Drug mixing device for biomedical research
By designing quantitative mechanisms and mixing mechanisms in the drug mixing device for biomedical research, the problems of inaccurate addition of medicines and unstable mixing ratios in the prior art are solved, and the precise control and uniform mixing of drugs are achieved, and the accuracy of biomedical research is improved.
Patent Information
- Application Number
- CN202422170737.X
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-09-05
- Publication Date
- 2025-06-10
- Estimated Expiration
- 2034-09-05
AI Technical Summary
Due to the inaccurate measurement method of existing drug mixing devices, it is difficult to achieve accurate control of drug addition, resulting in unstable mixing ratios and affecting the accuracy of biomedical research.
A drug mixing device for biomedical research is designed, including a quantitative mechanism and a mixing mechanism. The quantification mechanism realizes accurate measurement and addition of drugs through a combination of measuring cylinder, conical groove, observation port and scale mark; the mixing mechanism ensures full mixing and uniformity of drugs through a servo motor, agitating shaft and a crushing column.
Through precise measurement of the quantitative mechanism and sufficient stirring of the mixing mechanism, the precise control and uniform mixing of the drugs are achieved, and the accuracy of biomedical research is improved.
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Figure CN222956332U_ABST
Abstract
Description
Technical Field
[0001] The utility model relates to the technical field of biomedical research equipment, in particular to a medicine mixing device for biomedical research. Background Art
[0002] In the field of biomedical research, the research process is complex and delicate. Among many key links, it is necessary to mix a variety of drugs with different characteristics and effects extremely carefully and precisely. This is not just a simple physical fusion, but a crucial step related to the successful preparation of experimental samples. By reasonably mixing a variety of drugs, a complex physiological environment inside the human body can be simulated, providing an important experimental basis for studying the action mechanism and metabolic process of drugs in the body. At the same time, in the critical stage of drug research and development, the mixing of a variety of drugs plays a crucial role. Researchers need to mix different active ingredients, excipients and other drugs in a certain proportion and order according to specific research and development goals and theoretical bases to explore drug formulations with the best efficacy and safety. Therefore, there is a particular need for a medicine mixing device for biomedical research.
[0003] However, for existing medicine mixing devices, during use, due to inaccurate metering methods, it is difficult to achieve precise control of drug addition, resulting in unstable mixing ratios and thus affecting the accuracy of biomedical research. Content of the Utility Model
[0004] The purpose of the utility model is to provide a medicine mixing device for biomedical research to solve the problem that in the existing medicine mixing device, during use, due to inaccurate metering methods, it is difficult to achieve precise control of drug addition, resulting in unstable mixing ratios and thus affecting the accuracy of biomedical research as mentioned in the above background art.
[0005] To achieve the above purpose, the utility model provides the following technical solution: A medicine mixing device for biomedical research, including a bottom plate, a non-slip pad is fixedly connected to the lower surface of the bottom plate, a column is fixedly connected to the upper surface of the bottom plate, a panel is fixedly connected to the upper surface of the column, a metering mechanism is arranged on the upper surface of the panel, and a mixing mechanism is arranged on one side surface of the column;
[0006] The metering mechanism includes a connecting block, a hose, a clamping block, a discharge head, a sliding groove, a sliding block, a pulling block, a measuring cylinder, a conical groove, an observation port and scale lines. A connecting block is fixedly connected to the upper surface of the panel. A hose is fixedly connected to the lower surface of the connecting block. A clamping block is fixedly connected to the outer surface of the hose. One end of the hose is fixedly connected to a discharge head. A sliding groove is formed in the upper surface of the connecting block. A sliding block is slidably connected to the inner surface of the sliding groove. A pulling block is fixedly connected to one side surface of the sliding block. A measuring cylinder is fixedly connected to the upper surface of the connecting block. A conical groove is formed in the inner surface of the measuring cylinder. An observation port is fixedly connected to the outer surface of the measuring cylinder. Scale lines are fixedly connected to the outer surface of the measuring cylinder.
[0007] Preferably, multiple groups of anti-slip pads are arranged on the lower surface of the bottom plate, and the columns are symmetrically arranged with respect to the central axis of the panel.
[0008] Preferably, the connecting blocks are symmetrically arranged with respect to the central axis of the panel, and the inner size of the sliding groove matches the outer size of the sliding block.
[0009] The mixing mechanism preferably includes a servo motor, a rotating shaft, a mixing tank, a top plate, a feed inlet, a sealing cover, a driving motor, a stirring shaft, stirring blades, crushing columns and a discharge port. A servo motor is fixedly connected to one side surface of the column. A rotating shaft is fixedly connected to one side surface of the servo motor. One end of the rotating shaft is fixedly connected to a mixing tank. A top plate is fixedly connected to the upper surface of the mixing tank. A feed inlet is fixedly connected to the upper surface of the top plate. A sealing cover is rotatably connected to the upper surface of the feed inlet. A driving motor is fixedly connected to the upper surface of the top plate. A stirring shaft is fixedly connected to the lower surface of the driving motor. Stirring blades are fixedly connected to the outer surface of the stirring shaft. Crushing columns are fixedly connected to the outer surface of the stirring shaft. A discharge port is fixedly connected to the lower surface of the mixing tank.
[0010] Preferably, the rotating shafts are symmetrically arranged with respect to the central axis of the top plate, and the outer size of the clamping block matches the inner size of the feed inlet.
[0011] Preferably, the feed inlets are symmetrically arranged with respect to the central axis of the top plate, and the feed inlet and the sealing cover form a sealed structure.
[0012] Preferably, multiple groups of stirring blades are evenly distributed on the outer surface of the stirring shaft at equal intervals, and multiple groups of crushing columns are evenly distributed on the outer surface of the stirring shaft at equal intervals.
[0013] Compared with the prior art, the beneficial effects of the present utility model are as follows: For this pharmaceutical mixing device for biomedical research, through the setting of the quantitative mechanism, during use, first insert the clamping block into the feed port to fix the flexible hose and the discharge head, and then pour the medicine into the conical groove in the measuring cylinder. This shape design is conducive to concentrating the medicine at the bottom for more accurate measurement. The liquid level of the medicine inside the measuring cylinder can be directly observed through the observation port, and the scale lines clearly mark the volume of the medicine. Thus, according to the requirements of experiments or mixing, the addition amount of the medicine can be precisely controlled. Then, pull the pulling block to drive the sliding block to slide inside the sliding groove, so that the sliding block no longer blocks the injection port. The medicine will pass through the connecting block and the flexible hose in sequence and finally be discharged from the discharge head and enter the mixing tank, realizing quantitative operation and improving the accuracy of biomedical research. BRIEF DESCRIPTION OF THE DRAWINGS
[0014] Figure 1 It is a schematic side view of the external structure of the present utility model;
[0015] Figure 2 It is a schematic diagram of the structure of the connecting block and the sliding groove of the present utility model in mutual cooperation;
[0016] Figure 3 It is a schematic diagram of the structure of the feed port and the sealing cover of the present utility model in mutual cooperation;
[0017] Figure 4 It is a schematic diagram of the structure of the stirring shaft and the stirring blades of the present utility model in mutual cooperation.
[0018] In the figure: 1, bottom plate; 2, anti-slip pad; 3, column; 4, panel; 5, quantitative mechanism; 501,
[0019] connecting block; 502, flexible hose; 503, clamping block; 504, discharge head; 505, sliding groove; 506, sliding block; 507, pulling block; 508, measuring cylinder; 509, conical groove; 510, observation port; 511, scale line; 6, mixing mechanism; 601, servo motor; 602, rotating shaft; 603, mixing tank; 604, top plate; 605, feed port; 606, sealing cover; 607, drive motor; 608, stirring shaft; 609, stirring blades; 610, crushing column; 611, discharge port. DETAILED DESCRIPTION OF THE EMBODIMENTS
[0020] The technical solutions in the embodiments of the present utility model will be clearly and completely described below with reference to the accompanying drawings in the embodiments of the present utility model. Obviously, the described embodiments are only a part of the embodiments of the present utility model, rather than all the embodiments. Based on the embodiments of the present utility model, all other embodiments obtained by those of ordinary skill in the art without creative efforts shall fall within the protection scope of the present utility model.
[0021] Please refer to Figures 1-4 , the present utility model provides a technical solution: a medicine mixing device for biomedical research, including a bottom plate 1, a non-slip pad 2 is fixedly connected to the lower surface of the bottom plate 1, and on the upper
[0022] surface of the bottom plate 1, a column 3 is fixedly connected, on the upper surface of the column 3, a panel 4 is fixedly connected, a quantitative mechanism 5 is arranged on the upper surface of the panel 4, and a mixing mechanism 6 is arranged on one side surface of the column 3; the quantitative mechanism 5 includes a connecting block 501, a hose 502, a clamping block 503, a discharge head 504, a sliding groove 505, a sliding block 506, a pulling block 507, a measuring cylinder 508, a conical groove 509, an observation port 510 and scale lines 511. A connecting block 501 is fixedly connected to the upper surface of the panel 4, a hose 502 is fixedly connected to the lower surface of the connecting block 501, a clamping block 503 is fixedly connected to the outer surface of the hose 502, one end of the hose 502 is fixedly connected to a discharge head 504, a sliding groove 505 is opened on the upper surface of the connecting block 501, a sliding block 506 is slidably connected to the inner surface of the sliding groove 505, a pulling block 507 is fixedly connected to one side surface of the sliding block 506, a measuring cylinder 508 is fixedly connected to the upper surface of the connecting block 501, a conical groove 509 is opened on the inner surface of the measuring cylinder 508, an observation port 510 is fixedly connected to the outer surface of the measuring cylinder 508, and scale lines 511 are fixedly connected to the outer surface of the measuring cylinder 508. Through the settings of the connecting block 501, the hose 502, the clamping block 503, the discharge head 504, the sliding groove 505, the sliding block 506, the pulling block 507, the measuring cylinder 508, the conical groove 509, the observation port 510 and the scale lines 511, when in use, first clamp the clamping block 503 into the feed inlet 605 to fix the hose 502 and the discharge head 504, then pour the medicine into the conical groove 509 in the measuring cylinder 508. This shape design is beneficial for the medicine to be concentrated at the bottom for more accurate measurement. The liquid level of the medicine inside the measuring cylinder 508 can be directly observed through the observation port 510, and the scale lines 511 clearly mark the volume of the medicine, so that the addition amount of the medicine can be accurately controlled according to the needs of the experiment or mixing. Then pull the pulling block 507 to drive the sliding block 506 to slide inside the sliding groove 505, so that the sliding block 506 no longer blocks the injection port. The medicine will pass through the connecting block 501 and the hose 502 in sequence and finally be discharged from the discharge head 504 and enter the mixing tank 603, realizing quantitative operation and improving the accuracy of biomedical research.
[0023] Furthermore, multiple groups of non-slip pads 2 are arranged on the lower surface of the bottom plate 1, and the columns 3 are symmetrically arranged with respect to the central axis of the panel 4. Through the setting of the non-slip pads 2, when in use, the non-slip pads 2 can increase the friction between the bottom plate 1 and the tabletop, ensuring the safety and accuracy of the operation.
[0024] Furthermore, the connecting block 501 is symmetrically arranged with respect to the central axis of the panel 4. The inner dimension of the sliding groove 505 matches the outer dimension of the sliding block 506. Through the arrangement of the sliding groove 505 and the sliding block 506, during use, the sliding block 506 slides inside the sliding groove 505, and the sliding groove 505 limits the sliding block 506, making the sliding of the sliding block 506 more stable.
[0025] Furthermore, the mixing mechanism 6 includes a servo motor 601, a rotating shaft 602, a mixing tank 603, a top plate 604, a feed inlet 605, a sealing cover 606, a driving motor 607, a stirring shaft 608, stirring blades 609, crushing columns 610, and a discharge port 611. One side surface of the column 3 is fixedly connected to a servo motor 601, one side surface of the servo motor 601 is fixedly connected to a rotating shaft 602, one end of the rotating shaft 602 is fixedly connected to a mixing tank 603, the upper surface of the mixing tank 603 is fixedly connected to a top plate 604, the upper surface of the top plate 604 is fixedly connected to a feed inlet 605, the upper surface of the feed inlet 605 is rotatably connected to a sealing cover 606, the upper surface of the top plate 604 is fixedly connected to a driving motor 607, the lower surface of the driving motor 607 is fixedly connected to a stirring shaft 608, the outer surface of the stirring shaft 608 is fixedly connected to stirring blades 609, the outer surface of the stirring shaft 608 is fixedly connected to crushing columns 610, and the lower surface of the mixing tank 603 is fixedly connected to a discharge port 611. Through the servo motor 601, the rotating shaft 602, the mixing tank 603, the top plate 604, the feed inlet 605, the sealing cover 606, the driving motor 607, the stirring shaft 608, the stirring blades 609, the crushing columns 610, and the discharge port
[0026] For the setting of 611, during use, open the sealing cover 606 above the feed inlet 605, and put the medicines to be mixed into the interior of the mixing tank 603 through the feed inlet 605. The sealing cover 606 can seal the mixing tank 603 after the feeding is completed, preventing the material from splashing out during the mixing process and the entry of external impurities. Then start the driving motor 607. The driving motor 607 starts to work and drives the stirring shaft 608 to rotate. The stirring blades 609 on the outer surface of the stirring shaft 608 perform a stirring action in the mixing tank 603 as the stirring shaft 608 rotates, so that the materials at different positions are fully mixed to ensure the uniformity of mixing. At the same time, the crushing columns 610 outside the stirring shaft 608 also rotate together with the stirring shaft 608. During the mixing process, there may be cases of caking or larger particles. The crushing columns 610 use the impact force and frictional force generated by their rotation to impact and crush these caked or large particles, making them into finer particles for better mixing with other materials evenly. When it is necessary to adjust the angle of the mixing tank 603 or perform some special mixing operations, start the servo motor 601. The servo motor 601 works and drives the rotating shaft 602 to rotate. The rotating shaft 602 then drives the mixing tank 603 fixedly connected thereto to rotate. By precisely controlling the rotation speed and rotation angle of the servo motor 601, the position and posture of the mixing tank 603 can be flexibly adjusted to meet the requirements of different mixing processes. When the mixing is completed, open the discharge port 611 on the lower surface of the mixing tank 603. The evenly mixed material flows out from the discharge port 611 under the action of its own gravity and enters the next technological process or storage container.
[0027] Furthermore, the rotating shaft 602 is symmetrically arranged with respect to the central axis of the top plate 604. The outer dimension of the clamping block 503 matches the inner dimension of the feed inlet 605. Through the settings of the clamping block 503 and the feed inlet 605, during use, the clamping block 503 is clamped into the feed inlet 605, which can fix the hose 502 and the discharge head 504 to make the feeding more stable.
[0028] Furthermore, the feed inlet 605 is symmetrically arranged with respect to the central axis of the top plate 604. The feed inlet 605 and the sealing cover 606 form a sealing structure. Through the setting of the feed inlet 605, during use, a quantitative mechanism 5 is provided on multiple groups of feed inlets 605, and different medicines can be added quantitatively.
[0029] Furthermore, multiple groups of stirring blades 609 are evenly distributed on the outer surface of the stirring shaft 608 at equal intervals, and multiple groups of crushing columns 610 are evenly distributed on the outer surface of the stirring shaft 608 at equal intervals. Through the setting of the crushing columns 610, during use, the crushing columns 610 use the impact force and frictional force generated by their rotation to impact and crush these caked or large particles, making them into finer particles for better mixing with other materials evenly.
[0030] Working principle: Open the sealing cover 606 above the feed inlet 605, insert the clamping block 503 into the feed inlet 605, fix the hose 502 and the discharge head 504, and then pour the medicine into the conical groove 509 in the measuring cylinder 508. This shape design is conducive to concentrating the medicine at the bottom for more accurate measurement. The liquid level of the medicine inside the measuring cylinder 508 can be visually observed through the observation port 510, and the scale line 511 clearly marks the volume of the medicine. Thus, the addition amount of the medicine can be precisely controlled according to the needs of the experiment or mixing. Then, pull the pulling block 507 to drive the sliding block 506 to slide inside the sliding groove 505, so that the sliding block 506 no longer blocks the filling port. The medicine will pass through the connecting block 501 and the hose 502 in sequence and finally be discharged from the discharge head 504 and enter the mixing tank 603, realizing quantitative operation and improving the accuracy of biomedical research. After the medicine is put into the mixing tank 603 through the feed inlet 605, the sealing cover 606 is closed to seal the mixing tank 603, preventing the material from splashing out during the mixing process and external impurities from entering. Then, start the driving motor 607. The driving motor 607 starts to work and drives the stirring shaft 608 to rotate. The stirring blades 609 on the outer surface of the stirring shaft 608 perform stirring actions inside the mixing tank 603 as the stirring shaft 608 rotates, making the materials at different positions fully mixed to ensure the uniformity of mixing. At the same time, the crushing columns 610 outside the stirring shaft 608 also rotate together with the stirring shaft 608. During the mixing process, there may be cases of caking or larger particles. The crushing columns 610 use the impact force and friction generated by their rotation to impact and crush these caking or large particles, making them into finer particles for better mixing with other materials. When it is necessary to adjust the angle of the mixing tank 603 or perform some special mixing operations, start the servo motor 601. The servo motor 601 works and drives the rotating shaft 602 to rotate. The rotating shaft 602 then drives the mixing tank 603 fixedly connected to it to rotate. By precisely controlling the rotation speed and rotation angle of the servo motor 601, the position and attitude of the mixing tank 603 can be flexibly adjusted to meet the requirements of different mixing processes. When the mixing is completed, open the discharge port 611 on the lower surface of the mixing tank 603. The uniformly mixed material flows out from the discharge port 611 under the action of its own gravity and enters the next process flow or storage container. Among them, the models of the servo motor 601 and the driving motor 607 are YE2-132S-4.
[0031] Although the embodiments of the present invention have been shown and described, for those of ordinary skill in the art, it can be understood that various changes, modifications, substitutions, and variations can be made to these embodiments without departing from the principle and spirit of the present invention. The scope of the present invention is defined by the appended claims and their equivalents.
Claims
1. A drug mixing device for biomedical research, comprising a bottom plate (1), characterized in that: The lower surface of the bottom plate (1) is fixedly connected to an anti-slip pad (2), the upper surface of the bottom plate (1) is fixedly connected to a column (3), the upper surface of the column (3) is fixedly connected to a panel (4), the upper surface of the panel (4) is provided with a quantitative mechanism (5), and a side surface of the column (3) is provided with a mixing mechanism (6); The quantitative mechanism (5) comprises a connecting block (501), a hose (502), a clamping block (503), A discharge head (504), a sliding groove (505), a sliding block (506), a pulling block (507), a measuring cylinder (508), a conical groove (509), an observation port (510) and a scale line (511); the upper surface of the panel (4) is fixedly connected with a connection block (501); the lower surface of the connection block (501) is fixedly connected with a hose (502); the outer surface of the hose (502) is fixedly connected with a clamping block (503); one end of the hose (502) is fixedly connected with a discharge head (504); the upper surface of the connection block (501) is provided with a sliding groove (505); the inner surface of the sliding groove (505) is slidably connected with a sliding block (506); one side surface of the sliding block (506) is fixedly connected with a pulling block (507); the connection block (501) A measuring cylinder (508) is fixedly connected to the upper surface, a conical groove (509) is provided on the inner surface of the measuring cylinder (508), an observation port (510) is fixedly connected to the outer surface of the measuring cylinder (508), and a scale line (511) is fixedly connected to the outer surface of the measuring cylinder (508).
2. A biomedical research drug mixing device according to claim 1, characterized in that: The anti-slip pads (2) are arranged in multiple groups on the lower surface of the base plate (1), and the upright posts (3) are arranged symmetrically about the central axis of the panel (4).
3. A biomedical research drug mixing device according to claim 1, characterized in that: The connecting block (501) is symmetrically arranged with respect to the central axis of the panel (4), and the inner dimension of the sliding groove (505) is consistent with the outer dimension of the sliding block (506).
4. A biomedical research drug mixing device according to claim 1, characterized in that: The mixing mechanism (6) comprises a servo motor (601), a rotating shaft (602), a mixing tank (603), a top plate (604), a feed port (605), a sealing cover (606), a driving motor (607), a stirring shaft (608), a stirring blade (609), a crushing column (610) and a discharge port (611); a servo motor (601) is fixedly connected to a surface of one side of the column (3); a rotating shaft (602) is fixedly connected to a surface of one side of the servo motor (601); one end of the rotating shaft (602) is fixedly connected to a mixing tank (603); and an upper surface of the mixing tank (603) is fixedly connected to a mixing tank (603). A top plate (604) is connected, a feed port (605) is fixedly connected to the upper surface of the top plate (604), a sealing cover (606) is rotatably connected to the upper surface of the feed port (605), a driving motor (607) is fixedly connected to the upper surface of the top plate (604), a stirring shaft (608) is fixedly connected to the lower surface of the driving motor (607), a stirring blade (609) is fixedly connected to the outer surface of the stirring shaft (608), a crushing column (610) is fixedly connected to the outer surface of the stirring shaft (608), and a discharge port (611) is fixedly connected to the lower surface of the mixing tank (603).
5. A biomedical research drug mixing device according to claim 4, characterized in that: The rotating shaft (602) is symmetrically arranged with respect to the central axis of the top plate (604), and the outer dimension of the clamping block (503) is consistent with the inner dimension of the feed port (605).
6. A biomedical research drug mixing device according to claim 4, characterized in that: The feed inlet (605) is symmetrically arranged with respect to the central axis of the top plate (604), and the feed inlet (605) and the sealing cover (606) form a sealing structure.
7. A biomedical research drug mixing device according to claim 4, characterized in that: The stirring blades (609) are distributed in multiple groups at equal intervals on the outer surface of the stirring shaft (608), and the crushing columns (610) are distributed in multiple groups at equal intervals on the outer surface of the stirring shaft (608).