Novel pharmaceutical granulator
By setting up granulation components and heating components in the pharmaceutical granulator, the problems of different sizes of the pharmaceutical particles and uneven content are solved, and the effects of consistent sizes of the pharmaceutical particles and uniform content are achieved, and the quality of the pharmaceutical products is improved.
Patent Information
- Application Number
- CN202421295581.1
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-06-07
- Publication Date
- 2025-03-11
- Estimated Expiration
- 2034-06-07
AI Technical Summary
During the production process of pharmaceutical pelletizers, the size of the pharmaceutical pellets is different and the internal content is uneven, resulting in a decrease in the quality of the pharmaceutical.
A new type of pharmaceutical pelletizer was designed. By setting up a granulation assembly and heating assembly, including a mixing box, a cutting knife and a heating tube, it ensures that the drug raw materials are evenly cut and heated, thereby forming a pharmaceutical pellet with uniform size and uniform medicine.
The uniform size and uniform content of the medicine particles are achieved, the quality of the medicine is improved, and the viscosity of the medicine particles is reduced by heating the components to prevent the medicine particles from sticking together.
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Figure CN222586478U_ABST
Abstract
Description
Technical Field
[0001] The utility model belongs to the technical field of medical equipment, in particular to a new type of pharmaceutical granulator. Background Art
[0002] Drug granules are a very important component of drugs. Granulation methods include wet granulation, dry granulation, one-step granulation and spray granulation. Among them, wet granulation is the most widely used. Generally, multiple drug powders are mixed and bonded together with a binder, and then granulated inside a granulator to obtain drug granules.
[0003] When using a pharmaceutical granulator to make granules, the raw materials are usually stirred inside the machine and cut directly by a cutting knife. Although the raw materials can be quickly cut into granules, the sizes of the granules after cutting are different, and the drug content inside the granules is not uniform, which reduces the quality of the medicine. Utility Model Content
[0004] The purpose of the utility model is to provide a new type of pharmaceutical granulator. By setting a granulation component, the device can cut the drug raw materials into particles of the same size, which solves the problem that the existing device usually stirs the drug raw materials inside the pharmaceutical machine and directly cuts the drug raw materials with a cutting knife. Although the drug raw materials can be quickly cut into granules, the sizes of the cut granules are different, and the drug content inside the granules is not uniform, which reduces the quality of the drug.
[0005] In order to solve the above technical problems, the utility model is realized by the following technical solutions:
[0006] The utility model is a novel pharmaceutical granulator, comprising a base, wherein the four corners of the bottom of the base are fixedly connected to support legs, the top of the base is fixedly connected to a controller, the top of the base is provided with a circular groove 1, the bottom of the inner wall of the circular groove 1 is fixedly connected to an outer box, the bottom of the inner wall of the outer box is provided with a slide groove, the inner wall of the slide groove is slidably connected to a collection drawer, a handle is fixedly connected to the right side of the collection drawer, a granulating component is arranged inside the outer box, a heating component is arranged inside the outer box, the granulating component comprises a stirring box, the top of the outer box is provided with a circular groove 2, the inner wall of the circular groove 2 is fixedly connected to the outer surface of the stirring box, the outer surface of the stirring box is provided with a plurality of grooves 1, and by arranging the granulating component, the drug raw materials can be cut into particles of the same size, thereby ensuring the size of the drug particles and the uniformity of the drug content.
[0007] Furthermore, a circular groove three is provided at the bottom of the mixing box, and the inner wall of the circular groove three is rotatably connected to a rotating shaft. A motor is provided under the mixing box, and the top output end of the motor is fixedly connected to the bottom of the rotating shaft. By providing the mixing box, the drug raw materials can be further mixed so that the drug and the raw materials can be mixed more evenly.
[0008] Furthermore, a rotating plate is fixedly connected to the outer surface of the rotating shaft, and there are four rotating plates. The four rotating plates are in contact with the inner wall of the mixing box on the side away from the rotating shaft. A rotating block is fixedly connected to the outer surface of the rotating shaft. By setting the rotating plate, the drug raw materials can be discharged from the interior of the mixing box through the groove during the rotation and mixing process.
[0009] Furthermore, the top of the rotating block contacts the bottom of the mixing box, and a rotating rod is fixedly connected to the outer surface of the rotating block. The number of the rotating rods is five, and a cutting knife is fixedly connected to the top of each of the five rotating rods. The five cutting knives are in contact with the outer surface of the mixing box on one side close to the rotating shaft. By setting the cutting knife, the cut medicinal particles can maintain consistent size.
[0010] Furthermore, the heating component includes a fixed plate, the outer surface of the fixed plate is fixedly connected to the inner wall of the outer box, the top of the fixed plate is fixedly connected to the bottom of the motor, and a plurality of fixed blocks are fixedly connected to the top of the fixed plate. By setting the heating component, the medicine particles can be quickly air-dried due to the heated fixed blocks during the rolling process, so that the viscosity of the surface of the medicine particles is reduced and they will not stick together, thereby improving the practicability of the device.
[0011] Furthermore, the fixed blocks are arranged in a circular array with the fixed plate as the center, several of the fixed blocks are provided with groove 2 inside, several inner walls of the groove 2 are fixedly connected with heating tubes, several diverter blocks 1 are fixedly connected to the top of the fixed plate, several of the diverter blocks 1 are arranged in a circular array with the fixed plate as the center, a baffle is fixedly connected to the top of the fixed plate, the outer surface of the baffle is fixedly connected to the side of the fixed block away from the inner wall of the outer box, the outer surface of the baffle is fixedly connected to the side of the diverter block 1 away from the inner wall of the outer box, and the heating tube is provided to prevent the medicine particles from sticking together.
[0012] Furthermore, the front and back sides of the diverter block 1 are fixedly connected to the outer surface of the fixed block, the tops of several diverter blocks 1 are fixedly connected to diverter blocks 2, and the tops of several diverter blocks 2 are fixedly connected to the top of the inner wall of the outer box. By setting the diverter blocks, the medicine particles can be diverted, reducing the probability of the medicine particles sticking together.
[0013] The utility model has the following beneficial effects:
[0014] The utility model sets a granulating component, specifically, firstly puts the mixed drug raw materials into the interior of a mixing box, turns on the motor through a controller to make the cutting knife rotate on the outer surface of the mixing box, and the cutting knife cuts the drug raw materials discharged from the interior of a groove while rotating, so that the drug raw materials can be cut into particles of the same size, thereby ensuring the size of the drug particles and the uniformity of the drug content.
[0015] The utility model sets a heating component, specifically, turns on the heating tube to increase the surface temperature of the fixed block. Since the top of the fixed block is an inclined surface, the medicine particles that fall onto the top of the fixed block will roll along the inclined surface into the second groove inside the fixed plate. During the rolling process of the medicine particles, they will be quickly air-dried due to the heated fixed block, which reduces the viscosity of the surface of the medicine particles and prevents them from sticking together, thereby improving the practicality of the device.
[0016] Of course, any product implementing this utility model does not necessarily need to achieve all of the advantages described above at the same time. BRIEF DESCRIPTION OF THE DRAWINGS
[0017] In order to more clearly illustrate the technical solution of the embodiment of the utility model, the drawings required for describing the embodiment will be briefly introduced below. Obviously, the drawings described below are only some embodiments of the utility model. For ordinary technicians in this field, other drawings can be obtained based on these drawings without paying creative work.
[0018] Figure 1 It is a schematic diagram of the overall structure of the utility model;
[0019] Figure 2 It is a schematic diagram of the overall left side structure of the utility model;
[0020] Figure 3 This is a front sectional structural diagram of the outer box of the utility model;
[0021] Figure 4 This is a front sectional structural diagram of the mixing box of the utility model;
[0022] Figure 5 It is a schematic diagram of the overall structure of the fixing plate of the utility model;
[0023] Figure 6 The utility model is a schematic diagram of the overall structure of the diverter block.
[0024] In the accompanying drawings, the components represented by the reference numerals are listed as follows:
[0025] 1. Base; 2. Support legs; 3. Controller; 4. Outer box; 5. Collection drawer; 6. Handle; 11. Granulating assembly; 111. Mixing box; 112. Rotating shaft; 113. Rotating plate; 114. Motor; 115. Rotating block; 116. Rotating rod; 117. Cutting knife; 22. Heating assembly; 221. Fixed plate; 222. Fixed block; 223. Diverter block 1; 224. Diverter block 2; 225. Heating tube; 226. Baffle. DETAILED DESCRIPTION
[0026] The following will be combined with the drawings in the embodiments of the utility model to clearly and completely describe the technical solutions in the embodiments of the utility model. Obviously, the described embodiments are only part of the embodiments of the utility model, not all of them. Based on the embodiments in 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.
[0027] See also Figure 1-6 As shown, the utility model is a novel pharmaceutical granulator, comprising a base 1, the four corners of the bottom of the base 1 are fixedly connected to support legs 2, the top of the base 1 is fixedly connected to a controller 3, the top of the base 1 is provided with a circular groove 1, the bottom of the inner wall of the circular groove 1 is fixedly connected to an outer box 4, the bottom of the inner wall of the outer box 4 is provided with a slide, the inner wall of the slide is slidably connected to a collection drawer 5, a handle 6 is fixedly connected to the right side of the collection drawer 5, a granulating component 11 is arranged inside the outer box 4, a heating component 22 is arranged inside the outer box 4, the granulating component 11 comprises a stirring box 111, a circular groove 2 is arranged on the top of the outer box 4, the inner wall of the circular groove 2 is fixedly connected to the outer surface of the stirring box 111, and the outer surface of the stirring box 111 is provided with a plurality of grooves 1.
[0028] A circular groove three is provided at the bottom of the mixing box 111 , and a rotating shaft 112 is rotatably connected to the inner wall of the circular groove three. A motor 114 is provided below the mixing box 111 , and the top output end of the motor 114 is fixedly connected to the bottom of the rotating shaft 112 .
[0029] A rotating plate 113 is fixedly connected to the outer surface of the rotating shaft 112 . There are four rotating plates 113 . One side of the four rotating plates 113 away from the rotating shaft 112 contacts the inner wall of the mixing box 111 . A rotating block 115 is fixedly connected to the outer surface of the rotating shaft 112 .
[0030] The top of the rotating block 115 contacts the bottom of the mixing box 111, and a rotating rod 116 is fixedly connected to the outer surface of the rotating block 115. There are five rotating rods 116, and the tops of the five rotating rods 116 are fixedly connected to cutting knives 117. The five cutting knives 117 are in contact with the outer surface of the mixing box 111 on one side close to the rotating shaft 112. By setting the granulating component 11, specifically, the mixed drug raw materials are first placed in the mixing box, and the motor 114 is turned on by the controller 3 to rotate the cutting knives 117 on the outer surface of the mixing box 111. The cutting knives 117 will cut the drug raw materials discharged from the groove 1 while rotating, so that the drug raw materials can be cut into particles of the same size, thereby ensuring the size of the drug particles and the uniformity of the drug content.
[0031] The heating assembly 22 includes a fixing plate 221 , the outer surface of the fixing plate 221 is fixedly connected to the inner wall of the outer box 4 , the top of the fixing plate 221 is fixedly connected to the bottom of the motor 114 , and a plurality of fixing blocks 222 are fixedly connected to the top of the fixing plate 221 .
[0032] A plurality of fixing blocks 222 are arranged in a circular array with the fixing plate 221 as the center. A groove 2 is opened inside each of the fixing blocks 222 . A heating tube 225 is fixedly connected to the inner wall of each of the grooves 2.
[0033] A plurality of diverter blocks 223 are fixedly connected to the top of the fixed plate 221, and the plurality of diverter blocks 223 are arranged in a circular array with the fixed plate 221 as the center. A baffle plate 226 is fixedly connected to the top of the fixed plate 221, and the outer surface of the baffle plate 226 is fixedly connected to the side of the fixed block 222 away from the inner wall of the outer box 4, and the outer surface of the baffle plate 226 is fixedly connected to the side of the diverter block 223 away from the inner wall of the outer box 4.
[0034] The front and back sides of several diverter blocks 223 are fixedly connected to the outer surface of the fixed block 222, the tops of several diverter blocks 223 are fixedly connected to diverter blocks 224, and the tops of several diverter blocks 224 are fixedly connected to the top of the inner wall of the outer box 4. The heating component 22 is set, specifically, the heating tube 225 is turned on to increase the surface temperature of the fixed block 222. Since the top of the fixed block 222 is an inclined surface, the medicine particles that fall into the top of the fixed block 222 will roll along the inclined surface into the groove 2 inside the fixed plate 221. During the rolling process of the medicine particles, they will be quickly dried due to the heated fixed block 222, so that the viscosity of the surface of the medicine particles is reduced and they will not stick together, thereby improving the practicability of the device.
[0035] A specific application of this embodiment is as follows: first, the mixed drug raw materials are placed in the mixing box, and the motor 114 is turned on by the controller 3. The motor 114 drives the rotating shaft 112 to rotate. When the rotating shaft 112 rotates, it drives several rotating plates 113 to rotate in the mixing box 111. When the rotating plates 113 rotate, the mixed drug raw materials are further mixed so that the drugs and raw materials can be mixed more evenly. At the same time, when the rotating plates 113 rotate, the drug raw materials are discharged from the grooves provided in the mixing box 111. When the rotating shaft 112 rotates, it drives the rotating block 115 to rotate. When the rotating block 115 rotates, it drives several rotating rods 116 to rotate, so that the cutting knife 117 rotates on the outer surface of the mixing box 111. The cutting knife 117 rotates on the outer surface of the mixing box 111. While rotating, the raw medicine material discharged from the groove 1 will be cut, so that the raw medicine material can be cut into particles of the same size, ensuring the size of the medicine particles and the uniformity of the medicine content. The cut medicine particles will fall to the top of several fixed blocks 222 due to gravity and the diversion block 1 223. The heating tube 225 is turned on to increase the surface temperature of the fixed block 222. Since the top of the fixed block 222 is an inclined surface, the medicine particles falling to the top of the fixed block 222 will roll along the inclined surface to the groove 2 inside the fixed plate 221. During the rolling process of the medicine particles, they will be quickly air-dried due to the heated fixed block 222, so that the viscosity of the surface of the medicine particles will be reduced and they will not stick together, thereby improving the practicality of the device. The air-dried medicine particles will fall into the collection drawer, which is convenient for the staff to collect them uniformly.
[0036] In the description of this specification, the description with reference to the terms "one embodiment", "example", "specific example", etc. means that the specific features, structures, materials or characteristics described in conjunction with the embodiment or example are included in at least one embodiment or example of the utility model. In this specification, the schematic representation of the above terms does not necessarily refer to the same embodiment or example. Moreover, the specific features, structures, materials or characteristics described can be combined in any one or more embodiments or examples in a suitable manner.
[0037] The preferred embodiments of the utility model disclosed above are only used to help explain the utility model. The preferred embodiments do not describe all the details in detail, nor do they limit the utility model to the specific implementation methods described. Obviously, many modifications and changes can be made according to the content of this specification. This specification selects and specifically describes these embodiments in order to better explain the principles and practical applications of the utility model, so that technicians in the relevant technical field can well understand and use the utility model. The utility model is limited only by the claims and their full scope and equivalents.
Claims
1. A novel pharmaceutical granulator, comprising a base (1), wherein the four corners of the bottom of the base (1) are fixedly connected to support legs (2), the top of the base (1) is fixedly connected to a controller (3), and the top of the base (1) is provided with a circular groove 1, characterized in that: An outer box (4) is fixedly connected to the bottom of an inner wall of the circular groove, a slide groove is provided at the bottom of the inner wall of the outer box (4), a collection drawer (5) is slidably connected to the inner wall of the slide groove, a handle (6) is fixedly connected to the right side of the collection drawer (5), a granulating component (11) is arranged inside the outer box (4), and a heating component (22) is arranged inside the outer box (4); The granulation assembly (11) comprises a mixing box (111), the top of the outer box (4) is provided with a second circular groove, the inner wall of the second circular groove is fixedly connected to the outer surface of the mixing box (111), and the outer surface of the mixing box (111) is provided with a plurality of first grooves.
2. A novel pharmaceutical granulator according to claim 1, characterized in that: A circular groove three is provided at the bottom of the mixing box (111), and a rotating shaft (112) is rotatably connected to the inner wall of the circular groove three. A motor (114) is provided below the mixing box (111), and a top output end of the motor (114) is fixedly connected to the bottom of the rotating shaft (112).
3. A novel pharmaceutical granulator according to claim 2, characterized in that: A rotating plate (113) is fixedly connected to the outer surface of the rotating shaft (112), and the number of the rotating plates (113) is four. The sides of the four rotating plates (113) away from the rotating shaft (112) are in contact with the inner wall of the mixing box (111), and a rotating block (115) is fixedly connected to the outer surface of the rotating shaft (112).
4. A novel pharmaceutical granulator according to claim 3, characterized in that: The top of the rotating block (115) contacts the bottom of the mixing box (111); a rotating rod (116) is fixedly connected to the outer surface of the rotating block (115); the rotating rods (116) are five in number; a cutting knife (117) is fixedly connected to the top of each of the five rotating rods (116); and the five cutting knives (117) are in contact with the outer surface of the mixing box (111) on one side close to the rotating shaft (112).
5. A novel pharmaceutical granulator according to claim 1, characterized in that: The heating component (22) comprises a fixing plate (221), the outer surface of the fixing plate (221) being fixedly connected to the inner wall of the outer box (4), the top of the fixing plate (221) being fixedly connected to the bottom of the motor (114), and a plurality of fixing blocks (222) being fixedly connected to the top of the fixing plate (221).
6. A novel pharmaceutical granulator according to claim 5, characterized in that: A plurality of the fixing blocks (222) are arranged in a circular array with the fixing plate (221) as the center, a plurality of the fixing blocks (222) are provided with grooves 2 inside, and a plurality of the inner walls of the grooves 2 are fixedly connected with heating tubes (225).
7. A novel pharmaceutical granulator according to claim 6, characterized in that: A plurality of flow diverter blocks (223) are fixedly connected to the top of the fixed plate (221); the plurality of flow diverter blocks (223) are arranged in a circular array with the fixed plate (221) as the center; a baffle (226) is fixedly connected to the top of the fixed plate (221); an outer surface of the baffle (226) is fixedly connected to a side of the fixed block (222) away from the inner wall of the outer box (4); and an outer surface of the baffle (226) is fixedly connected to a side of the flow diverter block (223) away from the inner wall of the outer box (4).
8. A novel pharmaceutical granulator according to claim 7, characterized in that: The front and back sides of a plurality of the diverter blocks (223) are fixedly connected to the outer surface of the fixed block (222), the tops of a plurality of the diverter blocks (223) are fixedly connected to the diverter blocks (224), and the tops of a plurality of the diverter blocks (224) are fixedly connected to the top of the inner wall of the outer box (4).