A kit

Abstract

A medicine box comprises a box body and an end cover, the box body has a center part and two side cavity parts. An inert cavity for placing inert medicine is formed in the center part; a connecting sleeve is arranged on the center part, the axis of the connecting sleeve is perpendicular to the main axis of the center part and is used for connecting an external driving member. The two side cavity parts are symmetrically arranged on both sides of the center part and are respectively used for placing precursor agent and activating agent; a first through hole is arranged on the cavity wall between the inert cavity and the side cavity part; the end cover is mounted on the outer end surface of the side cavity part, and a second through hole is formed in the end cover for the external liquid to enter the side cavity part. When the driving member drives the box body to rotate at high speed, the precursor agent and the activating agent can be mixed with the external liquid under the action of centrifugal force, and the inert medicine in the box is instantaneously dissolved when meeting water, a mixing channel is formed between the side cavity parts filled with the precursor agent and the activating agent through the first through hole, and the two phases cooperate and move in parallel, which greatly shortens the medicine dissolving time and significantly accelerates the generation speed of the disinfecting solution.

Description

Technical Field

[0001] This utility model belongs to the technical field of disinfection reaction reagent containers, specifically relating to a reagent box. Background Technology

[0002] Currently, most commercially available containers for holding pharmaceuticals are relatively traditional in design and function, with many limitations, especially in terms of poor mixing efficiency. Existing containers of this type are mostly simple in structure, typically just separating different pharmaceuticals into different areas within the container, or mixing multiple pharmaceuticals and sealing them in a single chamber. When preparing a disinfectant solution, the container is brought into contact with the external liquid, relying on natural diffusion or simple stirring to mix the pharmaceuticals with the liquid. However, this natural diffusion process is extremely slow; pharmaceutical molecules need a significant amount of time to gradually disperse in the liquid, resulting in excessively long dissolution times.

[0003] Therefore, based on some of the situations in the prior art described above, this application has made further designs and improvements. Utility Model Content

[0004] To solve the above-mentioned technical problems, the present invention provides the following technical solution.

[0005] A medicine box includes a box body and end caps. The box body has a central portion and two side cavities. An inert cavity for holding an inert medicine is formed within the central portion. A connecting sleeve is provided on the central portion, the axis of which is perpendicular to the main axis of the central portion and is used to connect an external drive component. Two side cavities are symmetrically arranged on both sides of the central portion and are used to hold a precursor and an activator, respectively. A first through hole is provided in the cavity wall between the inert cavity and the side cavities. An end cap is installed on the outer end face of each side cavity, and the end cap has a second through hole for external liquid to enter the side cavity. When the drive component rotates the box body at high speed, the precursor and activator are rapidly ejected along the through hole of the end cap under centrifugal force, instantly mixing with the external liquid.

[0006] In a preferred embodiment of a medicine box, the box body consists of two interlocking parts. Each part has an interlocking groove and a locking block on its interlocking surface. The interlocking groove is L-shaped. When interlocking, the locking block is inserted axially into the groove and then rotated circumferentially to achieve interlocking. Each part has a semi-cavity groove on its interlocking surface; after interlocking, the two semi-cavities combine to form the inert cavity. Each part also has a semi-circular groove perpendicular to the interlocking surface; the two semi-circular grooves combine to form the connecting sleeve. The box body can be opened and disassembled simply by rotating in the opposite direction, facilitating medicine filling.

[0007] As a preferred embodiment of the medicine box, it also includes a locking ring, which is sleeved on the outer periphery of the connecting sleeve to prevent the two parts from loosening or sliding relative to each other in the fastening direction, and to ensure that the medicine box remains reliably fastened when rotating.

[0008] Compared with the prior art, this application has the following beneficial technical effects: when the driving component drives the box to rotate at high speed, the precursor and activator can be quickly mixed with the external liquid under the action of centrifugal force. At the same time, the inert agent in the box dissolves instantly when it comes into contact with water, and a mixing channel is formed between the side cavity containing the precursor and activator through the first through hole. The two phases cooperate and run in parallel, which greatly shortens the dissolution time of the agent and significantly accelerates the generation speed of the disinfection solution. Attached Figure Description

[0009] Figure 1 This is a 3D view of a disinfection generator.

[0010] Figure 2 This is a top view of the disinfection generator.

[0011] Figure 3 This is an exploded view of the sterilization generator.

[0012] Figure 4 for Figure 3 A magnified view of a portion of point A in the middle.

[0013] Figure 5 This is a perspective view of the cover in one embodiment.

[0014] Figure 6 This is a perspective view of the cover in another embodiment.

[0015] Figure 7 This is a 3D view of the medicine box.

[0016] Figure 8 This is an exploded view of the medicine box.

[0017] Figure 9 This is a three-dimensional diagram of the components.

[0018] The following is an explanation of the reference numerals in the attached figures:

[0019] 100. Bottle body; 110. Cavity; 120. Joint; 121. Limiting groove; 122. Sealing ring groove; 130. Elastic locking ring; 131. Locking protrusion;

[0020] 200. Cover; 201. Sealing ring; 202. Locking block; 210. Nebulizer; 211. Suction tube; 220. Battery; 230. Control module; 240. Display module; 250. Charging interface;

[0021] 300. Granule container; 310. Motor; 320. Connecting rod; 330. Medicine box; 340. Box body; 341. Central part; 342. Side cavity; 343. Connecting sleeve; 344. First through hole; 345. Separate part; 346. Fastening groove; 347. Fastening block; 348. Half cavity groove; 349. Semicircular groove; 350. End cap; 351. Second through hole; 360. Locking ring; 370. Tube column; 371. Third through hole. Detailed Implementation

[0022] The present invention will now be described in further detail with reference to the accompanying drawings and specific embodiments.

[0023] In the following embodiments, the same or similar reference numerals denote the same or similar components or components with the same or similar functions throughout. The embodiments described below with reference to the accompanying drawings are exemplary and are only used to explain the present invention, and should not be construed as limiting the present invention.

[0024] In the description of this utility model, it should be understood that the terms such as center, longitudinal, transverse, length, width, thickness, upper, lower, front, back, left, right, vertical, horizontal, top, bottom, inner, outer, clockwise, and counterclockwise, indicating orientation or positional relationships, are based on the orientation or positional relationships shown in the accompanying drawings and are only for the convenience of describing this utility model and simplifying the description; therefore, they should not be construed as limitations on this utility model. Furthermore, the terms "first," "second," etc., are used for descriptive purposes only and should not be construed as indicating or implying relative importance or implicitly specifying the number of technical features shown. In the description of this utility model, unless otherwise expressly specified and limited, the terms "installation," "connection," "joining," etc., should be interpreted broadly, and those skilled in the art can understand the specific meaning of the above terms in this utility model according to the specific circumstances.

[0025] refer to Figures 1 to 4 A disinfection generator includes a bottle body 100 and a cap 200. The bottle body 100 has a cavity 110 for holding a reaction liquid, and the cap 200 is detachably and sealingly connected to the opening of the bottle body 100. The cap 200 is provided with an atomizer 210, a battery 220, a particle container, and a control module 230. The atomizer 210 has a suction tube 211, the inlet of which leads to the bottom of the cavity 110. The battery 220 is used to supply power to the atomizer 210. The particle container is used to hold reaction particles that can react with the reaction liquid to generate a disinfection solution. The control module 230 is electrically connected to the battery 220 and the atomizer 210 and is used to control the start and stop of the atomizer 210. This design integrates the particle container, battery 220, atomizer 210, and control module 230 into the cover 200, which completely isolates the solid reaction particles from the reaction liquid inside the bottle before use. When in use, the cover 200 is simply assembled onto the bottle 100.

[0026] This disinfection generator is suitable for occasions where oxidizing disinfectant solutions need to be prepared on-site, especially for chlorine dioxide systems: users only need to put water (reaction agent) into bottle 100 and put cap 200 on bottle 100. The solid particles (chlorine dioxide precursor + activator) pre-placed in cap 200 are released and react instantly to generate fresh disinfectant solution, which is then sprayed directly out by atomizer 210.

[0027] The bottle body 100 has a connecting portion 120 at its mouth, and an L-shaped limiting groove 121 is provided around the outer periphery of the connecting portion 120. The cap 200 has a locking block 202 that cooperates with the limiting groove 121. The locking block 202 can be quickly connected to the bottle body 100 by axial insertion and rotation, without the need for multiple turns of threading, making the operation convenient and simple. The connecting portion 120 also has a soft elastic locking ring 130, and the elastic locking ring 130 has a locking protrusion 131 corresponding to the limiting groove 121. The bottom of the limiting groove 121 has a corresponding through hole, and the locking protrusion 131 extends elastically into the limiting groove 121 through the through hole to prevent the locking block 202 from rotating out in the opposite direction. The locking protrusion 131 can increase the resistance to the sliding of the locking block 202, making it impossible for the cap 200 to unscrew itself.

[0028] To ensure the airtightness of the cavity 110, a sealing ring groove 122 is provided at the top of the joint 120, and a sealing protrusion 201 is provided on the cap 200 to press against the sealing ring groove 122, thereby achieving a seal of the cavity 110 while engaging in a snap-fit ​​connection. The sealing protrusion 201, in conjunction with the sealing ring groove 122, forms a double seal on the end face and radially, preventing the highly oxidizing disinfectant from evaporating or leaking along the gap between the bottle 100 and the cap 200.

[0029] In addition, the cover 200 is also provided with a display module 240 for displaying the battery 220's power level and operating status, as well as a charging interface for charging the battery 220. This design makes the power level and operating status visible, and the display and charging are all located on the cover 200, without compromising the sealing integrity of the bottle 100.

[0030] As one embodiment of the particle container, see reference Figure 5 The granule container 300 is a tube 370 with an open top, the opening of which is sealed by a cap. The sidewall of the tube 370 has third through holes 371. The cap 200 has a threaded opening, and the upper part of the tube 370 is detachably and sealingly connected to the threaded opening. The tube 370 can be removed as a whole for easy replacement or replenishment of granules.

[0031] As another embodiment of the particle container, see reference. Figures 6 to 9The particle container 300 is a reagent box 330. A motor 310 for driving the reagent box 330 to rotate is installed on the cover 200. The output shaft of the motor 310 is connected to the reagent box 330 via a connecting rod 320. The side wall of the reagent box 330 is provided with a second through hole 351 for the reaction liquid to flow in and accelerate dissolution. The motor 310 drives the reagent box 330 to rotate, which can greatly accelerate the particle disintegration and dissolution.

[0032] Specifically, the medicine box 330 includes a box body 340 and an end cap 350. The box body 340 has a central portion 341 and two side cavities 342. An inert cavity for holding an inert medicine is formed within the central portion 341. A connecting sleeve 343 is provided on the central portion 341, the axis of which is perpendicular to the main axis of the central portion 341 and is used to connect an external drive component. The two side cavities 342 are symmetrically arranged on both sides of the central portion 341 and are used to hold a precursor and an activator, respectively. A first through hole 344 is provided on the cavity wall between the inert cavity and the side cavities 342. An end cap 350 is installed on the outer end face of the side cavity 342, and a second through hole 351 is provided on the end cap 350 to allow external liquid to enter the side cavity 342. When the drive component rotates the box body 340 at high speed, the precursor and activator are rapidly ejected along the through hole of the end cap 350 under centrifugal force, instantly mixing with the external liquid. When the drive unit rotates the box 340 at high speed, the precursor and activator can quickly mix with the external liquid under the action of centrifugal force. At the same time, the inert agent in the box dissolves instantly in water and forms a mixing channel between the side cavity 342 containing the precursor and activator through the first through hole 344. The two phases work together in parallel, which greatly shortens the dissolution time of the agent and significantly accelerates the generation speed of the disinfection solution.

[0033] The box body 340 adopts a split design 345, which consists of two interlocking split parts 345. The interlocking surfaces of the two split parts 345 are respectively provided with a groove 346 and a block 347. The groove 346 is L-shaped. When interlocking, the block 347 is inserted axially into the groove 346 and then rotated circumferentially to achieve the interlocking of the split parts 345. Each of the interlocking surfaces of the two split parts 345 is provided with a semi-cavity groove 348. After interlocking, the two semi-cavity grooves 348 are joined to form the inert cavity. Each of the two split parts 345 has a semi-circular groove 349 in a direction perpendicular to the interlocking surface. The two semi-circular grooves 349 are joined to form the connecting sleeve 343. The box body 340 can be opened and disassembled simply by rotating in the opposite direction for easy medication loading. In addition, the box body 340 also includes a locking ring 360, which is sleeved on the outer periphery of the connecting sleeve 343 to prevent the two parts 345 from loosening or sliding relative to each other in the fastening direction, and to ensure that the medicine box remains reliably fastened when rotating.

[0034] The scope of protection of this utility model includes, but is not limited to, the above embodiments. The scope of protection of this utility model is defined by the claims. Any substitutions, modifications, or improvements to this technology that are easily conceived by those skilled in the art shall fall within the scope of protection of this utility model.

Claims

1. A medicine box, characterized in that, Includes a housing (340) and an end cap (350), said housing (340) having: A central portion (341) is provided with an inert cavity for placing an inert agent; a connecting sleeve (343) is provided on the central portion (341), the axis of the connecting sleeve (343) being perpendicular to the main axis of the central portion (341) and used to connect an external drive component; Two side chambers (342) are symmetrically arranged on both sides of the central part (341) and are used to place the precursor and activator respectively. A first through hole (344) is provided on the cavity wall between the inert cavity and the side chamber (342). An end cap (350) is installed on the outer end face of the side chamber (342), and a second through hole (351) is provided on the end cap (350) to allow external liquid to enter the side chamber (342).

2. A medicine box according to claim 1, characterized in that, The box body (340) is composed of two interlocking parts (345). The interlocking surfaces of the two parts (345) are respectively provided with a fastening groove (346) and a fastening block (347). The fastening groove (346) is L-shaped. When fastening, the fastening block (347) is inserted into the fastening groove (346) along the axial direction and then rotated circumferentially to achieve the fastening of the parts (345). The two split parts (345) are provided with a semi-cavity groove (348) on their fastening surfaces. After fastening, the two semi-cavity grooves (348) are joined together to form the inert cavity. The two split parts (345) are each provided with a semi-circular groove (349) in a direction perpendicular to the fastening surface. The two semi-circular grooves (349) are joined together to form the connecting sleeve (343).

3. A medicine box according to claim 2, characterized in that, It also includes a locking ring (360), which is sleeved on the outer periphery of the connecting sleeve (343) to prevent the two parts (345) from loosening or sliding relative to each other in the fastening direction.

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