Cervical cancer screening kit

Abstract

The utility model relates to the technical field of kits, in particular to a cervical cancer screening kit which comprises a detection rod and detection card bodies, a plurality of cavities are formed in the detection rod, the detection card bodies are fixedly connected to the inner walls of the cavities respectively, a sampling assembly is arranged on the detection rod, and the detection card bodies are fixedly connected to the inner walls of the cavities respectively. The sampling assembly comprises grooves and through holes, the multiple grooves are formed in the detection rod, the multiple through holes are formed in the inner walls of the multiple cavities, the two ends of the multiple through holes communicate with the multiple cavities and the multiple grooves correspondingly, a driving assembly is arranged on the detection rod, the driving assembly comprises a push plate, and the push plate is arranged on the detection rod. The multiple push plates are slidably connected to the interiors of the multiple grooves correspondingly. The vagina sampling kit can be directly placed in the vagina of a user for use, so that the problem that the user inconveniently samples liquid in the genital tract is solved, the problems of sanitation and pollution can be greatly avoided, and the detection accuracy of the kit is improved.

Description

TECHNICAL FIELD

[0001] The utility model relates to the technical field of reagent box, specifically is a cervical cancer screening reagent box. BACKGROUND

[0002] The reagent box is a medical product for detecting bacteria or virus, which detects diseases through biochemical reaction, and the reagent box can reflect whether infection through color reaction by only dropping liquid sample on the detection card.

[0003] The female reproductive system diseases can also be self-tested through the reagent box, and the cervical cancer can be detected through the HPV detection reagent box, but the female genital tract is relatively narrow, so the user is inconvenient to sample the liquid in the genital tract, and therefore a new type of reagent box is needed to solve the problem of difficult sampling for gynecological diseases such as cervical cancer. UTILITY MODEL CONTENT

[0004] In order to solve the above technical problems, the utility model provides a cervical cancer screening reagent box, which can be directly put into the user's vagina for use, thereby solving the problem of user's inconvenience to sample the liquid in the genital tract, and greatly avoiding the problems of hygiene and pollution, and improving the accuracy of reagent box detection.

[0005] The technical solution for achieving the purpose of the utility model is as follows: a cervical cancer screening reagent box, comprising a detection rod 1, a detection card body 3, a box body 7 and a reagent 8, the detection rod 1 and the reagent 8 are arranged in the inside of the box body 7, a plurality of cavities 2 are formed in the inside of the detection rod 1, a plurality of detection card bodies 3 are fixedly connected to the inner walls of the cavities 2 respectively, a sampling assembly 5 is arranged on the detection rod 1, the sampling assembly 5 comprises grooves 51 and through holes 52, a plurality of grooves 51 are formed on the detection rod 1, a plurality of through holes 52 are formed on the inner walls of the cavities 2, the two ends of the plurality of through holes 52 are communicated with the plurality of cavities 2 and the plurality of grooves 51 respectively, a driving assembly 6 is arranged on the detection rod 1, the driving assembly 6 comprises push plates 61, a plurality of push plates 61 are slidingly connected to the insides of the plurality of grooves 51 respectively.

[0006] Preferably, the sampling assembly further comprises sliding sheets, and the plurality of sliding sheets are slidingly connected to the plurality of detection card bodies respectively.

[0007] Preferably, the sampling assembly further comprises air holes, a plurality of air holes are formed on the detection rod, and the plurality of air holes are communicated with the plurality of cavities respectively.

[0008] Preferably, the driving assembly further comprises a connecting plate, the connecting plate is slidingly connected to the inside of the detection rod, a plurality of sliding rods are fixedly connected to the connecting plate, the plurality of sliding rods are slidingly connected with the detection rod, and the plurality of sliding rods are fixedly connected with the plurality of push plates respectively.

[0009] Preferably, the driving assembly further comprises a pull rod, the pull rod is slidingly connected to the detection rod, and the bottom end of the pull rod is fixedly connected with the connecting plate.

[0010] Preferably, a plurality of the grooves are arranged in an annular array on the detection rod.

[0011] Preferably, a plurality of transparent plates are arranged on the detection rod, and the plurality of transparent plates correspond to the plurality of detection card bodies respectively.

[0012] Compared with the prior art, the utility model has the following remarkable advantages:

[0013] Firstly, in the utility model, the whole detection rod can be inserted into the vagina during use, so that the spherical part at the top of the detection rod is close to the cervix, then the pull rod is manually pushed and pulled, when the pull rod is pushed and pulled, the connecting plate and the sliding rod are driven to move back and forth, so that the plurality of push plates move back and forth, the overall diameter of the detection rod is relatively large, and the female vaginal wall is usually wrinkled, so that the detection rod is tightly wrapped by the vaginal wall, and the push plates can scrape the mucus on the vaginal wall when moving back and forth, so that the mucus on the vaginal wall is scraped into the grooves.

[0014] Secondly, in the utility model, when the push plates move towards the through hole, the mucus in the grooves is pushed into the through hole, so that the mucus is poured into the cavity, and when the push plates move away from the through hole, because the mucus in the vagina has viscosity, the air in the cavity is preferentially extracted, so that the mucus remains in the cavity, and with the increase of the mucus and the decrease of the air, the sliding sheet moves back and forth to balance the air pressure, and the air hole can also intake or exhaust air, after the pull rod is pulled several times, enough mucus enters the cavity, and the detection area at the end of the plurality of detection card bodies is fully contacted with the mucus, so that the detection is started, at this time, the whole kit can be taken out from the vagina, the display on the detection card body is observed through the transparent plate, and whether some inflammation or disease is infected can be judged according to the display of the corresponding detection card body. BRIEF DESCRIPTION OF DRAWINGS

[0015] The utility model will be explained further in combination with the drawings and examples:

[0016] Figure 1 is the three-dimensional structure schematic diagram of the utility model;

[0017] Figure 2 is the three-dimensional structure schematic diagram of the detection rod in the utility model Figure One ;

[0018] Figure 3 is the three-dimensional structure schematic diagram of the detection rod in the utility model Figure Two ;

[0019] Figure 4 is the internal structure section view of the detection stick in the utility model;

[0020] Figure 5 is the explosion view of the connecting structure of the detection card body and the driving assembly in the utility model.

[0021] Mark explanation:

[0022] 1, detection stick;2, cavity;3, detection card body;4, transparent plate;5, sampling assembly;51, groove;52, through hole;53, air hole;54, sliding sheet;6, driving assembly;61, push plate;62, pull rod;63, connecting plate;64, sliding rod;7, box body;8, reagent. Specific implementation

[0023] The utility model is described in detail below, and the technical scheme of the embodiment of the utility model is clearly and completely described. Obviously, the described embodiment is only a part of the embodiment of the utility model, not all the embodiments. Based on the embodiment of the utility model, all other embodiments obtained by the ordinary skilled in the art without creative labor belong to the scope of protection of the utility model.

[0024] The utility model discloses a kind of screening kits for cervical cancer by improvement, and the technical scheme of the utility model is:

[0025] As shown in Figures 1-5 A kind of screening kits for cervical cancer, including detection stick 1, detection card body 3, box body 7 and reagent 8, detection stick 1 and reagent 8 are set to the inside of box body 7, the inside of detection stick 1 is opened with multiple cavities 2, multiple detection card body 3 is fixedly connected on the inner wall of multiple cavities 2 respectively, sampling assembly 5 is provided on detection stick 1, sampling assembly 5 includes groove 51 and through hole 52, multiple grooves 51 are opened on detection stick 1, multiple through holes 52 are opened on the inner wall of multiple cavities 2, the two ends of multiple through holes 52 are communicated multiple cavities 2 and multiple grooves 51 respectively, driving assembly 6 is provided on detection stick 1, driving assembly 6 includes push plate 61, multiple push plates 61 are slidably connected in the inside of multiple grooves 51 respectively, detection card body 3 is the reagent box commonly seen in the prior art, such as colloidal gold method reagent box, multiple detection card body 3 can be used to detect HPV virus, genital tract PH value, vaginitis, syphilis and other diseases, to comprehensively detect the gynecological disease condition of user, avoid missing and misjudgment and so on, detection stick 1 is detachable structure, needs to be opened first before use, reagent 8 is added on detection card body 3 first.

[0026] Further, sampling assembly 5 also includes sliding sheet 54, multiple sliding sheets 54 are slidably connected on multiple detection card body 3 respectively.

[0027] Further, the sampling assembly 5 further comprises air holes 53, a plurality of air holes 53 are arranged on the detection rod 1, and the plurality of air holes 53 are respectively communicated with the plurality of cavities 2. With the reciprocating movement of the push plate 61, when the push plate 61 moves to the through hole 52, the mucus in the groove 51 is pushed into the through hole 52, and then the mucus is filled into the cavity 2. When the push plate 61 moves away from the through hole 52, because the mucus in the vagina is sticky, the air in the cavity 2 is preferentially extracted, so that the mucus remains in the cavity 2. With the increase of the mucus and the decrease of the air, the slide 54 reciprocally slides to balance the air pressure, and the air hole 53 can also intake or exhaust air.

[0028] Further, the driving assembly 6 further comprises a connecting plate 63 which is slidingly connected to the inside of the detection rod 1, and a plurality of slide rods 64 are fixedly connected to the connecting plate 63, the plurality of slide rods 64 are slidingly connected with the detection rod 1, and the plurality of slide rods 64 are respectively fixedly connected with the plurality of push plates 61.

[0029] Further, the driving assembly 6 further comprises a pull rod 62 which is slidingly connected to the detection rod 1, and the bottom end of the pull rod 62 is fixedly connected with the connecting plate 63.

[0030] Further, the plurality of grooves 51 are arranged in a ring array on the detection rod 1. Because the user adopts a sitting or lying posture during use, if only one ring-shaped groove is arranged, the mucus scraped by the push plate 61 will be deposited on the lower side, and at this time, the mucus cannot fill each cavity 2. Therefore, the grooves 51 are arranged in multiple and arranged in a ring array.

[0031] Further, a plurality of transparent plates 4 are arranged on the detection rod 1, and the plurality of transparent plates 4 correspond to the plurality of detection card bodies 3 respectively. The transparent plate 4 is made of acrylic material. After use of the kit, the display of the detection card body 3 in the detection rod 1 can be observed through the transparent plate 4.

[0032] The specific working method is: first, detect the card body 3 is the reagent kit commonly used in the prior art, such as colloidal gold method reagent kit, and multiple detection card bodies 3 can be used to detect HPV virus, reproductive tract PH value, vaginitis, syphilis and the like, so as to comprehensively detect the gynecological disease of the user, avoid missed detection and misdiagnosis, and the like, and before use, the detection rod 1 needs to be opened, and the reagent 8 is first added on the detection card body 3, then when used, the whole detection rod 1 is inserted into the vagina, so that the spherical part at the top of the detection rod 1 is close to the cervix, then the pull rod 62 is manually pushed and pulled, when the pull rod 62 is pushed and pulled, the connecting plate 63 and the sliding rod 64 are reciprocated, so that the multiple push plates 61 are reciprocated, the overall diameter of the detection rod 1 is relatively thick, and the female vaginal wall is usually wrinkled, so that the detection rod 1 is tightly wrapped by the vaginal wall, and the push plate 61 can scrape the vaginal wall when reciprocating, so as to scrape the mucus on the vaginal wall into the groove 51, with the reciprocating movement of the push plate 61, when the push plate 61 moves to the through hole 52, the mucus in the groove 51 is pushed into the through hole 52, so that the mucus is poured into the cavity 2, and when the push plate 61 moves away from the through hole 52, because the mucus in the vagina has viscosity, the air in the cavity 2 is preferentially extracted, so that the mucus remains in the cavity 2, and with the increase of the mucus and the decrease of the air, the sliding sheet 54 slides back and forth to balance the air pressure, and the air hole 53 can also inhale or exhale, after the pull rod 62 is pulled several times, enough mucus enters the cavity 2, and the detection area at the end of the multiple detection card bodies 3 is in contact with the mucus, so that the detection is started, at this time, the whole reagent kit can be taken out from the vagina, the display on the detection card body 3 is observed through the transparent plate 4, and whether the user is infected with some inflammation or disease can be judged according to the display of the corresponding detection card body 3.

[0033] The technical means disclosed in the utility model scheme is not limited to the technical means disclosed in the above technical means, and also includes technical solutions composed of the above technical features and equivalent replacements. The unfinished matters of the utility model belong to the common knowledge of those skilled in the art.

Claims

1. A cervical cancer screening kit, comprising a detection rod (1), a detection card body (3), a box body (7) and reagents (8), the detection rod (1) and the reagents (8) are arranged in the inside of the box body (7), a plurality of cavities (2) are arranged in the inside of the detection rod (1), and a plurality of detection card bodies (3) are fixedly connected to the inner walls of the cavities (2), characterized in that: The detection rod (1) is of detachable structure; the top end of the detection rod (1) is of spherical structure; the detection rod (1) is provided with a sampling assembly (5), the sampling assembly (5) comprises grooves (51) and through holes (52), a plurality of grooves (51) are formed on the detection rod (1), a plurality of through holes (52) are formed on the inner walls of the plurality of cavities (2), the two ends of the plurality of through holes (52) are communicated with the plurality of cavities (2) and the plurality of grooves (51) respectively, the detection rod (1) is provided with a driving assembly (6), the driving assembly (6) comprises push plates (61), a plurality of push plates (61) are slidingly connected to the interiors of the plurality of grooves (51) respectively; the sampling assembly (5) further comprises sliding sheets (54), a plurality of sliding sheets (54) are slidingly connected to the plurality of detection card bodies (3) respectively; the sliding sheets (54) of the sampling assembly (5) can reciprocally slide. ​ 2. The cervical cancer screening kit according to claim 1, wherein: The sampling assembly (5) further comprises air holes (53), a plurality of air holes (53) are formed on the detection rod (1), and the plurality of air holes (53) are communicated with the plurality of cavities (2) respectively.

3. The cervical cancer screening kit as claimed in claim 1, wherein: The driving assembly (6) further comprises a connecting plate (63), the connecting plate (63) is slidingly connected to the interior of the detection rod (1), a plurality of slide rods (64) are fixedly connected to the connecting plate (63), the plurality of slide rods (64) are slidingly connected with the detection rod (1), and the plurality of slide rods (64) are fixedly connected with the plurality of push plates (61) respectively.

4. The cervical cancer screening kit according to claim 3, wherein: The driving assembly (6) further comprises a pull rod (62), the pull rod (62) is slidingly connected to the detection rod (1), and the bottom end of the pull rod (62) is fixedly connected with the connecting plate (63).

5. The cervical cancer screening kit as claimed in claim 1, wherein: The plurality of grooves (51) are arranged in annular array on the detection rod (1).

6. The cervical cancer screening kit as claimed in claim 1, wherein: A plurality of transparent plates (4) are arranged on the detection rod (1), and the plurality of transparent plates (4) correspond to the plurality of detection card bodies (3) respectively.

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