S-type and R-type glassine promotion collagen detection device

Abstract

The utility model provides an S-type and R-type glassine promotion collagen detection device, which belongs to the technical field of biomedicine and comprises a bearing mechanism, an isolation box, a driving component fixedly mounted in an inner cavity of the isolation box and an optical detection part fixedly mounted at the top of the driving component. The detection table is fixedly mounted at the top of the optical detection piece; the flushing mechanism comprises a cleaning box fixedly installed in an inner cavity of the isolation box. The flushing mechanism can effectively clean appliances such as a micropipettor after detection, the flushing assembly enables cleaning liquid to flow, the flushing assembly is matched with the cleaning assembly to brush the surfaces of components, sample residues and cross contamination are prevented, cleanliness of the device and reliability of follow-up detection are guaranteed, and the detection efficiency is improved. Therefore, components of a sample possibly remained on the surface of the appliance can be more effectively removed, the risk of cross contamination of the sample caused by incomplete cleaning of the appliance is reduced, and the accuracy of a detection result is improved.

Description

Technical Field

[0001] This invention belongs to the field of biomedical technology, specifically relating to an S-type and R-type serotonin-promoting collagen detection device. Background Technology

[0002] In related research fields, studies on the promotion of collagen by S-type and R-type serotonin have gradually attracted attention. As the exploration of the mechanism of action of serotonin continues to deepen, the differences between S-type and R-type serotonin in promoting collagen synthesis have become the focus of research. The aim is to conduct comparative studies on their efficacy in promoting collagen synthesis through detection devices, so as to clarify the specific performance and characteristics of the two in this aspect.

[0003] Currently, during sample collection and pretreatment, micropipettes are prone to incomplete cleaning when aspirating different samples, resulting in residual components from the previous sample. This can affect the accuracy of subsequent test results and lead to cross-contamination between different samples. Utility Model Content

[0004] The purpose of this invention is to provide an S-type and R-type BOXER collagen-promoting detection device, which aims to solve the problems mentioned in the background art.

[0005] To achieve the above objectives, this utility model provides the following technical solution:

[0006] A detection device for S-type and R-type serotonin-induced collagen production includes,

[0007] The support mechanism includes an isolation box, a drive assembly fixedly installed inside the isolation box, an optical detection component fixedly installed on the top of the drive assembly, and a detection stage fixedly installed on the top of the optical detection component;

[0008] The rinsing mechanism includes a cleaning tank fixedly installed inside the isolation box, a flushing assembly disposed outside the cleaning tank, a support plate fixedly installed at the bottom of the cleaning tank, a drive motor fixedly installed at the bottom of the support plate, an auxiliary wheel rotatably installed at the top of the support plate, and an output shaft fixedly installed at the output end of the drive motor.

[0009] As a preferred embodiment of this utility model, the supporting mechanism further includes an immunoassay device fixedly installed on the outside of the testing platform, and an observation window fixedly installed on the outside of the isolation box.

[0010] As a preferred embodiment of the present invention, the flushing mechanism further includes a transmission belt sleeved on the outer surface of the output shaft, a drive gear movably sleeved on the other end of the transmission belt, a driven gear meshing with the drive gear, a fixed seat fixedly installed on the top of the driven gear, a propeller blade fixedly installed on the top of the fixed seat, and a cleaning assembly disposed on the top of the drive gear.

[0011] As a preferred embodiment of this utility model, the cleaning assembly includes a vertical rod fixedly installed on the top of the drive gear, and a plurality of supporting diagonal rods fixedly installed on the outer surface of the vertical rod.

[0012] As a preferred embodiment of this utility model, the cleaning assembly further includes a plurality of brushes fixedly installed on the outer surface of the vertical rod, and through holes formed on the outer surface of the brushes.

[0013] As a preferred embodiment of this utility model, the flushing assembly includes a water pipe fixedly installed on the outside of the cleaning tank, and a nozzle fixedly installed at the end of the water pipe.

[0014] As a preferred embodiment of this utility model, the flushing assembly further includes a booster pump fixedly installed at the bottom of the water pipe, and a connecting pipe head fixedly installed at the other end of the water pipe.

[0015] Compared with the prior art, the beneficial effects of this utility model are: the rinsing mechanism can effectively clean instruments such as micropipettes after detection; the rinsing component makes the cleaning solution flow, and together with the cleaning component, it brushes the surface of the parts, preventing sample residue and cross-contamination, ensuring the cleanliness of the device and the reliability of subsequent detection, thereby more effectively removing components of the previous sample that may remain on the surface of the instrument, reducing the risk of sample cross-contamination caused by incomplete instrument cleaning, and improving the accuracy of the detection results. Attached Figure Description

[0016] To more clearly illustrate the technical solutions of the embodiments of this utility model, the drawings used in the description of the embodiments will be briefly introduced below. Obviously, the drawings described below are only some embodiments of this utility model. For those skilled in the art, other drawings can be obtained based on these drawings without creative effort. Among them:

[0017] Figure 1 This is a schematic diagram of the overall structure of this utility model;

[0018] Figure 2 This is a partial sectional view of the overall structure of this utility model;

[0019] Figure 3 This is a partial cross-sectional view of the rinsing mechanism structure of this utility model;

[0020] Figure 4 For the present utility model Figure 3 Enlarged view of the structure at point A in the middle;

[0021] Figure 5 This is a schematic diagram of the flushing component structure of this utility model.

[0022] In the diagram: 100, bearing mechanism; 101, isolation box; 102, drive assembly; 103, optical inspection component; 104, inspection table; 105, immunoassay component; 106, observation window; 200, rinsing mechanism; 201, cleaning box; 202, flushing assembly; 202a, water pipe; 202b, nozzle; 202c, booster pump; 202d, connecting pipe head; 203, support plate; 204, drive motor; 205, auxiliary wheel; 206, output shaft; 207, transmission belt; 208, drive gear; 209, driven gear; 210, fixed seat; 211, propeller blade; 212, cleaning assembly; 212a, vertical rod; 212b, support diagonal rod; 212c, brush; 212d, through hole. Detailed Implementation

[0023] To make the above-mentioned objectives, features and advantages of this utility model more apparent and understandable, the specific embodiments of this utility model will be described in detail below with reference to the accompanying drawings.

[0024] Many specific details are set forth in the following description in order to provide a full understanding of the present invention. However, the present invention may also be implemented in other ways different from those described herein. Those skilled in the art can make similar extensions without departing from the spirit of the present invention. Therefore, the present invention is not limited to the specific embodiments disclosed below.

[0025] Secondly, the term "an embodiment" or "embodiment" as used herein refers to a specific feature, structure, or characteristic that may be included in at least one implementation of the present invention. The phrase "in one embodiment" appearing in different places in this specification does not necessarily refer to the same embodiment, nor is it a single or selective embodiment that excludes other embodiments.

[0026] Example 1

[0027] Reference Figures 1-5 This is the first embodiment of the present invention, which provides an S-type and R-type serotonin-promoted collagen detection device, comprising,

[0028] The support mechanism 100 includes an isolation box 101, a drive assembly 102 fixedly installed inside the cavity of the isolation box 101, an optical detection component 103 fixedly installed on the top of the drive assembly 102, and a detection stage 104 fixedly installed on the top of the optical detection component 103.

[0029] The rinsing mechanism 200 includes a cleaning tank 201 fixedly installed inside the isolation box 101, a flushing assembly 202 disposed outside the cleaning tank 201, a support plate 203 fixedly installed at the bottom of the cleaning tank 201, a drive motor 204 fixedly installed at the bottom of the support plate 203, an auxiliary wheel 205 rotatably installed at the top of the support plate 203, and an output shaft 206 fixedly installed at the output end of the drive motor 204.

[0030] The driving component 102 drives the optical detector 103 to a suitable position, aligning it with the sample on the detection stage 104. The optical detector 103 then begins to detect the sample, potentially utilizing optical principles such as light absorption and scattering to obtain relevant optical information about S-type and R-type bosonic acid promoting collagen in the sample. This information will serve as the basis for subsequent analysis.

[0031] Specifically, the support mechanism 100 also includes an immunoassay device 105 fixedly installed on the outside of the testing station 104, and an observation window 106 fixedly installed on the outside of the isolation box 101.

[0032] The immunoassay unit 105, based on the principle of antigen-antibody specific binding, identifies and detects specific components in the sample, further obtaining relevant information on S-type and R-type positron-methyl-β-hydroxyl (PSH) promoting collagen in the sample. This complements the optical detection results, improving the accuracy and reliability of the detection. Operators can observe the detection process and record relevant test results through the observation window 106. The observation window 106 ensures that the internal environment of the isolation box 101 is relatively closed while allowing operators to understand the detection status in real time.

[0033] Furthermore, the flushing mechanism 200 also includes a transmission belt 207 sleeved on the outer surface of the output shaft 206, a drive gear 208 movably sleeved on the other end of the transmission belt 207, a driven gear 209 meshing with the drive gear 208, a fixed seat 210 fixedly mounted on the top of the driven gear 209, a propeller blade 211 fixedly mounted on the top of the fixed seat 210, and a cleaning assembly 212 disposed on the top of the drive gear 208.

[0034] When the drive motor 204 drives the output shaft 206 to rotate, the transmission belt 207 moves accordingly. The transmission belt 207 drives the drive gear 208 to rotate, and the drive gear 208 meshes with the driven gear 209, causing the driven gear 209 to start rotating as well. When the driven gear 209 rotates, the fixed seat 210 and propeller blade 211 fixedly installed on its top rotate accordingly. The rotation of the propeller blade 211 can make the cleaning liquid in the cleaning tank 201 flow to a certain extent, enhancing the rinsing effect. At the same time, the cleaning component 212 set on the top of the drive gear 208 also starts to work. The vertical rod 212a in the cleaning component 212 rotates with the rotation of the drive gear 208.

[0035] Preferably, the cleaning assembly 212 includes a vertical rod 212a fixedly mounted on the top of the drive gear 208, and a plurality of support diagonal rods 212b fixedly mounted on the outer surface of the vertical rod 212a. The cleaning assembly 212 also includes a plurality of brushes 212c fixedly mounted on the outer surface of the vertical rod 212a, and through holes 212d formed on the outer surface of the brushes 212c.

[0036] For some residual substances that are difficult to remove by simple rinsing, the brushing action of the brush 212c can further enhance the cleaning effect, while the design of the through hole 212d helps the rinsing liquid to penetrate and circulate better during the brushing process, taking away the residual substances washed off, thereby more thoroughly removing residual components that may cause cross-contamination, and further ensuring the reliability of the test results.

[0037] Furthermore, the flushing assembly 202 includes a water pipe 202a fixedly installed on the outside of the cleaning tank 201, and a nozzle 202b fixedly installed at the end of the water pipe 202a. The flushing assembly 202 also includes a booster pump 202c fixedly installed at the bottom of the water pipe 202a, and a connecting pipe head 202d fixedly installed at the other end of the water pipe 202a.

[0038] In the sample collection and pretreatment process, after the micropipette and other instruments have drawn different samples, they can be rinsed using the rinsing assembly 202. The booster pump 202c can provide sufficient water pressure so that the water jet from the nozzle 202b has a strong rinsing force, thereby more effectively removing any components of the previous sample that may remain on the surface of the instrument. This reduces the risk of cross-contamination of samples due to incomplete instrument cleaning and improves the accuracy of the test results.

[0039] When in use, the sample to be tested is placed on the testing stage 104, the isolation box 101 forms a closed testing space, the driving component 102 drives the optical detection component 103 to align with the sample for optical detection, the immunodetector 105 on the outside of the testing stage 104 performs immunodetection, and the operator observes and records the results through the observation window 106.

[0040] After the test is completed, the rinsing mechanism 200 starts to work. The booster pump 202c of the rinsing component 202 draws cleaning fluid through the connecting pipe head 202d and sprays it out through the nozzle 202b via the water pipe 202a to rinse instruments such as micropipettes. At the same time, the drive motor 204 drives the drive gear 208 to rotate through the output shaft 206 and the transmission belt 207. The drive gear 208 drives the driven gear 209 to rotate the propeller blade 211, which promotes the flow of cleaning fluid. The cleaning component 212 at the top of the drive gear 208 uses the vertical rod 212a, the support diagonal rod 212b, the brush 212c and the through hole 212d to clean the surface of the components. The auxiliary wheel 205 assists in the movement. Finally, the device returns to its initial state and waits for the next test.

[0041] In summary, the rinsing mechanism 200 effectively cleans instruments such as micropipettes after testing. The rinsing component 202 circulates the cleaning solution, which, together with the cleaning component 212, scrubs the surface of the components, preventing sample residue and cross-contamination. This ensures the cleanliness of the device and the reliability of subsequent tests, thereby more effectively removing any components of the previous sample that may remain on the surface of the instruments. This reduces the risk of sample cross-contamination caused by incomplete instrument cleaning and improves the accuracy of the test results.

[0042] It is important to note that the constructions and arrangements of this application shown in several different exemplary embodiments are merely illustrative. Although only a few embodiments are described in detail in this disclosure, those who consult this disclosure will readily understand that many modifications are possible (e.g., changes in the size, dimensions, structure, shape and proportion of various elements, as well as parameter values ​​(e.g., temperature, pressure, etc.), mounting arrangements, use of materials, color, orientation, etc.) without substantially departing from the novel teachings and advantages of the subject matter described in this application). For example, an element shown as integrally formed may be composed of multiple parts or elements, the position of elements may be inverted or otherwise altered, and the nature or number or position of discrete elements may be changed or altered. Therefore, all such modifications are intended to be included within the scope of this utility model. The order or sequence of any process or method steps may be changed or rearranged according to alternative embodiments. In the claims, any "device plus function" clause is intended to cover the structure described herein that performs the function, and not only structural equivalents but also equivalent structures. Without departing from the scope of this invention, other substitutions, modifications, alterations, and omissions may be made in the design, operation, and arrangement of the exemplary embodiments. Therefore, this invention is not limited to the specific embodiments, but extends to various modifications that still fall within the scope of the appended claims.

[0043] Furthermore, in order to provide a concise description of exemplary embodiments, not all features of actual embodiments (i.e., those features that are not relevant to the best mode of carrying out the present invention as currently considered, or those features that are not relevant to implementing the present invention) may be omitted.

[0044] It should be understood that numerous specific implementation decisions can be made during the development of any practical implementation, such as in any engineering or design project. Such development efforts may be complex and time-consuming, but for those skilled in the art who benefit from this disclosure, the development effort will be a routine work of design, manufacturing, and production without requiring much experimentation.

[0045] It should be noted that the above embodiments are only used to illustrate the technical solution of this utility model and are not intended to limit it. Although this utility model has been described in detail with reference to preferred embodiments, those skilled in the art should understand that modifications or equivalent substitutions can be made to the technical solution of this utility model without departing from the spirit and scope of the technical solution of this utility model, and all such modifications or substitutions should be covered within the scope of the claims of this utility model.

Claims

1. A detection device for S-type and R-type serotonin-promoted collagen, characterized in that: include, The support mechanism (100) includes an isolation box (101), a drive assembly (102) fixedly installed in the cavity of the isolation box (101), an optical detection element (103) fixedly installed on the top of the drive assembly (102), and a detection stage (104) fixedly installed on the top of the optical detection element (103). The rinsing mechanism (200) includes a cleaning tank (201) fixedly installed inside the isolation box (101), a flushing assembly (202) disposed outside the cleaning tank (201), a support plate (203) fixedly installed at the bottom of the cleaning tank (201), a drive motor (204) fixedly installed at the bottom of the support plate (203), an auxiliary wheel (205) rotatably installed at the top of the support plate (203), and an output shaft (206) fixedly installed at the output end of the drive motor (204).

2. The S-type and R-type serotonin-promoting collagen detection device according to claim 1, characterized in that: The support mechanism (100) also includes an immunoassay device (105) fixedly installed on the outside of the testing station (104) and an observation window (106) fixedly installed on the outside of the isolation box (101).

3. The S-type and R-type serotonin-promoted collagen detection device according to claim 2, characterized in that: The flushing mechanism (200) further includes a transmission belt (207) sleeved on the outer surface of the output shaft (206), a drive gear (208) movably sleeved on the other end of the transmission belt (207), a driven gear (209) meshing with the drive gear (208), a fixed seat (210) fixedly mounted on the top of the driven gear (209), a propeller blade (211) fixedly mounted on the top of the fixed seat (210), and a cleaning assembly (212) disposed on the top of the drive gear (208).

4. The S-type and R-type serotonin-promoting collagen detection device according to claim 3, characterized in that: The cleaning assembly (212) includes a vertical rod (212a) fixedly mounted on the top of the drive gear (208), and a plurality of support diagonal rods (212b) fixedly mounted on the outer surface of the vertical rod (212a).

5. The S-type and R-type BOXER collagen-promoting detection device according to claim 4, characterized in that: The cleaning assembly (212) also includes a plurality of brushes (212c) fixedly installed on the outer surface of the vertical rod (212a), and through holes (212d) formed on the outer surface of the brushes (212c).

6. The S-type and R-type BOXER collagen-promoting detection device according to claim 5, characterized in that: The flushing assembly (202) includes a water pipe (202a) fixedly installed on the outside of the cleaning tank (201) and a nozzle (202b) fixedly installed at the end of the water pipe (202a).

7. The S-type and R-type serotonin-promoting collagen detection device according to claim 6, characterized in that: The flushing assembly (202) also includes a booster pump (202c) fixedly installed at the bottom of the water pipe (202a) and a connecting pipe head (202d) fixedly installed at the other end of the water pipe (202a).

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