Double determination kit for human chorionic gonadotropin
By designing an HCG detection test paper box containing a sealing cover, multiple sets of reagent paper and urine buffer tank, the problems of unsafe use, inaccurate detection, and waste of resources in the prior art are solved, and multiple sets of simultaneous detection are realized. Reagent paper can be replaced with efficient and safe detection effect.
Patent Information
- Application Number
- CN202420915913.5
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- Filing Date
- 2024-04-29
- Publication Date
- 2025-02-11
- Estimated Expiration
- 2034-04-29
AI Technical Summary
The existing HCG test strips are not safe enough to perform multiple sets of tests at the same time. Single detection cannot ensure accuracy. Multiple reagents are required for multiple tests. The process is cumbersome and errors are prone to, and the safety is insufficient. It cannot be fully sealed and cannot be carried out. Reuse, waste of resources.
A dual determination kit for human chorionic gonadotropin is designed, including a sealing cover, the kit body, reagent paper and urine buffer tank. The sealing cover can be opened sideways through the hinged ears, and multiple detection panels are provided. The replacing reagent paper, the urine buffer tank and the reagent paper are connected through a flow guide, achieving multiple sets of testing and accurate judgment.
The safety and accuracy of the kit is realized, allowing multiple sets of tests to be performed simultaneously, and the reagent paper can be replaced and reused to avoid waste of resources. It also has a fully sealed design, which improves the safety and efficiency of the test.
Smart Images
Figure CN222461473U_ABST
Abstract
Description
Technical Field
[0001] The utility model relates to the relevant field of test kits, in particular to a human chorionic gonadotropin double determination test kit. Background Art
[0002] Human chorionic gonadotropin test strips refer to HCG test strips. Usually, the method of use is to soak it in urine for 5-10 seconds, lay it flat for 3-5 minutes, and read the results. The specific analysis is as follows:
[0003] HCG test strips can usually be used to self-detect whether you are pregnant. If the result is positive or weakly positive, it generally indicates that you are pregnant. If the result is negative, it indicates that you are not pregnant. When using the HCG test strips, you need to immerse the end marked with "MAX" in urine for 5-10 seconds, lay the HCG test strip flat, and wait for 3-5 minutes. If a bar appears in the C area and no red appears in the T area, the result is negative. If obvious red strips appear in both the C and T areas, the result is positive. If the colors of the two areas are one dark and one light, the result is weakly positive. If only a red strip appears in the T area, the result is invalid and needs to be retested. If the result is positive or weakly positive, it is recommended to go to the hospital immediately for a blood HCG test, a B-type ultrasound test, etc. to determine whether you are pregnant;
[0004] For example, the authorized patent with authorization announcement number CN216792249U (pregnancy test device for obstetrics and gynecology): including a pregnancy test stick body, a detection mechanism is fixedly installed in the pregnancy test stick body, a protective mechanism is arranged outside the pregnancy test stick body, the detection mechanism includes a plastic liner, the plastic liner is fixedly installed in the pregnancy test stick body, a pregnancy test paper for testing is fixedly installed in the plastic liner, an observation window for observing the pregnancy test paper is fixedly installed on the side wall of the pregnancy test stick body, a display slot for the exposed pregnancy test paper is provided on the side wall of the plastic liner, and the positions of the observation window and the display slot correspond to each other. The utility model realizes more accurate absorption of urine by controlling the movement of urine on the pregnancy test paper, and has strong protection for the pregnancy test paper, effectively preventing accidental touch, which causes urine to leave the pregnancy test stick body, and improves the detection effect of the equipment;
[0005] The above-mentioned existing technologies are not safe to use and cannot perform multiple groups of tests at the same time. The accuracy of a single test cannot be guaranteed. Multiple reagents are required for multiple tests, which is not only cumbersome, but also prone to errors. They are not safe enough, cannot be fully sealed, cannot be reused, and waste resources. Utility Model Content
[0006] The purpose of the utility model is to provide a human chorionic gonadotropin dual determination kit to solve the problems proposed in the above-mentioned background technology that the use is not safe enough, multiple groups of tests cannot be performed simultaneously, single word detection cannot ensure accuracy, multiple reagents are required for multiple tests, which is not only cumbersome, but also prone to errors, insufficient safety, cannot be fully sealed, cannot be reused, and wastes resources.
[0007] To achieve the above-mentioned purpose, the utility model provides the following technical solutions: a human chorionic gonadotropin dual determination kit, comprising a sealing cover, a kit body, reagent paper and a urine cache tank, the top of the kit body is provided with a sealing cover that can be controlled to be opened laterally through a hinged ear, the middle of the kit body is provided with a detection panel, the detection panel is provided with a plurality of reagent papers, and the reagent papers are configured to be replaceable, a urine cache tank is provided on one side of the top of the kit body, and a liquid filling fun is provided inside the urine cache tank.
[0008] In a further embodiment, an observation window is provided in the middle of the sealing cover, and a protective cover is provided on the side of the sealing cover.
[0009] In a further embodiment, a hinged ear is provided on one side of the reagent kit body, and the hinged ear is hinged to the side edge of the sealing cover.
[0010] In a further embodiment, a display port is provided on the reagent paper, and a protective groove is provided on the display port.
[0011] In a further embodiment, an ear frame is provided on one side of the top of the sealing cover, and the ear frame is hinged to the handle frame, and the ear frame is connected to the sealing cover through a connector.
[0012] In a further embodiment, a plurality of guide tubes are provided on the outer side of the urine buffer tank, and one ends of the plurality of guide tubes are respectively connected to a plurality of reagent papers.
[0013] Compared with the prior art, the beneficial effects of the utility model are:
[0014] 1. The outer side of the reagent box body of the utility model is sealed with a sealing cover, through which the reagent box body can be sealed and fixed, and can be safely protected. A handle frame is provided in the middle of the top of the sealing cover, and the handle frame is used to facilitate the carrying of the reagent box body.
[0015] 2. A detection panel is provided in the middle of the reagent box body of the utility model, and a plurality of reagent papers are provided on the detection panel. Display ports are provided on the reagent papers, and a urine cache groove is provided on one side of the top of the reagent box body, and a liquid filling hopper is provided in the middle of the top of the urine cache groove. The urine cache groove and the reagent paper are connected by a guide tube, so that multiple groups of tests can be carried out at the same time, and accurate judgments can be made according to the results of multiple groups of tests, and the reagent papers can be replaced and reused to avoid waste of resources. BRIEF DESCRIPTION OF THE DRAWINGS
[0016] Figure 1 This is a schematic diagram of the structure of a human chorionic gonadotropin dual determination kit of the utility model;
[0017] Figure 2 It is a top view of the main body of the test kit of the utility model;
[0018] Figure 3 This is a front view of the main body of the test kit of the utility model;
[0019] Figure 4 This is a top view of the handle frame of the utility model;
[0020] Figure 5 It is a structural schematic diagram of part A of the utility model.
[0021] In the figure: 1. Protective cover; 2. Sealing cover; 3. Articulated ear; 4. Reagent box body; 5. Detection panel; 6. Reagent paper; 7. Display port; 8. Observation window; 9. Urine buffer tank; 10. Liquid filling bucket; 11. Handle rack; 12. Guide tube; 13. Connector; 14. Ear rack. DETAILED DESCRIPTION
[0022] The technical solutions in the embodiments of the present invention will be described clearly and completely below in conjunction with the drawings in the embodiments of the present invention. Obviously, the described embodiments are only part of the embodiments of the present invention, rather than all of the embodiments.
[0023] See also Figure 1-5 The utility model provides an embodiment: a human chorionic gonadotropin dual determination kit, comprising a sealing cover 2, a kit body 4, a reagent paper 6 and a urine buffer tank 9, the top of the kit body 4 is provided with a sealing cover 2 which can be opened laterally through a hinged ear 3, the middle of the kit body 4 is provided with a detection panel 5, a plurality of reagent papers 6 are provided on the detection panel 5, and the reagent papers 6 are set to a replaceable structure, a urine buffer tank 9 is provided on one side of the top of the kit body 4, and a liquid adding funnel 10 is provided inside the urine buffer tank 9.
[0024] The top of the reagent box body 4 can be sealed by the sealing cover 2, and urine detection can be performed through the detection panel 5. Multiple reagent papers 6 can be installed, and urine can be cached through the urine buffer tank 9. The addition of urine is convenient through the liquid adding funnel 10, and urine can be diverted to multiple reagent papers 6 through the guide tube 12. The reagent paper 6 is provided with a display port 7, and the display port 7 is provided with a protective groove, and the display port 7 is used to display the test results. Multiple guide tubes 12 are provided on the outside of the urine buffer tank 9, and one end of the multiple guide tubes 12 is respectively connected to the multiple reagent papers 6, and the guide tubes 12 are used to divert urine.
[0025] An observation window 8 is provided in the middle of the sealing cover 2, and a protective cover 1 is provided on the side of the sealing cover 2. The observation window 8 is used to observe the test results. A hinged ear 3 is provided on one side of the reagent box body 4, and the hinged ear 3 is hinged to the side of the sealing cover 2. The hinged ear 3 facilitates the hinged connection with the sealing cover 2, and the hinged ear 3 facilitates the hinged connection between the reagent box body 4 and the sealing cover 2. An ear frame 14 is provided on one side of the top of the sealing cover 2, and the ear frame 14 is hinged to the handle frame 11, and the ear frame 14 is connected to the sealing cover 2 through a connector 13. This design facilitates the installation of the handle frame 11.
[0026] Working principle: When in use, urine is added into the urine buffer tank 9 from the liquid adding bucket 10 for buffering, and the urine is diverted to multiple reagent papers 6 through the guide tube 12. The urine is tested through the reagent papers 6, and the test results can be displayed on the display port 7. The reagent box body 4 can be sealed by the sealing cover 2, and the protective cover 1 is used to safely protect the outside of the sealing cover 2. The display port 7 on the reagent paper 6 can be observed through the observation window 8, and the reagent box body 4 can be conveniently carried by hand through the handle frame 11.
[0027] It is obvious to those skilled in the art that the present invention is not limited to the details of the exemplary embodiments described above, and that the present invention can be implemented in other specific forms without departing from the spirit or essential features of the present invention. Therefore, the embodiments should be regarded as exemplary and non-restrictive from any point of view, and the scope of the present invention is defined by the appended claims rather than the above description, and it is intended that all changes falling within the meaning and scope of the equivalent elements of the claims be included in the present invention. Any reference numeral in a claim should not be regarded as limiting the claim to which it relates.
Claims
1. A human chorionic gonadotropin double determination kit, comprising a sealing cover (2), a kit body (4), a reagent paper (6) and a urine buffer tank (9), characterized in that: The top of the reagent box body (4) is provided with a sealing cover (2) which can be opened laterally through a hinged ear (3), the middle of the reagent box body (4) is provided with a detection panel (5), a plurality of reagent papers (6) are provided on the detection panel (5), and the reagent papers (6) are designed to be replaceable, a urine buffer tank (9) is provided on one side of the top of the reagent box body (4), and a liquid adding hopper (10) is provided inside the urine buffer tank (9).
2. The human chorionic gonadotropin dual determination kit according to claim 1, characterized in that: An observation window (8) is provided in the middle of the sealing cover (2), and a protective cover (1) is provided on the side of the sealing cover (2).
3. The human chorionic gonadotropin dual determination kit according to claim 1, characterized in that: A hinged ear (3) is provided on one side of the reagent box body (4), and the hinged ear (3) is hinged to the side edge of the sealing cover (2).
4. The human chorionic gonadotropin dual determination kit according to claim 1, characterized in that: The reagent paper (6) is provided with a display port (7), and the display port (7) is provided with a protection groove.
5. The human chorionic gonadotropin dual determination kit according to claim 1, characterized in that: An ear frame (14) is provided on one side of the top of the sealing cover (2), and the ear frame (14) is hinged to the handle frame (11), and the ear frame (14) is connected to the sealing cover (2) via a connector (13).
6. The human chorionic gonadotropin dual determination kit according to claim 1, characterized in that: A plurality of flow guide tubes (12) are arranged on the outside of the urine buffer tank (9), and one end of the plurality of flow guide tubes (12) is respectively connected to a plurality of reagent papers (6).