A high-throughput device for detecting peri-implantitis bacterial flora

By designing a high-throughput device containing partitions and distribution chambers, the cumbersome problems of disassembly and installation and cleaning of the peri-implant bacterial flora detection device are solved, and rapid cleaning and uniform distribution of samples are achieved, which improves detection efficiency and accuracy .

CN114634859BActive Publication Date: 2024-12-24THE 980TH HOSPITAL OF THE CHINESE PEOPLES LIBERATION ARMY JOINT LOGISTICS SUPPORT FORCE
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Patent Information

Application Number
CN202210302874.7
Authority / Receiving Office
CN · China
Patent Type
Patents(China)
Current Assignee / Owner
Filing Date
2022-03-24
Publication Date
2024-12-24
Estimated Expiration
2042-03-24

AI Technical Summary

Technical Problem

The existing periimplant bacterial bacteria detection device is complicated during disassembly and installation and cleaning, resulting in uneven detection effects, low working efficiency, and difficulty in cleaning, which increases the workload and time.

Method used

A high-throughput device is designed, including the main body, connecting pipe, air pipe, output pipe, partition, distribution chamber, liquid inlet hole and pressure block, and is quickly cleaned by clean water infusion and gas source startup, and through the partition and The distribution chamber ensures even distribution of samples, simplifies operation and improves efficiency.

Benefits of technology

It realizes rapid disassembly and installation and cleaning, avoids sample confusion, improves detection efficiency and work efficiency, reduces workload and time, and ensures the accuracy and uniformity of the test results.

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Abstract

The present invention relates to the technical field of bacterial detection, and discloses a high-throughput device for detecting peri-implantitis bacterial flora, comprising a main body, a connecting tube fixedly connected to the upper outer surface of the main body near the middle position, a trachea fixedly connected to the upper outer surface of the main body near the edge of one side, an output tube fixedly connected to the lower outer surface of the main body, a partition fixedly connected to the middle position of the inner surface of the main body, a first distribution chamber opened inside the main body above the partition, and a second distribution chamber opened inside the main body below the partition. The high-throughput device for detecting peri-implantitis bacterial flora has the advantages of fast disassembly and installation, timely cleaning, avoiding detection errors caused by sample mixing, low workload, high work efficiency, and reduced time required for detection, and solves the problems of complex working process, low work efficiency, slow cleaning, and uneven input.
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Description

Technical Field

[0001] The invention relates to the technical field of bacteria detection, in particular to a high-throughput device for detecting peri-implantitis bacteria. Background Art

[0002] Peri-implant mucositis refers to a reversible inflammation of the soft tissue around oral implants, the root cause of which is the bacterial microorganisms on the implants.

[0003] In the existing process of detecting peri-implantitis bacteria, when using a high-throughput method for detection, multiple hoses are usually connected to the infusion point for hanging drop sample liquid. However, in the actual operation process, because there are a large number of hoses connected to the infusion tube, it is very troublesome to replace the hoses. The partial unified input method will result in uneven output during operation, resulting in reduced detection effect. In addition, when cleaning, the workload is large, cleaning is difficult, and the work efficiency is low. Summary of the invention

[0004] 1. Technical issues to be solved

[0005] In view of the shortcomings of the prior art, the present invention provides a high-throughput device for detecting peri-implantitis bacteria, which has the advantages of fast disassembly and installation, timely cleaning, avoiding detection errors caused by sample mixing, low workload, high work efficiency, and reduced time required for detection, solving the problems of complex working process, low work efficiency, slow cleaning, and uneven input.

[0006] (II) Technical solution

[0007] To achieve the above-mentioned objectives, the present invention provides the following technical solutions: a high-throughput device for detecting peri-implantitis bacterial flora, comprising a main body, a connecting tube fixedly connected to the upper outer surface of the main body near the middle position, a trachea fixedly connected to the upper outer surface of the main body near the side edge, and an output tube fixedly connected to the lower outer surface of the main body.

[0008] Preferably, a partition is fixedly connected to the middle position of the inner surface of the main body, a first distribution chamber is opened inside the main body above the partition, a second distribution chamber is opened inside the main body below the partition, an input pipe is fixedly connected to the inner surface of the lower end of the main body, a partition plate is fixedly connected to the outer circular surface of the input pipe, a liquid inlet hole is opened on the outer surface of the upper end of the partition, an air cavity is opened inside the partition, and a pressure block is slidably connected to the outer surface of the lower end of the partition.

[0009] Preferably, an inlay groove is provided on the inner surfaces of the upper and lower ends of the main body near the front end, a sealing layer is fixedly connected to the inner surface of the inlay groove in the main body, and a baffle is slidably connected to the inner surface of the inlay groove provided in the main body.

[0010] Preferably, there are several liquid inlet holes in the partition, and they are evenly distributed in the partition. The liquid inlet holes in the partition pass through the partition and are connected with the second distribution chamber below the partition. The first distribution chamber, the liquid inlet holes, and the second distribution chamber are connected to each other, and the liquid inlet holes are not connected to the air cavity.

[0011] Preferably, the number of the output tubes is several, the number of the input tubes is twice the number of the output tubes, one input tube is connected to two output tubes, and the air pipe passes through the main body and is connected to the air cavity in the partition.

[0012] Preferably, the pressing block is made of foam, and a sealing gasket is provided at the connection between the pressing block and the partition.

[0013] Compared with the prior art, the present invention provides a high-throughput device for detecting peri-implantitis bacterial flora, which has the following beneficial effects:

[0014] 1. The high-throughput device for detecting peri-implantitis bacterial flora can complete the cleaning by connecting clean water to the connecting pipe and injecting clean water into the main body, starting the air source to make the clean water flow out through the output pipe, and by pulling out the baffle on the main body, the inside of the main body can be detected to see whether it is clean. The operation is simple, the workload is reduced, and the work efficiency of the staff is improved.

[0015] 2. The high-throughput device for detecting peri-implantitis bacterial flora starts the sample tube connected to the connecting tube, and the sample liquid enters the first distribution chamber, passes through the various liquid inlet holes on the partition, and then allows the sample liquid to enter the bottom through the various liquid inlet holes, thereby avoiding the sample being concentrated in the middle, resulting in no sample output from the output tubes at other positions, ensuring the uniformity of the sample, and can enter the second distribution chamber through the liquid inlet holes on the partition. When the sample enters the second distribution chamber, the first distribution in the first distribution chamber allows the sample to be input into each input tube of the second distribution chamber, and can prevent the sample from converging between the second distribution chambers through the partition plate, thereby ensuring the uniformity of the sample in the second distribution chamber. BRIEF DESCRIPTION OF THE DRAWINGS

[0016] Figure 1 It is a schematic diagram of the overall internal structure of the present invention;

[0017] Figure 2 It is a schematic diagram of the overall structure of the present invention;

[0018] Figure 3 This is a schematic diagram of the internal structure of the partition of the present invention;

[0019] Figure 4 It is a schematic diagram of the overall structure of one side of the present invention.

[0020] Among them: 1. main body; 2. connecting pipe; 3. air pipe; 4. output pipe; 5. partition; 6. first distribution chamber; 7. second distribution chamber; 8. input pipe; 9. partition plate; 10. liquid inlet hole; 11. air cavity; 12. pressing block; 13. baffle; 14. inlay groove; 15. sealing layer. DETAILED DESCRIPTION

[0021] The following will be combined with the drawings in the embodiments of the present invention to clearly and completely describe the technical solutions in the embodiments of the present invention. Obviously, the described embodiments are only part of the embodiments of the present invention, not all of the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the present invention.

[0022] Embodiment 1, as Figure 1-4 As shown, it includes a main body 1, a connecting pipe 2 is fixedly connected to the upper outer surface of the main body 1 near the middle position, an air pipe 3 is fixedly connected to the upper outer surface of the main body 1 near the position of one side edge, and an output pipe 4 is fixedly connected to the lower outer surface of the main body 1. Inlay grooves 14 are provided on the inner surfaces of the upper and lower ends of the main body 1 near the front end, a sealing layer 15 is fixedly connected to the inner surface of the inlay groove 14 in the main body 1, and a baffle 13 is slidably connected to the inner surface of the inlay groove 14 provided in the main body 1. Cleaning can be completed by externally connecting clean water at the connecting pipe 2 to the inside of the main body 1 and starting the air source to make the clean water flow out through the output pipe 4. By pulling out the baffle 13 on the main body 1, the inside of the main body 1 can be inspected to see if it is clean. The operation is simple, the workload is reduced, and the work efficiency of the staff is improved.

[0023] Embodiment 2, as Figure 1-3As shown, a partition 5 is fixedly connected to the middle position of the inner surface of the main body 1, a first distribution chamber 6 is opened inside the main body 1 above the partition 5, and a second distribution chamber 7 is opened inside the main body 1 below the partition 5. An input pipe 8 is fixedly connected to the inner surface of the lower end of the main body 1, and a partition plate 9 is fixedly connected to the outer surface of the input pipe 8. A liquid inlet hole 10 is opened on the upper outer surface of the partition 5, and an air cavity 11 is opened inside the partition 5. A pressing block 12 is slidably connected to the outer surface of the lower end of the partition 5. By starting the sample tube connected to the connecting tube 2, the sample liquid enters the first distribution chamber 6. In the chamber 6, the sample liquid can enter the bottom through each liquid inlet hole 10 on the partition 5, so as to avoid the sample being concentrated in the middle, resulting in no sample output from the output tube 4 at other positions, thereby ensuring the uniformity of the sample. The sample can enter the second distribution chamber 7 through the liquid inlet hole 10 on the partition 5. When the sample enters the second distribution chamber 7, the first distribution of the first distribution chamber 6 is used to make each input tube 8 of the second distribution chamber 7 have the input of the sample, and the partition plate 9 can be used to prevent the sample from converging between the second distribution chambers 7, thereby ensuring the uniformity of the sample in the second distribution chamber 7.

[0024] Working principle: When using this device, first connect the sample tube to the upper end of the connecting tube 2, and connect the gas source to the upper end of the gas tube 3. When working, first move the main body 1 to the target position, start the sample tube connected to the connecting tube 2, and the sample liquid enters the first distribution chamber 6, through the various liquid inlet holes 10 on the partition 5, and then the sample liquid can enter the bottom through the various liquid inlet holes 10, avoiding the concentration of samples in the middle, resulting in no sample output from the output tubes 4 at other positions, ensuring the uniformity of the sample, and can enter the second distribution chamber 7 through the liquid inlet holes 10 on the partition 5. When the sample reaches the second distribution chamber 7, the first distribution of the first distribution chamber 6 allows each input tube 8 of the second distribution chamber 7 to have the input of the sample, and can pass through the partition plate 9 to prevent the sample from converging between the second distribution chamber 7, thereby ensuring the uniformity of the sample in the second distribution chamber 7, and by connecting two input tubes 8 to an output tube 4, it is ensured that the output tube 4 can output the sample. After the sample enters the second distribution chamber 7, when a hanging drop sample is required, the gas source gas connected to the air pipe 3 is started to enter the air cavity 11 of the partition plate 5 through the air pipe 3. With the input of the gas, the gas The pressure in the cavity 11 increases, and begins to apply pressure to the pressing block 12, which then moves the pressing block 12 downward. As the pressing block 12 moves, the pressing block 12 begins to squeeze the sample in the second distribution chamber 7, so that the sample enters the output tube 4 for hanging droplets. This is completed once, and the main body 1 continues to be moved to other targets for hanging droplets. During the movement of the main body 1, the gas source is turned off. At this time, as the sample at the connecting tube 2 continues to be input, the sample in the second distribution chamber 7 increases. The foam pressing block 12 lacks the input gas from the gas source, resulting in a decrease in the internal pressure, and the sample exerts pressure on the pressure. The buoyancy generated by the block 12 causes the pressing block 12 to rise. When the main body 1 moves to the target position, the pressing block 12 returns to its original position. At this time, continuing to start the air source can move the pressing block 12 downward, and the hanging drop can be continued until the sample is finished. When cleaning, it is only necessary to connect clean water to the connecting pipe 2 and pour clean water into the main body 1, and start the air source to make the clean water flow out through the output pipe 4 to complete the cleaning. By pulling out the baffle 13 on the main body 1, the inside of the main body 1 can be inspected to see if it is clean. The operation is simple, the workload is reduced, and the work efficiency of the staff is improved.

[0025] Although embodiments of the present invention have been shown and described, it will be appreciated by those skilled in the art that various changes, modifications, substitutions and variations may be made to the embodiments without departing from the principles and spirit of the present invention, and that the scope of the present invention is defined by the appended claims and their equivalents.

Claims

1. A high-throughput device for detecting peri-implantitis bacterial flora, comprising a main body (1), characterized in that: A connecting pipe (2) is fixedly connected to a position near the middle of the upper outer surface of the main body (1), an air pipe (3) is fixedly connected to a position near the edge of one side of the upper outer surface of the main body (1), an output pipe (4) is fixedly connected to a lower outer surface of the main body (1), a partition (5) is fixedly connected to a position in the middle of the inner surface of the main body (1), a first distribution chamber (6) is provided inside the main body (1) above the partition (5), a second distribution chamber (7) is provided inside the main body (1) below the partition (5), an input pipe (8) is fixedly connected to the inner surface of the lower end of the main body (1), a partition plate (9) is fixedly connected to the outer surface of the input pipe (8), a liquid inlet hole (10) is provided on the upper outer surface of the partition (5), an air cavity (11) is provided inside the partition (5), and a pressure block (12) is slidably connected to the lower outer surface of the partition (5); The number of the liquid inlet holes (10) in the partition (5) is several and evenly distributed in the partition (5); the liquid inlet holes (10) in the partition (5) penetrate the partition (5) and communicate with the second distribution chamber (7) below the partition (5); the first distribution chamber (6), the liquid inlet hole (10) and the second distribution chamber (7) are mutually communicated; the liquid inlet hole (10) and the air cavity (11) are not communicated; the number of the output pipes (4) is several; the number of the input pipes (8) is twice the number of the output pipes (4); one input pipe (8) is communicated with two output pipes (4); the air pipe (3) penetrates the main body (1) and communicates with the air cavity (11) in the partition (5); When using the high-throughput device for detecting peri-implantitis bacterial flora, the main body (1) is first moved to the target position, the sample tube connected to the connecting tube (2) is started, and the sample liquid enters the first distribution chamber (6), passes through the various liquid inlet holes (10) on the partition (5), and then the sample liquid can enter the bottom through the various liquid inlet holes (10). When the sample enters the second distribution chamber 7, when a hanging drop sample is required, the gas source connected to the air pipe (3) is started to enter the air cavity (11) of the partition (5) through the air pipe (3). As the gas is input, the air cavity (11) The pressure inside increases, and begins to exert pressure on the pressing block (12), which then causes the pressing block (12) to move downward. As the pressing block (12) moves, the pressing block (12) begins to squeeze the sample in the second distribution chamber (7), causing the sample to enter the output pipe (4) and form a hanging drop. The gas source is then turned off. At this time, as the sample at the connecting pipe (2) continues to be input, the sample in the second distribution chamber (7) increases. Due to the lack of input gas from the gas source, the internal pressure of the pressing block (12) decreases, and the buoyancy generated by the sample on the pressing block (12) causes the pressing block (12) to rise, and the pressing block (12) returns to its original position.

2. A high-throughput device for detecting peri-implantitis bacterial flora according to claim 1, characterized in that: The upper and lower inner surfaces of the main body (1) are provided with inlay grooves (14) near the front end, the inner surface of the inlay groove (14) in the main body (1) is fixedly connected to a sealing layer (15), and the inner surface of the inlay groove (14) provided in the main body (1) is slidably connected to a baffle (13).

3. A high-throughput device for detecting peri-implantitis bacterial flora according to claim 1, characterized in that: The material of the pressing block (12) is foam, and a sealing gasket is provided at the connection between the pressing block (12) and the partition (5).