Oscillating mixing device of blood type detector and blood type detector

Abstract

The present application relates to the technical field of biomedical equipment, and particularly provides a blood type detector and a shaking and mixing device of the blood type detector, aiming to solve the problem that the mixing effect of blood samples and detection reagents of the existing blood type detector is poor, thereby affecting the detection result. To this end, the shaking and mixing device comprises a shaking and mixing mechanism and a cup loading component mounted on the shaking and mixing mechanism, the cup loading component is used for loading a reaction cup, and the shaking and mixing mechanism can vibrate with the cup loading component and the reaction cup in the cup loading component to mix the blood sample and the detection reagent in the reaction cup. By arranging the cup loading component on the shaking and mixing mechanism, the reaction cup can be directly fixed on the shaking and mixing mechanism, so that the vibration generated by the shaking and mixing mechanism can be better transmitted to the reaction cup, thereby improving the mixing effect of the blood sample and the detection reagent in the reaction cup, and further improving the accuracy of the detector.

Description

TECHNICAL FIELD

[0001] The present application relates to the technical field of biomedical equipment, and particularly provides a shaking and mixing device of a blood type detector and the blood type detector. BACKGROUND

[0002] With the rapid development of social economy, people's cognition of their own blood type is becoming more and more clear. Blood type refers to the antigen type on the surface of blood components (including red blood cells, white blood cells and platelets). The commonly used blood type refers to the specific antigen type on the red blood cell membrane. In the human blood type system, the blood type systems currently found and recognized by the International Blood Transfusion Association mainly include ABO blood type system, Rh blood type system, MNS blood type system, P blood type system and the like. Among them, the ABO blood type system and the Rh blood type system are the most commonly used.

[0003] In some scenarios (such as blood donation room, emergency room, etc.), it is necessary to quickly obtain the blood type. In order to improve the blood type detection rate, the existing technology generally uses a blood type detector for detection. However, the mixing effect of the existing blood type detector on the blood sample and the detection reagent is not good, thereby affecting the accuracy of the detection result of the blood type detector.

[0004] Therefore, there is a need in the art for a new technical solution to solve the above problems. SUMMARY

[0005] The present application aims to solve the above technical problems, i.e., to solve the problem of the poor mixing effect of the existing blood type detector on the blood sample and the detection reagent, thereby affecting the detection result.

[0006] In a first aspect, the present application provides a shaking and mixing device of a blood type detector, which comprises a shaking and mixing mechanism and a cup carrying member mounted on the shaking and mixing mechanism, the cup carrying member is used to carry a reaction cup, and the shaking and mixing mechanism can vibrate with the cup carrying member and the reaction cup located in the cup carrying member to mix the blood sample and the detection reagent in the reaction cup. By providing the cup carrying member, the reaction cup can be directly fixed on the shaking and mixing mechanism, so that the vibration generated by the shaking and mixing mechanism can be better transmitted to the reaction cup, thereby improving the mixing effect of the blood sample and the detection reagent in the reaction cup, and further improving the accuracy of the detector.

[0007] In the preferred technical solution of the above-mentioned shaking and mixing device of the blood type detector, the cup carrying member has a carrying cavity capable of accommodating the reaction cup, the top of the carrying cavity is provided in an open manner, and one side of the cup carrying member is provided with a cup loading port in communication with the carrying cavity, and the cup loading port allows the reaction cup to pass through. Through such a setting, automatic loading of the reaction cup is facilitated.

[0008] In the preferred technical scheme of the oscillation and mixing device of the blood type detector, the cup loading member is provided with a first positioning structure at the cup loading opening, the first positioning structure can abut against one side end of the reaction cup to make the other side end of the reaction cup abut against a first inner side wall of the loading chamber, and the first inner side wall is arranged opposite to the cup loading opening. Through such arrangement, when the oscillation and mixing mechanism is in operation, the translation of the reaction cup relative to the cup loading member can be prevented, and thus the oscillation and mixing device can be better ensured.

[0009] In the preferred technical scheme of the oscillation and mixing device of the blood type detector, the cup loading member is provided with a second positioning structure on a second inner side wall of the loading chamber, the second positioning structure can abut against a top end of the reaction cup to make a bottom end of the reaction cup abut against an inner bottom wall of the loading chamber, and the second inner side wall is arranged perpendicular to the first inner side wall. Through such arrangement, when the oscillation and mixing mechanism is in operation, the vertical movement of the reaction cup relative to the cup loading member can be prevented, and thus the oscillation and mixing device can be better ensured.

[0010] In the preferred technical scheme of the oscillation and mixing device of the blood type detector, the second positioning structure comprises a plurality of positioning ribs, and the plurality of positioning ribs are arranged on the two second inner side walls respectively.

[0011] In the preferred technical scheme of the oscillation and mixing device of the blood type detector, the positioning rib comprises a horizontal positioning part and an arc-shaped guiding part, the horizontal positioning part abuts against the top end of the reaction cup, one end of the arc-shaped guiding part is connected with the horizontal positioning part, and the other end of the arc-shaped guiding part extends upward to make the reaction cup enter smoothly. Through such arrangement, the reaction cup can enter the loading chamber more smoothly, and the working efficiency is improved.

[0012] In the preferred technical scheme of the oscillation and mixing device of the blood type detector, the other side of the cup loading member is provided with a cup unloading push opening communicated with the loading chamber at a position opposite to the cup loading opening. Through such arrangement, the automatic unloading of the reaction cup is facilitated.

[0013] In the preferred technical scheme of the oscillation and mixing device of the blood type detector, the oscillation and mixing mechanism comprises a mixing motor and an oscillation rotor, the cup loading member is installed on the top of the mixing motor, and a driving shaft of the mixing motor is connected with the oscillation rotor and can drive the oscillation rotor to rotate.

[0014] In the preferred technical scheme of the oscillation and mixing device of the blood type detector, the oscillation and mixing device further comprises a damping rubber pad installed on the bottom of the mixing motor. Through such arrangement, the vibration noise can be reduced, and the user experience is improved.

[0015] In a second aspect, the application also provides a blood type detector comprising the oscillation mixing device. BRIEF DESCRIPTION OF DRAWINGS

[0016] The preferred embodiments of the present application will be described below in conjunction with the accompanying drawings, in which:

[0017] Figure 1 is a structural schematic diagram of the blood type detector of the present application Figure 1 ;

[0018] Figure 2 is a structural schematic diagram of the blood type detector of the present application Figure 2 , wherein the housing is not shown;

[0019] Figure 3 is a structural schematic diagram of the feeding device and liquid level detection mechanism of the blood type detector of the present application;

[0020] Figure 4 is a structural schematic diagram of the fixing mechanism and siphon of the blood type detector of the present application;

[0021] Figure 5 is a structural schematic diagram of the fixing mechanism of the blood type detector of the present application Figure 1 ;

[0022] Figure 2 is a structural schematic diagram of the fixing mechanism of the blood type detector of the present application Figure 2 , wherein the elastic clamping block is not shown;

[0023] Figure 7 is a structural schematic diagram of the elastic clamping block of the blood type detector of the present application;

[0024] Figure 8 is a structural schematic diagram of the fixing mechanism and sample filling device of the blood type detector of the present application;

[0025] Figure 9 is a structural schematic diagram of the filling rubber plug of the blood type detector of the present application;

[0026] Figure 10 is a structural schematic diagram of the reagent filling device, oscillation mixing device and translation device of the blood type detector of the present application Figure 1 ;

[0027] Figure 11 is a structural schematic diagram of the reagent filling device, oscillation mixing device and translation device of the blood type detector of the present application Figure 2 ;

[0028] Figure 12 is a structural schematic diagram of the unloading device, translation device, oscillation mixing device and consumable storage member of the blood type detector of the present application;

[0029] Figure 13 Figure 1 is a structural schematic diagram of the unloading device, translation device and oscillation mixing device of the blood type detector of the present application;

[0030] Figure 14 Figure 2 is a structural schematic diagram of the oscillation mixing device of the blood type detector of the present application;

[0031] Figure 15 Figure 3 is a structural schematic diagram of the reaction cup of the blood type detector of the present application;

[0032] Figure 16 Figure 4 is a structural schematic diagram of the consumable storage member of the blood type detector of the present application.

[0033] List of reference signs:

[0034] 10, siphon; 11, resistance member; 12, rubber sleeve; 13, first liquid level mark; 14, second liquid level mark;

[0035] 20, feeding device; 210, horizontal feeding mechanism; 211, horizontal feeding fixed seat; 212, horizontal feeding motor; 213, horizontal feeding screw; 214, horizontal feeding sliding block; 220, vertical feeding mechanism; 221, vertical feeding fixed seat; 222, vertical feeding motor; 223, vertical feeding screw; 224, vertical feeding sliding block; 230, fixing mechanism; 231, horizontal fixing plate; 2311, plate-shaped body; 2312, elastic clamping block; 23111, accommodating slot; 23112, accommodating hole; 23113, unloading slot; 23121, fixed through hole; 23122, unloading port; 23123, empty structure; 232, vertical fixing plate; 2321, unloading through hole; 240, connecting member; 241, first connecting plate; 242, second connecting plate; 243, third connecting plate; 244, reinforcing plate;

[0036] 30, sample filling device; 31, sample filling mechanism; 311, filling rubber plug; 312, air pipe; 313, pressure pump; 3111, channel; 3112, tapered hole; 32, liquid level detection mechanism; 321, detection support; 3211, columnar structure;

[0037] 40, reagent filling device; 41, reagent box; 42, reagent filling needle; 43, reagent pump;

[0038] 50, translation device; 51, translation fixed seat; 52, translation motor; 53, translation screw; 54, translation sliding block;

[0039] 60, oscillation mixing device; 61, oscillation mixing mechanism; 611, mixing motor; 612, oscillation rotor; 613, damping rubber pad; 62, cup carrying member; 621, carrying cavity; 622, cup loading port; 623, cup unloading pushing port; 624, first positioning structure; 625, horizontal positioning part; 626, arc-shaped guiding part; 6211, first inner side wall; 6212, second inner side wall;

[0040] 70, loading and unloading device; 71, loading and unloading driving mechanism; 711, loading and unloading fixing seat; 712, loading and unloading motor; 713, loading and unloading lead screw; 714, loading and unloading sliding block; 72, loading member; 721, loading rod; 722, loading connecting rod; 723, loading connecting plate; 73, unloading member; 731, unloading rod; 732, unloading connecting rod; 733, unloading connecting plate

[0041] 80, reaction cup; 801, plate-shaped base body; 802, reaction groove; 803, side plate; 804, first reinforcing structure; 805, second reinforcing structure; 806, third reinforcing structure;

[0042] 90, consumable storage member; 901, cup outlet; 902, cup pushing port; 91, cover body; 911, first clamping structure;

[0043] 100, shell; 101, display screen; 102, taking and placing port;

[0044] 110, image recognition device;

[0045] 120, label storage member. DETAILED DESCRIPTION

[0046] The preferred embodiments of the present application will be described below with reference to the accompanying drawings. It should be understood by those skilled in the art that these embodiments are only used to explain the technical principles of the present application, and are not intended to limit the protection scope of the present application.

[0047] It should be noted that in the description of the present application, the terms "left", "right", "up", "down", "top", "bottom", etc. indicating the direction or positional relationship of the terms are based on the direction or positional relationship shown in the drawings, which is only for the convenience of description, and does not indicate or imply that the device or element must have a specific orientation, be constructed and operated in a specific orientation, and therefore cannot be understood as a limitation on the present application. In addition, the terms "first", "second", "third" are only for descriptive purposes and cannot be understood as indicating or implying relative importance.

[0048] In addition, it should be noted that in the description of the present application, unless otherwise explicitly specified and limited, the terms "arrange", "connect", "mount" should be understood broadly, for example, it can be fixedly connected, or detachably connected, or integrally connected. For those skilled in the art, the specific meaning of the above terms in the present application can be understood according to the specific circumstances.

[0049] Specifically, the present application provides a blood type detector, as shown in Figure 1 and Figure 2 The blood type detector of the present application comprises a housing 100, and a feeding device 20 and a sample filling device 30 mounted in the housing 100.

[0050] The feeding device 20 can move with the blood collection tube to make the blood collection tube communicate with the sample filling device 30, and the sample filling device 30 can fill the blood sample in the blood collection tube into the reaction cup 80.

[0051] Specifically, after the staff collects the blood sample through the blood collection tube, the blood collection tube is placed in the feeding device 20, the feeding device 20 moves the blood collection tube from the placement position to the sample filling position, and the top end of the blood collection tube communicates with the sample filling device 30, the sample filling device 30 applies pressure to the blood collection tube to make the blood sample in the blood collection tube fill into the reaction cup 80 at the sample filling position.

[0052] Preferably, the blood collection tube of the present application is a siphon tube 10.

[0053] It should be noted that in actual application, those skilled in the art can also use other types of blood collection tubes, such as conical blood collection tubes, etc., which are not limited by the present application. Of course, the present application preferably uses the siphon tube 10, which has a faster blood collection speed. The technical solution of the present application will be introduced below with the siphon tube 10 as an example.

[0054] Preferably, as shown in Figure 1 and Figure 2 The blood type detector of the present application further comprises a reagent filling device 40 mounted in the housing 100, and the reagent filling device 40 can fill the detection reagent into the reaction cup 80.

[0055] After the blood sample in the siphon tube 10 is filled into the reaction cup 80, the detection reagent is also filled into the reaction cup 80 (at the reagent filling position) through the reagent filling device 40, and the blood type of the blood sample can be determined through the reaction result of the detection reagent and the blood sample.

[0056] It should be noted that in actual application, the sample filling position and the reagent filling position can be arranged at the same position, in which case, after the blood sample in the pipette 10 is filled into the reaction cup 80, the reaction cup 80 does not need to be moved, and the detection reagent can be directly filled into the reaction cup 80 through the reagent filling device 40; or, the sample filling position and the reagent filling position can be arranged separately, in which case, after the blood sample in the pipette 10 is filled into the reaction cup 80, the reaction cup 80 needs to be moved from the sample filling position to the reagent filling position, and then the detection reagent can be filled into the reaction cup 80 through the reagent filling device 40. Such flexible adjustment and change and deviation from the principles and scope of the present application should be limited within the protection scope of the present application.

[0057] Preferably, as shown in Figure 1 and Figure 2 The blood type detector of the present application further comprises a shaking and mixing device 60 installed in the housing 100, which can carry the reaction cup 80 and mix the blood sample filled into the reaction cup 80 with the detection reagent.

[0058] After the blood sample and the detection reagent are filled into the reaction cup 80, the reaction cup 80 is shaken by the shaking and mixing device 60 to mix the blood sample filled into the reaction cup 80 with the detection reagent, thereby improving the accuracy of the detection result.

[0059] Preferably, as shown in Figure 1 and Figure 2 The blood type detector of the present application further comprises an image recognition device 110 installed in the housing 100, which can collect the image of the blood sample mixed with the detection reagent in the reaction cup 80, so as to output the blood type according to the collected image.

[0060] The image recognition device 110 collects the image, and then analyzes and processes the collected image to output the blood type, which can avoid the situation of manual misjudgment and further improve the accuracy of the detection result.

[0061] It should be noted that in actual application, the image recognition device 110 can directly analyze and process the collected image and output the blood type, or the image recognition device 110 can transmit the collected image to the control device of the blood type detector, and the control device can analyze and process the collected image and output the blood type, and the like. Such flexible adjustment and change and deviation from the principles and scope of the present application should be limited within the protection scope of the present application.

[0062] Exemplarily, the image recognition device 110 comprises a camera acquisition module and a data transceiving module. The camera acquisition module can acquire images, and transmit image information to the control device of the blood type detector through the data transceiving module for analog-digital conversion, data analysis, and then output the blood type.

[0063] It should be noted that in actual application, the blood type can be output in the form of voice broadcast, or the blood type can also be displayed in the form of text on the display screen 101 of the blood type detector, etc. Such flexible adjustment and change and deviation from the principles and scope of the present application should be limited within the protection scope of the present application.

[0064] Preferably, as shown in Figure 1 and Figure 2 The blood type detector of the present application further comprises a plurality of label storage members 120 installed on the shell 100, and each of the label storage members 120 stores a different type of blood type label.

[0065] By providing the label storage members 120 capable of storing blood type labels, when the blood type detector displays the detection result, the staff can directly pick up the blood type label in the label storage member 120 corresponding to the detection result for labeling, which is very convenient and provides a better user experience.

[0066] It should be noted that in actual application, the specific number of the label storage members 120 can be flexibly set by those skilled in the art, for example, the number of the label storage members 120 can be set to two, three, or four, etc.

[0067] Preferably, as shown in Figure 1 and Figure 2 The number of the label storage members 120 of the present application is four, and each of the label storage members 120 stores an A-type label, a B-type label, an AB-type label, and an O-type label.

[0068] Preferably, the blood type detector of the present application further comprises an indicator light (not shown in the figure) provided on the front panel of the label storage member 120.

[0069] When the blood type detector detects the blood type of the blood sample, the corresponding indicator light is lit, which can prevent the staff from picking up the wrong blood type label, and further improves the user experience.

[0070] Preferably, as shown in Figure 1 The shell 100 is provided with a mounting port (not shown in the figure) at a position corresponding to the label storage member 120, and the label storage member 120 is inserted into the shell 100 from the mounting port.

[0071] Exemplarily, the number of the label storage members 120 is four, four installation openings are arranged on the front panel of the shell 100, and the four label storage members 120 are respectively inserted into the corresponding installation openings.

[0072] Preferably, as shown in Figure 1 , Figure 2 , the blood type detector of the application further comprises a consumable storage member 90 and a loading and unloading device 70 installed in the shell 100.

[0073] The consumable storage member 90 is capable of storing a plurality of reaction cups 80, and the loading and unloading device 70 is capable of loading the reaction cup 80 located in the consumable storage member 90 onto the oscillation and mixing device 60, and capable of unloading the reaction cup 80 from the oscillation and mixing device 60 after the image recognition device 110 completes image acquisition.

[0074] By arranging the loading and unloading device 70, the loading and unloading of the reaction cup 80 can be automatically realized.

[0075] It should be noted that in actual application, the loading and unloading device 70 can also be arranged to only be capable of loading the reaction cup 80 located in the consumable storage member 90 onto the oscillation and mixing device 60, or the loading and unloading device 70 can also be arranged to only be capable of unloading the reaction cup 80 from the oscillation and mixing device 60 after the image recognition device 110 completes image acquisition. Such flexible adjustment and change deviating from the principle and scope of the application should be limited within the protection scope of the application.

[0076] Of course, the loading and unloading device 70 of the application is preferably arranged to be capable of both loading the reaction cup 80 located in the consumable storage member 90 onto the oscillation and mixing device 60, and unloading the reaction cup 80 from the oscillation and mixing device 60 after the image recognition device 110 completes image acquisition.

[0077] Preferably, as shown in Figure 1 , Figure 2 and Figure 10 , the sample injection site and the reagent injection site of the blood type detector of the application are spaced apart along the X direction, the image recognition device 110 is located above the reagent injection site, and the image acquisition end thereof is arranged downward, and the blood type detector of the application further comprises a translation device 50 installed in the shell 100, and the translation device 50 is capable of moving the oscillation and mixing device 60 between the sample injection site and the reagent injection site.

[0078] The sample injection site and the reagent injection site of the application are arranged separately, as shown in Figure 2As shown, the translation device 50 moves the oscillation mixing device 60 to the sample adding position, the loading and unloading device 70 pushes the reaction cup 80 in the consumable storage member 90 out and loads the reaction cup 80 on the oscillation mixing device 60, the sample adding device 30 adds the blood sample in the pipette 10 into the reaction cup 80, as shown Figure 10 As shown, the translation device 50 moves the oscillation mixing device 60 and the reaction cup 80 on the oscillation mixing device 60 to the reagent adding position, the reagent adding device 40 adds the detection reagent into the reaction cup 80, the oscillation mixing device 60 is started to mix the blood sample and the detection reagent added into the reaction cup 80, and the image recognition device 110 collects images.

[0079] Preferably, as shown Figure 2 to Figure 4 The feeding device 20 of the present application comprises a feeding mechanism and a fixing mechanism 230 for carrying the pipette 10.

[0080] The feeding mechanism can move the fixing mechanism 230 and the pipette 10 fixed on the fixing mechanism 230 to communicate the pipette 10 with the sample adding device 30, and the feeding mechanism can also cooperate with the sample adding device 30 to unload the pipette 10 on the fixing mechanism 230 from the fixing mechanism 230.

[0081] Specifically, the staff places the pipette 10 on the fixing mechanism 230, the feeding mechanism moves the fixing mechanism 230 and the pipette 10 on the fixing mechanism 230 towards the sample adding device 30 to communicate the pipette 10 with the sample adding device 30, and after the sample adding device 30 adds the blood sample in the pipette 10 into the reaction cup 80, the feeding mechanism continues to move the pipette 10 towards the sample adding device 30 and cooperates with the sample adding device 30 to automatically unload the pipette 10 from the fixing mechanism 230, without the need for manual unloading of the pipette 10, and the user has a better experience.

[0082] Preferably, as shown Figure 2 and Figure 3 The feeding mechanism of the present application comprises a horizontal feeding mechanism 210 and a vertical feeding mechanism 220, and the fixing mechanism 230 is installed on the vertical feeding mechanism 220.

[0083] The horizontal feeding mechanism 210 can drive the vertical feeding mechanism 220 and the fixing mechanism 230 to move in the horizontal direction, and the vertical feeding mechanism 220 can drive the fixing mechanism 230 to move in the vertical direction; and the horizontal feeding mechanism 210 can also cooperate with the sample adding device 30 to unload the pipette 10 on the fixing mechanism 230 from the fixing mechanism 230.

[0084] Specifically, the staff places the siphon 10 on the fixing mechanism 230, and the horizontal feeding mechanism 210 moves the vertical feeding mechanism 220, the fixing mechanism 230 and the siphon 10 towards the sample adding device 30, and after moving to the set position, the siphon 10 is aligned with the sample adding device 30, and the vertical feeding mechanism 220 moves the fixing mechanism 230 and the siphon 10 vertically upwards, so that the top end of the siphon 10 is in communication with the sample adding device 30.

[0085] After the sample adding device 30 adds the blood sample in the siphon 10 to the reaction cup 80, the horizontal feeding mechanism 210 moves the vertical feeding mechanism 220, the fixing mechanism 230 and the siphon 10 towards the sample adding device 30, and the sample adding device 30 abuts against the siphon 10, so as to unload the siphon 10 from the fixing mechanism 230. Of course, before moving the horizontal feeding mechanism 210 with the siphon 10 towards the sample adding device 30, the vertical fixing mechanism 230 can also be moved downwards with the fixing mechanism 230 and the siphon 10, so as to separate the siphon 10 from the sample adding device 30.

[0086] Preferably, as shown in Figure 2 to Figure 8 The sample adding device 30 is provided with a columnar structure 3211 extending in the horizontal direction, and the fixing mechanism 230 includes a horizontal fixing plate 231 and a vertical fixing plate 232.

[0087] The number of the horizontal fixing plates 231 is two and they are spaced apart in the vertical direction, the top end and the bottom end of the vertical fixing plate 232 are connected with the corresponding horizontal fixing plate 231 respectively, the horizontal fixing plate 231 is provided with a fixing through hole 23121 for fixing the siphon 10, the horizontal fixing plate 231 is provided with an unloading opening 23122 in communication with the fixing through hole 23121 on the side away from the vertical fixing plate 232, the vertical fixing plate 232 is provided with an unloading through hole 2321 allowing the columnar structure 3211 to pass through at the position corresponding to the columnar structure 3211, and the unloading through hole 2321 is correspondingly provided with the fixing through hole 23121, so that the columnar structure 3211 passing through the unloading through hole 2321 can contact the siphon 10 located in the fixing through hole 23121, thereby pushing the siphon 10 out of the fixing through hole 23121 from the unloading opening 23122 during the process of continuously moving the horizontal feeding mechanism 210 with the siphon 10 towards the columnar structure 3211.

[0088] Specifically, when the siphon 10 needs to be unloaded, the columnar structure 3211 on the sample adding device 30 passes through the unloading through hole 2321 on the fixing mechanism 230, and the front end (from the left to the right in the figure) of the columnar structure 3211 abuts against the unloading opening 23122 of the fixing through hole 23121, so as to push the siphon 10 out of the fixing through hole 23121 from the unloading opening 23122. Figure 8The left end of the columnar structure 3211 abuts against the siphon 10, and the horizontal feeding mechanism 210 continues to move the siphon 10 towards the columnar structure 3211, so that the columnar structure 3211 pushes the siphon 10 out of the fixed hole 23121 through the unloading port 23122 of the fixed mechanism 230, and the unloading of the siphon 10 is completed. After being pressed by the siphon 10, the unloading port 23122 is enlarged in size, so that the siphon 10 can be smoothly pushed out.

[0089] Preferably, as shown in Figure 4 to Figure 7 The horizontal fixed plate 231 includes a plate-shaped body 2311 connected with the vertical fixed plate 232 and an elastic clamping block 2312 mounted on the plate-shaped body 2311, and the fixed hole 23121 and the unloading port 23122 are formed on the elastic clamping block 2312. The inner diameter of the fixed hole 23121 is not greater than the outer diameter of the siphon 10 so as to clamp and fix the siphon 10.

[0090] Preferably, the elastic clamping block 2312 is made of an elastic non-metallic material (such as rubber, etc.), and the inner diameter of the fixed hole 23121 is slightly smaller than the outer diameter of the siphon 10, so as to improve the stability of the siphon 10 and prevent the siphon 10 from falling during movement.

[0091] Preferably, as shown in Figure 7 The elastic clamping block 2312 is provided with a hollow structure 23123 near the fixed hole 23121, so that the opening size of the unloading port 23122 can be more easily enlarged when the siphon 10 is unloaded.

[0092] By providing the hollow structure 23123, deformation is more likely to occur near the fixed hole 23121, so that a very small force can be used to unload the siphon 10 from the fixed mechanism 230, preventing the siphon 10 from being damaged and unable to be smoothly unloaded.

[0093] Preferably, as shown in Figure 5 And Figure 6 The plate-shaped body 2311 is provided with a containing clamping groove 23111, and the elastic clamping block 2312 is clamped in the containing clamping groove 23111.

[0094] Preferably, the shape of the containing clamping groove 23111 matches the shape of the elastic clamping block 2312, so that the elastic clamping block 2312 can be clamped.

[0095] It should be noted that the elastic clamping block 2312 can be completely accommodated in the accommodation clamping groove 23111, or only a part of the elastic clamping block 2312 can be accommodated in the accommodation clamping groove 23111, and such flexible adjustment and change deviating from the principles and scope of the present application should be limited within the protection scope of the present application. Of course, it is preferred that the elastic clamping block 2312 is completely accommodated in the accommodation clamping groove 23111.

[0096] Preferably, as shown in Figure 5 to Figure 7 The accommodation clamping groove 23111 has a size smaller than the thickness of the plate-shaped body 2311 in the vertical direction, and the plate-shaped body 2311 is provided with an accommodation hole 23112 communicating with the accommodation clamping groove 23111 at a position corresponding to the fixed through hole 23121, and the accommodation hole 23112 allows the siphon pipe 10 to pass through.

[0097] That is, the accommodation clamping groove 23111 does not completely penetrate the plate-shaped body 2311, but is provided as a groove structure, and the accommodation hole 23112 is provided at the bottom of the accommodation clamping groove 23111, and the accommodation hole 23112 communicates with the fixed through hole 23121, and the siphon pipe 10 can pass through the fixed through hole 23121 and the accommodation hole 23112, and the inner diameter of the accommodation hole 23112 is preferably larger than the outer diameter of the siphon pipe 10.

[0098] Preferably, as shown in Figure 5 to Figure 7 The plate-shaped body 2311 is provided with an unloading groove 23113 communicating with the accommodation clamping groove 23111 at a position corresponding to the unloading port 23122, and the unloading groove 23113 is arranged to allow the siphon pipe 10 to pass through, but not to allow the elastic clamping block 2312 to pass through, so as to prevent the elastic clamping block 2312 from being detached from the accommodation clamping groove 23111.

[0099] Preferably, as shown in Figure 2 and Figure 3 The feeding device 20 of the present application further comprises a connecting member 240, and the horizontal feeding mechanism 210 and the vertical feeding mechanism 220 are connected through the connecting member 240.

[0100] It should be noted that in actual application, the connecting member 240 can be provided as a connecting plate, a connecting frame or a connecting beam, and such adjustment and change of the specific structure of the connecting member 240 does not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application.

[0101] Preferably, as shown in Figure 3As shown, the connecting member 240 comprises a first connecting plate 241 connected with the horizontal feeding mechanism 210, a second connecting plate 242 connected with the vertical feeding mechanism 220, and a third connecting plate 243 for connecting the first connecting plate 241 and the second connecting plate 242, the first connecting plate 241 and the second connecting plate 242 are both arranged along the horizontal direction and are distributed in the vertical direction with a staggered interval, and the third connecting plate 243 is arranged along the vertical direction.

[0102] Preferably, the first connecting plate 241, the second connecting plate 242 and the third connecting plate 243 are integrally arranged.

[0103] Preferably, as shown in the drawings, Figure 3 The second connecting plate 242 is located directly above the horizontal feeding mechanism 210.

[0104] Preferably, as shown in the drawings, Figure 3 The connecting member 240 of the present application further comprises a reinforcing plate 244 arranged between the first connecting plate 241 and the third connecting plate 243 and between the second connecting plate 242 and the third connecting plate 243.

[0105] Exemplarily, the reinforcing plate 244 is a right-angled triangle structure, the two right-angled edges of the reinforcing plate 244 arranged between the first connecting plate 241 and the third connecting plate 243 are fixedly connected with or integrally arranged with the first connecting plate 241 and the third connecting plate 243, respectively, and the two right-angled edges of the reinforcing plate 244 arranged between the second connecting plate 242 and the third connecting plate 243 are fixedly connected with or integrally arranged with the second connecting plate 242 and the third connecting plate 243, respectively.

[0106] It should be noted that in actual application, the reinforcing plate 244 can also be arranged only between the first connecting plate 241 and the third connecting plate 243, or can also be arranged only between the second connecting plate 242 and the third connecting plate 243, and such flexible adjustment and change does not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application.

[0107] Preferably, as shown in the drawings, Figure 3 The horizontal feeding mechanism 210 of the present application comprises a horizontal feeding fixed seat 211, a horizontal feeding motor 212 mounted on the horizontal feeding fixed seat 211, a horizontal feeding screw 213 arranged along the horizontal direction, and a horizontal feeding sliding block 214 in screwing cooperation with the horizontal feeding screw 213.

[0108] The horizontal feed motor 212 is connected with the horizontal feed screw 213 and can drive the horizontal feed screw 213 to rotate relative to the horizontal feed fixed base 211. The horizontal feed slide 214 can move along the horizontal feed screw 213 with the rotation of the horizontal feed screw 213. The top surface of the horizontal feed slide 214 is fixedly connected with the first connecting plate 241, and the bottom surface of the horizontal feed slide 214 is in contact with the horizontal feed fixed base 211 to prevent the horizontal feed slide 214 from rotating.

[0109] It should be noted that, in actual application, the horizontal feed mechanism 210 can also be a hydraulic cylinder driving mechanism, or the screw and slide block can be replaced by a gear and rack, etc. Such adjustment and change of the specific structure of the horizontal feed mechanism 210 does not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application. Of course, the horizontal feed mechanism 210 is preferably set to the structure as described above, which is simple in structure and better in stability.

[0110] Preferably, as shown in Figure 3 , the vertical feed mechanism 220 includes a vertical feed fixed base 221, a vertical feed motor 222 mounted on the vertical feed fixed base 221, a vertical feed screw 223 arranged in the vertical direction, and a vertical feed slide block 224 in screw connection with the vertical feed screw 223.

[0111] The bottom end of the vertical feed fixed base 221 is fixedly connected with the second connecting plate 242. The vertical feed motor 222 is connected with the vertical feed screw 223 and can drive the vertical feed screw 223 to rotate relative to the vertical feed fixed base 221. The vertical feed slide block 224 can move along the vertical feed screw 223 with the rotation of the vertical feed screw 223. One side surface of the vertical feed slide block 224 is fixedly connected with the fixing mechanism 230, and the other side surface of the vertical feed slide block 224 is in contact with the vertical feed fixed base 221 to prevent the vertical feed slide block 224 from rotating.

[0112] It should be noted that, in actual application, the vertical feed mechanism 220 can also be a hydraulic cylinder driving mechanism, or the screw and slide block can be replaced by a gear and rack, etc. Such adjustment and change of the specific structure of the vertical feed mechanism 220 does not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application. Of course, the vertical feed mechanism 220 is preferably set to the structure as described above, which is simple in structure and better in stability.

[0113] Preferably, as shown in Figure 2 , Figure 3 , and Figure 8 , the sample filling device 30 of the present application includes a sample filling mechanism 31 and a liquid level detection mechanism 32.

[0114] The sample adding mechanism 31 is capable of communicating with the siphon 10 and adding the blood sample in the siphon 10 into the reaction cup 80, the liquid level detecting mechanism 32 is capable of detecting the liquid level in the siphon 10 so as to ensure that the amount of the blood sample added into the reaction cup 80 meets the detection requirement, and the columnar structure 3211 is arranged on the liquid level detecting mechanism 32.

[0115] Specifically, before the sample adding mechanism 31 adds the blood sample in the siphon 10 into the reaction cup 80, the liquid level detecting mechanism 32 detects the blood sample in the siphon 10 first, and detects whether the amount of the blood sample in the siphon 10 is sufficient, and if the amount of the blood sample is sufficient, the sample adding mechanism 31 adds the blood sample in the siphon 10 into the reaction cup 80.

[0116] The columnar structure 3211 is arranged on the liquid level detecting mechanism 32, that is, the horizontal feeding mechanism 210 is capable of cooperating with the liquid level detecting mechanism 32 to unload the siphon 10 on the fixing mechanism 230 from the fixing mechanism 230.

[0117] It should be noted that in actual application, the columnar structure 3211 can also be arranged on the sample adding mechanism 31, that is, the horizontal feeding mechanism 210 is capable of cooperating with the sample adding mechanism 31 to unload the siphon 10 on the fixing mechanism 230 from the fixing mechanism 230, and this flexible adjustment and change deviating from the principle and scope of the present application should be limited within the protection scope of the present application. Of course, the present application preferably arranges the columnar structure 3211 on the liquid level detecting mechanism 32.

[0118] Preferably, as shown in Figure 2 , Figure 3 and Figure 8 , the liquid level detecting mechanism 32 comprises a detection bracket 321 and a liquid level detecting sensor (not shown in the figure).

[0119] The columnar structure 3211 is arranged on the detection bracket 321, the number of the columnar structures 3211 is two and is spaced apart in the vertical direction, the vertical fixing plate 232 of the fixing mechanism 230 is also provided with two unloading through holes 2321, the two unloading through holes 2321 are arranged correspondingly with the two columnar structures 3211 respectively, and the number of the liquid level detecting sensors is also two and is installed on the corresponding columnar structures 3211 respectively, the liquid level detecting sensor located at the upper side (referred to as the first liquid level detecting sensor) is used for detecting the lowest effective liquid surface in the siphon 10, and the liquid level detecting sensor located at the lower side (referred to as the second liquid level detecting sensor) is used for detecting the highest allowable residual liquid surface in the siphon 10.

[0120] Specifically, before the sample filling mechanism 31 fills the blood sample in the siphon tube 10 into the reaction cup 80, the first liquid level detection sensor is used to detect the blood sample in the siphon tube 10, and detect whether the blood sample in the siphon tube 10 is above the minimum effective liquid level. If the blood sample is above the minimum effective liquid level, it means that the amount of blood sample is sufficient. Then, the sample filling mechanism 31 fills the blood sample in the siphon tube 10 into the reaction cup 80.

[0121] During the process of filling the blood sample, the second liquid level detection sensor is used to detect the blood sample in the siphon tube 10, and detect whether the blood sample in the siphon tube 10 is below the maximum allowable residual liquid level. If the blood sample is below the maximum allowable residual liquid level, it means that the amount of blood sample filled into the reaction cup 80 is sufficient. Then, the sample filling mechanism 31 can stop filling. Of course, the sample filling mechanism 31 can also fill the blood sample in the siphon tube 10 into the reaction cup 80.

[0122] It should be noted that the liquid level detection sensor in the present application is a non-contact liquid level detection sensor, for example, a photoelectric liquid level sensor or a capacitive liquid level sensor, etc.

[0123] In addition, it should be noted that in actual application, the columnar structure 3211 can be integrally arranged with the detection support 321, or the columnar structure 3211 can be fixedly connected with the detection support 321. The present application preferably integrally arranges the columnar structure 3211 with the detection support 321.

[0124] Preferably, as shown in Figure 4 The present application provides a liquid level mark on the wall of the siphon tube 10.

[0125] By providing the liquid level mark on the wall of the siphon tube 10, the staff can accurately grasp the amount of blood sample in the siphon tube 10.

[0126] It should be noted that in actual application, those skilled in the art can set a scale on the outer wall of the siphon tube 10 to form the liquid level mark, or can draw a mark line at a set position to form the liquid level mark, etc. Such adjustment and change of the specific setting form of the liquid level mark does not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application.

[0127] Preferably, as shown in Figure 4 The liquid level mark includes a first liquid level mark 13, and the first liquid level mark 13 is arranged at the position of the minimum effective liquid level.

[0128] Exemplarily, a green line can be drawn on the outer wall of the siphon 10 at the position corresponding to the lowest effective liquid level, indicating the first liquid level mark 13.

[0129] Preferably, as shown in Figure 4 , the liquid level marks include a second liquid level mark 14, which is arranged at the position corresponding to the highest allowable residual liquid level.

[0130] Exemplarily, a red line can be drawn on the outer wall of the siphon 10 at the position corresponding to the highest allowable residual liquid level, indicating the second liquid level mark 14.

[0131] Preferably, as shown in Figure 4 , Figure 8 and Figure 9 , the sample filling mechanism 31 of the present application is provided with a first sealing structure, and the siphon 10 is provided with a second sealing structure, which cooperate to seal the sample filling mechanism 31 and the siphon 10.

[0132] It should be noted that in actual applications, the first sealing structure and the second sealing structure can be arranged in the structure of a sealing ring cooperating with a sealing groove, or in the structure of a sealing gasket cooperating with a sealing gasket, or in the structure of a sealing sleeve cooperating with a sealing groove, etc. Such adjustment and change of the specific structure of the first sealing structure and the second sealing structure do not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application.

[0133] Preferably, as shown in Figure 4 , Figure 8 and Figure 9 , the sample filling mechanism 31 of the present application includes a filling rubber plug 311, an air pipe 312 and a pressure pump 313. The filling rubber plug 311 has a hole 3111, the top end of which is communicated with the pressure pump 313 through the air pipe 312, and the bottom end of which is communicated with the siphon 10.

[0134] Exemplarily, the hole 3111 on the filling rubber plug 311 is arranged in the vertical direction, and the feeding device 20 can pass into the hole 3111 from the bottom end of the hole 3111 with the siphon 10, so as to communicate the siphon 10 with the hole 3111 of the filling rubber plug 311.

[0135] The first sealing structure is a tapered hole 3112 formed at the bottom end of the channel 3111 on the filling rubber stopper 311, and the second sealing structure is a rubber sleeve 12 provided on the siphon tube 10. The shape of the rubber sleeve 12 matches the shape of the tapered hole 3112 so as to seal the bottom end of the channel 3111 after the top end of the siphon tube 10 is inserted into the channel 3111.

[0136] Specifically, the feeding mechanism, carrying the siphon tube 10, is inserted into the channel 3111 from the bottom end of the filling rubber stopper 311. The rubber sleeve 12, which is set on the siphon tube 10, enters the tapered hole 3112 at the bottom end of the channel 3111. The outer wall of the rubber sleeve 12 is tightly fitted to the inner wall of the tapered hole 3112 to seal the bottom end of the channel 3111 and prevent air leakage during the blood sample filling process.

[0137] Preferably, such as Figure 4 As shown, the siphon tube 10 also has a minimum liquid level indicator.

[0138] When staff collect blood samples using the siphon tube 10, they can use the minimum aspiration level indicator to determine if the amount of blood sample collected is sufficient. Once the blood sample in the siphon tube 10 reaches the minimum aspiration level indicator, no further blood collection is necessary.

[0139] Preferably, such as Figure 4 As shown, the rubber sleeve 12 forms the lowest liquid absorption level indicator.

[0140] In other words, this application installs the rubber sleeve 12 at the position of the lowest liquid absorption level indicator, so that the rubber sleeve 12 itself also serves as a liquid level indicator. In this way, there is no need to set a separate lowest liquid absorption level indicator.

[0141] Preferably, such as Figure 4 As shown, a resistance member 11 is provided inside the siphon tube 10. The resistance member 11 divides the internal space of the siphon tube 10 into a first space and a second space. The first space is located above the resistance member 11, and the second space is located below the resistance member 11. The resistance member 11 is configured to prevent air in the first space from entering the second space to prevent blood samples in the second space from dripping when no pressure is applied to the first space. The resistance member 11 is also configured to allow air in the first space to enter the second space when pressure is applied to the first space.

[0142] The blood sample collected by the staff through the siphon tube 10 is all located in the second space of the siphon tube 10, and by arranging the resistance member 11 in the siphon tube 10, the blood sample in the siphon tube 10 can be prevented from leaking during the movement of the siphon tube 10 along with the feeding device 20. After the top of the siphon tube 10 is communicated with the hole 3111 of the filling rubber plug 311 of the sample filling mechanism 31, the sample filling mechanism 31 applies pressure to the first space, so that the air in the first space breaks through the resistance member 11 and enters the second space, thereby filling the blood sample in the second space into the reaction cup 80.

[0143] It should be noted that in actual application, the resistance member 11 can be arranged as resistance cotton or a microporous plug, and such adjustment and change of the specific structure type of the resistance member 11 do not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application.

[0144] Of course, the resistance member 11 is preferably arranged as resistance cotton or a microporous plug.

[0145] Preferably, as shown in Figure 2 , Figure 10 and Figure 11 , the reagent filling device 40 of the present application comprises a reagent box 41, a reagent sample needle 42 and a reagent pump 43.

[0146] The reagent box 41 is used for storing detection reagents, the reagent sample needle 42 is located between the image recognition device 110 and the reagent sample site, and the reagent sample needle 42 is arranged obliquely to reduce the influence on the image recognition device 110 when collecting images. The liquid inlet end of the reagent pump 43 is communicated with the reagent box 41, and the liquid outlet end of the reagent pump 43 is communicated with the reagent sample needle 42.

[0147] When it is needed to fill detection reagents into the reaction cup 80, the reagent pump 43 is started to pump the detection reagents in the reagent box 41 into the reagent sample needle 42, and then into the reaction cup 80. By arranging the reagent sample needle 42 obliquely, the influence on the image recognition device 110 when collecting images is small, thereby ensuring the accuracy of the detection results.

[0148] Preferably, the reagent pump 43 is a constant flow pump.

[0149] By adjusting the reagent pump 43, a specified amount of reagent (for example, 30-50 microliters) is pumped out per rotation, and the control is more convenient and accurate.

[0150] Preferably, as shown in Figure 10 and Figure 11 , the needle tip of the reagent sample needle 42 deviates from the reaction groove 802 of the reaction cup 80 located at the reagent sample site in the horizontal direction (for details, see Figure 13The center of the reaction groove 802 is indicated by the vertical dotted line in the figure, and the reagent injection needle 42 is inclined at an angle such that the detection reagent ejected from the reagent injection needle 42 falls in the center of the reaction groove 802 for containing the blood sample and the detection reagent.

[0151] Figure 10 The center of the reaction groove 802 is indicated by the vertical dotted line in the figure, and the reagent injection needle 42 is inclined at an angle such that the detection reagent ejected from the reagent injection needle 42 falls in the center of the reaction groove 802 for containing the blood sample and the detection reagent.

[0152] It should be noted that in actual applications, the horizontal distance between the tip of the reagent injection needle 42 and the center of the reaction groove 802 and the inclination angle of the reagent injection needle 42 can be flexibly set by the person skilled in the art according to experiments or experience.

[0153] The horizontal distance between the tip of the reagent injection needle 42 and the center of the reaction groove 802 is preferably set to any value in the range of 3 to 6 mm, for example, 3 mm, 4 mm, 5 mm, or 6 mm, etc.

[0154] Preferably, as shown in Figure 2 , Figure 12 and Figure 13 , the loading and unloading device 70 comprises a loading and unloading driving mechanism 71, a loading member 72, and an unloading member 73.

[0155] The loading member 72 is arranged corresponding to the sample injection site, and the loading and unloading driving mechanism 71 can drive the loading member 72 to move horizontally along the Y direction to push the reaction cup 80 out of the consumable storage member 90 while loading the reaction cup 80 into the oscillation and mixing device 60 at the sample injection site; the unloading member 73 is arranged corresponding to the reagent injection site, and the loading and unloading driving mechanism 71 can also drive the unloading member 73 to move horizontally along the Y direction to unload the reaction cup 80 from the oscillation and mixing device 60 at the reagent injection site; wherein the Y direction is perpendicular to the X direction.

[0156] As shown in Figure 12 , the translation device 50 moves the oscillation and mixing device 60 to the sample injection site, aligns with the consumable storage member 90, and the loading and unloading driving mechanism 71 drives the loading member 72 to move horizontally to push the reaction cup 80 out of the consumable storage member 90, and the reaction cup 80 enters the oscillation and mixing device 60, and the blood sample is injected, as shown in Figure 13As shown, the translation device 50 carries the oscillation mixing device 60 and the reaction cup 80 to the reagent filling position, after the reagent filling is completed, the oscillation mixing device 60 is started to shake the blood sample and the reagent in the reaction cup 80, then the image recognition device 110 collects images, and then the loading and unloading driving mechanism 71 drives the unloading member 73 to move horizontally to unload the reaction cup 80 from the oscillation mixing device 60, and complete a detection work.

[0157] It should be noted that in actual application, the loading member 72 can also be cancelled, that is, only the loading and unloading driving mechanism 71 and the unloading member 73 are provided, or the unloading member 73 can also be cancelled, that is, only the loading and unloading driving mechanism 71 and the loading member 72 are provided. Of course, it is preferred to be provided as the loading and unloading driving mechanism 71, the loading member 72 and the unloading member 73.

[0158] Preferably, as shown in Figure 12 and Figure 13 The loading and unloading driving mechanism 71 of the present application comprises a loading and unloading fixed seat 711, a loading and unloading motor 712 mounted on the loading and unloading fixed seat 711, a loading and unloading lead screw 713 horizontally arranged along the Y direction, and a loading and unloading sliding block 714 in screw connection with the loading and unloading lead screw 713.

[0159] The loading and unloading motor 712 is connected with the loading and unloading lead screw 713 and can drive the loading and unloading lead screw 713 to rotate relative to the loading and unloading fixed seat 711, the loading and unloading sliding block 714 can move along the loading and unloading lead screw 713 with the rotation of the loading and unloading lead screw 713, the top surface of the loading and unloading sliding block 714 is fixedly connected with the loading member 72 and the unloading member 73, and the bottom surface of the loading and unloading sliding block 714 is in contact with the loading and unloading fixed seat 711 to prevent the loading and unloading sliding block 714 from rotating.

[0160] It should be noted that in actual application, the loading and unloading driving mechanism 71 can also be provided as a hydraulic cylinder driving mechanism, or the above-mentioned lead screw and sliding block can be replaced by a gear and rack, etc. Such adjustment and change of the specific structure of the loading and unloading driving mechanism 71 does not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application. Of course, the present application preferably sets the loading and unloading driving mechanism 71 as the above-mentioned structure, which is simple in structure and better in stability.

[0161] Preferably, as shown in Figure 12 and Figure 16 The consumable storage member 90 has a storage chamber (not shown in the figure) capable of storing a plurality of reaction cups 80, one side of the consumable storage member 90 is provided with a cup outlet 901 communicating with the storage chamber at a position close to the bottom end of the storage chamber, the cup outlet 901 allows the reaction cup 80 to pass through, and the other side of the consumable storage member 90 is provided with a cup pushing port 902 communicating with the storage chamber at a position opposite to the cup outlet 901, and the cup pushing port 902 is arranged opposite to the loading member 72.

[0162] That is, the two opposite sides of the consumable storage member 90 are respectively provided with a cup outlet 901 and a cup pushing opening 902, the loading member 72 is located at the side of the consumable storage member 90 provided with the cup pushing opening 902, the consumable storage member 90 is located between the loading member 72 and the oscillation and mixing device 60, the loading and unloading driving mechanism 71 drives the loading member 72 to move horizontally towards the consumable storage member 90, the loading member 72 enters the storage chamber from the cup pushing opening 902, and pushes the reaction cup 80 to move from the cup outlet 901, so that the reaction cup 80 enters the oscillation and mixing device 60.

[0163] Preferably, as shown in Figure 12 to Figure 14 The oscillation and mixing device 60 of the present application comprises an oscillation and mixing mechanism 61 and a cup loading member 62 mounted on the oscillation and mixing mechanism 61.

[0164] The cup loading member 62 is used to carry the reaction cup 80, and the oscillation and mixing mechanism 61 can vibrate with the cup loading member 62 and the reaction cup 80 in the cup loading member 62 to mix the blood sample and the detection reagent in the reaction cup 80.

[0165] Specifically, the oscillation and mixing mechanism 61 is mounted on the translation device 50, the cup loading member 62 is mounted on the oscillation and mixing mechanism 61, and the reaction cup 80 is fixed on the cup loading member 62. After the blood sample and the detection reagent are filled, the oscillation and mixing mechanism 61 is started to vibrate with the cup loading member 62 and the reaction cup 80, so as to fully mix the blood sample and the detection reagent in the reaction cup 80.

[0166] It should be noted that in actual application, the cup loading member 62 can be set as a cup loading rack, a cup loading box, a cup loading plate, etc. The adjustment and change of the specific structure of the cup loading member 62 do not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application.

[0167] Preferably, as shown in Figure 12 and Figure 14 The cup loading member 62 of the present application has a carrying chamber 621 capable of accommodating the reaction cup 80, the top of the carrying chamber 621 is provided with an opening, and one side of the cup loading member 62 is provided with a cup loading opening 622 communicating with the carrying chamber 621, which allows the reaction cup 80 to pass through.

[0168] The top of the mounting chamber 621 is open to facilitate image acquisition by the image recognition device 110. The cup carrier 62 has a cup-filling port 622 on the side near the consumable storage component 90. After the loading component 72 pushes the reaction cup 80 out of the cup outlet 901 of the consumable storage component 90, the reaction cup 80 enters the mounting chamber 621 of the cup carrier 62 through the cup-filling port 622. The mounting chamber 621 is configured to completely accommodate the reaction cup 80.

[0169] Preferably, such as Figure 13 and Figure 14 As shown, on the other side of the cup carrier 62 of this application, a cup unloading port 623 communicating with the mounting chamber 621 is provided at a position opposite to the cup loading port 622.

[0170] In other words, the cup carrier 62 is provided with a cup loading port 622 and a cup unloading port 623 on two opposite sides. After the image recognition device 110 has acquired the image, the loading and unloading drive mechanism 71 drives the unloading component 73 to move horizontally toward the cup carrier 62. The unloading component 73 enters the loading chamber 621 from the cup unloading port 623 and pushes the reaction cup 80 out from the cup loading port 622, unloading the reaction cup 80 from the cup carrier 62 of the oscillating mixing device 60.

[0171] Preferably, such as Figure 12 and Figure 13 As shown, the loading component 72 includes a horizontally arranged loading rod 721, a vertically arranged loading connecting rod 722, and a horizontally arranged loading connecting plate 723.

[0172] The loading rod 721 is positioned directly opposite the push cup opening 902. The top and bottom ends of the loading connecting rod 722 are connected to the loading rod 721 and the loading connecting plate 723, respectively. The loading connecting plate 723 is fixedly connected to the top surface of the loading and unloading slider 714.

[0173] For example, the loading rod 721 has a rectangular cross-section, and the cup-pushing opening 902 is also rectangular. The size of the loading rod 721 is smaller than the size of the cup-pushing opening 902, so it can pass through the cup-pushing opening 902.

[0174] Preferably, such as Figure 12 and Figure 13 As shown, the unloading component 73 includes a horizontally arranged unloading rod 731, a vertically arranged unloading connecting rod 732, and a horizontally arranged unloading connecting plate 733.

[0175] The unloading rod 731 is positioned directly opposite the unloading cup push port 623 of the cup-carrying component 62 located at the reagent dispensing position. The top and bottom ends of the unloading connecting rod 732 are connected to the unloading rod 731 and the unloading connecting plate 733, respectively. The unloading connecting plate 733 is fixedly connected to the top surface of the loading and unloading slider 714.

[0176] Exemplarily, the cross section of the unloading rod 731 is rectangular, the unloading cup pushing opening 623 is also rectangular, and the size of the unloading rod 731 is smaller than the size of the unloading cup pushing opening 623, so that the unloading rod 731 can pass through the unloading cup pushing opening 623.

[0177] Preferably, as shown in Figure 2 and Figure 12 , the storage chamber of the consumable storage member 90 is arranged in a vertical direction, and there is a gap between the inner side wall of the storage chamber and the outer side wall of the reaction cup 80, so that the reaction cup 80 can slide towards the bottom of the storage chamber under the action of its own gravity.

[0178] Specifically, the reaction cups 80 are stacked in the storage chamber, and when the reaction cup 80 at the bottom end is pushed out, the reaction cups 80 in the storage chamber can automatically slide down one position under the action of their own gravity.

[0179] According to statistics, a blood donation house needs to consume about 25 reaction cups 80 per working day, so the storage capacity of the storage chamber can be set to 25.

[0180] As shown in Figure 1 , the shell 100 is provided with a taking and placing opening 102 at a position corresponding to the consumable storage member 90, and the staff can install the consumable storage member 90 through the taking and placing opening 102.

[0181] It should be noted that in actual application, the storage chamber can also be arranged obliquely, and there can also be no gap between the inner side wall of the storage chamber and the outer side wall of the reaction cup 80. In this case, in order to smoothly move the reaction cups 80 in the storage chamber towards the bottom end of the storage chamber, a pushing member (such as a spring) can be arranged at the top end of the storage chamber. When the reaction cup 80 at the bottom of the storage chamber is pushed out, the remaining reaction cups 80 move towards the bottom end of the storage chamber under the action of the pushing member. This flexible adjustment and change does not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application.

[0182] Of course, the present application preferably arranges the storage chamber in a vertical direction, and arranges a gap between the inner side wall of the storage chamber and the outer side wall of the reaction cup 80, which is simpler in structure and convenient to arrange.

[0183] Preferably, as shown in Figure 12 and Figure 16 , the top end of the consumable storage member 90 is provided with a cover 91, and the cover 91 can cover the top of the storage chamber.

[0184] Preferably, as shown in Figure 16 , one end of the cover 91 is pivotally connected with the consumable storage member 90.

[0185] Exemplarily, a pivoting shaft is arranged at one end of the cover 91, and a connecting seat is arranged at the top end of the consumable storage member 90, two opposite connecting holes are arranged on the connecting seat, and the two ends of the pivoting shaft are respectively inserted into the two connecting holes and can rotate relative to the connecting seat to achieve the pivoting connection of the cover 91 and the consumable storage member 90.

[0186] It should be noted that in actual application, the cover 91 and the consumable storage member 90 can also be arranged in a plug-in or screwing manner, and the like, and such flexible adjustment and change does not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application.

[0187] Of course, the cover 91 is preferably pivoted to the consumable storage member 90, and after the cover 91 is opened, the cover 91 can still be connected to the consumable storage member 90, which can avoid the loss of the cover 91 and the pollution of the cover 91.

[0188] Preferably, as shown in Figure 16 the other end of the cover 91 is provided with a first clamping structure 911, and the consumable storage member 90 is provided with a second clamping structure (not shown in the figure), and the first clamping structure 911 and the second clamping structure are clamped and matched to prevent the cover 91 from rotating relative to the consumable storage member 90.

[0189] Specifically, after the cover 91 is closed, the first clamping structure 911 and the second clamping structure are clamped and matched to prevent the cover 91 from being automatically opened.

[0190] It should be noted that in actual application, the first clamping structure 911 and the second clamping structure can be arranged in a structure in which a clamping jaw is matched with a clamping groove, or the first clamping structure 911 and the second clamping structure can be arranged in a structure in which a clamping jaw is matched with a clamping opening, or the first clamping structure 911 and the second clamping structure can be arranged in a structure in which two buckles are matched, and the like, and such adjustment and change of the specific structure of the first clamping structure 911 and the second clamping structure does not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application.

[0191] Preferably, as shown in Figure 16 the first clamping structure 911 is a clamping jaw arranged on the cover 91, and the second clamping structure is a clamping groove formed on the consumable storage member 90, and the clamping jaw and the clamping groove are matched.

[0192] Exemplarily, the clamping groove is formed on the inner side wall of the storage chamber, and after the cover 91 is closed, the clamping jaw is located in the clamping groove to lock the cover 91.

[0193] It should be noted that in actual application, the first clamping structure 911 can also be set as a clamping groove, and correspondingly, the second clamping structure can be set as a clamping claw.

[0194] Preferably, as shown in Figure 16 The consumable storage member 90 is a storage box.

[0195] It should be noted that in actual application, the consumable storage member 90 can also be set as other types of storage structures, such as a storage rack, etc. Of course, the consumable storage member 90 is preferably set as a storage box in the present application, which has better sealing performance and can prevent the reaction cup 80 from being contaminated.

[0196] Preferably, as shown in Figure 13 and Figure 14 The cup loading member 62 is provided with a first positioning structure 624 at the cup loading opening 622, which can abut against one side end of the reaction cup 80, so that the other side end of the reaction cup 80 abuts against the first inner side wall 6211 of the loading cavity 621, which is opposite to the cup loading opening 622.

[0197] Exemplarily, the first positioning structure 624 includes two vertical positioning ribs arranged opposite to each other in the horizontal direction, which are respectively located at the left and right sides of the cup loading opening 622, and the distance between the two vertical positioning ribs is slightly smaller than the width of the reaction cup 80. The cup loading member 62 is made of plastic material, and when the reaction cup 80 is loaded, the two vertical positioning ribs are extruded by the reaction cup 80, and the distance between them increases. After the reaction cup 80 completely passes through the cup loading opening 622 and enters the loading cavity 621, the two vertical positioning ribs reset and abut against the outer side wall of one end of the reaction cup 80, while the other end of the reaction cup 80 abuts against the first inner side wall 6211 of the loading cavity 621, thereby achieving horizontal positioning of the reaction cup 80.

[0198] It should be noted that the first positioning structure 624 is not limited to the two vertical positioning ribs described above, for example, the first positioning structure 624 can also be set as one vertical positioning rib, or can also be set as a plurality of positioning protrusions, etc. Such adjustment and change of the specific structure of the first positioning structure 624 do not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application.

[0199] Preferably, as shown in Figure 13 and Figure 14As shown in

[0200] Specifically, after the reaction cup 80 is completely pushed into the loading cavity 621 of the cup loading member 62, the second positioning structure is pressed against the top end of the reaction cup 80, thereby achieving vertical positioning of the reaction cup 80.

[0201] It should be noted that in actual applications, those skilled in the art can set the second positioning structure as a positioning rib, a positioning plate, or a positioning block, and the like. Such adjustment and change of the specific structure of the second positioning structure do not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application.

[0202] Preferably, as shown in Figure 13 and Figure 14 The second positioning structure includes a plurality of positioning ribs, and the plurality of positioning ribs are respectively arranged on the two second inner side walls 6212.

[0203] For example, the number of the positioning ribs is six, and three positioning ribs are respectively arranged on the two second inner side walls 6212, and the three positioning ribs are distributed along the length direction of the second inner side wall 6212.

[0204] It should be noted that the number of the positioning ribs is not limited to the above-mentioned six, for example, the number of the positioning ribs can also be set to two, three, four, or eight, and the like. Such adjustment and change of the specific number of the positioning ribs do not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application.

[0205] Preferably, as shown in Figure 13 and Figure 14 The positioning rib includes a horizontal positioning portion 625 and an arc-shaped guiding portion 626, the horizontal positioning portion 625 is arranged against the top end of the reaction cup 80, one end of the arc-shaped guiding portion 626 is connected with the horizontal positioning portion 625, and the other end of the arc-shaped guiding portion 626 extends upwardly so that the reaction cup 80 can be smoothly entered.

[0206] For example, the number of the arc-shaped guiding portions 626 is two, and the arc-shaped guiding portions 626 are respectively located on both sides of the horizontal positioning portion 625, and the bottom end of the arc-shaped guiding portion 626 is smoothly connected with the end of the horizontal positioning portion 625.

[0207] Preferably, as shown in Figure 14As shown in the figure, the oscillation mixing mechanism 61 of the present application comprises a mixing motor 611 and an oscillation rotor 612, the cup carrier member 62 is installed on the top of the mixing motor 611, the driving shaft of the mixing motor 611 is connected with the oscillation rotor 612 and can drive the oscillation rotor 612 to rotate.

[0208] Wherein, the bottom of the mixing motor 611 is fixedly connected with the translation device 50, the top of the mixing motor 611 is fixedly connected with the cup carrier member 62, after starting the mixing motor 611, the mixing motor 611 generates vibration in the process of rotating with the oscillation rotor 612, the vibration is transmitted to the reaction cup 80 through the cup carrier member 62, so that the blood sample and the detection reagent in the reaction cup 80 are fully mixed.

[0209] Preferably, as shown in the figure, Figure 14 As shown in the figure, the oscillation mixing device 60 of the present application further comprises a shock-absorbing rubber pad 613 installed on the bottom of the mixing motor 611.

[0210] Exemplarily, four shock-absorbing rubber pads 613 are arranged on the bottom of the mixing motor 611.

[0211] Preferably, as shown in the figure, Figure 11 and Figure 12 As shown in the figure, the translation device 50 of the present application comprises a translation fixed base 51, a translation motor 52 installed on the translation fixed base 51, a translation screw 53 arranged horizontally along the X direction, and a translation sliding block 54 screw-connected with the translation screw 53.

[0212] Wherein, the translation motor 52 is connected with the translation screw 53 and can drive the translation screw 53 to rotate relative to the translation fixed base 51, the translation sliding block 54 can move along the translation screw 53 with the rotation of the translation screw 53, the top surface of the translation sliding block 54 is fixedly connected with the oscillation mixing device 60 (specifically, the mixing motor 611 of the oscillation mixing device 60), and the bottom surface of the translation sliding block 54 is in contact with the translation fixed base 51 to prevent the translation sliding block 54 from rotating.

[0213] It should be noted that in actual application, the translation device 50 can also be set as a hydraulic cylinder driving device, or the above-mentioned screw and sliding block can be replaced by a gear and a rack, etc., and such adjustment and change of the specific structure form of the translation device 50 does not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application. Of course, the present application preferably sets the translation device 50 as the structure form introduced above, which is simple in structure and better in stability.

[0214] Preferably, as shown in the figure, Figure 13 and Figure 15As shown, the reaction cup 80 of the present application comprises a plate-shaped base 801, a reaction groove 802 arranged on the plate-shaped base 801, and a side plate 803 arranged at the edge of the plate-shaped base 801, the reaction groove 802 is used to contain a blood sample and a detection reagent, and the side plate 803 extends downward along the vertical direction.

[0215] Exemplarily, the number of the reaction grooves 802 is two, the two reaction grooves 802 are spaced apart, the blood sample in the siphon tube 10 is respectively added into the two reaction grooves 802, and the reagent adding device 40 is provided with two reagent boxes 41, two reagent adding needles 42 and two reagent pumps 43, the two reagent boxes 41 respectively store a detection reagent A and a detection reagent B, the two reagent adding needles 42 are respectively arranged corresponding to the two reaction grooves 802, and the two reagent pumps 43 are respectively used to add the detection reagent A and the detection reagent B.

[0216] Among them, the detection reagent A can react with type A blood and type AB blood, the detection reagent B can react with type B blood and type AB blood, and neither the detection reagent A nor the detection reagent B can react with type O blood, and the reagent adding device 40 can add the detection reagent A and the detection reagent B into the two reaction grooves 802 respectively. If the blood samples in the two reaction grooves 802 all react with the detection reagent, the blood type is AB type, if the blood samples in the two reaction grooves 802 do not react with the detection reagent, the blood type is O type, if the blood samples in the reaction groove 802 added with the detection reagent A all react with the detection reagent, the blood type is A type, and if the blood samples in the reaction groove 802 added with the detection reagent B all react with the detection reagent, the blood type is B type.

[0217] It should be noted that when adding the blood sample, the siphon tube 10 is close to the consumable storage member 90, the loading member 72 first pushes out a part (for example, half of the reaction cup 80) of the reaction cup 80, so that one reaction groove 802 of the reaction cup 80 is just located directly below the siphon tube 10, by controlling the sample adding device 30 (for example, controlling the air sending amount, running time of the sample adding device 30 or combining with the liquid level detection sensor), first adding about half of the blood sample in the siphon tube 10 into the first reaction groove 802, and then making the loading member 72 push out the reaction cup 80 completely, at this time, the second reaction groove 802 of the reaction cup 80 is just located directly below the siphon tube 10, and then the remaining blood sample can be added into the second reaction groove 802 of the reaction cup 80 completely.

[0218] Of course, in actual application, the reaction cup 80 can be pushed out completely first, and the reaction cup 80 is completely entered into the cup loading member 62, and then the blood sample is added into the reaction cup 80, in this case, the siphon 10 is first added with the blood sample to one of the reaction grooves 802, and then the feeding device 20 is moved with the siphon 10 above the other reaction groove 802, and the remaining blood sample is added into the reaction groove 802.

[0219] Since the rubber plug 311 has a certain elasticity, and the distance between the two reaction grooves 802 is very close, the bottom end of the rubber plug 311 can move a certain distance with the siphon 10, of course, the rubber plug 311 can also be arranged in a form of sliding in the horizontal direction, etc., and those skilled in the art can make flexible arrangement.

[0220] In addition, it should be noted that the number of reaction grooves 802 is not limited to the above two, for example, the number of reaction grooves 802 can also be set to one or three, etc., and the adjustment and change of the specific number of reaction grooves 802 do not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application.

[0221] Of course, the number of reaction grooves 802 of the present application is preferably at least two and is spaced apart.

[0222] Preferably, as shown in Figure 15 The reaction groove 802 is a groove formed by the downward recess of the plate-shaped base 801.

[0223] Preferably, as shown in Figure 15 The reaction cup 80 further comprises a first reinforcing structure 804 arranged between the two opposite side plates 803, and the two ends of the first reinforcing structure 804 are respectively connected with the corresponding side plates 803.

[0224] Exemplarily, the reaction cup 80 comprises two opposite long side plates and two opposite short side plates, and the first reinforcing structure 804 is arranged between the two opposite long side plates. Of course, the first reinforcing structure 804 can also be arranged between the two opposite short side plates.

[0225] It should be noted that those skilled in the art can arrange the first reinforcing structure 804 as a reinforcing plate or a reinforcing rib, etc., and the adjustment and change of the specific structure of the first reinforcing structure 804 do not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application.

[0226] Preferably, as shown in Figure 15As shown, the reaction cup 80 further comprises a second reinforcing structure 805 arranged between the outer sidewall of the reaction groove 802 and the inner sidewall of the side plate 803, and the two ends of the second reinforcing structure 805 are connected with the outer sidewall of the reaction groove 802 and the inner sidewall of the side plate 803 respectively.

[0227] Exemplarily, the second reinforcing structure 805 is arranged between the reaction groove 802 and the short side plate and between the reaction groove 802 and the long side plate.

[0228] Similarly to the first reinforcing structure 804, the second reinforcing structure 805 can be arranged as a reinforcing plate or a reinforcing rib, and the adjustment and change of the specific structure of the second reinforcing structure 805 do not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application.

[0229] Preferably, as shown, Figure 15 the outer bottom surface of the reaction groove 802 is a plane and is located at the same horizontal plane with the bottom surface of the side plate 803.

[0230] Similarly to the first reinforcing structure 804, the third reinforcing structure 806 can be arranged as a reinforcing plate or a reinforcing rib, and the adjustment and change of the specific structure of the third reinforcing structure 806 do not deviate from the principles and scope of the present application, and should be limited within the protection scope of the present application.

[0231] Preferably, as shown, Figure 15 the outer bottom surface of the reaction groove 802 is a plane and is located at the same horizontal plane with the bottom surface of the side plate 803.

[0232] Those skilled in the art can understand that the combination of the features of different embodiments means to be within the scope of the present application and form different embodiments, although some embodiments described herein include certain features rather than other features included in other embodiments. For example, in the claims of the present application, any one of the claimed embodiments can be used in any combination.

[0233] So far, the technical solutions of the present application have been described in combination with the preferred embodiments shown in the drawings, but those skilled in the art can easily understand that the protection scope of the present application is obviously not limited to these specific embodiments. Those skilled in the art can make equivalent changes or replacements to the related technical features without deviating from the principles of the present application, and the technical solutions after the changes or replacements will fall within the protection scope of the present application.

Claims

1. A shaking mixing device for a blood typing instrument, characterized in that, The oscillating mixing device includes an oscillating mixing mechanism and a cup carrier component mounted on the oscillating mixing mechanism. The cup carrier is used to hold the reaction cup, and the oscillating mixing mechanism can vibrate the cup carrier and the reaction cup located in the cup carrier to mix the blood sample in the reaction cup with the test reagent. The cup carrier has a mounting chamber capable of accommodating the reaction cup, the top of the mounting chamber is open, and a cup-filling port communicating with the mounting chamber is provided on one side of the cup carrier, the cup-filling port allowing the reaction cup to pass through; The cup carrier is provided with a first positioning structure at the cup opening. The first positioning structure can abut against one side of the reaction cup so that the other side of the reaction cup abuts against the first inner wall of the mounting chamber. The first inner wall is disposed opposite to the cup opening. The cup carrier is provided with a second positioning structure on the second inner sidewall of the mounting chamber. The second positioning structure can abut against the top of the reaction cup so that the bottom of the reaction cup abuts against the inner bottom wall of the mounting chamber. The second inner sidewall is perpendicular to the first inner sidewall. On the other side of the cup-carrying component, at a position opposite to the cup-filling opening, there is a cup-unloading port that communicates with the loading chamber.

2. The shaking and mixing device of the blood typing instrument according to claim 1, characterized in that, The second positioning structure includes multiple positioning ribs, which are respectively disposed on the two second inner sidewalls.

3. The shaking and mixing device of the blood typing instrument according to claim 2, characterized in that, The positioning rib includes a horizontal positioning part and an arc-shaped guide part. The horizontal positioning part abuts against the top of the reaction cup, one end of the arc-shaped guide part is connected to the horizontal positioning part, and the other end of the arc-shaped guide part extends upward to allow the reaction cup to enter smoothly.

4. The shaking and mixing device of the blood typing instrument according to any one of claims 1 to 3, characterized in that, The oscillating mixing mechanism includes a mixing motor and an oscillating rotor. The cup carrier is mounted on top of the mixing motor, and the drive shaft of the mixing motor is connected to the oscillating rotor and can drive the oscillating rotor to rotate.

5. The shaking and mixing device of the blood typing instrument according to claim 4, characterized in that, The oscillating mixing device also includes a shock-absorbing rubber pad installed at the bottom of the mixing motor.

6. A blood typing instrument, characterized in that, The oscillating mixing device includes any one of claims 1 to 5.

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