Internal secretion hydrops sampler

By designing an endocrine effusion sampler, using the combined structure of the test tube and the bottom plate, the effective interception and output of the middle section of the endocrine effusion is achieved, which solves the problem of inaccurate sampling in the existing technology and improves the detection results. accuracy.

CN222466950UInactive Publication Date: 2025-02-14余娜
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Patent Information

Application Number
CN202322849501.4
Authority / Receiving Office
CN · China
Patent Type
Utility models(China)
Current Assignee / Owner
Filing Date
2023-10-23
Publication Date
2025-02-14
Estimated Expiration
Not applicable · inactive patent

AI Technical Summary

Technical Problem

Existing samplers are not easy to select the middle-section fluid of endocrine effusion, resulting in inaccurate detection results.

Method used

An endocrine effusion sampler is designed. Through the combination of test tube, bottom plate, liquid aspirator and syringe, the structure of slope and sealing ring is used to realize the liquid interception and output in the test tube, so that the middle section of liquid can be effectively extracted.

Benefits of technology

By intercepting the middle section of liquid, the accuracy of the detection results is improved, and the problem of inaccurate sampling in the prior art is solved.

✦ Generated by Eureka AI based on patent content.

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Abstract

The utility model discloses an endocrine effusion sampler, which belongs to the field of samplers and comprises a test tube, a bottom plate is movably mounted on the test tube, a liquid suction needle is movably connected to one side of the bottom plate, an injector is movably connected to the other side of the bottom plate, an inner table is fixedly connected to the bottom plate, and a connecting ring is fixedly connected to the edge of the bottom plate. The inner table is located on the inner side of the connecting ring, a first sealing ring is fixedly connected to the inner table, a second sealing ring is fixedly connected to the upper portion of the inner wall of the connecting ring, the liquid suction needle is inserted into a corresponding organ or tissue, then the injector is pulled, negative pressure is formed in the test tube, effusion enters the test tube, and after part of the effusion flows into the test tube, the liquid suction needle is inserted into the test tube. The opening of the test tube is moved to the position of the slope, so that liquid in the tube flows out through the outlet, then the test tube is reset downwards, the injection tube continues to be drawn, and effusion continues to be extracted, so that the test tube is convenient to intercept interrupted liquid, and the detection result is more accurate through the intercepted middle-section liquid.
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Description

Technical Field

[0001] The utility model relates to the field of samplers, in particular to an endocrine effusion sampler. Background Art

[0002] Endocrine system, an anatomical term, is referred to as endocrine system for short. It refers to the endocrine glands throughout the body. It is another important functional regulation system besides the nervous system. It can be divided into two categories: one is the visible organs that exist independently in morphology and structure, namely endocrine organs, such as pituitary gland, pineal gland, thyroid gland, parathyroid gland, thymus gland and adrenal gland; the other is the endocrine cell clusters dispersed in other organs and tissues, namely endocrine tissues, such as islets in the pancreas, interstitial cells in the testicles, etc. Effusion refers to the situation where there is an increase in the amount of fluid in some parts or organs of the body where there should not be fluid or there should be a small amount of fluid. When fluid accumulates in an organ or tissue in the endocrine system, it is necessary to sample it through a sampler. However, since the liquid drawn by the sampler is easily contaminated by external impurities, such as impurities in the sampler pipe, most samplers use mid-section liquid when sampling to make the results more accurate. However, it is not easy for existing samplers to select mid-section liquid, so it needs to be improved. Utility Model Content

[0003] The main purpose of the utility model is to provide an endocrine effusion sampler, which can effectively solve the problems in the background technology.

[0004] In order to achieve the above purpose, the technical solution adopted by the utility model is:

[0005] An endocrine effusion sampler comprises a test tube, wherein the test tube is movably mounted with a base plate, a pipette needle is movably connected to one side of the base plate, a syringe is movably connected to the other side of the base plate, an inner platform is fixedly connected to the base plate, a connecting ring is fixedly connected to the edge of the base plate, and the inner platform is located on the inner side of the connecting ring, a No. 1 sealing ring is fixedly connected to the inner platform, a No. 2 sealing ring is fixedly connected to the upper part of the inner wall of the connecting ring, and a No. 1 connecting tube and a No. 2 connecting tube are fixedly connected to the middle part of the base plate.

[0006] Preferably, the test tube is movably mounted on the No. 1 sealing ring, and the No. 1 sealing ring is located inside the test tube, the No. 2 sealing ring is located on the outer wall of the test tube, and the test tube is located between the No. 1 sealing ring and the No. 2 sealing ring.

[0007] Preferably, a slope is provided at the upper portion of the No. 1 sealing ring, and the slope is also located at the inner side of the test tube.

[0008] Preferably, one end of the No. 1 connecting tube and the No. 2 connecting tube passes through the inner platform and extends into the test tube.

[0009] Preferably, the other end of the No. 1 connecting tube is fixedly connected to the No. 1 hose, and the No. 1 connecting tube is fixedly connected to the pipetting needle via the No. 1 hose.

[0010] Preferably, the other end of the No. 2 connecting tube is fixedly connected to a No. 2 hose, and the No. 2 connecting tube is fixedly connected to the syringe via the No. 2 hose.

[0011] Preferably, an outlet is fixedly mounted on the connecting ring.

[0012] Compared with the prior art, the utility model has the following beneficial effects:

[0013] In the utility model, the aspiration needle is inserted into the corresponding organ or tissue, and then the syringe is pulled to form a negative pressure in the test tube, so that the accumulated fluid enters the test tube through a No. 1 hose and a No. 1 connecting tube. After part of the accumulated fluid flows into the test tube, the test tube is pulled upward to move the test tube mouth to a slope position, so that the liquid in the tube flows out, enters the bottom plate, and flows out through the outlet position. Then the test tube is reset downward, and the injection tube is continuously pulled to form a negative pressure, thereby continuing to extract the accumulated fluid, making it easy for the test tube to intercept the interrupted liquid, and the detection result is more accurate by intercepting the middle section of the liquid. BRIEF DESCRIPTION OF THE DRAWINGS

[0014] Figure 1 It is a schematic diagram of the overall structure of the utility model;

[0015] Figure 2 It is a structural schematic diagram of the bottom plate and the connecting ring of the utility model;

[0016] Figure 3 It is a structural schematic diagram of the No. 2 hose of the utility model.

[0017] In the figure: 1. test tube; 2. bottom plate; 3. connecting ring; 4. inner platform; 5. sealing ring No. 1; 6. ramp; 7. sealing ring No. 2; 8. outlet; 9. connecting tube No. 1; 10. connecting tube No. 2; 11. flexible tube No. 1; 12. pipetting needle; 13. flexible tube No. 2; 14. syringe. DETAILED DESCRIPTION

[0018] In order to make the technical means, creative features, objectives and effects achieved by the present invention easy to understand, the present invention is further described below in conjunction with specific implementation methods.

[0019] like Figure 1-3As shown, an endocrine effusion sampler comprises a test tube 1, on which a bottom plate 2 is movably mounted, a liquid aspiration needle 12 is movably connected to one side of the bottom plate 2, a syringe 14 is movably connected to the other side of the bottom plate 2, an inner platform 4 is fixedly connected to the bottom plate 2, a connecting ring 3 is fixedly connected to the edge of the bottom plate 2, and the inner platform 4 is located at the inner side of the connecting ring 3, a No. 1 sealing ring 5 is fixedly connected to the inner platform 4, a No. 2 sealing ring 7 is fixedly connected to the upper part of the inner wall of the connecting ring 3, the test tube 1 is movably mounted on the No. 1 sealing ring 5, and the No. 1 sealing ring 5 is located in the test tube 1, the No. 2 sealing ring 7 is located on the outer wall of the test tube 1, and the test tube 1 is fixedly connected to the inner platform 4. A slope 6 is provided on the upper portion of the No. 1 sealing ring 5 between the No. 1 sealing ring 5 and the No. 2 sealing ring 7. The slope 6 is also located on the inner side of the test tube 1. An outlet 8 is fixedly installed on the connecting ring 3. The No. 1 sealing ring 5 and the No. 2 sealing ring 7 are provided on the inner and outer sides of the test tube 1 for sealing. When the test tube 1 moves upward, the inner and outer walls of the test tube 1 move on the No. 1 sealing ring 5 and the No. 2 sealing ring 7 respectively. When the mouth of the test tube 1 moves to the position of the slope 6, the sealing state between the test tube 1 and the No. 1 sealing ring 5 is released, and the sealing between the test tube 1 and the No. 2 sealing ring 7 continues to prevent the liquid from flowing to the upper position of the connecting ring 3.

[0020] A connecting tube No. 1 9 and a connecting tube No. 2 10 are fixedly connected to the middle position of the bottom plate 2, one end of the connecting tube No. 1 9 and the connecting tube No. 2 10 passes through the inner platform 4 and extends into the test tube 1, the other end of the connecting tube No. 1 9 is fixedly connected to a hose No. 11, and the connecting tube No. 1 9 is fixedly connected to a liquid-pipetting needle 12 via the hose No. 11, the other end of the connecting tube No. 2 10 is fixedly connected to a hose No. 2 13, and the connecting tube No. 2 10 is fixedly connected to a syringe 14 via the hose No. 2 13, one side of the test tube 1 is connected to the liquid-pipetting needle 12 via the connecting tube No. 1 9 and the hose No. 11, and the other side of the test tube 1 is connected to the syringe 14 via the connecting tube No. 2 10 and the hose No. 2 13, so that the syringe 14 forms a negative pressure by sucking the gas in the test tube 1, so that the test tube 1 is convenient for sucking the accumulated fluid.

[0021] It should be noted that the utility model is an endocrine effusion sampler. The test tube 1 is inserted into the connecting ring 3. The test tube 1 is movably connected to the No. 2 sealing ring 7. The No. 1 sealing ring 5 is movably connected to the outer wall of the test tube 1, so that two layers of sealing are formed on the inner and outer sides of the test tube 1 through the No. 2 sealing ring 7 and the No. 1 sealing ring 5. Then the push rod of the syringe 14 is pulled. After the push rod is pulled partially, the syringe 14 sucks part of the gas in the test tube 1 through the No. 2 hose 13, so that the gas in the test tube 1 is Negative pressure is formed, and the negative pressure in the test tube 1 causes the test tube 1 to draw the accumulated fluid in a certain organ or tissue of the endocrine system through the No. 1 hose 11 and the aspiration needle 12. The accumulated fluid enters the test tube 1 through the No. 1 hose 11 and the No. 1 connecting tube 9, and the accumulated fluid accumulates on the inner platform 4. Then the test tube 1 is pulled upward, so that the mouth of the test tube 1 moves upward to the position of the slope 6 of the No. 1 sealing ring 5, so that the sealing state between the test tube 1 and the No. 1 sealing ring 5 is released, so that the liquid in the test tube 1 flows out from between the slope 6 and the test tube 1. The liquid flows out of the gap and flows into the bottom plate 2 and is located in the connecting ring 3. The outer position of the connecting ring 3 is fixedly connected with an outlet 8, so that the liquid flows out through the outlet 8. An external container is arranged below the outlet 8 to receive the accumulated liquid. Since the sealing state of the test tube 1 and the No. 1 sealing ring 5 is released, the negative pressure in the test tube 1 is eliminated, and the power for sucking the accumulated liquid disappears. When the accumulated liquid in the test tube 1 flows out, the test tube 1 is worked downward, so that the test tube 1 moves downward on the No. 1 sealing ring 5, so that the test tube 1 The mouth of the tube moves downward and contacts the bottom surface of the bottom plate 2, so that the test tube 1 and the No. 1 sealing ring 5 are sealed again, and then the syringe 14 continues to suck the gas through the push rod, so that the gas in the test tube 1 forms a negative pressure again, so that the test tube 1 sucks the accumulated liquid again, thereby drawing the middle liquid. When an appropriate amount of accumulated liquid is drawn, the liquid aspiration needle 12 is pulled out, and the test tube 1, the bottom plate 2 and other structures are inverted to collect the accumulated liquid in the test tube 1. By detecting the accumulated liquid in the middle section of the test tube 1, the result is more accurate.

[0022] The above shows and describes the basic principle and main features of the utility model and the advantages of the utility model. It is only a preferred embodiment of the utility model, and its description is more specific and detailed, but it cannot be understood as limiting the scope of the utility model. The technicians in this industry should understand that the utility model is not limited by the above embodiments. The embodiments can be changed, modified, replaced and deformed without departing from the principle and purpose of the utility model. These changes and improvements fall within the scope of the utility model to be protected. The scope of protection of the utility model is defined by the attached claims and their equivalents.

Claims

1. An endocrine effusion sampler, comprising a test tube (1), wherein the test tube (1) is movably mounted with a bottom plate (2), a liquid aspiration needle (12) is movably connected to one side of the bottom plate (2), and a syringe (14) is movably connected to the other side of the bottom plate (2), characterized in that: The bottom plate (2) is fixedly connected to an inner platform (4), the edge of the bottom plate (2) is fixedly connected to a connecting ring (3), and the inner platform (4) is located inside the connecting ring (3), the inner platform (4) is fixedly connected to a first sealing ring (5), the upper part of the inner wall of the connecting ring (3) is fixedly connected to a second sealing ring (7), and the middle part of the bottom plate (2) is fixedly connected to a first connecting pipe (9) and a second connecting pipe (10).

2. The endocrine effusion sampler according to claim 1, characterized in that: The test tube (1) is movably mounted on the No. 1 sealing ring (5), and the No. 1 sealing ring (5) is located inside the test tube (1), the No. 2 sealing ring (7) is located on the outer wall of the test tube (1), and the test tube (1) is located between the No. 1 sealing ring (5) and the No. 2 sealing ring (7).

3. An endocrine effusion sampler according to claim 2, characterized in that: The upper portion of the No. 1 sealing ring (5) is provided with a slope (6), and the slope (6) is also located at the inner side of the test tube (1).

4. The endocrine effusion sampler according to claim 3, characterized in that: One end of the No. 1 connecting tube (9) and the No. 2 connecting tube (10) passes through the inner platform (4) and extends into the test tube (1).

5. The endocrine effusion sampler according to claim 4, characterized in that: The other end of the No. 1 connecting tube (9) is fixedly connected to a No. 1 hose (11), and the No. 1 connecting tube (9) is fixedly connected to the liquid aspiration needle (12) via the No. 1 hose (11).

6. The endocrine effusion sampler according to claim 5, characterized in that: The other end of the No. 2 connecting tube (10) is fixedly connected to a No. 2 hose (13), and the No. 2 connecting tube (10) is fixedly connected to the syringe (14) via the No. 2 hose (13).

7. The endocrine effusion sampler according to claim 6, characterized in that: An outlet (8) is fixedly mounted on the connecting ring (3).