Medical intermediate sampling device
By designing the connection method of the ring plug and slot, and combining the cross chute and slide rod mechanism, the rapid disassembly and cleaning of the medical intermediate sampling device is achieved, solving the problem of difficult disassembly of drug residues and threaded connections, and improving the accuracy of inspection and convenience of operation.
Patent Information
- Application Number
- CN202420482095.4
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-03-12
- Publication Date
- 2025-03-11
- Estimated Expiration
- 2034-03-12
AI Technical Summary
The existing medical intermediate sampling devices have problems such as drug residues and threaded connections that are difficult to disassemble during cleaning, which affects the accuracy of intermediate inspection and the user's operational convenience.
A medical intermediate sampling device is designed, using the connection method of an annular plug and slot, and the cross chute and slide rod mechanism is used to achieve rapid disassembly and cleaning, avoiding the difficulty of threaded connection.
The rapid disassembly and cleaning of the sampling device is realized, which prevents drug residues and mutual contamination, solves the problem of difficulty for users with less strength to open, and improves the accuracy of intermediate physical examination and the convenience of operation.
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Figure CN222599252U_ABST
Abstract
Description
Technical Field
[0001] The utility model belongs to the technical field of pharmaceutical intermediates, and specifically relates to a pharmaceutical intermediate sampling device. Background Art
[0002] Pharmaceutical intermediates refer to chemical raw materials or chemical products that play a bridging role in the process of drug synthesis. They are compounds required in one or more intermediate steps in the drug production chain. At present, pharmaceutical intermediates need to use special pharmaceutical intermediate sampling devices to detect them during the production process.
[0003] Existing pharmaceutical intermediate sampling devices usually use a needle to extract pharmaceutical intermediates. However, in this way, after the sampling is completed, the pharmaceutical paste in the sampling cavity is not easy to clean. If it is not cleaned thoroughly, there will be residues in the cavity. When it is used next time, this residue will be mixed with the new drug, affecting the accuracy of the intermediate inspection. Secondly, there are also devices that can disassemble the tube body, but most of them use a threaded connection. If this connection method is screwed too tight, it will be difficult for users with less strength to open it for cleaning. Utility Model Content
[0004] In view of this, the utility model provides a pharmaceutical intermediate sampling device, which can be disassembled by a relevant user with just one press through a fixing mechanism, making it more convenient to clean the pharmaceutical intermediate sampling device, preventing the problem of mutual contamination when sampling different pharmaceutical intermediates, and solving the problem that it is difficult for users with less strength to open the device due to the threaded connection method.
[0005] In order to solve the above technical problems, the utility model provides a pharmaceutical intermediate sampling device, including a sampling tube and a container head and a connecting assembly arranged between the sampling tube and the container head, the connecting assembly including an annular plug arranged on the upper end surface of the sampling tube, the lower end surface of the container head is provided with a slot adapted to the annular plug, the middle part of the container head is also provided with a sampling assembly, the sampling assembly includes a cross slide groove arranged in the middle part of the container head, a cross slide rod is slidably connected in the cross slide groove, a piston is threadedly connected in a screw hole arranged in the middle part of the lower surface of the cross slide rod, the whole composed of the sampling tube and the container head is arranged in cooperation with the piston, a fixing mechanism is also provided between the sampling tube and the container head, and an ejection assembly is also provided in the slot.
[0006] A scale line is arranged on the right side of the outer arc surface of the sampling tube near the transparent window.
[0007] A transparent window is arranged in the opening arranged on the right side of the outer arc surface of the sampling tube.
[0008] The lower end of the sampling tube is movably plugged with a movable connector.
[0009] The fixing mechanism includes an assembly groove which is longitudinally symmetrically arranged at the lower end of the outer arc surface of the container head. The upper side of the inner cavity of the assembly groove is rotatably connected to a limit clamp. The upper end surface of the sampling tube is provided with a limit plate which is longitudinally symmetrically distributed. The limit plates are respectively matched with the limit clamps adjacent to the same side; the fixing mechanism also includes spring pieces which are respectively arranged at the upper end of the inner wall surface of the assembly groove. The lower ends of the spring pieces are respectively matched with the limit clamps adjacent to the same side.
[0010] The ejection assembly comprises a spring arranged on the top wall of the slot, a rubber sealing top ring is arranged at the lower end of the spring, the rubber sealing top ring is slidably connected to the slot, and the rubber sealing top ring is matched with the annular plug.
[0011] The beneficial effects of the above technical solution of the utility model are as follows:
[0012] 1. When other samples need to be taken after the sampling of the pharmaceutical intermediate sample is completed, the relevant staff only needs to press the limit clamp at the same time, and the limit clamp overcomes the elastic force of the spring and retracts into the assembly groove, so that the limit clamp is separated from the limit plate, and then the annular plug and the sampling tube are separated from the container head through the rubber sealing top ring under the action of the spring rebound force. The sampling tube and the container head can be opened with just one press, and then the sampling tube and the container head and their ancillary mechanisms can be cleaned. The relevant user only needs to press it to disassemble, which makes it more convenient to clean the pharmaceutical intermediate sampling device, prevents the problem of mutual contamination when sampling different pharmaceutical intermediates, and solves the problem that users with less strength are difficult to open due to the threaded connection method.
[0013] 2. After cleaning, just align the limit plate with the assembly groove, and then flexibly connect the annular plug on the sampling tube with the slot on the container head. After the limit plate contacts the limit clamp, the limit plate will slide relative to the limit clamp, and the limit clamp will overcome the elastic force of the spring piece to avoid. After the sampling tube and the container head are fully matched, the limit clamp will immediately reset under the action of the spring piece's rebound force and connect with the limit plate, thereby locking the sampling tube and the container head. At this time, the spring is compressed and exerts a reverse force on the rubber sealing top ring, so that the rubber sealing top ring tightly contacts the annular plug. Disassembly and installation can be achieved by one click and one plug, making it more convenient for relevant users to operate. BRIEF DESCRIPTION OF THE DRAWINGS
[0014] Figure 1 This is a schematic diagram of the main structure of a pharmaceutical intermediate sampling device of the utility model;
[0015] Figure 2 This is a schematic diagram of the fixing mechanism structure of the utility model;
[0016] Figure 3 A schematic diagram of the structure of the utility model;
[0017] Figure 4 It is a schematic diagram of the B structure of the utility model.
[0018] Explanation of the reference numerals in the accompanying drawings: 100, sampling tube; 200, container head; 300, annular plug; 301, slot; 400, cross slide rod; 401, piston; 500, movable connector; 600, assembly groove; 601, limit clamp; 602, limit plate; 603, spring; 700, spring; 701, rubber sealing top ring; 800, transparent window; 900, scale line. DETAILED DESCRIPTION
[0019] In order to make the purpose, technical scheme and advantages of the embodiment of the utility model clearer, the following will be combined with the appended drawings of the embodiment of the utility model. Figure 1-4 , the technical scheme of the embodiment of the utility model is clearly and completely described. Obviously, the described embodiment is a part of the embodiment of the utility model, not all of the embodiments. Based on the described embodiment of the utility model, all other embodiments obtained by ordinary technicians in this field belong to the scope of protection of the utility model.
[0020] like Figure 1-4 As shown:
[0021] The present embodiment provides a pharmaceutical intermediate sampling device, including a sampling tube 100 and a container head 200 and a connecting assembly arranged between the sampling tube 100 and the container head 200, the connecting assembly includes an annular plug 300 arranged on the upper end surface of the sampling tube 100, the lower end surface of the container head 200 is provided with a slot 301 adapted to the annular plug 300, and the middle part of the container head 200 is also provided with a sampling assembly, the sampling assembly includes a cross slide groove arranged in the middle part of the container head 200, a cross slide rod 400 is slidably connected in the cross slide groove, a piston 401 is threadedly connected in a screw hole arranged in the middle part of the lower surface of the cross slide rod 400, and the sampling tube 100 and the container head 200 assembly are connected. The whole is arranged in cooperation with the piston 401, a fixing mechanism is also arranged between the sampling tube 100 and the container head 200, and an ejection component is also arranged in the slot 301; the fixing mechanism includes an assembly groove 600 which is longitudinally symmetrically arranged at the lower end of the outer arc surface of the container head 200, and the upper side of the inner cavity of the assembly groove 600 is rotatably connected to the limit clamp 601, and the upper end surface of the sampling tube 100 is provided with a longitudinally symmetrically distributed limit plate 602, and the limit plate 602 is respectively arranged in cooperation with the limit clamp 601 adjacent to the same side; the fixing mechanism also includes spring pieces 603 which are respectively arranged at the upper end of the inner wall surface of the assembly groove 600, and the lower ends of the spring pieces 603 are respectively arranged in cooperation with the limit clamp 601 adjacent to the same side.
[0022] like Figure 1As shown, the ejection assembly includes a spring 700 arranged on the top wall of the slot 301, and a rubber sealing top ring 701 is provided at the lower end of the spring 700. The rubber sealing top ring 701 is slidably connected to the slot 301, and the rubber sealing top ring 701 is matched with the annular plug 300.
[0023] like Figure 1-4 As shown, a transparent window 800 is provided in the opening on the right side of the outer arc surface of the sampling tube 100 to facilitate observation by relevant users.
[0024] like Figure 1-2 As shown, a movable connector 500 is movably connected to the lower end of the sampling tube 100 to facilitate replacement by relevant users.
[0025] The working principle of the pharmaceutical intermediate sampling device provided by the utility model is as follows: when sampling is required, the relevant user holds the sampling tube 100 and its auxiliary mechanism, and then inserts the movable connecting head 500 into the storage place of the pharmaceutical intermediate required for sampling, and then the relevant user pulls the cross slide bar 400 outward, and the cross slide bar 400 drives the piston 401 to move to generate negative pressure suction, so that the pharmaceutical intermediate is drawn into the cavity formed by the sampling tube 100 and the container head 200, and then only needs to press the cross slide bar 400 to move the pharmaceutical intermediate sample into the specified inspection tube. After the sampling of the pharmaceutical intermediate sample is completed, when other samples need to be taken, the relevant staff only needs to press the limit clamp 601 at the same time, and the limit clamp 601 overcomes the elastic force of the spring 603 and retracts into the assembly groove 600, so that the limit clamp 601 is separated from the limit plate 602, and then the annular plug 300 and the sampling tube 100 are separated from the container head 200 through the rubber sealing top ring 701 under the action of the rebound force of the spring 700. The sampling tube 100 and the container head 200 can be opened with just one press, and then the sampling tube 100, the container head 200 and their attached mechanisms can be cleaned. , it can be disassembled by the relevant user with just one click, making it more convenient to clean the pharmaceutical intermediate sampling device, preventing the problem of mutual contamination when sampling different pharmaceutical intermediates, and solving the problem that it is difficult for users with less strength to open due to the threaded connection method. After cleaning, it is only necessary to align the limiting plate 602 with the assembly groove 600, and then flexibly connect the annular plug 300 on the sampling tube 100 with the slot 301 on the container head 200. After the limiting plate 602 contacts the limiting clamp 601, the limiting plate 602 will slide relative to the limiting clamp 601, and The limit clamp 601 overcomes the elastic force of the spring piece 603 and avoids it. After the sampling tube 100 and the container head 200 are fully matched, the limit clamp 601 is immediately reset under the action of the rebound force of the spring piece 603 and clamped on the limit plate 602, thereby locking and limiting the sampling tube 100 and the container head 200. At this time, the spring 700 is compressed and applies a reverse force to the rubber sealing top ring 701, so that the rubber sealing top ring 701 tightly contacts the annular plug 300. Disassembly and installation can be achieved by just pressing and plugging, making it more convenient for relevant users to operate.
[0026] like Figure 1 As shown, a scale line 900 is provided on the right side of the outer arc surface of the sampling tube 100 near the transparent window 800, so that the relevant user can intuitively determine the amount of sampling required according to the scale line 900.
[0027] In addition, it should be noted that in the description of the present invention, unless otherwise clearly specified and limited, the terms "installation", "connection" and "connection" should be understood in a broad sense, for example, it can be a fixed connection, a detachable connection, or an integral connection; it can be a mechanical connection or an electrical connection; it can be a direct connection, or it can be indirectly connected through an intermediate medium, or it can be the internal communication of two components. For those skilled in the art, the specific meanings of the above terms in the present invention can be understood according to the specific circumstances.
[0028] The above is a preferred embodiment of the present invention. It should be pointed out that, for ordinary technicians in this technical field, several improvements and modifications can be made without departing from the principles of the present invention. These improvements and modifications should also be regarded as the protection scope of the present invention.
Claims
1. A pharmaceutical intermediate sampling device, characterized in that: The invention comprises a sampling tube (100), a container seal (200), and a connection assembly arranged between the sampling tube (100) and the container seal (200), wherein the connection assembly comprises an annular plug (300) arranged on the upper end surface of the sampling tube (100), a slot (301) adapted to the annular plug (300) is arranged on the lower end surface of the container seal (200), a sampling assembly is also arranged in the middle of the container seal (200), and the sampling assembly comprises a slot (301) arranged on the container seal A cross slide groove is provided in the middle of the sealing head (200), a cross slide rod (400) is slidably connected in the cross slide groove, a piston (401) is threadedly connected in a screw hole provided in the middle of the lower surface of the cross slide rod (400), the sampling tube (100) and the container sealing head (200) are integrally arranged with the piston (401), a fixing mechanism is also provided between the sampling tube (100) and the container sealing head (200), and an ejection assembly is also provided in the slot (301).
2. A pharmaceutical intermediate sampling device as claimed in claim 1, characterized in that: The fixing mechanism comprises an assembly groove (600) longitudinally symmetrically arranged at the lower end of the outer arc surface of the container head (200), the upper side of the inner cavity of the assembly groove (600) is rotatably connected to a limit clamp (601), and the upper end surface of the sampling tube (100) is provided with a limit plate (602) longitudinally symmetrically distributed, and the limit plate (602) is respectively arranged in cooperation with the limit clamps (601) adjacent to the same side.
3. A pharmaceutical intermediate sampling device as claimed in claim 2, characterized in that: The fixing mechanism further comprises spring pieces (603) respectively arranged on the upper ends of the inner wall surfaces of the assembly grooves (600), and the lower ends of the spring pieces (603) are respectively arranged in cooperation with the adjacent limiting clamps (601) on the same side.
4. A pharmaceutical intermediate sampling device as claimed in claim 1, characterized in that: The ejection assembly comprises a spring (700) arranged on the top wall of the slot (301), a rubber sealing top ring (701) is provided at the lower end of the spring (700), the rubber sealing top ring (701) is slidably connected to the slot (301), and the rubber sealing top ring (701) is arranged in cooperation with the annular plug (300).
5. A pharmaceutical intermediate sampling device as claimed in claim 1, characterized in that: A transparent window (800) is provided in an opening arranged on the right side of the outer arc surface of the sampling tube (100).
6. A pharmaceutical intermediate sampling device as claimed in claim 5, characterized in that: A scale mark (900) is provided on the right side of the outer arc surface of the sampling tube (100) near the transparent window (800).
7. A pharmaceutical intermediate sampling device as claimed in claim 1, characterized in that: The lower end of the sampling tube (100) is movably plugged with a movable connector (500).