CN114323835A - Rapid drug detection kit - Google Patents

Rapid drug detection kit Download PDF

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Publication number
CN114323835A
CN114323835A CN202111453301.6A CN202111453301A CN114323835A CN 114323835 A CN114323835 A CN 114323835A CN 202111453301 A CN202111453301 A CN 202111453301A CN 114323835 A CN114323835 A CN 114323835A
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China
Prior art keywords
top end
feeding
fixed block
groove
sides
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Granted
Application number
CN202111453301.6A
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Chinese (zh)
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CN114323835B (en
Inventor
韩雅君
李卓
张科林
薛文英
贾燕妮
邓克廷
王瑶
井发红
高娟
马梦影
安西宁
王迎
刘岩
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Xi'an Liangsheng Biology Technology Co ltd
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Xi'an Liangsheng Biology Technology Co ltd
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Priority to CN202111453301.6A priority Critical patent/CN114323835B/en
Publication of CN114323835A publication Critical patent/CN114323835A/en
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Publication of CN114323835B publication Critical patent/CN114323835B/en
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Abstract

The invention 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 fact that the drug halving process is complicated, and comprises a kit, wherein a halving mechanism is installed at the top end of the kit, a fixing mechanism is installed at the top end of the halving mechanism, limiting grooves are symmetrically installed on two sides of the kit, limiting blocks are installed on two sides of the halving mechanism, a rotary disc is installed at the bottom end inside the kit, a fixed block is installed at the top end of the rotary disc, and test tubes are installed in the fixed 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 invention 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.
Disclosure of Invention
Aiming at the situation, in order to overcome the defects of the prior art, the invention 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 invention provides the following technical scheme: a rapid drug detection kit comprises a kit, wherein an equal division mechanism is installed at the top end of the kit, a fixing mechanism is installed at the top end of the equal division mechanism, limiting grooves are symmetrically installed on two sides of the kit, limiting blocks are installed on two sides of the equal division mechanism, a rotating disc is installed at the bottom end of the interior of the kit, a fixed block is installed at the top end of the rotating disc, and test tubes are installed in the fixed block at equal angles; the halving mechanism comprises a top cover arranged at the top end of the kit, a feeding groove is arranged at the top end of the top cover, a baffle plate positioned in the feeding groove is arranged at the top end of the top cover, a feeding rod positioned in the baffle plate is arranged at the top end of the fixed block, feeding holes are symmetrically formed in two sides of the feeding rod, a discharging pipe is arranged at the bottom end of the feeding hole, a material storage device is arranged on the outer side of the feeding rod, sliding grooves are symmetrically formed in two sides of the baffle plate, sliding plates are arranged on two sides of the material storage device, the sliding plates penetrate to the outer portion of the baffle plate through the sliding grooves, and a feeding spring is arranged at the bottom end of the sliding plates; 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 inside symmetry in movable groove installs the clamping bar, 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, 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, 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 invention 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 invention and are incorporated in and constitute a part of this specification, illustrate embodiments of the invention and together with the description serve to explain the principles of the invention and not to limit the invention.
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 at two sides of the kit 1, limiting blocks 5 are installed at two sides of the equal division mechanism 2, a rotating disc 6 is installed at the bottom end inside the kit 1, a fixed block 7 is installed at the top end of the rotating disc 6, and test tubes 8 are installed inside the fixed block 7 at equal angles; the halving mechanism 2 comprises a top cover 201 arranged at the top end of the kit 1, a feeding groove 202 is arranged at the top end of the top cover 201, a baffle plate 203 positioned in the feeding groove 202 is arranged at the top end of the top cover 201, a feeding rod 204 positioned in the baffle plate 203 is arranged at the top end of a fixed block 7, feeding ports 205 are symmetrically arranged at two sides of the feeding rod 204, a discharging pipe 206 is arranged at the bottom end of the feeding port 205, a material storage device 207 is arranged at the outer side of the feeding rod 204, sliding grooves 208 are symmetrically arranged at two sides of the baffle plate 203, sliding plates 209 are arranged at two sides of the material storage device 207, the sliding plates 209 penetrate through the outer part of the baffle plate 203 through the sliding grooves 208, a feeding spring 210 is arranged at the bottom end of the sliding plates 209, the top end of a 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 retaining ring attached to the bottom end of the material storage device 207, installing a top cover 201 at the top end of the kit 1, placing drugs into a material storage device 207, moving the material storage device 207 downwards under the pressure of the drugs to enable a feeding spring 210 to contract, after the material storage device 207 is fixed, opening a rotary disc 6 to enable the rotary disc 6 to drive a fixed block 7 and test tubes 8 inside the fixed block 7 to rotate, delivering the drugs downwards from a feeding hole 205 and outputting the drugs from a 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, and after the rotary disc 6 drives the fixed block 7 to rotate for a circle, the drugs in the material storage device 207 are completely output, and because the contact time of the discharging pipe 206 and each test tube 8 is the same, the amount of the drugs entering each test tube 8 is the same, and the rotary disc 6 is closed; the fixing mechanism 3 comprises a top plate 301 arranged at the top end of the feeding groove 202, a movable groove 302 is symmetrically arranged at the top end of the top plate 301, clamping rods 303 are symmetrically arranged inside the movable groove 302, clamping blocks 304 are arranged at the bottom end of the clamping rods 303, extrusion grooves 305 are arranged on the outer sides of the clamping blocks 304 at equal angles, extrusion blocks 306 are arranged inside the extrusion grooves 305, grooves 307 are formed in the front faces of the clamping blocks 304, ejector blocks 308 are arranged inside the grooves 307, ejector block springs 309 are arranged on the back faces of the ejector blocks 308, clamping grooves 310 are arranged inside the sliding grooves 208, springs are arranged between the clamping rods 303 and the movable groove 302, the clamping rods 303 and the movable groove 302 are clamped, one ends, located inside the clamping blocks 304, of the ejector blocks 308 are hemispherical and matched with the extrusion grooves 305, the top cover 201 is clamped with the limiting blocks 5 through the limiting grooves 4, the clamping rods 303 at the top end of the top plate 301 are pulled towards two sides, the clamping rods 303 are inserted between the feeding groove 202 and the baffle 203, at this moment, the clamping rods 303 are loosened, the clamping rods 303 move back under the action of the springs, 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 this moment, the two clamping blocks 304 are mutually abutted after being contacted, the jacking blocks 308 inside the clamping blocks 304 are mutually extruded, the jacking block springs 309 are contracted, at this moment, the jacking blocks 308 are extruded from the extrusion grooves 305 after moving towards the insides of the clamping blocks 304, and then the sliding plate 209 is fixed after the extrusion blocks 306 are tightly attached to the inner walls of the clamping grooves 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 invention, the scope of which is defined in the appended claims and their equivalents.

Claims (5)

1. A rapid drug detection kit comprises a kit (1) and is characterized in that: the reagent box is characterized in that an equal division mechanism (2) is installed at the top end of the reagent box (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 reagent box (1), limiting blocks (5) are installed on two sides of the equal division mechanism (2), a rotary disc (6) is installed at the bottom end of the interior of the reagent box (1), a fixed block (7) is installed at the top end of the rotary disc (6), and test tubes (8) are installed in the interior of the fixed block (7) at equal angles; the equal-dividing mechanism (2) comprises a top cover (201) arranged at the top end of the kit (1), a feeding groove (202) is arranged at the top end of the top cover (201), a baffle plate (203) located inside the feeding groove (202) is arranged at the top end of the top cover (201), a feeding rod (204) located inside the baffle plate (203) is arranged at the top end of a fixing block (7), feeding holes (205) are symmetrically formed in two sides of the feeding rod (204), a discharging pipe (206) is arranged at the bottom end of the feeding hole (205), a material storage device (207) is arranged on the outer side of the feeding rod (204), sliding grooves (208) are symmetrically formed in two sides of the baffle plate (203), sliding plates (209) are arranged on two sides of the material storage device (207), the sliding plates (209) penetrate through the baffle plate (203) through the sliding grooves (208), and feeding springs (210) are arranged at the bottom end of the sliding plates (209); 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).
2. The rapid drug detection kit according to claim 1, 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.
3. The rapid drug detection kit according to claim 1, 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).
4. The rapid drug detection kit according to claim 1, 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).
5. The rapid drug detection kit according to claim 1, wherein: one end of the top block (308) positioned in the clamping block (304) is hemispherical and is matched with the extrusion groove (305).
CN202111453301.6A 2021-11-30 2021-11-30 Drug rapid detection kit Active CN114323835B (en)

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CN114323835B CN114323835B (en) 2023-08-08

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CN213715240U (en) * 2020-12-05 2021-07-16 西安良升生物科技有限公司 Blood type detection microdisk
CN214097487U (en) * 2020-12-21 2021-08-31 保定市天齐生物试剂技术有限公司 IgG blood group antibody titer rapid detection kit
CN214183977U (en) * 2020-11-10 2021-09-14 江苏联瑞新材料股份有限公司 Preparation device of silica micropowder granularity test sample
CN214357448U (en) * 2020-12-31 2021-10-08 芯朗道(天津)医疗科技有限责任公司 Creatine kinase isoenzyme detection kit
CN214496321U (en) * 2021-01-30 2021-10-26 周玉玲 Kit for detecting multi-drug resistant gene mutation of hepatitis B virus
CN113588830A (en) * 2021-08-03 2021-11-02 四川大学 Screening identification and confirmation standard, screening method and kit for common toxicants

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CN106442085A (en) * 2016-10-19 2017-02-22 闫玉荣 Standard sample divider
CN207717779U (en) * 2017-12-28 2018-08-10 天津绿禾益民生物质利用科技有限公司 A kind of biotinylation kit convenient for quickly detecting
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CN208328016U (en) * 2018-02-09 2019-01-04 深圳莱赛生物科技有限公司 A kind of Bone mineral density kit
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CN214496321U (en) * 2021-01-30 2021-10-26 周玉玲 Kit for detecting multi-drug resistant gene mutation of hepatitis B virus
CN113588830A (en) * 2021-08-03 2021-11-02 四川大学 Screening identification and confirmation standard, screening method and kit for common toxicants

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