusion blocks 306 are installed inside the extrusion grooves 305, a groove 307 is formed in the front surface of the clamping block 304, a top block 308 is installed inside the groove 307, a top block spring 309 is installed on the back surface of the top block 308, a clamping groove 310 is formed inside the sliding groove 208, a spring is installed between the clamping rod 303 and the movable groove 302, the clamping rod 303 and the movable groove 302 are clamped, one end of the top block 308, which is located inside the clamping block 304, is hemispherical and matched with the extrusion grooves 305, the top cover 201 is clamped with a limiting groove 4 and a limiting block 5, the clamping rod 303 at the top end of the top plate 301 is pulled open towards two sides, insert clamping bar 303 between feed chute 202 and baffle 203, loosen clamping bar 303 this moment, clamping bar 303 moves back under the spring action back, make the clamp splice 304 of the clamping bar 303 bottom of both sides press from both sides in the draw-in groove 310 on slide 209, because two clamp splices 304 support each other after the contact this moment, make the inside kicking block 308 of clamp splice 304 extrude each other, make kicking block spring 309 shrink, kicking block 308 extrudes pressing block 306 from extrusion groove 305 after to the inside removal of clamp splice 304 this moment, thereby make pressing block 306 fixed slide 209 after closely laminating with the inner wall of draw-in groove 310.

The working principle is as follows: when in work, firstly, the top cover 201 is clamped with the limiting block 5 through the limiting groove 4, the top cover 201 is arranged at the top end of the reagent kit 1, drugs are put into the material storage device 207, at this time, the container 207 is pressed by the drug and moves downwards to make the feeding spring 210 contract, the clamping bar 303 at the top end of the top plate 301 is pulled to both sides, the clamping bar 303 is inserted between the feeding chute 202 and the baffle plate 203, at this time, the clamping bar 303 is released, after the clamping bar 303 moves back under the action of the spring, so that the clamping blocks 304 at the bottom ends of the clamping rods 303 at the two sides are clamped in the clamping grooves 310 on the sliding plate 209, at the moment, because the two clamping blocks 304 are contacted and then mutually abutted, the top blocks 308 inside the clamping blocks 304 are pressed against each other, so that the top block springs 309 contract, at this time, the top blocks 308 move towards the inside of the clamping blocks 304 to extrude the extrusion blocks 306 from the extrusion grooves 305, so that the sliding plate 209 is fixed after the extrusion block 306 is tightly attached to the inner wall of the clamping groove 310;

because the material storage device 207 is fixed, the rotary disc 6 is opened, the rotary disc 6 drives the fixed block 7 and the test tubes 8 in the fixed block 7 to rotate, drugs are conveyed downwards from the feed inlet 205 and are output from the discharge pipe 206, when the bottom end of the discharge pipe 206 is contacted with the test tubes 8, the drugs enter the test tubes 8, when the discharge pipe 206 is contacted with the top end of the fixed block 7, the discharge pipe 206 is closed, after the rotary disc 6 drives the fixed block 7 to rotate for a circle, the drug output in the material storage device 207 is finished, because the contact time of the discharge pipe 206 and each test tube 8 is the same, the drug entering amount in each test tube 8 is the same, and the rotary disc 6 is closed;

open top cap 201, add detect reagent to the test tube 8 in, open carousel 6 once more for carousel 6 drives the inside test tube 8 rotation of fixed block 7 and fixed block 7, makes narcotic drug and detect reagent rapid mixing in the test tube 8, thereby improves detection speed.

It is noted that, herein, relational terms such as first and second, and the like may be used solely to distinguish one entity or action from another entity or action without necessarily requiring or implying any actual such relationship or order between such entities or actions. Also, the terms "comprises," "comprising," or any other variation thereof, are intended to cover a non-exclusive inclusion, such that a process, method, article, or apparatus that comprises a list of elements does not include only those elements but may include other elements not expressly listed or inherent to such process, method, article, or apparatus.

Although embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that changes, modifications, substitutions and alterations can be made in these embodiments without departing from the principles and spirit of the utility model, the scope of which is defined in the appended claims and their equivalents.

Claims

1. A rapid drug detection kit comprises a kit (1) and is characterized in that: equal division mechanism (2) are installed on the top of kit (1), and fixed establishment (3) are installed on the top of equal division mechanism (2), and spacing groove (4) are installed to the bilateral symmetry of kit (1), and stopper (5) are all installed to the both sides of equal division mechanism (2), and carousel (6) are installed to the inside bottom of kit (1), and fixed block (7) are installed on the top of carousel (6), and test tube (8) are installed to the inside equal angle of fixed block (7).

2. The rapid drug detection kit according to claim 1, wherein: halving mechanism (2) is including installing in top cap (201) on kit (1) top, feed chute (202) are installed on the top of top cap (201), baffle (203) that are located feed chute (202) inside are installed on the top of top cap (201), feed rod (204) that are located baffle (203) inside are installed on the top of fixed block (7), feed inlet (205) have been seted up to the bilateral symmetry of feed rod (204), discharging pipe (206) are installed to the bottom of feed inlet (205), hopper (207) are installed in the outside of feed rod (204), spout (208) have been seted up to the bilateral symmetry of baffle (203), slide (209) are installed to the both sides of hopper (207), slide (209) run through to baffle (203) outside through spout (208), feeding spring (210) are installed to the bottom of slide (209).

3. The rapid drug detection kit according to claim 2, wherein: the top of test tube (8) and the top parallel and level of fixed block (7), the bottom of discharging pipe (206) and the top of fixed block (7) closely laminate.

4. The rapid drug detection kit according to claim 2, wherein: the bottom end of the stocker (207) is tightly attached to the outer wall of the feeding rod (204), and the bottom end of the stocker (207) is provided with a baffle ring attached to the outer side of the feeding rod (204).

5. The rapid drug detection kit according to claim 1, wherein: fixed establishment (3) including installing in roof (301) on feed chute (202) top, movable groove (302) have been seted up to roof (301) top symmetry, clamping bar (303) are installed to the inside symmetry of movable groove (302), clamp splice (304) are installed to the bottom of clamping bar (303), extrusion groove (305) have been seted up to the angle such as the outside of clamp splice (304), the internally mounted of extrusion groove (305) has extrusion piece (306), the front of clamp splice (304) is seted up flutedly (307), the internally mounted of flutedly (307) has kicking block (308), the back mounted of kicking block (308) has kicking block spring (309), draw-in groove (310) have been seted up to the inside of spout (208).

6. The rapid drug detection kit according to claim 5, wherein: a spring is arranged between the clamping rod (303) and the movable groove (302), and the clamping rod (303) is clamped with the movable groove (302).

7. The rapid drug detection kit according to claim 5, wherein: one end of the top block (308) positioned in the clamping block (304) is hemispherical and is matched with the extrusion groove (305).