Particle Sorting Kit

Abstract

Provided is a particle isolation kit that comprises a filter which causes minimal particle loss and which functions even when the flow is low.　A particle isolation kit comprising: a sample accommodation part for accommodating a sample liquid that includes particles; a microchip comprising a sample channel through which the sample liquid flows and an isolation channel through which target particles are isolated from the sample liquid; and a filter part comprising a filter and a tapered part that narrows the channel diameter along the flow direction downstream of the filter.

Description

[Technical field]

[0001] The present technology relates to a particle sorting kit used for sorting particles using a microchip equipped with a microchannel. [Background technology]

[0002] Currently, a technology called flow cytometry is used to analyze microparticles such as cells and microorganisms. Flow cytometry is an analytical technique that analyzes and separates microparticles by irradiating light onto microparticles that flow as if they are contained in a sheath flow that is sent through a flow channel, and detecting the fluorescence and scattered light emitted from each microparticle. The device used for flow cytometry is called a flow cytometer.

[0003] This flow cytometer uses a microchip with regions and channels for chemical or biological analysis on a silicon or glass substrate. Such an analysis system using a microchip is called a μ-TAS (micro-total-analysis system), a lab-on-a-chip, or a biochip.

[0004] An example of the application of μ-TAS to microparticle measurement technology is a microparticle sorting device that measures the characteristics of microparticles optically, electrically, or magnetically within a flow channel or area arranged on a microchip and sorts them. In such a flow cytometer that applies μ-TAS (microchip-type flow cytometer), the flow channel system is configured using a microchip, which has the advantage of preventing cross-contamination of samples between measurements.

[0005] For example, Patent Document 1 discloses a microchip that "has a main flow path through which a liquid containing microparticles flows, a capture chamber in which the microparticles are taken in and a pressure chamber in which negative pressure is generated, and a separation flow path that communicates with the main flow path, wherein a cross section perpendicular to the flow direction of the liquid in the capture chamber and the pressure chamber is larger than a cross section perpendicular to the flow direction of the liquid in other parts of the separation flow path." [Prior art documents] [Patent documents]

[0006] [Patent Document 1] JP 2017-058375 A Summary of the Invention [Problem to be solved by the invention]

[0007] When analyzing and separating microparticles such as cells and microorganisms, the presence of foreign matter such as particle aggregates and fiber debris in the sample liquid leads to a decrease in the accuracy of analysis and separation. Therefore, it is desirable to remove such foreign matter before passing it through the microchannel. Since the sample liquid passed through the microchannel is small in volume and at a low flow rate, the filter used to remove foreign matter needs to minimize particle loss and function even at a low flow rate.

[0008] However, typical filters have a large dead volume and a wide surface area, which means that a large amount of liquid remains inside the filter during use.In addition, due to the small flow rate, there is a problem that microparticles such as cells and microorganisms settle and accumulate inside the filter.

[0009] Therefore, a primary object of the present technology is to provide a particle sorting kit equipped with a filter that reduces particle loss and functions even at low flow rates. [Means for solving the problem]

[0010] In the present technology, first, a sample container for containing a sample liquid containing particles is provided. a microchip including a sample flow path through which the sample liquid flows and a sorting flow path through which target particles are sorted from the sample liquid; A filter section including a filter and a tapered section that narrows a flow path diameter in a flow direction downstream of the filter; A particle sorting kit is provided, comprising: In the particle sorting kit according to the present technology, the taper angle of the tapered portion can be 50 to 80°. In the particle sorting kit according to the present technology, the sample storage section, the microchip, and the filter section can be hermetically connected. In the particle sorting kit according to the present technology, the filter section can be provided upstream of the sample storage section. The filter portion may also be provided between the sample storage portion and the microchip. Furthermore, the filter section may be provided upstream of the sample storage section and between the sample storage section and the microchip. In the particle sorting kit according to the present technology, a tube pump section may be provided between the sample storage section and the filter section. In the particle sorting kit according to the present technology, the filter section can include a fitting section for fitting externally with a tube for connecting to the sample storage section and / or the microchip. The fitting portion can be designed to have a tapered structure in which the diameter narrows toward the filter. In this case, the taper angle of the taper structure of the fitting portion can be set to 80 to 90°.

[0011] In the present technology, the term "particles" may broadly include biologically relevant microparticles such as cells, microorganisms, and liposomes, as well as synthetic particles such as latex particles, gel particles, and industrial particles.

[0012] The bio-related microparticles include chromosomes, liposomes, mitochondria, organelles (cell organelles), and the like that constitute various cells. The cells include animal cells (e.g., blood cells, etc.) and plant cells. The microorganisms include bacteria such as Escherichia coli, viruses such as tobacco mosaic virus, and fungi such as yeast. Furthermore, the bio-related microparticles also include bio-related polymers such as nucleic acids, proteins, and complexes thereof. The industrial particles may be, for example, organic or inorganic polymer materials, metals, and the like. The organic polymer materials include polystyrene, styrene-divinylbenzene, polymethyl methacrylate, and the like. The inorganic polymer materials include glass, silica, magnetic materials, and the like. The metals include gold colloids, aluminum, and the like. The shape of these microparticles is generally spherical, but in the present technology, they may be non-spherical, and their size, mass, and the like are not particularly limited. [Brief description of the drawings]

[0013] [Figure 1] 1 is a conceptual diagram that illustrates a first embodiment of a particle sorting kit 1 according to the present technology. [Diagram 2] FIG. 2 is an enlarged conceptual diagram illustrating an example of an embodiment of a microchip 12 that can be used in a particle sorting kit 1 according to the present technology. [Diagram 3] 1 is an enlarged perspective cross-sectional view that illustrates a schematic diagram of an example of an embodiment of a filter portion 13 used in a particle sorting kit 1 according to the present technology. [Figure 4] 1 is an enlarged cross-sectional view that illustrates a schematic example of a method for laminating a filter 131 used in the present technology. [Diagram 5] FIG. 2 is an enlarged cross-sectional view showing a schematic example of an embodiment of a filter unit 13 used in a particle sorting kit 1 according to the present technology. [Figure 6] 6A and 6B are conceptual diagrams showing a method for connecting filter portion 13 and tube 15. Fig. 6A shows filter portion 13 and tube 15 before they are connected, and Fig. 6B is a conceptual diagram showing a state in which filter portion 13 and tube 15 are connected. [Figure 7]FIG. 2 is a conceptual diagram illustrating a second embodiment of the particle sorting kit 1 according to the present technology. [Figure 8] FIG. 11 is a conceptual diagram that illustrates a third embodiment of the particle sorting kit 1 according to the present technology. [Figure 9] FIG. 1 is a conceptual diagram illustrating an example of an embodiment of a particle sorting device 2 according to the present technology. [Figure 10] FIG. 1 is a conceptual diagram illustrating an example of an embodiment of a particle sorting system 3 according to the present technology. [Figure 11] 11 is a conceptual diagram illustrating a schematic example of an embodiment of a particle sorting system 3 according to the present technology, which is different from that shown in FIG. 10. FIG. [Figure 12] FIG. 1 is a cross-sectional view of a filter structure that has been conventionally and commonly used. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0014] Hereinafter, preferred embodiments of the present technology will be described with reference to the drawings. The embodiment described below is an example of a typical embodiment of the present technology, and is not intended to narrow the scope of the present technology. The description will be given in the following order. 1. Particle Sorting Kit 1 (1) Sample storage section 11 (2) Microchip 12 (3) Filter section 13 (4) Tube pump section 14 (5) Target particle storage unit 16 (6) Disposal Section 17 (7) Sheath liquid storage section 18 (8) Gate liquid storage section 19 2. Particle sorting device 2, particle sorting system 3 (1) Particle sorting kit 1 (2) Light irradiation unit 21 (3) Light detection unit 22 (4) Information Processing Unit 23 (5) Storage section 24 (6)Display section 25 (7) User Interface 26

[0015] 1. Particle Sorting Kit 1 1 is a conceptual diagram showing a schematic diagram of a first embodiment of a particle sorting kit 1 according to the present technology. The particle sorting kit 1 according to the present technology includes at least a sample storage section 11, a microchip 12, and a filter section 13. In addition, it is possible to include a tube pump section 14, a target particle storage section 16, a waste section 17, a sheath liquid storage section 18, a gate liquid storage section 19, and the like, as necessary. The particle sorting kit 1 will be described in detail below.

[0016] (1) Sample storage section 11 The sample container 11 contains a sample liquid containing particles to be separated. The sample container 11 can be formed, for example, from a cylindrical body with one open end and a lid part that fits into the lid part and closes the opening. The lid part is formed with a plurality of opening valves for containing the sample liquid in the lid part, and each opening valve has a check valve configuration. Therefore, when the sample liquid is contained in the sample container 11 through the opening valves, the sample liquid does not flow out of the sample container 11. The opening valve configuration also seals the sample liquid from the outside atmosphere.

[0017] The sample liquid is not particularly limited as long as it is a sample containing target particles to be separated using the particle separation kit 1 according to the present technology. Specific examples include liquids containing patient-derived cells, such as whole blood, peripheral blood mononuclear cells contained in whole blood, and cell suspensions containing only lymphocytes.

[0018] The sample storage section 11 may be provided with a substance that suppresses the aggregation of particles in the sample liquid. By using the substance that suppresses the aggregation of particles in the sample liquid, the aggregation of particles in the sample liquid can be suppressed, and any aggregates that still occur can be removed by the filter section 13 described below, so that impurities in the sample liquid can be removed more reliably.

[0019] Examples of substances that inhibit particle aggregation include deoxyribonuclease (DNase), ethylenediaminetetraacetic acid (EDTA), and poloxamer (eg, "Pluronic F68" manufactured by BASF).

[0020] When a substance that inhibits particle aggregation is included, the solution used for the sample liquid can be any commonly used solution as long as it does not impair the effects of the present technology, but it is preferable to use phosphate buffered saline (PBS) in the present technology.

[0021] When using PBS, it is preferable to use PBS that does not contain calcium ions and magnesium ions. However, when using a substance that inhibits particle aggregation as described above, it is also possible to use PBS that contains calcium ions and magnesium ions depending on the type of substance used. Specifically, in the present technology, PBS (without Ca 2+ ,Mg 2+ ), PBS (with Ca 2+ ,Mg 2+ ) + DNase, PBS (without Ca 2+ ,Mg 2+ It is preferable to use a combination of EDTA and the like, and it is also possible to add poloxamer to these combinations. Also, albumin such as bovine serum albumin or human serum albumin can be added at a concentration of, for example, about 0.5%.

[0022] In addition, in the particle sorting kit 1 according to the present technology, a pre-sample storage section 111 may be provided upstream of the sample storage section 11, and the pre-sample storage section 111 may contain a substance that suppresses aggregation of particles in the sample liquid or other drugs, etc.

[0023] (2) Microchip 12 2 is an enlarged conceptual diagram showing a schematic example of an embodiment of a microchip 12 that can be used in the particle sorting kit 1 according to the present technology. The microchip 12 that can be used in the present technology includes at least a sample flow path 121 through which a sample liquid flows, and a sorting flow path 122 through which target particles are sorted from the sample liquid.

[0024] Sample liquid containing particles is introduced into the sample flow path 121 from the sample inlet 1211. In addition, sheath liquid introduced from the sheath inlet 1231 is divided and sent into two sheath flow paths 123a and 123b. The sample flow path 121 and the sheath flow paths 123a and 123b join together to form the main flow path 124. The sample liquid laminar flow sent through the sample flow path 121 and the sheath liquid laminar flow sent through the sheath liquid paths 123a and 123b join together in the main flow path 124 to form a sheath flow in which the sample liquid laminar flow is sandwiched between the sheath liquid laminar flows.

[0025] 2 indicates a detection region 125 where excitation light is irradiated by a light irradiating unit 21 described later and where fluorescence and scattered light are detected by a light detecting unit 22 described later. The particles are sent to the detection region 125 in a state where they are aligned in a line in the sheath flow formed in the main flow channel 124 and are irradiated with excitation light from the light irradiating unit 21.

[0026] The main channel 124 branches into three channels downstream of the detection region 125. The main channel 124 communicates with three branch channels, the sorting channel 122 and the waste channels 126a and 126b, downstream of the detection region 125. Of these, the sorting channel 122 is a channel into which particles determined to satisfy predetermined optical characteristics (also referred to as "target particles") are taken in. On the other hand, particles determined not to satisfy predetermined optical characteristics (also referred to as "non-target particles") are not taken in the sorting channel 122, but flow into one of the two waste channels 126a and 126b.

[0027] The target particles are taken into the sorting channel 122 by generating a negative pressure in the sorting channel 122 with a piezoelectric element such as a piezo element, and using this negative pressure to suck the sample containing the target particles and the sheath liquid into the sorting channel 122. The piezoelectric element is placed in contact with the surface of the microchip 12, and is disposed at a position corresponding to the sorting channel 122. More specifically, the piezoelectric element is placed at a position corresponding to a pressure chamber 1221 provided as a region with an expanded inner space in the sorting channel 122.

[0028] 2, the inner space of the pressure chamber 1221 is expanded in the planar direction (the width direction of the sorting channel 122) and also in the cross-sectional direction (the height direction of the sorting channel 122). That is, the sorting channel 122 is expanded in the width direction and the height direction in the pressure chamber 1221. In other words, the sorting channel 122 is formed so that the cross section perpendicular to the flow direction of the sample and sheath liquid in the pressure chamber 1221 is large.

[0029] The piezoelectric element generates an expansion and contraction force in response to a change in the applied voltage, causing a pressure change in the sorting channel 122 via the surface (contact surface) of the microchip 12. When a flow occurs in the sorting channel 122 in response to a change in pressure in the sorting channel 122, the volume in the sorting channel 122 changes at the same time. The volume in the sorting channel 122 changes until it reaches a volume determined by the amount of displacement of the piezoelectric element corresponding to the applied voltage. More specifically, when the piezoelectric element is in a state in which it is expanded by the application of a voltage, it presses a displacement plate that constitutes the pressure chamber 1221, thereby maintaining the volume of the pressure chamber 1221 small. Then, when the applied voltage decreases, the piezoelectric element generates a force in a contracting direction, and generates a negative pressure in the pressure chamber 1221 by weakening the pressure on the displacement plate.

[0030] In this technology, in order to efficiently transmit the expansion and contraction force of the piezoelectric element to the inside of the pressure chamber 1221, it is preferable to form a recess in the surface of the microchip 12 at a position corresponding to the pressure chamber 1221 and place the piezoelectric element in the recess. This allows the displacement plate, which is the contact surface of the piezoelectric element, to be thin, and the displacement plate can be easily displaced by the change in pressing force accompanying the expansion and contraction of the piezoelectric element, causing a change in the volume of the pressure chamber 1221.

[0031] The microchip 12 is formed by bonding substrate layers on which the sample channel 121, the fractionation channel 122, etc. are formed. The sample channel 121, the fractionation channel 122, etc. can be formed on the substrate layers by injection molding of a thermoplastic resin using a mold. As the thermoplastic resin, a plastic conventionally known as a material for a microchip, such as polycarbonate, polymethylmethacrylate resin (PMMA), cyclic polyolefin, polyethylene, polystyrene, polypropylene, polydimethylsiloxane (PDMS), etc., can be used. The number of substrate layers constituting the microchip 12 is not particularly limited, and the microchip 12 can be made up of a plurality of layers, for example, two or more layers.

[0032] The microchip 12 used in the present technology may further include a gate liquid inlet 1271 into which a gate liquid is introduced, and a gate flow channel 127 through which the gate liquid introduced from the gate liquid inlet 1271 flows. The gate flow channel 127 is provided to connect one or more of the three branch flow channels, the separation flow channel 122 and the waste flow channels 126a and 126b, to the separation flow channel 122 just before the pressure chamber 1221, or to intersect perpendicularly, for example. The "gate liquid" is a liquid that is passed through the gate flow channel 127, and serves as the main solvent for the sample of microparticles or the like recovered after separation, so that various liquids can be selected according to the application. For example, a liquid medium used for the particle-containing liquid, a sheath liquid, or a buffer liquid containing a surfactant and having an adjusted pH, etc., in the case where the particles are proteins, can be passed at a constant flow rate according to the particles.

[0033] In particular, when the particles are cells, cell culture fluid, cell preservation fluid, etc. can be used as the gate fluid. When a cell culture fluid is used, it is suitable for carrying out subsequent processes on the cells recovered after sorting, such as cell culture, cell activation, gene transfer, etc. When a cell preservation fluid is used, it is suitable for storing and transporting the recovered cells. Furthermore, when the cells to be sorted and recovered are undifferentiated cells such as iPS cells, a differentiation induction fluid can be used, allowing the next process to proceed efficiently.

[0034] Similarly, various liquids can be selected as the sheath liquid. In this specification, the flow formed by the gate liquid is called a "gate flow."

[0035] The upstream side of the gate flow channel 127 can be introduced at an appropriate flow rate independently from the gate flow inlet 1271. In this technology, the flow rate of the liquid introduced into the gate flow channel 127 is smaller than the flow rate of the liquid introduced into the sheath flow channels 123a and 123b, so that it is economical when expensive liquids such as cell culture fluid, cell preservation fluid, and differentiation induction fluid are used only in the gate flow channel 127.

[0036] The gate flow can also be generated by branching off from the sheath liquid flow. For example, the sheath flow paths 123a and 123b after the sheath liquid inlet can be connected to the upstream end of the gate flow path 127, and the sheath liquid flow can be branched off and flow into the gate flow path 127 to generate the gate flow. In this case, it is necessary to appropriately design the flow path resistance of the gate flow path 127 so that the gate flow rate is an appropriate flow rate.

[0037] At the intersection of the gate channel 127 and the sorting channel 122, along with the gate flow that tries to proceed straight through the gate channel 127, gate flows toward the detection region 125 side and the pressure chamber 1221 side are also generated. The latter gate flow can prevent particles that should not be acquired (non-target particles) from entering the pressure chamber 1221 side of the sorting channel 122. The gate flow that has flowed through the gate channel 127 flows out into the sorting channel 122 and branches into gate flows toward the detection region 125 side and the pressure chamber 1221 side of the sorting channel 122. The former gate flow can prevent non-target particles from entering the pressure chamber 1221 side of the sorting channel 122.

[0038] The microchip 12 according to the present technology is connected to a sample storage section 11, a filter section 13 described later, etc., and may be distributed as a part of an article such as a cartridge, unit, device, kit, or instrument for a closed cell sorter.

[0039] (3) Filter section 13 3 is an enlarged perspective cross-sectional view showing a schematic example of an embodiment of the filter unit 13 used in the particle sorting kit 1 according to the present technology. The filter unit 13 includes at least a filter 131 and a tapered portion 132. If necessary, a fitting portion 133 may also be included.

[0040] (3-1) Filter 131 The material, inner diameter, pore size, etc. of filter 131 that can be used in filter section 13 of particle sorting kit 1 according to the present technology can be designed according to the size and form of the target particles to be sorted.

[0041] The material of the filter 131 used in the present technology may be nylon, polyethylene terephthalate (PET), polyethylene (PE), etc. Among these, in the present technology, it is preferable to manufacture the filter using nylon from the viewpoints of pore size, sterility, and adhesiveness.

[0042] Moreover, the inner diameter of the filter 131 used in the present technology is preferably 0.5 to 10 mm, and more preferably 2 to 7 mm. The smaller the area of ​​the filter 131, the smaller the amount of loss of target particles can be kept.

[0043] Furthermore, the pore size of the filter 131 used in the present technology can be designed according to the type of target particles. For example, when the target particles are blood cells, the pore size is preferably 20 to 100 μm. Also, when the target particles are iPS cells or the like, the pore size can be 100 μm or more. In this way, by designing the pore size of the filter 131 according to the type of target particles, it is possible to efficiently remove impurities while preventing the particles from being damaged or killed.

[0044] It is also possible to use a plurality of filters 131 stacked together. By stacking two or more filters 131, it is possible to more reliably prevent particle aggregates and foreign matter from leaking out. When stacking a plurality of filters 131, they can be stacked as is, but as shown in FIG. 4, it is also possible to stack filters 131a and 131b via an O-ring.

[0045] (3-2) Tapered section 132 The filter section 13 of the particle sorting kit 1 according to the present technology includes a tapered section 132 downstream of the filter 131. This tapered section 132 has a shape that narrows the flow path diameter along the flow direction F of the sample liquid.

[0046] Fig. 12 is a cross-sectional view of a filter structure that has been generally used in the past. In the conventional filter structure, particles in the sample liquid that has passed through the filter 1311 settle in the area indicated by the dashed line in Fig. 12, causing a problem of particle loss.

[0047] On the other hand, the filter section 13 of the particle sorting kit 1 according to the present technology has a tapered section 132 downstream of the filter 131, thereby preventing particles in the sample liquid that has passed through the filter 131 from settling on the inner wall surface of the filter section 13, thereby reducing the amount of particle loss.

[0048] Fig. 5 is an enlarged cross-sectional view showing a schematic example of an embodiment of filter section 13 used in particle sorting kit 1 according to the present technology. In particle sorting kit 1 according to the present technology, taper angle α of tapered section 132 shown in Fig. 5 is preferably 50 to 80°. By setting taper angle α of tapered section 132 to 50° or more, it is possible to more effectively prevent particles in the sample liquid that has passed through filter 131 from settling on the inner wall surface of filter section 13. Furthermore, by setting taper angle α of tapered section 132 to 80° or less, it is possible to realize a reduction in the size of filter section 13.

[0049] (3-3) Fitting portion 133 The filter section 13 of the particle sorting kit 1 according to the present technology can be provided with a fitting section 133 for fitting the outer diameter of the tube 15 for connection to the sample storage section 11 and / or the microchip 12. The tube 15 used in the present technology has a very thin inner diameter, so a tube connection using a barb shape like that of a general tube cannot be made. Therefore, by providing the filter section 13 used in the present technology with a fitting section 133 that presses the tube 15 from the outer diameter and fits the outer diameter, it becomes possible to connect even a tube 15 with a narrow inner diameter.

[0050] Fig. 6 is a conceptual diagram showing a method for connecting the filter portion 13 and the tube 15. Fig. 6A shows the filter portion 13 and the tube 15 before they are connected, and Fig. 6B is a conceptual diagram showing the filter portion 13 and the tube 15 in a connected state. As shown in Fig. 6B, the filter portion 13 and the tube 15 can be connected by pushing the tube 15 into the fitting portion 133 of the filter portion 13.

[0051] The fitting portion 133 preferably has a tapered structure in which the diameter narrows toward the filter 131. The taper angle β of the tapered structure can be designed according to the form of the tube 15 to be connected, but in the present technology, the taper angle β of the tapered structure is preferably set to 80 to 90°. By designing the taper angle β of the tapered structure within this range, a reliable connection can be achieved even if there is some variation in the outer diameter dimension of the tube 15 or in the dimension of the fitting portion 133 during manufacturing.

[0052] Furthermore, the inner diameter d1 of the fitting portion 133 on the filter 131 side and the length L in the long axis direction can be designed according to the form of the tube 15 used. For example, when using a tube 15 with an outer diameter d2 of 3.4 to 3.5 mm, it is preferable to design the inner diameter d1 of the fitting portion 133 on the filter 131 side to 3.3 to 3.6 mm and the length L of the fitting portion 133 in the long axis direction to 15 to 25 mm. By designing the inner diameter d1 of the fitting portion 133 on the filter 131 side and the length L of the fitting portion 133 in the long axis direction according to the form of the tube 15 used, a reliable connection can be achieved even if there is some variation in the dimensions of the fitting portion 133 during manufacturing.

[0053] The filter section 13 described above can be positioned at any position as long as it does not impair the effects of the present technology. For example, by providing it upstream of the sample holding section 11, as in the first embodiment of the particle sorting kit 1 related to the present technology shown in Figure 1, it is possible to prevent foreign matter from entering the sample holding section 11 at an early stage.

[0054] Also, for example, as in a second embodiment of a particle sorting kit 1 according to the present technology shown in Fig. 7, a filter unit 13 can be disposed between the sample storage unit 11 and the microchip 12. In this case, it is preferable to dispose the filter unit 13 immediately before the microchip 12. By disposing the filter unit 13 immediately before the microchip 12, it is possible to reliably prevent foreign matter from entering the microchip 12, and as a result, it is possible to improve the accuracy of the analysis performed in the microchip 12 and the sorting of the target particles.

[0055] Furthermore, for example, as in a third embodiment of the particle sorting kit 1 according to the present technology shown in Fig. 8, filter units 13a and 13b can be arranged at two locations, upstream of the sample storage unit 11 and between the sample storage unit 11 and the microchip 12. With this arrangement, the filter unit 13a arranged upstream of the sample storage unit 11 can prevent foreign matter from entering the sample storage unit 11 at an early stage, while the filter unit 13b arranged between the sample storage unit 11 and the microchip 12 can remove aggregates formed while the particles in the sample liquid are flowing from the sample storage unit 11 to the microchip 12. As a result, the accuracy of the analysis performed in the microchip 12 and the sorting of the target particles can be improved.

[0056] (4) Tube pump section 14 The filter section 13 of the particle sorting kit 1 according to the present technology can be equipped with a tube pump section 14. In the particle sorting kit 1 according to the present technology, the tube pump section 14 can be formed of an elastic material. Note that, although a roller for squeezing the elastic tube may be provided in the particle sorting kit 1 according to the present technology, it is also possible to pass the sample liquid in the tube 15 by installing the tube pump section 14 of the particle sorting kit 1 according to the present technology in a roller portion provided on the side of the particle sorting device 2 described later.

[0057] In the particle sorting kit 1 according to the present technology, the tube pump section 14 can be placed at any position as long as the effect of the present invention is not impaired. However, as in a second embodiment of the particle sorting kit 1 according to the present technology shown in FIG. 7 and a third embodiment of the particle sorting kit 1 according to the present technology shown in FIG. 8, it is preferable to place the tube pump section 14 between the sample storage section 11 and the filter section 13 (13b) provided between the sample storage section 11 and the microchip 12. In the tube pump section 14, particles in the sample liquid are in a state where they are likely to aggregate. By placing the tube pump section 14 in this manner, even if aggregates of particles are formed during flow through the tube pump section 14, the formed aggregates can be removed by the filter section 13 (13b) before the microchip 12. As a result, the accuracy of the analysis performed in the microchip 12 and the sorting of the target particles can be improved.

[0058] (5) Target particle storage unit 16 The particle sorting kit 1 according to the present technology may include a target particle storage section 16 as necessary. The sorted target particles are stored in the target particle storage section 16. The target particle storage section 16 is formed, for example, in a bag shape in which the target particles are stored, and includes an opening valve connected to the sorting flow path 122 of the microchip 12. The opening valve employs a so-called check valve configuration, and in a state in which the target particles are stored in the target particle storage section 16 via the opening valve, the target particles are prevented from exiting to the outside of the target particle storage section 16. In addition, the configuration of the opening valve prevents the target particles from coming into contact with the external atmosphere.

[0059] The above-mentioned configuration of the target particle reservoir 16 is merely an example, and any known configuration can be adopted as long as the target particles are not exposed to the external atmosphere.

[0060] (6) Disposal Section 17 In the particle sorting kit 1 according to the present technology, when only target particles are sorted from a sample liquid by the microchip 12, it is necessary to eliminate non-target particles. In addition, since a sheath flow is formed in the microchip 12 to sort the target particles, it is necessary to eliminate the sample liquid containing the non-target particles. For this reason, the particle sorting kit 1 according to the present technology may be provided with a disposal unit 17 as necessary. Particles other than the target particles are disposed of in the disposal unit 17.

[0061] (7) Sheath liquid storage section 18 In the particle sorting kit 1 according to the present technology, a sheath flow is formed in the microchip 12, and target particles are sorted from a sample liquid. Therefore, the particle sorting kit 1 according to the present technology may include a sheath liquid storage section 18 as necessary. The sheath liquid storage section 18 stores sheath liquid.

[0062] The sheath fluid storage section 18 includes, for example, a tubular member into which the sheath fluid flows, and the tubular member communicates with the sheath inlet 1231 of the microchip 12. As a result, the sheath fluid flows into the flow path of the microchip 12, forming a sheath flow.

[0063] There is no particular limitation on the configuration of the sheath fluid storage unit 18, and any known configuration may be used. In addition, there is no particular limitation on the configuration for discharging the sheath fluid from the sheath fluid storage unit 18, and for example, a drive source such as an actuator may be used.

[0064] (8) Gate liquid storage section 19 Furthermore, the particle sorting kit 1 according to the present technology may include a gate liquid storage section 19 as necessary. A gate liquid is stored in the gate liquid storage section 19. The "gate liquid" is the same as that described above, and therefore will not be described here.

[0065] The gate liquid storage section 19 includes, for example, a tubular member into which the gate liquid flows, and the tubular member communicates with the gate liquid inlet 1271 of the microchip 12. As a result, the gate liquid flows into the flow path of the microchip 12, and the target particles are separated.

[0066] The configuration of the gate liquid storage section 19 is not particularly limited, and may be a known configuration. In addition, the configuration for discharging the gate liquid from the gate liquid storage section 19 is not particularly limited, and may be, for example, a drive source such as an actuator.

[0067] Each part of the particle sorting kit 1 according to the present technology described above can be connected in part or in whole in a sealed manner. Therefore, the sorting and storage of target particles can be performed in a sealed space, thereby improving the degree of purification of the sorted target particles. In addition, it is possible to prevent contamination of the particle sorting kit itself by mist containing target particles and / or the inclusion of other substances in the sorted target particles. As a result, the particle sorting kit 1 according to the present technology can be applied to clinical applications such as immune cell therapy, which require high purity of target particles.

[0068] Furthermore, the particle sorting kit 1 according to the present technology itself can be made disposable, which can avoid the risk of contamination between samples and improve usability.

[0069] Furthermore, each part of the particle sorting kit 1 according to the present technology may be provided in multiple units. For example, although not shown, by providing a microchip 12 downstream of the target particle storage unit 16, the target particles sorted from the sample liquid may be further sorted.

[0070] 2. Particle sorting device 2, particle measurement system 3 Fig. 9 is a conceptual diagram showing an example of an embodiment of a particle sorting device 2 according to the present technology. Figs. 10 and 11 are conceptual diagrams showing an example of an embodiment of a particle sorting system 3 according to the present technology. Note that, due to space limitations, Figs. 9 to 11 show only a microchip 12 portion of a particle sorting kit 1 according to the present technology.

[0071] The particle sorting device 2 and the particle sorting system 3 according to the present technology at least include the particle sorting kit 1 according to the present technology described above, a light irradiation unit 21, and a light detection unit 22. In addition, they may also include an information processing unit 23, a storage unit 24, a display unit 25, a user interface 26, and the like, as necessary.

[0072] The information processing unit 23, the storage unit 24, the display unit 25, the user interface 26, etc. may be provided in the particle sorting device 2 as shown in Fig. 9, or a particle measuring system 3 may be formed including the particle sorting device 2 and an information processing device 4 including the information processing unit 23, the storage unit 24, the display unit 25, and the user interface 26 as shown in Fig. 10. Alternatively, the particle measuring system 3 may be formed by connecting the independent information processing unit 23, the storage unit 24, the display unit 25, and the user interface 26 to the light detection unit 22 of the particle sorting device 2 via a network as shown in Fig. 11.

[0073] Furthermore, the information processing unit 23, the storage unit 24, and the display unit 25 can be provided in a cloud environment and connected to the particle sorting device 2 via a network. In this case, records of information processing in the information processing unit 23 can be stored in the storage unit 24, and various pieces of information stored in the storage unit 24 can be shared by multiple users.

[0074] (1) Particle sorting kit 1 The particle sorting device 2 includes a particle sorting kit 1 that sorts and stores target particles. The particle sorting kit 1 includes a microchip 12. Note that the particle sorting kit 1 is similar to that described above, and therefore a description thereof will be omitted here.

[0075] (2) Light irradiation unit 21 The light irradiating unit 21 irradiates a sample to be separated with light. Specifically, the light irradiating unit 21 irradiates light (excitation light) to particles passing through a detection region 125 provided on a main flow channel 124 of the microchip 12.

[0076] The light irradiation unit 21 includes, for example, a light source that emits excitation light, and an objective lens that focuses the excitation light on the sample liquid flowing through the main flow path 124. The light source can be appropriately selected from a laser diode, an SHG laser, a solid-state laser, a gas laser, and a high-brightness LED depending on the purpose of the analysis. Furthermore, the light irradiation unit 21 may have optical elements other than the light source and the objective lens as necessary.

[0077] (3) Light detection unit 22 The light detection unit 22 detects the fluorescence and scattered light emitted from the sample to be separated when the excitation light is irradiated. Specifically, the light detection unit 22 detects the fluorescence and scattered light emitted from the sample and converts them into electrical signals. The electrical signals are then output to the information processing unit 23, which will be described later.

[0078] The configuration of the light detection unit 22 is not particularly limited, and any known configuration can be adopted, and the method of conversion into an electrical signal is also not particularly limited.

[0079] (4) Information Processing Unit 23 The information processing unit 23 receives the electrical signal converted by the light detection unit 22. Specifically, the information processing unit 23 determines the optical characteristics of the sample liquid and the target particles contained in the sample liquid based on the input electrical signal.

[0080] Furthermore, the information processing unit 23 includes a gating circuit for calculating a threshold value for separating target particles from the sample liquid, a threshold value for determining whether or not a required number of target particles or more have been separated, etc. When the threshold value for separating target particles from the sample liquid is calculated by this gating circuit configuration, it converts it into an electrical signal for separation and outputs the separation signal to a piezoelectric element included in the microchip 12.

[0081] The configuration of the information processing section 23 is not particularly limited, and may be any known configuration. Furthermore, the information processing method performed by the gating circuit of the information processing section 23 may be any known method.

[0082] (5) Storage section 24 The particle sorting device 2 and the particle sorting system 3 according to the present technology may include a memory unit 24 for storing various data. The memory unit 24 may store all items related to the measurement, such as optical information of the particles detected by the light detection unit 22, records of information processing in the information processing unit 23, and the like.

[0083] Furthermore, as mentioned above, in the present technology, the memory unit 24 can be provided in a cloud environment, so that each user can share various information recorded in the memory unit 24 on the cloud via the network.

[0084] In addition, in the present technology, the storage unit 24 is not essential, and various data can be stored using an external storage device or the like.

[0085] (6)Display section 25 The particle sorting device 2 and the particle sorting system 3 according to the present technology can be provided with a display unit 25 that displays various information. The display unit 25 can display all items related to the measurement, such as optical information of the particles detected by the light detection unit 22, various data processed by the information processing unit 23, and the like.

[0086] In the present technology, the display unit 25 is not essential, and an external display device may be connected. As the display unit 25, for example, a display or a printer may be used.

[0087] (7) User Interface 26 The particle sorting device 2 and the particle sorting system 3 according to the present technology may further include a user interface 26, which is a portion for a user to operate. The user can access and control each part through the user interface 26.

[0088] In the present technology, the user interface 26 is not essential, and an external operating device may be connected. As the user interface 26, for example, a mouse, a keyboard, etc. may be used.

[0089] In addition, the present technology can also have the following configuration. (1) a sample container for containing a sample liquid containing particles; a microchip including a sample flow path through which the sample liquid flows and a sorting flow path through which target particles are sorted from the sample liquid; A filter section including a filter and a tapered section that narrows a flow path diameter in a flow direction downstream of the filter; A particle sorting kit comprising: (2) The particle sorting kit according to (1), wherein the taper angle of the tapered portion is 50 to 80°. (3) The particle sorting kit according to (1) or (2), wherein the sample storage section, the microchip, and the filter section are hermetically connected. (4) The particle sorting kit according to any one of (1) to (3), wherein the filter section is provided upstream of the sample storage section. (5) The particle sorting kit according to any one of (1) to (4), wherein the filter section is provided between the sample storage section and the microchip. (6) The particle sorting kit according to any one of (1) to (5), wherein the filter section is provided upstream of the sample storage section and between the sample storage section and the microchip. (7) The particle sorting kit according to (5) or (6), further comprising a tube pump section between the sample storage section and the filter section. (8) A particle sorting kit according to any one of (1) to (7), wherein the filter section is provided with a fitting section for fitting externally with a tube for connecting to the sample storage section and / or the microchip. (9) The particle sorting kit according to (8), wherein the fitting portion has a tapered structure in which the diameter narrows toward the filter. (10) The particle sorting kit according to (9), wherein the taper angle of the taper structure of the fitting portion is 80 to 90°. [Explanation of symbols]

[0090] 1. Particle sorting kit 11 Sample storage section 12. Microchip 13 Filter section 14 Tube pump section 15 Tubes 16 Target particle storage section 17 Disposal Department 18 Sheath fluid storage section 19 Gate liquid storage section 2 Particle separation device 3. Particle sorting system 21 Light irradiation unit 22 Light detection unit 23 Information Processing Section 24 Memory section 25 Display section 26 User Interface

Claims

1. A sample container for containing a sample liquid containing biologically relevant microparticles; a microchip including a sample flow path through which the sample liquid flows and a sorting flow path through which target particles are sorted from the sample liquid; A filter section including a filter and a tapered section that narrows a flow path diameter in a flow direction downstream of the filter; Equipped with The filter unit is provided upstream of the sample storage unit and between the sample storage unit and the microchip, A particle sorting kit, comprising a tube pump section provided between the sample storage section and the filter section.

2. 2. The particle sorting kit according to claim 1, wherein the taper angle of the tapered portion is 50 to 80 degrees.

3. The particle sorting kit according to claim 1 , wherein the sample storage section, the microchip, and the filter section are hermetically connected.

4. 2. The particle sorting kit according to claim 1, wherein the filter section is provided with a fitting section for fitting an outer diameter of a tube for connection to the sample storage section and / or the microchip.

5. The particle sorting kit according to claim 4 , wherein the fitting portion has a tapered structure in which the diameter narrows toward the filter.

6. 6. The particle sorting kit according to claim 5, wherein the taper angle of the tapered structure of the fitting portion is 80 to 90 degrees.

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