CN220040157U - Transdermal cream granularity analyzer - Google Patents
Transdermal cream granularity analyzer Download PDFInfo
- Publication number
- CN220040157U CN220040157U CN202321517339.XU CN202321517339U CN220040157U CN 220040157 U CN220040157 U CN 220040157U CN 202321517339 U CN202321517339 U CN 202321517339U CN 220040157 U CN220040157 U CN 220040157U
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- China
- Prior art keywords
- granularity
- particle size
- dispersing
- dispersing device
- transdermal cream
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- 239000006071 cream Substances 0.000 title claims abstract description 36
- 239000002245 particle Substances 0.000 claims abstract description 138
- 239000011521 glass Substances 0.000 claims abstract description 19
- 230000006835 compression Effects 0.000 claims abstract description 18
- 238000007906 compression Methods 0.000 claims abstract description 18
- 239000006185 dispersion Substances 0.000 claims description 30
- 238000002347 injection Methods 0.000 claims description 14
- 239000007924 injection Substances 0.000 claims description 14
- 238000009434 installation Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 4
- 239000000843 powder Substances 0.000 description 3
- 230000009286 beneficial effect Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000012567 medical material Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
Abstract
The utility model discloses a transdermal cream granularity analyzer, which comprises an operation table, wherein a pair of supporting blocks are arranged on the operation table, a first sliding rail is arranged in each of the pair of supporting blocks, a first sliding block is connected in a sliding manner in the first sliding rail, a compression spring is arranged in the first sliding rail, one end of the compression spring is fixedly connected to the upper side wall of the first sliding block, a granularity dispersing device is fixedly connected to one side wall of the first sliding block far away from the supporting blocks, the lower end of the granularity dispersing device is provided with a granularity dispersing plate, and a plurality of dispersing holes are uniformly formed in the granularity dispersing plate. According to the utility model, the transdermal cream particles are placed into the particle size dispersing device, the particle size dispersing device is pulled upwards, the particle size dispersing device moves downwards under the action of the compression spring after being loosened, and the transdermal cream falls on the glass slide through the dispersing holes on the particle size dispersing plate under the action of inertia, so that the particles are uniformly distributed on the glass slide, and the particle size is conveniently detected.
Description
Technical Field
The utility model belongs to the technical field of particle size analyzers, and particularly relates to a transdermal cream particle size analyzer.
Background
Particle size is a main performance index of various materials, and particle size detection has become an important basic work for the production, application and research of medical materials. The existing dynamics analyzer is convenient for analyzing the common granularity, but is difficult to process the semisolid granularity, and the transdermal cream belongs to the semisolid granularity, so the analysis processing of the granularity is more difficult.
When the existing transdermal cream granularity analyzer is used, a small amount of transdermal cream is taken by a conventional medicine spoon to be directly flicked onto a microscope slide, but most of the transdermal cream is gathered together by powder, only a small amount of powder particles are monodisperse, so that the transdermal cream granularity analyzer is convenient for dispersing the powder, and can be dispersed in a manual mode, the workload of workers is increased by manual dispersion, and the particle dispersing effect is poor.
Accordingly, in view of the above-described technical problems, it is necessary to provide a transdermal cream particle size analyzer.
Disclosure of Invention
The utility model aims to provide a transdermal cream granularity analyzer for solving the problems.
In order to achieve the above object, an embodiment of the present utility model provides the following technical solution:
the utility model provides a transdermal cream granularity analyzer, includes the operation panel, be provided with a pair of supporting shoe on the operation panel, a pair of first slide rail has all been seted up in the supporting shoe, sliding connection has first slider in the first slide rail, install compression spring in the first slide rail, compression spring's one end fixedly connected with granularity dispersion devices on the upper side wall of first slider, fixedly connected with granularity dispersion devices on a lateral wall that the supporting shoe was kept away from to first slider, granularity dispersion devices's lower extreme is provided with the granularity dispersion board, a plurality of dispersion holes have evenly been seted up on the granularity dispersion board, be provided with the slide glass on the operation panel, the slide glass sets up the below at the granularity dispersion board.
Further, a pair of mounting blocks are arranged on two side walls of the lower end of the particle size dispersing device, and second sliding rails are arranged in the pair of mounting blocks.
Further, second sliding blocks are fixedly connected to the two side walls of the granularity dispersing plate, and the second sliding blocks are slidably connected in the second sliding rail.
Further, a plurality of air nozzles are arranged on the particle size dispersing device, and outlets of the air nozzles are arranged in the particle size dispersing device.
Further, the particle size dispersing device is provided with a sample injection hole, and the sample injection hole is connected with a sample injection cover in a threaded manner.
Further, the first handles are fixedly connected to the front side wall and the rear side wall of the particle size dispersing device, and the second handles are fixedly connected to one side wall of the particle size dispersing plate, which is arranged outside the particle size dispersing device.
Further, supporting legs are fixedly connected to the front side wall and the rear side wall of the supporting block, and one end, far away from the supporting block, of each supporting leg is fixedly connected to the operating platform.
Compared with the prior art, the utility model has the following advantages:
according to the utility model, the transdermal cream particles are placed into the particle size dispersing device, the particle size dispersing device is pulled upwards, the particle size dispersing device is released to move downwards rapidly under the action of the compression spring, and under the action of inertia, the transdermal cream falls on the glass slide through the dispersing holes on the particle size dispersing plate, so that the particles are uniformly distributed on the glass slide, and the particle size is conveniently detected.
Drawings
In order to more clearly illustrate the embodiments of the present utility model or the technical solutions in the prior art, the drawings that are required to be used in the embodiments or the description of the prior art will be briefly described below, and it is obvious that the drawings in the following description are only some embodiments described in the present utility model, and other drawings may be obtained according to the drawings without inventive effort to those skilled in the art.
FIG. 1 is a front view of a transdermal cream size analyzer according to an embodiment of the present utility model;
FIG. 2 is a perspective view of a transdermal cream size analyzer according to an embodiment of the present utility model;
FIG. 3 is a state diagram of a transdermal cream size analyzer according to an embodiment of the present utility model;
FIG. 4 is a schematic view of an embodiment of the installation of a particle size distribution plate;
FIG. 5 is a cross-sectional view of a transdermal cream size analyzer according to an embodiment of the present utility model.
In the figure: 1. the device comprises an operating platform, a supporting block, a first sliding rail, a first sliding block, a particle size dispersing device, a particle size dispersing plate, dispersing holes, a second sliding block, a mounting block and a second sliding block, wherein the operating platform, the supporting block, the first sliding rail, the first sliding block, the particle size dispersing device, the particle size dispersing plate, the dispersing holes, the second sliding block, the mounting block and the mounting block are arranged in sequence, and the operating platform, the supporting block, the first sliding rail, the first sliding block, the 5, the particle size dispersing device, the particle size dispersing plate the device comprises a first sliding rail, a second sliding rail, a compression spring, a gas nozzle, a sample inlet hole, a sample inlet cover, a first handle, a second handle, a glass slide and supporting legs.
Detailed Description
The present utility model will be described in detail below with reference to the embodiments shown in the drawings. The embodiments are not intended to limit the utility model, but structural, methodological or functional modifications from the embodiments are within the scope of the utility model.
The utility model discloses a transdermal cream particle size analyzer, which is shown in figures 1-5, and comprises an operation table 1, wherein transdermal cream belongs to semisolid particles, the particle size analyzer is difficult to analyze the particle size of the semisolid particles, and in order to facilitate the analysis of the particles on a glass slide by a microscope, the particles can be uniformly distributed, and the particles are prevented from being accumulated together, so that the particle size analyzer convenient for dispersing the particles is provided. The stage 1 is a stage for dispersing particles.
Referring to fig. 2 and 5, a pair of support blocks 2 are disposed on the console 1, a first sliding rail 3 is disposed in each of the pair of support blocks 2, a first sliding block 4 is slidably connected in the first sliding rail 3, a compression spring 11 is mounted in the first sliding rail 3, and one end of the compression spring 11 is fixedly connected to an upper side wall of the first sliding block 4. Because the first slider 4 is slidably connected in the first sliding rail 3, the first slider 4 can slide in the first sliding rail 3, and the shape of the section of the first slider 4 slidably connected in the first sliding rail 3 is the same as the shape of the first sliding rail 3, so that the first slider 4 is stable when sliding in the first sliding rail 3. By installing the compression spring 11 in the first slide rail 3, when the first slider 4 slides upward in the first slide rail 3, the compression spring 11 is compressed so that the compression spring 11 has a downward elastic force on the first slider 4.
Referring to fig. 3 and 5, a particle size dispersing device 5 is fixedly connected to a side wall of the first slider 4 far away from the supporting block 2, a particle size dispersing plate 6 is arranged at the lower end of the particle size dispersing device 5, a plurality of dispersing holes 7 are uniformly formed in the particle size dispersing plate 6, a glass slide 17 is arranged on the operating platform 1, and the glass slide 17 is arranged below the particle size dispersing plate 6. Since the first sliding block 4 can slide in the first sliding rail 3, the particle size dispersing device 5 is fixedly connected to the first sliding block 4, and therefore the first sliding block 4 and the particle size dispersing device 5 can drive each other to slide. The particle size dispersing device 5 is a device for dispersing particles, in order to achieve the dispersion of the particles by the particle size dispersing device 5, a particle size dispersing plate 6 is arranged at the lower end of the particle size dispersing device 5, dispersing holes 7 are formed in the particle size dispersing plate 6, the diameter of the dispersing holes 7 is matched with the particle size, and the diameter of the dispersing holes 7 is slightly larger than the particle size of the particles, so that the particles can pass through the dispersing holes 7.
Further, as shown in fig. 5, the particles of the transdermal cream to be dispersed are placed in the particle size dispersing device 5, the particle size dispersing device 5 drives the first slider 4 to slide upwards, the first slider 4 can compress the compression spring 11 when sliding upwards, after the particle size dispersing device 5 is lifted, the particle size dispersing device 5 and the first slider 4 can rapidly move downwards under the action of the compression spring 11 by loosening the particle size dispersing device 5, when the first slider 4 contacts with the lower end of the supporting block 2, the particle size dispersing device 5 can be subjected to larger inertia force, so that the particles on the particle size dispersing plate 6 pass through the dispersing holes 7 under the action of the inertia force, and the particles passing through the dispersing holes 7 can fall on the glass slide 17, so that the particles are uniformly distributed on the glass slide 17.
Referring to fig. 1 to 3, the particle size dispersing device 5 is provided with a plurality of air nozzles 12, and the outlets of the air nozzles 12 are all arranged in the particle size dispersing device 5. By installing the air nozzles 12 on the particle size dispersing device 5, the air nozzles 12 are used for being connected with compressed air, the compressed air can be supplied into the particle size dispersing device 5 through the air nozzles 12, so that the particles in the particle size dispersing device 5 can be purged through the compressed air, and the particles on the particle size dispersing plate 6 can fall on the glass slide 17 through the dispersing holes 7 under the action of the compressed air.
Referring to fig. 3 and 4, a pair of mounting blocks 9 are provided on two sidewalls of the lower end of the particle size dispersing device 5, a second slide rail 10 is provided in each of the pair of mounting blocks 9, and a second slide block 8 is fixedly connected to two sidewalls of the particle size dispersing plate 6, and the second slide block 8 is slidably connected in the second slide rail 10. In order to be convenient for install particle size dispersion board 6, through be provided with installation piece 9 at the lateral wall lower extreme of particle size dispersion device 5 to set up second slide rail 10 in installation piece 9, fixedly connected with second slider 8 on the both sides wall of particle size dispersion board 6, with second slider 8 sliding connection in second slide rail 10, so that accomplish the installation to particle size dispersion board 6, make the installation of particle size dispersion board 6 convenient.
Preferably, in order to facilitate the dispersion of particles having different particle sizes, different particle size dispersing plates 6 are provided, and the size of the diameter of the dispersion holes 7 formed in the different particle size dispersing plates 6 is different, and the diameter of the dispersion holes 7 is selected to be close to the particle size according to the size of the particles in accordance with the particle size range corresponding to the size of the diameter of the dispersion holes 7. When the particle size is out of the screening range of the dispersion holes 7, the particle size dispersing plate 6 needs to be replaced, and the particle size dispersing plate 6 is convenient to replace because the particle size dispersing plate 6 is installed in a sliding connection mode. When the particle size diameter is larger than the dispersion holes 7, particles cannot pass through the dispersion holes 7, and when the particle size diameter is far smaller than the dispersion holes 7, the number of particles passing through the dispersion holes 7 is too large, so that the particles are accumulated, and the dispersion is not facilitated.
Referring to fig. 1-3, the particle size dispersing device 5 is provided with a sample injection hole 13, and the sample injection hole 13 is in threaded connection with a sample injection cover 14. The sample injection hole 13 is used for adding transdermal cream particles into the particle size dispersing device 5, the sample injection cover 14 is used for closing the sample injection hole 13, and when the particles are added into the particle size dispersing device 5, the sample injection hole 13 is closed through the sample injection cover 14.
Referring to fig. 3, a first handle 15 is fixedly connected to both front and rear side walls of the particle size dispersing device 5, and a second handle 16 is fixedly connected to a side wall of the particle size dispersing plate 6 disposed outside the particle size dispersing device 5. First handles 15 are fixedly connected to the front and rear side walls of the particle size dispersing device 5, and the particle size dispersing device 5 is conveniently lifted up by the first handles 15 when the particles in the particle size dispersing device 5 are dispersed, so that the particle size dispersing device 5 falls down with enough inertia force. The second handle 16 is fixedly connected to one end of the particle size dispersing plate 6, which is arranged outside the particle size dispersing device 5, and the particle size dispersing plate 6 is convenient to assemble and disassemble through the second handle 16.
Referring to fig. 1-4, support legs 18 are fixedly connected to the front and rear side walls of the support block 2, and one end, away from the support block 2, of each support leg 18 is fixedly connected to the operation table 1. Since the support block 2 should be stable after being mounted so as to ensure stability when the particle size dispersing device 5 slides, the support block 2 is supported by the support legs 18, and stability of the support block 2 when in use is ensured.
When the device is used, firstly, the matched granularity dispersing plate 6 is selected according to the possible range of the granularity of the transdermal cream particles to be measured, so that the granularity dispersing plate 6 is arranged in the second sliding rail 10, then the transdermal cream particles are added into the granularity dispersing device 5, the particles are spread on the granularity dispersing plate 6 under the action of the air nozzle 12, then the granularity dispersing device 5 is driven to ascend by pulling the first handle 15 upwards, then the first handle 15 is loosened, the granularity dispersing device 5 moves downwards rapidly under the action of the compression spring 11, and when the granularity dispersing device 5 moves to the bottom, the particles on the granularity dispersing plate 6 fall on the surface of the glass slide 17 through the dispersing holes 7 under the action of inertia force, so that the particles are uniformly dispersed on the glass slide 17, and the granularity of the transdermal cream is conveniently analyzed by a microscope.
The technical scheme shows that the utility model has the following beneficial effects:
according to the utility model, the transdermal cream particles are placed into the particle size dispersing device, the particle size dispersing device is pulled upwards, the particle size dispersing device is released to move downwards rapidly under the action of the compression spring, and under the action of inertia, the transdermal cream falls on the glass slide through the dispersing holes on the particle size dispersing plate, so that the particles are uniformly distributed on the glass slide, and the particle size is conveniently detected.
It will be evident to those skilled in the art that the utility model is not limited to the details of the foregoing illustrative embodiments, and that the present utility model may be embodied in other specific forms without departing from the spirit or essential characteristics thereof. The present embodiments are, therefore, to be considered in all respects as illustrative and not restrictive, the scope of the utility model being indicated by the appended claims rather than by the foregoing description, and all changes which come within the meaning and range of equivalency of the claims are therefore intended to be embraced therein. Any reference sign in a claim should not be construed as limiting the claim concerned.
Furthermore, it should be understood that although the present disclosure describes embodiments, not every embodiment contains only one independent technical solution, and that such description is provided for clarity only, and that the technical solutions of the embodiments may be appropriately combined to form other embodiments that will be understood by those skilled in the art.
Claims (7)
1. The utility model provides a transdermal cream granularity analyzer, includes operation panel (1), its characterized in that, be provided with a pair of supporting shoe (2) on operation panel (1), a pair of first slide rail (3) have all been seted up in supporting shoe (2), sliding connection has first slider (4) in first slide rail (3), install compression spring (11) in first slide rail (3), the one end fixedly connected with of compression spring (11) is on the last lateral wall of first slider (4), fixedly connected with granularity dispersion devices (5) on one lateral wall that supporting shoe (2) were kept away from to first slider (4), the lower extreme of granularity dispersion devices (5) is provided with granularity dispersion board (6), a plurality of dispersion holes (7) have evenly been seted up on granularity dispersion board (6), be provided with slide glass (17) on operation panel (1), slide glass (17) set up in the below of granularity dispersion board (6).
2. The transdermal cream granularity analyzer according to claim 1, wherein a pair of mounting blocks (9) are provided on both side walls of the lower end of the granularity dispersing device (5), and a second slide rail (10) is provided in each of the pair of mounting blocks (9).
3. The transdermal cream granularity analyzer according to claim 2, wherein the two side walls of the granularity dispersing plate (6) are fixedly connected with second sliding blocks (8), and the second sliding blocks (8) are slidably connected in second sliding rails (10).
4. A transdermal cream particle size analyzer according to claim 1, characterized in that the particle size dispersing device (5) is provided with a plurality of air nozzles (12), and the outlets of the air nozzles (12) are all arranged in the particle size dispersing device (5).
5. The transdermal cream granularity analyzer according to claim 4, wherein the granularity dispersing device (5) is provided with a sample injection hole (13), and the sample injection hole (13) is connected with a sample injection cover (14) in a threaded manner.
6. The transdermal cream granularity analyzer according to claim 5, wherein the front and rear side walls of the granularity dispersing device (5) are fixedly connected with first handles (15), and the granularity dispersing plate (6) is arranged on one side wall outside the granularity dispersing device (5) and is fixedly connected with second handles (16).
7. The transdermal cream granularity analyzer according to claim 1, wherein the front and rear side walls of the support block (2) are fixedly connected with support legs (18), and one end of the support legs (18) far away from the support block (2) is fixedly connected to the operation table (1).
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202321517339.XU CN220040157U (en) | 2023-06-14 | 2023-06-14 | Transdermal cream granularity analyzer |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN202321517339.XU CN220040157U (en) | 2023-06-14 | 2023-06-14 | Transdermal cream granularity analyzer |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN220040157U true CN220040157U (en) | 2023-11-17 |
Family
ID=88732482
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN202321517339.XU Active CN220040157U (en) | 2023-06-14 | 2023-06-14 | Transdermal cream granularity analyzer |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN220040157U (en) |
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2023
- 2023-06-14 CN CN202321517339.XU patent/CN220040157U/en active Active
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