Lipid blood detection device for medical sample

Abstract

The utility model discloses a lipemia detection device for a medical sample. The lipemia detection device is used for reducing the difficulty of blood sample detection. The centrifugal machine comprises a centrifugal machine shell, a sealing cover, a centrifugal motor, a rotating seat, a rotating column, a condensate spraying device, a centrifugal tank and at least two blood sample plates, the centrifugal motor is installed in the center of the outer side of the bottom face of the centrifugal machine shell. The rotating base is arranged in the center of the inner side of the bottom face of the centrifugal machine shell. The centrifugal motor is connected with the rotating base. The rotating column is arranged in the center of the rotating seat; the centrifugal tank is arranged on the rotating column, a first sample fixing module is arranged at the bottom of the centrifugal tank, and a second sample fixing module is arranged on the side wall of the centrifugal tank; the blood sample plate comprises at least one blood test tube arranged at intervals; fixing blocks are arranged on the upper side and the lower side of the blood sample plate, and the blood sample plate is detachably fixed to the first fixing module and the second fixing module through the fixing blocks on the upper side and the lower side respectively; the sealing cover is positioned at the top of the centrifuge shell; and the condensate spraying device is arranged on the sealing cover.

Description

Technical Field

[0001] The embodiments of the present application relate to the field of lipemia detection, and in particular to a lipemia detection device for medical samples. Background Art

[0002] As people pay more attention to their physical health, more and more people evaluate their physical condition through regular blood tests, or draw blood and store it for future use.

[0003] With the storage of large quantities of blood samples, their condition needs to be constantly monitored, and abnormal blood samples need to be screened out. In existing technologies, waste blood samples require personnel to assess the quality of each blood sample in turn and screen out the waste blood samples. Specifically, testers must extract blood samples one by one from a blood test tube storage box and visually inspect them. This method is extremely labor-intensive and inefficient.

[0004] Therefore, at present, the method of detecting blood tubes stored in the equipment is gradually leaning towards automated detection. In the existing automated waste blood detection equipment, the blood tubes can only be automatically transferred to the detection personnel through the clamping device, or the image is taken and then sent to the display device of the detection personnel, and then the detection personnel perform unified identification. This method requires the detection personnel to pay close attention and very professional identification ability. That is, the above-mentioned automated waste blood detection method still requires human labor for detection. As the detection time increases, the possibility of human error is high, which greatly increases the difficulty of blood sample detection. Utility Model Content

[0005] The present application discloses a device for detecting blood lipids in medical samples, which is used to reduce the difficulty of detecting blood samples.

[0006] The present application provides a device for detecting blood lipids in medical samples, comprising:

[0007] Centrifuge housing, sealing cover, centrifugal motor, rotating base, rotating column, condensate spraying device, centrifuge tank, at least two blood sample plates;

[0008] The centrifugal motor is installed at the center of the outer side of the bottom surface of the centrifuge housing;

[0009] The rotating seat is arranged at the center position of the inner side of the bottom surface of the centrifuge housing, and the centrifugal motor is connected to the rotating seat;

[0010] The rotating column is arranged at the center of the rotating seat;

[0011] The centrifuge tank is arranged on the rotating column, the bottom of the centrifuge tank is provided with a first sample fixing module, and the side wall of the centrifuge tank is provided with a second sample fixing module;

[0012] The blood sample plate includes at least one blood test tube arranged at intervals;

[0013] The upper and lower sides of the blood sample plate are both provided with fixing blocks, and the blood sample plate is detachably fixed to the first fixing module and the second fixing module through the fixing blocks on the upper and lower sides respectively;

[0014] The sealing cover is located on the top of the centrifuge housing;

[0015] The condensate spraying device is arranged on the sealing cover.

[0016] Optionally, the condensate spraying device includes a condensate transmission column, a condensate annular transmission pipe and an oblique spray nozzle;

[0017] The condensate transmission column is fixed on the sealing cover, and the first end of the condensate transmission column is connected to the condensate storage tank;

[0018] The condensate annular transmission pipe is connected to the second end of the condensate transmission column;

[0019] At least two oblique spray nozzles are arranged on the condensate annular transmission pipe.

[0020] Optionally, the condensate spraying device further comprises at least one condensate vertical drip nozzle;

[0021] At least one condensate vertical drip nozzle is provided on the condensate annular transmission pipe.

[0022] Optionally, the lipemia detection device further includes a mounting base, a column, and a rotating disk;

[0023] The mounting base is arranged on the rotating column;

[0024] The column is installed on the mounting base;

[0025] The rotating disk is in the shape of a disk with high peripheries and a low center. The rotating disk is installed on a column, and spiral stripes are arranged on the inner side of the rotating disk.

[0026] Optionally, the lipemia detection device further comprises a swaying table;

[0027] The spraying platform is set on the pillar;

[0028] The spreading table is set with a rotating disk underneath.

[0029] Optionally, the lipemia detection device further includes a detection light source and a light source receiving device;

[0030] The detection light source is arranged on the inner side wall of the centrifuge tank, and an output light source is arranged on the detection light source. The number of the output light sources is consistent with the number of the blood test tube mounting slots on the blood sample plate;

[0031] The light source receiving device is arranged inside the centrifugal tank, and the number of receiving chips on the light source receiving device is the same as the number of the output light sources.

[0032] Optionally, the bottom of the centrifuge tank is designed to be truncated cone-shaped, with the bottom forming an acute angle with the horizontal plane;

[0033] The side wall of the centrifuge tank forms an acute angle with the horizontal plane.

[0034] Optionally, the centrifuge housing further includes a condensate return pipe;

[0035] The centrifugal tank is also designed with a condensate discharge port;

[0036] The condensate return pipe is arranged on the inner wall of the centrifuge housing, the first end of the condensate return pipe is located at the inner bottom of the centrifuge housing, and the second end of the condensate return pipe passes through the sealing cover and is connected to the condensate spraying device;

[0037] The condensate outlet is designed at the junction of the centrifugal tank side wall and the ground.

[0038] Optionally, the lipemia detection device further includes a shock absorber and an adsorption disk;

[0039] The shock absorber is arranged on the outer bottom of the centrifuge housing;

[0040] The adsorption plate is arranged at the bottom of the shock absorber.

[0041] Optionally, the blood test tube comprises a plastic test tube body, a one-way inlet plug and a one-way outlet nozzle;

[0042] The one-way inlet plug is provided with a groove adapted to the plastic test tube body, and a plastic seal is provided on the one-way inlet plug;

[0043] A through hole is provided at the bottom of the plastic test tube body, and a one-way outlet nozzle is provided on the through hole.

[0044] It can be seen from the above technical solutions that the embodiments of the present application have the following advantages:

[0045] In the present application, a device for detecting blood lipids in medical samples specifically includes a centrifuge housing, a sealing cover, a centrifuge motor, a rotating seat, a rotating column, a condensate spraying device, a centrifuge tank, and at least two blood sample plates. The connection relationship between the various components is as follows: the centrifuge motor is installed at the center position of the outer bottom surface of the centrifuge housing. The rotating seat is set at the center position of the inner bottom surface of the centrifuge housing, and the centrifuge motor is connected to the rotating seat. The rotating column is set at the center of the rotating seat. The centrifuge tank is set on the rotating column, and a first sample fixing module is set at the bottom of the centrifuge tank, and a second sample fixing module is set on the side wall of the centrifuge tank. The blood sample plate includes at least one blood test tube arranged at intervals. Fixed blocks are set on the upper and lower sides of the blood sample plate, and the blood sample plate is detachably fixed to the first fixing module and the second fixing module via the upper and lower fixing blocks respectively. The sealing cover is located at the top of the centrifuge housing, and the condensate spraying device is set on the sealing cover.

[0046] By placing the blood sample plate at an angle in the centrifuge tank, the blood test tubes on the blood sample plate are also placed at an angle. During the centrifugation process, the centrifugal motor drives the rotating seat and the rotating column, which drives the centrifuge tank to rotate. The centrifuge tank then drives the blood test tubes on the blood sample plate to centrifuge through the first and second fixed modules. During this process, the condensate spraying device sprays condensate from top to bottom on the sealing cover. During the centrifugation process, the condensate is evenly sprayed onto each blood test tube on the blood sample plate, causing the blood in the blood test tubes to condense and centrifuge simultaneously. The uniform and circulating condensate sprayed in the centrifuge can accelerate the separation of lipids in the blood test tubes, allowing ordinary centrifuges to efficiently classify blood test tubes, detect lipemia more quickly, and improve the efficiency of lipemia detection. BRIEF DESCRIPTION OF THE DRAWINGS

[0047] In order to more clearly illustrate the technical solutions in the embodiments of the present application, the following briefly introduces the drawings required for use in the embodiments or descriptions of the prior art. Obviously, the drawings described below are only some embodiments of the present application. For ordinary technicians in this field, other drawings can be obtained based on these drawings without any creative work.

[0048] Figure 1 A schematic diagram of the internal structure of a device for detecting lipemia in medical samples in this application;

[0049] Figure 2 A schematic diagram of the structure of a blood sample plate in the device for detecting lipemia of medical samples in this application;

[0050] Figure 3 This is another structural schematic diagram of a blood test tube in the device for detecting lipemia of medical samples in this application. DETAILED DESCRIPTION

[0051] In the following description, specific details such as specific system structures and techniques are provided for purposes of illustration rather than limitation to facilitate a thorough understanding of the embodiments of the present application. However, it will be apparent to those skilled in the art that the present application may be implemented in other embodiments without these specific details. In other cases, detailed descriptions of well-known systems, devices, circuits, and methods are omitted to avoid obscuring the description of the present application with unnecessary detail.

[0052] It should be understood that when used in the present specification and the appended claims, the term "comprising" indicates the presence of described features, integers, steps, operations, elements and / or components, but does not preclude the presence or addition of one or more other features, integers, steps, operations, elements, components and / or collections thereof.

[0053] It will also be understood that the term "and / or" used in this specification and the appended claims refers to and includes any and all possible combinations of one or more of the associated listed items.

[0054] As used in this specification and the appended claims, the term "if" can be interpreted as "when" or "upon" or "in response to determining" or "in response to detecting," depending on the context. Similarly, the phrase "if it is determined" or "if [described condition or event] is detected" can be interpreted as meaning "upon determination" or "in response to determining" or "upon detection of [described condition or event]" or "in response to detecting [described condition or event]," depending on the context.

[0055] In addition, in the description of the present application specification and the appended claims, the terms "first", "second", "third", etc. are only used to distinguish the descriptions and cannot be understood as indicating or implying relative importance.

[0056] References to "one embodiment" or "some embodiments" in this specification mean that a particular feature, structure, or characteristic described in conjunction with that embodiment is included in one or more embodiments of the present application. Thus, phrases such as "in one embodiment," "in some embodiments," "in other embodiments," and "in other embodiments" appearing in various places in this specification do not necessarily refer to the same embodiment, but rather mean "one or more but not all embodiments," unless otherwise specifically emphasized. The terms "including," "comprising," "having," and variations thereof all mean "including but not limited to," unless otherwise specifically emphasized.

[0057] In existing technologies, as people pay more attention to their physical health, more and more people evaluate their physical condition through regular blood tests, or draw blood and store it for future use.

[0058] With the storage of large quantities of blood samples, their condition needs to be constantly monitored, and abnormal blood samples need to be screened out. In existing technologies, waste blood samples require personnel to assess the quality of each blood sample in turn and screen out the waste blood samples. Specifically, testers must extract blood samples one by one from a blood test tube storage box and visually inspect them. This method is extremely labor-intensive and inefficient.

[0059] Therefore, at present, the method of detecting blood tubes stored in the equipment is gradually leaning towards automated detection. In the existing automated waste blood detection equipment, the blood tubes can only be automatically transferred to the detection personnel through the clamping device, or the image is taken and then sent to the display device of the detection personnel, and then the detection personnel perform unified identification. This method requires the detection personnel to pay close attention and very professional identification ability. That is, the above-mentioned automated waste blood detection method still requires human labor for detection. As the detection time increases, the possibility of human error is high, which greatly increases the difficulty of blood sample detection.

[0060] Based on this, the present application discloses a device for detecting lipemia in medical samples, which is used to reduce the difficulty of blood sample detection.

[0061] The following will be combined with the drawings in the embodiments of this application to clearly and completely describe the technical solutions in this application. Obviously, the embodiments described are only part of the embodiments of this application, not all of them. Based on the embodiments in this application, all other embodiments obtained by ordinary technicians in this field without making creative efforts are within the scope of protection of this application.

[0062] See also Figure 1 、 Figure 2 and Figure 3 The present application provides an embodiment of a device for detecting blood lipids in medical samples, comprising:

[0063] The present application provides a device for detecting blood lipids in medical samples, comprising:

[0064] Centrifuge housing 1, sealing cover 2, centrifugal motor 3, rotating base 4, rotating column 5, condensate spraying device 6, centrifugal tank 7, at least two blood sample plates 8;

[0065] The centrifugal motor 3 is installed at the center of the outer side of the bottom surface of the centrifuge housing 1;

[0066] The rotating seat 4 is arranged at the center position of the inner side of the bottom surface of the centrifuge housing 1, and the centrifugal motor 3 is connected to the rotating seat 4;

[0067] The rotating column 5 is arranged at the center of the rotating base 4;

[0068] The centrifuge tank 7 is arranged on the spin column 5, the bottom of the centrifuge tank 7 is provided with a first sample fixing module 9, and the side wall of the centrifuge tank 7 is provided with a second sample fixing module 10;

[0069] The blood sample plate 8 includes at least one blood test tube arranged at intervals;

[0070] The blood sample plate 8 is provided with fixing blocks on the upper and lower sides, and the blood sample plate 8 is detachably fixed to the first fixing module and the second fixing module through the fixing blocks on the upper and lower sides respectively;

[0071] The sealing cover 2 is located on the top of the centrifuge housing 1;

[0072] The condensate spraying device 6 is arranged on the sealing cover 2 .

[0073] In this embodiment, the centrifuge housing 1 is an outer shell that wraps the centrifuge tank 7, ensuring that the centrifuge tank 7 is not disturbed by the outside world during operation and is mainly used to protect the internal devices. The sealing cover 2 is used to seal the entire centrifuge tank 7.

[0074] The centrifugal motor 3 is located outside and is mainly used to drive the internal rotating seat 4 and the rotating column 5 to rotate, thereby causing the centrifugal tank 7 to rotate and centrifuge.

[0075] In this embodiment, to allow the blood sample plate 8 to be tilted, a first sample fixing module 9 and a second sample fixing module 10 are installed on the bottom and side surfaces of the centrifuge tank 7. The first sample fixing module 9 is installed upward, and the second sample fixing module 10 is installed toward the inside of the centrifuge tank 7. In this embodiment, the first sample fixing module 9 and the second sample fixing module 10 are retractable connecting columns.

[0076] In this embodiment, the condensate spraying device 6 is provided on the sealing cover 2, which is provided with a condensate storage device. Alternatively, the condensate storage device may be provided outside the centrifuge. The condensate spraying device 6 is connected to the condensate storage device via a pipeline, so that the condensate spraying device 6 can suck the condensate from the condensate storage device and pass it into the centrifuge tank 7. The condensate spraying device 6 is provided near the center of the mouth of the centrifuge tank 7.

[0077] In this embodiment, by placing blood sample plate 8 at an angle within centrifuge tank 7, the blood test tubes on blood sample plate 8 are also placed at an angle. During centrifugation, centrifuge motor 3 drives rotating seat 4 and rotating column 5, which in turn rotates centrifuge tank 7. Centrifuge tank 7, in turn, through first and second fixing modules, centrifuges the blood test tubes on blood sample plate 8. During this process, condensate spraying device 6 sprays condensate from top to bottom on sealing cover 2. During centrifugation, the condensate is evenly sprayed onto each blood test tube on blood sample plate 8, causing the blood in the blood test tubes to condense while centrifuging. The uniform and circulating condensate sprayed within the centrifuge accelerates the separation of lipids in the blood test tubes, allowing even ordinary centrifuges to efficiently classify blood test tubes, enabling faster detection of lipemia and improving the efficiency of lipemia detection.

[0078] Optionally, the condensate spraying device 6 includes a condensate transmission column 11, a condensate annular transmission pipe 12 and an oblique spray nozzle 13;

[0079] The condensate transmission column 11 is fixed on the sealing cover 2, and the first end of the condensate transmission column 11 is connected to the condensate storage tank;

[0080] The condensate annular transmission pipe is connected to the second end of the condensate transmission column 11;

[0081] At least two oblique spray nozzles 13 are provided on the condensate annular transmission pipe 12 .

[0082] In this embodiment, the condensate spraying device 6 includes a condensate transmission column 11, a condensate annular transmission pipe 12 and an oblique spray nozzle 13. The interior of the condensate transmission column 11 is a hollow structure, which can allow the condensate in the condensate storage device to be sucked and transmitted, and then distributed through the condensate annular transmission pipe 12, and finally evenly sprayed through the oblique spray nozzle 13, so that the blood test tubes on the blood sample plate 8 in the centrifuge tank 7 are evenly cooled during the centrifugation process.

[0083] Optionally, the condensate spraying device 6 further includes at least one condensate vertical drip nozzle 14;

[0084] At least one condensate vertical drip nozzle 14 is provided on the condensate annular transmission pipe 12 .

[0085] In this embodiment, the condensate spraying device 6 also includes at least one condensate vertical drip nozzle 14. The function of the condensate vertical drip nozzle 14 is to drop the condensate drop by drop into the centrifuge tank 7. During the rotation and centrifugation process of the centrifuge tank 7, the condensate at the bottom can be thrown away.

[0086] Optionally, the lipemia detection device further includes a mounting base 15, a column 16 and a rotating disk 17;

[0087] The mounting base 15 is disposed on the rotating column 5;

[0088] The column is mounted on the mounting base 15;

[0089] The rotating disk is in the shape of a disk with high peripheries and a low center. The rotating disk is installed on a column, and spiral stripes are arranged on the inner side of the rotating disk.

[0090] In this embodiment, to ensure better contact between the condensate and the blood test tubes on the blood sample plate 8, a mounting base 15 is provided on the rotating column 5. A vertical column is also provided, and a rotating disk is mounted on the column. The rotating disk's function is to fling away vertically dripping condensate. Furthermore, the rotating disk can be adjusted in height, i.e., its position relative to the blood sample plate 8. This design allows the condensate to be flung by the rotating disk onto blood test tubes at different heights, improving the condensation effect.

[0091] Optionally, the lipemia detection device further includes a swaying table 18;

[0092] The spraying platform 18 is arranged on the column;

[0093] The sprinkling station 18 is arranged below the rotating disk.

[0094] In this embodiment, the spreading platform 18 is mainly used to throw away the condensate falling from the rotating disk, thereby improving the use efficiency of the condensate.

[0095] Optionally, the lipemia detection device further includes a detection light source 19 and a light source receiving device 20;

[0096] The detection light source 19 is provided on the inner side wall of the centrifuge tank 7. The detection light source 19 is provided with an output light source. The number of the output light sources is consistent with the number of the blood test tube mounting slots on the blood sample plate 8.

[0097] The light source receiving device 20 is disposed inside the centrifuge tank 7 , and the number of receiving chips on the light source receiving device 20 is the same as the number of the output light sources.

[0098] In this embodiment, after centrifugation, blood test tubes are tested for lipemia using a light source. Within centrifuge tank 7, a detection light source 19 is designed on the inner sidewall of the centrifuge tank 7. A light source receiving device 20 is located within the centrifuge tank 7. Specifically, a light source receiving device 20 is positioned diagonally in the center of the bottom of the centrifuge tank 7. Furthermore, detection light source 19 is provided with an output light source. The number of output light sources matches the number of blood test tube mounting slots on blood sample plate 8. The number of receiving chips on light source receiving device 20 is the same as the number of output light sources.

[0099] Optionally, the bottom of the centrifugal tank 7 is designed to be truncated cone-shaped, with the bottom forming an acute angle with the horizontal plane;

[0100] The side wall of the centrifuge tank 7 forms an acute angle with the horizontal plane.

[0101] Optionally, the centrifuge housing 1 further includes a condensate return pipe 21;

[0102] The centrifugal tank 7 is also designed with a condensate discharge port 22;

[0103] The condensate return pipe 21 is provided on the inner wall of the centrifuge housing 1. The first end of the condensate return pipe 21 is located at the inner bottom of the centrifuge housing 1. The second end of the condensate return pipe 21 passes through the sealing cover 2 and is connected to the condensate spraying device 6.

[0104] The condensate outlet 22 is designed at the junction of the side wall of the centrifugal tank 7 and the ground.

[0105] In this embodiment, the condensate can be discharged through the condensate discharge port 22 below the centrifuge tank 7, and the condensate can be recovered through the condensate reflux pipe 21 inside the centrifuge housing 1, repeatedly enter the condensate storage device, and then repeatedly sprayed through the condensate spraying device 6.

[0106] Optionally, the lipemia detection device further includes a shock absorber 23 and an adsorption disk 24;

[0107] The shock absorber 23 is arranged on the outer bottom of the centrifuge housing 1;

[0108] The adsorption plate 24 is disposed at the bottom of the shock absorber 23 .

[0109] In this embodiment, in order to ensure the stability of the entire device, a shock absorber 23 and an adsorption plate 24 are designed so that the entire device can be stably adsorbed on the water surface and shock absorption is performed by the shock absorber 23.

[0110] Optionally, the blood test tube includes a plastic test tube body 25, a one-way inlet plug 26 and a one-way outlet nozzle 27;

[0111] The one-way inlet plug 26 is provided with a groove adapted to fit the plastic test tube body 25 and a plastic seal is provided on the one-way inlet plug 26;

[0112] A through hole is provided at the bottom of the plastic test tube body 25 , and a one-way outlet nozzle 27 is provided on the through hole.

[0113] In this embodiment, since lipemia is stratified, the lower layer of blood in the test tube can still be stored, so it is necessary to extract the useful blood in the blood test tube for storage. In this embodiment, the blood test tube includes a plastic test tube body 25, a one-way inlet plug 26, and a one-way outlet nozzle 27. The plastic test tube body 25 itself stores the blood sample. The upper one-way inlet plug 26 is provided with a groove adapted to the plastic test tube body 25, which can be well installed on the top of the test tube. The one-way inlet plug 26 is provided with a plastic seal, which is used in conjunction with the one-way outlet nozzle 27 at the bottom of the plastic test tube body 25. The blood test tube containing lipemia can be inserted into the one-way inlet plug 26 of another blood test tube through the one-way outlet nozzle 27 at the bottom, and the blood flows to the new blood test tube.

[0114] In this application, the terms "upper", "lower", "left", "right", "front", "back", "top", "bottom", "inside", "outside", "middle", "vertical", "horizontal", "lateral", "longitudinal", etc., indicating the orientation or position relationship, are based on the orientation or position relationship shown in the accompanying drawings, and are only used to illustrate the relative position relationship between the various components or components, and do not particularly limit the specific installation orientation of the various components or components.

[0115] Furthermore, some of the above terms may be used to express other meanings besides indicating a position or location. For example, the term "on" may also be used to indicate a dependency or connection in certain circumstances. Those skilled in the art will understand the specific meanings of these terms in this application based on the specific circumstances.

[0116] Furthermore, the terms "installed," "disposed," "provided with," "connected," and "connected" should be interpreted broadly. For example, they can refer to fixed connections, removable connections, or integral structures; mechanical connections or electrical connections; direct connections, indirect connections through an intermediary, or internal communication between two devices, elements, or components. Those skilled in the art will understand the specific meanings of these terms in this application based on the specific circumstances.

[0117] In addition, the structures, proportions, sizes, etc. drawn in the drawings in this application are only used to match the contents disclosed in the specification for those skilled in the art to understand and read, and are not used to limit the conditions under which this application can be implemented. Therefore, they have no substantive technical significance. Any structural modification, change in proportional relationship or adjustment of size should still fall within the scope of the technical content disclosed in this application without affecting the efficacy and purpose that can be achieved by this application.

Claims

1. A device for detecting lipemia in medical samples, characterized in that: include: Centrifuge housing, sealing cover, centrifugal motor, rotating base, rotating column, condensate spraying device, centrifuge tank, at least two blood sample plates; The centrifugal motor is installed at the center of the outer side of the bottom surface of the centrifuge housing; The rotating seat is arranged at the center position of the inner side of the bottom surface of the centrifuge housing, and the centrifugal motor is connected to the rotating seat; The rotating column is arranged at the center of the rotating seat; The centrifuge tank is arranged on the spin column, a first sample fixing module is arranged at the bottom of the centrifuge tank, and a second sample fixing module is arranged on the side wall of the centrifuge tank; The blood sample plate includes at least one blood test tube arranged at intervals; The upper and lower sides of the blood sample plate are both provided with fixing blocks, and the blood sample plate is detachably fixed to the first fixing module and the second fixing module through the fixing blocks on the upper and lower sides respectively; The sealing cover is located on the top of the centrifuge housing; The condensate spraying device is arranged on the sealing cover.

2. The blood lipid detection device according to claim 1, characterized in that: The condensate spraying device includes a condensate transmission column, a condensate annular transmission pipe and an oblique spray nozzle; The condensate transmission column is fixed on the sealing cover, and the first end of the condensate transmission column is connected to the condensate storage tank; The condensate annular transmission pipe is connected to the second end of the condensate transmission column; At least two oblique spray nozzles are provided on the condensate annular transmission pipe.

3. The device for detecting blood lipids according to claim 2, wherein: The condensate spraying device further comprises at least one condensate vertical drip nozzle; At least one condensate vertical drip nozzle is provided on the condensate annular transmission pipe.

4. The blood lipid detection device according to claim 3, characterized in that: The lipemia detection device also includes a mounting base, a column and a rotating disk; The mounting seat is arranged on the rotating column; The column is mounted on the mounting seat; The rotating disk is in the shape of a disk with high peripheries and a low center. The rotating disk is installed on the column, and spiral stripes are arranged on the inner side of the rotating disk.

5. The blood lipid detection device according to claim 4, characterized in that: The lipemia detection device also includes a sprinkling table; The sprinkling platform is arranged on the column; The sprinkling platform is arranged below the rotating disk.

6. The device for detecting blood lipids according to any one of claims 1 to 5, characterized in that: The lipemia detection device also includes a detection light source and a light source receiving device; The detection light source is arranged on the inner side wall of the centrifuge tank, and the detection light source is provided with an output light source, and the number of the output light sources is consistent with the number of the blood test tube mounting slots on the blood sample plate; The light source receiving device is arranged inside the centrifuge tank, and the number of receiving chips on the light source receiving device is the same as the number of the output light sources.

7. The device for detecting blood lipids according to any one of claims 1 to 5, characterized in that: The bottom of the centrifugal tank is designed in a frustum shape, and the bottom forms an acute angle with the horizontal plane; The side wall of the centrifugal tank forms an acute angle with the horizontal plane.

8. The device for detecting blood lipids according to claim 7, wherein: The centrifuge housing further includes a condensate return pipe; The centrifugal tank is also designed with a condensate discharge port; The condensate return pipe is arranged on the inner wall of the centrifuge housing, the first end of the condensate return pipe is located at the inner bottom of the centrifuge housing, and the second end of the condensate return pipe passes through the sealing cover and is connected to the condensate spraying device; The condensate discharge port is designed at the junction of the centrifugal tank side wall and the ground.

9. The device for detecting blood lipids according to any one of claims 1 to 5, wherein: The lipemia detection device further includes a shock absorber and an adsorption disk; The shock absorber is arranged on the outer bottom of the centrifuge housing; The adsorption plate is arranged at the bottom of the shock absorber.

10. The device for detecting blood lipids according to any one of claims 1 to 5, characterized in that: The blood test tube comprises a plastic test tube body, a one-way inlet plug and a one-way outlet nozzle; The one-way inlet plug is provided with a groove adapted to fit the plastic test tube body, and the one-way inlet plug is provided with a plastic seal; A through hole is provided at the bottom of the plastic test tube body, and the one-way outlet nozzle is provided on the through hole.

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