Semi-automatic blood coagulation detection analyzer
By designing a semi-automatic coagulation detection analyzer, the clamping assembly and auxiliary plate driven by servo motors can be used to realize the rotation and shaking of the test tube. Combined with multiple sets of syringes and disinfection components, the problems of cumbersome operation and error in the detection result are solved, and the detection efficiency and accuracy are improved.
Patent Information
- Application Number
- CN202510181691.8
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2025-02-19
- Publication Date
- 2025-03-18
- Estimated Expiration
- 2045-02-19
AI Technical Summary
The existing coagulation detection analyzers are cumbersome to operate and require professional operators to frequently shake the test tube, resulting in low operation fatigue and low detection efficiency, and manual shaking is difficult to ensure consistency, resulting in errors in the detection result.
A semi-automatic coagulation detection analyzer is designed, using a clamping assembly and auxiliary plate driven by a servo motor to realize the rotation and shaking of the test tube, so that the blood sample and the anticoagulant are fully mixed. At the same time, through multiple sets of syringes and disinfection components, automatic addition of reagents and automatic disinfection of needles are achieved.
It reduces the work burden of operators, improves the detection efficiency and accuracy of results, avoids errors caused by manual shaking, and ensures the uniformity of inspection results.
Smart Images

Figure CN119643891A_ABST
Abstract
Description
Technical Field
[0001] The present invention relates to the technical field of medical devices, and in particular to a semi-automatic blood coagulation detection analyzer. Background Art
[0002] A coagulation detection analyzer is a medical device clinically used to measure the content of various components in human blood and quantitative biochemical analysis results, providing a reliable digital basis for clinical diagnosis of various diseases in patients. Its working principle is to use optical, magnetic or fluid technology to detect and measure various parameters in the blood coagulation process to evaluate whether the patient's coagulation function is normal. During the use of existing coagulation detection analyzers, professional operators are required to shake the test tubes containing patient blood samples before testing. However, when there are many samples to be tested, the operator's manual shaking will cause certain fatigue to the operator's limbs, thereby affecting the efficiency of the test. At the same time, during the test process, multiple reagents need to be added and shaken manually. Since the time and frequency of each shaking are difficult to achieve consistency, certain errors will occur in the test results, and the process is relatively cumbersome when manually processed. Therefore, the present application provides a semi-automatic coagulation detection analyzer to meet the needs. Summary of the invention
[0003] The technical problem to be solved by the present invention is to provide a semi-automatic coagulation detection analyzer to solve the problems that the existing operation process is complicated and manual fatigue and mistakes are prone to occur when the number of test samples is large, which affects the detection efficiency.
[0004] In order to solve the above technical problems, the present invention provides the following technical solutions: A semi-automatic coagulation detection analyzer comprises a detector, wherein the detector comprises a detection box, a cover plate is installed at the front end of the detector, and transmission rollers are rotatably connected at four corners of the detection box, wherein the top of one of the transmission rollers is fixedly connected to the output shaft of a servo motor, an auxiliary plate is fixedly connected to the detection box, a clamping assembly is arranged above the auxiliary plate, and the clamping assembly is used to clamp a detection test tube, wherein the test tube contains blood to be detected by a patient, and three groups of adjacent syringes are arranged above the test tube, and needles are rotatably connected at the bottom of the syringes. The three groups of syringes are arranged in sequence clockwise, and the three groups of syringes are respectively meshed and connected with a rotating assembly, and the rotating assembly is used to rotate the needles of the syringes, and the bottoms of the three groups of syringes are respectively slidably connected with a disinfection assembly, and the disinfection assembly is used to disinfect the needles of the syringes. The three groups of syringes are respectively located on different sides of the detection box, and a detection sensor is arranged on the remaining side of the detection box.
[0005] Optionally, three groups of evenly spaced serrated structures are provided on the top of the auxiliary plate, the sides of the auxiliary plate are fixedly connected to guide plates, the middle positions of the three sides of the auxiliary plate are fixedly connected to pads, the pads correspond to the syringes one by one, and the pads are located directly below the syringes.
[0006] Optionally, a piston is slidably connected to the syringe, a group of evenly spaced trigger plates are fixedly connected to the top of the piston, an electric push rod is fixedly connected to the top of the trigger plate, a hollow rod is fixedly connected to the side of the syringe, an inclined block is fixedly connected to the hollow rod, the opening of the hollow rod is located above the piston, a trigger rod is slidably connected to the hollow rod, one end of the trigger rod is provided with an inclined surface, a first spring is sleeved on the trigger rod, the inclined surface of the trigger rod is located below the trigger plate, and a first gear is provided on the needle.
[0007] Optionally, the clamping assembly includes a conveyor belt, a connecting column is fixedly connected to the surface of the conveyor belt, and a clamping plate is provided on one side of the connecting column.
[0008] Optionally, one side of the clamping plate is fixedly connected to the second gear via a rubber rod, the second gear is connected to the connecting column via a bearing, the clamping plate clamps a test tube, a sealing cover is provided on the top of the test tube, and the inner side of the conveyor belt is connected to four transmission rollers.
[0009] Optionally, the rotating assembly includes an auxiliary roller, the auxiliary roller is connected to a gear shaft via a belt, and a gear is provided on the top of the gear shaft.
[0010] Optionally, the auxiliary roller is connected to the transmission roller via a belt, the top of the gear shaft is meshed with the first gear of the needle via a gear, and the length of the gear on the gear shaft is greater than the length of the first gear.
[0011] Optionally, the disinfection component includes a storage tank, in which a cotton roll is rotatably connected, the cotton roll in the storage tank is immersed in disinfectant alcohol, the other end of the cotton roll is located on a winding shaft in a collection tank, and a winding plate is provided on one side of the winding shaft.
[0012] Optionally, a circular array of pawls is provided on the winding shaft, a ratchet is rotatably connected to the winding shaft, the ratchet is cooperatively connected to the winding shaft via the pawl, a serrated structure with uniform intervals is provided at one end of one side of the winding plate, a group of circular array of serrated structures is provided on the side of the ratchet, and the ratchet is meshingly connected to the winding plate.
[0013] Optionally, the storage tank and the collection tank are both fixedly connected to one side of the detection box, one side of the cotton cloth roll is close to the needle, the length of the needle is greater than the width of the cotton cloth roll, and the top of the winding plate is provided with an inclined surface, which drives the inclined surface of the top of the winding plate to fit the inclined surface of the bottom of the inclined block, one side of the winding plate is slidably connected to the detection box, and a second spring is provided between the winding plate and the detection box.
[0014] Compared with the prior art, the present invention has at least the following beneficial effects: In the above scheme, by setting up a clamping assembly and an auxiliary plate, when testing the patient's blood sample, the test tube can be rotated and shaken so that the blood sample and anticoagulant in the test tube can be evenly mixed, avoiding the need for the operator to frequently shake the test tube when performing the inspection operation, reducing the operator's workload and improving the efficiency of the inspection. Furthermore, by setting up multiple groups of syringes, different reagents can be added to the test tube in sequence, and after adding each reagent, the test tube can be shaken to make the solution in the test tube more evenly mixed, so that the result of the patient's blood sample can be more accurate when the final test is performed.
[0015] By setting up a disinfection component and a rotating component, when the syringe injects the internal reagent into the test tube, the needle can be automatically disinfected. At the same time, the cotton roll can also be automatically reeled in, so that the needle can be disinfected after each use, avoiding the operator's frequent disinfection of the needle during actual operation.
[0016] When the rubber rod hits the guide plate, the test tube rotates and shakes, so that the blood sample and anticoagulant in the test tube are fully mixed. By shaking the test tube the same way each time, the consistency of the mixing of the blood sample and anticoagulant in each test tube is improved, and the mixing error caused by the difficulty in achieving consistency in time and frequency when shaking by hand, and the error in the test results caused by this, are prevented. The uniformity of the test results of the blood samples in each test tube is improved. At the same time, multiple groups of syringes can inject the same volume of reagent as required at the same time each time, so that the reaction time and concentration are more uniform, thereby improving the accuracy of detection. BRIEF DESCRIPTION OF THE DRAWINGS
[0017] The accompanying drawings, which are incorporated herein and constitute a part of the specification, illustrate embodiments of the invention and, together with the description, further serve to explain the principles of the invention and to enable those skilled in the relevant art to make and use the invention.
[0018] Figure 1 It is a schematic diagram of the three-dimensional structure of a semi-automatic coagulation detection analyzer; Figure 2This is a structural schematic diagram of a semi-automatic coagulation test analyzer with its cover opened; Figure 3 This is a diagram showing the internal structure of the detector of the present invention; Figure 4 It is a partial structural schematic diagram of the present invention; Figure 5 This is a schematic diagram of the auxiliary plate structure of the present invention; Figure 6 This is a schematic diagram of the connection structure between the auxiliary plate and the clamping assembly of the present invention; Figure 7 It is a schematic diagram of the structure of the clamping assembly of the present invention; Figure 8 This is a schematic diagram of the connection structure between the clamping assembly and the test tube of the present invention; Fig. 9 It is a schematic diagram of the connection structure between the syringe and the rotating assembly of the present invention; Fig.10 An exploded view of the syringe of the present invention; Fig.11 This is a schematic diagram of the connection structure between the syringe and the disinfection assembly of the present invention; Fig.12 It is a cross-sectional view of the top of the reel of the present invention.
[0019] Reference numerals: 1. Detector; 101. Cover plate; 11. Servo motor; 12. Drive roller; 13. Detection box; 2. Auxiliary plate; 21. Guide plate; 22. Pad; 3. Syringe; 31. Needle; 311. First gear; 32. Piston; 321. Trigger plate; 322. Electric push rod; 33. Hollow rod; 331. Bevel block; 332. Trigger rod; 333. First spring; 4. Clamping assembly; 41. Conveyor belt; 42. Connecting column; 43. Clamping plate; 431. Rubber rod; 432. Second gear; 433. Bearing; 5. Detection test tube; 51. Sealing cover; 6. Rotating assembly; 61. Auxiliary roller; 62. Gear shaft; 7. Disinfection assembly; 71. Storage tank; 72. Cotton roll; 73. Collection tank; 74. Reeling shaft; 741. Ratchet; 742. Ratchet; 75. Reeling plate; 751. Second spring.
[0020] As shown in the figure, in order to clearly implement the structure of the embodiment of the present invention, specific structures and devices are marked in the figure, but this is only for illustrative purposes and is not intended to limit the present invention to the specific structure, device and environment. According to specific needs, ordinary technicians in this field can adjust or modify these devices and environments. DETAILED DESCRIPTION
[0021] The following is a detailed description of a semi-automatic coagulation detection analyzer provided by the present invention in conjunction with the accompanying drawings and specific embodiments. At the same time, it is explained here that in order to make the embodiments more detailed, the following embodiments are the best and preferred embodiments, and those skilled in the art may also adopt other alternative methods to implement some known technologies; and the accompanying drawings are only for a more specific description of the embodiments, and are not intended to specifically limit the present invention.
[0022] It should be noted that the references to "one embodiment", "embodiment", "exemplary embodiments", "some embodiments" and the like in the specification indicate that the embodiments described may include specific features, structures or characteristics, but not every embodiment may include the specific features, structures or characteristics. In addition, when a specific feature, structure or characteristic is described in conjunction with an embodiment, it should be within the knowledge of a person skilled in the art to implement such feature, structure or characteristic in conjunction with other embodiments (whether or not explicitly described).
[0023] In general, a term can be understood, at least in part, from its use in context. For example, depending, at least in part, on the context, the term "one or more" as used herein can be used to describe any feature, structure, or characteristic in the singular sense, or can be used to describe a combination of features, structures, or characteristics in the plural sense. Additionally, the term "based on" can be understood as not necessarily intended to convey an exclusive set of factors, but can instead, depending, at least in part, on the context, allow for the presence of other factors that are not necessarily explicitly described.
[0024] It will be understood that the meanings of “on,” “over,” and “above” in the present invention should be interpreted in the broadest manner, so that “on” not only means “directly on” something, but also includes the meaning of being “on” something with intervening features or layers therebetween, and “on” or “over” not only means “on” or “above” something, but also includes the meaning of being “on” or “above” something with no intervening features or layers therebetween.
[0025] Additionally, spatially relative terms such as "under," "beneath," "lower," "above," "upper," and the like may be used herein for descriptive convenience to describe the relationship of one element or feature to another element or features, as shown in the accompanying drawings. Spatially relative terms are intended to encompass different orientations of the device in use or operation in addition to the orientation depicted in the accompanying drawings. The device may be oriented in other ways, and the spatially relative descriptors used herein may be similarly interpreted accordingly.
[0026] like Figures 1 to 12As shown, an embodiment of the present invention provides a semi-automatic coagulation detection analyzer, including a detector 1, wherein the detector 1 includes a detection box 13, a cover plate 101 is installed at the front end of the detector 1, and transmission rollers 12 are rotatably connected to the four corners of the detection box 13, and the top of one of the transmission rollers 12 is fixedly connected to the output shaft of the servo motor 11, and an auxiliary plate 2 is fixedly connected to the detection box 13, and a clamping assembly 4 is arranged above the auxiliary plate 2, and the clamping assembly 4 is used to clamp a detection test tube 5, and the detection test tube 5 contains blood to be tested by the patient, and three groups of adjacent syringes 3 are arranged above the detection test tube 5, and the bottom of the syringe 3 is rotatably connected to The three groups of syringes 3 are arranged in sequence clockwise, and the three groups of syringes 3 are respectively meshed and connected with a rotating assembly 6, and the rotating assembly 6 is used to rotate the needle 31 of the syringe 3. The bottoms of the three groups of syringes 3 are respectively slidably connected with a disinfection assembly 7, and the disinfection assembly 7 is used to disinfect the needle 31 of the syringe 3. The three groups of syringes 3 are respectively located on different sides of the detection box 13, and the remaining side of the detection box 13 is provided with a detection sensor. When the staff first opens the cover 101 and puts the test tube 5 containing the patient's blood sample on the clamping assembly 4, the servo motor 11 starts to rotate. When the servo motor 11 rotates, the clamping assembly 4 will The motor 11 starts to rotate under the action of the test tube 5, and at the same time drives the test tube 5 to move in the detector 1. During the movement of the test tube 5, it will rotate and vibrate under the action of the auxiliary plate 2, so that the blood sample in the test tube 5 is mixed with the anticoagulant. When the test tube 5 moves to just below the first syringe 3, the servo motor 11 stops rotating, the first syringe 3 is inserted into the test tube 5, and the first reagent inside is injected into the test tube 5. When the first syringe 3 has finished injecting, the servo motor 11 will continue to rotate, so that the test tube 5 continues to move, and rotates and vibrates again, so that the solution inside is fully mixed with the first reagent. When the detection test tube 5 moves to the bottom of the second syringe 3, the servo motor 11 will stop again, and the second syringe 3 will inject the second reagent inside into the detection test tube 5. When the injection is completed, the detection test tube 5 will move to the bottom of the third syringe 3 under the action of the servo motor 11 and be injected with the third reagent. Finally, after mixing, the detection test tube 5 will stay on one side of the detection sensor. When the detection sensor finishes the detection, the detection result will be displayed on the display screen at the top of the detector 1. At the same time, the detection test tube 5 will return to the initial position under the action of the servo motor 11. At this time, the operator can remove the detected detection test tube 5.
[0027] In this embodiment, if Figures 1 to 7As shown, the top of the detector 1 is a numerical control operation area, and the operator can adjust the rotation speed of the servo motor 11 according to different situations. The sides of the detector 1 are provided with movable doors, and the state of the detection box 13 can be observed and the reagents in the three syringes 3 can be added by opening the movable doors.
[0028] As an implementation method in this embodiment, Figures 3 to 8 As shown, the top of the auxiliary plate 2 is provided with three groups of uniformly spaced serrated structures, the side of the auxiliary plate 2 is fixedly connected with a guide plate 21, the middle positions of the three sides of the auxiliary plate 2 are fixedly connected with pads 22, the pads 22 and the syringes 3 correspond one to one, and the pads 22 are located directly below the syringes 3. The clamping assembly 4 includes a conveyor belt 41, the surface of the conveyor belt 41 is fixedly connected with a connecting column 42, a clamping plate 43 is provided on one side of the connecting column 42, one side of the clamping plate 43 is fixedly connected to the second gear 432 through a rubber rod 431, and the second gear 432 is connected to the connecting column 42 through a bearing 433. The clamping plate 43 clamps a test tube 5, and a sealing cover 51 is provided on the top of the test tube 5. The inner side of the conveyor belt 41 is connected to four transmission rollers 12. When the servo motor 11 rotates, When the rubber rod 431 hits the guide plate 21, the rubber rod 431 moves on the inclined surface at the top of the guide plate 21 and gradually bends. When the rubber rod 431 moves to the end of the inclined surface, the rubber rod 431 loses the effect of the inclined surface and thus quickly recovers. In this process, the test tube 5 experiences shaking. Through the self-rotation of the test tube 5 and the shaking of the test tube 5, the blood sample and the anticoagulant in the test tube 5 are fully mixed.
[0029] In this embodiment, if Figures 4 to 8 As shown, the guide plates 21 are provided with a plurality of them. Whenever the syringe 3 injects the internal reagent into the test tube 5, the rubber rod 431 will come into contact with the guide plate 21, and make the test tube 5 shake during the rotation, thereby increasing the mixing degree between the solution and the reagent in the test tube 5. When the syringe 3 inserts the needle 31 into the test tube 5, the bottom of the test tube 5 is located on the pad 22. At this time, the pad 22 provides support for the test tube 5, thereby preventing the rubber rod 431 from bending.
[0030] As an implementation method in this embodiment, Figures 9 to 12As shown, the syringe 3 is slidably connected with a piston 32, the top of the piston 32 is fixedly connected with a group of trigger plates 321 with uniform intervals, the top of the trigger plate 321 is fixedly connected with an electric push rod 322, the side of the syringe 3 is fixedly connected with a hollow rod 33, one end of the hollow rod 33 is limitedly slidably connected to the detection box 13, an inclined block 331 is fixedly connected to the hollow rod 33, the opening of the hollow rod 33 is located above the piston 32, a trigger rod 332 is slidably connected to the hollow rod 33, one end of the trigger rod 332 is provided with an inclined surface, the trigger rod 332 is sleeved with a first spring 333, the inclined surface of the trigger rod 332 is located below the trigger plate 321, and the needle 31 is provided with a first Gear 311, the rotating assembly 6 includes an auxiliary roller 61, the auxiliary roller 61 is connected to the gear shaft 62 through a belt, a gear is arranged on the top of the gear shaft 62, the auxiliary roller 61 is connected to the driving roller 12 through a belt, the auxiliary roller 61 is rotatably connected in the detection box 13, the top of the gear shaft 62 is meshed with the first gear 311 of the needle 31 through a gear, the gear length on the gear shaft 62 is greater than the length of the first gear 311, the disinfection assembly 7 includes a storage tank 71, a cotton roll 72 is rotatably connected in the storage tank 71, the cotton roll 72 in the storage tank 71 is not immersed in disinfection alcohol, the other end of the cotton roll 72 is located on the reel 74 in the collection tank 73, and one side of the reel 74 A winding plate 75 is provided, and a circular array of ratchet pawls 741 is provided on the winding shaft 74. A ratchet 742 is rotatably connected to the winding shaft 74. The ratchet 742 is connected to the winding shaft 74 through the ratchet 741. One end of one side of the winding plate 75 is provided with a serrated structure with uniform intervals. The side of the ratchet 742 is provided with a group of serrated structures in an annular array. The ratchet 742 is meshed and connected with the winding plate 75. The storage tank 71 and the collection tank 73 are both fixedly connected to one side of the detection box 13. One side of the cotton roll 72 is close to the needle 31. The length of the needle 31 is greater than the width of the cotton roll 72. The top of the winding plate 75 is provided with an inclined surface, which drives the inclined surface at the top of the winding plate 75 to contact the bottom of the inclined block 331. The inclined surface of the winding plate 75 fits together, one side of the winding plate 75 is slidably connected to the detection box 13, and a second spring 751 is arranged between the winding plate 75 and the detection box 13. When the servo motor 11 rotates, the transmission roller 12 drives the auxiliary roller 61 to rotate through the belt. When the auxiliary roller 61 rotates, the gear shaft 62 is rotated through the belt. During the rotation of the gear shaft 62, the needle 31 is driven to rotate through the top gear, so that the needle 31 can rotate on one side of the cotton cloth roll 72. When the detection test tube 5 is located below the syringe 3, when the servo motor 11 stops rotating, the needle 31 also stops rotating at the same time. At this time, the electric push rod 322 extends and pushes the trigger plate 321.
[0031] When the syringe 3 is in the state of being pressed down, the trigger plate 321 is pressed against the inclined surface of the trigger rod 332, and the trigger rod 332 is gradually pressed into the hollow rod 33. When the piston 32 moves downward for a certain distance, the trigger plate 321 is separated from the inclined surface of the trigger rod 332, and the trigger rod 332 is ejected under the action of the first spring 333 and is stuck between the two trigger plates 321. At this time, the electric push rod 322 stops moving, and the reagent in the syringe 3 is also injected into the test tube 5. When the electric push rod 322 is contracted, the trigger rod 332 is always stuck between the two trigger plates 321. When the syringe 3 moves downward, the inclined block 331 on the hollow rod 33 will be pressed on the winding plate 75, and the winding plate 75 will move under the action of the inclined block 331. When the winding plate 75 moves, the winding plate 75 will drive the ratchet 742 to rotate. When the ratchet 742 rotates, the winding shaft 74 will rotate through the pawl 741. When the winding shaft 74 rotates, the cotton cloth roll 72 will be rolled up, so that the clean alcohol cotton cloth in the storage tank 71 will contact the needle 31. When the hollow rod 33 moves upward, the winding plate 75 will move in the opposite direction under the action of the second spring 751, and drive the ratchet 742 to reverse. At this time, due to the reverse rotation of the ratchet 742, the winding shaft 74 will not be driven to rotate through the pawl 741, so the winding shaft 74 remains stationary. When the test tube 5 moves, the needle 31 will rotate on the alcohol cotton cloth under the action of the servo motor 11, thereby disinfecting the needle 31.
[0032] The working principle of the technical solution provided by the present invention is as follows: When the staff first opens the cover 101 and places the test tube 5 containing the patient's blood sample on the clamping assembly 4, the servo motor 11 starts to rotate. When the servo motor 11 rotates, the clamping assembly 4 will start to rotate under the action of the servo motor 11, and at the same time drive the test tube 5 to move in the detector 1. During the movement of the test tube 5, it will rotate and vibrate under the action of the auxiliary plate 2, so that the blood sample in the test tube 5 is mixed with the anticoagulant. When the test tube 5 moves to just below the first syringe 3, the servo motor 11 stops rotating, the first syringe 3 is inserted into the test tube 5, and the first reagent inside is injected into the test tube 5. When the first syringe 3 is injected, the servo motor 11 will continue to rotate to make the test tube 5 move. The test tube 5 then moves, and rotates and vibrates again to fully mix the solution inside with the first reagent. When the test tube 5 moves to the bottom of the second syringe 3, the servo motor 11 will stop again, and the second syringe 3 will inject the second reagent inside into the test tube 5. When the injection is completed, the test tube 5 will move to the bottom of the third syringe 3 under the action of the servo motor 11, and be injected with the third reagent. Finally, after mixing, the test tube 5 will stay on one side of the detection sensor. When the detection sensor inside the detector 1 is finished, the detection result will be displayed on the display screen at the top of the detector 1. At the same time, the test tube 5 will return to its initial position under the action of the servo motor 11. At this time, the operator can remove the tested test tube 5.
[0033] At the same time, when the servo motor 11 rotates, the transmission roller 12 located below the servo motor 11 will rotate, so that the conveyor belt 41 will rotate around the detection box 13. When the conveyor belt 41 rotates, the second gear 432 will rotate under the action of the auxiliary plate 2. When the second gear 432 rotates, the detection test tube 5 located on the clamping plate 43 will rotate synchronously with the second gear 432. When the rubber rod 431 hits the guide plate 21, the rubber rod 431 will move on the inclined surface at the top of the guide plate 21 and gradually bend. When the rubber rod 431 moves to the end of the inclined surface When the servo motor 11 rotates, the transmission roller 12 drives the auxiliary roller 61 to rotate through the belt. When the auxiliary roller 61 rotates, the gear shaft 62 is rotated through the belt. During the rotation of the gear shaft 62, the needle 31 is driven to rotate through the gear on the top, so that the needle 31 can rotate on one side of the cotton cloth roll 72.
[0034] When the test tube 5 is located below the syringe 3, the servo motor 11 stops rotating, and the needle 31 also stops rotating. At this time, the electric push rod 322 extends and pushes the trigger plate 321. At this time, since the inclined surface of the trigger rod 332 is stuck between the piston 32 and the trigger plate 321, the trigger plate 321 will drop synchronously with the syringe 3. When the hollow rod 33 moves to the bottom of the slide groove on the detection box 13, the hollow rod 33 cannot move downward further, and the syringe 3 cannot move. At this time, the needle 31 is inserted into the sealing cover 5. 1, as the electric push rod 322 continues to extend, the trigger plate 321 will be pressed on the inclined surface of the trigger rod 332, and gradually press the trigger rod 332 into the hollow rod 33. When the piston 32 moves downward for a certain distance, the trigger plate 321 will separate from the inclined surface of the trigger rod 332, and the trigger rod 332 will pop out under the action of the first spring 333 and get stuck between the two trigger plates 321. At this time, the electric push rod 322 stops moving, and the reagent in the syringe 3 is also injected into the test tube 5. When the electric push rod 322 shrinks, the trigger plate 321 will be pressed against the inclined surface of the trigger rod 332. During the process of the syringe 3 rising, the trigger rod 332 will always be stuck between the two trigger plates 321. During the rising process, the volume of the reagent inside the syringe 3 remains unchanged. When the syringe 3 moves downward, the inclined block 331 on the hollow rod 33 will be pressed on the winding plate 75. The winding plate 75 will move under the action of the inclined block 331. When the winding plate 75 moves, the winding plate 75 will drive the ratchet 742 to rotate. When the ratchet 742 rotates, the winding shaft 74 will rotate through the ratchet 741. When the winding shaft 74 rotates, , the cotton cloth roll 72 will be rolled up, so that the clean alcohol cotton cloth in the storage tank 71 will contact the needle 31. When the hollow rod 33 moves upward, the winding plate 75 will move in the opposite direction under the action of the second spring 751, and drive the ratchet 742 to reverse. At this time, due to the reverse rotation of the ratchet 742, the winding shaft 74 will not be driven to rotate through the pawl 741, so the winding shaft 74 remains stationary. When the test tube 5 moves, the needle 31 will rotate on the alcohol cotton cloth under the action of the servo motor 11, thereby disinfecting the needle 31.
[0035] The present invention covers any substitution, modification, equivalent method and scheme made on the essence and scope of the present invention. In order to make the public have a thorough understanding of the present invention, specific details are described in detail in the following preferred embodiments of the present invention, but those skilled in the art can fully understand the present invention without the description of these details. In addition, in order to avoid unnecessary confusion about the essence of the present invention, well-known methods, processes, procedures, components and circuits are not described in detail.
[0036] The above is only a preferred embodiment of the present invention. It should be pointed out that for ordinary technicians in this technical field, several improvements and modifications can be made without departing from the principle of the present invention. These improvements and modifications should also be regarded as the scope of protection of the present invention.
Claims
1. A semi-automatic coagulation detection analyzer, characterized in that: The detector comprises a detection box, a cover plate is installed at the front end of the detector, and transmission rollers are rotatably connected at the four corners of the detection box, and the top of one of the transmission rollers is fixedly connected to the output shaft of the servo motor; An auxiliary plate is fixedly connected to the detection box, and a clamping assembly is arranged above the auxiliary plate. The clamping assembly is used to clamp a detection test tube, and the detection test tube contains blood to be detected by a patient. Three groups of adjacent syringes are arranged above the detection test tube, and needles are rotatably connected to the bottom of the syringes. The three groups of syringes are arranged in a clockwise manner, and the three groups of syringes are respectively meshed and connected with a rotating assembly, and the rotating assembly is used to rotate the needles of the syringes; The bottoms of the three groups of syringes are slidably connected with disinfection components respectively, and the disinfection components are used to disinfect the needles of the syringes. The three groups of syringes are respectively located on different sides of the detection box, and the remaining side of the detection box is provided with a detection sensor.
2. The semi-automatic coagulation detection analyzer according to claim 1, characterized in that: The top of the auxiliary plate is provided with three groups of sawtooth structures with uniform intervals, the side of the auxiliary plate is fixedly connected with a guide plate, the middle positions of the three sides of the auxiliary plate are fixedly connected with pads, the pads correspond to the syringes one by one, and the pads are located directly below the syringes.
3. The semi-automatic coagulation detection analyzer according to claim 2, characterized in that: A piston is slidably connected to the syringe, a group of trigger plates with uniform intervals are fixedly connected to the top of the piston, an electric push rod is fixedly connected to the top of the trigger plate, a hollow rod is fixedly connected to the side of the syringe, an inclined block is fixedly connected to the hollow rod, the opening of the hollow rod is located above the piston, a trigger rod is slidably connected to the hollow rod, one end of the trigger rod is provided with an inclined surface, a first spring is sleeved on the trigger rod, the inclined surface of the trigger rod is located below the trigger plate, and a first gear is provided on the needle.
4. The semi-automatic coagulation detection analyzer according to claim 3, characterized in that: The clamping assembly comprises a conveyor belt, a connecting column is fixedly connected to the surface of the conveyor belt, and a clamping plate is arranged on one side of the connecting column.
5. The semi-automatic coagulation detection analyzer according to claim 4, characterized in that: One side of the clamping plate is fixedly connected to the second gear through a rubber rod, the second gear is connected to the connecting column through a bearing, the clamping plate clamps a test tube, a sealing cover is provided on the top of the test tube, and the inner side of the conveyor belt is connected to four transmission rollers.
6. The semi-automatic coagulation detection analyzer according to claim 5, characterized in that: The rotating assembly comprises an auxiliary roller, the auxiliary roller is connected to a gear shaft through a belt, and a gear is arranged on the top of the gear shaft.
7. The semi-automatic coagulation detection analyzer according to claim 6, characterized in that: The auxiliary roller is connected to the transmission roller through a belt, the top of the gear shaft is meshed and connected with the first gear of the needle through a gear, and the length of the gear on the gear shaft is greater than the length of the first gear.
8. The semi-automatic blood coagulation analysis instrument according to claim 7, characterized in that: The disinfection component includes a storage tank, in which a cotton roll is rotatably connected. The cotton roll in the storage tank is immersed in disinfectant alcohol. The other end of the cotton roll is located on a winding shaft in a collection tank, and a winding plate is provided on one side of the winding shaft.
9. The semi-automatic coagulation detection analyzer according to claim 8, characterized in that: The winding shaft is provided with a circular array of pawls, the winding shaft is rotatably connected with a ratchet, the ratchet is connected to the winding shaft through the pawl, one end of one side of the winding plate is provided with a uniformly spaced serrated structure, the side of the ratchet is provided with a group of circular array of serrated structures, and the ratchet is meshingly connected with the winding plate.
10. The semi-automatic blood coagulation analysis instrument according to claim 9, characterized in that: The storage tank and the collection tank are both fixedly connected to one side of the detection box, one side of the cotton cloth roll is close to the needle, the length of the needle is greater than the width of the cotton cloth roll, and the top of the winding plate is provided with an inclined surface, which drives the inclined surface of the top of the winding plate to fit the inclined surface of the bottom of the inclined block, and one side of the winding plate is slidably connected to the detection box, and a second spring is provided between the winding plate and the detection box.
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