JP2018163169A - Cartridge for measurement and liquid feeding method - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a cartridge for measurement and a liquid feeding method capable of increasing quantitative properties of plasma components separated by centrifugal separation in the case of transferring the plasma components to increase measurement accuracy of the plasma components.SOLUTION: A cartridge 10 for measurement comprises: a separation chamber 30 for separating corpuscle components and plasma components contained in a blood specimen by using a centrifugal force generated by rotating the cartridge 10 for measurement: a housing chamber 40 for housing the plasma components; a first channel 51 extended in a direction going from the separation chamber 30 to a rotation axis 20; a second channel 52 extended from an end opposite to a side of the separation chamber 30 of the first channel 51 in a direction separating from the rotation axis 20 so as to be connected to the housing chamber 40; and an air introduction passage 65 capable of introducing air from a connection position between the first channel 51 and the second channel 52 into the second channel 52.SELECTED DRAWING: Figure 1

Description

  The present invention relates to a measurement cartridge and a liquid feeding method for separating a liquid component from a specimen by centrifugation and using it for measurement.

  Patent Document 1 discloses a configuration for analyzing a sample using a disk-shaped bioanalytical device.

  Specifically, as shown in FIG. 20A, the blood 402 injected into the blood reservoir 401 is subjected to a centrifugal force generated by the rotation of the biological analysis device 400 via the blood channel 403. 404. The inside of the blood separation unit 404 is divided into a plasma storage unit 406 and a blood cell storage unit 407 by a blood separation wall 405. In addition, a plasma collection capillary 408 and a ventilation channel 409 are formed in the blood separation wall 405 so as to connect the plasma reservoir 406 and the blood cell reservoir 407. As shown in FIG. 20B, the blood 402 transferred to the blood separation unit 404 is further separated into a plasma component 410 and a blood cell component 411 by centrifugal force. Thereafter, the rotation of the bioanalytical device 400 is decelerated or stopped, so that the separated plasma component 410 is transferred to the plasma metering unit 412 through the siphon channel 412a by capillary force. Thereafter, the plasma component 410 is transferred to the reagent reaction unit 413 by centrifugal force and used for analysis.

US Patent Application Publication No. 2010/0240142

  An object of the present invention is to provide a measurement cartridge and a liquid feeding method capable of improving the measurement accuracy of a plasma component by increasing the quantitativeness of the plasma component when transferring the plasma component separated by centrifugation. And

  A first aspect of the present invention relates to a measurement cartridge (10, 200, 320) that is mounted on a measurement device (100) so as to be rotatable about a rotation axis (20, 103). The measurement cartridge (10, 200, 320) according to the present aspect uses blood force components contained in the blood sample (70, 280) by utilizing the centrifugal force generated by rotating the measurement cartridge (10, 200, 320). (71, 281) and a plasma component (72, 282) are separated from each other (30, 210), a plasma chamber (72, 282) is contained in a chamber (40, 241), and a separation chamber ( 30, 210) extending from the first flow path (51, 221) in the direction toward the rotation axis (20, 103), and the end of the first flow path (51, 221) opposite to the separation chamber (30, 210). Part, a second flow path (52, 222) extending in a direction away from the rotation shaft (20, 103) and connected to the storage chamber (40, 241), a first flow path (51, 221), and a second flow Road (52 Comprises 222) connected to the position (50a, 220a) from possible introduction of air into the second flow path (52,222) in the air introduction path and (65,207), the.

  According to the measurement cartridge according to this aspect, when the measurement cartridge is rotated in a state where the first flow path and the second flow path are filled with the plasma component, air enters the second flow path from the air introduction path, The plasma component filled in the first channel and the second channel is divided at the connection position. Thereby, the plasma component in the first flow path is returned to the separation chamber by centrifugal force, and the plasma component in the second flow path moves to the accommodation chamber by centrifugal force. Therefore, since the plasma component that moves to the storage chamber becomes a plasma component that fills the second flow path, the quantitativeness of the plasma component that moves to the storage chamber is improved.

  In the measurement cartridge (10, 200, 320) according to this aspect, the second flow path (52, 222) includes the plasma component (72, 282) separated in the separation chamber (30, 210) by capillary action. Then, the plasma components (72, 282) quantified by introducing air into the second flow path (52, 222) from the connection position (50a, 220a) by centrifugal force are stored in the storage chamber (40, 241). ).

  In the measurement cartridge (10, 200, 320) according to this aspect, the movement of the plasma components (72, 282) due to capillary action is stopped on the side of the accommodation chamber (40, 241) of the second flow path (52, 222). A valve (208c) may be provided.

  The measurement cartridge (10, 200, 320) according to this aspect includes a waste chamber (234) for discarding the plasma components (72, 282), a separation chamber (30, 210), and a waste chamber (234). The plasma components (72, 282) remaining in the separation chamber (30, 210) after the plasma components (72, 282) are transferred from the separation chamber (30, 210) to the receiving chamber (40, 241) Other flow paths (233) that move from the separation chamber (30, 210) toward the waste chamber (234) according to the siphon principle can be configured.

  A second aspect of the present invention relates to a liquid feeding method. In the liquid feeding method according to this aspect, the separation chamber (30, 210) included in the measurement cartridge (10, 200, 320) mounted on the measurement device (100) so as to be rotatable about the rotation shaft (20, 103). ), The blood sample (70, 280) is separated from the blood cell component (71, 281) and the plasma component (72, 282) using the centrifugal force generated by the rotation around the rotation axis (20, 103) (S102). ), The plasma components (72, 282) separated in the separation chamber (30, 210) are connected to the separation chamber (30, 210) and the storage chamber (40, 241) by capillary action (50, 200). ) (S103), and plasma components (72, 282) quantified by introducing air into the flow path (50, 200) by centrifugal force are contained in the storage chambers (40, 241). To transfer to (S104).

  According to the liquid feeding method according to this aspect, the same effects as those of the first aspect are achieved.

  In the liquid feeding method according to this aspect, the movement of the plasma components (72, 282) due to capillary action is stopped on the side of the storage chamber (40, 241) of the flow path (50, 200) (S103).

  In the liquid feeding method according to this aspect, the plasma components (72, 282) remaining in the separation chamber (30, 210) after the plasma components (72, 282) are moved from the separation chamber (30, 210) to the storage chambers (40, 241). 72, 282) is moved from the separation chamber (30, 210) toward the waste chamber (234) according to the siphon principle (S104).

  ADVANTAGE OF THE INVENTION According to this invention, when transferring the plasma component isolate | separated by centrifugation, the quantitative property of a plasma component can be improved and the measurement precision of a plasma component can be improved.

FIG. 1 is a schematic diagram illustrating a configuration of a measurement cartridge according to the first embodiment. 2A and 2B are diagrams for explaining a procedure for separating a solid component and a liquid component contained in a specimen according to Embodiment 1 and storing the liquid component in a storage chamber. FIGS. 3A and 3B are diagrams for explaining a procedure for separating the solid component and the liquid component contained in the specimen according to the first embodiment and storing the liquid component in the storage chamber. 4A and 4B are schematic views illustrating the configuration of a measurement cartridge according to a modification of the first embodiment. FIG. 5A is a schematic diagram illustrating a configuration of a measurement cartridge according to the second embodiment. FIGS. 5B and 5C are schematic views illustrating the configuration of a measurement cartridge according to a modification of the second embodiment. FIG. 6A is a schematic diagram illustrating a configuration of a measurement cartridge according to the third embodiment. 6B and 6C are schematic views illustrating the configuration of a measurement cartridge according to a modification of the third embodiment. FIG. 7A is a schematic diagram illustrating a configuration of a measurement apparatus according to a specific configuration example of the second embodiment. FIG. 7B is a schematic diagram illustrating a configuration of a measurement cartridge according to a specific configuration example of the second embodiment. FIG. 8 is an enlarged view schematically showing a partial configuration of the measurement cartridge according to the specific configuration example of the second embodiment. FIG. 9A is a schematic diagram illustrating a C1-C2 cross section according to a specific configuration example of the second embodiment. FIGS. 9B and 9C are schematic views illustrating a C1-C2 cross section according to a modified example of the specific configuration example of the second embodiment. FIG. 10A is an enlarged view schematically showing a configuration of a valve according to a specific configuration example of the second embodiment. FIGS. 10B to 10D are diagrams for explaining that the valve according to the specific configuration example of the second embodiment suppresses the liquid component from entering the storage chamber due to capillary action. FIG. 11 is a diagram illustrating a configuration when the main body according to the specific configuration example of the second embodiment is viewed obliquely from above, and a diagram illustrating a configuration when the lid is viewed from diagonally below. FIG. 12 is a schematic diagram when a cross section of the measuring device is viewed from the side when cut along a plane parallel to the YZ plane passing through the rotation axis according to the specific configuration example of the second embodiment. FIG. 13 is a block diagram illustrating a configuration of a measurement apparatus according to a specific configuration example of the second embodiment. FIG. 14 is a flowchart illustrating the operation of the measurement apparatus according to the specific configuration example of the second embodiment. FIG. 15 is a flowchart illustrating in detail a process of separating a specimen and transferring a liquid component to a storage chamber according to a specific configuration example of the second embodiment. FIG. 16A is a schematic diagram illustrating a state in which a sample is stored in the sample storage unit according to the specific configuration example of the second embodiment. FIG. 16B is a schematic diagram illustrating a state in which the sample in the sample storage unit according to the specific configuration example of Embodiment 2 is transferred to the separation chamber. FIG. 17A is a schematic diagram illustrating a state in which the specimen in the separation chamber according to the specific configuration example of Embodiment 2 is separated into a solid component and a liquid component by centrifugal force. FIG. 17B is a schematic diagram illustrating a state where the liquid component in the separation chamber according to the specific configuration example of Embodiment 2 is transferred to the flow path. FIG. 18A is a schematic diagram illustrating a state in which the liquid component in the second channel according to the specific configuration example of the second embodiment is being transferred to the storage chamber. FIG. 18B is a schematic diagram illustrating a state where the transfer of the liquid component according to the specific configuration example of Embodiment 2 is completed. FIG. 19 is a schematic diagram illustrating a configuration when the support member and the measurement cartridge according to the fourth embodiment are viewed from above. FIG. 20 is a schematic diagram for explaining a configuration according to related technology.

<Embodiment 1>
As shown in FIG. 1, the measurement cartridge 10 is a measurement cartridge for separating a liquid component from a specimen by centrifugation and using the liquid component for measurement. The measurement cartridge 10 is a replaceable part that summarizes functions necessary for separating a liquid component from a specimen by centrifugation. The measurement cartridge 10 is mounted on a measurement device so as to be rotatable around a rotation shaft 20 provided in the measurement device, and is configured to be able to separate a specimen contained therein into a solid component and a liquid component by centrifugal force. The measurement device rotates the rotation shaft 20 to rotate the attached measurement cartridge 10 around the rotation shaft 20.

  In the first embodiment, the sample is a whole blood sample collected from the subject. The liquid component is a plasma component contained in a blood sample of whole blood. The solid component is a blood cell component contained in a blood sample of whole blood. Note that the sample is not limited to a whole blood sample, but may be any sample collected from a subject. The liquid component is not limited to a plasma component, and may be a liquid component contained in a specimen collected from a subject. The solid component is not limited to a blood cell component, and may be a solid component contained in a specimen collected from a subject.

  FIG. 1 is a schematic view of a measurement cartridge 10 mounted on a measurement device as viewed vertically downward. In FIG. 1, the XYZ axes are orthogonal to each other. The X-axis positive direction indicates the rear, the Y-axis positive direction indicates the left direction, and the Z-axis positive direction indicates the vertically downward direction. In the following drawings, the XYZ axes are the same as the XYZ axes in FIG. Hereinafter, the radial direction of the circle centered on the rotating shaft 20 is simply referred to as “radial direction”. The circumferential direction of the circle around the rotation axis 20, that is, the rotation direction around the rotation axis 20, is simply referred to as “rotation direction”. Of the rotation directions, the counterclockwise direction when viewed in the positive direction of the Z axis is the T1 direction, and the clockwise direction when viewed in the positive direction of the Z axis is the T2 direction.

  As shown in FIG. 1, the measurement cartridge 10 is constituted by a plate-like and disc-like substrate 10a. Each part in the measurement cartridge 10 is formed by bonding a recess formed on the substrate 10a and a film (not shown) covering the substrate 10a. The measurement cartridge 10 is not limited to a plate shape but may include a protruding portion or the like. The measurement cartridge 10 is not limited to a disk shape and may have another shape such as a rectangular shape. The substrate 10a is provided with a hole 10b penetrating the substrate 10a at the center of the substrate 10a. The measurement cartridge 10 is installed in the measurement apparatus so that the center of the hole 10b coincides with the rotation shaft 20 of the measurement apparatus.

  The measurement cartridge 10 includes a separation chamber 30, a storage chamber 40, a flow path 50, a sample inlet 61, a sample storage portion 62, a flow path 63, a hole 64, an air introduction path 65, and a flow path. 66.

  The sample insertion port 61 is provided on the inner side in the radial direction of the sample storage unit 62 and opens the radial inner side of the sample storage unit 62 to the outside of the measurement cartridge 10. The sample storage unit 62 stores the sample input from the sample input port 61. The flow path 63 is provided on the outer side in the radial direction of the sample container 62 and connects the sample container 62 and the separation chamber 30.

  The separation chamber 30 includes a first reservoir 31 and a second reservoir 32 disposed in a direction away from the rotary shaft 20 with respect to the first reservoir 31. The second storage part 32 is connected to the first storage part 31. The 1st storage part 31 is extended in the direction which goes to the rotating shaft 20, and the 2nd storage part 32 is extended along the rotation direction. The rotation direction width L2 of the second storage unit 32 is larger than the rotation direction width L1 of the first storage unit 31. The 1st storage part 31 is arrange | positioned in the rotation direction with respect to the 2nd storage part 32 in the position biased in the T2 direction.

  The 1st storage part 31 is provided with inner wall 31a, 31b. The inner walls 31a and 31b are portions of the first reservoir 31 that are located on the opposite side of the rotary shaft 20 from the end of the first reservoir 31 that is positioned on the rotary shaft 20 side. The inner wall 31 a is located on the T1 direction side of the first reservoir 31, and the inner wall 31 b is located on the T2 direction side of the first reservoir 31. In plan view, the inner walls 31a and 31b extend in the radial direction. The inner wall 31b is connected on the same plane as the inner wall of the second reservoir 32 on the T2 direction side. The flow path 63 is connected to the inner wall 31b. The second storage part 32 includes an inner wall 32 a connected to the first storage part 31. The inner wall 32 a is located at the end of the second reservoir 32 on the rotating shaft 20 side, and is located on the T1 direction side of the first reservoir 31. In a plan view, the inner wall 32a extends in the rotational direction. The flow path 50 is connected to the inner wall 32a.

  The flow path 50 connects the separation chamber 30 and the storage chamber 40. The flow path 50 extends in a direction from the separation chamber 30 toward the rotary shaft 20. Specifically, a flow path 51 of a flow path 50 connected to a separation chamber 30 described later extends in a direction toward the rotary shaft 20. The flow path 51 shown in FIG. 1 extends in the direction toward the rotation axis 20, but the flow path 51 only needs to extend in the direction toward the rotation axis 20, and is not necessarily accurate toward the rotation axis 20. It does not have to extend. That is, the flow path 51 does not necessarily extend in the radial direction. Further, the flow path 50 does not necessarily extend in the direction toward the rotation axis 20 over the entire length, and extends in the direction toward the rotation axis 20 at least in a range where the specimen can enter before centrifugation. That's fine.

  The channel 50 includes a channel 51 and a channel 52. The flow path 51 extends linearly in the direction from the separation chamber 30 toward the rotary shaft 20. The flow path 52 extends linearly from the end of the flow path 51 opposite to the separation chamber 30 in a direction away from the rotary shaft 20. The end of the flow path 51 on the T2 direction side is connected to the separation chamber 30, and the end of the flow path 52 on the T1 direction side is connected to the storage chamber 40. The end of the flow path 51 opposite to the separation chamber 30 and the end of the flow path 52 opposite to the accommodation chamber 40 are connected to each other at the connection position 50a. The flow path 50 is configured such that the liquid component separated in the separation chamber 30 moves from the separation chamber 30 toward the storage chamber 40 through the flow path 50 by capillary action. For this reason, the inner diameter of the flow path 50 is set small enough to allow the liquid component to move by capillary action.

  The hole 64 is provided inside the air introduction path 65 in the radial direction, and opens the inside in the radial direction of the air introduction path 65 to the outside of the measurement cartridge 10. The air introduction path 65 is connected to the connection position 50a of the flow path 50, and introduces air into the flow path 50 at the connection position 50a. Specifically, the air introduction path 65 introduces air into the flow path 51 from the connection position 50a, and introduces air into the flow path 52 from the connection position 50a. The storage chamber 40 is a chamber for storing the liquid component separated by the separation chamber 30. The flow channel 66 is connected to the accommodation chamber 40. The liquid component transferred to the storage chamber 40 via the flow path 50 is transferred to another storage chamber via the flow path 66, and measurement regarding the liquid component is performed in the other storage chamber.

  Next, a procedure for separating the solid component 71 and the liquid component 72 contained in the specimen 70 and storing the liquid component 72 in the storage chamber 40 will be described with reference to FIGS. 2 (a) to 3 (b). To do.

  The operator inputs the sample 70 into the sample insertion port 61 in advance and stores the sample 70 in the sample storage unit 62. The operator attaches the measurement cartridge 10 to the measurement apparatus and starts an operation by the measurement apparatus. The measurement apparatus rotates the measurement cartridge 10 around the rotation shaft 20 and transfers the specimen 70 accommodated in the specimen accommodation portion 62 to the separation chamber 30 via the flow path 63 by centrifugal force. At this time, as shown in FIG. 2A, the interface between the specimen 70 and the gas layer in the separation chamber 30 is positioned radially inward from the position where the flow path 51 is connected to the inner wall 32a of the separation chamber 30. It is done. As a result, the specimen 70 enters the vicinity of the end of the flow path 51 on the separation chamber 30 side.

  Subsequently, the measurement apparatus rotates the measurement cartridge 10 around the rotation shaft 20 from the state shown in FIG. 2A, and the centrifugal force generated by the rotation around the rotation shaft 20 is applied to the specimen 70 accommodated in the separation chamber 30. Utilizing this, the solid component 71 and the liquid component 72 are separated. As a result, as shown in FIG. 2B, in the separation chamber 30, the solid component 71 moves radially outward and the liquid component 72 moves radially inward. Here, since the flow path 50 extends in the direction from the separation chamber 30 toward the rotary shaft 20, the solid component 71 that has entered the flow path 50 from the separation chamber 30 before centrifugation as shown in FIG. 2A. Moves from the flow path 50 to the separation chamber 30 by the centrifugal force at the time of centrifugal separation. Therefore, it is possible to suppress the solid component 71 from remaining in the flow path 50 after centrifugation.

  Moreover, since the flow path 51 is connected to the inner wall 32a, the flow path 51 can be extended from the inner wall 32a in the radial direction. As shown in FIG. 1, the flow path 51 of the first embodiment extends in the radial direction from the inner wall 32a. Thereby, the solid component 71 that has entered the flow path 51 from the separation chamber 30 and collected in the flow path 51 before the centrifugal separation is more smoothly moved to the first storage portion 31 by the centrifugal force during the centrifugal separation. Can do. Therefore, it can suppress more reliably that the solid component 71 remains in the flow path 50 after centrifugation.

  Subsequently, the measurement apparatus waits for a predetermined time from the state of FIG. 2B without rotating the measurement cartridge 10. Thereby, as shown in FIG. 3A, the liquid component 72 in the separation chamber 30 enters the flow path 50 by capillary action, and the flow path 50 is filled with the liquid component 72. Here, as described above, since the length of the first reservoir 31 is shorter than the length of the second reservoir 32 in the rotation direction, the liquid component 72 and the gas layer that appear in the first reservoir 31 after the centrifugation. Is greatly separated from the second reservoir 32 toward the rotary shaft 20. For this reason, the distance between this interface and the liquid layer of the solid component 71 after centrifugation can be increased, and the flow path 50 can be connected to a position away from the liquid layer of the solid component 71. Specifically, the flow path 50 can be connected to the inner wall 32a of the second reservoir 32 as in the first embodiment. Thereby, it can avoid that the solid component 71 after centrifugation is involved in the flow produced by the capillary phenomenon.

  As described above, according to the first embodiment, it is possible to prevent the solid component 71 from remaining in the flow path 50 after centrifugation, and to prevent the solid component 71 after centrifugation from being caught in the flow path 50. Thereby, it can suppress that the solid component 71 mixes in the liquid component 72 which moves the flow path 50 from the separation chamber 30 toward the storage chamber 40 by capillary action. Therefore, the measurement accuracy for the liquid component 72 performed in the subsequent stage of the storage chamber 40 can be increased.

  Subsequently, the measurement device rotates the measurement cartridge 10 around the rotation shaft 20 from the state of FIG. As a result, as shown in FIG. 3B, a centrifugal force is applied to the liquid component 72 in the flow path 50, and the liquid component 72 in the flow path 51 is returned to the separation chamber 30 by the centrifugal force and flows. The liquid component 72 in the path 52 moves to the storage chamber 40 by centrifugal force. At this time, air enters the flow path 50 from the air introduction path 65, and the liquid component 72 filled in the flow path 50 from the inside of the flow path 50 is divided at the connection position 50a, so that the liquid component 72 is smoothly moved. In other words, the flow path 50 introduces air into the flow path 50 from the connection position 50a, and transfers the liquid component 72 filled between the connection position 50a and the separation chamber 30 to the separation chamber 30. The liquid component 72 filled between 50 a and the storage chamber 40 is transferred to the storage chamber 40. Since the liquid component 72 moving to the storage chamber 40 becomes the liquid component 72 filled in the flow path 52, the quantitativeness of the liquid component 72 moving to the storage chamber 40 is improved. That is, the liquid component 72 in an amount necessary for measurement can be transferred to the storage chamber 40 without excess or deficiency.

  In addition, as shown in FIG. 1, the 1st storage part 31 of Embodiment 1 was arrange | positioned in the rotation direction with respect to the 2nd storage part 32 in the position biased in T2 direction. However, the present invention is not limited to this, and the first reservoir 31 may be arranged near the center position of the second reservoir 32 as shown in FIG. 4A in the rotational direction, as shown in FIG. Thus, it may be arranged at a position deviated in the T1 direction with respect to the second reservoir 32.

  When the 1st storage part 31 is arrange | positioned as shown to Fig.4 (a), in addition to the inner wall 32a, the 2nd storage part 32 is located in the T2 direction side of the 1st storage part 31, and is the 1st storage part. An inner wall 32 b connected to 31 is provided. In a plan view, the inner wall 32b extends in the rotational direction. When the 1st storage part 31 is arrange | positioned as shown in FIG.4 (b), the 2nd storage part 32 is provided with only the inner wall 32b among the inner walls 32a and 32b compared with Fig.4 (a). In this case, the inner wall 31a of the first reservoir 31 is connected to the inner wall of the second reservoir 32 on the T1 direction side in the same plane. The flow path 50 is connected to the inner wall 31a.

  The flow path 50 is not limited to being connected to the inner wall 32a as shown in FIG. 1 and FIG. 4A, but rotates more than the end of the second reservoir 32 located on the opposite side of the rotary shaft 20. You may connect to the part of the 2nd storage part 32 located in the axis | shaft 20 side. Specifically, the flow path 50 may be connected to the inner wall 32b in FIGS. 4 (a) and 4 (b), and in the T1 direction of the second reservoir 32 in FIGS. 1 and 4 (a) and 4 (b). It may be connected to the inner wall on the side or the T2 direction side.

  Further, the flow path 50 is not limited to being connected to the inner wall 31a as shown in FIG. 4 (b), but rather to the rotation shaft 20 than the end of the first storage portion 31 located on the rotation shaft 20 side. You may connect to the part of the 1st storage part 31 located in the other side. Specifically, the flow path 50 may be connected to the inner wall 31a in FIGS. 1 and 4 (a), or may be connected to the inner wall 31b in FIGS. 1, 4 (a), and (b).

  The flow path 50 may be connected to the separation chamber 30 at the connecting portion between the inner wall 31a and the inner wall 32b. The flow path 50 may be connected to the separation chamber 30 at the connecting portion between the inner wall 31b and the inner wall 32b. The flow path 50 may be connected to the separation chamber 30 at a connecting portion between the first storage portion 31 and the second storage portion 32 in a plane including the inner wall 31b shown in FIG. The flow path 50 may be connected to the separation chamber 30 at a connecting portion between the first storage portion 31 and the second storage portion 32 in a plane including the inner wall 31a shown in FIG.

  1 and FIGS. 4A and 4B, the flow path 63 is connected to the separation chamber 30 on the inner wall 31b of the first reservoir 31. However, the present invention is not limited to this, and the flow path 63 may be connected to the separation chamber 30 on the inner wall 31a of the first storage section 31, and is connected to the separation chamber 30 on the inner wall of the first storage section 31 located on the rotating shaft 20 side. It may be connected.

<Embodiment 2>
As shown in FIG. 5A, in the second embodiment, the separation chamber 30 has a radial direction among the inner walls of the second storage portion 32 on the T2 direction side as compared with the configuration of the first embodiment shown in FIG. The outer wall portion further includes a protrusion 30a protruding in the T2 direction. In other words, the second storage unit 32 of the second embodiment includes the first region 81 and the second region 82 disposed on the rotating shaft 20 side with respect to the first region 81. The width L2 of the second region 82 in the rotational direction is smaller than the width L3 of the first region 81 in the rotational direction. The second region 82 is disposed at a position that is biased in the T1 direction with respect to the first region 81. The first region 81 includes an inner wall 81a extending along the rotation direction in plan view. The inner wall 81 a is located on the T2 direction side in the first region 81 and is connected to the second region 82. The inner wall 81a is located at the end of the first region 81 on the rotating shaft 20 side.

  When the first region 81 and the second region 82 are configured in this manner, the solid component 71 can be efficiently accommodated in the wide first region 81 during centrifugation. Further, the provision of the protruding portion 30 a allows the interface between the specimen 70 and the gas layer to be positioned radially outside in the separation chamber 30 as compared with the first embodiment. Thereby, the specimen 70 can be centrifuged in a short time. In addition, the provision of the protruding portion 30 a allows the liquid layer of the solid component 71 to be kept away from the rotating shaft 20 as compared with the first embodiment. Thereby, it can suppress that the solid component 71 is caught in the flow to the flow path 50 by a capillary phenomenon.

  Further, since the width L2 of the second region 82 is smaller than the width L3 of the first region 81, compared to the case where the entire inner wall on the T2 direction side of the second storage portion 32 protrudes in the T2 direction from the configuration of FIG. The interface between the air layer after centrifugation and the liquid component 72 is positioned closer to the rotating shaft 20 side. In this case, since the connection position of the flow path 50 with respect to the separation chamber 30 can be brought closer to the rotating shaft 20, the connection position of the flow path 50 is far from the liquid layer of the solid component 71. Thereby, it can suppress more reliably that the solid component 71 is caught in the flow to the flow path 50 by a capillary phenomenon.

  In addition, the first reservoir 31 of the second embodiment is disposed at a position that is biased toward the T2 direction with respect to the second region 82, and the flow path 50 is located on the T1 direction with respect to the first reservoir 31. The second region 82 is connected to the position. Thus, when the flow path 50 is connected to the inner wall 32a, the liquid component 72 can be prevented from leaving the connection position on the inner wall 32a of the flow path 50 while the liquid component 72 flows into the flow path 50 by capillary action. . Thereby, while the liquid component 72 flows into the flow path 50 by capillary action, the liquid component 72 can be continuously supplied to the flow path 50 stably. In this case, the way of the interface between the gas layer and the liquid component 72 will be described in detail in a specific configuration example described later.

  As shown in FIG. 5A, the separation chamber 30 according to the second embodiment is configured by providing a protruding portion 30a on the inner wall of the second storage portion 32 on the T2 direction side in the configuration shown in FIG. It was done. However, the present invention is not limited to this, and as shown in FIG. 5 (b), the separation chamber 30 is configured by providing the protrusion 30a in the configuration shown in FIG. 4 (a) as in FIG. 5 (a). May be. Further, as shown in FIG. 5 (c), the separation chamber 30 may be configured by providing a protruding portion 30a in the configuration shown in FIG. 4 (b) similarly to FIG. 5 (a). In the case of the configuration illustrated in FIG. 5C, the flow path 51 is connected to a boundary position between the first storage unit 31 and the second storage unit 32, for example.

<Embodiment 3>
As shown in FIG. 6A, in the third embodiment, compared to the configuration of the second embodiment shown in FIG. 5A, the separation chamber 30 is included in the inner wall of the second reservoir 32 on the T1 direction side. The inner wall portion on the radially outer side further includes a protruding portion 30b protruding in the T1 direction. In other words, the first region 81 of the third embodiment has a shape extending in the T1 direction as compared with the second embodiment. The first region 81 further includes an inner wall 81b extending in the rotation direction in plan view. The inner wall 81 b is located on the T1 direction side and the radial inner side in the first region 81 and is connected to the second region 82.

  In the third embodiment, the width L3 of the first region 81 is longer than the width L3 of the second embodiment. Thereby, the solid component 71 can be more efficiently accommodated in the first region 81 during centrifugation. Further, by providing the protrusion 30 b, the interface between the specimen 70 and the gas layer can be positioned further radially outward in the separation chamber 30 as compared with the second embodiment. Thereby, the specimen 70 can be centrifuged in a shorter time. In addition, the provision of the protruding portion 30 b allows the liquid layer of the solid component 71 to be further away from the rotating shaft 20 as compared with the second embodiment. Thereby, it can further suppress that the solid component 71 is caught in the flow to the flow path 50 by capillary action.

  As shown in FIG. 6A, the separation chamber 30 of the third embodiment is provided with a protrusion 30b on the inner wall on the T1 direction side of the second reservoir 32 in the configuration shown in FIG. 5A. Was made up of. However, the present invention is not limited to this, and as shown in FIG. 6 (b), the separation chamber 30 is configured by providing the protrusion 30b in the configuration shown in FIG. 5 (b) as in FIG. 6 (a). May be. Further, as shown in FIG. 6C, the separation chamber 30 may be configured by providing a protruding portion 30b in the configuration shown in FIG. 5C as in FIG. 6A.

<Specific configuration example>
Hereinafter, a specific configuration of the measurement apparatus and a specific configuration of the measurement cartridge according to the second embodiment illustrated in FIG. 5A will be described. In the following description, the description of the same configuration as that of the measurement cartridge 10 of Embodiment 2 described with reference to FIG.

  As shown in FIG. 7A, the measuring apparatus 100 uses the measurement cartridge 200 to separate the liquid component from the sample, detects the test substance in the liquid component using an antigen-antibody reaction, An immunoanalyzer that analyzes a test substance based on a detection result. Also in the specific configuration example, the sample is a blood sample of whole blood collected from the subject. The liquid component is a plasma component contained in a blood sample of whole blood. The solid component is a blood cell component contained in a blood sample of whole blood.

  The measuring apparatus 100 includes a main body 101 and a lid 102. In the main body 101, the portion other than the portion facing the lid 102 is covered with the housing 101 a. In the lid part 102, the part other than the part facing the main body part 101 is covered with the housing 102 a. The main body 101 supports the lid 102 so that it can be opened and closed. When the measurement cartridge 200 is attached or detached, the lid 102 is opened as shown in FIG. A measurement cartridge 200 is mounted on the upper portion of the main body 101. The main body 101 includes a rotation shaft 103 that extends parallel to the Z-axis direction. The rotating shaft 103 corresponds to the rotating shaft 20 of FIG. The measuring apparatus 100 rotates the attached measurement cartridge 200 about the rotation shaft 103. The internal configuration of the measuring apparatus 100 will be described later with reference to FIGS.

  As shown in FIG. 7B, the measurement cartridge 200 corresponds to the measurement cartridge 10 of the second embodiment shown in FIG. The measurement cartridge 200 is constituted by a plate-shaped and disk-shaped substrate 200a. FIG. 5A shows a part of the measurement cartridge 200. Each part in the measurement cartridge 200 is formed by bonding a recess formed on the substrate 200a and a film (not shown) covering the substrate 200a. The substrate 200a and the film attached to the substrate 200a are formed using a light-transmitting member. The thickness of the substrate 200a is, for example, several millimeters, specifically 1.2 mm. The substrate 200a is provided with a hole 200b penetrating the substrate 200a at the center of the substrate 200a. The measurement cartridge 200 is installed in the measurement apparatus 100 so that the center of the hole 200b coincides with the rotation shaft 103 of the measurement apparatus 100.

  The measurement cartridge 200 includes a sample inlet 201, a sample storage unit 202, a channel 203, holes 204 and 206, air introduction channels 205 and 207, valves 208a, 208b, and 208c, a separation chamber 210, A flow path 220, a flow path 231, an overflow chamber 232, a flow path 233, a disposal chamber 234, storage chambers 241 to 246, a flow path 250, a liquid storage portion 261, and a hole 262 are provided.

  As shown in FIG. 8, the sample insertion port 201, the sample storage unit 202, and the flow path 203 correspond to the sample input port 61, the sample storage unit 62, and the flow path 63 shown in FIG. The valve 208 a is provided between the specimen storage unit 62 and the flow path 203. The valve 208 a prevents the sample stored in the sample storage unit 202 from moving to the flow path 203 before the measurement cartridge 200 is rotated.

  The separation chamber 210 includes a first storage unit 211 and a second storage unit 212, and the second storage unit 212 includes a first region 271 and a second region 272. The separation chamber 210 corresponds to the separation chamber 30 shown in FIG. 5 (a), and the first storage part 211 and the second storage part 212 are respectively the first storage part 31 and the second storage part shown in FIG. 5 (a). The first region 271 and the second region 272 corresponding to the part 32 correspond to the first region 81 and the second region 82 shown in FIG.

  The 1st storage part 211 is provided with the inner wall 211a, and the 2nd storage part 212 is provided with the inner wall 212a. The inner walls 211a and 212a correspond to the inner walls 31a and 32a shown in FIG. Further, the inner wall 211a is connected to the inner wall 212a by a curved inner wall 211b that is inclined so as to gradually become parallel to the inner wall 212a from the edge of the inner wall 211a on the inner wall 212a side and is connected to the inner wall 212a. That is, the inner wall 211a extending in the radial direction in plan view and the inner wall 212a extending in the rotation direction in plan view are smoothly connected by the curved inner wall 211b.

  The first region 271 includes an inner wall 271a. The inner wall 271a corresponds to the inner wall 81a shown in FIG. The width in the rotation direction of the inner wall 271a is larger than the width in the rotation direction of the inner wall 212a. The protruding portion 210a is a portion of the first region 271 that protrudes in the T2 direction with respect to the second region 272. The protrusion 210a corresponds to the protrusion 30a shown in FIG.

  An air introduction path 205 is connected to the inner wall of the separation chamber 30 that is located on the inner side in the radial direction and extends in the rotational direction in plan view. The hole 204 is provided inside the air introduction path 205 in the radial direction, and opens the inside in the radial direction of the air introduction path 205 to the outside of the measurement cartridge 200.

  An air introduction path 207 is connected to the connection position 220 a of the flow path 220. The hole 206 is provided inside the air introduction path 207 in the radial direction, and opens the inside in the radial direction of the air introduction path 207 to the outside of the measurement cartridge 200. The air introduction path 207 introduces air into the flow path 220 at the connection position 220a. The hole 206, the air introduction path 207, and the connection position 220a correspond to the hole 64, the air introduction path 65, and the connection position 50a shown in FIG. 1, respectively. The valve 208b is provided between the air introduction path 207 and the connection position 220a. The valve 208 b prevents the liquid component that has entered the flow path 220 due to the capillary phenomenon from entering the air introduction path 207.

  The channel 220 includes a channel 221 and a channel 222. The flow path 220 corresponds to the flow path 50 shown in FIG. 5A, and the flow paths 221 and 222 correspond to the flow path 51 and the flow path 52 shown in FIG. 5A, respectively. The valve 208 c is provided between the flow path 222 and the storage chamber 241 on the storage chamber 241 side of the flow path 222. The valve 208c is provided to stop the movement of the liquid component due to capillary action. In other words, the valve 208 c prevents the liquid component that has entered the flow path 220 from the separation chamber 210 due to capillary action from entering the accommodation chamber 241.

  The channel 231 connects the channel 221 and the overflow chamber 232. Specifically, the end of the flow channel 231 on the flow channel 221 side is connected to a branch position 221 a closer to the separation chamber 210 than the center of the flow channel 221. The channel 231 is provided with a storage portion 231a. The overflow chamber 232 contains unnecessary specimens and unnecessary liquid components. That is, the overflow chamber 232 is provided for discarding unnecessary specimens and unnecessary liquid components.

  The flow path 233 connects the first region 271 and the waste chamber 234. Specifically, one end of the flow path 233 is connected to the inner wall 271 a of the first region 271. The flow path 233 moves the liquid component remaining in the separation chamber 210 after moving the liquid component from the separation chamber 210 to the accommodating chamber 241 from the first region 271 toward the waste chamber 234 by the principle of siphon. The waste chamber 234 contains unnecessary liquid components. That is, the disposal chamber 234 is provided for discarding unnecessary liquid components.

  Returning to FIG. 7B, the accommodation chambers 241 to 246 are arranged in the rotation direction in the vicinity of the outer periphery of the substrate 200a. The accommodation chamber 241 corresponds to the accommodation chamber 40 shown in FIG. The flow path 250 includes an arc-shaped region extending in the rotation direction and a region for moving the reagent in the liquid storage unit 261 toward the corresponding storage chamber. The liquid storage unit 261 stores a reagent and includes sealing bodies 261a and 261b. The sealing bodies 261a and 261b are configured to be able to be opened by being pressed from above by a pressing portion 124 described later. When the sealing bodies 261 a and 261 b are opened, the radially inner side of the liquid storage portion 261 is opened to the outside of the measurement cartridge 200 through the hole 262, and the radially outer side of the liquid storage portion 261 becomes the flow path 250. Connected. Thereby, the reagent in the liquid storage unit 261 can be transferred to the corresponding storage chamber among the storage chambers 241 to 246 through the flow path 250 by centrifugal force.

  Note that each configuration of the measurement cartridge 200 illustrated in FIG. 7B is formed only in one third of the substrate 200a. However, the present invention is not limited to this, and the group of configurations may be formed in the remaining two thirds of the regions, and three groups of configurations may be provided on the substrate 200a.

  FIG. 9A is a diagram schematically showing the configuration of the separation chamber 210 when the C1-C2 cross section shown in FIG. 8 is viewed in the negative Y-axis direction. In FIG. 9A, the X axis positive direction indicates a direction toward the rotation axis 103, and the X axis negative direction indicates a direction away from the rotation axis 103.

  As shown in FIG. 9A, the separation chamber 210 includes a lower surface 273 as an inner wall located on the Z-axis positive direction side, and an upper surface 274 as an inner wall located on the Z-axis negative direction side. The lower surface 273 is a plane parallel to the XY plane. The upper surface 274 includes a first inclined portion 274a, a second inclined portion 274b, and flat portions 274c, 274d, 274e.

  The first inclined portion 274 a increases the thickness of the space in the second storage portion 212 as the distance from the rotation shaft 103 increases. The first inclined portion 274 a is provided in the first region 271 of the separation chamber 210. The second inclined portion 274 b decreases the thickness of the space in the second storage portion 212 as it moves away from the rotation shaft 103. The second inclined portion 274 b is provided in the second region 272 of the separation chamber 210. The flat portion 274c is a plane parallel to the XY plane, and connects the first inclined portion 274a and the second inclined portion 274b.

  The flat part 274d is a plane parallel to the XY plane, and the thickness of the space in the second storage part 212 in the first region 271 is defined as H1. The flat part 274e is a plane parallel to the XY plane, and the thickness of the space in the second storage part 212 in the second region 272 and the thickness of the space in the first storage part 211 are defined as H2. The flat portion 274c defines the thickness of the space in the second storage portion 212 at the boundary between the first region 271 and the second region 272 as H3. The relationship between the thicknesses H1 to H3 is H1> H2> H3.

  By providing the first inclined portion 274a, the thickness of the region radially outside the first inclined portion 274a can be increased, and the capacity of the region radially outside the first inclined portion 274a can be increased. This makes it easier for the solid component to stay in the radially outer region than the first inclined portion 274a due to the boycott effect during centrifugation, thereby increasing the efficiency of centrifugation. In addition, since the liquid component can be smoothly moved from the radially outer side of the second reservoir 212 to the radially inner side along the first inclined portion 274a, the liquid component is solid in a region radially outward from the first inclined portion 274a. Ingredients can be collected efficiently.

  By providing the second inclined portion 274b, the thickness of the region radially outside the second inclined portion 274b can be reduced, and the thickness of the region radially outward from the second inclined portion 274b can be reduced. Thereby, the solid component which moved to the radial direction outer side from the 2nd inclination part 274b by centrifugal force becomes difficult to return to a radial direction inner side. Therefore, it can suppress effectively that the solid component after centrifugation mixes in the flow path 220. FIG. Further, during the centrifugation, the solid component can be smoothly moved along the second inclined portion 274b to the radially outer side of the second inclined portion 274b.

  By providing the first inclined portion 274a and the second inclined portion 274b, the convex portion is disposed between the first region 271 in which the solid component is stored and the second region 272 in which the liquid component is stored. Become. Specifically, a flat portion 274 c that protrudes in the direction of reducing the thickness of the separation chamber 30 is provided between the first region 271 and the second region 272. Thereby, it can prevent more effectively that a solid component mixes in a liquid component.

  The thickness of the space in the second storage part 212 in the first region 271 is H1, and the thickness of the space in the second storage part 212 in the second region 272 is H2 smaller than H1. Thereby, the solid component can be efficiently retained in the first region 271.

  The first inclined portion 274a and the second inclined portion 274b are connected by a flat portion 274c. As a result, the solid component is less likely to move in the range where the flat portion 274c is provided, so that the solid component staying radially outward from the first inclined portion 274a by the centrifugal separation passes through the flat portion 274c and becomes a liquid component. Mixing is suppressed. Therefore, it can prevent more effectively that a solid component mixes in the liquid component taken in into the flow path 220 by capillary action.

  Note that the separation chamber 210 is not limited to the configuration illustrated in FIG. 9A, and may be configured, for example, as illustrated in FIGS. 9B and 9C. In the configuration shown in FIG. 9B, the first inclined portion 274a and the flat portion 274c are omitted from the upper surface 274 of the separation chamber 210 as compared with FIG. 9A. Also in this case, the effect by the 2nd inclination part 274b is show | played. In the configuration shown in FIG. 9C, the second inclined portion 274b and the flat portion 274c are omitted from the upper surface 274 of the separation chamber 210 as compared with FIG. 9A. Also in this case, the effect by the 1st inclination part 274a is show | played.

  In addition, in the configuration illustrated in FIG. 9A, the flat portion 274c may be omitted, and the first inclined portion 274a and the second inclined portion 274b may be adjacent to each other. Further, the configuration such as the inclined portion and the flat portion is not limited to being provided on the upper surface 274 but may be provided on the lower surface 273 or may be provided on both the lower surface 273 and the upper surface 274. Further, the inclined surface of the first inclined portion 274a and the inclined surface of the second inclined portion 274b do not necessarily have to be flat as shown in FIG. 9A, and may have irregularities.

  In the configuration shown in FIG. 9A, the first inclined portion 274a may be omitted, and the flat portion 274c and the flat portion 274d may be connected by a plane parallel to the YZ plane. In the configuration shown in FIG. 9C, the first inclined portion 274a may be omitted, and the flat portion 274d and the flat portion 274e may be connected by a plane parallel to the YZ plane. In the configuration shown in FIG. 9A, the second inclined portion 274b may be omitted, and the flat portion 274c and the flat portion 274e may be connected by a plane parallel to the YZ plane. In the configuration shown in FIG. 9B, the second inclined portion 274b may be omitted, and the flat portion 274d and the flat portion 274e may be connected by a plane parallel to the YZ plane.

  FIG. 10A is an enlarged view schematically showing the vicinity of the valve 208c.

  As shown in FIG. 10A, the valve 208c includes a flow path 275a, a space 275b, and a flow path 275c. The flow path 275 a is connected to the flow path 222, and the flow path 275 c is connected to the accommodation chamber 241. The space 275b connects the flow path 275a and the flow path 275c.

  The flow path 275a is configured such that the width of the flow path 275a is sharply smaller than the width of the flow path 222 at the connection portion 276a between the flow path 222 and the flow path 275a. The space 275b is configured such that the width of the space 275b is abruptly larger than the width of the flow path 275a at the connecting portion 276b between the flow path 275a and the space 275b. The flow path 275 c is configured such that, at a connection portion 276 c between the flow path 275 c and the storage chamber 241, the width of the flow path 275 c is sharply smaller than the width of the storage chamber 241. The cross-sectional areas of the flow paths 275a and 275c are constant. Note that the cross-sectional areas of the flow paths 275a and 275c are not necessarily constant. The flow paths 275a and 275c and the space 275b are configured to have low wettability with respect to the liquid.

  In the connection portion 276a, the width of the flow path 275a is abruptly smaller than the width of the flow path 222, and the flow path 275a has low wettability with respect to the liquid. As a result, as shown in FIG. 10B, even if the liquid component 282 in the flow path 222 reaches the connection portion 276a due to capillary action, the liquid component 282 is less likely to enter the flow path 275a. Therefore, the liquid component 282 in the flow path 222 can be prevented from entering the storage chamber 241 due to capillary action.

  Here, normally, the liquid component 282 in the flow path 222 does not enter the flow path 275a for the reason described above. However, the liquid component 282 in the flow path 222 may enter the flow path 275a due to capillary action. Therefore, the valve 208c is further provided with a space 275b and a flow path 275c in addition to the flow path 275a.

  In the connection portion 276b, the width of the space 275b is abruptly larger than that of the flow path 275a, and the space 275b has low wettability with respect to the liquid. As a result, as shown in FIG. 10C, even when the liquid component 282 reaches the connection portion 276b due to capillary action, the liquid component 282 in the flow path 275a enters the space 275b due to the surface tension of the liquid component 282. It becomes difficult to do. Therefore, it is possible to reliably suppress the liquid component 282 of the flow path 222 from entering the storage chamber 241 due to the capillary phenomenon.

  Further, in the connection portion 276c, the width of the storage chamber 241 is rapidly increased as compared with the width of the flow path 275c. As a result, as shown in FIG. 10D, even if the liquid component 282 reaches the connection portion 276c due to capillary action, the liquid component 282 in the flow path 275c is brought into the storage chamber 241 due to the surface tension of the liquid component 282. It becomes difficult to enter. Therefore, it is possible to reliably suppress the liquid component 282 of the flow path 222 from entering the storage chamber 241 due to the capillary phenomenon.

  The valve 208a also includes channels 275a and 275c and a space 275b, like the valve 208c. That is, the width of the flow path in the valve 208a is abruptly smaller than the width of the specimen storage unit 202 and the flow path 203, and the width of the space in the valve 208a is the flow path in the valve 208a. Compared to the size of, it is growing rapidly. Thereby, the valve 208a can suppress the sample in the sample container 202 from entering the flow path 203 due to a capillary phenomenon. In addition, the valve 208b includes flow paths 275a and 275c and a space 275b, similar to the valve 208c. That is, the width of the flow path in the valve 208b is abruptly smaller than the width of the air introduction path 207 and the flow path 220, and the width of the space in the valve 208b is the flow path in the valve 208b. Compared to the size of, it is growing rapidly. Accordingly, the valve 208b can suppress the liquid component in the flow path 220 from entering the air introduction path 207 due to a capillary phenomenon.

  Next, the internal configuration of the measurement apparatus 100 will be described with reference to FIGS.

  The main body 101 includes an installation member 111, a plate member 112, a support member 113, a magnetic force application unit 114, a detection unit 115, a container 116, a motor 117, and an encoder 118.

  The installation member 111 has a shape that fits into the housing 101a. The plate member 112 is installed at the center of the upper surface of the installation member 111. The plate member 112 is made of a metal having high thermal conductivity. A heater 131 described later is installed on the lower surface of the plate member 112. The support member 113 is installed at the center of the installation member 111 via an installation member 119 described later. The support member 113 is constituted by a turntable, for example.

  The magnetic force application unit 114 is installed on the lower surface of the installation member 111 so as to face the lower surface of the measurement cartridge 200 installed on the support member 113 through a hole formed in the installation member 111 and the plate member 112. . The magnetic force application unit 114 includes a magnet and a mechanism for moving the magnet in the Z-axis direction and the radial direction. The detection unit 115 is installed on the lower surface of the installation member 111 so as to face the lower surface of the measurement cartridge 200 installed on the support member 113 through a hole formed in the installation member 111 and the plate member 112. The detection unit 115 includes a photodetector. The photodetector of the detection unit 115 optically detects the test substance accommodated in the accommodation chamber 246. The photodetector of the detection unit 115 is configured by, for example, a photomultiplier tube, a phototube, a photodiode, or the like.

  The container 116 is installed on the lower surface of the installation member 111. The accommodating body 116 includes a lower surface 116a and accommodating portions 116b and 116c. A hole 116d to be described later is formed at the center of the upper surface of the container 116. The hole 116d penetrates from the upper surface to the lower surface 116a of the container 116 in the vertical direction. The rotation shaft 103 is passed through the hole 116d. The accommodating portions 116b and 116c are configured by concave portions that are recessed downward from the upper surface of the accommodating body 116. The accommodating portions 116b and 116c accommodate the magnetic force applying portion 114 and the detecting portion 115, respectively. The motor 117 is configured by a stepping motor. The motor 117 is installed on the lower surface 116a and rotates the rotation shaft 103 with the Z axis as the center of rotation. The encoder 118 is installed on the lower surface of the motor 117, and detects the rotation of a drive shaft 117a of the motor 117 described later.

  FIG. 11 shows a state in which the lid 102 is viewed from below. The lid portion 102 includes an installation member 121, a plate member 122, a clamper 123, and two pressing portions 124.

  The installation member 121 has a shape that fits into the housing 102a. The plate member 122 is installed at the center of the bottom surface of the installation member 121. The plate member 122 is made of a metal having high thermal conductivity, like the plate member 112. A heater 132 described later is installed on the upper surface of the plate member 122. The clamper 123 is installed at the center of the installation member 121. The two pressing portions 124 are installed on the upper surface of the installation member 121. The two pressing portions 124 are arranged in the radial direction of the measurement cartridge 200 installed on the support member 113 when the lid portion 102 is closed. The pressing portion 124 on the radially inner side presses the sealing body 261a from above through a hole formed in the installation member 121 and the plate member 122, and opens the sealing body 261a by pressing force. The pressing portion 124 on the radially outer side presses the sealing body 261b from above through a hole formed in the installation member 121 and the plate member 122, and opens the sealing body 261b by pressing force.

  When the measuring apparatus 100 is assembled, the installation member 111 and the container 116 assembled as shown in FIG. 11 are installed in the housing 101a, and the main body 101 is completed. Then, the lid portion 102 assembled as shown in FIG. 11 is installed so that it can be opened and closed with respect to the installation member 111 of the main body portion 101, whereby the lid portion 102 is installed on the main body portion 101. In this way, the measuring apparatus 100 is completed.

  FIG. 12 is a schematic diagram showing a cross section of the measuring apparatus 100 when cut along a plane parallel to the YZ plane passing through the rotation shaft 103. FIG. 12 shows a state where the measurement cartridge 200 is installed in the measurement apparatus 100 and the lid 102 is closed. As described above, the magnetic force application unit 114 and the detection unit 115 are installed on the lower surface of the installation member 111, and the two pressing units 124 are installed on the upper surface of the installation member 121. In FIG. 12, positions corresponding to the arrangement positions of these parts are indicated by broken lines.

  As shown in FIG. 12, the drive shaft 117a of the motor 117 extends into the hole 116d. An installation member 119 is installed above the hole 116d. The installation member 119 rotatably supports a rotary shaft 103 extending in the vertical direction. The rotation shaft 103 is fixed to the drive shaft 117a of the motor 117 by a fixing member 117b inside the hole 116d.

  A support member 113 for supporting the lower surface of the measurement cartridge 200 is fixed to the upper portion of the rotating shaft 103 via a predetermined member. When the motor 117 is driven and the drive shaft 117 a rotates, the rotational driving force is transmitted to the support member 113 through the rotation shaft 103. As a result, the measurement cartridge 200 installed on the support member 113 rotates about the rotation shaft 103. When the measurement cartridge 200 is installed on the support member 113 and the lid portion 102 is closed, the clamper 123 presses the inner peripheral portion of the upper surface of the measurement cartridge 200 in a rotatable state.

  A heater 131 is installed on the lower surface of the plate member 112, and a heater 132 is installed on the upper surface of the plate member 122. The heaters 131 and 132 are disposed so that the heat generation surface is flat and the heat generation surface is parallel to the measurement cartridge 200. Thereby, the measurement cartridge 200 can be efficiently heated. The plate members 112 and 122 are provided with temperature sensors 141 and 142 shown in FIG. 13, respectively. The temperature sensors 141 and 142 detect the temperatures of the plate members 112 and 122, respectively. The control unit 151 to be described later, when performing the measurement, causes the heaters 131 and 132 so that the temperature of the plate member 112 detected by the temperature sensor 141 and the temperature of the plate member 122 detected by the temperature sensor 142 become a predetermined temperature. Drive.

  The magnetic force application unit 114 applies a magnetic force to the measurement cartridge 200 using a magnet, as indicated by an upward dotted arrow in FIG. The detection unit 115 receives light generated from the accommodation chamber 246 of the measurement cartridge 200 as indicated by a downward dotted arrow in FIG. When the lid 102 is closed, the passage of light is prevented between the space where the measurement cartridge 200 is located and the outside. Thereby, even if the light generated in the reaction process in the storage chamber 246 is very weak, light does not enter from the outside into the space where the measurement cartridge 200 is located. Therefore, the light generated by the reaction is detected by the photodetector of the detection unit 115. It becomes possible to detect with high accuracy.

  As shown in FIG. 13, the measuring apparatus 100 includes a magnetic force application unit 114, a detection unit 115, a motor 117, an encoder 118, a pressing unit 124, heaters 131 and 132, temperature sensors 141 and 142, and a control. Unit 151, display unit 152, input unit 153, drive unit 154, and sensor unit 155.

  Control unit 151 includes, for example, an arithmetic processing unit and a storage unit. The arithmetic processing unit is configured by, for example, a CPU, an MPU, and the like. The storage unit is configured by, for example, a flash memory or a hard disk. The control unit 151 receives signals from each unit of the measurement apparatus 100 and controls each unit of the measurement apparatus 100. The display unit 152 and the input unit 153 are provided, for example, on the side surface portion of the main body unit 101 or the upper surface portion of the lid unit 102. The display unit 152 is configured by, for example, a liquid crystal panel. The input unit 153 includes, for example, buttons and a touch panel. The drive unit 154 includes other mechanisms arranged in the measurement apparatus 100. The sensor unit 155 includes a sensor for detecting a predetermined part of the measurement cartridge 200 installed on the support member 113 and another sensor arranged in the measurement apparatus 100.

  Next, the operation of the measuring apparatus 100 will be described with reference to FIG.

  First, the operator inputs a sample collected from the subject through the sample insertion port 201 and installs the measurement cartridge 200 on the support member 113. A sample input from the sample input port 201 is stored in the sample storage unit 202. The test substance in the specimen includes, for example, an antigen. As an example, the antigen is hepatitis B surface antigen (HBsAg). The test substance may be one or more of an antigen, an antibody, or a protein.

  A predetermined reagent is previously stored in the seven liquid storage portions 261 and the storage chamber 241 of the measurement cartridge 200. Specifically, the R1 reagent is stored in the liquid storage unit 261 located in the radial direction of the storage chamber 241. The storage chamber 241 stores the R2 reagent. The liquid storage unit 261 located in the radial direction of the storage chamber 242 stores the R3 reagent. A cleaning liquid is stored in the liquid storage portion 261 located in the radial direction of the storage chambers 243 to 245. The liquid storage unit 261 located in the radial direction of the storage chamber 246 stores the R4 reagent. The liquid storage unit 261 adjacent to the T1 direction side of the liquid storage unit 261 storing the R4 reagent stores the R5 reagent.

  In the following control, the control unit 151 acquires the rotational position of the drive shaft 117a of the motor 117 based on the output signal of the encoder 118 connected to the motor 117. The controller 151 acquires a position in the rotation direction of the measurement cartridge 200 by detecting a predetermined part of the rotating measurement cartridge 200 with a sensor. Alternatively, the measurement cartridge 200 may be installed at a predetermined position with respect to the support member 113. As a result, the control unit 151 can position each part of the measurement cartridge 200 at a predetermined position in the rotation direction.

  Upon receiving a start instruction from the operator via the input unit 153, the control unit 151 starts the process illustrated in FIG. In step S <b> 11, the control unit 151 separates the specimen and transfers the liquid component to the storage chamber 241.

  Here, the process of step S11 will be described in detail with reference to FIG. The flowchart in FIG. 15 is a flowchart showing in detail the processing in step S11 in FIG. In the following description, FIG. 15 will be mainly referred to, and the state transition diagrams of FIGS. 16A to 18B will be appropriately referred to.

  Before the process of step S11 of FIG. 14 and step S101 of FIG. 15 are started, the sample storage unit 202 stores the sample 280 as shown in FIG. In step S101, the control unit 151 drives the motor 117 to rotate the measurement cartridge 200, and as shown in FIG. 16B, the sample 280 in the sample storage unit 202 is transferred to the separation chamber 210 by centrifugal force. To do.

  During the transfer of the specimen 280, the interface between the specimen 280 and the gas layer approaches the rotation shaft 103 in the separation chamber 210, the flow path 233, and the flow path 221. However, since the flow path 231 is connected to the flow path 221 at the branch position 221a, if the interface between the sample 280 and the air layer crosses the branch position 221a radially inward, the sample that has crossed the branch position 221a. 280 is discarded through the flow path 231 into the overflow chamber 232. Thereby, even if the amount of the sample 280 input from the sample input port 201 varies, a predetermined amount of the sample 280 is stored in the separation chamber 210, and the interface between the sample 280 and the gas layer in the separation chamber 210 is , Positioned at a predetermined position in the radial direction.

  In step S102, the control unit 151 drives the motor 117 to rotate the measurement cartridge 200, and the solid component 281 and the liquid component are separated from the specimen 280 in the separation chamber 210 by centrifugal force as shown in FIG. 282. At this time, the interface between the solid component 281 and the liquid component 282 is positioned in the first region 271. Here, since the flow path 220 extends radially inward from the separation chamber 210, the specimen 280 that has entered the flow path 221 before the centrifugation as shown in FIG. As a result, the flow smoothly moves from the flow path 221 to the separation chamber 210. Therefore, the solid component 281 can be prevented from remaining in the flow path 220 after centrifugation.

  Subsequently, in step S103, the control unit 151 waits for a predetermined time without rotating the measurement cartridge 200, whereby the liquid component 282 in the separation chamber 210 is caused by capillary action as shown in FIG. Is transferred to the flow path 220. In step S103, when the liquid component 282 in the separation chamber 210 moves to the flow path 220, the interface between the gas layer and the liquid component 282 gradually moves outward in the radial direction as shown by a dotted line in FIG. Go ahead. At the same time, the liquid component 282 in the separation chamber 210 is filled in the flow path 233 by capillary action.

  Here, since the length of the first reservoir 211 is shorter than the length of the second reservoir 212 in the rotation direction, the interface between the liquid component 282 and the gas layer that appears in the first reservoir 211 after centrifugation is solid. Large separation from the liquid layer of component 281. Thus, when the interface between the liquid component 282 and the gas layer is far away from the liquid layer of the solid component 281, the position where the flow path 220 is connected to the separation chamber 210 is the position far away from the liquid layer of the solid component 281. Can be set. Thereby, it is possible to avoid the solid component 281 after the centrifugation from being caught in the flow generated by the capillary phenomenon in the flow path 50.

  In addition, a curved inner wall 211 b is provided between the inner wall 211 a of the first reservoir 211 and the inner wall 212 a of the second reservoir 212. As a result, when the liquid component 282 moves from the first reservoir 211 to the flow path 50 by capillary action, the flow of the liquid component 282 changes smoothly along the curved inner wall 211b, and therefore T2 of the inner wall 212a. The occurrence of turbulent flow of the liquid component 282 near the end on the direction side is suppressed. For this reason, it can suppress that the solid component 281 is caught in such a turbulent flow, and mixes in the flow path 220.

  The first reservoir 211 is disposed at a position that is biased in the T2 direction with respect to the second region 272, and the flow path 50 is at a position of the second region 272 on the T1 direction side with respect to the first reservoir 211. Thus, while the liquid component 282 flows into the flow path 220 by capillary action, the interface between the gas layer and the liquid component 282 is on the flow path 220 side as shown by a dotted line in FIG. The end portion of the head is inclined in a state closer to the rotation shaft 103 than the end portion on the side opposite to the flow path 220, and proceeds in a direction away from the rotation shaft 103. That is, the interface advances in a direction away from the rotation shaft 103 in a state where the end of the interface on the T1 direction side is closer to the radially inner side than the end of the interface on the T2 direction side. Thereby, it can suppress that the liquid component 282 leaves | separates from the connection position in the inner wall 212a of the flow path 220. FIG. Therefore, the liquid component 282 can be stably supplied to the flow path 50 while the liquid component 282 flows into the flow path 50 by capillary action.

  In the vicinity of the inner wall 212a, the interface between the gas layer and the liquid component 282 advances in the T1 direction. Therefore, in order to transfer a sufficient amount of the liquid component 282 to the flow path 220, the flow path 50 is preferably connected to the inner wall 212a as close to the T1 direction as possible.

  In the rotation direction, the inner wall 271a is longer than the inner wall 212a. Thus, the portion of the first region 271 that protrudes in the T2 direction with respect to the second region 272, that is, the protruding portion 210a shown in FIG. The solid component 281 accumulated in the protruding portion 210a by centrifugation is not easily affected by the flow due to the capillary phenomenon, and is likely to remain in the protruding portion 210a even after centrifugation. For this reason, the solid component 281 accumulated in the protruding portion 210a by centrifugation is hardly mixed into the flow generated by the capillary phenomenon. Therefore, the amount of the solid component 281 accumulated in the protrusion 210a can be increased by increasing the length of the protrusion 210a by lengthening the inner wall 271a. Therefore, it can prevent more effectively that the solid component 281 after centrifugation flows into the flow path 220 by capillary action.

  In addition, a valve 208 c is provided on the side of the accommodation chamber 241 of the flow path 222. The valve 208 c prevents the liquid component 282 transferred to the flow path 50 from moving to the storage chamber 241 as shown in FIG. As a result, the liquid component 282 can be accumulated by capillary action in the range of the flow path 222 from the connection position 220a to the valve 208c, and in the next step S104, the amount of the liquid component 282 defined in the range of the flow path 222 is obtained. Can be transferred to the storage chamber 241. Therefore, the quantitative property of the liquid component 282 moving to the storage chamber 241 is improved.

  Subsequently, in step S104, the control unit 151 drives the motor 117 to rotate the measurement cartridge 200, and centrifuges the liquid component 282 in the flow path 222 as shown in FIGS. 18 (a) and 18 (b). Transfer to the storage chamber 241 by force. 18A is a diagram illustrating a state in the middle of transferring the liquid component 282 in the flow path 222 to the storage chamber 241, and FIG. 18B is a diagram illustrating a state in which the transfer of the liquid component 282 is completed. It is. Thus, the liquid component 282 determined by the flow path 222 is transferred to the storage chamber 241.

  When the measurement cartridge 200 is rotated in step S104, the liquid component 282 in the flow path 221 is transferred to the overflow chamber 232 through the flow path 231 by centrifugal force. A part of the liquid component 282 in the flow path 221 is returned to the separation chamber 210 by centrifugal force.

  In step S104, when a centrifugal force is applied to the measurement cartridge 200 from the state of FIG. 17B, the liquid component 282 in the separation chamber 210 is applied according to the siphon principle as shown in FIG. 18A. Is transferred to the waste chamber 234 through the flow path 233. As a result, as shown in FIG. 18B, the liquid component 282 remaining in the separation chamber 210 is transferred to the waste chamber 234, and the interface between the gas layer in the separation chamber 210 and the liquid component 282 reaches the inner wall 212a. It is moved away from the connecting position of the flow path 220 radially outward. Therefore, after the liquid component 282 is moved from the separation chamber 210 to the storage chamber 241, the liquid component 282 remaining in the separation chamber 210 is prevented from flowing into the flow path 220 again toward the storage chamber 241 due to capillary action. it can. Therefore, the amount of the liquid component 282 transferred to the storage chamber 241 can be stabilized, and the measurement accuracy of the liquid component 282 can be increased.

  The flow path 233 is connected to the inner wall 271a. Accordingly, as shown in FIG. 18A, when the liquid component 282 in the separation chamber 210 is discarded into the disposal chamber 234, the solid component 281 is mixed into the flow path 233, and the flow path 233 becomes a solid component. 281 can prevent clogging.

  Returning to FIG. 14, in step S12, the control unit 151 transfers the reagent to the storage chamber. Specifically, the control unit 151 drives the motor 117 to rotate the measurement cartridge 200, and positions the sealing bodies 261a and 261b aligned in the radial direction directly below the two pressing units 124. And the control part 151 drives the two press parts 124, pushes down sealing body 261a, 261b, and opens sealing body 261a, 261b. The controller 151 repeatedly performs such a plug opening operation to open the six sealing bodies 261a and the six sealing bodies 261b located in the radial direction of the storage chambers 241 to 246. Then, the control unit 151 drives the motor 117 to rotate the measurement cartridge 200, and the reagent stored in the six liquid storage units 261 positioned in the radial direction of the storage chambers 241 to 246 is caused to flow by centrifugal force. They are transferred to the storage chambers 241 to 246 through the passage 250, respectively.

  Thereby, the R1 reagent is transferred to the storage chamber 241, and the liquid component, the R1 reagent, and the R2 reagent are mixed in the storage chamber 241. The R3 reagent is transferred to the storage chamber 242, the cleaning liquid is transferred to the storage chambers 243 to 245, and the R4 reagent is transferred to the storage chamber 246.

  Furthermore, when the transfer of the reagent is finished in step S12, the control unit 151 performs a stirring process. Specifically, the control unit 151 drives the motor 117 so as to switch between two different rotation speeds at a predetermined time interval while rotating in a predetermined direction. Thereby, the liquid in the storage chambers 241 to 246 is stirred by changing the Euler force generated in the rotation direction at predetermined time intervals. Such a stirring process is similarly performed not only in step S12 but also in steps S13 to S18 after the transfer process.

  Here, the R1 reagent includes a capture substance that binds to the test substance. The capture substance includes, for example, an antibody that binds to the test substance. The antibody is, for example, a biotin-conjugated HBs monoclonal antibody. The R2 reagent includes magnetic particles and a magnetic particle suspension. The magnetic particles are, for example, streptavidin-coupled magnetic particles whose surfaces are coated with avidin. In step S12, when the liquid component separated from the specimen, the R1 reagent, and the R2 reagent are mixed and stirred, the test substance and the R1 reagent are bound by an antigen-antibody reaction. And the test substance couple | bonded with the capture | acquisition substance of R1 reagent couple | bonds with a magnetic particle through a capture substance by reaction of an antigen-antibody reactant and a magnetic particle. In this way, a complex in which the test substance and the magnetic particles are combined is generated.

  Next, in step S <b> 13, the control unit 151 transfers the complex in the storage chamber 241 from the storage chamber 241 to the storage chamber 242.

  Specifically, the control unit 151 drives the motor 117 to rotate the measurement cartridge 200 and positions the accommodation chamber 241 immediately above the magnet of the magnetic force application unit 114. The control unit 151 drives the magnetic force application unit 114 to bring the magnet closer to the lower surface of the measurement cartridge 200 and collect the composites that spread in the accommodation chamber 241. The control unit 151 drives the magnetic force application unit 114 to move the magnet inward in the radial direction, and transfers the composite in the accommodation chamber 241 to the arc-shaped region of the flow path 250. The control unit 151 drives the motor 117 to rotate the measurement cartridge 200 and transfers the composite along the arc-shaped region of the flow path 250. The control unit 151 drives the magnetic force application unit 114 to move the magnet outward in the radial direction, and transfers the composite to the accommodation chamber 242. Then, the control unit 151 drives the magnetic force application unit 114 to separate the magnet from the lower surface of the measurement cartridge 200.

  As described above, the process of step S13 is performed. In addition, the transfer of the complex in steps S14 to S17 is performed in the same manner as in step S13.

  Thus, in the storage chamber 242, the complex generated in the storage chamber 241 and the R3 reagent are mixed. Here, the R3 reagent contains a labeling substance. The labeling substance includes a capture substance that specifically binds to the test substance and a label. For example, the labeling substance is a labeled antibody in which an antibody is used as a capture substance. In step S13, when the complex generated in the storage chamber 241 and the R3 reagent are mixed and stirred, the complex and the labeled antibody contained in the R3 reagent react. As a result, a complex in which the test substance, the capture antibody, the magnetic particles, and the labeled antibody are bound to each other is generated.

  In step S <b> 14, the control unit 151 transfers the complex in the storage chamber 242 from the storage chamber 242 to the storage chamber 243. Thereby, in the storage chamber 243, the composite produced in the storage chamber 242 and the cleaning liquid are mixed. In step S <b> 14, when the composite generated in the storage chamber 242 is mixed with the cleaning liquid and a stirring process is performed, the composite and the unreacted substance are separated in the storage chamber 243. That is, in the storage chamber 243, unreacted substances are removed by cleaning.

  In step S <b> 15, the control unit 151 transfers the complex in the storage chamber 243 from the storage chamber 243 to the storage chamber 244. Thereby, in the storage chamber 244, the composite produced in the storage chamber 242 and the cleaning liquid are mixed. Also in the storage chamber 244, unreacted substances are removed by cleaning.

  In step S <b> 16, the control unit 151 transfers the complex in the storage chamber 244 from the storage chamber 244 to the storage chamber 245. Thereby, in the storage chamber 245, the composite produced in the storage chamber 242 and the cleaning liquid are mixed. Also in the storage chamber 245, unreacted substances are removed by cleaning.

  In step S <b> 17, the control unit 151 transfers the complex in the storage chamber 245 from the storage chamber 245 to the storage chamber 246. Thereby, in the storage chamber 246, the complex produced in the storage chamber 242 and the R4 reagent are mixed. Here, the R4 reagent is a reagent for dispersing the complex generated in the storage chamber 242. The R4 reagent is, for example, a buffer solution. In step S17, the complex generated in the storage chamber 242 is mixed with the R4 reagent, and when the stirring process is performed, the complex generated in the storage chamber 242 is dispersed.

  In step S <b> 18, the control unit 151 transfers the R5 reagent to the storage chamber 246. Specifically, the control unit 151 drives the motor 117 to rotate the measurement cartridge 200, and positions the sealing bodies 261a and 261b positioned closest to the T1 direction side immediately below the two pressing units 124. And the control part 151 drives the two press parts 124, pushes down sealing body 261a, 261b, and opens sealing body 261a, 261b. Then, the control unit 151 drives the motor 117 to rotate the measurement cartridge 200, and the R5 reagent stored in the liquid storage unit 261 located on the most T1 direction side by the centrifugal force is passed through the flow path 250. Transfer to storage chamber 246. Thereby, in the storage chamber 246, the R5 reagent is further mixed with the liquid mixture generated in step S17.

  Here, the R5 reagent is a luminescent reagent containing a luminescent substrate that generates light by reaction with the labeled antibody bound to the complex. In step S18, the mixed solution generated in step S17 and the R5 reagent are mixed and a stirring process is performed to prepare a sample. This sample emits chemiluminescence by the reaction between the labeling substance bound to the complex and the luminescent substrate.

  In step S19, the control unit 151 drives the motor 117 to rotate the measurement cartridge 200, positions the storage chamber 246 directly above the photodetector of the detection unit 115, and detects light generated from the storage chamber 246 by light detection. Detect with a vessel. In step S <b> 20, the control unit 151 performs immunity analysis processing based on the light detected by the photodetector of the detection unit 115. When the photodetector of the detection unit 115 is configured by a photomultiplier tube, a pulse waveform corresponding to reception of a photon is output from the photodetector. The detection unit 115 counts photons at regular intervals based on the output signal of the photodetector, and outputs a count value. The control unit 151 analyzes the presence / absence and amount of the test substance based on the count value output from the detection unit 115 and causes the display unit 152 to display the analysis result.

<Embodiment 4>
In the fourth embodiment, as shown in FIG. 19, a support member 310 is disposed instead of the support member 113, and a measurement cartridge 320 is used instead of the measurement cartridge 200. About another structure, it is the same as that of said specific structural example.

  The support member 310 includes a hole 311 and three installation parts 312. The hole 311 is provided at the center of the support member 310. The support member 310 is installed on the rotation shaft 103. As a result, the support member 310 can rotate about the rotation shaft 103. Three installation sections 312 are provided in the rotation direction. The installation unit 312 includes a surface 312a and a hole 312b. The surface 312 a is a surface that is one step lower than the upper surface of the support member 310. The hole 312b is formed at the center of the surface 312a and penetrates the support member 310 in the vertical direction. The measurement cartridge 320 has a rectangular shape. The measurement cartridge 320 has the same configuration as the measurement cartridge 200 except for the outer shape.

  When starting the measurement, the operator places the sample into the sample insertion port of the measurement cartridge 320 and places the measurement cartridge 320 in the installation unit 312 as in the case of the measurement cartridge 200. Then, similarly to the specific configuration example described above, the control unit 151 drives the motor 117, the magnetic force application unit 114, and the detection unit 115. In the third embodiment, the measurement cartridges 320 can be installed in the three installation units 312, respectively, and therefore the three measurement cartridges 320 can be measured simultaneously.

10, 200, 320 Measuring cartridge 20, 103 Rotating shaft 30, 210 Separation chamber 31, 211 First reservoir 31a, 31b, 211a Inner wall 32, 212 Second reservoir 32a, 32b, 212a Inner wall 40, 241 Housing chamber 50 , 220 Channel 50a, 220a Connection position 51, 221 Channel 52, 222 Channel 61, 201 Sample inlet 63, 203 Channel 65, 207 Air introduction channel 70, 280 Sample 71, 281 Solid component 72, 282 Liquid component 81, 271 First region 81a, 81b, 271a Inner wall 82, 272 Second region 100 Measuring device 208c Valve 211b Inner wall 233 Channel 234 Waste chamber 274a First inclined part 274b Second inclined part 274c Flat part

Claims (7)

A measurement cartridge mounted on a measurement device so as to be rotatable about a rotation axis,
A separation chamber for separating a blood cell component and a plasma component contained in a blood sample using a centrifugal force generated by rotating the measurement cartridge;
A storage chamber for storing the plasma component;
A first flow path extending in a direction from the separation chamber toward the rotation axis;
A second flow path extending from the end of the first flow path opposite to the separation chamber in a direction away from the rotation shaft and connected to the storage chamber;
A measurement cartridge comprising: an air introduction path capable of introducing air into the second flow path from a connection position between the first flow path and the second flow path.   The second flow path is quantified by filling the plasma component separated in the separation chamber by capillary action and then introducing air from the connection position into the second flow path by the centrifugal force. The measurement cartridge according to claim 1, wherein the plasma component is transferred to the storage chamber.   The measurement cartridge according to claim 1, wherein a valve for stopping movement of the plasma component due to capillary action is provided on the storage chamber side of the second flow path. A disposal chamber for discarding the plasma component;
The separation chamber and the waste chamber are connected, and the plasma component remaining in the separation chamber after moving the plasma component from the separation chamber to the receiving chamber is transferred from the separation chamber to the waste chamber by the principle of siphon. The measurement cartridge according to any one of claims 1 to 3, further comprising another flow path that is moved toward the center. In a separation chamber included in a measurement cartridge that is mounted on a measurement device so as to be rotatable about a rotation axis, a blood sample is separated into a blood cell component and a plasma component using centrifugal force generated by rotation around the rotation axis. ,
Filling the plasma component separated in the separation chamber into a flow path connecting the separation chamber and the storage chamber by capillary action;
A liquid feeding method of transferring the plasma component quantified by introducing air into the flow path by the centrifugal force to the storage chamber.   The liquid feeding method according to claim 5, wherein movement of the plasma component due to capillary action is stopped on the storage chamber side of the flow path.   The plasma component remaining in the separation chamber after moving the plasma component from the separation chamber to the storage chamber is moved from the separation chamber toward the waste chamber according to a siphon principle. Liquid feeding method.

Images