High-sensitivity cardiac troponin I detection reagent card

Abstract

The utility model discloses a high-sensitivity cardiac troponin I detection reagent card, and relates to the field of reagent cards. The sample pad comprises a shell, a rotating groove is formed in one side of the top of the shell, a convex groove is rotationally connected to the interior of the rotating groove through a rotating shaft, a sliding groove is formed in the bottom of the convex groove, and a sample pad is clamped in the sliding groove in a sliding mode. The sample pad can absorb temporarily stored blood and ensure that a sample can be subsequently transferred to the test paper strip, after the overturning convex groove is buckled back to the containing groove, the test paper strip is in close contact with the supporting block, and it is ensured that the blood can uniformly flow to the test paper strip; therefore, the accuracy and reliability of detection are improved, and the accuracy and integrity of subsequent operation are ensured.

Description

Technical Field

[0001] The utility model relates to the field of reagent cards, in particular to a high-sensitivity cardiac troponin I detection reagent card. Background Art

[0002] Troponin (Tn) is a group of contractile proteins present in skeletal muscle and myocardial cells. Cardiac troponin (cTn) is a group of proteins in the troponin complex that are related to myocardial contractile function. It consists of cardiac troponin T (cTnT, which is the part of the regulatory protein), troponin I (cTnI, which contains inhibitory factors) and troponin C (cTnI, which contains inhibitory factors). cTnI is a protein complex composed of three subunits: cTnC, cTnI subunit, and cTnI subunit. Under normal circumstances, the content of troponin TnI and TnT in the blood is very small. When myocardial cells are damaged, cardiac troponin I and T are released into the blood circulation. If a large area of ​​damage occurs, high concentrations of cardiac troponin I and T will appear in the blood, which determines its specificity in indicating myocardial damage. cTnI is the only TnI isomer in human myocardial fibers. About 3% of cTnI is free in the cytoplasm, and the rest is bound to myocardial structural proteins. When myocardial damage occurs, early free The isolated cTnI is rapidly released into the blood, and the cTnI level increases 4-6 hours after myocardial injury. Subsequently, the myocardial structural protein is degraded, and cTnI is continuously released, reaching a peak after 12-18 hours and maintaining for 5-7 days. cTnI is not expressed in skeletal muscle. Its biochemical properties determine its high specificity and sensitivity as an indicator of myocardial injury. Therefore, cTnI has been used as a standard diagnostic method for acute myocardial infarction, especially when there is no abnormality in the electrocardiogram test, the cTnI indicator can be used as a diagnostic method. Therefore, a highly sensitive cTnI kit is needed clinically.

[0003] The existing high-sensitivity cardiac troponin I detection reagent card requires a finger to be squeezed with a wire when in use, and then the blood is dripped into the interior of the receiving groove. During the operation, the blood drop may drip crookedly, causing contamination of the surrounding environment. Utility Model Content

[0004] Based on this, the purpose of the utility model is to provide a high-sensitivity cardiac troponin I detection reagent card to solve the technical problem that blood drops may drip crookedly during operation, causing pollution to the surrounding environment.

[0005] To achieve the above-mentioned purpose, the utility model provides the following technical solution: a high-sensitivity cardiac troponin I detection reagent card, comprising a shell, a top side of the shell is provided with a rotating groove, the interior of the rotating groove is rotatably connected to a convex groove via a rotating shaft, a sliding groove is provided at the bottom of the convex groove, and a sample pad is slidably engaged inside the sliding groove.

[0006] By adopting the above technical solution, by opening a rotating groove on one side of the top of the shell and rotating the connecting convex groove inside the rotating groove through a rotating shaft, the user can easily flip the convex groove to collect and test blood samples, making the operation easier and improving the user experience.

[0007] Furthermore, a limiting plate is fixedly connected to one side of the top of the convex groove, and the limiting plate is a key-shaped structure.

[0008] By adopting the above technical solution and setting a limit plate, the lifting operation of the convex groove can be facilitated, thereby facilitating the subsequent blood dripping operation, reducing the complexity of lifting the convex groove and improving the convenience of use.

[0009] Furthermore, a top block is fixedly connected to the inner bottom of the shell, and a test paper is arranged on the top of the top block.

[0010] By adopting the above technical solution, the design of the top block enables the test paper to reliably contact the sample pad, ensuring that blood can be reliably transferred to the test paper and realizing subsequent detection operations.

[0011] Furthermore, a support block is provided on one side of the top block, and a plurality of the support blocks are provided, and the plurality of the support blocks are linearly and evenly arranged.

[0012] By adopting the above technical solution, by setting a plurality of support blocks on one side of the top block, these support blocks are arranged linearly and evenly, which can more stably support the test paper and prevent it from bending or deformation during transportation and testing, which helps to improve the accuracy and reliability of the test.

[0013] Furthermore, a receiving groove is provided on one side of the rotating groove, and the receiving groove is matched with the convex groove.

[0014] By adopting the above technical solution, a receiving groove is opened on one side of the rotating groove and matched with the convex groove, a stable return space is provided for the convex groove, so that the convex groove can be accurately embedded in the receiving groove after flipping, ensuring the stability and reliability of the structure.

[0015] Furthermore, a mounting groove is provided at the bottom of the convex groove, and the mounting groove is fixedly connected to the sample pad.

[0016] By adopting the above technical solution, by opening a mounting groove at the bottom of the convex groove and fixedly connecting it to the sample pad, the stability and reliability of the sample pad are ensured, so that the sample pad can be firmly fixed on the convex groove and will not move or fall off during operation, thereby ensuring the accuracy and repeatability of the detection.

[0017] Furthermore, a support block is provided below the accommodating groove, and the top of the support block abuts against the test paper.

[0018] By adopting the above technical solution, by arranging a support block under the accommodating groove, it can be ensured that when the convex groove is engaged in the accommodating groove, the test paper can be stably supported. The top of the support block abuts against the test paper, providing a flat and solid supporting surface for the test paper, which helps to maintain the flatness and stability of the test paper.

[0019] In summary, the utility model mainly has the following beneficial effects:

[0020] 1. The utility model is provided with a shell and a convex groove, and the sample pad is turned upward by flipping the convex groove, so that the user can directly drop blood for sampling. The operation is simple and can effectively prevent blood from contaminating the surrounding environment. The sample pad can absorb and temporarily store blood to ensure that the sample can be transferred to the test strip later. After the convex groove is flipped back to the receiving groove, the test paper is in close contact with the support block, ensuring that the blood can flow evenly to the test paper, thereby improving the accuracy and reliability of the test, and further ensuring the accuracy and integrity of subsequent operations;

[0021] 2. The utility model provides a mounting groove and a support block, and directly fixes the sample pad by providing the mounting groove, thereby ensuring the stability of the sample pad and the accuracy of the position, avoiding the looseness or position deviation that may occur in the sliding engagement method, improving the reliability of the contact between the test paper and the sample pad, ensuring that the sample can be smoothly and accurately transferred from the sample pad to the test paper, and further improving the accuracy and efficiency of the test. BRIEF DESCRIPTION OF THE DRAWINGS

[0022] Figure 1 It is a three-dimensional structural schematic diagram of the utility model;

[0023] Figure 2 This is a bottom-up three-dimensional structural schematic diagram of the utility model;

[0024] Figure 3 It is a schematic diagram of a half-section structure of the utility model;

[0025] Figure 4 This is a schematic diagram of a half-section structure of the second embodiment of the present utility model;

[0026] Figure 5 It is a schematic diagram of the three-dimensional structure of the closed rotating groove of the first embodiment of the utility model.

[0027] In the figure: 1. shell; 2. rotating groove; 3. convex groove; 4. sliding groove; 5. sample pad; 6. limit plate; 7. top block; 8. test paper; 9. support block; 10. receiving groove; 11. installation groove; 12. support block. DETAILED DESCRIPTION

[0028] The following will be combined with the drawings in the embodiments of the utility model to clearly and completely describe the technical solutions in the embodiments of the utility model. The embodiments described below with reference to the drawings are exemplary and are only used to explain the utility model, and cannot be understood as limiting the utility model.

[0029] The following describes an embodiment of the utility model based on its overall structure.

[0030] Embodiment 1:

[0031] A high-sensitivity cardiac troponin I detection reagent card, such as Figure 1-Figure 5 As shown, it includes a shell 1, a rotating groove 2 is opened on one side of the top of the shell 1, a convex groove 3 is rotatably connected to the inside of the rotating groove 2 through a rotating shaft, a sliding groove 4 is opened at the bottom of the convex groove 3, and a sample pad 5 is slidably engaged inside the sliding groove 4. By opening the rotating groove 2 on one side of the top of the shell 1 and connecting the convex groove 3 to the rotating groove 2 through a rotating shaft, the user can easily flip the convex groove 3 to collect and test blood samples, making the operation easier and improving the user experience. At the same time, the sliding groove 4 opened at the bottom of the convex groove 3 and the sample pad 5 slidably engaged inside reduce the difficulty of production, and the sample pad 5 can be easily slid and engaged in the sliding groove 4, which is convenient for installation during production.

[0032] See also Figure 1 , Figure 2 , Figure 3 and Figure 5 A limiting plate 6 is fixedly connected to one side of the top of the convex groove 3, and the limiting plate 6 is a key-shaped structure. By setting the limiting plate 6, the lifting operation of the convex groove 3 can be facilitated, and then the subsequent blood dripping operation can be facilitated, which reduces the complexity of lifting the convex groove 3 and improves the convenience of use. At the same time, the key-shaped structure design of the limiting plate 6 increases the structural strength, so that the convex groove 3 will not be pressed into the accommodating groove 10 during transportation.

[0033] See also Figure 3A top block 7 is fixedly connected to the inner bottom of the shell 1, and a test strip 8 is arranged on the top of the top block 7. The design of the top block 7 enables the test strip 8 to reliably contact the sample pad 5, ensuring that the blood can be reliably transferred to the test strip 8 to achieve subsequent detection operations. At the same time, by fixing the top block 7 on the inner bottom of the shell 1, it can be ensured that the test strip 8 is stably supported and positioned, so that the test strip 8 can remain flat and stable during the detection process, thereby improving the accuracy and reliability of the detection.

[0034] See also Figure 3 A support block 9 is arranged on one side of the top block 7, and a plurality of support blocks 9 are arranged, and the plurality of support blocks 9 are arranged linearly and evenly. By arranging a plurality of support blocks 9 on one side of the top block 7, the support blocks are arranged linearly and evenly, which can more stably support the test paper 8 and prevent it from bending or deformation during transportation and detection, thereby helping to improve the accuracy and reliability of detection. At the same time, the arrangement of the plurality of support blocks 9 also increases the contact area between the test paper 8 and the housing 1, so that the test paper 8 can more reliably absorb and transfer the detection liquid, thereby further improving the accuracy and efficiency of the detection.

[0035] See also Figure 1 , Figure 2 , Figure 3 and Figure 5 A receiving groove 10 is provided on one side of the rotating groove 2, and the receiving groove 10 is matched with the convex groove 3. By providing the receiving groove 10 on one side of the rotating groove 2 and matching it with the convex groove 3, a stable return space is provided for the convex groove 3, so that the convex groove 3 can be accurately embedded in the receiving groove 10 after flipping, ensuring the stability and reliability of the structure. At the same time, the design of the receiving groove 10 also helps to protect the convex groove 3 and the sample pad 5 inside it from external contamination or damage. When the convex groove 3 is embedded in the receiving groove 10, it is within the protection of the shell 1, reducing contact with the outside world, thereby reducing the risk of contamination.

[0036] The implementation principle of the utility model is as follows: first, before the test is needed, the convex groove 3 is turned over so that the bottom of the convex groove 3 can be on the surface, and then the blood drop directly touches the sample pad 5 so that the sample pad 5 can absorb the blood, and then the convex groove 3 is turned over so that the convex groove 3 is buckled back into the inside of the receiving groove 10. At this time, the test paper 8 lifted by the support block 9 is in contact with each other, and the blood flows to the test paper 8. Then a diluent is added, and the diluent dilutes the blood and moves along the test paper 8 to complete the test. The support block 9 can ensure that the test paper 8 remains stable and is placed inside the housing 1.

[0037] Embodiment 2:

[0038] See also Figure 4A mounting groove 11 is provided at the bottom of the convex groove 3, and the mounting groove 11 is fixedly connected to the sample pad 5. By providing the mounting groove 11 at the bottom of the convex groove 3 and fixing it with the sample pad 5, the stability and reliability of the sample pad 5 are ensured, so that the sample pad 5 can be firmly fixed on the convex groove 3 and will not move or fall off during operation, thereby ensuring the accuracy and repeatability of the detection. At the same time, the fixed connection between the mounting groove 11 and the sample pad 5 improves the structural strength of the reagent card, and the manufacturer can glue the sample pad 5 in the mounting groove 11, thereby improving the production efficiency.

[0039] See also Figure 4 A support block 12 is provided below the receiving groove 10, and the top of the support block 12 abuts against the test paper 8. By providing the support block 12 below the receiving groove 10, it can be ensured that when the convex groove 3 is buckled in the receiving groove 10, the test paper 8 can be stably supported. The top of the support block 12 abuts against the test paper 8, providing a flat and solid supporting surface for the test paper 8, which helps to maintain the flatness and stability of the test paper 8. At the same time, the support block 12 helps to facilitate the transfer of blood in the test paper 8. When the convex groove 3 is buckled, the sample pad 5 and the test paper 8 are tightly fitted, and the sample on the sample pad 5 is transferred to the test paper 8, thereby improving the accuracy and efficiency of the detection.

[0040] The implementation principle of the utility model is as follows: firstly, as a replacement for the method of installing the sample pad 5 by sliding engagement in the first embodiment, a directly protruding fixed sample pad 5 is adopted to avoid using a protruding top block 7 to ensure contact, thereby improving the reliability of contact.

[0041] Parts not involved in the present invention are the same as the prior art or can be implemented by using the prior art, and will not be described in detail here.

[0042] Although an embodiment of the utility model has been shown and described, this specific embodiment is only an explanation of the utility model and is not a limitation of the utility model. The specific features, structures, materials or characteristics described may be combined in a suitable manner in any one or more embodiments or examples. After reading this specification, those skilled in the art may make modifications, substitutions and variations to the embodiments without creative contribution as needed without departing from the principles and purpose of the utility model. However, as long as they are within the scope of the claims of the utility model, they are protected by patent law.

Claims

1. A high-sensitivity cardiac troponin I detection reagent card, characterized in that: The invention comprises a housing (1), wherein a rotating groove (2) is provided on one side of the top of the housing (1), a convex groove (3) is rotatably connected to the interior of the rotating groove (2) via a rotating shaft, a sliding groove (4) is provided at the bottom of the convex groove (3), and a sample pad (5) is slidably engaged in the interior of the sliding groove (4).

2. The high-sensitivity cardiac troponin I detection reagent card according to claim 1, characterized in that: A limiting plate (6) is fixedly connected to one side of the top of the convex groove (3), and the limiting plate (6) is in a key-shaped structure.

3. The high-sensitivity cardiac troponin I detection reagent card according to claim 1, characterized in that: A top block (7) is fixedly connected to the inner bottom of the housing (1), and a test paper (8) is arranged on the top of the top block (7).

4. The high-sensitivity cardiac troponin I detection reagent card according to claim 3, characterized in that: A support block (9) is provided on one side of the top block (7), and a plurality of the support blocks (9) are provided, and the plurality of the support blocks (9) are linearly and evenly arranged.

5. The high-sensitivity cardiac troponin I detection reagent card according to claim 1, characterized in that: A receiving groove (10) is provided on one side of the rotating groove (2), and the receiving groove (10) is matched with the convex groove (3).

6. The high-sensitivity cardiac troponin I detection reagent card according to claim 1, characterized in that: A mounting groove (11) is provided at the bottom of the convex groove (3), and the mounting groove (11) is fixedly connected to the sample pad (5).

7. The high-sensitivity cardiac troponin I detection reagent card according to claim 5, characterized in that: A support block (12) is provided below the containing groove (10), and the top of the support block (12) is in contact with the test paper (8).

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