Channel structure, fluid agitation method, and lipid particle manufacturing method

Abstract

To provide a channel structure, a fluid agitation method, and a lipid particle manufacturing method in which a fluid can be more uniformly mixed by generating a lateral vortex.SOLUTION: A channel structure according to an embodiment comprises a first channel, and a second channel confluent with the first channel. An end of a first channel side of the second channel has a region with a depth shallower than the first channel. The direction of the first channel is bent when viewed from the direction of the second channel, and in a mixed region of the second channel and the first channel, the first channel is closed relative to a longer direction of the second channel.SELECTED DRAWING: Figure 1

Description

[Technical field]

[0001] FIELD OF THE DISCLOSURE The present invention relates to a flow path structure, a fluid agitation method, and a method for producing lipid particles. [Background technology]

[0002] Stirring is an appropriate method to mix two liquids quickly and uniformly. In recent years, microchannels have been used to handle fluids, but when the amount of two liquids is small, turbulence is unlikely to occur in the microchannel, which has a small Reynolds number, making it difficult to stir and mix the two liquids. Therefore, attempts have been made to promote mixing by generating a steady swirling flow (vortex, swirl) in the microchannel. Three-dimensional fluid control is required to generate a swirling flow in a microchannel, which requires delicate molds and channel processing, or highly accurate layered molding of multiple channels.

[0003] On the other hand, microchannels used in situations where it is desirable to avoid cross-contamination, such as medical applications, are preferably disposable. In such cases, microchannels with low-cost designs that do not require high precision are required. [Prior art documents] [Patent documents]

[0004] [Patent Document 1] Special Publication No. 2019-506286 [Patent Document 2] Special Publication No. 2019-503271 [Non-patent literature]

[0005] [Non-Patent Document 1] Stroock, Abraham D., et al. Science, Jan 2002, 295.5555: 647-651 Summary of the Invention [Problem to be solved by the invention]

[0006] The problem to be solved by the present invention is to provide a flow path structure, a fluid agitation method, and a method for producing lipid particles that can mix fluids more uniformly by generating transverse vortices. [Means for solving the problem]

[0007] A flow path structure according to an embodiment comprises a first flow path and a second flow path merging into the first flow path, an end of the second flow path on the first flow path side has a region that is shallower than the first flow path, the direction of the first flow path is bent when viewed from the direction of the second flow path, and in a mixing region between the second flow path and the first flow path, the first flow path is closed in the longitudinal direction of the second flow path. [Brief description of the drawings]

[0008] [Figure 1] FIG. 1 is a plan view and a cross-sectional view showing an example of a flow path structure according to a first embodiment. [Diagram 2] FIG. 2 is a perspective view illustrating an example of the flow path structure of the first embodiment. [Diagram 3] FIG. 3 is a cross-sectional view showing an example of a flow channel cross section of the flow channel structure of the embodiment. [Figure 4] FIG. 4 is a plan view showing an example of a flow path structure according to the second embodiment. [Diagram 5] FIG. 5 is a plan view showing an example of a flow path structure according to the third embodiment. [Figure 6] FIG. 6 is a plan view showing an example of a flow path structure according to the fourth embodiment. [Figure 7] FIG. 7 is a plan view showing an example of a flow path structure according to the fourth embodiment. [Figure 8] FIG. 8 is a plan view showing an example of a flow path structure according to the fourth embodiment. [Figure 9] FIG. 9 is a plan view showing an example of a flow path structure according to the fifth embodiment. [Figure 10] FIG. 10 is a cross-sectional view showing an example of a flow path structure according to an embodiment. [Figure 11] FIG. 11 is a diagram showing an example of a lipid particle according to an embodiment. [Figure 12] FIG. 12 is a flowchart showing an example of a method for producing lipid particles according to an embodiment. [Figure 13] FIG. 13 is a diagram showing an example of a flow path structure used in the method for producing lipid particles according to the embodiment. [Figure 14] FIG. 14 is an image showing the experimental results of Example 1. [Figure 15] FIG. 15 is an image showing the experimental results of Example 2. [Figure 16] FIG. 16 is an image showing the simulation results of Example 2. [Figure 17] FIG. 17 is a photograph showing the experimental results of Example 3. [Figure 18] FIG. 18 is a photograph showing the experimental results of Example 4. [Figure 19] FIG. 19 is a photograph showing the experimental results of Example 4. [Figure 20] FIG. 20 is a graph showing the experimental results of Example 4. [Figure 21] FIG. 21 is a graph showing the experimental results of Example 4. [Figure 22] FIG. 22 is an image showing the simulation results of Example 5. [Diagram 23] FIG. 23 is a plan view showing the flow path structure used in Example 6. As shown in FIG. [Figure 24] FIG. 24 is a graph showing the experimental results of Example 6. [Diagram 25] FIG. 25 is a plan view showing the flow path structure used in Example 7. As shown in FIG. [Figure 26] FIG. 26 is an image showing the simulation results of Example 10. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

[0009] Hereinafter, the embodiments will be described with reference to the accompanying drawings. In each embodiment, the same components are denoted by the same reference numerals, and the description thereof may be omitted. The drawings are schematic, and the relationship between the thickness of each part and the planar dimensions, the thickness ratio of each part, etc. may differ from the actual ones.

[0010] (First embodiment) As shown in the plan view of Fig. 1(a), the flow path structure 1 of the first embodiment includes a first flow path 2 and a second flow path 3 that merges with the first flow path 2. The first flow path 2 and the second flow path 3 are cavities formed inside the flow path structure 1, that is, the top surface of each of the flow paths has a lid and is configured to be liquid-tight. The third and fourth flow paths described below also have the same shape as cavities formed inside the flow path structure.

[0011] The end of the second flow path 3 on the side of the first flow path 2 has a first region that is shallower than the first flow path 2. The first region is also referred to as the first shallow portion 4 below. As shown in FIG. 1(b), which is a cross-sectional view taken along B-B' in FIG. 1(a), for example, the first shallow portion 4 has a bottom surface that protrudes from the region upstream of the first shallow portion 4 (hereinafter referred to as the "deep portion 5") and the first flow path 2, narrowing the inner cavity of the flow path. The deep portion 5 and the first flow path 2 may have the same depth. In this figure, the direction of travel of the fluid is indicated by an arrow. As shown in the figure, the direction of travel of the fluid in the first flow path 2 is different from that in the second flow path 3. The region of the first flow path 2 where the fluid from the second flow path 3 joins is referred to as the "mixing region 6".

[0012] For example, the first flow channel 2 and the second flow channel 3 are microflow channels.

[0013] Figure 2 shows the state when a fluid is flowed from the second flow path 3. The arrow indicates the direction of travel of the fluid. As the fluid passes through the first shallow section 4 and flows into the first flow path 2, a transverse vortex is generated. A transverse vortex is a swirling flow whose axis of rotation coincides with the long axis of the first flow path 2. In this example, the end of the first flow path 2 to the right of the second flow path 3 is closed and forms a wall, so the fluid flows to the left while generating a transverse vortex (to the right while generating a transverse vortex in Figure 2) along the long axis of the first flow path 2. The generation of transverse vortices allows the fluid to be thoroughly mixed and stirred.

[0014] 1(b), the depth d1 of the first shallow portion 4 is preferably less than 1 / 2 the depth d2 of the first flow path 2. It is more preferable that d1 / d2 is 1 / 3 or less. By setting the depth in this manner, the flow velocity of the fluid when it flows from the first shallow portion 4 into the first flow path 2 increases, making it easier for lateral vortices to occur.

[0015] Although a shallower depth d1 of the first shallow portion 4 can obtain a flow velocity that generates a larger and stronger transverse vortex, making it too shallow can cause excessive pressure loss and can also lead to blockage if a foreign object is present. Therefore, for example, when d1 / d2 is designed to be shallower, such as 1 / 3, 1 / 4, 1 / 5, etc., through experiments or simulations, an appropriate depth d1 can be finally determined based on the machining accuracy of the flow path or robustness against pressure loss and foreign objects.

[0016] In practice, since the accuracy of the mold molding or cutting process, which are the preferred techniques used to manufacture this flow path structure, is generally 5 μm, it is desirable that the depth of the shallow portion 4 be at least 10 μm or more in order to avoid blockage of the flow path due to error.

[0017] Furthermore, in order to form steadily stable transverse vortices and to prevent unexpected reactions due to cavitation, it is advisable to avoid reducing the depth of the shallow portion 4 to a depth so shallow that the flow velocity reaches the turbulent region.

[0018] The length of the first shallow portion 4 is preferably equal to or longer than the flow path width of the second flow path 3. This allows the flow turbulence that occurs when the fluid flows from the deep portion 5 to the first shallow portion 4 to be appropriately contained within the first shallow portion 4. By suppressing the flow turbulence, the transverse vortex can be generated more efficiently. However, it is not preferable to unnecessarily lengthen the first shallow portion 4 because it may excessively increase the pressure (fluid resistance), and the length of the first shallow portion 4 is usually preferably about three times the flow path width at the longest. However, if the discharge performance of the pump allows, it is also possible to make it longer than three times if necessary for convenience of the flow path arrangement, etc.

[0019] The second flow path 3 merges with the first flow path 2 at a right angle, for example. The angle θ1 between the second flow path 3 and the first flow path 2 does not necessarily have to be a right angle, but the larger the angle θ1, the more likely it is that the laminar flow merges. Therefore, it is preferable that the angle θ1 is as close to a right angle as possible. In the example of FIG. 1, the first flow path 2 is configured so that the flow bends to the left when viewed from the second flow path 3, but it may also be configured so that the flow bends to the right.

[0020] The cross section of the first flow channel 2 is preferably a square with the same width and depth as shown in FIG. 3(a). However, it is not necessary to make it a square precisely, and it may be an approximately square with one side slightly longer. If possible, it is also preferable to make the two corners of the bottom of the cross section round as shown in FIG. 3(b), or the bottom of the cross section may be rounded with a radius of half the distance of the side of the square as shown in FIG. 3(c). With such a cross-sectional shape, the transverse vortex becomes closer to a perfect circle, and the transverse vortex is maintained for a longer period. As a result, the fluid can be well mixed and stirred. It is not necessary to make the cross-sectional shape like this over the entire area of ​​the first flow channel 2, and it is sufficient that at least the mixing region 6 has such a cross-sectional shape.

[0021] The flow path width and depth of the deep portion 5 of the second flow path 3 and the first flow path 2, the depth of the first shallow portion 4, and the supply amount of the fluid are not limited and are determined according to the type of fluid. For example, in order to prevent laminar flow in order to generate a transverse vortex, it is preferable to adjust the Reynolds number in the flow path portion having a normal depth other than the first shallow portion 4 to be 10 or more. Also, in order to avoid turbulence in order to create a uniform transverse vortex, it is preferable to set the Reynolds number to at least less than 2300. More preferably, taking into account the performance of a commonly available pump and the strength of the effective transverse vortex, the Reynolds number is preferably 50 to about 1000.

[0022] For example, when the cross section of the deep portion 5 and the first flow channel 2 is 0.3 mm square, the flow velocity is preferably about 0.5 m / s or more. If the fluid is assumed to be similar to water, the Reynolds number in this case is about 100 at room temperature.

[0023] For example, if the length of one side of the flow passage cross section is shortened while maintaining the Reynolds number constant, the pressure is affected by a square. Therefore, for example, in a flow passage with one side of 0.3 mm, the pressure loss in the first shallow portion 4 increases tenfold by setting the depth d1 of the first shallow portion 4 to 0.1 mm. Furthermore, a tenfold increase in pressure in the first shallow portion 4 increases the need to change the specifications of the pump applicable to the flow rate range, and in that case, the types of pumps are limited. Therefore, it is desirable to design the depth of the deep portion 5 and the first flow passage 2 so that the depth d1 of the first shallow portion 4 is 0.1 mm or more. Furthermore, in order to reduce the burden on the pump, it is preferable to set the upper limit of the pressure increase to about 10 times.

[0024] On the other hand, when using a pump in this flow path structure, it is preferable to use a pump that does not cause pulsation. Such pumps are easily available with a liquid delivery rate of about 1 ml / sec. In consideration of this, the appropriate upper limit for the width and depth of the cross section of the deep portion 5 and the first flow path 2 may be about 3 mm.

[0025] As described above, according to the flow path structure 1 of the embodiment, it is possible to mix and stir the fluids more effectively by generating a transverse vortex. As will be described in detail later, when this flow path structure is manufactured, it is not necessary to form a tunnel structure in the base material, and it is possible to adopt a configuration in which a flat lid is placed on a groove-shaped flow path (i.e., a configuration in which the flow paths are not stacked on each other). Therefore, it is possible to manufacture the flow path structure simply and at low cost without requiring high machining accuracy.

[0026] Second embodiment The flow path structure of the second embodiment further includes a third flow path 7 connected in series to the first flow path immediately upstream of the junction with the second flow path. For example, as in a flow path structure 10 shown in Fig. 4(a), the third flow path 7 and the first flow path 2 form an integrated linear flow path, and the second flow path 3 merges with the first flow path 2 at a right angle. In this case, the angle θ1 between the second flow path 3 and the first flow path 2 and the angle θ2 between the second flow path 3 and the third flow path 7 are both right angles.

[0027] In a further embodiment, as in the flow path structure 11 shown in FIG. 4(b), the second flow path 3 and the third flow path 7 merge into the first flow path 2 at, for example, the same angle, forming a Y-shape as a whole. The angle θ2 between the second flow path 3 and the third flow path 7 is preferably a right angle. Moreover, these two flow paths merge into the first flow path 2 at the same angle, in other words, the second flow path 3 and the third flow path 7 are connected symmetrically to each other with the major axis of the first flow path 2 as the axis of symmetry. For example, when the angle θ2 is a right angle, the angle θ1 between the second flow path 3 and the first flow path 2 is, for example, 135°.

[0028] In the flow channel structures 10 and 11, in addition to the second flow channel 3, the fluid is also caused to flow from the third flow channel 7. As a result, the two fluids join in the mixing region 6. In addition, the first shallow portion 4 generates a transverse vortex in the mixing region 6, so that the two fluids are mixed and stirred.

[0029] The flow path structure 11 can cause less turbulence in the flow immediately after merging from the second flow path 3 than the flow path structure 10. Although flow turbulence increases the stirring effect, more uniform mixing can be achieved by reducing the turbulence, and in this case, the life (energy) of the transverse vortex is not wasted and the transverse vortex can be sustained for a longer period. Therefore, when uniform mixing is desired more than the stirring effect, it is preferable to use the flow path structure 11 rather than the flow path structure 10. Conversely, when more rapid mixing is desired, it is preferable to use the flow path structure 10.

[0030] In the flow path structures 10 and 11 of the second embodiment, the depth d1 of the first shallow portion 4 is preferably less than 1 / 2 the depth d2 of the first flow path 2. For example, if the first shallow portion 4 is not provided, and fluids are flowed from the second flow path 3 and the third flow path 7 at approximately the same flow rate, the fluids each occupy 1 / 2 of the cross-sectional area after merging, and the tendency to form a laminar flow after merging becomes stronger. Therefore, if d1 / d2 is set to 1 / 2, a similar situation is realized, and it is possible that transverse vortices are less likely to be generated. Therefore, by setting d1 / d2 to less than 1 / 2, transverse vortices may be more likely to be generated.

[0031] The flow path structures 10 and 11 of the second embodiment can be used for mixing, for example, two fluids, and can mix the two fluids more efficiently and uniformly.

[0032] Third embodiment The flow path structure of the third embodiment further includes a flow path group (mixing unit) for mixing fluids at the downstream end of the first flow path of the flow path structure of the first or second embodiment. Fig. 5 shows an example of a flow path structure 20 of the third embodiment. The flow path structure 20 includes a merging unit 21 and a mixing unit 22. In this figure, for convenience, the shallow portions (first shallow portion 4a to third shallow portion 4c) are shown by a diagonal line pattern. Also, the flow direction of the fluid is shown by an arrow.

[0033] The confluence unit 21 includes a group of flow paths for two fluids to merge. The confluence unit 21 has the same structure as the flow path structure 10 or 11 of the second embodiment, for example. Here, the same structure as the flow path structure 11 is illustrated. In the confluence unit 21, as described in the second embodiment, a transverse vortex is generated in the mixing region 6a by the fluid passing through the first shallow portion 4a, and the two fluids flowing from the second flow path 3 and the third flow path 7, respectively, are mixed in the first flow path 2. Thereafter, the fluid flows to the mixing unit 22 downstream.

[0034] The mixing unit 22 is connected downstream of the confluence unit 21 and includes a group of flow paths that further mix and stir the fluids that have been confluenced at the confluence unit 21. The group of flow paths includes, for example, a first branch-and-confluence flow path 23 and a second branch-and-confluence flow path 24 that branch the fluid flowing in from the first flow path 2 into two to form two separate flows, and that merge the two aliquots into a fourth flow path.

[0035] For example, the second branching / merging channel 24 has a second region (second shallow portion 4b) in its middle portion that is shallower than its upstream and downstream sides, and its downstream portion is bent to merge with the fourth channel. The second shallow portion 4b and the bend generate a transverse vortex, which allows the fluids to be mixed and stirred. The end of the first branching / merging channel 23 on the fourth channel side has a third region (third shallow portion 4c) that is shallower than the fourth channel. The third shallow portion 4c generates a transverse vortex when the fluids merge in the fourth channel, which allows the fluids to be mixed and stirred.

[0036] The structures of the first branching and merging channel 23 and the second branching and merging channel 24 will be described in more detail below. The first branching and merging channel 23 includes, for example, a branching portion 23a, an intermediate portion 23b, and a merging portion 23c from upstream to downstream. Similarly, the second branching and merging channel 24 includes, for example, a branching portion 24a, an intermediate portion 24b, and a merging portion 24c.

[0037] The branching portion 23a and the branching portion 24a are connected to the downstream end of the first flow path 2 and are portions that branch the fluid. In order to make the flow rates equal, the branching portion 23a and the branching portion 24a are preferably connected to each other symmetrically with respect to the axis of the first flow path 2, for example, at the same angle, and have the same flow path width and depth. The angle formed by the branching portion 23a and the branching portion 24a is not limited, but is, for example, a right angle.

[0038] However, since it is possible to generate a lateral vortex in the downstream second shallow portion 4b, 4c without necessarily making the flow rates of the two branches equal, it is also possible to make the size or angle of the flow paths different from each other. However, in that case, the flow rate of one path will be reduced, and the difficulty (required accuracy) of pressure adjustment may increase in the path with the lower flow rate. Therefore, it is preferable to branch the paths in roughly equal amounts in terms of product robustness.

[0039] At intermediate portions 23b and 24b downstream of branching portion 23a and branching portion 24a, respectively, the flow path is bent at an angle parallel to the longitudinal axis of first flow path 2. Then, at junctions 23c and 24c downstream thereof, it is further bent inward and connected to fourth flow path 25.

[0040] The intermediate portion 24b is, for example, a second shallow portion 4b having a depth less than 1 / 2 of the depth of the confluence portion 24c. Since one of the flow paths in the mixing unit 22 has the third shallow portion 4c, the pressure balance may be biased when branching, and the flow may not be branched evenly. Therefore, for example, by disposing the second shallow portion 4b, the pressure of the two branched flows can be made the same. Although the second shallow portion 4b can be provided in the branching portion 24a, it is preferable to dispose it in the intermediate portion 24b because branching is simpler. Since the flow path is bent at the confluence portion 24c downstream of the second shallow portion 4b, a transverse vortex is generated near the upstream of the confluence portion 24c (mixing region 6b). This allows the fluid to be further agitated there. The cross-sectional shape of the flow path in the mixing region 6b is preferably any of the shapes shown in FIG. 3.

[0041] The confluence portion 23c and the confluence portion 24c are connected to the fourth flow path 25, for example, at the same angle to each other, that is, symmetrically to each other about the axis of the fourth flow path 25. The angle formed by the confluence portion 23c and the confluence portion 24c is preferably a right angle.

[0042] For example, the confluence 23c is a third shallow portion 4c having a depth less than half the depth of the fourth flow path 25. The third shallow portion 4c generates a transverse vortex near the inlet of the fourth flow path 25 (mixing region 6c). This allows the fluid to be further mixed and stirred. The cross-sectional shape of the flow path in the mixing region 6c is preferably any one of the shapes shown in FIG.

[0043] If the only purpose is to generate a transverse vortex, the second shallow portion 4b is not necessarily provided, and it is also possible to adjust the pressure and make the depth the same throughout the second branch-junction channel 24. However, the configuration in which shallow portions are provided in both the first branch-junction channel 23 and the second branch-junction channel 24 shown in Fig. 5 is preferable because, even if one of the channels is blocked by the intrusion of foreign matter, the fluids can be mixed and stirred by passing through the shallow portion in one of the channels.

[0044] In Figure 5, a flow path (here, the second branching and merging flow path 24) arranged diagonally to a flow path (here, the second flow path 3) having a shallow portion 4a of the merging unit 21 has a second shallow portion 4b in an intermediate portion 24b, but the first branching and merging flow path 23 and the second branching and merging flow path 24 may be arranged in an inverted manner as shown in Figure 6 described later.

[0045] (Fourth embodiment) The flow path structure according to the fourth embodiment includes a plurality of mixing units 22. For example, as shown in Fig. 6(a), the flow path structure 30 includes three mixing units arranged in series, that is, a first mixing unit 22a, a second mixing unit 22b, and a third mixing unit 22c.

[0046] 6(b), in a second mixing unit 22b, the first branching and merging channel 23 (having the third shallow portion 4c at the merging portion) and the second branching and merging channel 24 (having the second shallow portion 4b at the intermediate portion) are arranged in an inverted manner about the axis of the fourth channel 25. By alternately arranging mixing units in which the arrangements of the first branching and merging channel 23 and the second branching and merging channel 24 are inverted as in this example, the fluids can be mixed more evenly.

[0047] The number of mixing units 22 is not limited to three, but may be two, four, five, six or more.

[0048] According to a further embodiment, a flow path structure may be used in which a plurality of mixing units 22a-2c are arranged in parallel, as in the flow path structure 40 shown in Fig. 7. For example, the fluid is branched upstream, passes through the plurality of mixing units 22a-2c, and then merges into one flow path downstream. This arrangement can reduce the resistance to liquid delivery even when the flow rate is high, compared to a case where the units are arranged in series. When a liquid delivery pump is used, the load on the pump is smaller.

[0049] A structure using both serial and parallel arrangements may also be used. In this case, the resistance of the liquid supply can be adjusted, and the effect of stirring and mixing can be enhanced. For example, the flow path structure 50 shown in FIG. 8 has four flow path structures each including two mixing units 22 arranged in series, and these four flow path structures are arranged in parallel. In addition, in a portion where the fluids join downstream of the parallel-arranged mixing units 22, it is preferable to arrange a shallow portion on one of the joining flow paths in order to promote mixing and stirring. The flow path structure using both serial and parallel arrangements is not limited to the example shown in FIG. 8, and can be modified according to the type or application of the fluid.

[0050] According to the flow path structure of the fourth embodiment, the fluids can be mixed and stirred further than in the case where one mixing unit 22 is provided.

[0051] Fifth embodiment In the flow path structure of the fifth embodiment, like a flow path structure 60 shown in Fig. 9, the third flow path 7 and the first flow path 2 of the merging unit 21 form an integrated linear flow path. The second flow path 3 merges with the first flow path 2 at a right angle (i.e., the same flow path structure as in (a) of Fig. 4).

[0052] Furthermore, the junction 23c of the first mixing unit 22a is connected in series to the fourth flow path 25, and forms a straight flow path integral with the fourth flow path 25. The junction 24c joins at a right angle to the fourth flow path 25. In the second mixing unit 22b, the first branching / junction flow path 23 and the second branching / junction flow path 24 are arranged in an inverted manner, but similarly the junction 23c and the fourth flow path 25 form a straight flow path, and the junction 24c joins thereat at a right angle.

[0053] The first flow path 2 and the fourth flow path 25 are bent so as to follow the axis of symmetry of the two branched flow paths just before the next branch. Alternatively, the first flow path 2 and the fourth flow path 25 may be directly connected in series to the next branch portion 23a without being bent.

[0054] In this example, any number of mixing units 22 may be connected, for example, one, three, four, five, six or more.

[0055] By merging two shallow flow paths at a right angle in this way, the fluids can be mixed and stirred more quickly. One reason for this is thought to be that the turbulence of the flow increases when the flows merge. Although the turbulence of the flow has little effect on the uniformity of the mixing, it can increase the effect of stirring. Therefore, when speed of stirring is more important than uniformity, this type of flow path structure is preferable.

[0056] (Method of Manufacturing Flow Channel Structure) A method for manufacturing the flow path structure described above (hereinafter collectively referred to as "flow path structure 100") will be described below with reference to Fig. 10. As shown in (a) of Fig. 10, the flow path structure 100 includes a substrate 102 having a groove 101 formed therein that functions as a flow path, and a plate-shaped cover portion 103 joined to the substrate 102 so as to cover the top surface of the groove 101.

[0057] The material of the substrate 102 may be selected from resins such as acrylic, polyethylene, polypropylene, glass, ceramics, metals, etc., depending on the application. For example, if the flow path structure is for medical applications, cycloolefin polymers and the like are also preferred. If it is to be reused many times, ceramics such as glass and quartz are preferred from the perspective of stability, and if temperature and other factors are to be adjusted, metals whose surfaces have been treated for corrosion resistance may be used. The grooves 101 can be formed, for example, by pressing or cutting using a mold. In the area corresponding to the shallow portion, the grooves 101 may be formed or cut shallower than in other areas.

[0058] The material of the lid portion 103 can be, for example, the same material as that described for the substrate 102. The lid portion 103 can be, for example, plate-shaped. Alternatively, a thin film-shaped lid portion 104 may be used as shown in FIG. 10(b).

[0059] A sensor terminal 105 for monitoring the state of the fluid can be attached to the film-like lid 104. Alternatively, the lid 104 can be endowed with various functions or characteristics, such as high thermal conductivity or a function for performing a specific process on a specific substance (not shown).

[0060] If there is concern that the lid 104 may expand due to internal pressure, the expansion may be suppressed by pressing a pressing plate 106 against the lid 104 from above, as shown in (c) of Fig. 10. The pressing plate 106 may include a heat medium flow path 107 for heat exchange disposed therein, or an electric terminal (not shown) having a sensor function.

[0061] In this manner, the flow channel structure 100 can be manufactured by a simple procedure of forming the groove 101 in the substrate 102 and joining the lid portion 103 or 104. Therefore, for example, it is not necessary to form grooves in both the substrate 102 and the lid portion 103, and therefore it is not necessary to precisely align the two, which makes it highly suitable for mass production.

[0062] According to a further embodiment, the shallow groove 101 may be formed by making the depth of the shallow groove 101 the same as that of the other portions, and attaching a lid 104 having a protrusion at the corresponding portion. That is, the flow passage inner cavity of the shallow portion 4 formed in this manner is recessed from above, thereby narrowing the flow passage. This structure requires more manufacturing steps, such as forming and aligning the lid, compared to the above-mentioned structure with a protruding bottom, but it is possible to generate a transverse vortex in the same way.

[0063] (Method of stirring fluid) According to an embodiment, a fluid agitation method is provided. The fluid agitation method includes flowing a fluid to be agitated through the flow path structure of the embodiment. According to the fluid agitation method, by using the flow path structure of the embodiment, the fluid can be mixed and agitated more effectively.

[0064] When the flow path structure of the first embodiment is used, this method includes flowing a first fluid from the second flow path 3 to the first flow path 2. When the flow path structure of the second to fifth embodiments is used, this method further includes flowing a second fluid into the third flow path 7. The first fluid and the second fluid may be different types of fluid, and according to the flow path structures of the second to fifth embodiments, the first fluid and the second fluid can be mixed and stirred more effectively. Also, more uniform mixing is possible.

[0065] (Method for producing lipid particles containing drugs) Hereinafter, a method for producing lipid particles encapsulating a drug using the flow path structure of the embodiment will be described.

[0066] First, the lipid particles produced by this method will be described. As shown in Fig. 11, the lipid particle 200 is made of a lipid membrane formed by arranging lipid molecules, and has a hollow, roughly spherical shape. A drug 202 is encapsulated in the lumen 201 of the lipid particle 200. The lipid particle 200 can be used, for example, to deliver the drug 202 into a cell.

[0067] The manufacturing method includes the following steps, for example as shown in FIG. Condensing the drug (in the case of a nucleic acid) (condensation step S1); Using the flow channel structure of the embodiment, a first solution containing lipids as materials for lipid particles in an organic solvent is flowed from one of the second flow channel 3 and the third flow channel 7, and a second solution containing a drug in an aqueous solvent is flowed from the other of the second flow channel 3 and the third flow channel 7, thereby mixing the first solution with the second solution to obtain a mixed solution (mixing step S2); A particle formation step S3 is a step of forming lipid particles containing a drug by reducing the concentration of the organic solvent in the mixture. Concentrating the lipid particle solution (concentration step S4).

[0068] This production method can be carried out, for example, by using the flow path structure shown in Fig. 13. In Fig. 13, (a) shows an aggregation flow path structure 301 having a configuration for performing the condensation step S1, (b) shows a flow path structure 302 of an embodiment for performing the mixing step S2, (c) shows a particulation flow path structure 303 having a configuration for performing the particulation step S3, and (d) shows a concentration flow path structure 304 having a configuration for performing the concentration step S4.

[0069] An example of the procedure of this manufacturing method will now be described.

[0070] First, a first solution and a second solution are prepared. The first solution contains lipids in an organic solvent. The lipids are lipids that are materials that constitute the lipid particles 200. The second solution contains a drug 202 in an aqueous solvent.

[0071] Condensation process S1 The drug 202 is, for example, a nucleic acid, but is not limited thereto. The nucleic acid drug 202 may be, for example, a nucleic acid containing DNA, RNA and / or other nucleotides, and may be, for example, an mRNA of a specific gene, a DNA encoding a gene, a DNA containing a gene expression cassette containing a gene and other sequences for expressing the gene, such as a promoter, a vector, etc. When the drug 202 is a nucleic acid, an aggregation step S1 may be performed first to aggregate the nucleic acid (drug 202).

[0072] Condensation of nucleic acids is carried out, for example, using a nucleic acid-condensing peptide. The nucleic acid-condensing peptide can condense nucleic acids into smaller particles, thereby making it possible to make the particle size of the lipid particle 200 smaller and to encapsulate more nucleic acids within the lipid particle 200. As a result, there can be less nucleic acid remaining outside the lipid particle 200, which may cause the lipid particle 200 to aggregate.

[0073] A preferred nucleic acid-condensing peptide is, for example, a peptide containing 45% or more cationic amino acids in total. A more preferred nucleic acid-condensing peptide has RRRRRR (first amino acid sequence) at one end and the sequence RQRQR (second amino acid sequence) at the other end. Between the first amino acid sequence and the second amino acid sequence, there is contained 0 or 1 or more intermediate sequences consisting of RRRRRR or RQRQR. In addition, there are contained two or more neutral amino acids between two adjacent sequences of the first amino acid sequence, the second amino acid sequence, and the intermediate sequence. The neutral amino acid is, for example, G or Y. The other end may have RRRRRR (first amino acid sequence) instead of the second amino acid sequence.

[0074] The nucleic acid-condensing peptide preferably has the following amino acid sequence: RQRQRYYRQRQRGGRRRRRR (SEQ ID NO:1) RQRQRGGRRRRRR (SEQ ID NO:2) RRRRRRYYRQRQRGGRRRRRR (sequence number 3).

[0075] Furthermore, a nucleic acid-condensing peptide having the following amino acid sequence can be used in combination with any of the above nucleic acid-condensing peptides. This peptide can further condense the nucleic acid condensate condensed with the above nucleic acid-condensing peptide.

[0076] GNQSSNFGPMKGGNFGGRSSGPYGGGGQYFAKPRNQGGY (M9) (SEQ ID NO: 4) As shown in FIG. 13(a), the aggregation flow channel structure 301 for performing the aggregation step S1 is, for example, a Y-shaped flow channel. For example, an aggregating agent inlet 312 is provided at the upstream end of one of the Y-shaped branched flow channels 311, from which an aggregating agent containing a nucleic acid condensing peptide is flowed. A drug inlet 314 is provided at the upstream end of the other flow channel 313, from which a solution containing nucleic acid (drug 202) in an aqueous solvent is flowed. The aqueous solvent is, for example, water, a saline solution such as physiological saline, an aqueous glycine solution, or a buffer solution. As a result, the aggregating agent and the solution containing the drug 202 are mixed in a flow channel 315 where the flow channels 311 and 313 join. By the mixing, a second solution containing the condensed drug 202 is obtained.

[0077] The condensation step S1 does not necessarily have to be performed using a flow path, but may be performed by mixing and stirring the flocculant and a solution containing nucleic acid (drug 202) in an aqueous solvent.

[0078] In view of the above effects, it is preferable to perform the condensation step S1 when the drug 202 is a nucleic acid. However, when the drug 202 is not a nucleic acid, or when the drug is a nucleic acid but does not need to be condensed, it is not necessary to perform the condensation step S1.

[0079] ·Mixing process S2 The first and second solutions are then mixed.

[0080] The second solution may be prepared as described above when the drug 202 is a nucleic acid. Alternatively, when a non-condensing nucleic acid or a drug 202 that is not a nucleic acid is used, the second solution can be prepared by mixing the drug 202 with any of the above aqueous solvents selected according to the type of drug. The non-nucleic acid drug 202 includes, for example, proteins, peptides, amino acids, other organic compounds, inorganic compounds, etc. as active ingredients. The drug 202 may be, for example, a therapeutic drug or diagnostic drug for a disease. However, the drug 202 is not limited to these, and may be any substance that can be encapsulated in the lipid particle 200.

[0081] The drug 202 may further include reagents such as a pH adjuster, an osmotic pressure adjuster, and / or a drug activator, as necessary. The pH adjuster is, for example, an organic acid such as citric acid and its salt. The osmotic pressure adjuster is, for example, a sugar or an amino acid. The drug activator is, for example, a reagent that supports the activity of an active ingredient. These may be added after the condensation step S1, if performed.

[0082] The drug 202 may be one kind of substance or may contain a plurality of substances. The concentration of the drug 202 in the second solution is preferably, for example, 0.01% to 1.0% (by weight).

[0083] The first solution can be prepared by mixing a lipid with an organic solvent. The lipid can be, for example, a lipid that is a main component of a biological membrane. The lipid can also be artificially synthesized. The lipid can include, for example, a base lipid such as a phospholipid or sphingolipid, for example, diacylphosphatidylcholine, diacylphosphatidylethanolamine, ceramide, sphingomyelin, dihydrosphingomyelin, cephalin, or cerebroside, or a combination thereof.

[0084] For example, as a base lipid, 1,2-dioleoyl-sn-glycero-3-phosphoethanolamine (DOPE), 1,2-stearoyl-sn-glycero-3-phosphoethanolamine (DSPE), 1,2-dipalmitoyl-sn-glycero-3-phosphatidylcholine (DPPC), 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphatidylcholine (POPC), 1,2-di-O-octadecyl-3-trimethylammonium propane (DOTMA), 1,2-dioleoyl-3-dimethylammonium propane (DODAP), 1,2-Dimyristoyl-3-dimethylammonium propane (14:0 DAP), 1,2-dipalmitoyl-3-dimethylammonium propane (16:0 DAP), 1,2-distearoyl-3-dimethylammonium propane (18:0 DAP), N-(4-carboxybenzyl)-N,N-dimethyl-2,3-bis(oleoyloxy)propane (DOBAQ), 1,2-dioleoyl-3-trimethylammonium propane (DOTAP), 1,2-dioleoyl-sn-glycero-3-phosphochorin (DOPC), 1,2-dilinoleoyl-sn-glycero-3-phosphochorin (DLPC), 1,2-dioleoyl-sn-glycero-3-phospho-L-serine (DOPS), or cholesterol, Alternatively, it is preferable to use any combination of these, and it is particularly preferable to use DOTAP and / or DOPE.

[0085] Preferably, the lipid further comprises a first lipid compound and / or a second lipid compound that is a biodegradable lipid. The first lipid compound can be represented by the formula Q-CHR2. (In the formula, Q is a nitrogen-containing aliphatic group containing two or more tertiary nitrogen atoms and no oxygen; R is independently C 12 ~C 24 is an aliphatic group of At least one R contains, in its main chain or in a side chain, a linking group L-R selected from the group consisting of -C(=O)-O-, -OC(=O)-, -OC(=O)-O-, -SC(=O)-, -C(=O)-S-, -C(=O)-NH-, and -NHC(=O)-.

[0086] The first lipid compound is, for example, a lipid having a structure represented by the following formula: [ka] [ka] [ka] [ka]

[0087] In particular, it is preferable to use a lipid compound of formula (1-01) and / or a lipid compound of formula (1-02).

[0088] The second lipid compound can be represented by the formula P-[XWY-W'-Z]2. (In the formula, P is an alkyleneoxy containing one or more ether bonds in the main chain; Each X is independently a divalent linking group containing a tertiary amine structure, Each W is independently a C1-C6 alkylene; each Y is independently a divalent linking group selected from the group consisting of a single bond, an ether bond, a carboxylate bond, a thiocarboxylate bond, a thioester bond, an amide bond, a carbamate bond, and a urea bond; Each W' is independently a single bond or a C1-C6 alkylene; Z is independently a fat-soluble vitamin residue, a sterol residue, or C 12 ~C 22 (an aliphatic hydrocarbon group).

[0089] The second lipid compound is, for example, a lipid having a structure represented by the following formula: [ka] [ka] [ka]

[0090] In particular, it is preferable to use the compound of formula (2-01).

[0091] When the lipid particle 200 contains the first lipid compound and the second lipid compound, it is possible to increase the amount of the drug 202 encapsulated in the lipid particle 200 and to increase the efficiency of introducing the drug 202 into cells. In addition, cell death of the introduced cells can be reduced. The base lipid is preferably contained in an amount of 30% to about 80% (molar ratio) of the total lipid material. Alternatively, the lipid material may be nearly 100% composed of the base lipid. The first and second lipid compounds are preferably contained in an amount of about 20% to about 70% (molar ratio) of the total lipid material.

[0092] The lipid preferably includes a lipid that prevents aggregation of the lipid particles 200. For example, the lipid that prevents aggregation preferably further includes a PEG-modified lipid, such as polyethylene glycol (PEG) dimyristoyl glycerol (DMG-PEG), a polyamide oligomer derived from an omega-amino(oligoethylene glycol)alkanoic acid monomer (U.S. Pat. No. 6,320,017), or a monosialoganglioside. Such a lipid is preferably included in the total lipid material of the lipid particle 200 at about 1% to about 10% (molar ratio).

[0093] The lipid may further include lipids such as lipids with relatively low toxicity for adjusting toxicity, lipids having functional groups for binding ligands to the lipid particle 200, and lipids for suppressing leakage of encapsulated substances such as sterols, e.g., cholesterol. In particular, it is preferable to include cholesterol.

[0094] For example, the lipid particle 200 preferably contains a compound of formula (1-01) or formula (1-02) and / or a compound of formula (2-01), DOPE and / or DOTAP, cholesterol, and DMG-PEG.

[0095] The type and composition of lipids are appropriately selected in consideration of the acid dissociation constant (pKa) or size of the lipid particles 200 of interest, the type of encapsulation, or the stability in the cells to be introduced, etc. For example, in order to obtain a desired composition of lipids constituting the lipid particles 200, the composition of lipids contained in the first solution may be set to the same ratio.

[0096] The organic solvent of the first solution is, for example, ethanol, methanol, isopropyl alcohol, ether, chloroform, benzene, acetone, etc. The concentration of the lipid in the organic solvent is preferably, for example, 0.1% to 0.5% (by weight).

[0097] The first solution and the second solution are mixed using a flow path structure 302 of an embodiment as shown in (b) of Fig. 13. Here, the flow path structure 302 is shown as the flow path structure of the fourth embodiment, but the flow path structure 302 is not limited thereto, and it is also possible to use, for example, the flow path structure of the second, third or fifth embodiment.

[0098] When the aggregation step S1 is performed, the downstream end of the flow path 315 of the aggregation flow path structure 301 is connected to the upstream end of the second flow path 3 of the flow path structure 302 of the embodiment, and the second solution is supplied to the second flow path 3. When the condensation step S1 is not performed, a second solution inlet (not shown) is provided at the upstream end of the second flow path 3, and the second solution is supplied from there. The third flow path 7 is provided, for example, with a first solution inlet 321 at its upstream end, and the first solution is supplied from there. As a result, the first solution and the second solution are mixed, and a mixed solution 8 is obtained. When the mixing unit 22 is provided, the mixed solution 8 is further mixed and stirred therein. For example, when the condensation step S1 is not performed, the first solution may be flowed into the second flow path 3, and the second solution may be flowed into the third flow path 7.

[0099] ·Particleization process S3 Next, in the particulation step S3, the concentration of the organic solvent in the mixed liquid 8 is reduced. For example, it is preferable to relatively reduce the organic solvent concentration by adding a large amount of an aqueous solution to the mixed liquid 8. For example, an aqueous solution three times the amount of the mixed liquid 8 is added to the mixed liquid 8. The aqueous solution may be the same as the aqueous solvent used in the first solution. By reducing the organic solvent concentration, the lipids are particulated, and lipid particles 200 encapsulating the drug 202 can be generated. As a result, a lipid particle solution 9 containing the lipid particles 200 is obtained.

[0100] As shown in (c) of FIG. 13, the particulation flow channel structure 303 for carrying out the particulation step S3 is, for example, a Y-shaped flow channel. The upstream end of one of the Y-shaped branched flow channels 331 is connected to, for example, the most downstream end of the flow channel structure 302 (the fourth flow channel 25 in this example), from which the mixed liquid 8 is supplied. The upstream end of the other flow channel 332 is provided with, for example, an aqueous solution inlet 333, from which the aqueous solution flows. As a result, the aqueous solution is mixed with the mixed liquid 8 in a flow channel 334 where the flow channels 331 and 332 join. As a result, the lipid is particulated, lipid particles 200 encapsulating the drug 202 are generated, and a lipid particle solution 9 containing the lipid particles 200 is obtained.

[0101] The particulate formation step S3 does not necessarily have to be performed using a flow path, and for example, an aqueous solution may be added to the mixed liquid 8 collected in the container.

[0102] In this manner, the lipid particles 200 can be produced.

[0103] ·Concentration process S4 The lipid particle production method of the embodiment may further include concentrating the lipid particle solution 9 as necessary (concentration step S4). The concentration is performed, for example, by removing a part of the solvent and / or the remaining lipid and drug 202 from the lipid particle solution 9. The concentration can be performed, for example, by ultrafiltration. For ultrafiltration, it is preferable to use an ultrafiltration filter having a pore size of, for example, 2 nm to 100 nm. For example, Amicon (registered trademark) Ultra-15 (Merck) or the like can be used as the filter. By performing the concentration step S4, it is possible to obtain a lipid particle solution 9 with high purity and concentration. The concentration of the lipid particles 200 in the lipid particle solution 9 after concentration is 1×10 13 pieces / mL~5×10 13 It is preferable that the concentration is about 1 / mL. However, it is not always necessary to carry out the concentration step S4.

[0104] 13(d), the concentration flow path structure 304 performing the concentration step S4 includes a flow path 341 and a filter 342 provided on the wall surface of the flow path 341. An upstream end of the flow path 341 is connected to, for example, the flow path 335 of the particulation flow path structure 303.

[0105] The filter 342 is provided, for example, in place of a part of the wall surface of the flow path 341. As the filter 342, any of the ultrafiltration filters described above can be used.

[0106] By flowing the lipid particle solution 9 through the flow path 341, the remaining materials and excess solvent, etc., pass through the filter 342 and are discharged to the outside of the flow path 341, while the lipid particles 200 remain in the flow path 341 and flow downstream, concentrating the lipid particle solution 9. The downstream end of the flow path 341 may be provided with an outlet 343 for collecting the lipid particle solution 9 after concentration, or may be connected to a tank for collecting the lipid particle solution 9.

[0107] The concentration step S4 does not necessarily have to be performed using a flow path, and for example, the lipid particle solution 9 collected in a container may be filtered through a filter.

[0108] Furthermore, in the lipid particle production method of the embodiment, a process for improving the quality of the lipid particles 200 may be further carried out as necessary. The improvement in quality may be, for example, prevention of leakage of the drug 202 from the lipid particles 200, improvement of the amount of the drug 202 encapsulated in the lipid particles 200, improvement of the ratio of the lipid particles 200 encapsulating the drug 202 (encapsulation rate), reduction and prevention of aggregation of the lipid particles 200, and / or reduction of variation in size of the lipid particles. For example, a process for cooling the lipid particle solution 9 may be carried out. Such a process may also be carried out using a flow path.

[0109] Each of the above-mentioned flow paths described above is, for example, a micro flow path. The flow of the fluid in the flow path, the injection of the fluid into the flow path, the removal of the fluid from the tank, and / or the storage of the lipid particle solution 9 in the container can be performed, for example, by a pump or an extrusion mechanism configured and controlled so that these operations are performed automatically.

[0110] The method for producing lipid particles according to the embodiment does not necessarily have to include the condensation step S1 and the concentration step S4 as described above, but may include at least the mixing step S2 and the particulation step S3.

[0111] According to the lipid particle manufacturing method of the embodiment, since the mixing step S2 is performed using the flow path structure of the embodiment, the first solution and the second solution can be mixed and stirred uniformly and well, and it is possible to manufacture higher quality lipid particles 200. For example, effects such as an increase in the amount of drug 202 encapsulated, a reduction in the average particle size of the lipid particles 200, and an increase in the ratio of lipid particles encapsulating the drug 202 can be obtained.

[0112] [example] Example 1 A flow channel structure similar to that shown in FIG. 4(a) was manufactured. The cross-sectional width × depth of the first flow channel 2 was 0.3 mm × 0.3 mm, and the depth of the shallow portion 4 was 1 / 3 (0.1 mm). Water was flowed from the upstream of the third flow channel 7 (the right side in the figure) toward the left side in the figure, and water containing a fluorescent dye was flowed from the second flow channel 3, and the flow channel structure was photographed with a fluorescent microscope. The flow rate in each flow channel was the same, and the linear velocity of the first flow channel 2 was set so that the Reynolds number was 50 or more.

[0113] The captured image is shown in Figure 14. It became clear that a transverse vortex was generated in the first flow channel 2 over a distance of several mm from the mixing region 6.

[0114] Example 2 A Y-shaped flow channel structure similar to that shown in Fig. 4(b) was manufactured. The third flow channel 7 and the first flow channel 2 had sides each measuring 0.3 mm square. The second flow channel 3 had a depth just before the mixing region 6 of 1 / 3 (0.1 mm).

[0115] Water was allowed to flow from the third flow channel 7, and water containing a fluorescent dye was allowed to flow from the second flow channel 3, and photographs were taken with an optical microscope. The flow rates in each flow channel were the same. A similar experiment was also carried out using the flow channel structure manufactured in Example 1, and the two were compared.

[0116] The photographed image of the flow path structure of Example 1 is shown in Fig. 15(a), and the photographed image of the flow path structure of Example 2 is shown in Fig. 15(b). It was revealed that the flow path structure of Example 2 had less turbulence in the flow immediately after merging than the flow path structure of Example 1, which is preferable for uniform mixing.

[0117] In addition, the generation of transverse vortices in the flow channel structure of FIG. 4(b) was simulated. The simulation was performed using ANSYS (registered trademark) Fluent (registered trademark), which is a fluid analysis software. The simulation image is shown in FIG. 16. It is clear from the image that transverse vortices are generated in the mixing region 6.

[0118] Example 3 A mixing unit 22 was joined downstream of the flow path structure (junction unit 21) of Example 2 to manufacture a flow path structure similar to that shown in Fig. 5. The flow paths other than the shallow portion had sides of 0.3 mm square, and the shallow portion had a depth of 1 / 3 (0.1 mm). A fluid containing a fluorescent dye was flowed from the second flow path 3 of the junction unit 21, and water was flowed from the third flow path 7.

[0119] A photograph of the first flow path 2 of the confluence unit 21 through the mixing unit 22 is shown in Fig. 17. Transverse vortices were observed over a distance of about 1 mm in the confluence 24c immediately after the second shallow portion 4b and in the fourth flow path 25 immediately after the third shallow portion 4c, and it became clear that mixing was promoted there. This result showed that further mixing could be achieved by providing the mixing unit 22.

[0120] Example 4 Three mixing units 22 were arranged in series downstream of the flow path (junction unit 21) of Example 2 to manufacture a flow path structure similar to that shown in FIG. 6(a). The normal flow paths other than the shallow portion had sides of 0.3 mm square, and the shallow portion had a depth of 1 / 3 (0.1 mm). Ethanol was flowed from the second flow path 3 of the junction unit, and water was flowed from the third flow path 7. Schlieren images were taken of the junction unit, the junction of the first mixing unit, the junction of the second mixing unit, and the junction of the third mixing unit.

[0121] The captured images are shown in Figure 18. The generation of lateral vortices was observed downstream of the shallow parts of each unit. In addition, as the water flowed from the confluence unit to the third mixing unit, the unevenness (cloudy areas) observed due to the difference in the refractive index between water and ethanol disappeared, indicating that the water was well mixed.

[0122] In addition, in a flow path structure of a similar configuration, water containing a fluorescent dye was flowed in one flow path of the merging unit, and water was flowed in the other, and photographed with a fluorescent microscope. The photographed image is shown in Figure 19. The image shows that as the water flows from the first mixing unit to the third mixing unit, the streaky shadows that appear when the fluorescent dye and water mix disappear, indicating that the water is mixed evenly.

[0123] FIG. 20 shows a graph illustrating the fluorescence intensity (normalized values) of the branching point of the first mixing unit (FIG. 19(a)), the flow path connecting the first mixing unit and the second mixing unit (FIG. 19(b)), the branching point of the second mixing unit (FIG. 19(c)), the flow path connecting the second mixing unit and the third mixing unit (FIG. 19(d)), the branching point of the third mixing unit (FIG. 19(e)), and the flow path most downstream of the third mixing unit (FIG. 19(f)). FIG. 21 shows a graph illustrating the brightness variance (normalized value), i.e., the squared value of the difference from the average value of the fluorescence intensity.

[0124] FIG. 20 clearly shows that the variation in fluorescence intensity is reduced as the flow progresses from (a) to (f).

[0125] 21, the brightness variance was approximately 0.46 at point (a), approximately 0.05 at points (b) and (c), approximately 0.02 at points (d) and (e), and approximately 0.05 at point (f). These results show that the fluorescence intensity approaches the average value as it moves from point (a) to point (f).

[0126] Therefore, it became clear that the two liquids were uniformly mixed as they flowed from the first mixing unit to the third mixing unit.

[0127] Example 5 In Examples 1 to 4, the shallow portion was set to a depth of 1 / 3 of the depth of the rest of the flow path, but in Example 5, the depth of the shallow portion for a flow path structure having the same shape as Example 1 was set to 1 / 1, 1 / 2, 1 / 3 or 1 / 6, and the dependence of lateral vortex generation on the depth of the shallow portion was simulated.

[0128] Simulation images are shown in Figure 22. At 1 / 1, almost no transverse vortices were generated. At 1 / 2, the generation of transverse vortices was very small. From 1 / 3, significant transverse vortices were generated, and at the thinner 1 / 6, even stronger transverse vortices were generated.

[0129] Therefore, it became clear that the depth of the shallow portion is preferably less than 1 / 2, and more preferably 1 / 3 or less.

[0130] Example 6 A flow path structure A (Example 1) and a flow path structure B (Example 2) shown in FIG. 23 were manufactured, and mixing of two liquids was simulated using these flow path structures for comparison.

[0131] In the flow path structure A, two mixing units 22 are arranged in series downstream of a junction unit 21. The first flow path of the junction unit of the flow path structure A is designated as α1, the flow path connecting the first mixing unit and the second mixing unit is designated as α2, and the flow path after the junction of the second mixing unit (fourth flow path) is designated as α3.

[0132] The flow path structure B is configured such that two mixing units 22 are provided downstream of the junction unit 21, and two flow paths intersect at right angles at the junction unit and the junction of the mixing units (similar to the flow path structure shown in FIG. 9). The first flow path of the junction unit of the flow path structure B is designated as β1, the flow path after the junction at the junction of the first mixing unit is designated as β2, and the flow path after the junction at the junction of the second mixing unit is designated as β3. The flow path after the bend downstream of flow path β1 (immediately before the branching part of the first mixing unit) is designated as γ1, the flow path after the bend downstream of flow path β2 (immediately before the branching part of the second mixing unit) is designated as γ2, and the flow path after the bend downstream of flow path β3 is designated as γ3.

[0133] Ethanol and water were introduced in equal amounts from each confluence unit under the condition that the Reynolds number was at least 50, and the ethanol concentration at each position in the flow paths α1-3, β1-5, and γ1-3 was simulated. The results are shown in Figure 24. The maximum ethanol concentration in each of α, β, and γ progressed as mixing progressed from 1 to 3, and finally converged to about 44%, which is the completely mixed concentration, but the convergence was clearly faster in the flow path structure B (β, γ) than in the flow path structure A (α).

[0134] One of the reasons for this is thought to be that flow turbulence increases when a flow channel with a shallow portion is joined at a right angle to a normal flow channel. Since flow turbulence is expected to have a mixing effect, if speed of mixing is desired rather than uniformity, a structure like flow channel structure B, in which a flow channel with a shallow portion is joined at a right angle to a normal flow channel, is desirable.

[0135] Example 7 In Example 7, an experiment will be described in which DNA-encapsulated lipid particles were produced using the flow channel structure of the embodiment, and the amount of DNA encapsulated in the lipid particles was measured.

[0136] As shown in FIG. 25, a flow path structure C (Comparative Example 1) having a Y-shaped structure without a shallow portion, a flow path structure D (Example 3) in which three mixing units are arranged in series in a confluence unit, and a flow path structure E (Example 4) in which six mixing units are arranged in series in a confluence unit were manufactured.

[0137] 180μl of 0.1mg / ml nLuc plasmid DNA was dissolved in 1620μl of 10mM HEPES (pH7.3) to obtain a DNA solution (solution 2). Six types of lipids were mixed as lipid particle materials in a molar ratio of FFT10:FFT20:DOPE:DOTAP:cholesterol:DNG-PEG2000=35:70:21:9.4:88.5:9.4, and dissolved in 1800μl of ethanol to obtain a lipid solution (solution 1).

[0138] The DNA solution (second solution) and the lipid solution (first solution) were filled in syringes and connected to a syringe pump. A liquid delivery tube was connected to each syringe connected to the syringe pump, and the liquid delivery tube was connected to the two input ports of the merging units of the flow channel structures C to E, respectively. A liquid delivery tube was also connected to the output port, and connected to a tube for recovering the mixed solution. Then, the liquid was delivered using a syringe pump and mixed in the flow channel. Of the fluid recovered from the output port, the first 800 μl was discarded, and finally 2400 μl was recovered as a DNA-lipid mixture. 7.2 ml of 10 mM HEPES (pH 7.3) was added to 2.4 ml of this DNA-lipid mixture to form particles, thereby obtaining a dilute lipid particle solution. 9.6 ml of the dilute lipid particle solution was centrifuged and concentrated to 240 μl using an ultrafiltration filter (Amicon (registered trademark) Ultra15, Merck) to obtain a lipid particle solution.

[0139] 890 μl of purified water (water for injection, manufactured by Otsuka Pharmaceutical Co., Ltd.) was mixed with 10 μl of lipid particle solution, and the resulting mixture was placed in a cuvette for particle size measurement, and the particle size and polydispersity index (pdi) were measured using a Zetasaizer® Nano ZSP (Malvern) in particle size measurement mode. Next, the zeta potential of the diluted solution was measured in the zeta potential measurement mode using a cuvette for zeta potential measurement.

[0140] In addition, Quant-iT TM The concentration of DNA encapsulated in the lipid particles of the lipid particle solution was measured using a PicoGreen (registered trademark) ds DNA Assay kit (Thermo Fisher Scientific). A solution (liquid A) was prepared by mixing 0.5 μl of lipid particle solution with 99.5 μl of 10 mM HEPES (pH 7.3) in advance. In addition, a solution (liquid A) was prepared by mixing 0.5 μl of lipid particle solution with 84.5 μl of 10 mM HEPES (pH 7.3), 1% Triton TM 10 μl of -X 100 and 5 μl of heparin were mixed to prepare a solution in which DNA was eluted from the lipid particles (liquid B).

[0141] After leaving each solution at room temperature for 30 minutes, 100 μl of PicoGreen solution was added, and the amount of fluorescence was measured using QuantiFlour (registered trademark) (Promega). The calibration curve sample was measured at the same time, and the amount of DNA in each sample was calculated. The difference between the amount of DNA in solution B and the amount of DNA in solution A was taken as the amount of DNA encapsulated in the lipid particles. The measurement results are shown in Table 1.

[0142] [Table 1]

[0143] Compared to the Y-shaped flow path structure C without a shallow portion, the amount of DNA encapsulated was improved by about 190% by using the flow path structures D and E of the embodiments. Furthermore, when the flow path structures D and E of the embodiments were used, the average particle size could be further reduced, and lipid particles with an even smaller average particle size were obtained with the flow path structure E having six mixing units.

[0144] Example 8 In Example 8, an experiment will be described in which mRNA-encapsulating lipid particles were produced using the flow channel structure of the embodiment, and the amount of mRNA encapsulated in the lipid particles was measured.

[0145] 180μl of mRNA encoding 0.1mg / ml NanoLuc® was dissolved in 1620μl of 10mM HEPES (pH7.3) to obtain an mRNA solution (second solution). Six types of lipids for lipid particle preparation were mixed in a molar ratio of FFT10:FFT20:DOPE:DOTAP:cholesterol:DNG-PEG2000=35:70:21:9.4:88.5:9.4 and dissolved in 1800μl of ethanol to obtain a lipid solution (first solution).

[0146] The mRNA solution (second solution) and the lipid solution (first solution) were filled in syringes and connected to a syringe pump. A liquid delivery tube was connected to each syringe connected to the syringe pump, and the liquid delivery tube was connected to the two input ports of the flow path structures D and E manufactured in Example 7. A liquid delivery tube was also connected to the output port, and connected to a tube for recovering the mixed solution. Then, the liquid was delivered using a syringe pump and mixed in the flow path. Of the fluid recovered from the output port, the first 800 μl was discarded, and finally 2400 μl was recovered as an mRNA-lipid mixture. 7.2 ml of 10 mM HEPES (pH 7.3) was added to 2.4 ml of this mRNA-lipid mixture to form particles, and a dilute lipid particle solution was obtained. 9.6 ml of the dilute lipid particle solution was centrifuged and concentrated to 240 μl using an ultrafiltration filter (AmiconUltra15) to obtain a lipid particle solution.

[0147] 890μl of purified water (water for injection, manufactured by Otsuka Pharmaceutical Co., Ltd.) was mixed with 10μl of lipid particle solution, and placed in a cuvette for particle size measurement. The particle size and polydispersity index (pdi) were measured using the particle size measurement mode of the Zetasaizer Nano ZSP. Next, the zeta potential of the same diluted solution was measured using a cuvette for zeta potential measurement in the zeta potential measurement mode. The results are shown in Table 2.

[0148] [Table 2]

[0149] It was revealed that the lipid particles produced by the flow path structure E having six mixing units had a smaller average particle size and further mixing was achieved compared to the flow path structure D having three mixing units.

[0150] Example 9 In Example 9, an experiment will be described in which the proportion of lipid particles encapsulating mRNA among lipid particles produced using the flow channel structure of the embodiment is measured.

[0151] 180μl of mRNA encoding 0.1mg / ml NanoLuc® was dissolved in 1620μl of 10mM HEPES (pH7.3) to obtain an mRNA solution (second solution). Six types of lipids for lipid particle preparation were mixed in a molar ratio of FFT10:FFT20:DOPE:DOTAP:cholesterol:DNG-PEG2000=35:70:21:9.4:88.5:9.4 and dissolved in 1800μl of ethanol to obtain a lipid solution (first solution).

[0152] The mRNA solution (second solution) and the lipid solution (first solution) were filled in syringes and connected to a syringe pump. A liquid delivery tube was connected to each syringe connected to the syringe pump, and the liquid delivery tube was connected to the two input ports of the flow channel structures C to E manufactured in Example 7. A liquid delivery tube was also connected to the output port, and connected to a tube for recovering the mixed solution. Then, the liquid was delivered using a syringe pump and mixed in the flow channel. Of the fluids recovered from the output port, the first 800 μl was discarded, and finally 2400 μl was recovered as an mRNA-lipid mixture. 7.2 ml of 10 mM HEPES (pH 7.3) was added to 2.4 ml of this mRNA-lipid mixture to form particles, and a dilute lipid particle solution was obtained. 9.6 ml of the dilute lipid particle solution was centrifuged and concentrated to 240 μl using an ultrafiltration filter (Amicon Ultra 15) to obtain a lipid particle solution.

[0153] The abundance of lipid particles encapsulating mRNA was measured using NanoSight (registered trademark) NS300 (Malvern). 10 μl of lipid particle solution was mixed with 990 μl of 10 mM HEPES (pH 7.3) and diluted. 5 μl of QantiFlour (RNAdye) and 985 μl of HEPES (pH 7.3) were mixed with 10 μl of dilute lipid particle solution, vortexed, and left at room temperature for 30 minutes in the dark. Thereafter, the lipid particle staining solution was irradiated with a laser using NanoSight NS300, and the number of particles that obtained a certain level of intensity of side scattered light or more was taken as the total number of lipid particles (C). Furthermore, the same sample was excited with a laser to cause fluorescence, and the number of particles with a certain level of fluorescence intensity or more was taken as the number of lipid particles encapsulating mRNA (D). The ratio of D to C was calculated and taken as the abundance of nucleic acid-encapsulating lipid particles. The results are shown in Table 3.

[0154] [Table 3]

[0155] It was revealed that the presence rate of lipid particles encapsulating mRNA is significantly improved in the flow channel structures D and E of the embodiments, compared to the flow channel structure C that does not have a shallow portion. This result shows that the mRNA solution and the lipid solution are mixed uniformly with the flow channel structures D and E of the embodiments.

[0156] Example 10 We simulated vortex generation in a flow path structure in which multiple mixing units 22 are connected in series after the confluence unit 21. The simulation image is shown in Figure 26. This image makes it clear that transverse vortices are generated downstream of the shallow part of each mixing unit.

[0157] Although some embodiments of the present invention have been described, these embodiments are presented as examples and are not intended to limit the scope of the invention. These novel embodiments can be implemented in various other forms, and various omissions, substitutions, and modifications can be made without departing from the spirit of the invention. These embodiments and their modifications are included in the scope and spirit of the invention, and are included in the scope of the invention and its equivalents described in the claims. The inventions described in the claims of the parent application as originally filed are set forth below. [1] A first flow path and a second flow path that merges with the first flow path, A flow path structure, wherein an end of the second flow path on the first flow path side has a first region that is shallower in depth than the first flow path. [2] The flow path structure according to [1], wherein the first flow path and the second flow path are cavities formed inside the flow path structure. [3] The flow path structure according to [1] or [2], wherein a depth of the first region is less than half a depth of the first flow path. [4] The flow path structure according to any one of [1] to [3], wherein the second flow path merges with the first flow path at a right angle. [5] The flow path structure according to any one of [1] to [4], further comprising a third flow path connected in series to the first flow path immediately upstream of a junction with the second flow path. [6] The flow path structure according to [5], wherein the third flow path is a cavity formed inside the flow path structure. [7] The flow path structure according to [5] or [6], wherein the third flow path and the first flow path form an integrated linear flow path, and the second flow path merges at a right angle with the first flow path. [8] The flow path structure according to [5] or [6], wherein the second flow path and the third flow path are connected to the first flow path symmetrically with respect to a longitudinal axis of the first flow path, and an angle between the second flow path and the third flow path is a right angle. [9] a mixing unit connected to a downstream end of the first flow path; the mixing unit includes a first branching and merging flow path and a second branching and merging flow path that branch the fluid flowing in from the first flow path into two to form two branched flows and merge the two branched flows into a fourth flow path; The second branch / junction flow path has a second region in an intermediate portion thereof that is shallower than the upstream and downstream sides thereof, and the downstream portion thereof bends and joins the fourth flow path. an end of the first branch / junction flow path on the side of the fourth flow path has a third region that is shallower in depth than the fourth flow path, The flow path structure according to any one of [1] to [8].

[10] The flow path structure according to [9], wherein the fourth flow path is a cavity formed inside the flow path structure.

[11] The depth of the second region is less than half the depth of the flow channels upstream and downstream of the second region; The depth of the third region is less than half the depth of the fourth flow channel. The flow path structure according to [9] or

[10] .

[12] The flow path structure according to any one of [9] to

[11] , wherein the junctions of the first branching / merging flow path and the second branching / merging flow path to the fourth flow path are connected to the fourth flow path at angles symmetrical to each other with respect to a longitudinal axis of the fourth flow path.

[13] The flow path structure according to any one of [9] to

[11] , wherein a junction portion of the second branching / merging flow path into the fourth flow path is connected in series to the fourth flow path and forms a straight flow path integral with the fourth flow path, and the junction portion of the first branching / merging flow path joins the fourth flow path at a right angle.

[14] The flow path structure according to any one of [9] to

[13] , comprising a plurality of the mixing units connected in series.

[15] The flow path structure according to any one of [9] to

[13] , comprising a plurality of the mixing units connected in parallel.

[16] A method for stirring a fluid using a flow path structure, comprising: the flow path structure includes a first flow path and a second flow path merging with the first flow path, and an end of the second flow path on the first flow path side has a first region having a depth shallower than that of the first flow path, flowing a first fluid from the second flow path to the first flow path; A method for agitating a fluid.

[17] The method according to

[16] , wherein the depth of the first region is less than half the depth of the first flow path.

[18] The flow path structure further includes a third flow path connected in series to the first flow path immediately upstream of a junction with the second flow path, further comprising flowing a second fluid from the third flow path to the first flow path. The method according to

[16] or

[17] .

[19] The flow path structure further includes a mixing unit downstream of the first flow path, the mixing unit includes a first branching and merging flow path and a second branching and merging flow path that branch the fluid flowing in from the first flow path into two to form two branched flows and merge the two branched flows into a fourth flow path; an end of the first branch / junction flow path on the side of the fourth flow path has a second region that is shallower in depth than the fourth flow path, The second branch / junction flow path has a third region in an intermediate portion thereof, the third region being shallower than the upstream and downstream portions thereof, and the downstream portion thereof is bent to join the fourth flow path. The method according to any one of

[16] to

[18] .

[20] The depth of the second region is less than half the depth of the flow channels upstream and downstream of the second region; The depth of the third region is less than half the depth of the fourth flow channel. The method described in

[19] . [twenty one] The method according to

[19] or

[20] , wherein the flow path structure comprises a plurality of the mixing units connected in series. [twenty two] The method according to

[19] or

[20] , wherein the flow path structure comprises a plurality of the mixing units connected in parallel. [twenty three] A method for producing lipid particles encapsulating a drug by using the flow channel structure according to any one of [5] to

[15] , flowing a first solution containing lipids as materials for the lipid particles in an organic solvent through one of the second flow path and the third flow path, and flowing a second solution containing the drug in an aqueous solvent through the other of the second flow path, thereby mixing the first solution and the second solution to obtain a mixed solution; and reducing the concentration of the organic solvent in the mixture to granulate the lipids and generate lipid particles encapsulating the drug; Including, Method for producing lipid particles. [twenty four] The method according to

[23] , wherein the drug is a nucleic acid, and further comprising agglomerating the nucleic acid prior to mixing the first solution with the second solution. [twenty five] The method according to

[23] or

[24] , further comprising a step of concentrating a lipid particle solution containing the lipid particles after the particulation. [Explanation of symbols]

[0158] 1, 10, 11, 20, 30, 31, 40, 50, 60, 100...flow path structure, 2...first flow path, 3...second flow path, 4, 4a...first shallow portion, 4b...second shallow portion, 4c...third shallow portion, 7...third flow path, 8...mixture, 9...lipid particle solution, 21...Mixing unit, 22...Mixing unit, 22a…first mixing unit, 22b…Second mixing unit, 22c…3rd mixed unit, 23...first branching and merging passage, 24...second branching and merging passage, 25...fourth channel, 200...lipid particles, 202...drug.

Claims

1. A first flow path and a second flow path that merges with the first flow path, an end of the second flow path on the side of the first flow path has a first region having a depth shallower than that of the first flow path; a direction of the first flow path is bent when viewed from a direction of the second flow path, A flow channel structure, wherein the first flow channel is closed in a longitudinal direction of the second flow channel in a mixing region of the second flow channel and the first flow channel.

2. The flow path structure according to claim 1 , wherein a direction of the first flow path intersects with a plane formed by a depth direction of the first region and a direction of the second flow path.

3. The flow path structure according to claim 1 , wherein the first flow path and the second flow path are cavities formed inside the flow path structure.

4. 4. The flow path structure according to claim 1, wherein a depth of the first region is less than half a depth of the first flow path.

5. The flow path structure according to claim 1 , wherein the second flow path merges with the first flow path at a right angle.

6. The flow path structure according to claim 1 , further comprising a third flow path connected in series to the first flow path immediately upstream of a junction with the second flow path.

7. The flow path structure according to claim 6 , wherein the third flow path is a cavity formed inside the flow path structure.

8. The flow path structure according to claim 6 or 7, wherein the third flow path and the first flow path form an integrated linear flow path, and the second flow path joins the first flow path at a right angle.

9. 8. The flow path structure according to claim 6, wherein the second flow path and the third flow path are connected to the first flow path symmetrically with respect to a major axis of the first flow path, and an angle formed between the second flow path and the third flow path is a right angle.

10. a mixing unit connected to a downstream end of the first flow path; the mixing unit includes a first branching and merging flow path and a second branching and merging flow path that branch a fluid flowing in from the first flow path into two to form two branched flows and merge the two branched flows into a fourth flow path; the second branch / junction flow path has a second region in an intermediate portion thereof that is shallower than the upstream and downstream portions thereof, and the downstream portion thereof bends and joins the fourth flow path; an end of the first branch / junction flow path on the side of the fourth flow path has a third region that is shallower in depth than the fourth flow path, The flow path structure according to any one of claims 1 to 9.

11. The flow path structure according to claim 10 , wherein the fourth flow path is a cavity formed inside the flow path structure.

12. The depth of the second region is less than half the depth of the flow passages upstream and downstream of the second region; The depth of the third region is less than half the depth of the fourth flow path. The flow path structure according to claim 10 or 11.

13. The flow path structure according to any one of claims 10 to 12, wherein the junctions of the first branching and merging flow path and the second branching and merging flow path to the fourth flow path are connected to the fourth flow path at angles symmetrical to each other with respect to a longitudinal axis of the fourth flow path.

14. The flow path structure according to any one of claims 10 to 12, wherein a junction portion of the second branching / merging flow path to the fourth flow path is connected in series to the fourth flow path and forms a straight flow path integral with the fourth flow path, and the junction portion of the first branching / merging flow path merges at a right angle to the fourth flow path.

15. The flow path structure according to any one of claims 10 to 14, comprising a plurality of the mixing units connected in series.

16. The flow path structure according to any one of claims 10 to 14, comprising a plurality of the mixing units connected in parallel.

17. A method for stirring a fluid using a flow path structure, comprising: the flow path structure includes a first flow path and a second flow path joining the first flow path, the second flow path having an end on the first flow path side that has a first region that is shallower in depth than the first flow path, a direction of the first flow path is bent when viewed from a direction of the second flow path, In a mixing region of the second flow path and the first flow path, the first flow path is closed in a longitudinal direction of the second flow path, flowing a first fluid from the second flow path to the first flow path; A method for agitating a fluid.

18. The fluid stirring method according to claim 17 , wherein the direction of the first flow path intersects with a plane formed by the depth direction of the first region and the direction of the second flow path.

19. 19. The method of claim 17 or 18, wherein the depth of the first region is less than half the depth of the first flow channel.

20. The flow path structure further includes a third flow path connected in series to the first flow path immediately upstream of a junction with the second flow path, further comprising flowing a second fluid from the third flow path to the first flow path. The method according to any one of claims 17 to 19.

21. The flow path structure further includes a mixing unit downstream of the first flow path, the mixing unit includes a first branching and merging flow path and a second branching and merging flow path that branch a fluid flowing in from the first flow path into two to form two branched flows and merge the two branched flows into a fourth flow path; an end of the first branch / junction flow path on the side of the fourth flow path has a second region that is shallower in depth than the fourth flow path; the second branch / junction flow path has a third region in an intermediate portion thereof, the third region being shallower than the upstream and downstream portions thereof, and the downstream portion thereof is bent to join the fourth flow path; The method according to any one of claims 17 to 20.

22. The depth of the second region is less than half the depth of the flow passages upstream and downstream of the second region; The depth of the third region is less than half the depth of the fourth flow path.

22. The method of claim 21.

23. 23. The method of claim 21 or 22, wherein the flow path structure comprises a plurality of the mixing units connected in series.

24. 23. The method of claim 21 or 22, wherein the flow path structure comprises a plurality of the mixing units connected in parallel.

25. A method for producing lipid particles encapsulating a drug using the flow path structure according to any one of claims 6 to 9, comprising the steps of: flowing a first solution containing lipids as materials for the lipid particles in an organic solvent through one of the second flow path and the third flow path, and flowing a second solution containing the drug in an aqueous solvent through the other of the second flow path, thereby mixing the first solution and the second solution to obtain a mixed solution; and reducing the concentration of the organic solvent in the mixture to granulate the lipids and generate lipid particles encapsulating the drug; Including, Method for producing lipid particles.

26. 26. The method of claim 25, wherein the agent is a nucleic acid, and further comprising aggregating the nucleic acid prior to combining the first solution with the second solution.

27. 27. The method of claim 25 or 26, further comprising concentrating the lipid particle solution containing the lipid particles after the particulation.

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