Detection device for cat pancreatic lipase

Abstract

The utility model relates to the technical field of lipase detection devices, and discloses a cat pancreas lipase detection device which comprises a kit, a placing frame is fixed in the kit, and three groups of first placing grooves and second placing grooves are sequentially formed in the top surface of the placing frame from front to back in the width direction; each group comprises a first placing groove and three second placing grooves, and the fixing assembly comprises a fixed clamping plate arranged in the first placing groove and a movable clamping plate arranged in the second placing groove. According to the kit, the three groups of detection reagents and detection tools are respectively clamped and fixed by adopting the three groups of fixed clamping plates and movable clamping plates, and when one group of detection reagents and detection tools is unfastened, the detection reagents and detection tools of other groups are still in a clamped and fixed state, so that the stability of the reagents during transportation of the kit is improved; meanwhile, the situation that when a group of cat pancreatic lipase blood samples are detected, a worker mistakenly takes reagents and detection tools of other test groups, and detection work is affected is prevented.

Description

Technical Field

[0001] The utility model relates to the technical field of lipase detection devices, in particular to a detection device for cat pancreatic lipase. Background Art

[0002] Lipase is an important enzyme for animals to digest fat. Its secretion amount and activity are related to the digestion, absorption and utilization of fat by animals. The hepatopancreas or pancreas of aquatic animals is the main secretory organ of lipase, and the gastrointestinal mucosa and liver can also secrete it. The lipase activity in the pyloric trichomes of some fish is the highest. Determining the lipase activity in various parts of aquatic animals is helpful to study and analyze their ability to digest fat and the digestive function of various parts. For cats, pancreatitis often occurs, and the determination of pancreatitis requires the detection of lipase in the body.

[0003] An existing high-efficiency cat pancreatic-specific lipase detection kit (publication number: CN210506301U) has at least the following disadvantages: although the device is equipped with multiple groups of detection reagents inside the kit to achieve the effect of multiple tests in one box, the detection reagents are not effectively grouped, making it easy for staff to take the wrong reagents or detection tools when using them, and take reagents from other test groups for testing, thereby affecting the test results. In addition, the kit is not equipped with an effective fixing mechanism for the reagents or detection tools, which may cause collision damage during transportation of the kit. For this reason, the present utility model is proposed. Utility Model Content

[0004] The purpose of the utility model is to solve the shortcomings of the prior art and to propose a detection device for cat pancreatic lipase.

[0005] In order to achieve the above purpose, the present invention adopts the following technical solutions:

[0006] A detection device for cat pancreatic lipase, a test kit, wherein a placement rack is fixed inside the test kit, and three groups of first placement slots and second placement slots are respectively opened on the top surface of the placement rack in sequence from front to back along the width direction, each group having one first placement slot and three second placement slots, a test card is placed inside the first placement slot, and a buffer, a mixing test tube and a rubber-tipped dropper are placed inside the three second placement slots in sequence, and a fixing assembly is provided inside each of the first placement slot and the second placement slot, and the fixing assembly includes a fixed splint arranged inside the first placement slot and a movable splint arranged inside the second placement slot.

[0007] As a further solution of the present invention, three movable grooves are provided inside the test kit, which are connected to the first placement groove and the second placement groove. A rack is slidably provided inside the movable groove, and a gear is rotatably connected to the inner bottom surface of the movable groove. The gear is engaged with the rack, and one end of the fixed splint is fixed to the front side of the rack. Three connecting rods are also fixed to the front side of the gear. A plug-in cylinder is fixed to the right side of the movable splint, and the connecting rod is slidably inserted into the interior of the plug-in cylinder. A spring is fixed between one end of the connecting rod and one side of the interior of the plug-in cylinder.

[0008] As a further solution of the present invention, a square rod is rotatably inserted into the top surface of the test kit, the bottom end of the square rod is slidably inserted into the top surface of the gear, a rotating head is fixed to the top end of the square rod, and two limit rods are fixed on the top surface of the test kit at the position of the rotating head, and the top end of the limit rod is slidably inserted into the bottom surface of the rotating head.

[0009] As a further solution of the present invention, an adsorption sheet is fixed to the top surface of the reagent box at the position of the rotating head, and the adsorption sheet is adsorbed to the bottom surface of the rotating head.

[0010] As a further solution of the present invention, a sealing strip is fixed to the top surface of the reagent box, and a sealing cover is connected to the rear side of the reagent box via a hinge. A buckle and a buckle seat are respectively provided on the rear side of the sealing cover and the front side of the reagent box.

[0011] As a further solution of the present invention, a foam board is fixed to the top surface of the sealing cover.

[0012] Compared with the prior art, the present invention has the following beneficial effects:

[0013] By arranging three groups of first placement slots and second placement slots on a placement rack, three groups of test cards, buffers, mixing test tubes and rubber-tipped droppers can be stored respectively, so that the test kit can perform at least three tests on feline pancreatic lipase blood samples, and the three groups of test reagents and test tools are clamped and fixed by using three groups of fixed splints and movable splints respectively. When one group of test reagents and test tools are untied, the test reagents and test tools of other test groups are still in a clamped and fixed state, thereby increasing the stability of the reagents during transportation of the test kit and preventing staff from mistakenly taking reagents and test tools of other test groups when performing the test on one group of feline pancreatic lipase blood samples, thereby affecting the progress of the test work. BRIEF DESCRIPTION OF THE DRAWINGS

[0014] Figure 1 This is a schematic diagram of the three-dimensional structure of a detection device for cat pancreatic lipase proposed by the utility model;

[0015] Figure 2 This is a schematic diagram of the three-dimensional disassembled structure of a detection device for cat pancreatic lipase proposed in the utility model;

[0016] Figure 3 This is a schematic diagram of the three-dimensional cross-sectional structure of the placement frame of a cat pancreatic lipase detection device proposed by the present invention;

[0017] Figure 4 This is a schematic diagram of the three-dimensional cross-sectional structure of the placement frame of a cat pancreatic lipase detection device proposed by the utility model.

[0018] In the figure: 1. Test kit; 101. Placement rack; 102. First placement slot; 103. Second placement slot; 104. Test card; 105. Buffer; 106. Mixing test tube; 107. Rubber-tipped dropper; 2. Fixed splint; 201. Movable splint; 202. Movable slot; 203. Rack; 204. Gear; 205. Connecting rod; 206. Plug-in cylinder; 207. Spring; 208. Square rod; 209. Rotating head; 210. Limiting rod; 3. Adsorption sheet; 4. Sealing strip; 401. Sealing cover; 5. Foam board. DETAILED DESCRIPTION

[0019] In order to make the technical means, creative features, objectives and effects achieved by the present invention easier to understand, the present invention is further described below in conjunction with specific implementation methods.

[0020] In the description of this utility model, it should be noted that the terms "upper," "lower," "inner," "outer," "front end," "rear end," "both ends," "one end," "the other end," and the like, indicating orientations or positional relationships, are based on the orientations or positional relationships shown in the accompanying drawings and are intended solely to facilitate the description of this utility model and simplify the description. They are not intended to indicate or imply that the devices or components referred to must have a specific orientation, be constructed, or operate in a specific orientation. Therefore, they should not be construed as limitations on this utility model. Furthermore, the terms "first" and "second" are used for descriptive purposes only and should not be construed as indicating or implying relative importance.

[0021] In the description of this utility model, it should be noted that, unless otherwise expressly specified or limited, the terms "installed," "provided with," "connected," etc. should be understood in a broad sense. For example, "connected" can mean a fixed connection, a detachable connection, or an integral connection; it can be a mechanical connection or an electrical connection; it can be a direct connection or an indirect connection through an intermediate medium, or it can be internal communication between two components. Those skilled in the art will be able to understand the specific meanings of the above terms in this utility model based on the specific circumstances.

[0022] Reference Figure 1-Figure 4, a detection device for cat pancreatic lipase, a test kit 1, a placement rack 101 is fixed inside the test kit 1, and three groups of first placement slots 102 and second placement slots 103 are respectively opened on the top surface of the placement rack 101 along the width direction from front to back, each group has a first placement slot 102 and three second placement slots 103, a test card 104 is placed inside the first placement slot 102, and a buffer 105, a mixing test tube 106 and a rubber-tipped dropper 107 are placed inside the three second placement slots 103 in sequence, and a fixing component is provided inside the first placement slot 102 and the second placement slot 103, and the fixing component includes a fixed splint 2 arranged inside the first placement slot 102 and a movable splint 201 arranged inside the second placement slot 103.

[0023] Reference Figure 2-Figure 4 In this embodiment, three movable grooves 202 are provided inside the reagent box 1, and the movable groove 202 is connected to the first placement groove 102 and the second placement groove 103. A rack 203 is slidably provided inside the movable groove 202, and a gear 204 is rotatably connected to the inner bottom surface of the movable groove 202. The gear 204 is meshed with the rack 203. One end of the fixed splint 2 is fixed to the front side of the rack 203. Three connecting rods 205 are also fixed to the front side of the gear 204. A plug-in cylinder 206 is fixed to the right side of the movable splint 201. The connecting rod 205 is slidably inserted into the interior of the plug-in cylinder 206. A spring 207 is fixed between one end of the connecting rod 205 and one side of the interior of the plug-in cylinder 206. By rotating the gear clockwise Wheel 204, under the action of meshing of gear 204 and rack 203, makes rack 203 move laterally, thereby driving fixed splint 2 away from test card 104, and movable splint 201 away from buffer 105, mixing test tube 106 and rubber-tipped dropper 107. During this process, connecting rod 205 slides inside plug-in tube 206 and pulls spring 207. At this time, staff can take out a set of testing tools, and then use rubber-tipped dropper 107 to take an appropriate amount of blood sample and an appropriate amount of buffer solution, mix them in mixing test tube 106, and then drip them onto test card 104. After waiting for fifteen minutes, place test card 104 in fluorescence analyzer for analysis, and then carry out control tests of the second and third groups in turn to complete the entire testing process.

[0024] Reference Figure 2-Figure 4In this embodiment, a square rod 208 is rotatably inserted into the top surface of the reagent box 1. The bottom end of the square rod 208 is slidably inserted into the top surface of the gear 204. A rotating head 209 is fixed to the top of the square rod 208. Two limiting rods 210 are fixed to the top surface of the reagent box 1 at the position of the rotating head 209. The top end of the limiting rod 210 is slidably inserted into the bottom surface of the rotating head 209. The rotation of the rotating head 209 is restricted by the insertion of the rotating head 209 and the limiting rod 210. The positions of the gear 204 and the rack 203 are locked to ensure that the fixed splint 2 and the movable splint 201 stably clamp the reagents and detection tools. When the reagents and detection tools need to be used, pull up the rotating head 209 to disengage the rotating head 209 from the limiting rod 210. At this time, the rotating head 209 can be rotated clockwise, thereby driving the square rod 208 and the gear 204 to rotate synchronously. At this time, the reagents and detection tools can be released, making it convenient to take the reagents and detection tools.

[0025] Reference Figure 2-Figure 4 In this embodiment, an adsorption sheet 3 is fixed on the top surface of the reagent box 1 at the position of the rotating head 209. The adsorption sheet 3 is adsorbed on the bottom surface of the rotating head 209. By being arranged on the rotating head 209 and adsorbed on the adsorption sheet 3, the rotating head 209 is adsorbed and restricted, preventing the rotating head 209 from escaping from the limiting rod 210, resulting in loosening of the clamping of the reagent and the detection tool.

[0026] Reference Figure 2-Figure 4 In this embodiment, a sealing strip 4 is fixed to the top surface of the reagent box 1, and a sealing cover 401 is connected to the rear side of the reagent box 1 through a hinge. A buckle and a buckle seat are respectively provided on the rear side of the sealing cover 401 and the front side of the reagent box 1. By providing the sealing cover 401 and the sealing strip 4, when the sealing cover 401 and the reagent box 1 are buckled, the interior of the reagent box 1 can be kept sealed, thereby increasing the preservation effect of the reagents and detection tools.

[0027] Reference Figure 2-Figure 4 In this embodiment, a foam plate 5 is fixed to the top surface of the sealing cover 401. By providing the foam plate 5, when the sealing cover 401 and the reagent box 1 are fastened together using a snap, the foam plate 5 can be respectively abutted against the top surfaces of the test card 104, the buffer 105, the mixing test tube 106 and the rubber-tipped dropper 107, thereby further enhancing the fixing effect of the reagents and the detection tools.

[0028] From the above description, it can be seen that the above embodiment of the present invention achieves the following technical effects: in use, by pulling the rotating head 209 upwards, the rotating head 209 is driven to disengage from the limit rod 210. In this process, the square rod 208 slides on the gear 204. At this time, the rotating head 209 is rotated clockwise, so that the square rod 208 drives the gear 204 to rotate. Under the action of the gear 204 and the rack 203 meshing, the rack 203 moves laterally, thereby driving the fixed splint 2 away from the test card 104, and the movable splint 201 away from the buffer 105, the mixing test tube 106 and the rubber-tipped dropper 107. In this process, the connecting rod 205 slides inside the plug-in tube 206 and pulls the spring 207. At this time, the staff can take out a set of testing tools, and then use the rubber-tipped dropper 107 to take an appropriate amount of blood sample and an appropriate amount of buffer solution to mix them in the mixing test tube 106, and then drip them into the test Card 104, wait for fifteen minutes and then place the test card 104 in the fluorescence analyzer for analysis, and then carry out the second and third group control tests in turn to complete the entire detection process, by setting the rotating head 209 and the adsorption sheet 3 to be adsorbed, so that the rotating head 209 is adsorbed and restricted, preventing the rotating head 209 from escaping from the limit rod 210, resulting in loosening of the clamping of the reagents and the detection tools, by setting the sealing cover 401 and the sealing strip 4, when the sealing cover 401 and the reagent box 1 are fastened with a snap, it can be ensured that the inside of the reagent box 1 remains sealed, thereby increasing the preservation effect of the reagents and the detection tools, by setting the foam board 5, when the sealing cover 401 and the reagent box 1 are fastened with a snap, the foam board 5 can be respectively abutted against the top surfaces of the test card 104, the buffer 105, the mixing test tube 106 and the rubber-tipped dropper 107, thereby further increasing the fixation effect of the reagents and the detection tools.

[0029] The above shows and describes the basic principles, main features and advantages of the present invention. Those skilled in the art should understand that the present invention is not limited to the above embodiments. The above embodiments and descriptions are merely illustrative of the principles of the present invention. Various changes and improvements may be made to the present invention without departing from the spirit and scope of the present invention. Such changes and improvements are intended to fall within the scope of the present invention. The scope of protection claimed in this invention is defined by the appended claims and their equivalents.

Claims

1. A detection device for cat pancreatic lipase, comprising a kit (1), characterized in that: The reagent kit (1) is fixed with a placement rack (101) inside. The top surface of the placement rack (101) is provided with three groups of first placement slots (102) and second placement slots (103) in sequence from front to back along the width direction. Each group has one first placement slot (102) and three second placement slots (103). A detection card (104) is placed inside the first placement slot (102). A buffer (105), a mixing test tube (106) and a rubber-tipped dropper (107) are placed inside the three second placement slots (103). A fixing assembly is provided inside the first placement slot (102) and the second placement slot (103). The fixing assembly includes a fixed splint (2) arranged inside the first placement slot (102) and a movable splint (201) inside the second placement slot (103).

2. A detection device for cat pancreatic lipase according to claim 1, characterized in that: The reagent box (1) is provided with three movable grooves (202) inside, the movable grooves (202) are connected with the first placement groove (102) and the second placement groove (103), a rack (203) is slidably provided inside the movable groove (202), a gear (204) is rotatably connected to the inner bottom surface of the movable groove (202), the gear (204) is meshed with the rack (203), one end of the fixed splint (2) is fixed to the front side of the rack (203), three connecting rods (205) are also fixed to the front side of the gear (204), an inserting cylinder (206) is fixed on the right side of the movable splint (201), the connecting rod (205) is slidably inserted into the inside of the inserting cylinder (206), and a spring (207) is fixed between one end of the connecting rod (205) and one side of the inside of the inserting cylinder (206).

3. A detection device for cat pancreatic lipase according to claim 1, characterized in that: The top surface of the reagent box (1) is rotatably inserted with a square rod (208), the bottom end of the square rod (208) and the top surface of the gear (204) are slidably inserted, the top end of the square rod (208) is fixed with a rotating head (209), and the top surface of the reagent box (1) is located at the position of the rotating head (209) and fixed with two limiting rods (210), and the top end of the limiting rod (210) and the bottom surface of the rotating head (209) are slidably inserted.

4. The detection device for cat pancreatic lipase according to claim 1, characterized in that: An adsorption sheet (3) is fixed on the top surface of the reagent box (1) at the position of the rotating head (209), and the adsorption sheet (3) is adsorbed on the bottom surface of the rotating head (209).

5. The detection device for cat pancreatic lipase according to claim 1, characterized in that: A sealing strip (4) is fixed to the top surface of the reagent box (1), and a sealing cover (401) is connected to the rear side of the reagent box (1) via a hinge. A buckle and a buckle seat are respectively provided on the rear side of the sealing cover (401) and the front side of the reagent box (1).

6. A detection device for cat pancreatic lipase according to claim 5, characterized in that: A foam plate (5) is fixed to the top surface of the sealing cover (401).

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