This application claims priority from prior Japanese Patent Application No. 2023-035980, filed on Mar. 8, 2023, entitled “SPECIMEN ANALYZER AND SPECIMEN ANALYSIS METHOD”, the entire content of which is incorporated herein by reference.
The present invention relates to a specimen analyzer and a specimen analysis method for agitating a specimen in a container, suctioning the agitated specimen from inside the container, and analyzing the suctioned specimen.
Japanese Laid-Open Patent Publication No. 2012-173251 discloses a specimen analyzer including: a specimen transport device which transports a rack accommodating a plurality of specimen containers; and a measurement unit. The measurement unit includes a hand part, a specimen container transfer part, and a piercer. In Japanese Laid-Open Patent Publication No. 2012-173251, when any of the specimen containers accommodated in the rack is placed at a specimen container take-out position by the specimen transport device, the hand part grips and takes out the specimen container from the rack and is rotated as a pendulum while gripping the specimen container, to agitate a specimen in the specimen container. After the agitation is ended, the hand part sets the specimen container onto the specimen container transfer part. The specimen container transfer part transfers the specimen container to a suction position. At the suction position, the piercer suctions the specimen in the specimen container. The specimen container having been subjected to suctioning of the specimen is transferred to a specimen setting position by the specimen container transfer part, is taken out from the specimen container transfer part by the hand part, and then is returned to the original position in the rack. Thereafter, when a next specimen container accommodated in the rack is placed at the specimen container take-out position, the measurement unit executes the above operations on the next specimen container.
In the above Japanese Laid-Open Patent Publication No. 2012-173251, the series of operations described above is repeated by being performed on each of the specimen containers. The series of operations includes: taking out the specimen container from the rack; performing agitation; transferring the specimen container to the suction position; suctioning a specimen therefrom; transferring the specimen container to the specimen setting position; taking out the specimen container from the specimen container transfer part; and returning the specimen container to the rack. In order to improve the efficiency of specimen testing work, further increase in the number of specimens to be processed per unit time by such a specimen analyzer in the case of analyzing a plurality of specimens has been desired.
The scope of the present invention is defined solely by the appended claims, and is not affected to any degree by the statements within this summary.
In order to attain the above object, as shown in
A specimen analysis method according to the present invention is, as shown in
Hereinafter, an embodiment will be described with reference to the drawings. Firstly, an overall configuration of a specimen analyzer 100 will be described with reference to
As shown in
Hereinafter, two directions orthogonal to each other in a horizontal plane are defined as an X direction and a Y direction. In the X direction, a direction to one side and a direction to the other side are respectively defined as an X1 direction and an X2 direction. In the Y direction, a direction to one side and a direction to the other side are respectively defined as a Y1 direction and a Y2 direction. An up-down direction orthogonal to the X direction and the Y direction is defined as a Z direction, and an upward direction and a downward direction in the Z direction are respectively defined as a Z1 direction and a Z2 direction.
As shown in
As shown in
Each of the specimen containers 1 is a cylindrical container that has a cylindrical shape and that has an opened upper end and a closed bottom portion. A specimen collected from a subject is contained in the specimen container 1. The specimen is a whole blood specimen. The specimen container 1 has an upper end portion to which a cap 1a for closing the opening is attached. A portion or the entirety of the cap 1a is made from a flexible material such as rubber, and the cap 1a can be pierced (penetrated) by a suction tube. A barcode label 1b indicating identification information for identifying the specimen container 1 is pasted on the side surface of the specimen container 1. The barcode label 1b may be a label indicating a two-dimensional code instead of a barcode.
As shown in
The transport path 23 extends in the X direction and is connected to the pre-analysis rack holding part 21 and the post-analysis rack holding part 22. The transport path 23 is configured to transport the specimen containers 1, which are held by each of the racks 2 received from the pre-analysis rack holding part 21, to a take-out position P0 at which the measurement unit 10 takes in a specimen. In addition, the transport path 23 is configured to, before transporting each of the specimen containers 1 to the take-out position P0, transport the specimen container 1 to a rack reading position P0a at which the information reading part 24 reads information. The information reading part 24 is a barcode reader that optically reads the barcode label 1b on each of the specimen containers 1 transported to the rack reading position P0a. The transport path 23 transports, to the rack send-out part 25, each of racks 2 holding specimen containers 1 having been subjected to suctioning of specimens.
The rack send-out part 25 is disposed so as to be opposed to the post-analysis rack holding part 22 with the transport path 23 interposed therebetween and is configured to move in the Y1 direction horizontally. In addition, the rack send-out part 25 is configured to, by moving in the Y1 direction horizontally, push out the rack 2 on the transport path 23 to the post-analysis rack holding part 22 side.
The post-analysis rack holding part 22 is configured to be able to hold a plurality of the racks 2 each accommodating specimen containers 1 containing post-analysis specimens. The post-analysis rack holding part 22 receives and accumulates the racks 2 sent out from a position on the transport path 23 by the rack send-out part 25. Each of the racks 2 holding the post-analysis specimen containers 1 is collected from the post-analysis rack holding part 22 by the user.
As shown in
The suction part 11 is configured to suction a specimen from each of the specimen containers 1. The suction part 11 is disposed above a suction position P6 on the rear side (Y2 direction side) of the inside of the unit cover 18. The suction part 11 suctions the specimen from the specimen container 1 transported to the suction position P6 by the container transport part 13. The suction part 11 is configured to supply the suctioned specimen to reaction parts (81a to 81e; see
The agitating part 12 is configured to agitate the specimen in the specimen container 1. The agitating part 12 performs agitation processing for the specimen as a pretreatment that precedes suctioning of the specimen by the suction part 11. Particles sedimented in the specimen container 1 are dispersed in the liquid component of the specimen through the agitation processing. The agitating part 12 is disposed on the front side (Y1 direction side) of the inside of the unit cover 18. The agitating part 12 is configured to perform the agitation processing on the specimen container 1 relayed from the container transport part 13.
As shown in
The container transport part 13 is configured to transport each of the specimen containers 1 between the rack 2 on the rack transport part 20, the agitating part 12, and the suction position P6 for specimen suctioning by the suction part 11. The container transport part 13 includes a hand part 13a and a container transfer part 13b.
The hand part 13a can be placed above the transport path 23 of the rack transport part 20 and is configured to grip each of the specimen containers 1 and move in the up-down direction. The hand part 13a can take out, from the rack 2 on the transport path 23, the specimen container 1 placed at the take-out position P0 among the specimen containers 1 held by the rack 2 and insert the specimen container 1 into the rack 2. The hand part 13a can insert the gripped specimen container 1 into the container transfer part 13b and take out the specimen container 1 from the container transfer part 13b. The hand part 13a can insert the gripped specimen container 1 into the agitating part 12 and take out the specimen container 1 from the agitating part 12. The operations of inserting and taking out the specimen container 1 will be described in detail later.
The container transfer part 13b is configured to receive, from the hand part 13a, the specimen container 1 having been agitated by the agitating part 12 and transfer the specimen container 1 to the suction position P6. The agitating part 12 is configured to receive, from the hand part 13a, the specimen container 1 having been taken out from the rack 2 and agitate the specimen in the specimen container 1. Thus, the hand part 13a can execute the operations of taking out a specimen container 1 from the rack 2, relaying the specimen container 1 to the container transfer part 13b, and relaying the specimen container 1 to the agitating part 12. Therefore, the device configuration can be simplified as compared to a case where these operations are executed by separate mechanisms.
The reading part 14 is configured to read identification information from the barcode label 1b (see
The sample preparation part 15 prepares a sample, for detection, from the specimen suctioned by the suction part 11. The sample preparation part 15 is configured to prepare a measurement sample by reacting the specimen suctioned by the suction part 11 and a reagent with each other. The measurement sample prepared by the sample preparation part 15 is supplied to the measurement part 16.
The measurement part 16 is configured to measure the measurement sample prepared from the specimen suctioned by the suction part 11. Information indicating presence of detection-target components contained in the measurement sample (i.e., specimen) is detected. The detection-target components include particles such as red blood cells (RBC), white blood cells (WBC), and platelets (PLT). In addition, the detection-target components include a blood pigment (specifically, hemoglobin (HGB)) in blood. Data of a measurement result obtained in the measurement part 16 is transmitted through a communication part 93 (
The controller 91 is configured to control the agitating part 12, the suction part 11, and the container transport part 13. In the present embodiment, the controller 91 controls not only the agitating part 12, the suction part 11, and the container transport part 13 but also each of parts (the measurement part 16, the reading part 14, the sample preparation part 15, and the like) accommodated in the measurement unit 10. In addition, the controller 91 transmits the data of the measurement result obtained in the measurement part 16, through the communication part 93 (
The analysis part 30 is configured to analyze the data of the measurement result obtained from the measurement unit 10, to obtain an analysis result (a red blood cell count, a platelet count, a hemoglobin amount, a white blood cell count, or the like) regarding each of measurement items.
Next, a detailed configuration of the measurement unit 10 will be described.
As shown in
The hand part 13a includes: a pair of gripping pieces 41a and 41b opposed to each other in a horizontal direction (Y direction); and an actuator 42 which actuates the pair of gripping pieces 41a and 41b so as to cause opening/closing therebetween. The actuator 42 is an air cylinder. The actuator 42 may be an electric motor. In addition, the hand part 13a includes a hand movement mechanism which moves the pair of gripping pieces 41a and 41b and the actuator 42 in the up-down direction. The hand movement mechanism includes: a guide rail 43 extending in the Z direction; a hand lifting/lowering motor 44; a pair of pulleys 45a and 45b; and an annular belt 46. A movable part 41 composed of the pair of gripping pieces 41a and 41b and the actuator 42 is slidably attached to the guide rail 43. The hand lifting/lowering motor 44 is a stepping motor. The hand lifting/lowering motor 44 rotationally drives the pulley 45a, to perform circulation drive of the belt 46 extended on and between the pulley 45a and the pulley 45b. The movable part 41 is connected to a portion of the belt 46 and is moved in the Z1 direction and the Z2 direction along the guide rail 43 in association with circulation drive of the belt 46. The hand movement mechanism is a linear motion mechanism which moves the hand part 13a (movable part 41) in only the Z direction.
Inside the protruding portion 18a of the unit cover 18, an opening 18b is formed at a position immediately below the hand part 13a. The hand part 13a moves through the opening 18b in the downward direction (Z2 direction) to grip, by the pair of gripping pieces 41a and 41b, the specimen container 1 held by the rack 2 on the transport path 23 (the specimen container 1 placed at the take-out position P0). Then, the hand part 13a directly moves in the upward direction (Z1 direction) to take out the specimen container 1 from the rack 2. Meanwhile, the hand part 13a in a state of gripping the specimen container 1 moves through the opening 18b in the downward direction (Z2 direction) to insert the gripped specimen container 1 into the rack 2. Then, the hand part 13a releases the specimen container 1 being gripped by the pair of gripping pieces 41a and 41b and moves in the upward direction (Z1 direction) to return, to the rack 2, the specimen container 1 having been taken out. Relaying of a specimen container 1 with respect to the container transfer part 13b and the agitating part 12 is also performed at the respective height positions for the container transfer part 13b and the agitating part 12 through operations of gripping the specimen container 1 by the gripping pieces 41a and 41b and releasing the gripped specimen container 1.
The hand part 13a is provided with an origin sensor 47 which detects an origin position in the Z direction of the movable part 41. Control is performed so as to position the hand part 13a at each of: a position at which the specimen container 1 is taken out from and inserted (returned) into the rack 2 by the hand part 13a; a position at which the specimen container 1 is inserted into and taken out from the container transfer part 13b by the hand part 13a; a position at which the specimen container 1 is inserted into and taken out from the agitating part 12 by the hand part 13a; and the like. This control is performed by the controller 91 (see
As shown in
Consequently, the container transfer part 13b linearly moves the container holding part 51 in the Y direction as shown in
The second position P2 is a position at which the hand part 13a executes insertion and taking-out of the specimen container 1 with respect to the container transfer part 13b. That is, in the top view, the second position P2 coincides with the take-out position P0 (see
As shown in
As shown in
As shown in
As shown in
The agitating part 12 is disposed away from the hand part 13a in the X2 direction. The agitating part 12 has a holding part 130 for holding the specimen container 1 and can move the holding part 130 in the X1 direction and the X2 direction. The agitating part 12 is configured to linearly move to the first position P1 and a third position P3 along a first direction (X direction) in the horizontal plane. The position of the agitating part 12 is based on a position at which the specimen container 1 is held by the holding part 130 (the center position of a holding hole 131a of a holding member 131 described later).
The first position P1 is a position at which the hand part 13a executes insertion and taking-out of the specimen container 1 with respect to the agitating part 12 (holding part 130). That is, in the top view, the first position P1 coincides with the take-out position P0 (see
In this manner, the agitating part 12 is configured to linearly move to the first position P1 and the third position P3 along the first direction (X direction) in the horizontal plane, and the container transfer part 13b is configured to linearly move to the second position P2 and the fourth position P4 along a second direction (Y direction) intersecting with the first direction (X direction) in the top view. Further, the first position P1 and the second position P2 are each a position at which a movement path of the container transfer part 13b and a movement path of the agitating part 12 intersect with each other in the top view. Consequently, the specimen container 1 can be relayed and retracted merely by causing linear reciprocating movement of each of the agitating part 12 and the container transfer part 13b. Thus, the structure for moving the agitating part 12 and the container transfer part 13b can be simplified. In addition, in the case of a simple linear reciprocating movement as in the present embodiment, the mechanisms related to the movement easily lead to obtainment of rigidity and accuracy, and the operation speed can be set to be high, whereby the processing time can be shortened owing to the increased operation speed.
Therefore, in the present embodiment, the hand part 13a is configured to execute, at the first position P1, insertion and taking-out of the specimen container 1 with respect to the agitating part 12 and execute, at the second position P2, insertion and taking-out of the specimen container 1 with respect to the container transfer part 13b. Consequently, the hand part 13a can execute, at positions (the first position P1 and the second position P2) coinciding with each other in the top view, insertion and taking-out of the specimen container 1 with respect to the agitating part 12 and insertion and taking-out of the specimen container 1 with respect to the container transfer part 13b merely through upward/downward movement. Thus, the movement range of the hand part 13a can be made small, whereby the structure of the hand part 13a can be simplified. In addition, since the movement range of the hand part 13a is made small, the times required for insertion and taking-out of the specimen container 1 with respect to the agitating part 12 and the container transfer part 13b can be shortened.
In addition, the hand part 13a is configured to perform taking-out and insertion of the specimen container 1 with respect to the rack 2, insertion and taking-out of the specimen container 1 with respect to the agitating part 12 placed at the first position P1, and insertion and taking-out of the specimen container 1 with respect to the container transfer part 13b placed at the second position P2, through upward/downward movement without moving in the horizontal direction. Consequently, the hand part 13a only has to move upward/downward, and thus no mechanism for moving the hand part 13a in the horizontal direction needs to be provided. As a result, the structure of the hand part 13a can be effectively simplified.
The third position P3 is a position at which the agitating part 12 executes agitation processing on the specimen container 1. Third position P3 is also a shunt position separated in the horizontal direction (XY direction) from the container transfer part 13b present at the second position P2. That is, in the present embodiment, the first position P1 for the agitating part 12 and the second position P2 for the container transfer part 13b are set to positions at which the agitating part 12 and the container transfer part 13b interfere (i.e., come into contact) with each other. To prevent this interference, control by the controller 91 causes the agitating part 12 to be placed at the third position P3 while the container transfer part 13b (container holding part 51) is present at the second position P2 or the reading position P5. Meanwhile, control by the controller 91 causes the container transfer part 13b to be placed at the fourth position P4 or the suction position P6 while the agitating part 12 is present at the first position P1.
As shown in
The linear motion mechanism 111 is configured to linearly move the slide part 120 in the X direction. The linear motion mechanism 111 includes a guide rail 112 and a slide drive part 113 which are provided on the base part 110 and which extend in the X direction. The slide part 120 is movably attached on the guide rail 112 via a slider block 112a (see
As shown in
The slide part 120 is an intermediate support plate supporting the holding part 130 and a drive part 121 which drives the holding part 130. As shown in
As shown in
The drive part 121 has an electric rotation motor 122 and a transmission mechanism 123. The transmission mechanism 123 has: a pulley 123a attached to an output shaft of the rotation motor 122; a pulley 123b attached to the rotation shaft 125; an annular belt 123c wound on the pulley 123a and the pulley 123b; and an arm 124 provided so as to rotate together with the pulley 123b around the rotation shaft 125. The rotation motor 122 rotates the pulley 123a, to rotate the pulley 123b via the annular belt 123c. The arm 124 has one end portion provided so as to be rotatable around the rotation shaft 125. The arm 124 has another end portion provided with an engagement protrusion 124a inserted into an engagement hole 130e of the holding part 130. When the arm 124 is rotated around the rotation shaft 125 in association with rotation of the pulley 123b, the engagement protrusion 124a in the engagement hole 130e is brought into contact with the holding part 130 (i.e., an inner peripheral edge of the engagement hole 130e) so as to move the holding part 130. As a result, the holding part 130 is rotated (see
Consequently, as shown in
As shown in
The holding member 131 is provided so as to be adjacent to the front surface portion 130c on the X1 side of the holding part 130. The holding member 131 has the holding hole 131a (see
The fixation part 132 is configured to fix the specimen container 1 placed in the holding part 130 and release the fixed specimen container 1. Specifically, the fixation part 132 has: a pair of (two) contact members 133a and 133b having the shapes of rollers; a support part 134 supporting the contact members 133a and 133b; and a fixation drive part 135 which moves the support part 134 in the X direction to a fixation position and a release position.
The pair of contact members 133a and 133b are supported at X2-side positions relative to the holding member 131 by the support part 134 configured to be linearly movable in the X direction. The pair of contact members 133a and 133b are provided at positions opposed, in the X direction, to the side surface of the specimen container 1 supported by the holding member 131. As shown in
The fixation drive part 135 advances the rod part in the X1 direction, to move the support part 134 and the contact members 133a and 133b in the X1 direction toward the holding member 131 (i.e., specimen container 1). As shown in
The fixation drive part 135 retracts the rod part in the X2 direction, to move the support part 134 and the contact members 133a and 133b in the X2 direction and retract each of the contact members 133a and 133b to the release position (the position shown in
As shown in
In addition, the holding part 130 is provided with a container detector 137. As shown in
As described above, the agitating part 12 includes: the holding part 130 which holds the lower portion of each of the specimen containers 1; and the drive part 121 which causes reciprocating movement of the holding part 130 in the predetermined direction. The drive part 121 causes reciprocating movement of the holding part 130 in the predetermined direction (the R1 direction and the R2 direction), whereby the agitating part 12 performs agitation. Consequently, it is possible to shake and agitate the specimen through the reciprocating movement while stably holding the specimen container 1 from below.
As shown in
In addition, the drive part 121 is configured to cause reciprocating rotation of the holding part 130 around the rotation shaft 125 extending in the horizontal direction (Y direction). The holding part 130 is configured to hold the lower portion of the specimen container 1 oriented so as to extend along the up-down direction at an origin position Q0 for the reciprocating rotation. The holding part 130 is rotated around the rotation shaft 125 extending in the horizontal direction, and thus, can more effectively agitate the specimen by utilizing the effect of gravity at the time of reciprocating rotation.
The controller 91 is configured to control the drive part 121 to rotate the holding part 130 from the origin position Q0 to a predetermined angle Q1 larger than 90 degrees. As shown in
Here, as shown in
Specifically, the predetermined angle Q1 is larger than 90 degrees, and thus, when the holding part 130 reaches the predetermined angle Q1, the specimen container 1 is stopped in such an orientation as to be obliquely tilted downward such that the cap 1a at the upper end portion is at a lower position than the bottom portion of the specimen container 1. At this time, the fall-off object reception part 115 is present below the cap 1a. Therefore, adhesion matter E adhered on the upper surface of the cap 1a falls off from the cap 1a onto the fall-off object reception part 115 owing to the effect of inertia exhibited when the rotation is stopped.
Thus, the adhesion matter E adhered when the specimen has been contained in the specimen container 1 can be shaken off from the specimen container 1 onto the fall-off object reception part 115 by utilizing the agitation operation. The adhesion matter E is, for example, powdered blood resulting from coagulation of a blood specimen. Consequently, when the specimen is suctioned from the specimen container 1 having been agitated, a minute amount of the adhesion matter E can be inhibited from adhering on the suction tube or from entering the specimen that is suctioned. In the present embodiment, the fall-off object reception part 115 is configured to be detachable and re-attachable. Thus, at the time of regular maintenance or the like, the fall-off object reception part 115 can be detached from the mount 117, and the adhesion matter E received on the fall-off object reception part 115 can be removed, whereby workability in maintenance is excellent.
In order to ascertain the rotational position of the holding part 130, the agitating part 12 is provided with: an origin position detector 126 (see
As shown in
As shown in
Here, the agitating part 12 is configured to abruptly stop rotation of the holding part 130 when the holding part 130 reaches the predetermined angle Q1 from the origin position Q0. Consequently, the specimen in the specimen container 1 can be effectively agitated. Further, the adhesion matter E adhered on the specimen container 1 can be effectively caused to fall off from the specimen container 1 owing to inertia.
Specifically, in the agitation operation, the controller 91 controls the drive part 121 to stop rotation of the arm 124 and stop the holding part 130 at the predetermined angle Q1 when it is detected that the holding part 130 has reached the predetermined angle Q1 from the origin position Q0 as shown in
Here, the arm 124 is connected to the holding part 130 in a state of allowing relative movement in the rotation direction by a predetermined amount CL (see
When the holding part 130 is rotated in the R1 direction from the origin position Q0 to the predetermined angle Q1, the engagement protrusion 124a of the arm 124 comes into contact with an inner peripheral edge 130e1 on the R1 side of the engagement hole 130e so as to press the holding part 130, whereby the holding part 130 is rotated in the R1 direction. When the holding part 130 reaches the predetermined angle Q1 and rotation of the arm 124 is stopped, the holding part 130 continues to rotate by the gap of the predetermined amount CL owing to inertia. An inner peripheral edge 130e2 on the R2 side of the engagement hole 130e comes into contact (collides) with the engagement protrusion 124a, whereby the holding part 130 is stopped. In this manner, when the arm 124 rotated to the predetermined angle Q1 is stopped, the holding part 130 moves by the predetermined amount CL and collides with the arm 124 (engagement protrusion 124a) owing to inertia, to be abruptly stopped.
Consequently, as compared to a configuration in which the holding part 130 is stopped by merely stopping rotation of the rotation motor 122 of the drive part 121, a larger extent of deceleration (negative acceleration) can be applied to the holding part 130, whereby the adhesion matter E adhered on the specimen container 1 can be effectively removed. In addition, an operation of abruptly stopping the holding part 130 can be realized by utilizing coupling portions (the engagement protrusion 124a and the engagement hole 130e) of the arm 124 and the holding part 130. Thus, the configuration for abruptly stopping the holding part 130 can be realized without increasing the number of components of the agitating part 12, unlike in a case where a stopper for stopping the holding part 130 rotated to the predetermined angle Q1 is provided to the base part 110 or the like separately from the arm 124 and the holding part 130.
In addition, the controller 91 is configured to perform control to abruptly stop rotation of the holding part 130 when the holding part 130 reaches the origin position Q0 from the predetermined angle Q1 at a time of end of agitation.
The time of end of agitation mentioned herein refers to the time of end of rotation in the R2 direction from the predetermined angle Q1 to the origin position Q0 during the last time (i.e., eighth time) of reciprocating rotation among eight times of repetitively executed reciprocating rotation. Each time of reciprocating rotation is composed of: rotation in the R1 direction from the origin position Q0 to the predetermined angle Q1; and rotation in the R2 direction from the predetermined angle Q1 to the origin position Q0.
As shown in
As shown in
As a result, at the origin position Q0, inertial force is exerted substantially vertically downward (in the Z2 direction) to the specimen container 1 held by the holding part 130, owing to the abrupt stop. Consequently, droplets of the specimen adhered on the inner surface of the cap 1a of the specimen container 1 through the agitation operation can be caused to fall off to the bottom portion side inside the specimen container 1 owing to inertia. In a case where the specimen is left on the inner surface of the cap 1a even at the time of suctioning of the specimen, fine droplets of the specimen adhered on the inner surface of the cap 1a might leak to outside upon insertion of the suction tube 71 into the specimen container 1 owing to a difference in pressure between the inner side and the outer side of the specimen container 1. Such fine droplets of the specimen adhered on the inner surface of the cap 1a can be inhibited from leaking upon insertion of the suction tube 71 by causing the droplets to fall off.
The controller 91 causes, for the first to seventh times of reciprocating rotation and rotation in the R1 direction from the origin position Q0 to the predetermined angle Q1 during the eighth time of reciprocating rotation, the holding part 130 to move through rotation at a predetermined high speed in the relevant directions. The controller 91 performs, only for rotation in the R2 direction from the predetermined angle Q1 to the origin position Q0 during the eighth time of reciprocating rotation, control to execute low-speed rotation to the preparatory position Q2 and high-speed rotation from the preparatory position Q2 to the origin position Q0 described above. Control to drive the rotation motor 122 in each of rotation in the R1 direction and rotation in the R2 direction is, for example, trapezoidal drive in which the target speed (angular speed) is set in two levels, i.e., a predetermined high-speed level and a predetermined low-speed level, and is switched according to the number of times of reciprocation in the agitation operation. Although the time of acceleration/deceleration (in particular, the time of deceleration) to the target speed from a stopped state can be set as appropriate, the time of acceleration/deceleration is preferably set to be short within a range of possible setting in order to effectively cause the holding part 130 to abruptly stop.
The agitating part 12 is configured as described above.
As shown in
Each of the plurality of reaction parts 81a to 81e receives the specimen suctioned by the suction part 11 and a reagent and reacts the specimen and the reagent with each other, to prepare a measurement sample. The suction part 11 includes the metering part 73 connected to the suction tube 71. The metering part 73 has a function of suctioning and ejecting a predetermined amount of specimen through the suction tube 71. The metering part 73 is implemented by a syringe pump. Consequently, the specimen contained in the specimen container 1 is suctioned and ejected by the suction part 11 to one or more supply-target reaction parts among the reaction parts 81a to 81e.
The reagent supply part 82 holds a reagent container 3 containing a predetermined amount of reagent. The reagent supply part 82 includes: a reagent container holder 83; a metering part 84a implemented by a diaphragm pump; and electromagnetic valves 85a and 85b which open/close a flow path through which the reagent having been suctioned is transferred to the metering part 84a and the reaction part 81a. In addition, the reagent supply part 82 includes a metering part 84b and electromagnetic valves 85c and 85d for transferring a reagent (a hemolytic agent or the like) from a large-capacity reagent container 4 disposed outside of the measurement unit 10.
The number of the reagent container holders 83 provided is two or more, and each of the reagent container holders 83 is configured such that a corresponding reagent container 3 is held so as to be detachable therefrom and re-attachable thereto. Consequently, the reagent supply part 82 holds a plurality of the reagent containers 3 containing a plurality of respective types of reagents corresponding to a measurement item. Each of the reagent containers 3 is replaced with a new reagent container 3 when the contained reagent runs out.
Control by the controller 91 causes the electromagnetic valve 85a to be opened and causes the electromagnetic valve 85b to be closed, whereby the metering part 84a suctions a predetermined amount of reagent in the reagent container 3 through the flow path into the metering part 84a. Consequently, the predetermined amount of reagent necessary for preparing a measurement sample is metered. In addition, control by the controller 91 causes the electromagnetic valve 85a to be closed and causes the electromagnetic valve 85b to be opened, whereby the metering part 84a can transfer the reagent metered in the metering part 84a to the reaction part 81a.
For the metering part 84b, the electromagnetic valve 85c, and the electromagnetic valve 85d which are connected to the large-capacity reagent container 4, operations of these respective parts are also controlled by the controller 91 in the same manner as the operations of the metering part 84a, the electromagnetic valve 85a, and the electromagnetic valve 85b. Consequently, respective types of reagents are transferred into the reaction parts 81a to 81e. In addition, a waste liquid chamber 86 for disposing of a measured (prepared) sample is provided inside the measurement unit 10 and is connected to each of the reaction parts 81a to 81e via an electromagnetic valve 85e. The measured (prepared) sample is disposed of in the waste liquid chamber 86 through opening/closing of the electromagnetic valve 85e by the controller 91.
As shown in
The plurality of reaction parts 81a to 81e are provided correspondingly to measurement items. To each of the reaction parts 81a to 81e, a reagent (a staining liquid or the like) of a type corresponding to the relevant measurement item is supplied by the corresponding reagent supply part 82 (see
For example, each of the reaction part 81a and the reaction part 81b prepares a measurement sample for WBC detection (detection of white blood cells). To the reaction part 81a and the reaction part 81b, a hemolytic agent and a staining liquid are supplied as reagents. The hemolytic agent contains a surfactant, and red blood cells and platelets are dissolved therein by action of the surfactant. The staining liquid contains a fluorescent dye. The reaction part 81a and the reaction part 81b are connected to the first detector 16a of the measurement part 16. Each of cells in the measurement sample supplied to the first detector 16a is converted into electric signals corresponding to scattered light and fluorescence through flow cytometry. The electric signals are plotted on a scattergram in the analysis part 30, and statistical analysis processing is performed, whereby a count value of the number of white blood cells and values resulting from classification of the white blood cells are calculated.
The reaction part 81c prepares a measurement sample for RBC detection (detection of red blood cells) and PLT detection (detection of platelets). The reaction part 81c is connected to the second detector 16b which performs RBC detection (detection of red blood cells) and PLT detection (detection of platelets) through the sheath flow DC detection method. The reaction part 81d is connected to the third detector 16c which performs HGB detection (detection of blood pigments in blood) through the SLS-hemoglobin method. The reaction part 81e prepares a measurement sample for RET detection (detection of reticulocytes) and a measurement sample for PLT high-sensitivity detection (PLT-F detection). The reaction part 81e is connected to the first detector 16a. In an ordinary measurement order, WBC detection, RBC detection, HGB detection, and PLT detection are performed, and either the reaction part 81a or the reaction part 81b, the reaction part 81c, and the reaction part 81d each prepare a sample. The reaction part 81e is used only when a measurement item of RET and/or PLT-F is included in a measurement order.
(Configuration regarding Control of Specimen Analyzer)
As shown in
The controller 91 includes: a processor implemented by a CPU; and a memory. The controller 91 executes a control program stored in the storage 92, to control each part of the measurement unit 10 and the rack transport part 20. The storage 92 is implemented by a semiconductor memory element and stores therein: the program to be executed by the controller 91; data of identification information and a measurement order; data (detection signal) of a measurement result obtained by the measurement part 16; a state of the agitating part 12 described later; and a state of the container transfer part 13b described later. The communication part 93 includes a communication interface for performing communication with the analysis part 30. Alternatively, the controller 91 and the storage 92 may each be implemented by an FPGA.
The analysis part 30 is mainly composed of: a controller 31 implemented by a CPU; a storage 32 including a ROM, a RAM, and a solid-state drive (SSD); a display part 33 implemented by a liquid crystal display; an input part 34 implemented by a keyboard and a mouse; and a communication part 35 implemented by a communication interface.
The analysis part 30 is communicably connected to the communication part 93 of the measurement unit 10 and the host computer 300 via the communication part 35. The analysis part 30 obtains, via the communication part 93, identification information read by each of the information reading part 24 of the rack transport part 20 and the reading part 14 of the measurement unit 10. The analysis part 30 identifies each of the specimen containers 1 held by the rack 2, on the basis of the identification information on the specimen container 1. The analysis part 30 inquires of the host computer 300 about the identification information, to obtain a measurement order for the specimen in the specimen container 1 held by the container transfer part 13b.
The analysis part 30 transmits the obtained measurement order to the controller 91 via the communication part 35 and the communication part 93. The controller 91 controls each part of the measurement unit 10 and the rack transport part 20 according to the transmitted measurement order. The controller 91 controls the suction part 11 and the sample preparation part 15 to prepare a measurement sample corresponding to a measurement item specified in the measurement order. Then, the controller 91 controls the measurement part 16 to perform measurement, corresponding to the measurement item, on the prepared measurement sample.
The controller 91 causes the measurement part 16 to measure the specimen in the specimen container 1, and obtains a detection signal from the measurement part 16. The controller 91 transmits the detection signal via the communication part 93 to the analysis part 30. The analysis part 30 analyzes the analyte content of the specimen or the like on the basis of the obtained detection signal. In addition, the analysis part 30 causes an analysis result to be displayed on the display part 33 and to be transmitted to the host computer 300.
Next, the flow of a measurement operation executed on one specimen container 1 by the specimen analyzer 100 will be described with reference to
As shown in
In the present embodiment, the specimen analyzer 100 is configured such that control by the controller 91 causes, during a period from start to end of agitation of one of the specimen containers 1, transferring to the suction position P6 (S8), suctioning of a specimen (S9), and returning to the rack 2 (S11) to be executed on another one of the specimen containers 1.
Consequently, agitation processing for the one specimen container 1 by the agitating part 12 and processing for the other specimen container 1 (transferring to the suction position P6, suctioning of a specimen, and returning to the rack 2) can be executed as concurrent processing operations that coincide in time with each other. Therefore, as compared to a case where the processing for the one specimen container 1 and the processing for the other specimen container 1 are executed separately and sequentially, the number of specimens to be processed per unit time by the specimen analyzer 100 in the case of analyzing a plurality of specimens can be increased by a number corresponding to the period during which the agitation processing for the one specimen container 1 and the processing for the other specimen container 1 coincide in time with each other. Ordinarily, among a series of operations of taking out a specimen container 1 from the rack 2, agitating the specimen container 1, suctioning a specimen from the specimen container 1, and returning the specimen container 1 to the rack 2, the operation of agitating the specimen container 1 requires the longest time. The purpose of setting the time for this operation to be longest is to evenly distribute components of the specimen inside the specimen container 1 and improve the accuracy of analysis. For example, in the automatic multi-item blood cell analyzer XN-1000 (manufactured by Sysmex Corporation) as a conventional analyzer, the time required for the above series of operations from the operation of taking out a specimen container to the operation of returning the specimen container is about 36 seconds, and the time required for the operation of agitating the specimen container among the series of operations is about 12 seconds. That is, in the automatic multi-item blood cell analyzer XN-1000, an (N+1)th specimen container can be taken out from the rack about 36 seconds after an Nth specimen container is taken out from the rack, and up to 100 specimens can be processed per hour. Meanwhile, in the specimen analyzer 100 in the present embodiment, while the agitation processing requiring the longest time is being performed on one specimen container 1, transferring to the suction position P6, suctioning of a specimen, and returning to the rack 2 are performed on another specimen container 1. Consequently, in a case where each of the operations requires a time equivalent to that required in the automatic multi-item blood cell analyzer XN-1000, the (N+1)th specimen container 1 can be taken out from the rack 2 about 18 seconds after the Nth specimen container 1 is taken out from the rack 2, whereby up to 200 specimens can be processed per hour.
Hereinafter, the flow of a measurement operation to be executed on one specimen container 1 by the specimen analyzer 100 will be specifically described. First, in step S1, the rack transport part 20 transports one of a plurality of specimen containers 1 held by a rack 2 to the take-out position P0 (see
In step S2, with the hand part 13a and the agitating part 12, the specimen container 1 having been taken out from the rack 2 is relayed from the hand part 13a to the agitating part 12. Specifically, the hand part 13a (see
In step S3, the agitating part 12 agitates a specimen in the specimen container 1. The agitating part 12 moves the fixation part 132 to the fixation position (see
In step S4, the agitating part 12 moves from the third position P3 to the first position P1 (see
In step S5, with the agitating part 12, the hand part 13a, and the container transfer part 13b, the specimen container 1 having been agitated is relayed from the agitating part 12 to the container transfer part 13b. First, the agitating part 12 moves the fixation part 132 to the release position (see
After the agitating part 12 moves to the third position P3, the container transfer part 13b moves to the second position P2 (see
In step S6, the container transfer part 13b moves the specimen container 1 to the reading position P5 (see
In step S8, the container transfer part 13b moves the specimen container 1 to the suction position P6 (see
In step S10, the container transfer part 13b moves the specimen container 1 to the second position P2 (see
In step S12, with the suction part 11 and the sample preparation part 15, a measurement sample is prepared. Specifically, the suction part 11 ejects, to one of the reaction parts 81a and 81b, the specimen suctioned (in step S9) from the specimen container 1. In an ordinary measurement order, the suction part 11 ejects the specimen to each of the reaction parts 81c and 81d. The sample preparation part 15 supplies reagents to the respective reaction parts each containing the specimen and mixes the specimen and the reagents with each other in the reaction parts, to prepare measurement samples.
In step S13, the measurement part 16 measures each of the measurement samples. Specifically, the measurement part 16 supplies the measurement sample prepared in the reaction part 81a or 81b to the first detector 16a and performs measurement through flow cytometry. In addition, the measurement part 16 supplies the measurement sample prepared in the reaction part 81c and the measurement sample prepared in the reaction part 81d to the corresponding second detector 16b and third detector 16c, respectively, and executes detection according to the sheath flow DC detection method and detection according to the SLS-hemoglobin method.
In step S14, the controller 91 outputs, to the analysis part 30, measurement data based on electric signals obtained from the respective detectors through the measurement in step S13. The analysis part 30 having received the measurement data performs analysis processing on the measurement data. As a result of the analysis processing, an analysis result regarding each of measurement items specified in the measurement order is generated.
As described above, the present embodiment is such that, in the case of consecutively measuring specimens in a plurality of specimen containers, the specimen analyzer 100 executes, while the agitation operation in step S3 is being executed on one of the specimen containers 1, transferring to the suction position P6 (S8), suctioning of a specimen (S9), and returning to the rack 2 (S11) on another one of the specimen containers 1. Hereinafter, control to be executed by the controller 91 in order to realize this feature will be described with reference to
The controller 91 concurrently executes a series of control operations for the suction part 11 (suction part control), a series of control operations for the agitating part 12 (agitating part control), a series of control operations for the hand part 13a (hand part control), a series of control operations for the container transfer part 13b (container transfer part control), a series of control operations for the reading part 14 (reading part control), a series of control operations for the sample preparation part 15 (sample preparation part control), a series of control operations for the measurement part 16 (measurement part control), and a series of control operations for the rack transport part 20 (rack transport part control).
The suction part control is control in which the suction part 11 suctions a specimen from each specimen container 1 placed at the suction position P6 and ejects the suctioned specimen to relevant ones of the reaction parts 81a to 81e. The agitating part control is control in which the agitating part 12 receives each specimen container 1 at the first position P1 (pickup position), agitates the received specimen container 1, and transfers the agitated specimen container 1 to the first position P1 again. The container transfer part control is control in which the container transfer part 13b receives each specimen container 1 at the pickup position P2, transfers the received specimen container 1 to the reading position P5 and the suction position P6, and transfers the specimen container 1 having been subjected to suctioning of a specimen to the pickup position P2 again. The hand part control is control in which: each specimen container 1 placed at the take-out position P0 is transferred (picked up) from the rack 2 to the agitating part 12; the specimen container 1 placed at the first position P1 is transferred from the agitating part 12 to the container transfer part 13b; and the specimen container 1 placed at the second position P2 is transferred (returned) from the container transfer part 13b to the rack 2.
The reading part control is control in which identification information is read from the barcode on each specimen container 1 placed at the reading position P5. The sample preparation part control is control in which specimens and reagents contained in the reaction parts 81a to 81e are mixed with each other so that measurement samples are prepared. The measurement part control is control in which the measurement samples are supplied to the first detector 16a, the second detector 16b, and the third detector 16c, and measurement data is obtained. The rack transport part control is control in which: the rack 2 placed on the pre-analysis rack holding part 21 is transported such that a specimen container 1 to be subjected to suctioning is placed at the take-out position P0; after the specimen container 1 is taken into the measurement unit 10, the rack 2 is, in order to receive the specimen container 1 for which suctioning has been completed, transported such that the holding hole 2a having held this specimen container 1 is placed at the take-out position P0 again; and, after this specimen container 1 is returned to the rack 2, the rack 2 is transported to the post-analysis rack holding part 22.
Hereinafter, the agitating part control, the container transfer part control, the hand part control, the suction part control, and the reading part control among the above control operations to be concurrently executed by the controller 91 will be further described.
The state of the agitating part 12 is transitioned according to the process shown in
As shown in
In step S1005, the controller 91 causes the agitating part 12 to move from the first position P1 (pickup position) to the third position P3 (agitation position). In step S1006, the controller 91 transitions the state of the agitating part 12 from M1 to M2. The processing in step S1003 and the processing in step S1005 correspond to the operation in step S2 in
In step S1008, the controller 91 determines whether or not completion of agitation of the specimen container 1 by the agitating part 12 has been reported. Completion of agitation of the specimen container 1 by the agitating part 12 is reported when the last time of reciprocating rotation by the agitating part 12 is completed. The controller 91 stands by (step S1008: No) until completion of agitation of the specimen container 1 by the agitating part 12 is reported. Meanwhile, when completion of agitation of the specimen container 1 by the agitating part 12 is reported (step S1008: Yes), the controller 91 advances the process to step S1010. In step S1010, the controller 91 determines whether or not a specimen container 1 is held by the container transfer part 13b at a timing immediately after agitation of the specimen container 1 is completed, i.e., a timing at which completion of agitation of the specimen container 1 by the agitating part 12 is reported. Specifically, in step S1010, the controller 91 determines whether or not the state of the container transfer part 13b is A0 described later at the timing at which completion of agitation of the specimen container 1 by the agitating part 12 is reported. The controller 91 controls operation of the agitating part 12 according to whether or not the state of the container transfer part 13b is A0.
On one hand, in a case where, at the timing at which completion of agitation of the specimen container 1 by the agitating part 12 is reported, a specimen container 1 is held by the container transfer part 13b, i.e., the state of the container transfer part 13b is not A0 (step S1010: container being present), the controller 91 transitions the state of the agitating part 12 from M2 to M3 in step S1011. The controller 91 stands by (step S1012: No) until the specimen container 1 in the container transfer part 13b is returned to the rack in step S1012. Meanwhile, when the specimen container 1 in the container transfer part 13b is returned to the rack 2, i.e., the state of the container transfer part 13b becomes A0 (step S1012: Yes), the controller 91 advances the process to step S1013. In step S1013, the controller 91 transitions the state of the agitating part 12 from M3 to M4 and advances the process to step S1015.
On the other hand, in a case where, at the timing at which completion of agitation of the specimen container 1 by the agitating part 12 is reported, no specimen container 1 is held by the container transfer part 13b, i.e., the state of the container transfer part 13b is A0 (step S1010: container being absent), the controller 91 transitions the state of the agitating part 12 from M2 to M4 in step S1014 and advances the process to step S1015 without standing by. In step S1015, the controller 91 causes the agitating part 12 to move from the third position P3 (agitation position) to the first position P1 (pickup position). The processing in step S1015 corresponds to the operation in step S4 in
In step S1016, the controller 91 determines whether or not there is a request to take out a specimen container 1 from the rack 2. A request to take out a specimen container 1 from the rack 2 in the present step is reported when a specimen container 1 containing a specimen that needs to be measured next to the specimen container 1 having been taken into the measurement unit 10 is placed at the take-out position P0. When there is a request to take out a specimen container 1 from the rack 2 (step S1016: Yes), the controller 91 transitions the state of the agitating part 12 from M4 to M5 in S1017. Meanwhile, when there is no request to take out a specimen container 1 from the rack 2 (step S1016: No), the controller 91 skips step S1017 and advances the process to step S1018.
In step S1018, the controller 91 causes the agitating part 12 to move from the first position P1 (pickup position) to the third position P3 (agitation position) after the hand part 13a takes out the specimen container 1 from the agitating part 12 through processing in step S3008 of the hand part control described later. The processing in step S1018 corresponds to the operation in step S5 in
In step S1020, the controller 91 determines whether the state of the agitating part 12 is M5 or M4. When the state of the agitating part 12 is M5 (step S1020: M5), the controller 91 returns the process to step S1002, transitions the state of the agitating part 12 from M5 to M1 in step S1002, and executes processing for the specimen container 1 containing the specimen that needs to be measured next. Meanwhile, when the state of the agitating part 12 is M4 (step S1020: M4), the controller 91 transitions the state of the agitating part 12 from M4 to M0 in step S1021, returns the process to step S1001, and awaits a request to take out a next specimen container 1 from the rack 2.
Next, the container transfer part control will be described. The state of the container transfer part 13b is transitioned according to the process shown in
As shown in
In step S2003, the controller 91 determines whether or not completion of relaying of the specimen container 1 from the agitating part 12 to the container transfer part 13b has been reported (completion of transference of the specimen container 1 has been reported). Completion of relaying of the specimen container 1 from the agitating part 12 to the container transfer part 13b is reported when the hand part 13a takes out the specimen container 1 from the agitating part 12 and relays the specimen container 1 to the container transfer part 13b through the processing in step S3008 of the hand part control described later. This reporting is the same as the reporting in step S1019 shown in
The controller 91 stands by (step S2003: No) until completion of relaying of the specimen container 1 from the agitating part 12 to the container transfer part 13b has been reported (completion of transference of the specimen container 1 has been reported). Meanwhile, when completion of transference of the specimen container 1 is reported (step S2003: Yes), the controller 91 transitions the state of the container transfer part 13b from A0 to A1 in step S2004. In step S2005, the controller 91 causes the container transfer part 13b to move from the second position P2 (pickup position) to the fourth position P4 (shunt position). The processing in step S2005 corresponds to the operation in step S6 in
In step S2006, the controller 91 determines whether or not there is a request to take out a next specimen container 1 from the rack 2. A request to take out a next specimen container 1 from the rack 2 is reported when, at the present timing, a specimen container 1 containing a specimen that needs to be measured next to the specimen in the specimen container 1 placed in the container transfer part 13b is placed at the take-out position P0 and the state of the agitating part 12 is M0. When there is no request to take out a next specimen container 1 from the rack 2 (step S2006: No), the controller 91 skips the processing in step S2007 and advances the process to step S2008. Meanwhile, when there is a request to take out a next specimen container 1 from the rack 2 (step S2006: Yes), the controller 91 determines in step S2007 whether or not completion of relaying of the next specimen container 1 from the rack 2 to the agitating part 12 has been reported (completion of pickup of the next specimen container 1 has been reported), i.e., whether or not the state of the agitating part 12 is M2. Completion of pickup of the specimen container 1 is reported when, through the processing in step S3004 of the hand part control described later, the hand part 13a relays the next specimen container 1 having been taken out from the rack 2 to the agitating part 12, and the agitating part 12 moves to the third position P3 (agitation position). The controller 91 stands by (step S2007: No) until completion of pickup of the next specimen container 1 is reported, i.e., until the state of the agitating part 12 becomes M2. Meanwhile, when completion of pickup of the next specimen container 1 is reported, i.e., the state of the agitating part 12 becomes M2 (step S2007: Yes), the controller 91 advances the process to step S2008. In this manner, the controller 91 controls operation of the container transfer part 13b according to whether or not the state of the agitating part 12 is M2. In the processing in steps S2006 to S2007, the container transfer part 13b stands by at the fourth position P4 (shunt position) until relaying of the next specimen container 1 from the rack 2 to the agitating part 12 is completed. Consequently, it is possible to avoid collision between the container transfer part 13b and the agitating part 12 which has moved to the first position P1 (pickup position) in order to receive the next specimen container 1.
In step S2008, the controller 91 transitions the state of the container transfer part 13b from A1 to A2. In step S2009, the controller 91 causes the container transfer part 13b to move from the fourth position P4 (shunt position) to the reading position P5. The processing in step S2009 corresponds to the operation in step S6 in
In step S2012, the controller 91 transitions the state of the container transfer part 13b from A3 to A4. In step S2013, the controller 91 causes the container transfer part 13b to move from the reading position P5 to the suction position P6. The processing in step S2013 corresponds to the operation in step S8 in
In step S2015, the controller 91 determines whether or not start of suctioning of the specimen from the specimen container 1 by the suction part 11 has been reported. Start of suctioning of the specimen from the specimen container 1 by the suction part 11 is reported when the suction tube 71 of the suction part 11 starts to be lowered from above the specimen container 1 through processing in step S4002 of the suction part control described later. The controller 91 stands by (step S2015: No) until start of suctioning of the specimen from the specimen container 1 by the suction part 11 has been reported. Meanwhile, when start of suctioning of the specimen from the specimen container 1 by the suction part 11 has been reported (step S2015: Yes), the controller 91 transitions the state of the container transfer part 13b from A5 to A6 in step S2016.
In step S2017, the controller 91 determines whether or not completion of suctioning of the specimen from the specimen container 1 by the suction part 11 has been reported. Completion of suctioning of the specimen from the specimen container 1 by the suction part 11 is reported when the suction tube 71 of the suction part 11 is, after suctioning of the specimen, lifted so as to be positioned above the specimen container 1 through the processing in step S4002 of the suction part control described later. The controller 91 stands by (step S2017: No) until completion of suctioning of the specimen from the specimen container 1 by the suction part 11 is reported. Meanwhile, when completion of suctioning of the specimen from the specimen container 1 by the suction part 11 is reported (step S2017: Yes), the controller 91 advances the process to step S2018. In step S2018, the controller 91 transitions the state of the container transfer part 13b from A6 to A7.
In step S2019, the controller 91 determines whether or not there is a request to take out a next specimen container 1 from the rack 2. A request to take out a next specimen container 1 from the rack 2 is reported when, at the present timing, a specimen container 1 containing a specimen that needs to be measured next to the specimen in the specimen container 1 placed in the container transfer part 13b is placed at the take-out position P0 and the state of the agitating part 12 is M0. When there is no request to take out a next specimen container 1 from the rack 2 (step S2019: No), the controller 91 skips processing in step S2020 and advances the process to step S2021. Meanwhile, when there is a request to take out a next specimen container 1 from the rack 2 (step S2019: Yes), the controller 91 determines in step S2020 whether or not completion of relaying of the next specimen container 1 from the rack 2 to the agitating part 12 has been reported (completion of pickup of the next specimen container 1 has been reported), i.e., whether or not the state of the agitating part 12 is M2. Completion of pickup of the specimen container 1 is reported when, through the processing in step S3004 of the hand part control described later, the hand part 13a relays the next specimen container 1 having been taken out from the rack 2 to the agitating part 12, and the agitating part 12 moves to the third position P3 (agitation position). The controller 91 stands by (step S2020: No) until completion of pickup of the next specimen container 1 is reported, i.e., until the state of the agitating part 12 becomes M2. Meanwhile, when completion of pickup of the next specimen container 1 is reported, i.e., the state of the agitating part 12 becomes M2 (step S2020: Yes), the controller 91 advances the process to step S2021. In this manner, the controller 91 controls operation of the container transfer part 13b according to whether or not the state of the agitating part 12 is M2. In the processing in steps S2014 to S2020, the container transfer part 13b stands by at the suction position P6 until relaying of the next specimen container 1 from the rack 2 to the agitating part 12 is completed. Consequently, it is possible to avoid collision between the container transfer part 13b and the agitating part 12 which has moved to the first position P1 (pickup position) in order to receive the next specimen container 1.
In step S2021, the controller 91 transitions the state of the container transfer part 13b from A7 to A8. In step S2022, the controller 91 causes the container transfer part 13b to move from the suction position P6 to the second position P2 (pickup position). The processing in step S2022 corresponds to the operation in step S10 in
In step S2026, the controller 91 causes the container transfer part 13b to move from the second position P2 (pickup position) to the fourth position P4 (shunt position) after the hand part 13a takes out the specimen container 1 from the container transfer part 13b through processing in step S3012 of the suction part control described later. In step S2027, the controller 91 determines whether or not completion of returning of the specimen container 1 having been present in the container transfer part 13b to the rack 2 has been reported. Completion of returning of the specimen container 1 having been present in the container transfer part 13b to the rack 2 is reported when relaying of the specimen container 1 into the holding hole 2a of the rack 2 by the hand part 13a is completed through the processing in step S3012 of the suction part control described later. The controller 91 stands by (step S2027: No) until completion of returning of the specimen container 1 having been present in the container transfer part 13b to the rack 2 has been reported. Meanwhile, when completion of returning of the specimen container 1 having been present in the container transfer part 13b to the rack 2 is reported (step S2027: Yes), the controller 91 advances the process to step S2028. In step S2028, the controller 91 transitions the state of the container transfer part 13b from A10 to A0, returns the process to step S2001, and awaits a request to transfer a specimen container 1 from the agitating part 12 to the container transfer part 13b.
About 12 seconds are required from start of the processing in step S2008 to end of the processing in step S2027 with the result of the determination being Yes. In a case where a plurality of specimens are being consecutively measured, the result of the determination in step S2007 becomes Yes at a timing at which the state of the agitating part 12 is transitioned to M2 through the processing in step S1006. Therefore, the timing of start of the agitation processing in step S1007 and the timing of start of the processing in step S2008 coincide with each other. As described above, about 12 seconds are required from start to end of the agitation processing in step S1007. Thus, during the period from start to end of agitation of one specimen container 1, processing of transferring to the suction position P6 (step S2013), processing of suctioning of a specimen (steps S2015 to S2017/step S4002 described later), and processing of returning to the rack 2 (steps S2026 and S2027/S3012 described later) are executed on another specimen container 1 that precedes the one specimen container 1.
Next, the hand part control will be described. As shown in
In step S3004, the controller 91 controls the hand part 13a to execute pickup processing of: taking out, from the rack 2, the specimen container 1 placed at the take-out position P0; lifting the movable part 41 to the position above the first position P1 (pickup position); lowering the movable part 41 after the agitating part 12 moves to the first position P1 (pickup position); and relaying the specimen container 1 to the agitating part 12. The processing in step S3004 corresponds to the operation in step S4 in
In step S3005, the controller 91 determines whether or not there is a request to transfer the specimen container 1 from the agitating part 12 to the container transfer part 13b. A request to transfer the specimen container 1 from the agitating part 12 to the container transfer part 13b is reported when: agitation of a specimen in the specimen container 1 by the agitating part 12 is completed; and the state of the container transfer part 13b is A0. On one hand, when there is a request to transfer the specimen container 1 from the agitating part 12 to the container transfer part 13b (step S3005: Yes), the controller 91 determines in step S3006 whether or not the hand part 13a is executing another operation other than an operation of transferring the specimen container 1 from the agitating part 12 to the container transfer part 13b. When the hand part 13a is executing another operation (step S3006: Yes), the controller 91 stands by (step S3007: No) until the other operation is completed, and, when the other operation is completed (step S3007: Yes), the controller 91 advances the process to step S3008. Meanwhile, when the controller 91 determines in step S3006 that the hand part 13a is not executing another operation (step S3006: No), the controller 91 skips step S3007 and advances the process to step S3008. On the other hand, when the controller 91 determines in step S3005 that there is no request to transfer the specimen container 1 from the agitating part 12 to the container transfer part 13b (step S3005: No), the controller 91 skips steps S3006 and S3007 and advances the process to step S3008.
In step S3008, the controller 91 controls the hand part 13a to execute transfer processing of: taking out, from the agitating part 12 having moved to the first position P1 (pickup position), the specimen container 1 held by the agitating part 12; lifting the movable part 41 to the position above the first position P1 (pickup position); lowering the movable part 41 after the agitating part 12 moves to the third position (agitation position) and the container transfer part 13b moves to the second position P2 (pickup position); and relaying the specimen container 1 to the container transfer part 13b. The processing in step S3008 corresponds to the operation in step S5 in
In step S3009, the controller 91 determines whether or not there is a request to return the specimen container 1 present in the container transfer part 13b to the rack 2. A request to return the specimen container 1 present in the container transfer part 13b to the rack 2 is reported when: the holding hole 2a, of the rack 2, having held this specimen container 1 is placed at the take-out position P0; and the state of the container transfer part 13b is A9. On one hand, when there is a request to return the specimen container 1 present in the container transfer part 13b to the rack 2 (step S3009: Yes), the controller 91 determines in step S3010 whether or not the hand part 13a is executing another operation other than a returning operation of returning the specimen container 1 present in the container transfer part 13b to the rack 2. When the hand part 13a is executing another operation (step S3010: Yes), the controller 91 stands by (step S3011: No) until the other operation is completed, and, when the other operation is completed (step S3011: Yes), the controller 91 advances the process to step S3012. Meanwhile, when the controller 91 determines in step S3010 that the hand part 13a is not executing another operation (step S3010: No), the controller 91 skips step S3011 and advances the process to step S3012. On the other hand, when the controller 91 determines in step S3009 that there is no request to return the specimen container 1 present in the container transfer part 13b to the rack 2 (step S3009: No), the controller 91 skips steps S3010 and S3011 and advances the process to step S3012.
In step S3012, the controller 91 controls the hand part 13a to execute returning processing of: taking out, from the container transfer part 13b having moved to the second position P2 (pickup position), the specimen container 1 held by the container transfer part 13b; lifting the movable part 41 to a position above the second position P2 (pickup position); lowering the movable part 41 after the container transfer part 13b moves to the fourth position P4 (shunt position); and relaying the specimen container 1 to the rack 2. The processing in step S3012 corresponds to the operation in step S11 in
Next, the suction part control will be described. As shown in
Next, the reading part control will be described. As shown in
Next, description will be given regarding the timing and the manner of operation of each of the hand part 13a, the agitating part 12a, the container transfer part 13b, and the suction part 11 performed through concurrent processing operations which are the suction part control, the agitating part control, the hand part control, the container transfer part control, the reading part control, the sample preparation part control, the measurement part control, and the rack transport part control described above, in the case of consecutively processing a plurality of specimen containers 1.
In
During a period from the time point t6 (see
During a period from the time point t7 of end of the agitation to a time point t8 (see
The above operations during a period from the time point t1 to the time point t16 are processing for the first specimen container 1, and there is no specimen container 1 to be subjected to agitation processing prior to the first specimen container 1. Thus, there is no operation that is executed concurrently with the agitation operation. After the time point t16, processing operations in
In
During a period that is subsequent to the movement of the container transfer part 13b to the fourth position P4 and that lasts from a time point t17 (see
During this period, the agitating part 12 moves (move (1)) from the third position P3 to the first position P1 at a time point t19 after the hand part 13a takes out the specimen container 1 from the rack 2. During a period from a time point t20 (see
During a period from the time point t22 to a time point t23, the agitating part 12 executes the agitation operation. That is, the agitating part 12 performs the agitation operation on the one subsequent specimen container 1 (second container) in a state where the other specimen container 1 (first container) having been taken in first is held by the container transfer part 13b.
In
First, at the time point t24, the container transfer part 13b holding the other specimen container 1 (first container) moves (move (5)) the container holding part 51 from the fourth position P4 to the reading position P5. During a period from the time point t25 (see
During a period that is subsequent to completion of the movement and that lasts from a time point t28 (see
During a period that is subsequent to end of the suctioning and that lasts from the time point t31 to a time point t32, the suction part 11 moves the suction tube 71 (see
During a period that is subsequent to completion of the movement and that lasts from the time point t35 (see
The above operations are operations executed during the agitation operation for the one specimen container 1 (second container) by the agitating part 12.
During a period that is subsequent to end of the agitation and that lasts from the time point t23 to a time point t39, the agitating part 12 moves (move (1)) from the third position P3 to the first position P1. Then, during a period from a time point t40 (see
During a period from the time point t32 to a time point t48, the suction part 11 moves from the suction position P6 to the ejection position for any of the reaction parts (81a to 81e). Then, during a period from the time point t48 to a time point t49, the suction part 11 moves the suction tube 71 downward into the reaction part (81a to 81e). Then, from the time point t49, the suction part 11 performs an operation of ejecting the suctioned specimen (the specimen from the first specimen container 1).
Processing for third and subsequent specimen containers 1 is performed through repetition of the operations during the period from the time point t17 to the time point t47 shown in
Therefore, the specimen analyzer 100 is configured such that control by the controller 91 causes the following operations before agitation of the one specimen container 1 (third container). That is, during the period from the time point t40 to the time point t41, the hand part 13a transfers the other specimen container 1 (second container) having been agitated by the agitating part 12, from the agitating part 12 to the container transfer part 13b, and then, during a period from the time point t17 to the time point t18, the hand part 13a transfers the one specimen container 1 (third container) having yet to be agitated, from the rack 2 to the agitating part 12. Consequently, the hand part 13a can relay the other specimen container 1 having been agitated, from the agitating part 12 to the container transfer part 13b, and furthermore, the same hand part 13a can relay the one specimen container 1 having yet to be agitated, from the rack 2 to the agitating part 12. For example, an unnecessary operation does not need to be performed, and thus the processing efficiency can be improved as compared to a case where, after the other specimen container 1 is agitated by the agitating part 12, the specimen container 1 is returned to the rack 2 once, and then, relayed from the rack 2 to the container transfer part 13b.
When one specimen container 1 as an (N+1)th container is taken in, the following operations are performed in the same manner as that for the third container. That is, during the agitation process (from the time point t22 to the time point t23) for the one specimen container 1 as the (N+1)th container, another specimen container 1 as an Nth container is subjected to each of the operations of transferring to the reading position P5 (from the time point t24 to the time point t25), reading of information (from the time point t25 to the time point t26), transferring to the suction position P6 (from the time point t26 to the time point t27), suctioning of a specimen (from the time point t30 to the time point t31), transferring to the second position P2 (from the time point t33 to the time point t34), and returning to the rack 2 (from the time point t35 to the time point t36).
As described above, the specimen analyzer 100 in the present embodiment is configured such that control by the controller 91 causes, during the period from start (time point t22) to end (time point t23) of agitation of the one specimen container 1, the container transport part 13 to perform transferring of the other specimen container 1 to the suction position P6 (from the time point t26 to the time point t27). Thus, during the agitation of the one specimen container 1, the transferring of the other specimen container 1 to the suction position P6 can be concurrently executed, whereby the processing efficiency can be improved as compared to a case where the agitation and the transferring to the suction position P6 are separately executed.
In addition, the specimen analyzer 100 is configured such that control by the controller 91 causes, during the period from start (time point t22) to end (time point t23) of agitation of the one specimen container 1, completion of the transferring of the other specimen container 1 to the suction position P6 (from the time point t26 to the time point t27) and causes, during said period, the suction part 11 to start (time point t30) suctioning of a specimen from the other specimen container 1 transferred to the suction position P6. Thus, during the agitation of the one specimen container 1, the suctioning of the specimen from the other specimen container 1 can be concurrently executed, whereby the processing efficiency can be improved as compared to a case where the agitation and the suctioning of the specimen are separately executed.
In addition, the specimen analyzer 100 is configured such that control by the controller 91 causes, during the period from start (time point t22) to end (time point t23) of agitation of the one specimen container 1, completion of the transferring of the other specimen container 1 to the suction position P6 (from the time point t26 to the time point t27) and the suctioning of the specimen from the other specimen container 1 (from the time point t30 to the time point t31) and causes, during said period, the container transport part 13 to start (time point t35) returning of the other specimen container 1 having been subjected to the suctioning to the rack 2. Thus, during the agitation of the one specimen container 1, the returning of the other specimen container 1 to the rack 2 can be concurrently executed, whereby the processing efficiency can be improved as compared to a case where the agitation and the returning to the rack 2 are separately executed.
In addition, the specimen analyzer 100 is configured such that control by the controller 91 causes, during the period from start (time point t22) to end (time point t23) of agitation of the one specimen container 1, execution of: movement of the other specimen container 1 to the reading position P5 by the container transport part 13 (from the time point t24 to the time point t25); and reading of the identification information on the other specimen container 1 by the reading part 14 (from the time point t25 to the time point t26). Thus, during the agitation of the one specimen container 1, the reading of the identification information on the other specimen container 1 can be concurrently executed, whereby the processing efficiency can be improved as compared to a case where the agitation and the reading of the identification information are separately executed.
In addition, the specimen analyzer 100 is configured such that control by the controller 91 causes the hand part 13a to: return the other specimen container 1 (Nth container) having been subjected to suctioning by the suction part 11, from the container transfer part 13b to the rack 2 (from the time point t35 to the time point t36); and, after agitation of the one specimen container 1 ((N+1)th container), transfer the one specimen container 1 having been agitated by the agitating part 12, from the agitating part 12 to the container transfer part 13b (from the time point t40 to the time point t41). Thus, the hand part 13a can perform an operation of: returning the other specimen container 1 (Nth container) having been subjected to suctioning, from the container transfer part 13b to the rack 2; and furthermore, relaying the one specimen container 1 ((N+1)th container) having been agitated, from the agitating part 12 to the container transfer part 13b which has become vacant. Therefore, an unnecessary operation does not need to be performed, and thus the processing efficiency can be improved as compared to a case where, after the one specimen container 1 ((N+1)th container) is agitated by the agitating part 12, the specimen container 1 is returned to the rack 2 once, and then, relayed from the rack 2 to the container transfer part 13b.
In addition, as shown in
Next, an example of processing times in
Therefore, in a case where the series of operations is repeated without parallel processing, the series of operations which are reading of information, suctioning of the specimen, and returning of the specimen container 1 to the rack 2 is further executed for 12 seconds after agitation processing is executed for 12 seconds. However, in the present embodiment, agitation processing for one specimen container 1, and each of reading of information about another specimen container 1, suctioning of a specimen from the other specimen container 1, and returning of the other specimen container 1 to the rack 2, are executed simultaneously and in a parallel manner, whereby the number of specimens to be processed per unit time can be increased.
Meanwhile, for a plurality of specimen containers 1, suctioning of a specimen is executed in a cycle of 18 seconds, and thus it is important to set also the cycle of sample preparation and measurement per specimen to fall within the cycle of 18 seconds.
To this end, the reaction part 81a and the reaction part 81b receive the same type of reagent in the present embodiment (see
Consequently, a measurement sample is prepared in one of the reaction part 81a and the reaction part 81b, and, before an operation of making ready for reception of a next specimen is completed, a measurement sample can be prepared from the next specimen by using the other one of the reaction part 81a and the reaction part 81b. Therefore, in a case where agitation processing for one of the specimen containers 1 and processing for another one of the specimen containers 1 are executed as concurrent processing operations so that suctioning of a specimen in the one specimen container 1 and suctioning of a specimen in the other specimen container 1 are executed at a short time interval, it is also made possible for preparation of measurement samples to be executed in a parallel manner by the plurality of reaction parts 81, whereby the number of specimens to be processed per unit time can be effectively increased.
Specifically, as shown in
Thus, even in a case where the cycle of sample preparation per specimen cannot be set to fall within the cycle of 18 seconds with one reaction part, the cycle can be set to fall within the cycle of 18 seconds by, before completing an operation of making ready for the next sample preparation in the one reaction part 81a, preparing a sample from the next specimen by using the other reaction part 81b.
As shown in
The embodiment and examples disclosed herein are merely illustrative in all aspects and should not be considered as being restrictive. The scope of the present disclosure is defined not by the description of the above embodiment or examples but by the scope of the claims, and further includes meaning equivalent to the scope of the claims and all modifications within said scope.
For example, in the above embodiment, an example has been described in which, during agitation processing for the one specimen container 1 as the (N+1)th container (from the time point t22 to the time point t23), each processing, i.e., each of transferring to the reading position P5 (from the time point t24 to the time point t25), reading of information (from the time point t25 to the time point t26), transferring to the suction position P6 (from the time point t26 to the time point t27), suctioning of a specimen (from the time point t30 to the time point t31), transferring to the second position P2 (from the time point t33 to the time point t34), and returning to the rack 2 (from the time point t35 to the time point t36), is performed on the other specimen container 1 as the Nth container. However, the present disclosure is not limited thereto. In the present disclosure, during the period from start to end of agitation of the one specimen container 1, only at least one of transferring to the suction position P6, suctioning of a specimen, and returning to the rack 2 has to be executed on the other specimen container 1. In this case as well, completion of the processing for the specimen containers 1 can be hastened by the period of said operation that can be executed on the other specimen container 1 during the agitation of the one specimen container 1. Consequently, the number of specimens to be processed per unit time by the specimen analyzer 100 in the case of analyzing a plurality of specimens can be increased.
For example, a first modification shown in
A second modification shown in
A third modification shown in
A fourth modification shown in
A fifth modification shown in
In addition, in the above embodiment, an example has been described in which the first position P1 at which each specimen container 1 is taken out from or put into the agitating part 12, the second position P2 at which the specimen container 1 is taken out from or put into the container transfer part 13b, and the take-out position P0 for taking out the specimen container 1 from the rack 2 are aligned in the up-down direction. However, the present disclosure is not limited thereto. The first position P1, the second position P2, and the take-out position P0 do not have to be aligned in the up-down direction. The first position P1, the second position P2, and the take-out position P0 may be present at positions different from one another in the top view. The first position P1 and the second position P2 may be the same position in the top view, and the take-out position P0 may be a position different from the first position P1 and the second position P2 in the top view. Alternatively, one of the first position P1 and the second position P2 may be the same position as the take-out position P0 in the top view, and the other one of the first position P1 and the second position P2 may be a position different from the take-out position P0 in the top view.
In addition, in the above embodiment, an example has been described in which the container transfer part 13b linearly moves in the Y direction, and the agitating part 12 linearly moves in the X direction. However, the present disclosure is not limited thereto. The container transfer part 13b may move in a direction other than the Y direction and may move in a curved manner. Likewise, the agitating part 12 may move in a direction other than the X direction and may move in a curved manner. The container transfer part 13b and the agitating part 12 may move in directions parallel to each other. In this case, the hand part 13a may be configured to be horizontally movable so as to extend on and between the container transfer part 13b and the agitating part 12. Alternatively, a mechanism for relaying the specimen container 1 between the container transfer part 13b and the agitating part 12 may be provided separately from the hand part 13a.
In addition, in the above embodiment, an example has been described in which the hand part 13a performs taking-out and insertion of the specimen container 1 with respect to each of the rack 2, the agitating part 12, and the container transfer part 13b, through upward/downward movement without moving in the horizontal direction. However, the present disclosure is not limited thereto. The hand part 13a may be configured to move not only upward/downward but also horizontally. For example, the agitating part 12 may be fixed at the third position P3, and the hand part 13a may move horizontally between the take-out position P0 and the third position P3 in the top view.
In addition, in the above embodiment, an example has been described in which the agitating part 12 includes the holding part 130 which holds the lower portion of the specimen container 1 and the drive part 121 which causes reciprocating movement of the holding part 130 in the predetermined direction. However, the present disclosure is not limited thereto. The agitating part 12 may be configured to perform agitation in a manner in which: the upper portion of the specimen container 1 is held such that the specimen container 1 is hung; and the specimen container 1 is rotated around a horizontal axis as a pendulum.
In addition, in the above embodiment, an example has been described in which the drive part 121 causes reciprocating rotation of the holding part 130 around the rotation shaft 125 extending in the horizontal direction. However, the present disclosure is not limited thereto. The drive part 121 may be configured to perform agitation by rotating the holding part 130 around a rotation shaft extending in a direction other than the horizontal direction, e.g., the vertical direction. Alternatively, the agitating part 12 does not have to rotate the holding part 130 around a specific rotation shaft. For example, the agitating part 12 may include a linear motion mechanism for causing reciprocating movement of the holding part 130 in a linear trajectory and may perform agitation by causing linear reciprocating movement of the holding part 130.
In addition, in the above embodiment, an example has been described in which the drive part 121 rotates the holding part 130 from the origin position Q0 to the predetermined angle Q1 larger than 90 degrees. However, the present disclosure is not limited thereto. In the present disclosure, the predetermined angle Q1 may be 90 degrees or smaller. The predetermined angle Q1 may be another angle other than 140 degrees. When the origin position Q0 is defined as the horizon (0 degrees), the upper limit of the predetermined angle Q1 is, for example, 270 degrees. When the predetermined angle Q1 is larger than 270 degrees, the upper end portion (cap 1a) of the specimen container 1 is oriented upward, whereby it becomes difficult to cause adhesion matter to fall off. In a case where the fall-off object reception part 115 is not provided, the predetermined angle Q1 may be any angle smaller than 360 degrees. The drive part 121 may cause, instead of reciprocating rotation, rotation by 360 degrees or larger in a direction around the rotation shaft.
In addition, in the above embodiment, an example has been described in which the fall-off object reception part 115 for receiving adhesion matter having fallen off from the specimen container 1 is provided at a position that is present below the upper end portion of the specimen container 1 in a state of having been rotated to the predetermined angle Q1. However, the present disclosure is not limited thereto. In the present disclosure, the fall-off object reception part 115 does not have to be provided.
In addition, in the above embodiment, an example has been described in which the agitating part 12 is configured to abruptly stop rotation of the holding part 130 when the holding part 130 reaches the predetermined angle Q1 from the origin position Q0. However, the present disclosure is not limited thereto. The agitating part 12 may slowly stop rotation of the holding part 130.
In addition, in the above embodiment, an example has been described in which: the arm 124 of the agitating part 12 is connected to the holding part 130 in a state of allowing relative movement in the rotation direction by the predetermined amount CL; and, when the arm 124 is stopped, the holding part 130 moves by the predetermined amount CL and collides with the arm 124 owing to inertia, to be abruptly stopped. However, the present disclosure is not limited thereto. In the present disclosure, the arm 124 and the holding part 130 may be connected so as not to move relative to each other. In the case of abruptly stopping the holding part 130, a stopper that is to collide with a rotating portion (the arm 124 or the holding part 130) may be separately provided to the agitating part 12. Alternatively, a braking device may be provided to the pulley 123b which is rotated together with the arm 124, and rotation of the pulley 123b may be forcedly stopped so as to abruptly stop the holding part 130. The holding part 130 may be abruptly stopped through only drive control of the rotation motor 122
In addition, in the above embodiment, an example has been described in which the holding part 130 is abruptly stopped at the time of end of agitation. However, the present disclosure is not limited thereto. In the present disclosure, the holding part 130 does not have to be abruptly stopped at the origin position Q0 at the time of end of agitation.
In addition, in the above embodiment, an example has been described in which: the plurality of reaction parts 81a and 81b which receive the same type of reagent are provided; and the specimen suctioned from the specimen container 1 is selectively ejected to one of the plurality of reaction parts 81a and 81b. However, the present disclosure is not limited thereto. In the present disclosure, the number of provided reaction parts which receive the same type of reagent may be only one or may be three or more.
In the above embodiment, an example has been described in which the slide drive part 113 which moves the holding part 130 of the agitating part 12 to the first position P1 and the third position P3 is an air cylinder. However, the present disclosure is not limited thereto. The slide drive part 113 may be an electric motor. In this case, drive force of the slide drive part 113 is converted into drive force in the front-rear direction by a belt-pulley mechanism, whereby the slide part 120 can be moved.
In the above embodiment, the measurement unit 10 includes the reading part 14, and the container transport part 13 positions the specimen container 1 at the reading position P5, whereby identification information on the specimen container 1 is read. However, reading of identification information in the measurement unit 10 may be omitted. That is, the measurement unit 10 does not have to include the reading part 14. In this case, the identification information read by the information reading part 24 may be used for identifying the specimen in the specimen container 1.
In the above embodiment, the controller 91 controls operation of each of the parts of the measurement unit 10 and the rack transport part 20. However, the controller 31 may control operations of some of the parts of the measurement unit 10 and the rack transport part 20. Alternatively, the measurement unit 10 does not have to include the controller 91, and the controller 31 may control the operations of the measurement unit 10 and the rack transport part 20. The analysis part 30 does not have to include the controller 31, and the controller 91 may perform analysis processing for measurement data.
In the above embodiment, an example has been described in which the specimen analyzer 100 is provided with one measurement unit 10. However, the present disclosure is not limited thereto. The specimen analyzer 100 may be provided with a plurality of measurement units 10. For example, with respect to the one rack transport part 20, two measurement units 10 may be arranged side-by-side.
In the above embodiment, an example has been described in which specimens contained in a plurality of specimen containers 1 (ordinary specimens) held by a rack 2 transported by the rack transport part 20 are measured. However, the present disclosure is not limited thereto. The specimen analyzer 100 may measure, in preference to the plurality of specimen containers 1 (ordinary specimens) held by the rack 2 transported by the rack transport part 20, a specimen contained in a specimen container 1 (interruption specimen) having been placed on the container holding part 51 by a user.
In a case where the controller 91 determines in step S101 that a specimen container 1 is present in the container transfer part 13b (step S101: Yes), the controller 91 determines in step S102 whether or not a specimen is being suctioned. The determination as to whether or not a specimen is being suctioned may be performed according to, for example, whether or not the operation in step S9 (
In a case where the controller 91 determines in step S101 that no specimen container is present in the container transfer part 13b (step S101: No), or after step S104 is executed, the controller 91 determines in step S105 whether or not a specimen container 1 is present in the agitating part 12. The determination as to whether or not a specimen container 1 is present in the agitating part 12 is performed on the basis of an output from a sensor (container detector 137) for detecting a specimen container 1 held by the holding part 130 or may be performed by means of software. In the case of performing the determination by means of software, the controller 91 may perform the determination according to, for example, whether or not any of the operations in steps S1 to S3 (
In a case where the controller 91 determines in step S105 that a specimen container is present in the agitating part 12 (step S105: Yes), the controller 91 causes the agitating part 12 to stop agitating the specimen container 1 in step S106 even when the predetermined number of times of agitation has not yet been completed. Through this processing, the agitating part 12 is stopped in a state where the specimen container 1 held by the holding part 130 is placed at the third position P3. In step S107, the controller 91 causes the specimen container 1 in the agitating part 12 to be returned to the original holding hole 2a of the original rack 2. Through this processing, the specimen container 1 held by the holding part 130 is placed at the first position P1, and the hand part 13a returns this specimen container 1 to the rack 2 transported to the position at which this specimen container 1 has been taken out. Alternatively, the processing in step S107 may be executed after step S108 is executed.
In a case where the controller 91 determines in step S105 that no specimen container 1 is present in the agitating part 12 (step S105: No), or after step S107 is executed, the controller 91 controls the container transfer part 13b such that the container holding part 51 moves to the container placement position P7 in step S108. Next, processing in step S109 is started when the user places an agitated interruption specimen into the container holding part 51 placed at the container placement position P7 and presses the switch 95. In step S109, the controller 91 executes measurement processing in the interruption specimen measurement mode. Specifically, in step S109, the controller 91 causes the container transfer part 13b to move the interruption specimen placed in the container holding part 51 from the container placement position P7 to the reading position P5, and then, controls the suction part 11, the hand part 13a, the container transfer part 13b, the reading part 14, the sample preparation part 15, and the measurement part 16 to execute the operations in steps S7 to S14 (
In this manner, the specimen analyzer 100 in the sixth modification can be operated in a first mode of measuring a plurality of ordinary specimens accommodated in the rack 2 on the rack transport part 20 and a second mode of measuring an interruption specimen in preference to the plurality of ordinary specimens. The controller 91 is configured to, when the second mode is set, perform control to return the ordinary specimens present in the agitating part 12 and the container transport part 13 to the rack 2. That is, in the case of measuring the interruption specimen, each specimen container 1 taken into the unit cover 18 is returned to the corresponding original holding hole 2a of the original rack 2. Consequently, the specimen analyzer in the sixth modification can swiftly perform measurement of the interruption specimen even during measurement of the plurality of ordinary specimens.
In the above embodiment, an example has been described in which the specimen analyzer 100 is a blood cell counter. However, the specimen analyzer 100 may be another type of analyzer such as an immunoassay device, a biochemical measurement device, a blood coagulation measurement device, or a urine analyzer. Therefore, the specimen in the present disclosure is not limited to a blood specimen and may be urine, tissue fluid, another body fluid (such as cerebrospinal fluid, ascitic fluid, pleural fluid, synovial fluid, or peritoneal dialysis effluent), or the like.
The present disclosure includes the following items 1-44.
Item 1: A specimen analyzer comprising:
Item 2: The specimen analyzer of item 1, wherein
Item 3: The specimen analyzer of item 2, wherein
Item 4: The specimen analyzer of item 2, wherein
Item 5: The specimen analyzer of item 2, wherein
Item 6: The specimen analyzer of item 5, wherein
Item 7: The specimen analyzer of item 6, wherein
Item 8: The specimen analyzer of item 7, wherein
Item 9: The specimen analyzer of item 1, wherein
Item 10: The specimen analyzer of item 9, wherein
Item 11: The specimen analyzer of item 10, wherein
Item 12: The specimen analyzer of item 11, further comprising
Item 13: The specimen analyzer of item 2, further comprising
Item 14: The specimen analyzer of item 1, wherein
Item 15: The specimen analyzer of item 14, wherein
Item 16: The specimen analyzer of item 15, wherein
Item 17: The specimen analyzer of item 16, wherein
Item 18: The specimen analyzer of item 17, wherein
Item 19: The specimen analyzer of item 18, wherein
Item 20: The specimen analyzer of item 19, wherein
Item 21: The specimen analyzer of item 1, further comprising
Item 22: The specimen analyzer of item 21, wherein
Item 23: The specimen analyzer of item 1, wherein
Item 24: The specimen analyzer of item 1, wherein
Item 25: A specimen analysis method to be performed by a specimen analyzer configured to analyze a specimen contained in a specimen container, the specimen analysis method comprising:
Item 26: The specimen analysis method of item 25, wherein
Item 27: The specimen analysis method of item 25, further comprising:
Item 28: The specimen analysis method of item 27, wherein
Item 29: The specimen analysis method of item 28, wherein
Item 30: The specimen analysis method of item 29, further comprising:
Item 31: The specimen analysis method of item 25, wherein
Item 32: The specimen analysis method of item 31, wherein,
Item 33: The specimen analysis method of item 32, wherein,
Item 34: The specimen analysis method of item 33, further comprising:
Item 35: The specimen analysis method of item 27, further comprising:
Item 36: The specimen analysis method of item 25, wherein
Item 37: The specimen analysis method of item 36, wherein
Item 38: The specimen analysis method of item 37, wherein
Item 39: The specimen analysis method of item 38, wherein
Item 40: The specimen analysis method of item 39, wherein
Item 41: The specimen analysis method of item 40, wherein
Item 42: The specimen analysis method of item 41, wherein
Item 43: The specimen analysis method of item 25, further comprising
Item 44: The specimen analysis method of item 43, wherein
Number | Date | Country | Kind |
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2023-035980 | Mar 2023 | JP | national |