Drug reference substance analysis and detection device

Abstract

The utility model relates to the technical field of drug analysis and detection, in particular to a drug reference substance analysis and detection device which comprises a chassis, the upper end of the chassis is fixedly connected with the supporting column, the top end of the supporting column is fixedly provided with a display screen, the outer side of the middle of the supporting column is fixedly connected with a supporting ring, and the upper end of the supporting ring is provided with the test disc; by arranging the supporting column, the display screen, the test disc, the partition plate, the transparent baffle ring, the video recording module and the like, at most seven groups of medicine samples can be rapidly and conveniently arranged for testing, the operation is simple and convenient, the conversion is rapid, the interval time of adding reagents into each group of samples is shortened, and the observation efficiency is improved; each group of test conditions can be recorded in detail and transmitted to the display screen for unified display, so that visual observation is facilitated, the change conditions of each group of samples can be quickly found, the good observation effect of the test is improved, and relatively accurate judgment is given.

Description

TECHNICAL FIELD

[0001] The utility model relates to medicine analysis and detection technical field especially relates to a medicine control analysis and detection device. BACKGROUND

[0002] Medicine is the pharmacy important component, its kind is various, according to its containing different component can cure and prevent different types of disease, and the effect of some drugs is similar, in order to observe the similar drug effect time and effect, need to carry out analysis and detection, carries out medicine control under the same environment.

[0003] Under the existing test condition, it is difficult to simultaneously test and observe multiple groups of medicines under the same environment, and the operation of adding reagents to each group of samples is complicated and troublesome, and the conversion is slow, which affects the relative synchronous observation of the test personnel, and each group of samples is placed in a row during observation, which is difficult to observe comprehensively, and the sample changes cannot be found in time.

[0004] Therefore, in view of the above problems that it is difficult to simultaneously test and observe multiple groups of medicines under the same environment under the existing test condition, the test operation process is complicated and troublesome, which affects the observation efficiency of the test personnel, and the samples are placed disorderly, which cannot be observed uniformly, it is difficult to observe comprehensively, and the sample changes cannot be found in time, a medicine control analysis and detection device can be designed, by setting support column, display screen, test disc, partition plate, transparent baffle ring and video recording module, etc., up to seven groups of medicine samples can be arranged for testing quickly and conveniently, the observation efficiency is improved, the test conditions of each group can be recorded in detail and transmitted to the display screen for unified display, which is convenient for intuitive observation. CONTENT OF THE UTILITY MODEL

[0005] In order to overcome the problems that it is difficult to simultaneously test and observe multiple groups of medicines under the same environment under the existing test condition, the test operation process is complicated and troublesome, which affects the observation efficiency of the test personnel, and the samples are placed disorderly, which cannot be observed uniformly, it is difficult to observe comprehensively, and the sample changes cannot be found in time.

[0006] The utility model discloses a technical scheme for a drug reference substance analysis and detection device, which comprises a base plate, a support column and a test plate.

[0007] Preferably, the test plate, the fixing ring, the transparent baffle ring and the eight partition plates divide eight intervals of the same size, and at most seven intervals are selected to place each group of samples. After placing, the test plate is rotated, and each sample interval is sequentially moved under the reagent bottle. The reagent for detection is dropped, and finally each interval with the dropped reagent is moved under each video module. Each corresponding interval is monitored by the video module, and the video image is transmitted to the display screen for display, which is convenient for the tester to intuitively view.

[0008] Preferably, a lifting ring is fixedly connected to the outer side of the upper end of the support column, and a transparent isolation cover is fixedly connected to the outer side of the lifting ring. A notch is formed in the front surface of the transparent isolation cover.

[0009] Preferably, an extension block is fixedly connected to the front end of the support ring, and a motor electrically connected to the display screen is fixedly installed at the bottom of the extension block and the support ring. An output shaft of the motor is fixedly connected with a gear.

[0010] Preferably, an inner tooth ring is fixedly connected to the bottom of the test plate, and the inner tooth ring is meshingly connected with the gear.

[0011] Preferably, air cylinders electrically connected to the display screen are fixedly installed at the bottom of the transparent baffle ring and symmetrically on the left and right sides of the test plate. L-shaped connecting plates are fixedly connected to the movable ends of the two air cylinders, and the sides of the two L-shaped connecting plates away from the movable ends of the air cylinders are fixedly connected to the bottom of the transparent baffle ring.

[0012] Preferably, a limiting ring is fixedly connected to the outer side of the middle of the support column, and the limiting ring is arranged on the upper side of the test plate.

[0013] Preferably, seven labels one are pasted on the outer side of the transparent baffle ring at equal intervals, and seven labels two are pasted on the ends of the seven support plates away from the support column.

[0014] The beneficial effects of this utility model are:

[0015] This device, equipped with support columns, a display screen, a test tray, a partition plate, a transparent retaining ring, and a video recording module, can quickly and conveniently arrange up to seven groups of drug samples for testing. It is simple and convenient to operate, with rapid switching, shortening the interval between adding reagents to each group of samples, improving observation efficiency, and recording the detailed test results of each group of samples and transmitting them to the display screen for unified display. This facilitates intuitive observation, helps to quickly identify changes in each group of samples, improves the observation effect of the test, and provides more accurate judgments. Attached Figure Description

[0016] Figure 1 The diagram shown is a three-dimensional structural schematic of a pharmaceutical reference standard analysis and detection device according to this utility model.

[0017] Figure 2 The diagram shown is a schematic representation of the support column structure of a pharmaceutical reference standard analysis and detection device according to this utility model.

[0018] Figure 3 The diagram shown illustrates the structure of the fixing ring in a pharmaceutical reference standard analysis and detection device according to this utility model. Figure 1 ;

[0019] Figure 4 The diagram shown illustrates the structure of the fixing ring in a pharmaceutical reference standard analysis and detection device according to this utility model. Figure 2 ;

[0020] Figure 5 The diagram shown is a schematic representation of the transparent isolation cover structure of a pharmaceutical reference standard analysis and detection device according to this utility model.

[0021] Explanation of reference numerals in the attached diagram: 1. Chassis; 2. Support column; 3. Display screen; 4. Support ring; 5. Test tray; 6. Fixing ring; 7. Divider plate; 8. Transparent retaining ring; 9. Support plate; 10. Video recording module; 11. Support frame; 12. Reagent bottle; 13. Lifting ring; 14. Transparent isolation cover; 15. Notch; 16. Extension block; 17. Motor; 18. Gear; 19. Internal gear ring; 20. Cylinder; 21. L-shaped connecting plate; 22. Limiting ring; 23. Label 1; 24. Label 2. Detailed Implementation

[0022] The present invention will be further described below with reference to the accompanying drawings and embodiments.

[0023] Please see Figures 1-5This utility model provides an embodiment: a drug reference standard analysis and detection device, including a chassis 1; it also includes a support column 2 and a test tray 5. The support column 2 is fixedly connected to the upper end of the chassis 1, and a display screen 3 is fixedly installed at the top of the support column 2. A support ring 4 is fixedly connected to the outer side of the middle part of the support column 2. The test tray 5 is provided at the upper end of the support ring 4, and the middle part of the test tray 5 is movably penetrated by the support column 2. A fixing ring 6 is fixedly connected to the middle of the upper end of the test tray 5. Eight partition plates 7 are fixedly connected in a ring array to the outer side of the fixing ring 6. The bottom of each of the eight partition plates 7 is fixedly connected to the upper surface of the test tray 5. Transparent retaining rings 8 are movably arranged on the outer side of the eight partition plates 7 and the test tray 5. Seven equidistantly distributed support plates are installed around the outer side of the upper end of the support column 2. A test plate 9 and a support frame 11 are provided. A video recording module 10, which is electrically connected to the display screen 3, is fixedly connected to the bottom of each support plate 9 on the side away from the support column 2. A reagent bottle 12 is installed on the side of the support frame 11 away from the support column 2. The test plate 5, the fixing ring 6, the transparent retaining ring 8, and the eight partition plates 7 divide the test plate into eight equal-sized intervals. Up to seven intervals are selected to place each group of samples. After placement, the test plate 5 is rotated to move each interval where the samples are placed to the bottom of the reagent bottle 12 in turn. The test reagent is dripped in. Finally, each interval with the test reagent dripped is moved to the bottom of the corresponding video recording module 10. The video recording module 10 monitors each corresponding interval and transmits the video footage to the display screen 3 for easy viewing by the test personnel.

[0024] Please see Figure 2 , Figure 4 and Figure 5 In this embodiment, a hanging ring 13 is fixedly connected to the upper outer side of the support column 2 and the fixed ring 6. A transparent isolation cover 14 is fixedly connected to the outer side of the hanging ring 13. A notch 15 is opened on the front surface of the transparent isolation cover 14. The transparent isolation cover 14 seals each test area to prevent experimental errors caused by air. The notch 15 is used for the dripping of reagents and subsequent cleaning of the area. An extension block 16 is fixedly connected to the front end of the support ring 4. A motor 17 electrically connected to the display screen 3 is fixedly installed together with the extension block 16 and the bottom of the support ring 4. A gear 18 is fixedly connected to the output shaft of the motor 17. The operation on the display screen 3 can control the start of the motor 17 to work. The motor 17 drives the gear 18 to rotate. An internal gear ring 19 is fixedly connected to the bottom of the test disk 5, and the internal gear ring 19 and the gear 18 are meshed. When the motor 17 drives the gear 18 to rotate, the gear 18 drives the meshing internal gear ring 19 to rotate, thereby controlling the test disk 5 to rotate accurately.

[0025] Please see Figures 1-4In this embodiment, cylinders 20 electrically connected to the display screen 3 are symmetrically fixed on the left and right sides of the bottom of the test pan 5. L-shaped connecting plates 21 are fixedly connected to the movable ends of both cylinders 20. The sides of the two L-shaped connecting plates 21 away from the movable ends of the cylinders 20 are fixedly connected to the bottom of the transparent retaining ring 8. Operation on the display screen 3 allows the two cylinders 20 to work synchronously. By pushing the two L-shaped connecting plates 21, the transparent retaining ring 8 is raised. When the top of the transparent retaining ring 8 descends to the surface height of the test pan 5, the corresponding section can be cleared at the notch 15 on the transparent isolation cover 14. The washing process is carried out, and then the washing water is drained. A limiting ring 22 is fixedly connected to the outer side of the middle part of the support column 2, and the limiting ring 22 is set on the upper side of the test plate 5. The limiting ring 22 is used to restrict the test plate 5 from moving upward, so that the test plate 5 can only rotate. Seven labels 1 23 are pasted around the outer side of the transparent baffle ring 8, and labels 24 are pasted on the ends of the seven support plates 9 away from the support column 2. Labels 1 23 mark the corresponding intervals, and labels 24 mark the recording content of the video recording module 10 on the corresponding support plate 9, so as to facilitate the differentiation and marking of the reference drugs and record the test conditions of the corresponding samples.

[0026] During operation, the test tray 5, fixing ring 6, transparent retaining ring 8, and eight partition plates 7 divide the sample into eight equal sections. Up to seven sections are selected for each sample group. After placement, the motor 17 is activated via the display screen 3. The motor 17 drives the gear 18, which in turn drives the meshing internal gear ring 19, thus controlling the precise rotation of the test tray 5. Each sample section is then moved below the reagent bottle 12, and the test reagent is added. Finally, each section with the test reagent added is moved below its corresponding video recording module 10 and sealed to the outside environment by the transparent isolation cover 14. Labels 23 and 24 are pre-marked with the corresponding sample sections. The video recording module 10 monitors each section and transmits the recorded footage to the display screen 3 for observation of changes in the samples. After the test, the corresponding sections can be cleaned at the notch 15 on the transparent isolation cover 14, and the cleaning water can be drained.

[0027] Through the above steps, the device can quickly and conveniently arrange up to seven groups of drug samples for testing. It is simple and convenient to operate, and the switching is rapid. It shortens the interval between adding reagents to each group of samples, improves the efficiency of observation, and can record and transmit the test results of each group in detail to the display screen 3 for unified display. This facilitates intuitive observation, helps to quickly discover changes in each group of samples, improves the observation effect of the test, and provides a more accurate judgment. This solves the problem that under the existing test conditions, it is difficult to conduct simultaneous test detection and observation of multiple groups of drugs under the same environment. The test operation is relatively cumbersome and troublesome, which affects the observation efficiency of the test personnel. In addition, the samples are placed in a messy manner, which makes it difficult to conduct unified observation, make it difficult to observe comprehensively, and fail to detect changes in samples in a timely manner.

Claims

1. A drug reference standard analysis detection device comprising a base plate (1); characterized in that: Also include support column (2) and test disc (5), the upper end of the base (1) is fixedly connected with support column (2), the top of support column (2) is fixedly installed with display screen (3), the middle part of the outer side of support column (2) is fixedly connected with support ring (4), the upper end of support ring (4) is provided with test disc (5), and the middle part of test disc (5) is movably penetrated by support column (2), the upper end of test disc (5) is fixedly connected with fixed ring (6), the outer side of fixed ring (6) is annularly arranged and fixedly connected with eight partition plates (7), the bottom of eight partition plates (7) is fixedly connected to the upper end surface of test disc (5), the outer side of eight partition plates (7) and test disc (5) is movably provided with transparent blocking ring (8), the upper end of the outer side of support column (2) is installed with seven equidistantly distributed support plates (9) and a support frame (11), the bottom of each support plate (9) is fixedly connected with a video recording module (10) electrically connected with display screen (3) on the side away from support column (2), and reagent bottle (12) is installed on the side away from support column (2) of support frame (11).

2. The drug reference standard analysis testing device of claim 1, wherein: The upper end of the outer side of support column (2) is fixedly connected with a lifting ring (13), and the outer side of lifting ring (13) is fixedly connected with a transparent isolation cover (14), and the front surface of transparent isolation cover (14) is provided with a notch (15).

3. The drug reference standard analysis testing device of claim 1, wherein: The front end of support ring (4) is fixedly connected with an extension block (16), and the bottom of extension block (16) and support ring (4) is fixedly installed with a motor (17) electrically connected with display screen (3), and the output shaft of motor (17) is fixedly connected with a gear (18).

4. The drug reference standard analysis testing device of claim 3, wherein: The bottom of test disc (5) is fixedly connected with an inner tooth ring (19), and the inner tooth ring (19) is meshedly connected with the gear (18).

5. The drug reference standard analysis testing device of claim 1, wherein: The bottom of test disc (5) is fixedly installed with a gas cylinder (20) electrically connected with display screen (3) on the left and right sides, and the movable end of the two gas cylinders (20) is fixedly connected with an L-shaped connecting plate (21), and the side away from the movable end of the two L-shaped connecting plates (21) is fixedly connected to the bottom of transparent blocking ring (8).

6. The drug reference standard analysis testing device of claim 1, wherein: The middle part of the outer side of support column (2) is fixedly connected with a limiting ring (22), and the limiting ring (22) is arranged on the upper side of test disc (5).

7. The drug reference standard analysis testing device of claim 1, wherein: The outer side of transparent blocking ring (8) is pasted with seven equally spaced labels (23), and the end away from support column (2) of seven support plates (9) is pasted with label (24).

Images