CN220751696U - Sampler for high-viscosity liquid bulk drug - Google Patents
Sampler for high-viscosity liquid bulk drug Download PDFInfo
- Publication number
- CN220751696U CN220751696U CN202322245940.4U CN202322245940U CN220751696U CN 220751696 U CN220751696 U CN 220751696U CN 202322245940 U CN202322245940 U CN 202322245940U CN 220751696 U CN220751696 U CN 220751696U
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- CN
- China
- Prior art keywords
- bulk drug
- sampling
- viscosity liquid
- wall
- sampler
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000003814 drug Substances 0.000 title claims abstract description 65
- 229940079593 drug Drugs 0.000 title claims abstract description 61
- 239000007788 liquid Substances 0.000 title claims abstract description 24
- 238000005070 sampling Methods 0.000 claims abstract description 72
- 238000000605 extraction Methods 0.000 claims description 13
- 238000003860 storage Methods 0.000 claims description 6
- 239000008186 active pharmaceutical agent Substances 0.000 claims 5
- 229940088679 drug related substance Drugs 0.000 claims 5
- 238000000034 method Methods 0.000 abstract description 7
- 206010044565 Tremor Diseases 0.000 abstract description 3
- 230000003028 elevating effect Effects 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- 239000002994 raw material Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 5
- 238000004140 cleaning Methods 0.000 description 3
- 239000003242 anti bacterial agent Substances 0.000 description 2
- 229940088710 antibiotic agent Drugs 0.000 description 2
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 description 2
- 230000005574 cross-species transmission Effects 0.000 description 2
- BSYNRYMUTXBXSQ-UHFFFAOYSA-N Aspirin Chemical compound CC(=O)OC1=CC=CC=C1C(O)=O BSYNRYMUTXBXSQ-UHFFFAOYSA-N 0.000 description 1
- LPHGQDQBBGAPDZ-UHFFFAOYSA-N Isocaffeine Natural products CN1C(=O)N(C)C(=O)C2=C1N(C)C=N2 LPHGQDQBBGAPDZ-UHFFFAOYSA-N 0.000 description 1
- 208000007107 Stomach Ulcer Diseases 0.000 description 1
- 229960001138 acetylsalicylic acid Drugs 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 229960001948 caffeine Drugs 0.000 description 1
- VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- WIIZWVCIJKGZOK-RKDXNWHRSA-N chloramphenicol Chemical compound ClC(Cl)C(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 WIIZWVCIJKGZOK-RKDXNWHRSA-N 0.000 description 1
- 229960005091 chloramphenicol Drugs 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- GXGAKHNRMVGRPK-UHFFFAOYSA-N dimagnesium;dioxido-bis[[oxido(oxo)silyl]oxy]silane Chemical compound [Mg+2].[Mg+2].[O-][Si](=O)O[Si]([O-])([O-])O[Si]([O-])=O GXGAKHNRMVGRPK-UHFFFAOYSA-N 0.000 description 1
- 230000006806 disease prevention Effects 0.000 description 1
- 208000000718 duodenal ulcer Diseases 0.000 description 1
- 238000000855 fermentation Methods 0.000 description 1
- 230000004151 fermentation Effects 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 150000002484 inorganic compounds Chemical class 0.000 description 1
- 229910010272 inorganic material Inorganic materials 0.000 description 1
- 239000000391 magnesium silicate Substances 0.000 description 1
- 229940099273 magnesium trisilicate Drugs 0.000 description 1
- 229910000386 magnesium trisilicate Inorganic materials 0.000 description 1
- 235000019793 magnesium trisilicate Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229940127557 pharmaceutical product Drugs 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 235000017807 phytochemicals Nutrition 0.000 description 1
- 229930000223 plant secondary metabolite Natural products 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000003908 quality control method Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
Landscapes
- Sampling And Sample Adjustment (AREA)
Abstract
The utility model relates to the technical field of bulk drug sampling equipment, and discloses a sampler for high-viscosity liquid bulk drug. According to the utility model, the control shaft, the control button, the gear support frame and the lifting table can be twisted to control and rotate the control shaft, the control shaft drives the gears to rotate together, and the lifting table meshed with the gears is driven to lift through the rotation of the gears, so that a sampling tube fixed in the support frame can sample bulk drug, the sampling tube is fixed in the support frame, and is not easy to shake during sampling, and larger force is not required to pull, so that the phenomenon that sampling deviation is caused due to shaking of hands in the sampling process is avoided.
Description
Technical Field
The utility model relates to the technical field of bulk drug sampling equipment, in particular to a sampler for high-viscosity liquid bulk drug.
Background
The bulk drug is intended to be used as any substance or mixture of substances in pharmaceutical manufacturing, and is an active ingredient of a pharmaceutical product when used in pharmacy. The substance has pharmacological activity or other direct effect in diagnosis, treatment, symptomatic relief, treatment or prevention of disease, or can affect the function or structure of the body. The raw materials are divided into two main types of chemical synthetic drugs and natural chemical drugs according to the sources of the raw materials. The chemical synthetic drugs can be divided into inorganic synthetic drugs and organic synthetic drugs. Inorganic synthetic drugs are inorganic compounds (extremely individual elements) such as aluminum hydroxide, magnesium trisilicate, etc. for treating gastric and duodenal ulcers; the organic synthetic medicine is mainly prepared from basic organic chemical raw materials through a series of organic chemical reactions (such as aspirin, chloramphenicol, caffeine, etc.). Natural chemical drugs can be classified into biochemical drugs and phytochemical drugs according to their sources. Antibiotics are generally prepared by microbial fermentation and belong to the category of biochemistry. Various semisynthetic antibiotics have been developed in recent years, and are products combining biosynthesis and chemical synthesis. Among the raw materials, the organic synthetic medicine has the largest variety, yield and ratio of output value, and is the main support of the chemical pharmaceutical industry. The quality of the raw material medicine determines the quality of the preparation, so the quality standard is very strict, and strict national pharmacopoeia standards and quality control methods are formulated for the raw material medicine widely applied in various countries in the world.
Most of the existing sampling devices are hand-held syringe type sampling devices, and because high-viscosity liquid is high in viscosity, the hand-held syringe type sampling devices need to be pulled with great force, and sampling deviation can be caused by shaking hands in the sampling process; and when the sampling equipment is taken out from the high-viscosity liquid, the high-viscosity liquid is adhered to the outer side of the sampling equipment, and the high-viscosity liquid is difficult to remove from the sampling equipment, so that the workload of workers is increased.
Disclosure of Invention
(one) solving the technical problems
Aiming at the defects of the prior art, the utility model provides a sampler for high-viscosity liquid bulk drugs, which has the advantages of no need of hand holding, convenient sampling and easy cleaning, and solves the technical problems.
(II) technical scheme
In order to achieve the above purpose, the present utility model provides the following technical solutions: the utility model provides a sampler for high viscosity liquid bulk drug, includes the base, base top fixedly connected with crane, crane upper end position inner wall rotation is connected with the control axle, control axle outer wall fixedly connected with gear, crane inner wall sliding connection has the elevating platform, elevating platform top fixedly connected with support frame, support frame inner wall swing joint has the sampling tube, sampling tube inner wall sliding connection has the extraction pole, extraction pole top fixedly connected with extraction mounting, extraction pole bottom fixedly connected with rubber piece.
Preferably, the gear is meshed with the outer wall of one side of the lifting platform.
Through the technical scheme, the lifting platform can move up and down in the lifting frame through the meshing of the gears, so that the sampling tube fixed in the supporting frame can be used for sampling bulk drug, the sampling of the sampling tube is not needed to be held, the device does not need to be pulled with great effort, and the phenomenon that the sampling occurs due to shaking of hands in the sampling process is avoided.
Preferably, the outer wall of one end of the control shaft is fixedly connected with a control button.
Through above-mentioned technical scheme, accessible twist the control button and carry out the control rotation to controlling the axle, control the axle and drive the gear and rotate together, drive the elevating platform with gear engagement through the rotation of gear and go on elevating movement to simple easy operation, and equipment cost is low.
Preferably, the bottom of the sampling tube is sleeved with a conical cover.
Through above-mentioned technical scheme, through the sampling tube of bulk drug sample work can adhere to remaining bulk drug, the bulk drug of high viscosity liquid is more difficult to clean, if not thoroughly clean the sampling tube, can make the bulk drug remain in the sampling tube, make the next bulk drug sample result that goes on error appear, the effect of cone cover is after carrying out the bulk drug sample work of high viscosity liquid, alright take off the cone cover, carry out the degree of depth cleanness to sampling tube inside and cone cover to the convenience makes the more thorough cleanness of sealed sampling tube.
Preferably, the top surface of the base is provided with a storage groove.
Through above-mentioned technical scheme, place the bulk drug of cup dress on putting the thing groove, alright make cup dress bulk drug and put thing groove joint to make the bulk drug of cup dress be difficult for appearing rocking in the work of sample, thereby influence the bulk drug and get the work, and avoided leading to the bulk drug to spill over because of the rocking of bulk drug.
Preferably, a round hole is formed in the outer wall of one end, far away from the lifting table, of the supporting frame, and a fixing bolt is connected to the position, located in the round hole, of the supporting frame in a threaded mode.
Through above-mentioned technical scheme, the effect of fixed sampling tube has been played to the fixing bolt of here for the sampling tube is placed in the support frame fixedly, and at the during operation of sample, and the sampling tube is difficult for appearing rocking, thereby influences the collection to the bulk drug and has avoided the hand shake in the sampling process can lead to the sample to appear the deviation.
Compared with the prior art, the utility model provides a sampler for high-viscosity liquid bulk drugs, which has the following beneficial effects:
1. according to the utility model, the control shaft, the control button, the gear support frame and the lifting table can be twisted to control and rotate the control shaft, the control shaft drives the gears to rotate together, and the lifting table meshed with the gears is driven to lift through the rotation of the gears, so that a sampling tube fixed in the support frame can sample bulk drug, the sampling tube is fixed in the support frame, and is not easy to shake during sampling, and larger force is not required to pull, so that the phenomenon that sampling deviation is caused due to shaking of hands in the sampling process is avoided.
2. According to the utility model, the residual crude drug is adhered to the sampling tube through the conical cover sleeved at the bottom of the sampling tube, the crude drug in the high-viscosity liquid is more difficult to clean, if the sampling tube is not completely cleaned, the crude drug is left in the sampling tube, the error of the sampling result of the crude drug in the next time occurs, the conical cover is used for taking down the conical cover after the sampling operation of the crude drug in the high-viscosity liquid, and the inside of the sampling tube and the conical cover are deeply cleaned, so that the sealed sampling tube is more thoroughly cleaned conveniently.
Drawings
FIG. 1 is a schematic perspective view of the structure of the present utility model;
FIG. 2 is a schematic perspective view of the internal structure of the present utility model;
FIG. 3 is a schematic cross-sectional view of the structure of the present utility model.
Wherein: 1. a base; 2. a lifting frame; 3. a control shaft; 4. a gear; 5. a lifting table; 6. a support frame; 7. a sampling tube; 8. an extraction rod; 9. extracting the fixing piece; 10. a rubber block; 11. a control knob; 12. a conical cover; 13. a storage groove; 14. and (5) fixing bolts.
Detailed Description
The following description of the embodiments of the present utility model will be made clearly and completely with reference to the accompanying drawings, in which it is apparent that the embodiments described are only some embodiments of the present utility model, but not all embodiments. All other embodiments, which can be made by those skilled in the art based on the embodiments of the utility model without making any inventive effort, are intended to be within the scope of the utility model.
Referring to fig. 1-3, a sampler for high viscosity liquid bulk drug comprises a base 1, wherein a lifting frame 2 is fixedly connected to the top surface of the base 1, a control shaft 3 is rotatably connected to the inner wall of the upper end position of the lifting frame 2, a gear 4 is fixedly connected to the outer wall of the control shaft 3, a lifting table 5 is slidably connected to the inner wall of the lifting frame 2, a supporting frame 6 is fixedly connected to the top of the lifting table 5, a sampling tube 7 is movably connected to the inner wall of the supporting frame 6, an extraction rod 8 is slidably connected to the inner wall of the sampling tube 7, an extraction fixing piece 9 is fixedly connected to the top of the extraction rod 8, and a rubber block 10 is fixedly connected to the bottom of the extraction rod 8.
Specifically, the gear 4 is engaged with the outer wall of one side of the elevating platform 5. The advantage is, elevating platform 5 accessible gear 4's meshing elevating movement in crane 2 to can make the sampling tube 7 of support frame 6 internal fixation take a sample the bulk drug, need not handheld sampling tube 7 sample, make the device need not great strength pulling, avoid the in-process hand shake can lead to taking a sample to appear the deviation.
Specifically, the outer wall of one end of the control shaft 3 is fixedly connected with a control button 11. The advantage is, the control rotation to control the axle 3 is carried out to the accessible twist control button 11, controls the axle 3 and drives gear 4 and rotate together, drives the elevating platform 5 that meshes with gear 4 through the rotation of gear 4 and carries out elevating movement to simple easy operation, and equipment cost is low.
Specifically, the bottom of the sampling tube 7 is sleeved with a conical cover 12. The sampling tube 7 through the bulk drug sampling work can adhere to remaining bulk drug, and the bulk drug of high viscosity liquid is more difficult to clean, if not thoroughly clean sampling tube 7 completely, can make the bulk drug remain in sampling tube 7, makes the next bulk drug sampling result that goes on error appear, and the effect of cone cover 12 is after carrying out the bulk drug sampling work of high viscosity liquid, alright take off cone cover 12, carries out the deep cleaning to sampling tube 7 inside and cone cover 12 to the convenience makes the more thorough cleanness of sealed sampling tube 7.
Specifically, the top surface of the base 1 is provided with a storage groove 13. The advantage is, place the bulk drug of cup dress on putting thing groove 13, alright make cup dress bulk drug and put thing groove 13 joint to make the bulk drug of cup dress be difficult for appearing rocking in the work of sample, thereby influence the bulk drug and get the work, and avoided leading to the bulk drug to spill over because of the rocking of bulk drug.
Specifically, the outer wall of one end of the support frame 6 far away from the lifting platform 5 is provided with a round hole, and the position of the support frame 6 positioned in the round hole is in threaded connection with a fixing bolt 14. The advantage is, the effect of fixed sampling tube 7 has been played to the dead bolt 14 here for sampling tube 7 is placed in support frame 6 fixedly, and at the during operation of sample, and sampling tube 7 is difficult for appearing rocking, thereby influences the collection to the bulk drug and has avoided the hand shake in the sampling process can lead to the sample to appear the deviation.
When the device is used, the bulk drug in the cup is placed on the storage tank 13, so that the bulk drug in the cup is clamped with the storage tank 13, the lifting movement of the lifting table 5 is controlled by the control button 11, the conical cover 12 at the bottom of the sampling tube 7 is placed into the bulk drug, the fixing piece 9 is manually drawn, the drawing rod 8 is pulled, the bulk drug is drawn into the sampling tube 7, and after the bulk drug sampling work is carried out, the conical cover 12 can be taken down to carry out deep cleaning on the inside of the sampling tube 7 and the conical cover 12.
Although embodiments of the present utility model have been shown and described, it will be understood by those skilled in the art that various changes, modifications, substitutions and alterations can be made therein without departing from the principles and spirit of the utility model, the scope of which is defined in the appended claims and their equivalents.
Claims (6)
1. A sampler for high viscosity liquid bulk drug, includes base (1), its characterized in that: the surface of the top of the base (1) is fixedly connected with a lifting frame (2), the inner wall of the upper end position of the lifting frame (2) is rotationally connected with a control shaft (3), the outer wall of the control shaft (3) is fixedly connected with a gear (4), the inner wall of the lifting frame (2) is slidingly connected with a lifting table (5), the lifting platform is characterized in that a supporting frame (6) is fixedly connected to the top of the lifting platform (5), a sampling tube (7) is movably connected to the inner wall of the supporting frame (6), an extraction rod (8) is slidably connected to the inner wall of the sampling tube (7), an extraction fixing piece (9) is fixedly connected to the top of the extraction rod (8), and a rubber block (10) is fixedly connected to the bottom of the extraction rod (8).
2. A sampler for a high viscosity liquid drug substance as in claim 1 wherein: the gear (4) is meshed with the outer wall of one side of the lifting table (5).
3. A sampler for a high viscosity liquid drug substance as in claim 1 wherein: the outer wall of one end of the control shaft (3) is fixedly connected with a control button (11).
4. A sampler for a high viscosity liquid drug substance as in claim 1 wherein: the bottom of the sampling tube (7) is sleeved with a conical cover (12).
5. A sampler for a high viscosity liquid drug substance as in claim 1 wherein: the top surface of the base (1) is provided with a storage groove (13).
6. A sampler for a high viscosity liquid drug substance as in claim 1 wherein: the outer wall of one end of the supporting frame (6) far away from the lifting table (5) is provided with a round hole, and the position of the supporting frame (6) located in the round hole is in threaded connection with a fixing bolt (14).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202322245940.4U CN220751696U (en) | 2023-08-19 | 2023-08-19 | Sampler for high-viscosity liquid bulk drug |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202322245940.4U CN220751696U (en) | 2023-08-19 | 2023-08-19 | Sampler for high-viscosity liquid bulk drug |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN220751696U true CN220751696U (en) | 2024-04-09 |
Family
ID=90564000
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202322245940.4U Active CN220751696U (en) | 2023-08-19 | 2023-08-19 | Sampler for high-viscosity liquid bulk drug |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN220751696U (en) |
-
2023
- 2023-08-19 CN CN202322245940.4U patent/CN220751696U/en active Active
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| GR01 | Patent grant | ||
| GR01 | Patent grant |