A device for preventing rupture and mixing of whole blood cell marker diagnostic reagent
By using a multi-rotation chamber and a motor-driven rotation device in the whole blood cell marker diagnostic reagent, combining the mixing method of rotation and rotation, the problems of low efficiency and rupture in the existing technology are solved, and efficient and accurate whole blood cell mixing is achieved. deal with.
Patent Information
- Application Number
- CN202410419339.9
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Filing Date
- 2024-04-09
- Publication Date
- 2024-12-17
- Estimated Expiration
- 2044-04-09
AI Technical Summary
The existing mixing device is inefficient when processing whole blood cell marker diagnostic reagents and is prone to rupture of whole blood cells, affecting the accuracy of detection.
A whole blood cell marker diagnostic reagent anti-rupture mixing device is designed, and a rotating device driven by a multi-rotation chamber and a motor is used to mix whole blood cells in the reagent tube by combining revolution and rotation to control centrifugal strength and avoid rupture. And the reagent tube is stabilized and agitated by the matching of gears and ring gears.
It improves the mixing efficiency and quality of whole blood cells, avoids rupture, and enhances the accuracy of subsequent detection.
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Figure CN118304789B_ABST
Abstract
Description
Technical Field
[0001] The invention relates to the technical field of mixing devices, in particular to a rupture-proof mixing device for a whole blood cell marker diagnostic reagent. Background Art
[0002] Whole blood cell marker diagnostic reagents are reagents used to detect the levels of specific cells or molecules in the blood, usually for disease diagnosis, monitoring disease progression or evaluating treatment effects; these reagents are widely used in medical laboratories and clinical medicine and can provide important biological information; the reagents need to be mixed before testing;
[0003] Existing mixing devices usually consist of a conveying device and a shaking device. The mixing device can only mix a few reagent samples at a time, which is very inefficient. In addition, during the mixing process, whole blood cells may rupture due to excessive centrifugal force, thereby affecting subsequent testing and reducing the accuracy of the test. Summary of the invention
[0004] The object of the present invention is to provide a whole blood cell marker diagnostic reagent anti-rupture mixing device to solve the problems raised in the above background technology.
[0005] In order to solve the above technical problems, the present invention provides the following technical solutions:
[0006] A whole blood cell marker diagnostic reagent anti-rupture mixing device comprises: a body, a plurality of rotating chambers are arranged on the body, and the plurality of rotating chambers are equally arranged along the axis of the body, a rotating device is arranged in the rotating chamber, and the rotating device comprises: a placement plate, the placement plate is arranged in the rotating device, and the rotating plate is rotatably connected to the rotating chamber.
[0007] Preferably, a motor is provided in the rotating chamber, a driving shaft of the motor is connected to the bottom of the rotating device, and a reagent tube is placed in the placement tray;
[0008] The staff places the reagent tubes in the placement tray, and then the controller controls the motor to start. The drive shaft in the motor drives the rotating device to rotate, and the rotating device then rotates around the axis of the drive shaft. While the motor drives the rotating device to rotate, the controller controls the rotating device to start, and the rotating device then drives each reagent tube to rotate individually, so that while the rotating device rotates over a large range, the reagent tubes also rotate individually, thereby improving the mixing of the whole blood cells in the reagent tubes, thereby improving the mixing effect of the whole blood cells. At the same time, the speed of the motor and the rotating device can be used to control the mixing rate of the reagent tubes, thereby avoiding the rupture of the whole blood cells during the mixing process, thereby improving the quality of the whole blood cell mixing.
[0009] Preferably, a plurality of placement grooves are provided on the placement plate, and the plurality of placement grooves are arranged around the axis of the placement plate, a movable cavity is provided on one side of the placement groove close to the rotating cavity, the placement groove is connected with the movable cavity, and a placement tube is provided in the placement groove.
[0010] Preferably, a ring gear is provided on the shaft wall of the placement groove, tooth grooves are provided on the inner wall and the outer wall of the ring gear, the ring gear is rotatably connected to the placement groove, a micro motor is provided in the placement disk, an output gear is provided on the driving shaft of the micro motor, a driven gear is provided between the ring gear and the output gear, and the ring gear is meshed with the output gear through the driven gear.
[0011] Preferably, an annular gear ring is provided on one side of the placement tube close to the moving chamber, the annular gear ring is meshed with the inner wall of the annular gear, the length of the annular gear ring is greater than the length of the annular gear, a plurality of fixing rings are provided inside the placement tube, the fixing rings are connected to the inner wall of the placement tube through a bracket, a plurality of the fixing rings are vertically equally arranged along the axis of the placement tube, a support plate is provided at the bottom of the placement tube, and the bracket, fixing ring and support plate are all made of rubber.
[0012] Preferably, a plurality of movable plates are provided inside the movable cavity, the plurality of movable plates are combined into a circle, the plurality of movable plates are radially arranged along the axis of the movable cavity, a plurality of movable grooves are provided on the inner wall of the movable cavity, a movable block is provided on the side of the movable plate close to the movable groove, the movable plate is slidably connected to the movable groove through the movable block, and the bottom of the placement tube is in contact with the upper surface of the movable plate.
[0013] Preferably, a rotating shaft is provided on the side of the movable plate away from the placement groove, and a plurality of cams are provided on the rotating shaft. The plurality of cams are equally arranged along the axis of the rotating shaft, and the raised portion of each cam faces a different direction. The side wall of the cam contacts the lower surface of the movable plate, and the cam is slidably connected to the movable plate.
[0014] Preferably, one end of the rotating shaft passes through the moving cavity and is provided with a bevel gear, and an end face gear is provided inside the rotating cavity, and the bevel gear is meshed with the end face gear;
[0015] After whole blood cells are placed in the reagent tube, the staff puts the reagent tube into the placement slot, and the reagent tube passes through the fixing ring in turn, and the fixing ring then wraps and fixes the reagent tube. When the reagent tube moves to the bottom of the placement tube, the reagent tube contacts the support plate, and the support plate holds the reagent tube. The fixing ring and the support plate cooperate with each other, and the fixing ring and the support plate wrap the reagent tube, which prevents the reagent tube from colliding with the inner wall of the placement tube during the rotation and mixing process, thereby causing the reagent tube to collide and break, thereby ensuring the integrity of the reagent tube during the mixing process and improving the protection of the reagent tube;
[0016] When the reagent tube is placed, the control starts the motor in the rotating chamber. The drive shaft in the motor drives the placement plate to rotate. During the rotation of the placement plate, the placement plate drives the placement slot to rotate, and the placement slot drives the reagent tube to rotate, thereby realizing the revolution of the reagent tube around the axis of the rotating chamber;
[0017] While the reagent tube is revolving, the controller controls the micro motor in the placement plate to start, and the driving shaft in the micro motor drives the output gear to rotate. When the output gear rotates, it drives the driven gear to rotate. When the driven gear rotates, it drives the ring gear to rotate. During the rotation of the ring gear, the ring gear and the annular gear ring are meshed and transmitted, so that the annular gear ring rotates. During the rotation of the annular gear ring, the annular gear ring drives the placement tube to rotate, and the placement tube drives the reagent tube to rotate. The reagent tube mixes the whole blood cells under the condition of coordinated revolution and rotation, thereby improving the mixing efficiency of the whole blood cells. The rotation rate is regulated by the controller, so that the centrifugal intensity of the whole blood cells in the reagent tube can be small, thereby avoiding the whole blood cells being ruptured by high centrifugal force, which leads to poor subsequent detection results, thereby improving the accuracy of subsequent detection;
[0018] When the motor drives the placement plate to rotate, since the rotating shaft passes through the moving cavity and is provided with a bevel gear, during the rotation of the placement plate, the placement plate drives the rotating shaft to rotate, and the rotating shaft drives the bevel gear to rotate around the axis of the placement plate. Since the bevel gear and the end gear are in meshing rotation, when the bevel gear rotates around the placement plate, it meshes with the end gear, and during the meshing process, the bevel gear rotates around its own axis, so that when the bevel gear rotates, it drives the rotating shaft to rotate.
[0019] When the rotating shaft rotates, it drives several cams to rotate. During the rotation of the cam, the side wall of the cam contacts the moving plate. When the raised part of the cam rotates toward the side close to the moving cavity, the raised part of the cam immediately pushes the moving plate to move, and the moving block on the moving plate moves along the moving groove, and the moving plate moves toward the side close to the moving cavity. During the movement of the moving plate, the moving plate pushes the placement tube to move, and the placement tube moves to the side away from the moving plate, and the placement tube moves along the axis of the placement groove, and then the placement tube extends out of the placement groove; when the raised part of the cam rotates toward the side away from the moving plate, the moving plate moves toward the side close to the cam, and then the placement tube moves toward the side close to the cam, so that the placement tube makes a vertical reciprocating movement along the axis of the placement groove, thereby realizing the stirring of the whole blood cells in the reagent tube, further improving the efficiency of the mixing of the whole blood cells, and by coordinating the revolution, rotation and reciprocating movement of the axis of the reagent tube, the quality of the mixing of the whole blood cells in the reagent tube is improved.
[0020] Compared with the prior art, the beneficial effects achieved by the present invention are:
[0021] 1. When the reagent tube is placed, the controller starts the motor in the rotating chamber. The driving shaft in the motor drives the placement plate to rotate. During the rotation of the placement plate, the placement plate drives the placement slot to rotate, and the placement slot drives the reagent tube to rotate, so that the reagent tube revolves around the axis of the rotating chamber; while the reagent tube revolves, the controller controls the micro motor in the placement plate to start, and the driving shaft in the micro motor drives the output gear to rotate. When the output gear rotates, it drives the driven gear to rotate. When the driven gear rotates, it drives the ring gear to rotate. During the rotation of the ring gear, the ring gear meshes with the annular gear ring, so that the annular gear ring rotates. During the rotation of the annular gear ring, the annular gear ring drives the placement tube to rotate, and the placement tube drives the reagent tube to rotate. The reagent tube mixes the whole blood cells under the conditions of the coordination of revolution and rotation, thereby improving the efficiency of the whole blood cell mixing. The controller regulates the rotation rate, so that the whole blood cells can be centrifuged at a low intensity in the reagent tube, thereby avoiding the high centrifugal force that causes the whole blood cells to rupture, which leads to poor subsequent detection results, thereby improving the accuracy of subsequent detection.
[0022] 2. When the rotating shaft rotates, it drives several cams to rotate. During the rotation of the cam, the side wall of the cam contacts the moving plate. When the raised part of the cam rotates toward the side close to the moving cavity, the raised part of the cam immediately pushes the moving plate to move, and the moving block on the moving plate moves along the moving groove, and the moving plate moves toward the side close to the moving cavity. During the movement of the moving plate, the moving plate pushes the placement tube to move, and the placement tube moves toward the side away from the moving plate, and the placement tube moves along the axis of the placement groove, and then the placement tube extends out of the placement groove; when the raised part of the cam rotates toward the side away from the moving plate, the moving plate moves toward the side close to the cam, and then the placement tube moves toward the side close to the cam, so that the placement tube makes a vertical reciprocating movement along the axis of the placement groove, thereby realizing the stirring of the whole blood cells in the reagent tube, further improving the efficiency of the mixing of the whole blood cells, and by coordinating the revolution, rotation and reciprocating movement of the axis of the reagent tube, the quality of the mixing of the whole blood cells in the reagent tube is improved. BRIEF DESCRIPTION OF THE DRAWINGS
[0023] The accompanying drawings are used to provide a further understanding of the present invention and constitute a part of the specification. Together with the embodiments of the present invention, they are used to explain the present invention and do not constitute a limitation of the present invention. In the accompanying drawings:
[0024] Figure 1 It is the main figure of the present invention;
[0025] Figure 2 is a cross-sectional view of the present invention;
[0026] Figure 3 It is a schematic diagram of the structure of the rotating device;
[0027] Figure 4 is a schematic diagram of the cross-sectional structure of the rotating device;
[0028] Figure 5 is a cross-sectional front view of the rotating device;
[0029] Figure 6 It is a schematic diagram of the exploded structure of the rotating device;
[0030] Figure 7 is an exploded front view of the rotating device;
[0031] Figure 8 is a schematic diagram of the internal structure of the placement tube;
[0032] Fig. 9 is a schematic diagram of the structure of the ring gear and the placement tube;
[0033] In the figure: 1, machine body; 11, rotating chamber;
[0034] 2. Rotating device; 21. Placing plate; 22. Placing groove; 221. Ring gear; 23. Moving chamber; 24. Placing tube; 241. Annular gear ring; 242. Fixed ring; 243. Support plate; 25. Moving plate; 26. Moving groove; 27. Rotating shaft; 28. Cam; 30. Bevel gear; 31. Face gear. DETAILED DESCRIPTION
[0035] The following will be combined with the drawings in the embodiments of the present invention to clearly and completely describe the technical solutions in the embodiments of the present invention. Obviously, the described embodiments are only part of the embodiments of the present invention, not all of the embodiments. Based on the embodiments of the present invention, all other embodiments obtained by ordinary technicians in this field without creative work are within the scope of protection of the present invention.
[0036] See also Figure 1-Figure 9 , the present invention provides a technical solution:
[0037] A whole blood cell marker diagnostic reagent anti-rupture mixing device comprises: a body 1, a plurality of rotating chambers 11 are arranged on the body 1, and the plurality of rotating chambers 11 are equally arranged along the axis of the body 1, a rotating device 2 is arranged in the rotating chamber 11, and the rotating device 2 comprises: a placement plate 21, the placement plate 21 is arranged in the rotating device 2, and the rotating plate 21 is rotatably connected to the rotating chamber 11.
[0038] As a specific embodiment of the present invention, a motor is provided in the rotating chamber 11, the driving shaft of the motor is connected to the bottom of the rotating device 2, and a reagent tube is placed in the placement tray 21;
[0039] The staff places the reagent tubes in the placement tray 21, and then the controller controls the motor to start. The driving shaft in the motor drives the rotating device 2 to rotate, and the rotating device 2 then rotates around the axis of the driving shaft. While the motor drives the rotating device 2 to rotate, the controller controls the rotating device 2 to start, and the rotating device 2 then drives each reagent tube to rotate individually, so that while the rotating device 2 rotates over a large range, the reagent tubes also rotate individually, thereby improving the mixing of the whole blood cells in the reagent tubes. At the same time, the rotation speed of the motor and the rotating device 2 can be used to control the mixing rate of the reagent tubes, thereby avoiding the rupture of the whole blood cells during the mixing process.
[0040] As a specific embodiment of the present invention, a plurality of placement grooves 22 are arranged on the placement plate 21, and the plurality of placement grooves 22 are arranged around the axis of the placement plate 21. A movable cavity 23 is arranged on the side of the placement groove 22 close to the rotating cavity 11, and the placement groove 22 is connected to the movable cavity 23, and a placement tube 24 is arranged in the placement groove 22.
[0041] As a specific embodiment of the present invention, a ring gear 221 is arranged on the shaft wall of the placement groove 22, and tooth grooves are arranged on the inner wall and the outer wall of the ring gear 221. The ring gear 221 is rotatably connected with the placement groove 22. A micro motor is arranged in the placement plate 21, and an output gear is arranged on the driving shaft of the micro motor. A driven gear is arranged between the ring gear 221 and the output gear, and the ring gear 221 is meshed with the output gear through the driven gear.
[0042] As a specific embodiment of the present invention, an annular gear ring 241 is provided on one side of the placement tube 24 close to the moving chamber 23, and the annular gear ring 241 is meshed with the inner wall of the annular gear 221. The length of the annular gear ring 241 is greater than the length of the annular gear 221. A plurality of fixing rings 242 are provided inside the placement tube 24, and the fixing ring 242 is connected to the inner wall of the placement tube 24 through a bracket. A plurality of the fixing rings 242 are vertically equally arranged along the axis of the placement tube 24. A support plate 243 is provided at the bottom of the placement tube 24, and the bracket, fixing ring 242 and support plate 243 are all made of rubber.
[0043] As a specific embodiment of the present invention, a plurality of movable plates 25 are arranged inside the movable chamber 23, and the plurality of movable plates 25 are combined into a circle, and the plurality of movable plates 25 are radially arranged along the axis of the movable chamber 23, and a plurality of movable grooves 26 are arranged on the inner wall of the movable chamber 23, and a movable block is arranged on the side of the movable plate 25 close to the movable groove 26, and the movable plate 25 is slidably connected to the movable groove 26 through the movable block, and the bottom of the placement tube 24 is in contact with the upper surface of the movable plate 25.
[0044] As a specific embodiment of the present invention, a rotating shaft 27 is provided on the side of the movable plate 25 away from the placement groove 22, and a plurality of cams 28 are provided on the rotating shaft 27. The plurality of cams 28 are equally arranged along the axis of the rotating shaft 27, and the raised portion of each cam 28 faces a different direction. The side wall of the cam 28 contacts the lower surface of the movable plate 25, and the cam 28 is slidably connected to the movable plate 25.
[0045] As a specific embodiment of the present invention, one end of the rotating shaft 27 passes through the moving cavity 23 and is provided with a bevel gear 30, and an end face gear 31 is provided inside the rotating cavity 11, and the bevel gear 30 is meshed with the end face gear 31;
[0046] After whole blood cells are placed in the reagent tube, the staff puts the reagent tube into the placement slot 22, and the reagent tube passes through the fixing ring 242 in turn, and the fixing ring 242 then wraps and fixes the reagent tube. When the reagent tube moves to the bottom of the placement tube 24, the reagent tube contacts the support plate 243, and the support plate 243 holds the reagent tube. The fixing ring 242 and the support plate 243 cooperate with each other, and the fixing ring 242 and the support plate 243 wrap the reagent tube, thereby preventing the reagent tube from colliding with the inner wall of the placement tube 24 during the rotation and mixing process, thereby causing the reagent tube to collide and break;
[0047] When the reagent tube is placed, the control starts the motor in the rotating chamber 11. The drive shaft in the motor drives the placement plate 21 to rotate. During the rotation of the placement plate 21, the placement plate 21 drives the placement slot 22 to rotate, and the placement slot 22 drives the reagent tube to rotate, so that the reagent tube revolves around the axis of the rotating chamber 11;
[0048] While the reagent tube is revolving, the controller controls the micro motor in the placement plate 21 to start, and the driving shaft in the micro motor drives the output gear to rotate. When the output gear rotates, it drives the driven gear to rotate. The driven gear rotates and drives the ring gear 221 to rotate. During the rotation of the ring gear 221, the ring gear 221 meshes with the annular gear ring 241, so that the annular gear ring 241 rotates. During the rotation of the annular gear ring 241, the annular gear ring 241 drives the placement tube 24 to rotate, and the placement tube 24 drives the reagent tube to rotate. The reagent tube mixes the whole blood cells under the condition of the coordination of the revolution and the rotation, and the rotation rate is regulated by the controller;
[0049] During the process of the placement plate 21 being driven by the motor to rotate, since the rotating shaft 27 passes through the moving cavity 23 and is provided with a bevel gear 30, during the rotation of the placement plate 21, the placement plate 21 drives the rotating shaft 27 to rotate, and the rotating shaft 27 drives the bevel gear 30 to rotate around the axis of the placement plate 21. Since the bevel gear 30 and the end face gear 31 are in meshing rotation, when the bevel gear 30 rotates around the placement plate 21, it meshes with the end face gear 31, and during the meshing process, the bevel gear 30 rotates around its own axis, so that when the bevel gear 30 rotates, it drives the rotating shaft 27 to rotate.
[0050] When the rotating shaft 27 rotates, it drives several cams 28 to rotate. During the rotation of the cam 28, the side wall of the cam 28 contacts the moving plate 25. When the raised part of the cam 28 rotates toward the side close to the moving chamber 23, the raised part of the cam 28 immediately pushes the moving plate 25 to move, and the moving block on the moving plate 25 moves along the moving groove 26. The moving plate 25 moves toward the side close to the moving chamber 23. During the movement of the moving plate 25, the moving plate 25 pushes the placement tube 24 to move, and the placement tube 24 moves toward the side away from the moving plate 25. The placement tube 24 moves along the axis of the placement groove 22, and then the placement tube 24 extends out of the placement groove 22; when the raised part of the cam 28 rotates toward the side away from the moving plate 25, the moving plate 25 moves toward the side close to the cam 28, and then the placement tube 24 moves toward the side close to the cam 28, so that the placement tube 24 makes a vertical reciprocating movement along the axis of the placement groove 22, thereby realizing the stirring of the whole blood cells in the reagent tube.
[0051] Working principle of the present invention:
[0052] After whole blood cells are placed in the reagent tube, the staff puts the reagent tube into the placement slot 22, and the reagent tube passes through the fixing ring 242 in turn, and the fixing ring 242 then wraps and fixes the reagent tube. When the reagent tube moves to the bottom of the placement tube 24, the reagent tube contacts the support plate 243, and the support plate 243 holds the reagent tube. The fixing ring 242 and the support plate 243 cooperate with each other, and the fixing ring 242 and the support plate 243 wrap the reagent tube, thereby preventing the reagent tube from colliding with the inner wall of the placement tube 24 during the rotation and mixing process, thereby causing the reagent tube to collide and break;
[0053] When the reagent tube is placed, the control starts the motor in the rotating chamber 11. The drive shaft in the motor drives the placement plate 21 to rotate. During the rotation of the placement plate 21, the placement plate 21 drives the placement slot 22 to rotate, and the placement slot 22 drives the reagent tube to rotate, so that the reagent tube revolves around the axis of the rotating chamber 11;
[0054] While the reagent tube is revolving, the controller controls the micro motor in the placement plate 21 to start, and the driving shaft in the micro motor drives the output gear to rotate. When the output gear rotates, it drives the driven gear to rotate. The driven gear rotates and drives the ring gear 221 to rotate. During the rotation of the ring gear 221, the ring gear 221 meshes with the annular gear ring 241, so that the annular gear ring 241 rotates. During the rotation of the annular gear ring 241, the annular gear ring 241 drives the placement tube 24 to rotate, and the placement tube 24 drives the reagent tube to rotate. The reagent tube mixes the whole blood cells under the condition of the coordination of the revolution and the rotation, and the rotation rate is regulated by the controller;
[0055] During the process of the placement plate 21 being driven by the motor to rotate, since the rotating shaft 27 passes through the moving cavity 23 and is provided with a bevel gear 30, during the rotation of the placement plate 21, the placement plate 21 drives the rotating shaft 27 to rotate, and the rotating shaft 27 drives the bevel gear 30 to rotate around the axis of the placement plate 21. Since the bevel gear 30 and the end face gear 31 are in meshing rotation, when the bevel gear 30 rotates around the placement plate 21, it meshes with the end face gear 31, and during the meshing process, the bevel gear 30 rotates around its own axis, so that when the bevel gear 30 rotates, it drives the rotating shaft 27 to rotate.
[0056] When the rotating shaft 27 rotates, it drives several cams 28 to rotate. During the rotation of the cam 28, the side wall of the cam 28 contacts the moving plate 25. When the raised part of the cam 28 rotates toward the side close to the moving chamber 23, the raised part of the cam 28 immediately pushes the moving plate 25 to move, and the moving block on the moving plate 25 moves along the moving groove 26. The moving plate 25 moves toward the side close to the moving chamber 23. During the movement of the moving plate 25, the moving plate 25 pushes the placement tube 24 to move, and the placement tube 24 moves toward the side away from the moving plate 25. The placement tube 24 moves along the axis of the placement groove 22, and then the placement tube 24 extends out of the placement groove 22; when the raised part of the cam 28 rotates toward the side away from the moving plate 25, the moving plate 25 moves toward the side close to the cam 28, and then the placement tube 24 moves toward the side close to the cam 28, so that the placement tube 24 makes a vertical reciprocating movement along the axis of the placement groove 22, thereby realizing the stirring of the whole blood cells in the reagent tube.
[0057] It should be noted that, in this article, relational terms such as first and second, etc. are only used to distinguish one entity or operation from another entity or operation, and do not necessarily require or imply any such actual relationship or order between these entities or operations. Moreover, the terms "include", "comprise" or any other variants thereof are intended to cover non-exclusive inclusion, so that a process, method, article or device including a series of elements includes not only those elements, but also other elements not explicitly listed, or also includes elements inherent to such process, method, article or device.
[0058] Finally, it should be noted that the above description is only a preferred embodiment of the present invention and is not intended to limit the present invention. Although the present invention has been described in detail with reference to the aforementioned embodiments, those skilled in the art can still modify the technical solutions described in the aforementioned embodiments or replace some of the technical features therein by equivalents. Any modification, equivalent replacement, improvement, etc. made within the spirit and principle of the present invention shall be included in the protection scope of the present invention.
Claims
1. A device for preventing the rupture and mixing of a whole blood cell marker diagnostic reagent, characterized in that: include: A machine body (1), wherein a plurality of rotating chambers (11) are arranged on the machine body (1), and the plurality of rotating chambers (11) are equally spaced along the axis of the machine body (1); a rotating device (2) is arranged in the rotating chamber (11), and the rotating device (2) comprises: a placement plate (21), the placement plate (21) is arranged in the rotating device (2), and the placement plate (21) is rotatably connected to the rotating chamber (11); The placement plate (21) is provided with a plurality of placement grooves (22), the plurality of placement grooves (22) are arranged around the axis of the placement plate (21), a moving cavity (23) is provided on one side of the placement groove (22) close to the rotating cavity (11), the placement groove (22) is communicated with the moving cavity (23), and a placement tube (24) is provided in the placement groove (22); A ring gear (221) is arranged on the shaft wall of the placement groove (22), tooth grooves are arranged on the inner wall and the outer wall of the ring gear (221), the ring gear (221) is rotatably connected with the placement groove (22), a micro motor is arranged in the placement plate (21), an output gear is arranged on the driving shaft of the micro motor, a driven gear is arranged between the ring gear (221) and the output gear, and the ring gear (221) is meshed with the output gear through the driven gear; A ring gear ring (241) is provided on one side of the placement tube (24) close to the moving chamber (23), the ring gear ring (241) meshes with the inner wall of the ring gear (221), the length of the ring gear ring (241) is greater than the length of the ring gear (221), a plurality of fixing rings (242) are provided inside the placement tube (24), the fixing rings (242) are connected to the inner wall of the placement tube (24) through a bracket, and the plurality of fixing rings (242) are vertically equally arranged along the axis of the placement tube (24), a support plate (243) is provided at the bottom of the placement tube (24), and the bracket, the fixing ring (242) and the support plate (243) are all made of rubber; A plurality of movable plates (25) are arranged inside the movable chamber (23), the plurality of movable plates (25) are combined into a circle, the plurality of movable plates (25) are radially arranged along the axis of the movable chamber (23), a plurality of movable grooves (26) are arranged on the inner wall of the movable chamber (23), a movable block is arranged on one side of the movable plate (25) close to the movable groove (26), the movable plate (25) is slidably connected to the movable groove (26) via the movable block, and the bottom of the placement tube (24) is in contact with the upper surface of the movable plate (25); A rotating shaft (27) is arranged on one side of the movable plate (25) away from the placement groove (22), and a plurality of cams (28) are arranged on the rotating shaft (27). The plurality of cams (28) are equally spaced along the axis of the rotating shaft (27), and the protruding portion of each cam (28) faces a different direction. The side wall of the cam (28) contacts the lower surface of the movable plate (25), and the cam (28) is slidably connected to the movable plate (25); One end of the rotating shaft (27) passes through the moving cavity (23) and is provided with a bevel gear (30), and an end face gear (31) is provided inside the rotating cavity (11), and the bevel gear (30) is meshed with the end face gear (31).
2. The anti-rupture mixing device for whole blood cell marker diagnostic reagent according to claim 1, characterized in that: A motor is arranged in the rotating chamber (11), a driving shaft of the motor is connected to the bottom of the rotating device (2), and a reagent tube is placed in the placement tray (21).
