Disassembled medicine drying device
By employing multiple independent placement slots and racks in the disassembled medicine drying device, combined with drying and sealing components, the problems of mutual interference between medicines and moisture absorption caused by improper sealing are solved, achieving independent drying and safe storage of medicines.
Patent Information
- Application Number
- CN202520592592.4
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2025-03-31
- Publication Date
- 2026-02-24
- Estimated Expiration
- 2035-03-31
AI Technical Summary
Existing desiccant drying devices for disassembled medicines are prone to causing mutual interference between medicines during storage and retrieval, and medicines are easily exposed to moisture if the sealed door is not closed properly. They also lack the functions of sorting and precise drying.
Multiple independent placement slots and racks were designed, combined with drying and sealing components. Through the cooperation of fans and ultraviolet lamps, independent drying of medicines and reliable closure of the sealing door were achieved. Temperature and humidity sensors were used to monitor the status to ensure the drying effect and sealing of the medicines.
It enables independent and precise drying of medicines, avoids mutual interference between medicines, and can quickly determine whether the sealed door is closed to prevent medicines from getting damp, thus improving drying efficiency and safety.
Smart Images

Figure CN223939918U_ABST
Abstract
Description
Technical Field
[0001] This utility model relates to the field of pharmaceutical moisture-proof technology, specifically to a drying device for disassembled pharmaceuticals. Background Technology
[0002] Breaking down medications into smaller doses or units refers to dividing a full package of medicine into smaller doses or units to meet a patient's short-term or specific dosage needs. This practice helps reduce medication waste and allows patients to take medication accurately according to their doctor's orders. Breaking down medications into smaller units is often necessary in various situations. For example, for medications that chronic patients need to take long-term, doctors may adjust the dosage based on the patient's condition and medication response. Additionally, for expensive medications, breaking down medications into smaller units can reduce the financial burden on patients. However, after medications are broken down, the outer seal of the packaging becomes ineffective, and prolonged storage can lead to moisture absorption, affecting the drug's performance. Therefore, medication drying devices are needed for preservation and periodic drying. Existing medication drying devices... This device typically consists of a drying cabinet. Repackaged medications are placed inside, and a fan with heating elements periodically blows hot air to prevent moisture absorption, thus achieving dry preservation. Traditional drying devices for repackaged medications place all medications in the same cabinet and dry them by blowing hot air. Retrieving one medication requires opening the entire cabinet door, affecting the storage of other medications. If the door is not completely closed, all medications inside will become damp. Having all medications in one cabinet is inconvenient for categorization and retrieval, especially for medications packaged in aluminum-plastic composite panels, where stacking and the hot air further exacerbate the problem. Therefore, we propose a new drying device for repackaged medications. Utility Model Content
[0003] The technical problem to be solved by this utility model is to overcome the existing defects and provide a drying device for disassembled medicines. It is equipped with a drying mechanism and uses multiple independent racks to place disassembled medicines. It can independently, accurately and quickly perform precise drying of disassembled medicines, avoiding mutual interference between medicines. It can also determine whether the sealing door is closed properly by observing the state of the handle, avoiding the occurrence of medicines getting damp due to the sealing door not being closed properly. It can effectively solve the problems in the background art.
[0004] To achieve the above objectives, this utility model provides the following technical solution: a drying device for disassembled medicines, including a drying cabinet and a drying mechanism;
[0005] Drying cabinet: It has evenly distributed placement slots at the front of its interior, a flow guide channel at the rear of its interior, and mounting frames at both the top and bottom of the rear of the drying cabinet.
[0006] Drying mechanism: It includes a placement rack, slot, outer rail, inner rail, drying components, and sealing components. The placement slot is equipped with a sliding placement rack inside the placement slot. The slot is opened inside the placement rack. The outer rail is respectively set in the middle of the left and right side walls of the placement slot. The inner rail is respectively set in the middle of the left and right sides of the placement rack. The outer surface of the inner rail located in the same placement slot is slidably connected to the inner wall of the vertically adjacent outer rail, providing a basis for the placement and removal of different disassembled medicines. The drying components are all set inside the rear side of the drying cabinet, and the sealing components are all set in the front end of the placement slot. With the drying mechanism, disassembled medicines can be placed on multiple independent placement racks, and the disassembled medicines can be dried independently, accurately, and quickly, avoiding mutual interference between medicines. The state of the handle can also be observed to determine whether the sealing door is closed properly, avoiding the occurrence of medicines getting damp due to the sealing door not being closed properly.
[0007] Furthermore, the drying assembly includes a guide tube, a heating wire, and a fan. The guide tube is provided between the front and rear side walls of the guide channel. The heating wire is located inside the front side of the mounting frame, and the fan is located inside the rear side of the mounting frame. The placement rack, guide tube, heating wire, and fan are all longitudinally adjacent. The input ends of the heating wire and fan are electrically connected to the output end of the microcontroller, providing a basis for the initial drying of the disassembled medicine.
[0008] Furthermore, the drying assembly also includes an exhaust pipe and a second fan. The exhaust pipes are all located in the middle of the top wall of the placement slot, with the rear ends of the exhaust pipes facing downwards. The second fan is located inside the upper part of the guide slot. The input end of the second fan is electrically connected to the output end of the microcontroller, which can quickly exhaust humid air, accelerate air circulation, and improve the drying efficiency of disassembled medicines.
[0009] Furthermore, the drying assembly also includes ultraviolet lamps, all of which are located in the middle of the top wall of the placement tank. The input end of each ultraviolet lamp is electrically connected to the output end of the microcontroller, providing a basis for further drying of the disassembled medicines.
[0010] Furthermore, the sealing assembly includes a sealing door, a locking groove, a limiting post, and a spring. The sealing doors are all located on the front side of the bottom wall of the placement groove, the locking grooves are all opened in the middle of the interior of the sealing door, the limiting posts are all slidably connected to the interior of the locking groove, and the front side of the top wall of the placement groove is provided with a limiting hole. The upper end of the limiting post located in the same placement groove is inserted into the inner wall of the limiting hole, and the lower end of the limiting post is provided with a spring between it and the bottom wall of the placement groove, providing a basis for sealing the disassembled medicine.
[0011] Furthermore, the sealing assembly also includes a handle groove and a handle. The handle groove is located in the middle of the front side of the sealing door, and the handle is rotatably connected to the middle of the outer surface of the limiting post. The outer surface of the handle is engaged with the inner wall of the longitudinally adjacent handle groove, providing a driving effect for the sealing operation of disassembling medicines.
[0012] Furthermore, it also includes temperature and humidity sensors, all of which are located at the rear end of the sealed door and are bidirectionally electrically connected to a microcontroller, enabling real-time monitoring of the status of the disassembled medicines inside the drying cabinet.
[0013] Furthermore, it also includes a microcontroller, which is located on the upper right front side of the drying cabinet. The input terminal of the microcontroller is electrically connected to an external power supply to provide control for the drying of disassembled medicines.
[0014] Compared with the prior art, the beneficial effects of this utility model are as follows: This disassembled medicine drying device has the following advantages:
[0015] 1. Multiple placement slots allow for the independent placement of different types of medicines. The racks and slots ensure that medicines in different packages are neatly arranged with gaps between them. The combined use of fans one and two, utilizing pressure difference, improves air circulation inside the cabinet. Combined with ultraviolet light irradiation, the medicines can be dried quickly while preventing different types of medicines from affecting each other, facilitating subsequent sorting and retrieval.
[0016] 2. Secure and release the sealing door by moving the handle. Quickly determine if the sealing door is closed by observing whether the handle is inside the handle groove to avoid the medicine getting damp due to an improperly closed sealing door. Attached Figure Description
[0017] Figure 1 This is a schematic diagram of the structure of this utility model;
[0018] Figure 2 This is a schematic cross-sectional view of the drying mechanism of this utility model;
[0019] Figure 3 This is a schematic diagram of the sealing door structure of this utility model;
[0020] Figure 4 This is a schematic cross-sectional view of the sealing assembly of this utility model;
[0021] Figure 5 This is a schematic diagram of the placement rack structure of this utility model.
[0022] In the diagram: 1. Drying cabinet, 2. Placement slot, 3. Guide channel, 4. Mounting frame, 5. Drying mechanism, 51. Placement rack, 52. Slot, 53. Outer rail, 54. Inner rail, 55. Drying assembly, 551. Guide pipe, 552. Heating wire, 553. Fan 1, 554. Exhaust pipe, 555. Fan 2, 556. Ultraviolet lamp, 56. Sealing assembly, 561. Sealed door, 562. Locking groove, 563. Limiting post, 564. Spring, 565. Handle groove, 566. Handle, 6. Temperature and humidity sensor, 7. Microcontroller. Detailed Implementation
[0023] The technical solutions of the present utility model will be clearly and completely described below with reference to the accompanying drawings of the embodiments. Obviously, the described embodiments are only some embodiments of the present utility model, and not all embodiments. Based on the embodiments of the present utility model, all other embodiments obtained by those of ordinary skill in the art without creative effort are within the protection scope of the present utility model.
[0024] Please see Figure 1-5 This embodiment provides a technical solution: a drug drying device for dismantling and drying, including a drying cabinet 1 and a drying mechanism 5;
[0025] Drying cabinet 1: It has evenly distributed placement slots 2 at the front end of its interior, and a guide channel 3 is opened on the rear side of the interior of the drying cabinet 1. Both the upper and lower ends of the rear side of the drying cabinet 1 are equipped with mounting frames 4. It also includes a microcontroller 7, which is located on the upper front right side of the drying cabinet 1. The input end of the microcontroller 7 is electrically connected to an external power supply to provide control for the drying of disassembled medicines.
[0026] Drying mechanism 5 includes a rack 51, slots 52, outer rails 53, inner rails 54, drying components 55, and sealing components 56. The rack 51 is slidable inside the rack 2. Slots 52 are located inside the rack 51 and are evenly distributed on the left and bottom walls of the rack 51. Outer rails 53 are located in the middle of the left and right side walls of the rack 2, and inner rails 54 are located in the middle of the left and right sides of the rack 51. The outer and inner rails 53 form guide rails. The outer surface of the inner rails 54 located within the same rack 2 is slidably connected to the inner wall of the vertically adjacent outer rails 53, providing a basis for the placement and removal of different disassembled medicines. The drying components 55 are all located inside the rear side of the drying cabinet 1. Component 55 includes a guide pipe 551, a heating wire 552, and a first fan 553. Guide pipes 551 are located between the front and rear side walls of the guide channel 3. Heating wires 552 are all located inside the front side of the mounting frame 4, and first fans 553 are all located inside the rear side of the mounting frame 4. The placement frame 51, guide pipes 551, heating wires 552, and first fans 553 are all longitudinally adjacent. The input ends of heating wires 552 and first fans 553 are electrically connected to the output end of the microcontroller 7, providing a basis for the initial drying of disassembled medicines. The drying component 55 also includes an exhaust pipe 554 and a second fan 555. Exhaust pipes 554 are all located in the middle of the top wall of the placement slot 2, with their rear ends facing downwards. Second fans 555 are all located inside the upper part of the guide channel 3. The input terminals are all electrically connected to the output terminals of the microcontroller 7, which can quickly expel humid air, accelerate air circulation, and improve the drying efficiency of disassembled medicines. The drying component 55 also includes ultraviolet lamps 556, which are all located in the middle of the top wall of the placement slot 2. The input terminals of the ultraviolet lamps 556 are all electrically connected to the output terminals of the microcontroller 7, providing a basis for further drying of disassembled medicines. The sealing components 56 are all located at the front end of the placement slot 2. The sealing components 56 include sealing doors 561, locking grooves 562, limiting posts 563, and springs 564. The sealing doors 561 are all located on the front side of the bottom wall of the placement slot 2. The sealing strip is provided on the rear side of the sealing door 561, which improves the sealing effect of the sealing door 561. The locking grooves 562 are all opened in the sealing grooves. Inside the sealing door 561, the limiting posts 563 are slidably connected to the inside of the locking groove 562. Limiting holes are provided on the front side of the top wall of the placement groove 2. The upper ends of the limiting posts 563 located inside the same placement groove 2 are inserted into the inner wall of the limiting holes. Springs 564 are provided between the lower ends of the limiting posts 563 and the bottom wall of the placement groove 2, providing a basis for sealing the disassembled medicines. The sealing assembly 56 also includes handle grooves 565 and handles 566. The handle grooves 565 are all located in the middle of the front side of the sealing door 561. The handles 566 are rotatably connected to the middle of the outer surface of the limiting posts 563. The outer surface of the handles 566 engages with the inner wall of the longitudinally adjacent handle grooves 565, providing a driving effect for sealing the disassembled medicines. A temperature and humidity sensor 6 is also included.Temperature and humidity sensors 6 are all located at the rear end of the sealing door 561. These sensors are bidirectionally electrically connected to the microcontroller 7, allowing real-time monitoring of the status of the disassembled medicines inside the drying cabinet 1. A drying mechanism 5 is provided, using multiple independent racks 51 to hold the disassembled medicines. This allows for independent, precise, and rapid drying of the medicines, preventing mutual interference between them. The status of the handle 566 can also be used to determine if the sealing door 561 is properly closed, preventing the medicines from becoming damp due to an improperly closed door.
[0027] The working principle of the disassembled medicine drying device provided by this utility model is as follows: When drying disassembled medicines, first place the disassembled medicines inside the drying cabinet 1, deflect the handle 566 outwards to pull it out from inside the handle groove 565 until the lower end of the handle 566 is in contact with the rear end of the handle groove 565, then move the handle 566 downwards, causing the limiting post 563 to move downwards, the spring 564 to contract, the upper end of the limiting post 563 to leave the inside of the limiting hole, the sealing door 561 is no longer restricted, deflect the sealing door 561 outwards to open the sealing door 561, and quickly and smoothly pull out the placement rack 51 through the guide rail to place the disassembled medicines. Above the shelf 51, the aluminum-plastic composite medicines and bagged powder medicines, due to their thinner outer packaging edges, can be inserted into the left side of the slot 52 and remain upright, with gaps between the medicines. Bottled medicines can be placed on the right side of the shelf 51. After placing the disassembled medicines, push the shelf 51 back into the storage slot 2, move the handle 566 down to move the limiting post 563 down, then close the sealing door 561, release the handle 566, and the spring 564 will rebound without force until the upper end of the limiting post 563 is inserted into the locking slot 562. Then turn the handle 566 to engage the handle slot 56. Inside compartment 5, the sealing door 561 is engaged. Limited by the handle groove 565, the handle 566 and the limiting post 563 will not move. The sealing door 561 is also checked for tightness by observing whether the handle 566 is in the handle groove 565, preventing the medicine from getting damp due to an improperly closed sealing door 561. Then, the microcontroller 7 controls the temperature and humidity sensor 6 to monitor the status of the disassembled medicines in each compartment 2 in real time. When drying is required, the microcontroller 7 controls the heating wire 552 and fan 553 to operate. The heating wire 552 dissipates heat, and the fan 553 draws in outside air. After being heated by heating wire 552, external air enters the placement tank 2 through guide pipe 551. At this time, fan 2 555 works, drawing in and accelerating the external air. When the high-speed external air passes through the inside of guide 3, the air velocity and pressure inside guide 3 are high, allowing the air inside placement tank 2 to enter guide 3 more quickly through exhaust pipe 554 and then be blown out of drying cabinet 1, achieving rapid air circulation. At the same time, ultraviolet lamp 556 works, irradiating the surface of the disassembled medicine with ultraviolet radiation, evaporating the moisture inside the disassembled medicine, and further accelerating the drying efficiency of the disassembled medicine.
[0028] It is worth noting that the microcontroller 7 disclosed in the above embodiments is an STM32F103RCT6 microcontroller, the heating wire 552 is a YHYJ heating wire, the first fan 553 and the second fan 555 are both TG4020 fans, the ultraviolet lamp 556 is a UVLN81 T ultraviolet lamp, and the temperature and humidity sensor 6 is an HC2A-I C102 temperature and humidity sensor. The microcontroller 7 controls the operation of the heating wire 552, the ultraviolet lamp 556, the temperature and humidity sensor 6, the first fan 553 and the second fan 555 using methods commonly used in the prior art.
[0029] The above description is merely an embodiment of this utility model and does not limit the patent scope of this utility model. Any equivalent structural or procedural transformations made based on the content of this utility model specification and drawings, or direct or indirect applications in other related technical fields, are similarly included within the patent protection scope of this utility model.
Claims
1. A drying device for disassembled medicines, characterized in that: Includes a drying cabinet (1) and a drying mechanism (5); Drying cabinet (1): The front end of the interior is provided with evenly distributed placement slots (2), the rear side of the interior of the drying cabinet (1) is provided with a flow guide slot (3), and the upper and lower ends of the rear side of the drying cabinet (1) are provided with mounting frames (4). Drying mechanism (5): It includes a placement rack (51), a slot (52), an outer rail (53), an inner rail (54), a drying component (55), and a sealing component (56). The placement slot (2) is provided with a sliding placement rack (51) inside. The slot (52) is opened inside the placement rack (51). The outer rail (53) is respectively set in the middle of the left and right side walls of the placement slot (2). The inner rail (54) is respectively set in the middle of the left and right sides of the placement rack (51). The outer surface of the inner rail (54) located in the same placement slot (2) is slidably connected to the inner wall of the vertically adjacent outer rail (53). The drying components (55) are all set in the rear side of the inside of the drying cabinet (1). The sealing components (56) are all set in the front end of the placement slot (2).
2. The drug drying device for dismantling and drying according to claim 1, characterized in that: It also includes a microcontroller (7), which is located on the upper front side of the right side of the drying cabinet (1), and the input terminal of the microcontroller (7) is electrically connected to an external power supply.
3. The drug drying device for dismantling and drying according to claim 2, characterized in that: The drying assembly (55) includes a guide tube (551), a heating wire (552), and a fan (553). The guide tube (551) is provided between the front and rear side walls of the guide groove (3). The heating wire (552) is located inside the front side of the mounting frame (4). The fan (553) is located inside the rear side of the mounting frame (4). The placement frame (51), the guide tube (551), the heating wire (552), and the fan (553) are all longitudinally adjacent. The input ends of the heating wire (552) and the fan (553) are electrically connected to the output end of the microcontroller (7).
4. The drug drying device for dismantling and drying according to claim 2, characterized in that: The drying assembly (55) also includes an exhaust pipe (554) and a second fan (555). The exhaust pipe (554) is located in the middle of the top wall of the placement slot (2), with the rear end of the exhaust pipe (554) facing downwards. The second fan (555) is located inside the upper part of the guide slot (3), and the input end of the second fan (555) is electrically connected to the output end of the microcontroller (7).
5. The drug drying device for dismantling and drying according to claim 2, characterized in that: The drying assembly (55) also includes ultraviolet lamps (556), which are all located in the middle of the top wall of the placement slot (2). The input end of each ultraviolet lamp (556) is electrically connected to the output end of the microcontroller (7).
6. The drug drying device for dismantling and drying according to claim 2, characterized in that: The sealing assembly (56) includes a sealing door (561), a locking groove (562), a limiting post (563), and a spring (564). The sealing doors (561) are all located on the front side of the bottom wall of the placement groove (2). The locking grooves (562) are all opened in the middle of the interior of the sealing door (561). The limiting posts (563) are all slidably connected to the interior of the locking grooves (562). The front side of the top wall of the placement groove (2) is provided with limiting holes. The upper ends of the limiting posts (563) located in the same placement groove (2) are all inserted into the inner wall of the limiting holes. The lower ends of the limiting posts (563) are all provided with springs (564) between them and the bottom wall of the placement groove (2).
7. The drug drying device according to claim 6, characterized in that: The sealing assembly (56) also includes a handle groove (565) and a handle (566). The handle groove (565) is opened in the middle of the front side of the sealing door (561), and the handle (566) is rotatably connected to the middle of the outer surface of the limiting post (563). The outer surface of the handle (566) is engaged with the inner wall of the longitudinally adjacent handle groove (565).
8. The drug drying device according to claim 7, characterized in that: It also includes a temperature and humidity sensor (6), which is located at the rear end of the sealing door (561) and is bidirectionally electrically connected to the microcontroller (7).