CN220894281U - Medicine adverse reaction monitoring device - Google Patents

Abstract

The utility model discloses a medicine adverse reaction monitoring device, which relates to the technical field of monitoring devices and comprises a test box, a placement box, a partition plate and a first box door, wherein the placement plate is arranged in the test box at equal intervals, a pushing mechanism is arranged in the test box at equal intervals corresponding to the placement plate, a second box door is hinged to one side of the test box corresponding to the pushing mechanism, and the pushing mechanism comprises a motor. This medicine adverse reaction monitoring device, through push mechanism's setting, thereby in this medicine adverse reaction monitoring device use, can constitute an isolation space through isolation frame, division board, second chamber door, and can push the culture dish to the isolation space through the motor when taking, thereby greatly reduced the external influence to the test box inside, improved test data's accuracy, and avoided waiting for test environment to resume again, guaranteed this medicine adverse reaction monitoring device's test efficiency.

Description

Medicine adverse reaction monitoring device

Technical Field

The utility model relates to the technical field of monitoring devices, in particular to a monitoring device for adverse drug reactions.

Background

The generalized adverse drug reaction monitoring includes adverse reactions caused by drug quality problems or improper medication, including side effects, toxic effects (toxic effects), sequelae (post effects) and the like of drugs, which are often accompanied by symptoms such as shortness of breath, heart rate disturbance and the like, some of which occur when drugs themselves contain impurities or are improper for medication, some of which occur under the conditions of qualified quality inspection, clinically normal usage and dosage, and some of which are very concerned about drug safety worldwide from the viewpoint of adverse reactions, but how to prevent and control related risks caused by medication is a current challenge, so that adverse drug reaction monitoring can be performed by a device before drug delivery.

For example, chinese patent discloses a drug monitoring device. (grant bulletin No. CN 218272250U), the patent technology can realize the function of monitoring the control variable by arranging a test tank and a control tank, thereby better observing the adverse reaction of the medicine; the function of compressing and fixing the placing boxes with different sizes is realized by arranging the sliding blocks and the sliding plates; the temperature sensor, the humidity sensor, the fixed box and the hollow plate are arranged, so that the function of adjusting the temperature and the humidity in the test box is realized;

However, when the medicine is actually detected, sampling detection is carried out at intervals in the test process, the test environment is broken in the process of opening the box door by sampling, temperature and humidity conditions can change greatly in an instant manner, harmful substances such as dust and bacteria can fall into the medicine, the test data can deviate greatly, and the test efficiency is reduced because the test environment is required to be restored again.

Disclosure of utility model

The utility model aims to provide a medicine adverse reaction monitoring device so as to solve the problems in the background technology.

In order to achieve the above purpose, the present utility model provides the following technical solutions: the utility model provides a medicine adverse reaction monitoring devices, includes the test box, places case, baffle, first chamber door, the inside equidistance of test box is provided with places the board, and the inside of test box corresponds to places the board equidistance and is provided with push mechanism, one side of test box corresponds push mechanism and articulates there is the second chamber door;

The pushing mechanism comprises a motor, one end of the motor is arranged on one side inner wall of the test box, one end output shaft of the motor is fixedly connected with a screw, the outer wall of the screw is connected with a pushing frame in a threaded mode, the bottom of the pushing frame is attached to the bottom inner wall of the test box, one side of the pushing frame is fixedly connected to one side of the placing plate, isolation frames are correspondingly arranged on two sides of the partition plate, the bottom of the isolation frames are fixedly connected to the bottom inner wall of the test box, an auxiliary assembly is arranged at the top of the isolation frames, through grooves are formed in the top of the isolation frames in a penetrating mode, and isolation plates are arranged on the inner wall of the through grooves in an attached mode.

Preferably, the top fixedly connected with connecting rod of division board, and the other end fixedly connected with slide of connecting rod, one side fixedly connected with ejector pad of pushing away the frame, the both sides of slide set up to the inclined plane form.

Preferably, the two sides of the partition plate are fixedly connected with the fixing plates, the bottoms of the fixing plates are provided with telescopic springs at equal intervals, and the other ends of the telescopic springs are fixedly connected to the top of the sliding plate.

Preferably, the limiting plates are fixedly connected to the two sides of the fixing plate, one side of the sliding plate is slidably connected to one side of the limiting plates, and the outer wall of the connecting rod is slidably connected to one side of the limiting plates.

Preferably, the bottom of division board corresponds the propelling movement frame equidistance and leaves and be equipped with the recess, and the laminating of the top of propelling movement frame sets up the inner wall at the recess.

Preferably, the top of the placing plate is equidistantly separated from the placing groove.

Preferably, the auxiliary assembly comprises a suction pump, the bottom of the suction pump is arranged at the top of the isolation frame, the top of the suction pump is provided with a suction pipe, the outer wall of the suction pipe is provided with an electromagnetic valve, one side of the suction pump is provided with a conveying pipe, and the other end part of the conveying pipe is arranged at the top of the isolation frame.

Compared with the prior art, the utility model has the beneficial effects that: the medicine adverse reaction monitoring device comprises a medicine box;

1. Through pushing mechanism's setting to in this medicine adverse reaction monitoring devices use, can constitute an isolation space through isolation frame, division board, second chamber door, and can push the culture dish to the isolation space through the motor when taking, thereby greatly reduced the external influence to the test box inside, improved test data's accuracy, and avoided waiting for test environment to resume again, guaranteed this medicine adverse reaction monitoring devices's test efficiency.

2. Through auxiliary assembly's setting to in this medicine adverse reaction monitoring devices use, when placing the board with the culture dish again, can carry out the premix through air in the suction pump with the test box and isolation space, cause inside humiture to appear changing suddenly when avoiding the division board to open, further guaranteed the accuracy of this medicine adverse reaction monitoring devices's test data.

Drawings

FIG. 1 is a schematic overall structure of the present utility model;

FIG. 2 is a schematic view of the rear view of the interior of the experimental box of the present utility model;

FIG. 3 is a schematic diagram of a pushing mechanism according to the present utility model;

fig. 4 is a schematic structural view of an auxiliary assembly of the present utility model.

In the figure: 1. a test chamber; 2. placing a box; 3. a partition plate; 4. a first door; 5. placing a plate; 7. a second door; 6. a pushing mechanism; 601. a motor; 602. a screw; 603. pushing a frame; 604. an isolation frame; 605. a through groove; 606. a partition plate; 607. a connecting rod; 608. a slide plate; 609. a pushing block; 610. a fixing plate; 611. a telescopic spring; 612. a limiting plate; 613. a groove; 8. an auxiliary component; 801. a getter pump; 802. an air suction pipe; 803. an electromagnetic valve; 804. a conveying pipe.

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.

Embodiment one:

Referring to fig. 1-4, the present utility model provides a technical solution: the utility model provides a medicine adverse reaction monitoring device, which comprises a test box 1, place the case 2, baffle 3, first chamber door 4, the inside equidistance of test case 1 is provided with places board 5, and the inside of test case 1 is provided with push mechanism 6 corresponding to placing board 5 equidistance, and one side of test case 1 is articulated to have second chamber door 7 corresponding to push mechanism 6, further push mechanism 6 includes motor 601, and one end of motor 601 installs in one side inner wall of test case 1, and one end output shaft fixedly connected with screw 602 of motor 601, then the outer wall threaded connection of screw 602 has push frame 603, and the laminating of push frame 603 sets up in the bottom inner wall of test case 1, and one side fixedly connected with of push frame 603 is in one side of placing board 5, then both sides of baffle 3 are provided with spacer 604 correspondingly, and the bottom fixedly connected with of spacer 604 is in the bottom inner wall of test case 1, and the top of the isolation frame 604 is provided with a through groove 605 in a penetrating way, then the inner wall of the through groove 605 is provided with an isolation plate 606 in a fitting way, the top of the isolation plate 606 is fixedly connected with a connecting rod 607, the other end of the connecting rod 607 is fixedly connected with a slide plate 608, one side of the push frame 603 is fixedly connected with a push block 609, two sides of the slide plate 608 are provided with inclined planes, two sides of the partition plate 3 are fixedly connected with a fixed plate 610, then the bottom of the fixed plate 610 is provided with a telescopic spring 611 at equal distance, the other end of the telescopic spring 611 is fixedly connected with the top of the slide plate 608, two sides of the fixed plate 610 are fixedly connected with a limiting plate 612, one side of the slide plate 608 is connected with one side of the limiting plate 612 in a sliding way, the outer wall of the connecting rod 607 is connected with one side of the limiting plate 612, the bottom of the isolation plate 606 is provided with a groove 613 corresponding to the push frame 603 in an equal distance, meanwhile, the top of the pushing frame 603 is attached to the inner wall of the groove 613, and the top of the placing plate 5 is equidistantly separated from the placing groove;

More specifically, in this embodiment, in the present device, the inside of the test chamber 1 is divided into a test chamber and a control chamber by the partition board 3, and the pushing mechanism 6 is respectively disposed in the test chamber and the control chamber, and meanwhile, the prior art products for monitoring the inside of the test chamber 1 and adjusting the temperature and humidity of the inside of the test chamber 1 can refer to the cameras, the control panel, the temperature sensor, the humidity sensor, etc. in the above-mentioned comparison document, and will not be described further herein;

in the use process of the medicine adverse reaction monitoring device, the top of the placing plate 5 is equidistantly separated from the placing groove, so that a culture dish can be placed on the placing plate 5, when the culture dish in the test box 1 needs to be taken out for sampling detection, the motor 601 is started firstly, a screw 602 is fixedly connected with an output shaft at one end of the motor 601, the outer wall of the screw 602 is in threaded connection with a pushing frame 603, the bottom of the pushing frame 603 is attached to the inner wall of the bottom of the test box 1, the pushing frame 603 can be driven by the motor 601 to move linearly back and forth, then, isolation frames 604 are correspondingly arranged at two sides of the partition plate 3, the bottom of the isolation frames 604 is fixedly connected to the inner wall of the bottom of the test box 1, and an isolation plate 606 is attached to the inner wall of the through groove 605, and meanwhile, one side of the test box 1 is correspondingly hinged with a second box door 7 by the pushing mechanism 6, so that an isolation space can be formed by the isolation frames 604, the isolation plate 606 and the second box door 7, and then one side of the pushing frame 603 is fixedly connected to one side of the placing plate 5 by the motor 601, so that the placing plate 5 can be pushed out of the test box 1;

Then, the connecting rod 607 is fixedly connected with the top of the isolation plate 606, the other end part of the connecting rod 607 is fixedly connected with the slide plate 608, one side of the pushing frame 603 is fixedly connected with the pushing block 609, and meanwhile, both sides of the slide plate 608 are in an inclined plane shape, so that the pushing block 609 can be driven by the pushing frame 603 to move and contact with an inclined plane of one side of the slide plate 608, the limiting plate 612 is fixedly connected with both sides of the fixing plate 610, one side of the slide plate 608 is slidably connected with one side of the limiting plate 612, and the outer wall of the connecting rod 607 is slidably connected with one side of the limiting plate 612, so that the slide plate 608 is limited, the slide plate 608 is enabled to be linearly lifted, the isolation plate 606 is synchronously driven to lift, and a culture dish can be pushed into the isolation space, at this time, the push block 609 contacts with the inclined surface of the other side of the slide 608, the bottom of the fixed plate 610 is provided with the telescopic springs 611 at equal distance, and the other ends of the telescopic springs 611 are fixedly connected to the top of the slide 608, so that the telescopic springs 611 rebound to drive the slide 608 to descend;

Through the above, thereby in this medicine adverse reaction monitoring devices use, can constitute an isolation space through spacer 604, division board 606, second chamber door 7, and can push the culture dish to the isolation space through motor 601 when taking, thereby greatly reduced the external influence to test box 1 is inside, improved test data's accuracy, and avoid waiting for test environment to resume again, guaranteed this medicine adverse reaction monitoring devices's test efficiency.

Embodiment two:

On the basis of the above embodiment, the top of the isolation frame 604 is provided with the auxiliary assembly 8, the further auxiliary assembly 8 comprises the suction pump 801, the bottom of the suction pump 801 is mounted on the top of the isolation frame 604, the top of the suction pump 801 is provided with the suction pipe 802, then the outer wall of the suction pipe 802 is provided with the electromagnetic valve 803, one side of the suction pump 801 is provided with the conveying pipe 804, and the other end of the conveying pipe 804 is arranged on the top of the isolation frame 604;

More specifically, in this embodiment, in the use process of the apparatus for monitoring adverse drug reaction, when a inspector has detected that a culture dish is replaced on the placement plate 5, the second box door 7 is closed at this time, and the insulation space is opened and closed by the second box door 7 and has a temperature and humidity difference with the inside of the test box 1 at this time, in order to avoid sudden change of the temperature and humidity in the test box 1 caused by sudden large-area contact and mixing of the insulation space and the air in the test box 1 due to pushing of the culture dish to the original position at this time, an air suction pipe 802 is arranged at the top of the air suction pump 801, and an electromagnetic valve 803 is arranged at the outer wall of the air suction pipe 802, so that the air suction pipe 802 is opened by the electromagnetic valve 803, then a conveying pipe 804 is arranged at the top of the insulation frame 604 through the air suction pipe 802, and the air inside the test box 1 is conveyed into the insulation space through the conveying pipe 804 to be premixed, so as to avoid sudden change of the temperature and humidity in the inside when the insulation plate 606 is opened, and further ensure accuracy of test data of the apparatus for monitoring adverse drug reaction;

Through as described above to in this medicine adverse reaction monitoring devices use, when placing the board 5 with the culture dish again, can mix in advance with the isolation space through the air in the test chamber 1 of aspirator pump 801, avoid causing inside humiture to change suddenly when division board 606 is opened, further guaranteed the accuracy of this medicine adverse reaction monitoring devices's test data.

Working principle: when the medicine adverse reaction monitoring device is used, when a culture dish in the test box 1 is required to be taken out for sampling detection, the placing plate 5 is pushed out of the test box 1 through the motor 601, then the pushing block 609 is driven by the pushing frame 603 to move and contact with one inclined surface of the sliding plate 608, so that the sliding plate 608 is linearly lifted, the isolation plate 606 is synchronously driven to lift, the culture dish can be pushed into an isolation space, when the culture dish is pushed to a certain distance, the pushing block 609 is contacted with the inclined surface of the other side of the sliding plate 608 at the moment, when one side of the pushing block 609 is contacted with one side of the isolation frame 604, the sliding plate 608 drives the isolation plate 606 to descend to the lowest point, and meanwhile, the inner wall of the groove 613 is bonded through the top of the pushing frame 603, so that the isolation space can be completely sealed, the second box door 7 can be opened at the moment to take out the culture dish, the influence of the outside on the inside of the test box 1 is greatly reduced, the accuracy of test data is improved, and the test environment is prevented from being required to be restored again;

Then, when the inspector finishes detecting the culture dish and relocates the culture dish on the placement plate 5, the second box door 7 is closed at the moment, the air in the test box 1 is sucked through the suction pump 801 and is conveyed into the isolation space through the conveying pipe 804 to be premixed, so that the abrupt change of the internal temperature and humidity caused by the opening of the isolation plate 606 is avoided, and the accuracy of test data of the medicine adverse reaction monitoring device is further ensured.

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 (7)

1. The utility model provides a medicine adverse reaction monitoring devices, includes test box (1), places case (2), baffle (3), first chamber door (4), its characterized in that: the inside of the test box (1) is provided with a placing plate (5) at equal distance, the inside of the test box (1) is provided with a pushing mechanism (6) at equal distance corresponding to the placing plate (5), and one side of the test box (1) is hinged with a second box door (7) corresponding to the pushing mechanism (6);

Push mechanism (6) are including motor (601), and one end portion of motor (601) installs one side inner wall at test box (1), one end output shaft fixedly connected with screw rod (602) of motor (601), and the outer wall threaded connection of screw rod (602) has push frame (603), the bottom laminating of push frame (603) sets up the bottom inner wall at test box (1), and one side fixed connection of push frame (603) is in one side of placing board (5), the both sides of baffle (3) correspond and are provided with spacer frame (604), and the bottom fixed connection of spacer frame (604) is at the bottom inner wall of test box (1), the top of spacer frame (604) is provided with auxiliary assembly (8), and runs through at the top of spacer frame (604) and has seted up logical groove (605), the inner wall laminating of logical groove (605) is provided with division board (606).

2. The adverse drug reaction monitoring device according to claim 1, wherein a connecting rod (607) is fixedly connected to the top of the isolation plate (606), a slide plate (608) is fixedly connected to the other end of the connecting rod (607), and a push block (609) is fixedly connected to one side of the push frame (603).

3. The adverse drug reaction monitoring device according to claim 2, wherein two sides of the slide plate (608) are inclined, two sides of the partition plate (3) are fixedly connected with a fixing plate (610), telescopic springs (611) are equidistantly arranged at the bottom of the fixing plate (610), and the other end of each telescopic spring (611) is fixedly connected to the top of the slide plate (608).

4. A device for monitoring adverse drug reactions according to claim 3 wherein the two sides of the fixed plate (610) are fixedly connected with a limiting plate (612), one side of the slide plate (608) is slidably connected to one side of the limiting plate (612), and the outer wall of the connecting rod (607) is slidably connected to one side of the limiting plate (612).

5. The adverse drug reaction monitoring device according to claim 1, wherein grooves (613) are formed in the bottoms of the isolation plates (606) at equal intervals corresponding to the pushing frames (603), and the tops of the pushing frames (603) are attached to the inner walls of the grooves (613).

6. A device for monitoring adverse drug reactions according to claim 1 characterised in that the top of the placement plate (5) is provided with placement slots equidistant from it.

7. The adverse drug reaction monitoring device according to claim 1, wherein the auxiliary assembly (8) comprises a suction pump (801), the bottom of the suction pump (801) is mounted on the top of the isolation frame (604), the top of the suction pump (801) is provided with a suction pipe (802), the outer wall of the suction pipe (802) is provided with an electromagnetic valve (803), one side of the suction pump (801) is provided with a conveying pipe (804), and the other end of the conveying pipe (804) is arranged on the top of the isolation frame (604).