Fluid devices and their use

Abstract

A fluid device comprising: a base at least partially provided with a well array in which a plurality of wells that open to one face and have the same shape are regularly arranged; and a lid member arranged facing the well array, wherein a space between the well array and the lid member forms a flow passage through which a fluid flows, and a distance Dab between a center of gravity Ca of an opening portion of any well A of the well array and the center of gravity Cb of an opening portion of a well B closest to the well A and the diameter Da of a circle having the same area as the area of the opening portion of the well A satisfy the following formula (1):　(1): 0.8 ≤ Da / Dab < 1.

Description

Technical Field

[0001] The present invention relates to fluid devices and their use. More specifically, the present invention relates to fluid devices, a method for isolating an aqueous medium, and a method for detecting a detection target. This application claims priority to Japanese Patent Application No. 2020-147507 filed in Japan on September 2, 2020, the content of which is incorporated herein by reference.

Background Art

[0002] Techniques for detecting biomolecules in fluid devices are known. For example, in DNA microarray technology, biomolecules may be introduced into micropores and detected by performing a reaction involving heating. In addition, techniques for detecting biomolecules at the single-molecule level are known. Examples of such techniques include digital measurement techniques such as digital ELISA (Digital Enzyme-Linked ImmunoSorbent Assay), digital PCR (Digital Polymerase Reaction), and digital Invasive Cleavaged Assay (Digital ICA).

[0003] In these techniques, it is necessary to isolate an aqueous medium containing biomolecules in a minute reaction space. The inventors have previously developed a method for isolating an aqueous medium in which an aqueous medium is fed into a flow path of a reaction vessel having a flow path and a plurality of wells to fill the plurality of wells with the aqueous medium, and then an oily sealing liquid is fed into the flow path to seal the aqueous medium in the plurality of wells with the oily sealing liquid, so that each well becomes a plurality of independent reaction spaces (see, for example, Patent Document 1).

Prior Art Documents

Patent Documents

[0004]

Patent Document 1

Summary of the Invention

[0005] However, the inventors found that when the volume of the wells in a well array formed on a substrate becomes small, when reagents are introduced into each well, the air that was present inside the well may remain without being replaced by the reagents, which can hinder the detection of biomolecules.

[0006] Therefore, the present invention aims to provide a technique for suppressing the retention of air bubbles inside wells when introducing an aqueous medium into each well of a fluid device having a well array. [Means for solving the problem]

[0007] The present invention includes the following embodiments. [1] A substrate having at least a portion of a well array in which a plurality of wells of the same shape opening on one side are regularly arranged, and a lid member disposed opposite the well array, wherein the space between the well array and the lid member forms a fluid channel, and the distance Dab between the centroid Ca of the opening of any well A in the well array and the centroid Cb of the opening of the well B closest to well A, and the diameter Da of a circle having the same area as the area of ​​the opening of well A satisfy the following equation (1) Furthermore, the volume of each well is 10 fL or more and 100 pL or less, and the total volume of each well in the well array is 0.2 μL or more and 2.0 μL or less. , fluid devices. 0.8 ≤ Da / Dab < 1 …(1) [2] The fluid device according to [1], wherein the diameter of a circle having the same area as the opening of the well is 1 μm or more and 50 μm or less. [3] The fluid device according to [1] or [2], wherein the ratio of the total area of ​​the openings of each well in the well array to the area of ​​the well array on one side is 30% or more and 90% or less. 。 [4 [1]~[ 3 A fluid device as described in any of the following: [ 5[1]~[ 4 A fluid device as described in any of the following: [ 6 ] The contact angle between the one surface and water is 70 degrees or more and 180 degrees or less, [1]~[ 5 A fluid device as described in any of the following: [ 7 [1]~[ 6 A fluid device as described in any of the following: [ 8 ][1]~[ 7 A method for isolating an aqueous medium, comprising the steps of introducing an aqueous medium into the flow channel of a fluid device described in any of the [ ], and after introducing the aqueous medium, introducing a sealing liquid into the flow channel to isolate the aqueous medium in each well of the well array. [ 9 ][ 8 A method for detecting a target, comprising the steps of: isolating an aqueous medium containing a target to be detected and a detection reagent by the method described in [ ], heating the fluid device to cause a reaction inside the well to generate a signal for detecting the target to be detected; and detecting the signal. [ 10 The target of detection is a biomolecule, 9 The method used in [ ]. [ 11 The above reaction is an isothermal reaction, 9 ] or [ 10 The method used in [ ]. [ 12 The signal is fluorescent, 9 ]~[ 11 The method described in one of the following ways. [Effects of the Invention]

[0008] According to the present invention, a technique can be provided to suppress the retention of air bubbles inside the wells when introducing an aqueous medium into each well of a fluid device having a well array.

Brief Description of the Drawings

[0009] [Figure 1] (a) is a schematic cross-sectional view for explaining the structure of the fluid device, (b) is a top view of the fluid device, and (c) is a partially enlarged view (plan view) of the well array of the fluid device seen from the opening surface side of the well. [Figure 2] (a) and (b) are photographs of the well array obtained by feeding buffer to the fluid device of Example 1 and observing it in bright field in Experimental Example 1. [Figure 3] (a) to (c) are photographs of the well array obtained by feeding buffer to the fluid device of Comparative Example 1 and observing it in bright field in Experimental Example 1. [Figure 4] (a) to (e) are photographs of the well array obtained by feeding buffer to the fluid device of Comparative Example 2 and observing it in bright field in Experimental Example 1. [Figure 5] (a) to (e) are cross-sectional views of the fluid device showing the results of the simulation in Experimental Example 2. [Figure 6] (a) to (c) are cross-sectional views of the fluid device showing the results of the simulation in Experimental Example 3. [Figure 7] (a) to (c) are cross-sectional views of the fluid device showing the results of the simulation in Experimental Example 4. [Figure 8] (a) to (c) are cross-sectional views of the fluid device showing the results of the simulation in Experimental Example 5.

Embodiments for Carrying Out the Invention

[0010] Hereinafter, embodiments of the present invention will be described in detail with reference to the drawings as appropriate. In the drawings, the same or corresponding parts are denoted by the same or corresponding reference numerals, and duplicate descriptions are omitted. Note that the dimensional ratios in each figure are exaggerated for the purpose of explanation and do not necessarily match the actual dimensional ratios.

[0011] [Fluid Device] In one embodiment, the present invention provides a fluid device comprising a substrate having at least a portion of a well array in which a plurality of wells of the same shape opening on one side are regularly arranged, and a lid member disposed opposite the well array, wherein the space between the well array and the lid member forms a fluid channel, and the distance Dab between the centroid Ca of the opening of any well A in the well array and the centroid Cb of the opening of the well B closest to well A, and the diameter Da of a circle having the same area as the area of ​​the opening of well A, satisfy the following formula (1). 0.8 ≤ Da / Dab < 1 …(1)

[0012] As will be described later in the examples, the fluid device of this embodiment makes it possible to suppress the retention of air bubbles inside the wells when introducing an aqueous medium into each well of the well array.

[0013] Figure 1(a) is a schematic cross-sectional view illustrating the structure of the fluid device of this embodiment, Figure 1(b) is a top view of the fluid device of this embodiment, and Figure 1(c) is a partially enlarged view (plan view) of the well array of the fluid device of this embodiment as seen from the well opening side.

[0014] As shown in Figure 1(a), the fluid device 100 of this embodiment comprises a substrate 130 having at least a portion of a well array 120 in which a plurality of wells 110 of the same shape opening on one side are regularly arranged, and a lid member 140 positioned opposite the well array 120, the space 150 between the well array 120 and the lid member 140 forming a fluid channel. The fluid channel 150 is a continuous space between the surface 131 of the substrate 130 and the surface 141 of the lid member 140.

[0015] As shown in Figures 1(b) and (c), the distance Dab between the centroid Ca of the opening of any well A in the well array 120 (i.e., the centroid of the shape defined by the periphery of the opening) and the centroid Cb of the opening of the well B closest to well A, and the diameter Da of a circle with the same area as the opening of well A, satisfy the following equation (1). 0.8 ≤ Da / Dab < 1 …(1)

[0016] In the fluid device of this embodiment, the lower limit of the Da / Dab value is 0.8, but may be 0.83 or higher. The upper limit of the Da / Dab value is less than 1, but may be 0.92 or lower, or approximately 0.9. These lower and upper limits can be combined in any way.

[0017] As shown in Figure 1(a), the fluid device of this embodiment may include an inlet 160 for introducing fluid into the flow path 150 and an outlet 170 for discharging fluid from the flow path 150. In the example of Figure 1(a), the inlet 160 and outlet 170 are formed on the lid member 140, but the inlet 160 and outlet 170 may also be formed on a peripheral member 180 (described later) or on the substrate 130. The inlet 160 and outlet 170 are positioned on either side of the well array 120.

[0018] The shapes of the inlet 160 and outlet 170 are not particularly limited and can be any conceivable shape as long as they can transport fluid. For example, they may be circles, ellipses, triangles, squares, pentagons, hexagons, heptagons, and octagons.

[0019] As shown in Figure 1(a), the fluid device of this embodiment preferably includes a peripheral member 180. The peripheral member 180 functions as a spacer to separate the substrate 130 and the lid member 140 to form a flow path 150. The peripheral member 180 is also positioned between the substrate 130 and the lid member 140, surrounding the well array 120, and forms part of the wall surface of the flow path 150. That is, the flow path 150 is preferably surrounded by the peripheral member 180 located between the surface 131 of the substrate 130 and the surface 141 of the lid member 140. The peripheral member 180 may be provided as an integral member that is continuously connected to the lid member 140.

[0020] Furthermore, the cross-sectional shape of the flow path 150 in a plane perpendicular to the flow direction is not particularly limited, and any conceivable shape is acceptable as long as it is a shape that can deliver fluid. Examples include squares, rectangles, triangles, circles, and ellipses. In addition, the cross-sectional shape of the flow path 150 may be constant or change from the inlet 160 to the outlet 170, but it is preferable that it be constant.

[0021] The fluid device of this embodiment may be a microchannel, a small channel typically used when handling biomolecules. More specifically, the fluid device of this embodiment may have a maximum cross-sectional area of ​​0.01 to 1 mm². 2 That's fine.

[0022] The well array 120 may be formed by forming a plurality of wells 110 on one side 131 of the substrate 130, or the substrate 130 may be a laminate of a first layer having a plurality of through holes and a second layer which is a flat plate, wherein the through holes form the wells 110 and the plurality of through holes form the well array 120.

[0023] The material of the substrate 130 is not particularly limited and can be, for example, metals such as stainless steel, titanium, cobalt-chromium alloy, and magnesium alloy; glass; and resin materials such as general-purpose plastics, medical plastics, and cosmetic plastics. Multiple materials made of these materials may also be laminated. Examples of resin materials include polyethylene, polypropylene, polystyrene, polyamide, polycarbonate, cyclic polyolefin, polylactic acid, polyglycolic acid, polycaprolactone, acrylic, urethane resin, silicone resin, fluororesin, aromatic polyether ketone, epoxy resin, and copolymer materials of these resins. More specifically, ZEONEX® and CYTOP® can be used. The material of the lid member 140 is also not particularly limited and can be, for example, the same as the material of the substrate 130 described above.

[0024] The shape of the opening of the well 110 (i.e., the shape of the well 110 in the plan view of the fluid device 100 as seen from the opening side of the well 110) is not particularly limited and may be a circle, an ellipse, or a polygon such as a triangle, square, pentagon, hexagon, heptagon, or octagon. If the shape of the opening of the well 110 is a circle, the centroid of the opening of the well 110 will be the center of the circle.

[0025] Each of the multiple wells 110 constituting the well array 120 has the same shape and is arranged regularly. However, a small number of wells (e.g., 1 to 4) may have different shapes for use as alignment marks in imaging and device manufacturing. In this case, substantially all wells (i.e., all wells except the aforementioned small number) have the same shape and are arranged regularly.

[0026] Here, "regularly arranged wells" means that the centroids of the openings of the wells constituting the well array are arranged in a certain pattern. For example, the centroids of the well openings may be arranged in a square grid. In this case, the lines connecting the centroids of the openings of four adjacent wells form a rectangle, preferably a square.

[0027] Alternatively, the centroids of the well openings may be arranged in a triangular grid (also called a hexagonal grid). In this case, the lines connecting the centroids of three adjacent well openings form an equilateral triangle. When the wells are arranged in a triangular grid, the distance between the centroid of any well opening and the centroid of the opening of the well closest to that well is constant for all wells.

[0028] The wells shown in Figure 1(c) are arranged in a triangular grid. As shown in Figure 1(c), the centroids Ca, Cb, and Cc of the openings of any well A, the well B closest to well A, and the well C closest to both well A and well B, respectively, among the wells 110 that make up the well array 120, form an equilateral triangle with each of these points as vertices. In Figure 1(c), the lines connecting the centroids Ca, Cb, and Cc of the openings of wells A, B, and C, respectively, form an equilateral triangle.

[0029] In the fluid device of this embodiment, the diameter of a circle with the same area as the well opening is preferably 1 μm or more and 50 μm or less. That is, the lower limit of the diameter of a circle with the same area as the well opening is preferably 1 μm. The upper limit of the diameter of a circle with the same area as the well opening may be less than 20 μm, 19 μm or less, 18 μm or less, 17 μm or less, 16 μm or less, 15 μm or less, 14 μm or less, 13 μm or less, 12 μm or less, 11 μm or less, or 10 μm or less. These lower and upper limits can be combined arbitrarily.

[0030] In the fluid device of this embodiment, the area of ​​the well array 120 refers to the area of ​​the region on the surface 131 that inscribes the wells 110 located at the periphery of the well array 120. The ratio of the total area of ​​the openings of each well 110 of the well array 120 to the area of ​​the well array 120 on one surface 131 (hereinafter sometimes referred to as the "opening area ratio") is preferably 30% or more and 90% or less.

[0031] The lower limit of the opening area ratio may be 60%, 45%, or 30%. The upper limit of the opening area ratio may be 90%, 80%, or 70%. These lower and upper limits can be combined in any way. For example, the opening area ratio may be between 30% and 90%, between 45% and 80%, or between 60% and 70%.

[0032] In the fluid device of this embodiment, the volume of each well 110 is preferably 10 fL or more and 100 pL or less, and more preferably 100 fL or more and 30 pL or less. Furthermore, the total volume of each well 110 constituting the well array 120 is preferably 0.2 μL or more and 2.0 μL or less, and more preferably 0.4 μL or more and 1.5 μL or less. Furthermore, the ratio of the diameter of a circle with the same area as the opening area of ​​the well 110 to the depth of the well 110 is preferably 3% or more and 200% or less, more preferably 30% or more and 120% or less, and even more preferably 60% or more and 90% or less. When the size of the well 110 is within the above range, single-molecule detection of biomolecules can be suitably performed.

[0033] In the fluid device of this embodiment, it is preferable that the ratio of the total volume of each well 110 constituting the well array 120 to the volume of the flow path 150 is 5% or more and 40% or less.

[0034] In the fluid device of this embodiment, the contact angle between one surface 131 and water is preferably 70 degrees or more and 180 degrees or less. Furthermore, the contact angle between the surface 141 of the lid member 140 facing the well array 120 and water is preferably 70 degrees or more and 180 degrees or less. When the contact angles of surfaces 131 and 141 are within the above range, when the sealing liquid is introduced into the flow path 150, the aqueous medium tends to be easily isolated in each well of the well array.

[0035] The fluid device of this embodiment can be manufactured, for example, by the following procedure. First, a substrate is prepared, and a resin layer is formed on one side of the substrate. Wells are formed on the substrate by forming through holes in this resin layer. A second resin layer may be provided between the substrate and the resin layer. Alternatively, an anchor layer or the like may be provided to improve the adhesion between the substrate and the resin layer.

[0036] The resin layer may be formed from a material obtained by mixing a colored component with a resin material. When the resin material is a resist, the content of the colored component can be, for example, 0.5% by mass (also called mass%) or more and 60% by mass or less. With respect to the content, it is preferably 5% by mass or more and 55% by mass or less, and more preferably 20% by mass or more and 50% by mass or less.

[0037] The content of the colored component can be appropriately set to enable the construction of the desired pattern, taking into consideration the proportion of photosensitive components, etc., contained in the resist. The colored component may also be a pigment, and a dispersant may be added along with the pigment as appropriate. When the formed resin layer is made from a material in which the colored component is mixed with the resin material, the resin layer will have a color based on the colored component.

[0038] Next, through-holes are formed in the resin layer. Photolithography allows for the simple and accurate formation of through-holes. When the resin layer is formed by injection molding or the like, the formation of the resin layer and the formation of the through-holes can be performed in the same process. In addition, through-holes can also be formed by etching using a pattern mask. Once the through-holes are formed in the resin layer, a substrate 130 having a well array 120 is obtained.

[0039] Alternatively, the well array 120 may be formed by forming a plurality of wells 110 on one side 131 of the substrate 130. In this case, the substrate 130 having the well array 120 can be manufactured by injection molding the above-mentioned resin material using a mold corresponding to the shape of the well array 120.

[0040] Next, the peripheral member 180 is placed around the well array 120. Then, the lid member 140 is placed on the peripheral member 180. Subsequently, the substrate 130, peripheral member 180, and lid member 140 are joined together to obtain the fluid device 100. The flow path 150 is formed between the lid member 140 and the substrate 130 by the peripheral member 180.

[0041] The method for joining the substrate 130, the peripheral member 180, and the lid member 140 is not particularly limited, and known methods can be used, such as laser welding, bonding with double-sided tape, and bonding with adhesive.

[0042] Furthermore, in order to improve the adhesion between the substrate 130, the peripheral member 180, and the lid member 140, surface treatments may be performed on the surfaces of the substrate 130 and the lid member 140 before bonding to increase the adhesive effect. For example, surface treatments include (1) chemical surface modification and (2) processing of the surface shape.

[0043] Alternatively, the peripheral member 180 and the lid member 140 may be integrally molded. In this case, the fluid device 100 can be manufactured by joining a substrate 130 having at least a portion of the well array 120 with a lid member 140 from which the peripheral member 180 is integrally molded. The flow path 150 is formed between the lid member 140 and the substrate 130 by the peripheral member 180 integrally molded with the lid member 140.

[0044] By the above method, a fluid device can be manufactured. However, the method for manufacturing a fluid device is not limited to the one described above; other known methods that can be applied by analogy to each step can be used.

[0045] [Method for isolating aqueous media] In one embodiment, the present invention provides a method for isolating an aqueous medium, comprising the steps of introducing an aqueous medium into the flow channel of the fluid device described above, and, after introducing the aqueous medium, introducing a sealing liquid into the flow channel to isolate the aqueous medium in each well of the well array.

[0046] According to the method of this embodiment, when an aqueous medium is filled into each well of a well array and isolated, the retention of air bubbles inside the wells can be suppressed.

[0047] It is preferable that the aqueous medium and the sealing liquid are either immiscible or poorly miscible with each other. Specific examples of sealing liquids include fluorine-based liquids such as FC-40, FC-43, FC-770, FC-72, and FC-3283 (all manufactured by 3M).

[0048] The aqueous medium may contain the target to be detected and the detection reagent. Examples of the target to be detected include biomolecules such as nucleic acids, proteins, and lipids. The detection reagent is appropriately selected depending on the detection method.

[0049] In the method of this embodiment, the aqueous medium may contain a surfactant. This provides effects such as suppressing the retention of air bubbles inside the wells and suppressing non-specific adsorption to the regions between the wells on the surface 131 of the substrate 130.

[0050] In the method of this embodiment, the step of introducing a filling liquid is included before introducing the aqueous medium, and the filling liquid and the aqueous medium may be miscible with each other or easily miscible. This makes it easier to further suppress the retention of air bubbles inside the well. Specific filling liquids include aqueous media containing surfactants, aqueous media without surfactants, and organic solvents that mix easily with aqueous media.

[0051] The inclusion of a surfactant in the filler also provides effects such as suppressing the retention of air bubbles inside the wells and suppressing non-specific adsorption to the areas between wells on the surface 131 of the substrate 130. The surfactant may be included in both the aqueous medium and the filler, or in only one of them.

[0052] In the method of this embodiment, the aqueous medium and the sealing liquid may be introduced under pressure from the inlet of the fluid device. Introducing the aqueous medium and the sealing liquid under pressure may be done by injecting the aqueous medium and the sealing liquid using a syringe or pipette. According to the method of this embodiment, even when introduced under pressure, the effect of suppressing the retention of air bubbles inside the well is easily obtained.

[0053] [Method for detecting the target] In one embodiment, the present invention provides a method for detecting a target, comprising the steps of: isolating an aqueous medium containing the target to be detected and a detection reagent in the wells of a well array of a fluid device using the aqueous medium isolation method described above; heating the fluid device to cause a reaction to occur inside the wells to generate a signal for detecting the target to be detected; and detecting the signal.

[0054] According to the method of this embodiment, since the retention of air bubbles inside the well is suppressed, it is easy to detect the target object with high accuracy.

[0055] The aqueous medium contains the target to be detected and the detection reagent. Examples of the target to be detected include biomolecules such as nucleic acids, proteins, and lipids. The detection reagent is selected appropriately according to the detection principle.

[0056] The reaction that produces the signal may be a isothermal reaction. The signal may also be fluorescent. An example of such a reaction is Invasive Cleavaged Assay (ICA). In the case of ICA, the target of detection is nucleic acid, and the detection reagents include flap probes, flap endonucleases (FEN), and fluorescent substrates. A flap probe is a nucleic acid fragment designed to hybridize with the target nucleic acid to form a double-stranded nucleic acid with a flap structure. In the case of ICA, the reaction that produces the signal is preferably conducted at a reaction temperature of 55°C to 75°C.

[0057] In the method of this embodiment, the step of detecting a signal may involve capturing an image of the fluid device and analyzing the captured image to detect the signal.

[0058] In another aspect, the present invention encompasses the following embodiments. [1] A fluid device comprising a substrate having at least a portion of a well array in which a plurality of wells of the same shape opening on one side are regularly arranged, and a lid member disposed opposite to the well array, wherein the space between the well array and the lid member forms a fluid channel, and the distance Dab between the centroid Ca of the opening of any well A in the well array and the centroid Cb of the opening of the well B closest to well A, and the diameter Da of a circle having the same area as the area of ​​the opening of well A, satisfy the following equation (1). 0.8 ≤ Da / Dab < 0.92 …(1) [2] The fluid device according to [1], wherein the diameter of a circle having the same area as the opening of the well is 1 μm or more and 15 μm or less. [3] The fluid device according to [1] or [2], wherein the ratio of the total area of ​​the openings of each well in the well array to the area of ​​the well array on one side is 60% or more and 80% or less. [4] The fluid device according to any one of [1] to [3], wherein the volume of each well is 100 fL or more and 30 pL or less. [5] The fluid device according to any one of [1] to [4], wherein the total volume of each well in the well array is 0.4 μL or more and 1.5 μL or less. [6] The fluid device according to any one of [1] to [5], wherein the ratio of the sum of the volumes of each well in the well array to the volume of the flow path is 5% or more and 100% or less. [7] The fluid device according to any one of [1] to [6], wherein the ratio of the diameter of a circle having the same area as the area of ​​the opening of the well to the depth of the well is 60% or more and 90% or less. [8] The fluid device according to any one of [1] to [7], wherein the contact angle with water on one of the surfaces is 70 degrees or more and 120 degrees or less. [9] The fluid device according to any one of [1] to [8], wherein the contact angle between the surface of the lid member facing the well array and water is 70 degrees or more and 120 degrees or less. A method for isolating an aqueous medium, comprising the steps of introducing an aqueous medium into the channel of a fluid device described in any of

[10] [1] to [9], and introducing a sealing liquid into the channel after introducing the aqueous medium to isolate the aqueous medium in each well of the well array. A method for detecting a target, comprising the steps of: isolating an aqueous medium containing a target to be detected and a detection reagent by the method described in

[11]

[10] , then heating the fluid device to cause a reaction to occur inside the well to generate a signal for detecting the target to be detected; and detecting the signal.

[12] The method according to

[11] , wherein the target of detection is a biomolecule.

[13] The method according to

[11] or

[12] , wherein the reaction is an isothermal reaction.

[14] The method according to any one of

[11] to

[13] , wherein the signal is fluorescent. [Examples]

[0059] [Manufacturing Example 1] (Fabrication of the fluid device in Example 1) A substrate made of cyclic polyolefin (product code "ZEONOR1020R", manufactured by Nippon Zeon Co., Ltd.) and a lid component made of cyclic polyolefin (product code "ZEONOR1020R", manufactured by Nippon Zeon Co., Ltd.) were manufactured by injection molding.

[0060] The substrate thickness was 0.6 mm. A well array was formed on one side of the substrate. The well openings were circular. The wells had a diameter of 10 μm and a depth of 15 μm. The volume of each well was 824 fL, the total volume of all wells was 0.76 μL, and the ratio of the well opening diameter to the well depth was 66.7%. A well array was formed by arranging multiple wells in a triangular grid pattern in a 6.0 mm × 30.0 mm area on the substrate, such that the distance between the center of one well and the center of the nearest well was 12 μm. The contact angle with water on one side of the substrate was 89 degrees.

[0061] The lid member was formed integrally with the stepped portion (peripheral member). By adjusting the height of the stepped portion to 30 μm, the height of the flow path was set to 30 μm. The actual height of the flow path was measured using a contact-type measuring instrument (model number "TALYSURF PGI1240", manufactured by Taylor Hobson). The volume of the flow path was approximately 6 μL, and the ratio of the sum of the volumes of each well to the volume of the flow path was approximately 12.7%. The contact angle between the surface of the lid member facing the well array and the water was 89 degrees.

[0062] Next, the stepped portion of the substrate and the lid member were joined by laser welding to fabricate the microfluidic device of Example 1.

[0063] [Manufacturing Example 2] (Fabrication of fluid devices for Comparative Example 1 and Comparative Example 2) A microfluidic device for Comparative Example 1 was fabricated in the same manner as in Example 1, except that the distance between the center of one well and the center of the well closest to it was set to 16 μm. The area on which the well array was formed was the same as in Example 1, and the total volume of each well was 0.63 μL.

[0064] Furthermore, a microfluidic device for Comparative Example 2 was fabricated in the same manner as in Example 1, except that the distance between the center of one well and the center of the well closest to it was set to 20 μm. The area on which the well array was formed was the same as in Example 1, and the total volume of each well was 0.4 μL.

[0065] [Experimental Example 1] Aqueous media was introduced into each fluid device in Example 1, Comparative Example 1, and Comparative Example 2, and the likelihood of air bubbles remaining in the wells was evaluated.

[0066] First, an aqueous medium (i.e., a buffer) with the composition shown in Table 1 below was injected into the channel formed between the substrate and the lid member of each fluid device.

[0067] [Table 1]

[0068] Buffer injection was performed on each fluid device while observing it from the substrate side using a microscope (model number "BZ-710", manufactured by Keyence Corporation) under bright-field conditions. A 10x objective lens was used, and the exposure time was 20 milliseconds. The amount of buffer injected until all air bubbles in the well were completely removed was then measured.

[0069] Figures 2(a) and 2(b) are photographs showing the bright-field observation results of the well array when buffer was delivered to the fluid device of Example 1. Figure 2(a) is a photograph showing the result when 20 μL of buffer was delivered, and Figure 2(b) is a photograph showing the result when 50 μL of buffer was delivered. The size of the observation images in Figures 2(a) and 2(b) was 3,600 μm × 2,700 μm. As a result, the fluid device of Example 1 was able to sufficiently remove the air bubbles remaining in the wells with a delivery volume of 50 μL of buffer.

[0070] Furthermore, Figures 3(a) to 3(c) are photographs showing the bright-field observation results of the well array when buffer was delivered to the fluid device of Comparative Example 1. Figure 3(a) is a photograph showing the result when 100 μL of buffer was delivered, Figure 3(b) is a photograph showing the result when 200 μL of buffer was delivered, and Figure 3(c) is a photograph showing the result when 300 μL of buffer was delivered. The size of the observation images in Figures 3(a) to 3(c) was 3,600 μm × 2,700 μm. As a result, the fluid device of Comparative Example 1 required the delivery of 300 μL of buffer to sufficiently remove the air bubbles remaining in the wells.

[0071] Figures 4(a) to 4(e) show the bright-field observation results of the well array when buffer was delivered to the fluid device of Comparative Example 2. Figure 4(a) shows the result when 100 μL of buffer was delivered, Figure 4(b) shows the result when 200 μL of buffer was delivered, Figure 4(c) shows the result when 300 μL of buffer was delivered, Figure 4(d) shows the result when 400 μL of buffer was delivered, and Figure 4(e) shows the result when 500 μL of buffer was delivered. The size of the observation images in Figures 4(a) to 4(e) was 3,600 μm × 2,700 μm. As a result, the fluid device of Comparative Example 2 required the delivery of 500 μL of buffer to sufficiently remove the air bubbles remaining in the wells.

[0072] Table 2 below shows the well diameter, well depth, distance between the center of a well and the center of the nearest well (center-to-center distance), ratio of well diameter to center-to-center distance (diameter / center-to-center distance), flow path height, opening area ratio, amount of buffer required to completely remove air bubbles from the well, and evaluation results of the resistance to air bubble retention in the well for each fluid device.

[0073] The opening area ratio was defined as the ratio of the total area of ​​the well openings to the area of ​​the 6.0 mm × 30.0 mm region where the well array was formed. Furthermore, the evaluation of the resistance to air bubble retention within the wells was performed according to the following evaluation criteria. (Evaluation Criteria) Good: The amount of buffer required to completely remove air bubbles from the well is 50 μL or less. Failure: The amount of buffer required to completely remove air bubbles from the well exceeded 50 μL.

[0074] [Table 2]

[0075] From these results, it became clear that when the ratio of the well's diameter to the distance between the center of a well and the center of the well closest to it (intercenter distance) (diameter / intercenter distance) is 0.8 or higher, air bubbles tend to remain less likely to persist in the well.

[0076] [Experimental Example 2] (Simulation 1) The likelihood of air bubbles remaining in the wells of a fluid device was investigated through simulation. The simulation was performed using software (product name "Ansys Fluent," manufactured by ANSYS).

[0077] A simulation was conducted on a fluid device having a well array with the shape shown in Table 3, where a liquid with the physical properties shown in Table 4 was delivered through the flow path. Table 3 shows the well diameter, well depth, distance between the center of a well and the center of the nearest well (center-to-center distance), ratio of well diameter to center-to-center distance (diameter / center-to-center distance), flow path height, taper, and presence or absence of burrs and rounding of the fluid device's wells. In Table 4, the wettability value reflects the physical properties of the fluid device. Taper refers to a shape where the area of ​​the well opening and the area of ​​the well bottom are different, tapering from the opening to the bottom. The taper angle refers to the angle between one surface of the substrate including the well opening and the side of the well. When the taper angle is 0°, the angle between one surface of the substrate including the well opening and the side of the well is 90°.

[0078] The fluid device simulated in this experimental example was the same as the fluid device in Example 1.

[0079] [Table 3]

[0080] [Table 4]

[0081] The simulation was performed under two conditions: first, the liquid was delivered at a flow rate of 33 mm / second for 0.027 seconds after the start of delivery, and then at a flow rate of 330 mm / second from 0.027 seconds to 0.047 seconds after delivery.

[0082] Figures 5(a) to 5(e) are cross-sectional views of the fluid device showing the simulation results. Figure 5(a) shows the simulation results before the start of fluid delivery, Figure 5(b) shows the simulation results 0.02 seconds after the start of fluid delivery, Figure 5(c) shows the simulation results 0.03 seconds after the start of fluid delivery, Figure 5(d) shows the simulation results 0.04 seconds after the start of fluid delivery, and Figure 5(e) shows the simulation results 0.047 seconds after the start of fluid delivery. In Figures 5(a) to 5(e), the scales indicate the outlines of bubbles and liquid.

[0083] As a result, it became clear that after the start of liquid delivery, the bubbles in the well gather and merge, and these merged bubbles flow along, entraining other bubbles.

[0084] [Experimental Example 3] (Simulation 2) The likelihood of air bubbles remaining in the wells of a fluid device was investigated through simulation. The simulation was performed using software (product name "Ansys Fluent," manufactured by ANSYS).

[0085] We simulated the case where a liquid with the physical properties shown in Table 4 above is delivered through the flow path of a fluid device having a well array with the shape shown in Table 5 below.

[0086] The fluid device simulated in this experimental example was equivalent to the fluid device in Comparative Example 1.

[0087] [Table 5]

[0088] The simulation was performed under two conditions: first, the liquid was delivered at a flow rate of 33 mm / second for 0.02 seconds after the start of delivery, and then at a flow rate of 330 mm / second from 0.02 seconds after that.

[0089] Figures 6(a) to 6(c) are cross-sectional views of the fluid device showing the simulation results. Figure 6(a) shows the simulation results before the start of fluid delivery, Figure 6(b) shows the simulation results 0.02 seconds after the start of fluid delivery, and Figure 6(c) shows the simulation results 0.03 seconds after the start of fluid delivery. In Figures 6(a) to 6(c), the scales indicate the outlines of bubbles and liquid.

[0090] As a result, it became clear that even when liquid was pumped, the air bubbles in the well did not gather and merge, and the bubbles remained.

[0091] [Experimental Example 4] (Simulation 3) The likelihood of air bubbles remaining in the wells of a fluid device was investigated through simulation. The simulation was performed using software (product name "Ansys Fluent," manufactured by ANSYS).

[0092] We simulated the case where a liquid with the physical properties shown in Table 4 above is delivered through the flow path of a fluid device having a well array with the shape shown in Table 6 below.

[0093] [Table 6]

[0094] The simulation was performed under the case where the liquid was delivered at a flow rate of 33 mm / second for 0.02 seconds after the start of delivery.

[0095] Figures 7(a) to 7(c) are cross-sectional views of the fluid device showing the simulation results. Figure 7(a) shows the simulation results before the start of fluid delivery, Figure 7(b) shows the simulation results 0.01 seconds after the start of fluid delivery, and Figure 7(c) shows the simulation results 0.02 seconds after the start of fluid delivery. In Figures 7(a) to 7(c), the scales indicate the outlines of bubbles and liquid.

[0096] As a result, it became clear that when the diameter of the well is large, air bubbles are less likely to remain inside the well.

[0097] [Experimental Example 5] (Simulation 4) The likelihood of air bubbles remaining in the wells of a fluid device was investigated through simulation. The simulation was performed using software (product name "Ansys Fluent," manufactured by ANSYS).

[0098] We simulated the case where a liquid with the physical properties shown in Table 4 above is delivered through the flow path of a fluid device having a well array with the shape shown in Table 7 below.

[0099] [Table 7]

[0100] The simulation was performed under the case where the liquid was delivered at a flow rate of 33 mm / second for 0.02 seconds after the start of delivery.

[0101] Figures 8(a) to 8(c) are cross-sectional views of the fluid device showing the simulation results. Figure 8(a) shows the simulation results before the start of fluid delivery, Figure 8(b) shows the simulation results 0.01 seconds after the start of fluid delivery, and Figure 8(c) shows the simulation results 0.02 seconds after the start of fluid delivery. In Figures 8(a) to 8(c), the scales indicate the outlines of bubbles and liquid.

[0102] As a result, it became clear that when the diameter of the well is large, air bubbles are less likely to remain inside the well. [Industrial applicability]

[0103] According to the present invention, when an aqueous medium is introduced into each well of a fluid device having a well array, a technique can be provided to suppress the retention of air bubbles inside the wells. Furthermore, according to the method for detecting a target object of the present invention, when an aqueous medium is introduced into each well of a fluid device having a well array to isolate it and generate a signal for detection, the retention of air bubbles inside the wells can be suppressed, and the detection efficiency of the target object can be improved. [Explanation of symbols]

[0104] 100... Fluid device, 110... Well, 120-well array, 130... Substrate, 140... Lid member, 131, 141... Surface, 150... Flow channel, 160... Inlet, 170... Outlet, 180... Peripheral member, A, B, C... Well, Da... Diameter, Dab... Distance, Ca, Cb, Cc... Center of gravity.

Claims

1. A substrate having at least a portion of a well array in which multiple wells of the same shape opening on one side are regularly arranged, The well array comprises a lid member positioned opposite to the well array, The space between the well array and the lid member forms a fluid channel through which fluid flows. The distance Da between the centroid Ca of the opening of any well A in the well array and the centroid Cb of the opening of the well B closest to well A, and the diameter Da of a circle with the same area as the area of ​​the opening of well A, satisfy the following equation (1): The volume of each of the aforementioned wells is 10 fL or more and 100 pL or less. A fluid device in which the total volume of each well in the well array is 0.2 μL or more and 2.0 μL or less. 0.8≦Da / Dab<1 (1)

2. The fluid device according to claim 1, wherein the diameter of a circle having the same area as the opening of the well is 1 μm or more and 50 μm or less.

3. The fluid device according to claim 1 or 2, wherein the ratio of the total area of ​​the openings of each well in the well array to the total area of ​​the well array on one side is 30% or more and 90% or less.

4. The fluid device according to any one of claims 1 to 3, wherein the ratio of the total volume of each well in the well array to the volume of the flow path is 5% or more and 40% or less.

5. The fluid device according to any one of claims 1 to 4, wherein the ratio of the diameter of a circle with the same area as the area of ​​the opening of the well to the depth of the well is 3% or more and 200% or less.

6. The fluid device according to any one of claims 1 to 5, wherein the contact angle with water on one of the aforementioned surfaces is 70 degrees or more and 180 degrees or less.

7. The fluid device according to any one of claims 1 to 6, wherein the contact angle between the surface of the lid member facing the well array and water is 70 degrees or more and 180 degrees or less.

8. A step of introducing an aqueous medium into the flow channel of the fluid device according to any one of claims 1 to 7, A method for isolating an aqueous medium, comprising the steps of introducing the aqueous medium, and then introducing a sealing liquid into the flow path to isolate the aqueous medium in each well of the well array.

9. The method according to claim 8 involves isolating the target to be detected and the aqueous medium containing the detection reagent, then heating the fluid device to cause a reaction inside the well to generate a signal for detecting the target to be detected, A method for detecting the object to be detected, comprising the step of detecting the signal.

10. The method according to claim 9, wherein the target of detection is a biomolecule.

11. The method according to claim 9 or 10, wherein the reaction is an isothermal reaction.

12. The method according to any one of claims 9 to 11, wherein the signal is fluorescence.

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