This application claims priority from prior Japanese Patent Application No. 2022-030373, filed on Feb. 28, 2022, and Japanese Patent Application No. 2022-030375, filed on Feb. 28, 2022, the entire contents of which are incorporated herein by reference.
The disclosure relates to a specimen preparation apparatus, a specimen processing apparatus, a specimen preparation method and a specimen processing method.
Japanese Patent Publication No. 2021-162321 (Patent Document 1) discloses a specimen preparation apparatus provided with a centrifuge. In the specimen preparation apparatus of Patent Document 1, a user performs an operation to set a centrifuge tube in a centrifuge.
In the above Patent Document 1, there is room for improvement from a viewpoint of automation because a user needs to perform an operation to set a centrifuge tube in a centrifuge.
One or more embodiments may be to achieve further automation of a specimen preparation apparatus provided with a centrifuge.
A specimen preparation apparatus according to one or more embodiments that prepares a measurement specimen from a specimen may include a holder that holds a centrifuge tube, a transfer unit that transfers the centrifuge tube held by the holder, a dispenser that dispenses a specimen into the centrifuge tube before or after transfer by the transfer unit, and a centrifugation section that holds the centrifuge tube transferred by the transfer unit and centrifuges the specimen dispensed into the centrifuge tube by rotation.
A specimen preparation apparatus according to one or more embodiments may include a transfer unit that transfer the centrifuge tube between the holder and the centrifugation section. Since the transfer unit allows the centrifuge tube to be transferred to the centrifugation section, an operation that a user sets the centrifuge tube in the centrifugation section is reduced, and further automation is achieved.
A specimen processing apparatus according to one or more embodiments may include a container transport mechanism that includes a holder to hold a plurality of containers capable of storing specimens and a drive unit to move the holder, a processing section that processes containers or a specimen in the containers, and a controller, wherein the controller controls the container transport mechanism and the processing section, so that the plurality of containers are moved in the same direction by the drive unit, at least one type of container is provided at a predetermined position, and at least one type of container or a specimen in at least one type of container is performed with a predetermined process.
A specimen processing apparatus according to one or more embodiments may simplify the container transport mechanism and reduce the size of the apparatus since multiple types of containers are not necessary to be transported individually.
A method of preparing a specimen according to one or more embodiments may include transferring a centrifuge tube provided by a user is transferred to a centrifugation section, dispensing a sample into the centrifuge tube transferred to the centrifugation section, and centrifuging the sample stored in the centrifuge tube by the centrifugation section.
According to the method of preparing a specimen according to one or more embodiments, an operation that the user sets the centrifuge tube to the centrifugation section may be reduced, and further automation may be achieved.
A method of processing a specimen according to one or more embodiments using a specimen processing apparatus that may include: a container transport mechanism, which includes the holder to hold a plurality of containers capable of storing a specimen and the drive unit to move the holder; the processing section that processes the containers or a specimen in the containers; and the controller, may include moving a plurality of containers in the same direction by the drive unit, at least one type of container is provided at a predetermined processing position, and at least one type of container or a specimen in at least one type of container is performed with a predetermined process.
According to a method of processing a specimen according to one or more embodiments, since multiple types of containers do not need to be transported individually, the container transport mechanism may be simplified, and the apparatus may be downsized.
According to one or more embodiments, further automation of specimen preparation involving centrifugation may be achieved. Also, according to one or more embodiments, a container transport mechanism may be simplified, and an apparatus may be downsized.
One or more embodiments are described on the basis of a drawing.
First, with reference to
The specimen preparation apparatus 100 is an apparatus to prepare a measurement specimen for measurement by a flow cytometer by performing a pretreatment on a blood sample. The measurement specimen is an immunostained specimen of a white blood cell derived from a blood sample. More specifically, the measurement specimen is prepared in which a cell surface antigen (e.g., CD4, CD25, CD62L) and an intracellular antigen (e.g., FOXP3) of a T cell included in the blood sample are labeled by a labeled antibody.
The rack transporter 20 includes a common drive unit 21a to move the racks 10a to 10c integrally along an X direction.
The rack transporter 20 includes a magnet 23 that is provided between the rack 10a to hold the processing container 11 and the rack 10b to hold the centrifuge tube (reaction container) 12. The magnet 23 is used to collect a complex including red blood cells and a magnetic particle (solid phase substance) formed in the processing container 11 as described below.
The specimen preparation apparatus 100 includes a centrifugation section 30. The centrifugation section 30 includes a rotor 31 that rotates at a high speed and a plurality of holders 32 that are provided around the periphery of the rotor 31. The holder 32 has, for example, a cylindrical shape and may receive and hold the centrifuge tube 12 therein. Also, the holder 32 holds the centrifuge tube 12 with its opening facing upward when the rotor 31 is stopped.
The specimen preparation apparatus 100 includes a transfer unit 40 that transfers the centrifuge tube 12 between the rack transporter 20 and the centrifugation section 30. The transfer unit 40 is movably supported in a Y direction by a transfer axis 41. Also, the transfer unit 40 is movable in a Z direction (vertical direction).
The specimen preparation apparatus 100 includes a dispenser 50. The dispenser 50 is movably supported in the Y direction on the transfer axis 41 common to the transfer unit 40. Also, the dispenser 50 is movable in the Z direction (vertical direction). The dispenser 50 includes a pipette 50a, dispenses a sample stored in the sample container 13 into the processing container 11 using the pipette 50a.
The specimen preparation apparatus 100 includes an agitator 51 that agitates a blood sample. The agitator 51 agitates a blood sample in the container 13 by holding and removing the sample container 13 from the rack 10c and inverting and agitating the blood sample.
The specimen preparation apparatus 100 includes a dispenser 60. The dispenser 60 is movably supported in the X direction by a transfer axis 61. Also, the transfer axis 61 is movably supported in the Y direction by a transfer axis 62. As a result, the dispenser 60 is movable in a horizontal direction in the apparatus. Also, the dispenser 60 is movable in the Z direction (vertical direction). The dispenser 60 includes a pipette 60a, and dispenses a reagent installed in a reagent setting part 70a and a reagent setting part 70b to the processing container 11 of the rack transporter 20 or the centrifuge tube 12 in the centrifugation section 30. The dispenser 60 further aspirates a supernatant in the processing container 11, in a state in which magnetic particles are attracted by the magnet 23, and dispenses the supernatant into the centrifuge tube 12 transferred to the centrifugation section 30. The dispenser 60 discharges the reagent into the processing container 11, which is moved to a reagent discharging position by the drive unit 21a.
The specimen preparation apparatus 100 includes reagent setting parts 70a and 70b. The reagent setting part 70a includes a cold storage and holds the reagent at a low temperature. The reagent setting part 70b holds the reagent at a normal temperature.
The specimen preparation apparatus 100 includes a nozzle cleaner 80. The nozzle cleaner 80 cleans a nozzle of the dispenser 60.
The specimen preparation apparatus 100 includes a controller 90 that controls each part of the apparatus. The controller 90 includes a processor and a memory. The processor is configured with, for example, a CPU. The memory may include a memory and a storage. The processor controls each part of the specimen preparation apparatus 100 by executing a program stored in the memory.
The reagent setting part 70a includes a lid and a shutter member. The reagent setting part 70a is a box-shaped member with a lid comprising a top surface that may be opened and closed. The lid is provided to cover an upper part of the reagent setting part 70a. In the lid, a plurality of insertion holes through which nozzles are passed is formed at a position above the plurality of reagent containers. In the shutter member, an insertion hole of the nozzle and a shielding section are formed. The shutter member is provided on the lid so as to be opened and closed integrally with the lid.
In a layout of the specimen preparation apparatus 100 illustrated in
Referring to
The lower portion 230 of the rack transporter 20 includes a drive unit 21a comprising a motor, a pair of pulleys 212a, and a belt 212. An output axis of the drive unit 21a is connected to the pulley 212a on the left side (X1 direction side). The belt 212 extends along the X axis, and both ends of the belt 212 extend over the pair of pulleys 212a. A connecting member 213 is fixed to the belt 212. The connecting member 213 is connected to a slider 214. The slider 214 is movable in the X direction along a rail 215.
An upper end part of the side wall 214a projecting out of the slit 210 is connected to a fastener 221 that is screwed to a bottom part 10c1 of the rack 10c. The upper end part of the side wall 214b projecting from the slit 211 is connected to the fastener 221 that is screwed to the bottom part 10c1 of the rack 10c, a fastener 222 that is screwed to a bottom part 10b1 of the rack 10b, and a fastener 223 that is screwed to a bottom part 10a1 of the rack 10a.
In the above-described configuration, when side walls 214a, 214b of the slider 214 move in the X axis direction via the slits 210, 211 by driving of the drive unit 21a described above, the racks 10a to 10c connected to the side walls 214a, 214b move integrally in the X axis direction. In one or more embodiments, the slider 214 of the rack transporter 20 and the racks 10a to 10c are screwed and secured by the fasteners 221, 222, and 223, but screw fixing is not required as long as the slider 214 and the racks 10a to 10c are interlocked by engaging with each other. For example, projections provided downwardly on the bottom of the racks 10a to 10c and holes provided in the upper end parts of the side walls 214a, 214b may form respective convexities and concavities that may be engaged with each other.
As illustrated in
Referring to the perspective view illustrated in
The transfer unit 40 is attached to a sheet metal 41A constituting a transfer axis 41 in a Y axis and Z axis movable manner. AY axis motor 415 is attached to the sheet metal 41A. A belt 414 is stretched over an output axis of the Y axis motor 415. Also, a rail 411a extending horizontally is attached to the sheet metal 41A. A sheet metal 411 is slidably attached to the rail 411a. A part of the sheet metal 411 is fastened to the belt 414 by a fastener 413. Therefore, the belt is driven by the Y axis motor 415, and the sheet metal 411 moves along the Y axis accordingly.
A sheet metal 417 to support a part involved in a Z axis movement described below is attached to the sheet metal 411. The sheet metal 417 is a vertical plate extending in a vertical direction, and a Z axis motor 416 is attached on a lower back (X1 direction side) of the sheet metal 417. An open/close motor 420 is provided above the sheet metal 417. Also, a longitudinal rail 418 is attached to a front side of the sheet metal 417 (X2 direction side). An output of the Z axis motor 416 is transmitted to a belt 412 that is vertically bridged. A sheet metal 431 is fixed to the belt 412. The sheet metal 431 is slidably attached to a rail 418. The sheet metal 431 has a rail 433 extending horizontally. A slide section 432 is slidably attached to the rail 433. The slide section 432 is biased toward the Y2 direction along the rail 433 by a spring member 440 that is horizontally provided between the sheet metal 431 and the slide section 432, as illustrated by a white arrow in
At a lower end of the slide section 432 on the Y1 direction side, a first gripper 434 that consists of one of a pair of grippers to grip the upper part of the centrifuge tube 12 is attached. As shown in
At a rear (Y2 direction side) end of the slide section 432, a thick contacting section 432a is provided on the X2 direction side. An output axis of the open/close motor 420 provided above the sheet metal 417 is connected to the belt 421. When the driving force of the open/close motor 420 is transmitted to the belt 421, a first rod 423, which is provided to extend vertically against the sheet metal 417 and to be rotatable around an axis, rotates. The upper and lower ends of the first rod 423 are connected to a second rod 424, which is parallel to the first rod 423 and extends in the vertical direction, and when the first rod 423 rotates about its own axis, the second rod 424 rotates about the first rod 423, as illustrated by an arrow in
When the second rod 424 rotates about the first rod 423, the contacting section 432a of the sliding section 432 is pushed in the Y1 direction by the second rod 424. As a result, the slide section 432 moves in the Y1 direction against the force of the spring member 440. As described earlier, the slide section 432 and the first gripper 434 move integrally, and by the first gripper 434 moving in the Y1 direction, a space between the first gripper 434 and the second gripper 435 opens, and the centrifuge tube 12 may be gripped in the meantime.
The Z axis motor 416 is connected to a pair of grippers 434, 435 via the belt 412, sheet metal 431, and slide section 432. When the Z axis motor 416 is driven, the sheet metal 431 fixed to the belt 412 moves in the vertical direction. As the sheet metal 431 moves in the vertical direction, the grippers 434, 43 5 move in the vertical direction along the Z axis.
When moving the centrifuge tube 12 from the rack transporter 20 to the centrifugation section 30, the Z axis motor 416 and the open/close motor 420 lower the grippers 434, 435 to grip the centrifuge tube 12 in the rack transporter 20 and move the griped centrifuge tube 12 upward. The grippers 434, 435, which grip the centrifuge tube 12, are moved to an upper side of the centrifugation section 30 by the drive of the Y axis motor 415. After moving the grippers 434 and 435 to the upper side of the centrifugation section 30, the Z axis motor 416 lowers the centrifuge tube 12, and the centrifuge tube 12 is inserted into the holder 32 of the centrifugation section 30. The open/close motor 420 opens the grippers 434, 435, and the gripping is released. When the centrifuge tube 12 that stores the specimen prepared in the centrifugation section 30 is returned to the rack transporter 20, the reverse operation is performed. That is, by the Z axis motor 416 and the open/close motor 420, the grippers 434, 435 are lowered to grip the centrifuge tube 12 in the centrifugation section 30, and the gripped centrifuge tube 12 is moved upward. The grippers 434, 435, that grip the centrifuge tube 12, are moved to the upper side of the rack transporter 20 by the drive operation of the Y axis motor 415. After moving the grippers 434 and 435 to the upper side of the rack transporter 20, by the operation of the Z axis motor 416, the centrifuge tube 12 is lowered, and the centrifuge tube 12 is inserted into an original holding position of the rack 10b in the rack transporter 20. The grippers 434, 435 are opened by operation of the open/close motor 420, and the gripping is released.
When the centrifuge tube 12 is returned from the centrifugation section 30 to the rack transporter 20, a prepared specimen is stored in the centrifuge tube 12. Accordingly, it is necessary to avoid the centrifuge tube 12 from falling out during transfer so that the specimen does not spill into the apparatus. Thus, the transfer unit 40 illustrated in
Furthermore, in the transfer unit 40 illustrated in
The specimen preparation apparatus 100 is provided with the transfer unit 40 in such a configuration so that the centrifuge tube 12 set in the rack 10b of the rack transporter 20 may be transferred to the rotor 31 of the centrifugation section 30. Accordingly, there is no need for a user to access the centrifugation section 30. Thus, automation of the operation is achieved as compared to a conventional arrangement in which the user sets the centrifuge tube 12 in the centrifugation section 30. Furthermore, by restricting access such as by a user to the centrifugation section 30, an improvement in safety is achieved.
Referring to
Above the cover 33, a lid 34 is provided to close the openings 331 and 332. The lid 34 may slide in the horizontal direction (Y direction). The lid 34 is provided with an opening 341 and a notch 342. Also, the lid 34 is moved in the Y direction by a drive unit 35.
As illustrated in
Also, as illustrated in
Also, as illustrated in
Referring to
As illustrated in
Prior to a process of dispensing a sample, as illustrated in
In step S201 of
In step S202, a blood sample in the sample container 13 is agitated. As illustrated in
In step S203, a blood sample is aspirated from the sample container 13 and discharged into the processing container 11 of the rack 10a, and the blood sample is dispensed. As illustrated in
In step S204, an antibody is dispensed into the processing container 11 from which the blood sample is discharged. As illustrated in
When dispensing is completed to all the processing containers 11, in step S205, an agitation of the blood sample in the processing container 11 is performed. The rack is repeatedly moved back and forth in the X1 direction and the X2 direction by the rack transporter 20, and the blood sample in the processing container 11 is agitated. The rack 10a holding the processing container 11 is then allowed to stand still for a predetermined period of time (e.g., 20 minutes).
In step S206, a buffer solution is dispensed into the processing container 11. The rack transporter 20 moves the rack 10a, and at the position P3, a buffer is dispensed into each processing container 11 by the dispenser 60. The rack 10a is moved at a high speed by the rack transporter 20, and the blood sample in the processing container 11 is agitated. Thereafter, the blood sample is allowed to stand still. For example, a BSA solution and a phosphate buffered saline (PBS) are dispensed as buffer solutions. Also, the blood sample to which the buffer solution is dispensed is agitated.
In step S207, a magnetic particle is dispensed into the processing container 11. For example, a streptavidin-bound magnetic particle is dispensed as a magnetic particle. As illustrated in
In step S208, the blood sample in the processing container 11 is agitated, and a reaction is carried out. The time required is, for example, 5 minutes. The rack is moved at a high speed by the rack transporter 20, and the blood sample in the processing container 11 is agitated. Then, the blood sample is allowed to stand still. Therefore, a complex including red blood cells and a solid phase substance is formed in the processing container 11.
In step S209, magnetic attraction is performed. As illustrated in
In step S210, a supernatant (e.g., 700 µL) of the blood sample in the processing container 11, in which attraction is performed, is aspirated and discharged into the centrifuge tube 12 of the centrifugation section 30 to be dispensed. As illustrated in
In step S212, the specimen in the centrifuge tube 12 is centrifuged. In the centrifugation section 30, the rotor 31 is rotated at a high speed to settle the white blood cell at the bottom of the centrifuge tube 12.
In step S213, the supernatant in the centrifuge tube 12 is removed. The dispenser 60 aspirates and removes the supernatant (e.g., 600 µL) of the centrifuge tube 12, in which the white blood cell is settled by centrifugation.
In step S214, the specimen in the centrifuge tube 12 is agitated. The white blood cell is settled at the bottom of the centrifuge tube 12 by step S212 and step S213. In order to disperse the settled white blood cell, the centrifuge tube 12 is agitated. The centrifugation section 30 agitates the specimen in the centrifuge tube 12 by rotating the rotor 31 in one direction with repeated acceleration and deceleration. In one or more embodiments, repeated rotation with acceleration and deceleration in one direction as agitation by the centrifugation section 30 is explained as an example, but a rotation method for agitation may be intermittent rotation or rotation in both forward and reverse directions.
In step S215, an antibody reagent is dispensed into the centrifuge tube 12. The dispenser 60 dispenses a cocktail reagent including a CD25-labeled antibody, a CD4-labeled antibody, and a CD62-labeled antibody as the antibody reagent into the centrifuge tube 12 held in the centrifugation section 30.
In step S216, the centrifugation section 30 rotates the rotor 31 while repeatedly accelerating and decelerating in one direction to agitate the specimen in the centrifuge tube 12, and a reaction of the specimen proceeds. The predetermined time is, for example, 30 minutes.
In step S217, a cleaning liquid for the pre-fixation sample is dispensed into the centrifuge tube 12. The dispenser 60 dispenses a PBS as the cleaning liquid into the centrifuge tube 12.
In step S218, the centrifugation section 30 agitates the specimen in the centrifuge tube 12 by rotating the rotor 31 while repeatedly accelerating and decelerating in one direction.
In step S219, the centrifugation section 30 centrifuges the specimen in the centrifuge tube 12 by rotating the rotor 31 at a high speed in one direction. As a result, the white blood cell that reacts with the antibody reagent is settled.
In step S220, the dispenser 60 aspirates and removes the supernatant from the centrifuge tube 12. As a result, the surface antigens CD25, CD4 and CD62 are stained with the corresponding labeled substances.
In step S221, the dispenser 60 dispenses a fixation/permeabilization agent into the centrifuge tube 12.
In step S222, the centrifugation section 30 agitates the specimen in the centrifuge tube 12 by rotating the rotor 31 while repeatedly accelerating and decelerating in one direction, and the reaction is performed. The predetermined time is, for example, 30 minutes.
In step S223, the dispenser 60 dispenses a cleaning liquid for the post-fixation sample into the centrifuge tube 12.
In step S224, the centrifugation section 30 agitates the specimen in the centrifuge tube 12 by rotating the rotor 31 while repeatedly accelerating and decelerating in one direction.
In step S225, the centrifugation section 30 centrifuges the specimen in the centrifuge tube 12 by rotating the rotor 31 at a high speed.
In step S226, the dispenser 60 aspirates and removes the supernatant from the centrifuge tube 12.
In steps S227 to S230, dispensing of the cleaning liquid, agitation, centrifugation and removal of the supernatant are performed. In other words, a cleaning process of the sample is repeated. The cleaning process of the sample may be performed once, twice, three or more times. As a result, processes of fixation and permeabilization for the cell in the centrifuge tube 12 are performed.
In step S231, the dispenser 60 dispenses an antibody reagent into the centrifuge tube 12. For example, a reagent including a Foxp3-labeled antibody is dispensed as the antibody reagent.
In step S232, the centrifugation section 30 rotates the rotor 31 while repeatedly accelerating and decelerating in one direction to agitate the specimen in the centrifuge tube 12 and perform a reaction. The predetermined time is, for example, 30 minutes.
In step S233, the dispenser 60 dispenses a cleaning liquid for the post-fixation sample into the centrifuge tube 12. In steps S234 to S236, as described above, agitation, centrifugation and removal of the supernatant are performed, and in steps S237 to S240, a process of cleaning the sample including dispensing of the cleaning liquid, agitation, centrifugation, and removal of the supernatant is repeated. The process of cleaning the sample may be performed once, twice, three or more times. As a result, the FOXP3 in the centrifuge tube 12 is stained with the corresponding labeled substance.
In step S241, the dispenser 60 dispenses a buffer solution into the centrifuge tube 12. Dispensing adjusts the specimen in the centrifuge tube 12 to a predetermined volume of liquid and a predetermined ph suitable for supply to the measurement apparatus. For example, a BSA solution and a PBS are dispensed as buffer solutions.
In step S242, the centrifugation section 30 rotates the rotor 31 to perform agitation as described above.
In step S243, the transfer unit 40 removes the centrifuge tube 12 held in the centrifugation section 30 from the rotor 31 and sets the centrifuge tube 12 on the rack 10b held in the rack transporter 20. At this time, each centrifuge tube 12 is returned to its original position in the rack 10b. As described above, the controller 90 stores a correspondence between each holder 32 of the rotor 31 and the holding position in the rack 10b of the centrifuge tube 12 set in each holder 32. The transfer unit 40 transfers the centrifuge tube 12 held in each holder 32 back to its original holding position in the rack 10b based on the correspondence stored in the controller 90. For example, the centrifuge tube 12 that is held in the leftmost holding position in the initial position in
The above completes the specimen preparation using the specimen preparation apparatus 100.
Next, with reference to
The centrifugation section 30 positions the rotor 31 at a desired rotational position by adjusting a position of the rotor 31 at the origin and the rotational distance from the origin.
In step S301, the origin of the rotor 31 of the centrifugation section 30 is set out. Thereafter, a process of step S410 (steps S302 to 305) is processed.
As step S410, first, in step S302, a θ axis of the rotor 31 is moved to a set position of the centrifuge tube 12 as a reaction container. Specifically, a rotation angle of the rotor 31 is aligned with a position to which the centrifuge tube 12 is transferred. In step S303, a Y axis of the transfer unit 40 is moved to a catch position. Then, the centrifuge tube 12 is caught by the transfer section 40, and the centrifuge tube 12 is transferred to the rotor 31.
Thereafter, in step S304, the Y axis of the transfer unit 40 is moved to an origin position. In step S305, the θ axis of the rotor 31 is moved to the origin position. When there is a next sample, process of steps S302 to S305 (step S410) are repeated.
In step S306, the θ axis of the rotor 31 is moved to a pipette access position where the sample is dispensed, the reagent is dispensed or the supernatant is aspirated. In step S307, an XY axis of the dispenser 60 is moved to the pipette access position. Then, the sample is discharged into the centrifuge tube 12 of the rotor 31 by the dispenser 60.
Thereafter, in step S308, the XY axis of the dispenser 60 is moved to the origin position. In step S309, the θ axis of the rotor 31 is moved to the origin position. When there is a next sample, processes of steps S306 to S309 are repeated.
Thereafter, the process of step S420 (steps S310 to S324) is repeated twice.
As step S420, first, in step S310, a process of centrifugation is performed, followed by originating of the rotor 31. In step S311, the θ axis of the rotor 31 is moved to the pipette access position. In step S312, the XY axis of the dispenser 60 is moved to the pipette access position. Then, the supernatant is aspirated and removed from the centrifuge tube 12 of the rotor 31 by the dispenser 60.
In step S313, the XY axis of the dispenser 60 is moved to the origin position. In step S314, the θ axis of the rotor 31 is moved to the origin position. In step S315, the θ axis of the rotor 31 is driven to perform a strong agitation operation. Thereafter, the originating of the rotor 31 is performed.
In step S316, the θ axis of the rotor 31 is moved to the pipette access position. In step S317, the XY axis of the dispenser 60 is moved to the pipette access position. Then, the reagent is dispensed into the centrifuge tube 12 of the rotor 31 by the dispenser 60.
In step S318, the XY axis of the dispenser 60 is moved to the origin position. In step S319, the θ axis of the rotor 31 is moved to the origin position. When there is a next sample, processes of steps S316 to S319 are repeated.
In step S320, the θ axis of the rotor 31 is driven to perform a weak agitation operation. Thereafter, the originating of the rotor 31 is performed.
In step S321, the θ axis of the rotor 31 is moved to the pipette access position. In step S322, the XY axis of the dispenser 60 is moved to the pipette access position. Then, the reagent is discharged into the centrifuge tube 12 of the rotor 31 by the dispenser 60.
In step S323, the XY axis of the dispenser 60 is moved to the origin position. In step S324, the θ axis of the rotor 31 is moved to the origin position. When there is a next sample, processes of steps S321 to S324 are repeated.
After the process of step S420 (steps S310 to S324) is repeated twice, a process of step S430 (steps S325 to S334) is repeated twice.
As step S430, first, in step S325, the process of centrifugation is performed, followed by originating of the rotor 31. In step S326, the θ axis of the rotor 31 is moved to the pipette access position. In step S327, the XY axis of the dispenser 60 is moved to the pipette access position. Then, the supernatant is aspirated and removed from the centrifuge tube 12 of the rotor 31 by the dispenser 60.
In step S328, the XY axis of the dispenser 60 is moved to the origin position. In step S329, the θ axis of the rotor 31 is moved to the origin position. When there is a next sample, processes of steps S326 to S329 are repeated.
In step S330, the θ axis of the rotor 31 is driven to perform a strong agitation operation. Thereafter, the originating of the rotor 31 is performed.
In step S331, the θ axis of the rotor 31 is moved to the pipette access position. In step S332, the XY axis of the dispenser 60 is moved to the pipette access position. Then, the reagent is discharged into the centrifuge tube 12 of the rotor 31 by the dispenser 60.
In step S333, the XY axis of the dispenser 60 is moved to the origin position. In step S334, the θ axis of the rotor 31 is moved to the origin position. When there is a next sample, processes of steps S331 to S334 are repeated.
After the process of step S430 (steps S325 to S334) is repeated twice, in step S335, the θ axis of the rotor 31 is driven to perform a weak agitation operation. Thereafter, the originating of the rotor 31 is performed.
In step S336, the θ axis of the rotor 31 is moved to the pipette access position. In step S337, the XY axis of the dispenser 60 is moved to the pipette access position. Then, the reagent is discharged into the centrifuge tube 12 of the rotor 31 by the dispenser 60.
In step S338, the XY axis of the dispenser 60 is moved to the origin position. In step S339, the θ axis of the rotor 31 is moved to the origin position. When there is a next sample, processes of steps S336 to S339 are repeated.
Thereafter, the process of step S430 (steps S325 to S334) is performed twice. Thereafter, step S410 (steps S302 to S305) is performed. In step S340, the originating of the rotor 31 of the centrifugation section 30 is performed, and the operation is terminated.
Referring to
As illustrated in
Also, the specimen preparation apparatus 100 includes a sample table 15a that rotates and transfers the sample container 13, a removal processing table 15b that rotates and transfers the processing container 11, and a container transporting table 15c that rotates and transfers the centrifuge tube 12 as the container transport mechanism 22.
The specimen preparation apparatus 100 includes a common drive unit 21c that rotates and moves the sample table 15a, the removal processing table 15b, and the container transporting table 15c around a rotation axis extending in the vertical direction, respectively.
Also, the specimen preparation apparatus 100 includes a dispenser 44, a dispenser 45, a dispenser 46, and a dispenser 47. The dispenser 44 is rotatable around the rotation axis extending in the vertical direction. In addition, the dispenser 44 is movable in the Z direction (vertical direction). Moreover, the dispenser 44 aspirates a blood sample from the sample container 13 of the sample table 15a and discharges the blood sample to the processing container 11 of the removal processing table 15b to dispense the blood sample.
The dispenser 45 is rotatable around the rotation axis extending in the vertical direction. Also, the dispenser 45 is movable in the Z direction (vertical direction). Moreover, the dispenser 45 aspirates the reagent installed in a reagent setting part 70c and discharges the reagent into the processing container 11 of the removal processing table 15b to dispense the reagent. The dispenser 46 is rotatable around the rotation axis extending in the vertical direction. Also, the dispenser 46 is movable in the Z direction (vertical direction). Moreover, the dispenser 46 aspirates the reagent installed in the reagent setting part 70d and discharges the reagent into the processing container 11 of the removal processing table 15b to dispense the reagent.
The dispenser 47 is rotatable around the rotation axis extending in the vertical direction. Also, the dispenser 47 is movable in the Z direction (vertical direction). Moreover, the dispenser 47 aspirates the supernatant after processing from the processing container 11 of the removal processing table 15b and discharges the supernatant to the centrifuge tube 12 of the container transporting table 15c to dispense the supernatant after processing of the blood sample.
The specimen preparation apparatus 100 also includes a container transfer unit 48. The container transfer unit 48 is rotatable around the rotation axis extending in the vertical direction. Also, the container transfer unit 48 is movable in the Z direction (vertical direction). The container transfer unit 48 transfers the centrifuge tube 12 between the container transporting table 15c and the centrifugation section 30.
In addition, the specimen preparation apparatus 100 includes an agitator 51 that agitates a blood sample. The agitator 51 holds and vibrates the sample container 13 to agitate the blood sample in the sample container 13.
Also, the specimen preparation apparatus 100 includes a dispenser 63. The dispenser 63 is rotatable around the rotation axis extending in the vertical direction. In addition, the dispenser 63 is movable in the Z direction (vertical direction). Moreover, the dispenser 63 aspirates the reagent installed in a reagent setting part 70e, discharges the reagent into the centrifuge tube 12 of the centrifugation section 30 to dispense the reagent. Also, the dispenser 63 aspirates and removes the supernatant from the blood sample in the centrifuge tube 12 of the centrifugation section 30.
Also, the specimen preparation apparatus 100 includes reagent setting parts 70c, 70d and 70e.
The rack transporter 20 forms a complex including red blood cells and a solid phase substance and includes a magnet 23 that separates the formed complex from the supernatant of the blood sample. The magnet 23 is, for example, a BF separation section that performs BF separation.
The centrifugation section 30 is, for example, a centrifugation section capable of performing centrifugation. The centrifugation section 30 includes a first centrifugation section 30a and a second centrifugation section 30b. The first centrifugation section 30a and the second centrifugation section 30b are driven independently of each other and process the blood sample with a batch processing.
In the sample table 15a, the sample container 13 is set at a position P11. The specimen container 13 set at the position P11 is rotated counterclockwise as shown in
In the removal processing table 15b, the processing container 11 is set at a position P15. The processing container 11 set at the position P15 is rotated counterclockwise as shown in
In the container transporting table 15c, the centrifuge tube 12 is set at a position P22. The centrifuge tube 12 set at the position P22 is rotated counterclockwise as shown in
In the first centrifugation section 30a of the centrifugation section 30, the centrifuge tube 12 is transferred to a position P27 by the container transfer unit 48. Also, at a position P28, a reagent is discharged into the centrifuge tube 12 by the dispenser 63. Also, at the position P28, the supernatant is aspirated from the centrifuge tube 12 by the dispenser 63.
In the second centrifugation section 30b of the centrifugation section 30, the centrifuge tube 12 is transferred to a position P29 by the container transfer unit 48. Also, at a position P30, a reagent is discharged into the centrifuge tube 12 by the dispenser 63. Also, at the position P30, the supernatant is aspirated from the centrifuge tube 12 by the dispenser 63.
As illustrated in
As illustrated in
As illustrated in
In the centrifugation section 30, the process of dispensing the reagent, the process of centrifugation, and the process of removing the supernatant are repeated to immunostain cells of the blood sample.
As illustrated in
One or more embodiments disclosed above should be considered exemplary and not restrictive in all respects. The scope of the invention is indicated by the claims rather than by the description of the above-described embodiments, and further includes all modifications within the meaning and scope equivalent to the claims.
For example, one or more embodiments disclosed above may illustrate the rack transporter 20 that transports the racks 10a to 10c along the X axis as a holder that holds the centrifuge tube 12 to be set by the user, but the form of the holder is not limited thereto. For example, the holder and the centrifuge tube 12 held in the holder may not move within the apparatus. For example, the transfer unit 40 may be configured to move to the holding position where the user sets the centrifuge tube 12, take out the centrifuge tube 12, and transfer the centrifuge tube 12 to the centrifugation section 30.
In one or more embodiments described above, the centrifuge tube 12 after centrifugation is returned to the rack transporter 20, but the centrifuge tube 12 may be transferred to another location within the apparatus. For example, a specimen storage other than the rack transporter 20 may be provided in the apparatus, and the centrifuge tube 12 after centrifugation may be transferred there. In other words, the place where the centrifuge tube 12 is set by the user (i.e., the holder) and the place where the centrifuge tube 12 is taken out by the user after centrifugation may be separated.
In one or more embodiments described above, the dispenser 47 dispenses a sample into the centrifuge tube 12 transferred to the centrifugation section 30, but the dispenser 47 may dispense a sample into the centrifuge tube 12 held in the holder 32 before transferred by the transfer unit 40.
Number | Date | Country | Kind |
---|---|---|---|
2022-030373 | Feb 2022 | JP | national |
2022-030375 | Feb 2022 | JP | national |