A biological sample automatic detector
By adopting the three-dimensional storage form with double belt multi-position insertion in the biological sample automation detector and the design of the feeding mechanism, the problem of the small number of slides in the equipment is solved, and a large number of slides are provided in a limited space, improving the detection efficiency.
Patent Information
- Application Number
- CN202411487980.2
- Authority / Receiving Office
- CN · China
- Patent Type
- Patents(China)
- Current Assignee / Owner
- Filing Date
- 2024-10-24
- Publication Date
- 2025-03-18
- Estimated Expiration
- 2044-10-24
AI Technical Summary
The existing biofluorescence automated detection equipment has a small number of slides, which leads to the problem that a single detection activity can detect the small number of biological samples.
An automated biological sample detector is designed, using a three-dimensional storage form with double belts and multiple position inserts. The continuous supply of slides is achieved through the feeding mechanism, and the rapid and stable conveying of slides is achieved by using the suction cup and swing arm structure.
It effectively solves the problem of underutilizing the internal space of the equipment, and realizes the provision of a large number of slides for detection activities in limited equipment space, and increases the number of detectable biological samples in a single detection activity.
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Figure CN119001131B_ABST
Abstract
Description
Technical Field
[0001] The invention relates to the field of biological sample automatic detectors, in particular to a biological sample automatic detector. Background Art
[0002] Fluorescence detection of biological samples can detect human cells, bacteria, mold, food residues, etc. Specific components in biological samples are marked with fluorescent substances, the marked biological samples are added to optical glass slides, and the light source is stimulated to irradiate the marked parts to produce fluorescence effects, which are then detected and recorded through fluorescence detectors.
[0003] In a single batch detection activity, the existing bioluminescence automated detection equipment needs to arrange the glass slides neatly on the operating platform. However, the area of the operating platform is limited, and the number of glass slides placed at one time is restricted by the area of the operating platform, which leads to a small number of test samples that can be accommodated in a single detection activity. The internal space of the equipment is not fully utilized. Increasing the number of test samples in a single detection activity by increasing the size of the equipment will obviously lead to a surge in equipment costs. Therefore, in order to optimize the above problems, an automated biological sample detector is proposed. Summary of the invention
[0004] In view of the problem that the number of biological samples that can be detected in a single detection activity is small due to the small number of slides accommodated in the above-mentioned or prior art bioluminescence automated detection equipment, the present invention is proposed.
[0005] Therefore, an object of the present invention is to provide an automated biological sample detector.
[0006] In order to solve the above technical problems, the present invention provides the following technical solutions: an automated biological sample detector, comprising a detector and a glass slide, and also comprising a feeding mechanism arranged in the detector, which comprises a bottom plate, two long sides of the upper surface of the bottom plate are each provided with a belt 1, and both ends of the two belts 1 are each wound with a short shaft, and the four short shafts are respectively vertically rotatably connected to the four corners of the bottom plate, the outer wall of the belt 1 is provided with ribs along its width direction, the ribs are distributed at equal intervals about the outer wall of the belt 1, and the two belts 1 are parallel and symmetrical to each other about the bottom plate, the bottom end of the short shaft passes through the bottom of the bottom plate, and the middle positions at both ends of the bottom surface of the bottom plate are rotatably connected with rollers, and the rollers and the rollers are connected to the bottom of the bottom plate. A second belt is wound around two adjacent short shafts, and the two adjacent sides of the first belts are synchronously and arranged in the same direction when running, the glass slide is inserted between the two first belts, and the edge of the glass slide is slidably inserted between two adjacent ribs of the first belt; a swing arm is hinged at one end of the bottom plate, and a transfer ring is fixedly connected to the end of the swing arm, a suction cup is inserted at the top of the transfer ring, and a spring one is arranged between the suction cup and the end surface of the transfer ring, a slot is provided on the swing arm, and a shift block is slidably connected in the slot, a pin is inserted into the side wall of the transfer ring, and one end of the pin is fixedly connected to the shift block, and one end of the pin matches the plug-in suction cup, and the pin is located between the shift block and the outer wall of the transfer ring and a second spring is arranged.
[0007] As a preferred solution of the biological sample automated detector of the present invention, a bearing is embedded in the top of the short shaft, and a U-shaped bracket is provided at the top of the short shaft, the inner ring of the bearing is fixedly connected to the bracket, and the U-shaped opening of the bracket points to the swing arm.
[0008] As a preferred solution of the biological sample automated detector of the present invention, wherein: the base plate is fixedly connected to a hinge seat, the end of the swing arm away from the adapter ring is hinged to the hinge seat, and the bottom end of the hinge seat is provided with an L-shaped positioning buckle, the positioning buckle is buckled with the bottom edge of the base plate, and the end of the shift block away from the pin squeezes and resists the positioning buckle.
[0009] As a preferred solution of the biological sample automated detector of the present invention, wherein: the swing arm is connected with a screw along the hinge axis between it and the hinge seat, the screw passes through the swing arm and the hinge seat, the number of spiral turns of the screw spiral groove is one-half turn, and the lead specification of the screw is greater than twenty millimeters.
[0010] As a preferred solution of the biological sample automatic detector of the present invention, wherein: the bottom plate is fixedly connected to a micro cylindrical cylinder beside the hinged seat, and the end of the piston rod of the micro cylindrical cylinder is coaxially fixedly connected to the screw rod.
[0011] As a preferred solution of the biological sample automatic detector of the present invention, wherein: the end of the adapter ring away from the suction cup is sealed and fixedly connected with a gas joint.
[0012] As a preferred solution of the biological sample automatic detector of the present invention, a servo-driven dropper and a bioluminescence sensor are also provided in the detector, and a conveyor belt is provided at the bottom of the dropper and the bioluminescence sensor.
[0013] As a preferred solution of the biological sample automated detector of the present invention, one end of the conveyor belt is adjacent to the swing arm, and the conveying directions of the conveyor belt and belt one are parallel to each other, two belts three are arranged inside the conveyor belt and are distributed on both sides of the conveyor belt, and the conveyor belt is located within the rotation radius of the swing arm, suction cup and air joint and is hollowed out.
[0014] As a preferred solution of the biological sample automated detector of the present invention, when the swing arm is at the deflection lower dead point position, the suction cup suction port height is coplanar with the upper plane of belt three, the suction cup is located in the middle position between the two belts three, and the suction cup corresponds to the position of the dropper above.
[0015] As a preferred solution of the biological sample automatic detector of the present invention, wherein: the bottom surface of the conveyor belt is equipped with a fluorescence excitation light source at a position corresponding to the biological fluorescence sensor.
[0016] The beneficial effects of the biological sample automatic detector of the present invention are:
[0017] Compared with the traditional glass slide operation platform, the feeding mechanism of the device replaces the conventional flat slide storage form with a three-dimensional slide storage form with double belts and multiple positions, which can continuously provide a large number of slides for the biological sample fluorescence detection device during the detection activity, so that the slide capacity of the detection device is no longer a factor restricting the efficiency of the biological sample fluorescence automatic detection, and effectively solves the problem in the prior art that the biological fluorescence automatic detection device can detect a small number of biological samples in a single detection activity due to the small number of slides it can accommodate;
[0018] The feeding mechanism of the device uses a swing arm to manipulate the suction cup to transport the glass slide back and forth between belt one and belt three. The suction cup cooperates with the swing arm to move the glass slide horizontally when adsorbing the glass slide, so that the glass slide can be safely separated from belt one to avoid damage. The suction cup can also lock itself relative to the swing arm position after the glass slide reaches belt three, so that the glass slide is smoothly released on belt three. Therefore, the feeding mechanism can quickly and stably provide glass slides to the detection equipment. BRIEF DESCRIPTION OF THE DRAWINGS
[0019] In order to more clearly illustrate the technical solutions of the embodiments of the present invention, the following briefly introduces the drawings required for use in the description of the embodiments. Obviously, the drawings described below are only some embodiments of the present invention. For ordinary technicians in this field, other drawings can be obtained based on these drawings without creative work.
[0020] Figure 1 This is a schematic diagram of the overall structure of the biological sample automatic detector.
[0021] Figure 2 This is a schematic diagram of the assembly structure of the feeding mechanism and conveyor belt of the biological sample automatic detector.
[0022] Figure 3 This is a schematic diagram of the structure of the feeding mechanism of the biological sample automatic detector.
[0023] Figure 4 This is a structural cross-sectional screenshot of the feeding mechanism of the biological sample automated detector.
[0024] Figure 5 This is a schematic diagram of the bottom perspective structure of the feeding mechanism of the biological sample automatic detector.
[0025] Figure 6 For the automated detection of biological samples Figure 5 Schematic diagram of the structure of A.
[0026] Figure 7 This is a schematic diagram of the swing arm structure of the biological sample automated detector.
[0027] Figure 8 This is a cross-sectional view of the swing arm structure of the biological sample automated detector.
[0028] Fig. 9 This is a schematic diagram of the assembly structure of the conveyor belt and swing arm of the biological sample automatic detector.
[0029] Fig.10 This is a schematic diagram of the structure of the conveyor belt of the biological sample automated detector from the bottom perspective.
[0030] Fig.11 This is a disassembled diagram of the conveyor belt structure of the biological sample automated detector.
[0031] In the figure: 100, detector; 101, dropper; 102, bioluminescent sensor; 103, fluorescent excitation light source; 104, glass slide; 200, feeding mechanism; 201, bottom plate; 202, belt one; 203, short shaft; 204, roller; 205, belt two; 206, hinge seat; 207, swing arm; 208, adapter ring; 209, suction cup; 210, spring one; 211, shift block; 212, latch; 213, spring two; 214, screw; 215, micro cylindrical cylinder; 216, air joint; 202a, rib; 203a, bearing; 206a, positioning buckle; 207a, slot; 300, conveyor belt; 301, belt three. DETAILED DESCRIPTION
[0032] In order to make the above-mentioned objects, features and advantages of the present invention more obvious and easy to understand, the specific implementation methods of the present invention are described in detail below in conjunction with the accompanying drawings.
[0033] Example 1, reference Figure 1 to Figure 11 , which is the first embodiment of the present invention, provides an automated biological sample detector 100, which can provide a large number of glass slides 104 for detection activities within a limited device space, so as to carry a larger number of biological samples, thereby realizing the detection of a larger number of biological samples in a single detection activity of the device. It includes a detector 100 and a glass slide 104, and also includes a feeding mechanism 200 arranged in the detector 100.
[0034] refer to Figure 3 and Figure 4 The feeding mechanism 200 includes a bottom plate 201, and the two long sides of the upper surface of the bottom plate 201 are provided with a belt 202, and the two ends of the two belts 202 are wound with short shafts 203, and the four short shafts 203 are respectively connected to the four corners of the bottom plate 201 by vertical rotation, and the outer wall of the belt 202 is provided with ribs 202a along its width direction, and the ribs 202a are distributed at equal intervals with respect to the outer wall of the belt 202, and the two belts 202 are parallel and symmetrical with respect to the bottom plate 201, and the glass slide 104 is inserted between the two belts 202, and the edge of the glass slide 104 is slidably inserted between two adjacent ribs 202a of the belt 202; refer to Figure 5 and Figure 6 The bottom end of the short shaft 203 passes through the bottom of the bottom plate 201, and the middle positions of both ends of the bottom surface of the bottom plate 201 are rotatably connected with rollers 204, and a belt 205 is wound around the roller 204 and the two adjacent short shafts 203. The two belts 1 202 are synchronously arranged in the same direction when running on adjacent sides; Figure 7 and Figure 8A swing arm 207 is hinged at one end of the bottom plate 201, and an adapter ring 208 is fixedly connected to the end of the swing arm 207. A suction cup 209 is inserted at the top of the adapter ring 208, and a spring 210 is provided between the suction cup 209 and the end surface of the adapter ring 208.
[0035] Specifically, refer to Figure 7 and Figure 8 A bearing 203a is embedded in the top of the short shaft 203, and a U-shaped bracket is arranged at the top of the short shaft 203. The inner ring of the bearing 203a is fixedly connected to the bracket, and the U-shaped opening of the bracket points to the swing arm 207. The end of the adapter ring 208 away from the suction cup 209 is sealed and fixedly connected to the air joint 216. The base plate 201 is located next to the hinge seat 206 and is fixedly connected to a miniature cylindrical cylinder 215, and the end of the piston rod of the miniature cylindrical cylinder 215 is coaxially fixedly connected to the screw 214.
[0036] For further reference, Figure 7 and Figure 8 The swing arm 207 is provided with a slot 207a, and a shift block 211 is slidably connected in the slot 207a. A latch 212 is inserted into the side wall of the adapter ring 208, and one end of the latch 212 is fixedly connected to the shift block 211. One end of the latch 212 matches the plug-in suction cup 209. The latch 212 is located between the shift block 211 and the outer wall of the adapter ring 208 and a spring 213 is provided. The bottom plate 201 is fixedly connected to the hinge seat 206. The end of the swing arm 207 away from the adapter ring 208 is connected to the hinge seat 206 is hinged, and the bottom end of the articulated seat 206 is provided with an L-shaped positioning buckle 206a, and the positioning buckle 206a is buckled with the bottom edge of the bottom plate 201, and the end of the shift block 211 away from the pin 212 squeezes and resists the positioning buckle 206a, and the swing arm 207 is matched with the hinge axis of the articulated seat 206 and is plugged with a screw 214, and the screw 214 passes through the swing arm 207 and the articulated seat 206, the number of spiral turns of the spiral groove of the screw 214 is one-half turn, and the lead specification of the screw 214 is greater than twenty millimeters.
[0037] The structural principle and advantages of the device are further explained in combination with the existing technology: the existing automated biological sample detection equipment uses a servo system to drive the sampling mechanism to sample the biological sample and drip the sample on the carrier (glass slide 104). After the sampling is completed, the platform moves so that the carrier and the biological sample are moved to the detection area for detection. The platform area for placing the carrier is very limited, so the number of biological samples that the device can detect is also limited. When the number of biological samples that need to be detected exceeds the detection capacity of the device, it needs to be performed in batches for multiple times.
[0038] The present invention mainly provides a feeding mechanism 200 for providing glass slides 104 to a detector 100. The feeding mechanism 200 prepares a large number of glass slides 104 for use by vertically arranging and inserting. The feeding mechanism 200 releases the glass slides 104 one by one to a conveyor belt 300, and then the conveyor belt 300 sequentially transports the glass slides 104 to biological sample droplets and detection stations to complete biological sample sampling and detection. The feeding mechanism 200 of the glass slide 104 is different from the existing biological sample automatic detection equipment in terms of working form;
[0039] To achieve the above functions, firstly, the feeding mechanism 200 uses a high-strength bottom plate 201 as the structural basis, and two parallel belts 1 202 are installed on the bottom plate 201. A large number of vertical ribs 202a are designed on the surface of the belt 1 202. The gaps between the ribs 202a are used to insert the glass slide 104. The structure involves the following technical details:
[0040] The feeding mechanism 200 takes and delivers the glass slides 104 through the suction cup 209, and the glass slides 104 need not only to be parallel to each other, but also to be perpendicular to the belt 1 202. Figure 6 As shown, the suction cup 209 can correctly fit and absorb the surface of the glass slide 104. To achieve this function, the two belts 1 202 need to be debugged symmetrically and keep the symmetry unchanged during repeated operation. Therefore, the belt 1 202 and the belt 2 205 need to run synchronously, as shown in FIG. Figure 5 and Figure 6 As shown, the device adopts the method of winding the belt 205 to keep the two belts 1 202 in synchronization, wherein the roller 204 is provided with two belt grooves, and the bottom end of the short shaft 203 is provided with a belt groove, and the belt 205 is an annular PU round belt with a steel wire core. Figure 6 Taking the perspective as an example, the winding method is that the two sections of the belt 205 extending from the two sides of the short shaft 203 are respectively overlapped in the two belt grooves of the roller 204, and the belt 205 extending from the roller 204 is crossed and reversed in an X shape and then wound around another short shaft 203, so that when any belt 1 202 is dragged, the belt 1 202 can drive another belt 1 202 through the short shaft 203 and the belt 2 205 to realize synchronous and reverse operation (one belt 1 202 runs clockwise, and the other belt 1 202 runs counterclockwise), so that the two belts 1 202 and the contact side of the glass slide 104 run synchronously and in the same direction;
[0041] By setting one end of the belt 205 in a cross-reverse direction, the two short shafts 203 can be synchronized in reverse rotation, and the height difference between the two belt grooves on the roller 204 can be used to avoid contact friction and wear at the intersection of the belt 205. By selecting a PU round belt with a steel wire core, the elastic deformation and elongation of the belt 205 can be avoided to prevent the two short shafts 203 from running out of sync. In addition to being more economical than the traditional gear reversing structure, this structure also avoids the problem of virtual position caused by tooth clearance (the transmission clearance will cause the position difference between the two belts 1 202, which will cause the glass slide 104 to swing and become unstable).
[0042] Since the suction cup 209 moves in an arc path with the swing arm 207, the swing arm 207 cannot swing downward directly after the suction cup 209 absorbs the glass slide 104, which will cause the bottom of the glass slide 104 to be squeezed and broken by the bottom plate 201. Therefore, the device swings the swing arm 207 upward to make the suction port of the suction cup 209 contact the glass slide 104, and connects the suction cup 209 to the negative pressure source through the air joint 216, so that the negative pressure makes the suction cup 209 absorb the glass slide 104. Figure 8 As shown, after the glass slide 104 is adsorbed, the suction cup 209 tends to shrink into the adapter ring 208 under the negative pressure, thereby compressing the spring 1 210 to pull the glass slide 104 horizontally out from between the belts 1 202. After the glass slide 104 is separated from the belt 1 202, it can be safely deflected with the swing arm 207. During the process of the glass slide 104 being pulled out of the belt 1 202 horizontally, the belt 1 202 will be moved a short distance through the rib 202a, so that the adjacent glass slide 104 reaches the waiting position;
[0043] After the suction cup 209 successfully obtains the glass slide 104, the swing arm 207 deflects downward so that the glass slide 104 is converted from a vertical state to a horizontal state. Fig. 9 As shown, the suction cup 209 is between the belts 301, and the glass slide 104 is placed flat on the belts 301. The structure involves the following technical details:
[0044] The suction cup 209 should maintain internal negative pressure during the movement of the swing arm 207. When the swing arm 207 reaches the lower dead point, assuming that the suction port of the suction cup 209 reaches the designated position, and the suction port of the suction cup 209 is level with the belt 301, the negative pressure ends and the suction cup 209 releases the glass slide 104. The spring 1 210 will lift the suction cup 209 and the glass slide 104, and the glass slide 104 will be difficult to contact the belt 301, and thus cannot be transported to the next station by the belt 301. Therefore, a shift block 211 is designed between the swing arm 207 and the adapter ring 208. The shift block 211 is limited by the width of the slot 207a and can only slide in the slot 207a. It is also limited by the latch 212 to determine the direction of its sliding. Figure 6 and Figure 8As shown, when the swing arm 207 deflects downward by ninety degrees, the end face of the swing arm 207 abuts against the hinge seat 206 to limit the position. During the process, the shift block 211 abuts against the positioning buckle 206a at the bottom edge of the hinge seat 206, causing it to shrink into the slot 207a, thereby compressing the spring 213 so that the pin 212 is inserted into the side wall of the suction cup 209. At this time, the negative pressure ends so that the suction cup 209 releases the glass slide 104. The suction cup 209 will not bounce upward under the restriction of the pin 212, and the belt 3 301 can smoothly transport the glass slide 104 to the next workstation.
[0045] The up and down swing of the swing arm 207 is powered by a micro cylindrical cylinder 215, which drives the screw 214 to extend and retract, and drives the swing arm 207 to deflect through the high-lead spiral groove on the screw 214. Since the swing arm 207 only needs to deflect 90 degrees, the spiral groove of the screw 214 only needs to have about half a turn.
[0046] In summary, compared with the traditional glass slide 104 operating platform, the device replaces the conventional flat storage form with a three-dimensional storage form, which can continuously provide a large number of glass slides 104 for biological sample fluorescence detection equipment during detection activities, so that the glass slide 104 capacity of the detection equipment is no longer a factor restricting the efficiency of biological sample fluorescence automated detection.
[0047] Example 2, reference Figure 1 , Figure 2 , Figure 9~Figure 11 , which is the second embodiment of the present invention. Different from the previous embodiment, this embodiment provides a conveyor belt 300 of the biological sample automatic detection instrument 100, which cooperates with the feeding mechanism to move the glass slide 104 to the next process, and the glass slide 104 completes the acquisition and detection of the biological sample. Figure 1 The detector 100 is also provided with a servo-driven dropper 101 and a bioluminescent sensor 102, and the detector 100 is provided with a conveyor belt 300 at the bottom of the dropper 101 and the bioluminescent sensor 102. Figure 2 One end of the conveyor belt 300 is adjacent to the swing arm 207, and the conveying directions of the conveyor belt 300 and the belt 1 202 are parallel to each other. Fig. 9 and Fig.10 , two belts 301 are arranged inside the conveyor belt 300 and are distributed on both sides of the conveyor belt 300. The conveyor belt 300 is located in the rotation radius range of the swing arm 207, the suction cup 209 and the air joint 216 and is hollowed out. When the swing arm 207 is at the deflection lower dead point position, the suction port height of the suction cup 209 is coplanar with the upper plane of the belt 301, the suction cup 209 is located in the middle position between the two belts 301, and the suction cup 209 corresponds to the position of the dropper 101 above. Fig.10 and Fig.11The bottom surface of the conveyor belt 300 is equipped with a fluorescence excitation light source 103 at a position corresponding to the bioluminescence sensor 102 .
[0048] The feeding mechanism 200 works with the conveyor belt 300. The conveyor belt 300 uses two narrow belts 301 distributed on both sides thereof, so that the middle part is hollowed out to leave room for the swing arm 207 to move and avoid blocking the fluorescent excitation light source 103. Figure 1 The working process of the conveyor belt 300 is as follows: the suction cup 209 releases the glass slide 104 on the conveyor belt 300, the dropper 101 releases the biological sample on the glass slide 104, and the conveyor belt 300 moves the glass slide 104 and the biological sample to between the fluorescent excitation light source 103 and the biological fluorescence sensor 102 for detection. The above process is repeated until the biological sample to be detected is tested or all the glass slides 104 in the feeding mechanism 200 are used.
[0049] The rest of the structure is the same as that of Example 2.
[0050] It should be noted that the above embodiments are only used to illustrate the technical solutions of the present invention rather than to limit it. Although the present invention has been described in detail with reference to the preferred embodiments, those skilled in the art should understand that the technical solutions of the present invention may be modified or replaced by equivalents without departing from the spirit and scope of the technical solutions of the present invention, which should all be included in the scope of the claims of the present invention.
Claims
1. An automated biological sample detector, comprising a detector (100) and a glass slide (104), characterized in that: It also includes a feeding mechanism (200) arranged in the detector (100), which includes a bottom plate (201), two long sides of the upper surface of the bottom plate (201) are each provided with a belt 1 (202), and both ends of the two belts 1 (202) are each wound with a short shaft (203), and the four short shafts (203) are respectively connected to the four corners of the bottom plate (201) in a vertical rotation manner, and the outer wall of the belt 1 (202) is provided with ribs (202a) along its width direction, and the ribs (202a) are distributed at equal intervals with respect to the outer wall of the belt 1 (202), and the two belts 1 (202) are spaced apart with respect to each other. The bottom plates (201) are parallel and symmetrical to each other, the bottom ends of the short shafts (203) penetrate to the bottom of the bottom plate (201), the middle positions of both ends of the bottom surface of the bottom plate (201) are rotatably connected with rollers (204), and a belt 2 (205) is wound between the roller (204) and the two adjacent short shafts (203), the two adjacent sides of the belts 1 (202) are synchronously arranged in the same direction when running, the glass slide (104) is inserted between the two belts 1 (202), and the edge of the glass slide (104) is slidably inserted between two adjacent ribs (202a) of the belt 1 (202); A swing arm (207) is hingedly connected to one end of the bottom plate (201), and an adapter ring (208) is fixedly connected to the end of the swing arm (207). A suction cup (209) is inserted at the top of the adapter ring (208), and a spring 1 (210) is arranged between the suction cup (209) and the end surface of the adapter ring (208). A slot (207a) is provided on the swing arm (207), and a shift block (211) is slidably connected in the slot (207a). A latch (212) is inserted into the side wall of the adapter ring (208), and one end of the latch (212) is fixedly connected to the shift block (211). One end of the latch (212) matches the plug-in suction cup (209), and a spring 2 (213) is arranged between the latch block (211) and the outer wall of the adapter ring (208).
2. The biological sample automated detector according to claim 1, characterized in that: A bearing (203a) is embedded in the top end of the short shaft (203), and a U-shaped bracket is provided at the top end of the short shaft (203); the inner ring of the bearing (203a) is fixedly connected to the bracket, and the U-shaped opening of the bracket points to the swing arm (207).
3. The biological sample automated detector according to claim 2, characterized in that: The bottom plate (201) is fixedly connected to a hinge seat (206); one end of the swing arm (207) away from the adapter ring (208) is hinged to the hinge seat (206); an L-shaped positioning buckle (206a) is provided at the bottom end of the hinge seat (206); the positioning buckle (206a) is buckled with the bottom edge of the bottom plate (201); and one end of the shift block (211) away from the latch (212) presses against the positioning buckle (206a).
4. The biological sample automated detector according to claim 3, characterized in that: The swing arm (207) is plugged with a screw rod (214) along the hinge axis between the swing arm (207) and the hinge seat (206); the screw rod (214) passes through the swing arm (207) and the hinge seat (206); the number of spiral turns of the spiral groove of the screw rod (214) is one-half turn, and the lead specification of the screw rod (214) is greater than twenty millimeters.
5. The biological sample automated detector according to claim 4, characterized in that: The bottom plate (201) is fixedly connected to a micro cylindrical cylinder (215) located beside the hinge seat (206), and the end of the piston rod of the micro cylindrical cylinder (215) is coaxially fixedly connected to the screw rod (214).
6. The biological sample automated detector according to claim 5, characterized in that: One end of the adapter ring (208) away from the suction cup (209) is sealed and fixedly connected to a gas joint (216).
7. The biological sample automated detector according to claim 6, characterized in that: A servo-driven dropper (101) and a bioluminescence sensor (102) are also provided in the detector (100), and a conveyor belt (300) is provided at the bottom of the dropper (101) and the bioluminescence sensor (102) in the detector (100).
8. The biological sample automated detector according to claim 7, characterized in that: One end of the conveyor belt (300) is adjacent to the swing arm (207), and the conveying directions of the conveyor belt (300) and the belt one (202) are parallel to each other. Two belts three (301) are arranged inside the conveyor belt (300) and are distributed on both sides of the conveyor belt (300). The conveyor belt (300) is located within the rotation radius of the swing arm (207), the suction cup (209) and the air joint (216) and is hollowed out.
9. The biological sample automated detector according to claim 8, characterized in that: When the swing arm (207) is at the deflection lower dead point position, the suction opening height of the suction cup (209) is coplanar with the upper plane of the belt three (301), the suction cup (209) is located in the middle position between the two belts three (301), and the suction cup (209) corresponds to the position of the dropper (101) above.
10. The biological sample automated detector according to claim 9, characterized in that: The bottom surface of the conveyor belt (300) is located at a position corresponding to the bioluminescence sensor (102) and is equipped with a fluorescence excitation light source (103).
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