JP2011123050A - Filling method of solution to be inspected - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a filling method of a solution to be inspected capable of precisely and certainly dispensing the solution to be inspected at a low cost by a simple method while preventing the mixing of foreign matter. <P>SOLUTION: The filling method of the solution to be inspected includes the process for supplying the solution to be inspected to the first well 12 of a biochip 100 wherein the first well 12 and a large number of second wells 14 containing a reagent are provided to the first surface 10a of a substrate, the process for bringing a cover member 16 and the substrate to a close contact state in a looped region surrounding the first well and second wells of the contact surface of the cover member and the substrate in a state that the cover member is arranged on the substrate so as to cover the first well and the second wells with the cover member 16, the process for rotating the biochip centering around a rotation axis in a state that the distance from the second wells to the rotation axis becomes longer than the distance from the first well to the rotation axis and moving the solution to be inspected to the second wells from the first well in the region inside the looped region and the process for bringing the cover member into close contact with the substrate to hermetically close the first well and the second wells. <P>COPYRIGHT: (C)2011,JPO&amp;INPIT

Description

  The present invention relates to a method for filling a test liquid.

  A method of performing chemical analysis, chemical synthesis, bio-related analysis, or the like using a microfluidic chip in which a fine flow path is provided on a glass substrate or the like has attracted attention. Microfluidic chips are also called Micro Total Analytical System (Micro TAS), Lab-on-a-chip, etc., and require less sample and reagents than conventional devices, and reaction time Has a merit that it is short and has less waste, and is expected to be used in a wide range of fields such as medical diagnosis, on-site analysis of the environment and food, production of pharmaceuticals and chemicals, etc. (Patent Document 1). Since the amount of the reagent may be small, it is possible to reduce the cost of the inspection, and since the necessary amount of the sample and the reagent is small, the reaction time can be greatly shortened and the efficiency of the inspection can be improved. In particular, when used for medical diagnosis, it is possible to reduce the necessary amount of a sample such as blood as a sample, which has the advantage of reducing the burden on the patient.

  On the other hand, when the amount of the test liquid such as sample or reagent decreases, the measurement result may be reduced due to the decrease in dispensing accuracy or the large influence of the evaporation amount of the test liquid on the sample volume. Easy to vary. In addition, the dispensing operation of the test liquid is generally complicated and requires a long working time, and consumes a large amount of consumables such as pipettes and tips, thus increasing the cost of inspection. Further, manual dispensing of the test liquid is prone to mistakes, and there is a high possibility that an undesirable substance is mixed into the test liquid. From such a background, a technique for accurately and reliably dispensing a test solution is expected.

JP 2006-509199 A

  The present invention provides a method for filling a test liquid that can prevent the introduction of foreign substances and can dispense the test liquid accurately and reliably by a simple method at low cost.

A test method for a test liquid according to an aspect of the present invention includes:
Supplying a test solution to the first well of the biochip comprising a first well and a plurality of second wells containing reagents separated from the first well on a first surface of the substrate;
With the covering member disposed on the substrate such that the first well and the second well are covered with the covering member, the first well and the first of the joint surfaces between the covering member and the substrate are arranged. Adhering the covering member and the substrate in a loop-shaped region surrounding two wells;
The biochip is rotated around the rotation axis in a state where the biochip is arranged such that the distance from the second well to the rotation axis is longer than the distance from the first well to the rotation axis. Thus, the test solution is removed from the first well through the space formed between the covering member and the substrate in a region inside the loop-shaped region by utilizing centrifugal force. Moving to a well;
Sealing the first well and the second well by bringing the covering member into close contact with the substrate;
including.

  In the present invention, the “second well separated from the first well” means that the second well is provided independently of the first well. For example, the first well and the second well are flow paths. It is not connected via. Further, in the present invention, “adhesion” includes both “welding: melting and adhering joint portions of a plurality of members” and “adhesion: adhering a plurality of members using an adhesive”. It is a concept.

In the test method of the test solution, in the step of moving the test solution from the first well to the second well, the first surface faces the rotation shaft when the biochip is rotated. The biochip can be arranged as described above. Here, the term “opposing” not only means that the first surface faces parallel to the rotation axis, but also, for example, the acute angle θ ₁ of the angles formed by the first surface and the rotation axis is 0 <θ. _This is a concept including the case of ₁ <90.

In this case, in the step of moving the test solution from the first well to the second well, when the biochip is rotated, it is perpendicular to the rotation axis from the first surface to the rotation axis. The biochip can be arranged such that the distance in the direction is shorter than the distance in the direction perpendicular to the rotation axis from the second surface facing the first surface to the rotation axis. Here, the term “opposite” not only refers to the case where the first surface faces the second surface in parallel, but also, for example, an acute angle θ ₂ of the angles formed by the first surface and the second surface. Is a concept including the case of 0 <θ ₂ <90.

  In the test method of the test liquid, the covering member has a surface on which an adhesive is disposed, and in the step of closely contacting the covering member and the substrate in the loop-shaped region, the loop-shaped region is The substrate and the covering member can be bonded to each other in the loop-shaped region by applying pressure.

  Further, in the test method of the test liquid, the substrate and the covering member have a property of melting by heat, and in the step of closely contacting the covering member and the substrate in the loop-shaped region, the loop shape By irradiating the region with ultrasonic waves, the substrate and the covering member can be welded in the loop region.

  In the test method of the test liquid, the upper end portion of the second well is formed by a convex portion, and in the step of sealing the first well and the second well, the convex portion of the biochip and the covering member Can be in close contact with each other.

  In the test method for the test liquid, the covering member may have a property of elastic deformation.

  According to the test method of the test solution, the substrate is provided so that the test solution is supplied to the first well of the biochip, and the first well and the second well are covered with a covering member. The step of bringing the covering member and the substrate into close contact with each other in a loop-shaped region surrounding the first well and the second well in the joint surface between the covering member and the substrate with the covering member disposed thereon And in a state where the biochip is arranged so that the distance from the second well to the rotation axis is longer than the distance from the first well to the rotation axis, the biochip is moved around the rotation axis. By rotating, using the centrifugal force, the test solution is passed through the space formed between the covering member and the substrate in the region inside the loop-shaped region. And moving the test solution to the second well, and sealing the first well and the second well by bringing the covering member into close contact with the substrate. And can be filled by a simple method. In addition, foreign substances can be prevented from being mixed, and the test liquid can be dispensed accurately and reliably at low cost.

The figure explaining 1 process of the test | inspection method of the test liquid which concerns on 1st Embodiment of this invention (the upper figure is a top view, the lower figure is sectional drawing corresponding to the upper figure, FIG.2, FIG.5, FIG.7 and FIG.9) The same applies to the above). The figure explaining 1 process of the test | inspection method of the test liquid which concerns on 1st Embodiment of this invention. The figure explaining 1 process of the test | inspection method of the test liquid which concerns on 1st Embodiment of this invention. FIG. 4 is a perspective view schematically showing a pressure member shown in FIG. 3. Sectional drawing explaining 1 process of the test | inspection method of the test liquid which concerns on 1st Embodiment of this invention. The figure explaining 1 process of the test | inspection method of the test liquid which concerns on 1st Embodiment of this invention. The figure explaining 1 process of the test | inspection method of the test liquid which concerns on 1st Embodiment of this invention. Sectional drawing explaining 1 process of the test | inspection method of the test liquid which concerns on 1st Embodiment of this invention. The figure explaining 1 process of the test | inspection method of the test liquid which concerns on 1st Embodiment of this invention. The figure explaining 1 process of the test | inspection method of the test liquid which concerns on 2nd Embodiment of this invention (the upper figure is a top view, the lower figure is sectional drawing corresponding to an upper figure, and it is the same also in FIG.11 and FIG.13). The figure explaining 1 process of the test | inspection method of the test liquid which concerns on 2nd Embodiment of this invention. It is a figure explaining the process of welding the biochip shown in FIG. 10, and a coating | coated member using an ultrasonic welding apparatus. The figure explaining 1 process of the test | inspection method of the test liquid which concerns on 2nd Embodiment of this invention. It is a figure explaining the process of welding the biochip shown by FIG. 11, and a coating | coated member using an ultrasonic welding apparatus.

  Below, the test | inspection method of the test liquid which concerns on one Embodiment of this invention is demonstrated concretely.

1. First embodiment (test liquid inspection method)
1 to 3 and FIGS. 5 to 9 are diagrams for explaining one step of the test method for the test liquid according to the first embodiment of the present invention (FIGS. 1, 2, 5, 7, and 7). In FIG. 9, the upper diagram is a plan view, and the lower diagram is a cross-sectional view corresponding to the upper diagram). FIG. 4 is a perspective view schematically showing the pressing member shown in FIG.

  In the test method for a test liquid according to the first embodiment of the present invention, the first surface 12a of the substrate 10 is divided into the first well 12 and the plurality of second wells 14 separated from the first well 12 and containing the reagent. The step of supplying the test solution 20 to the first well 12 of the biochip 100 provided in FIG. 1 (FIGS. 1 and 2) and the substrate 10 so that the first well 12 and the second well 14 are covered with the covering member 16. A loop-shaped region 18 surrounding the first well 12 and the second well 14 (hereinafter also simply referred to as “region”) in the joint surface between the covering member 16 and the substrate 10 with the covering member 16 disposed thereon. In step (FIG. 3 to FIG. 5), and the distance from the second well 14 to the rotation axis A is longer than the distance from the first well 12 to the rotation axis A. State in which biochip 100 is arranged By rotating the biochip 100 about the rotation axis A, the centrifugal force is used to make a space 17 formed between the covering member 16 and the substrate 10 in a region inside the loop-shaped region 18. The test solution 20 is moved from the first well 12 to the second well 14 (FIGS. 6 and 7), the covering member 16 is brought into close contact with the biochip 100, and the first well 12 and the second well 14 are moved. Sealing step (FIGS. 8 and 9). In the present embodiment, a case where the biochip 100 is used for performing PCR (Polymerase Chain Reaction) on the test solution 20 will be described.

1.1. Step of Supplying Test Solution 20 The biochip 100 used in the test method for a test solution according to the present embodiment is a reagent separated from the first well 12 and the first well 12, as shown in FIG. Are provided on the first surface 10a of the substrate 10. As shown in FIG. 1, the first well 12 and the second well 14 are recesses (recesses) provided in the substrate 10, and these recesses do not penetrate the substrate 10. Further, in the substrate 10, the first well 12 is provided independently from the plurality of second wells 14, and the first well 12 and the second well 14 are not connected via a flow path or the like.

1.1.1. Substrate In the present embodiment, the first surface 10a is a surface on the substrate 10 where the first well 12 and the second well 14 are provided.

  A test solution 20 is stored in the first well 12 (see FIG. 2). The reagent contained in the second well 14 is used, for example, for testing the test solution 20. The reagent contained in the second well 14 can be arranged on the inner wall surface of the second well 14. In this case, after injecting the liquid containing the reagent into the second well 14, the reagent in the liquid can be disposed on the inner wall surface of the second well 14 by drying the solvent in the liquid.

  The volumes of the first well 12 and the second well 14 are appropriately determined according to conditions such as an inspection object and an inspection method. The volume of the first well 12 is larger than the total volume of the plurality of second wells 14 in that a sufficient amount of the test solution 20 can be accommodated to fill all the plurality of second wells 14 in a process described later. Larger is preferred.

  The plurality of second wells 14 can be arranged in a plurality of columns and rows as shown in FIG. The plurality of second wells 14 are provided independently, and the second wells 14 are not connected to each other through a flow path or the like. For example, the plurality of second wells 14 may be recesses having the same volume.

  When PCR is performed using the biochip 100, for example, the first well 12 does not contain a reagent, and the second well 14 can contain a reagent containing a fluorescent probe for amplifying a target nucleic acid contained in a specimen. . In this case, in the plurality of second wells 14 of the biochip 100, primers for amplifying different target nucleic acids are contained, and the reagent in the second well 14 is added to the test solution 20 in each second well 14. By performing PCR after elution, two or more nucleic acids can be amplified and analyzed at once using the biochip 100.

  The material of the substrate 10 is not particularly limited, but the substrate 10 is preferably made of a material that does not damage the components contained in the test solution 20, for example, an inorganic material (for example, single crystal silicon, Pyrex (registered trademark) glass). It can be made of an organic material (for example, a resin such as polycarbonate). For example, when the substrate 10 is made of an inorganic material, the first well 12 and the second well 14 can be formed in the substrate 10 by dry etching using a photolithography method. For example, when the substrate 10 is made of a resin, the first well 12 and the second well 14 can be formed on the substrate 10 by molding, injection molding, or hot embossing. In the present embodiment, a case where the substrate 10 is made of polycarbonate will be described.

1.1.2. Covering member 16
The material of the covering member 16 is not particularly limited, but the covering member 16 is preferably made of a material that does not damage the components contained in the test solution 20, and a step of rotating the biochip 100 described later (see FIG. 6). In order to reliably generate the space 17, it is more preferable that the covering member 16 has a property of elastic deformation. Examples of such a covering member 16 include resin and rubber.

  When the biochip 100 is used for measuring fluorescence intensity, it is preferable that at least the covering member 16 is made of a transparent and low autofluorescent material, and the substrate 10 and the covering member 16 are both transparent and made of a low autofluorescent material. Preferably it consists of. Further, when the biochip 100 is used for PCR, the substrate 10 and the covering member 16 are preferably made of materials that can withstand the heating in the PCR. As such materials, transparent and low autofluorescent resin (for example, polycarbonate) Is mentioned.

  The covering member 16 can have a surface 16a on which an adhesive is disposed. The covering member 16 having the surface 16a on which the adhesive is disposed is in close contact with the object by strongly pressing the surface 16a on which the adhesive is disposed against the object (the first surface 10a of the substrate 10 in the present embodiment). can do. As such a covering member 16, for example, trade name: LightCycler 480 Sealing Foil, model name: 04 729 757 001, manufactured by Roche Diagnostics, trade name: polyolefin microplate sealing tape, model name: 9793-3M Product name: Amplification tape 96, model name: 232702, manufactured by Nunc Corporation. Further, the surface 16a on which the adhesive of the covering member 16 is disposed may be porous in that the adhesive force is not exhibited in a state where no pressure is applied, and the adhesive force can be exerted by pressure. Or the adhesive agent arrange | positioned on the surface 16a of the coating | coated member 16 may exhibit adhesive force by addition of energy (for example, electron beam), for example.

1.1.3. Test solution 20
As shown in FIG. 2, the test solution 20 is supplied to the first well 12. The test solution 20 can be stored in the first well 12 by, for example, a manual operation (for example, using a pipette) or a machine. When the biochip 100 is used for PCR, for example, the test solution 20 includes a specimen that may contain the target nucleic acid, a primer for amplifying the target nucleic acid, and a fluorescent reagent for measuring the amount of amplification product (for example, SYBR GREEN ™). ), And a PCR master mix.

  The amount of the test solution 20 is appropriately determined according to the volumes of the first well 12 and the second well 14, but is preferably the same as or larger than the total volume of the plurality of second wells 14, for example. The amount of the test solution 20 is more preferably larger than the total volume of the plurality of second wells 14 in that the test solution 20 can be reliably filled by the plurality of second wells 14.

  The test solution 20 is prepared from a specimen. When the test solution 20 is a PCR target, the target nucleic acid to be measured is, for example, DNA extracted from a sample such as blood, urine, saliva, spinal fluid, or reverse transcription from RNA extracted from the sample. And the like.

1.2. Step of Adhering Covering Member 16 and Substrate 10 in Loop-Shaped Region 18 Next, as shown in FIG. 3, the covering member 16 is disposed on the biochip 100, and the first well 12 and the second well 14 is covered with a covering member 16. In this state, in a state where the substrate 10 and the covering member 16 are in contact with each other, a pressure is applied to the loop-shaped region 18 (the region indicated by diagonal lines in FIG. 5) surrounding the first well 12 and the second well 14 in the biochip 100. Then, the substrate 10 and the covering member 16 are brought into close contact (adhesion) in the region 18.

  As shown in FIG. 5, the region 18 surrounds the first well 12 and the second well 14 in a loop shape, and the pressure member 40 is arranged on the covering member 16 in the direction of the arrow in FIG. It is formed by applying pressure to bring the substrate 10 and the covering member 16 into close contact.

  For example, as shown in FIG. 4, the pressure member 40 includes a cavity portion 42 and a loop-shaped end surface 44 positioned at the entrance of the cavity portion 42. The pressure member 40 is pressed against the biochip 100 in a state where the end surface 44 of the pressure member 40 is in contact with the covering member 16. That is, when the covering member 16 is in contact with the end face 44 and pressed in the direction of the arrow in FIG. 3, the covering member 16 adheres to the substrate 10 and the loop-shaped region 18 is formed.

  Accordingly, the substrate 10 and the covering member 16 are bonded in the region 18, but the substrate 10 and the covering member 16 are merely in contact with each other in the inner and outer regions of the region 18 and are not bonded. That is, in the region inside the region 18, the substrate 10 and the covering member 16 are not bonded, and the covering member 16 is merely in contact with the substrate 10. Therefore, in the region inside the region 18, A space is formed when the test liquid enters between the substrate 10 and the covering member 16 by centrifugal force.

1.3. Step of moving the test solution 20 from the first well 12 to the second well 14 Next, as shown in FIG. 6, the distance from the second well 14 to the rotation axis A is the distance from the first well 12 to the rotation axis A. In a state where the biochip 100 is arranged so as to be longer than the distance, the biochip 100 is rotated around the rotation axis A, and as shown in FIG. The test solution 20 is moved from the first well 12 to the second well 14 through a space 17 formed between the covering member 16 and the substrate 10 in a region inside the region 18. Thereby, the test solution 20 is filled in the second well 14. Here, the distance from the first well 12 (second well 14) to the rotation axis A is the upper end of the first well 12 (second well 14) when the biochip 100 is rotated as shown in FIG. This is the distance from the part d ₁ (d ₂ ) to the rotation axis A. As a device for rotating the biochip 100 around the rotation axis A, for example, a commercially available centrifuge can be used.

  That is, since the substrate 10 and the covering member 16 are only in contact with each other in the region inside the region 18, when the biochip 100 is rotated as described above, the rotation axis A is separated from the rotation axis A in a plane perpendicular to the rotation axis A. Since centrifugal force is applied to the test solution 20 in a direction away from the test solution 20, the test solution 20 moves from the first well 12 to the second well 14 through the space 17 as shown in FIG. 7. On the other hand, since the substrate 10 and the covering member 16 are in close contact with each other in the region 18, the test solution 20 does not leak into the region outside the region 18, and the test solution 20 remains inside the region 18.

  More specifically, the coating member 16 is elastically deformed by the fluid pressure of the test solution 20 and the centrifugal force applied to the coating member 16, and the coating member 16 is distorted. A space 17 is formed. The test solution 20 moves from the first well 12 to the second well 14 through the space 17.

  When the biochip 100 is rotated, as shown in FIG. 6, the biochip is arranged so that the first surface 10a of the biochip 100 faces the rotation axis. More specifically, the distance in the direction perpendicular to the rotation axis from the first surface 10a to the rotation axis is relative to the rotation axis from the second surface 10b facing the first surface 10a to the rotation axis. The biochip 100 can be arranged to be shorter than the vertical distance.

1.4. Step of sealing the first well 12 and the second well 14 Next, the covering member 16 is brought into close contact with the substrate 10 to seal the first well 12 and the second well 14. Thereby, all the joint surfaces of the board | substrate 10 and the coating | coated member 16 are adhere | attached (refer FIG. 9).

  As a method of closely attaching the covering member 16 to the substrate 10, for example, as shown in FIG. 8, the roller 30 is rotated on the covering member 16 in the direction of the arrow (direction from the second well 14 toward the first well 12). The method of pressurizing while letting go is mentioned. By this method, the test solution 20 existing in the space 17 between the substrate 10 and the covering member 16 moves to the first well 12, and the bonding surface between the covering member 16 and the substrate 10 is bonded. As a result, the first well 12 and the second well 14 are sealed by the covering member 16. In addition, you may perform the same pressurization operation using a braid | blade (not shown) instead of the roller 30. FIG.

1.5. Applications of Biochip 100 Various inspections can be performed on the biochip 100 in which the second well 14 is filled with the test liquid 20 by the test liquid inspection method according to the present embodiment. When PCR is performed using the biochip 100, the biochip 100 in which the second well 14 is filled with the test solution 20 is placed in a thermal cycler (not shown) including a flat heat block (not shown). It can be set and PCR can be performed.

  In this case, since the second well 14 of the biochip 100 is sealed with the covering member 16, evaporation of the test solution 20 in the PCR temperature cycle process can be prevented. Further, since the covering member 16 is made of a transparent and low autofluorescent material, the target nucleic acid can be quantified (real-time PCR) by measuring the fluorescence luminance simultaneously with the amplification. In addition, the biochip 100 can be used to analyze various nucleic acids (DNA, RNA) using the principle of PCR, such as mutation of genes such as SNP and methylation of DNA.

1.6. Characteristics According to the test liquid inspection method according to the present embodiment, the first well 12 and the plurality of second wells 14 containing a reagent separated from the first well 12 are formed on the first surface 10a of the substrate 10. The step of supplying the test solution 20 to the first well 12 of the biochip 100 provided, and the covering member 16 on the first surface 10 a so that the first well 12 and the second well 14 are covered with the covering member 16. In a state where the covering member 16 and the substrate 10 are in close contact with each other in the loop-shaped region 18 surrounding the first well 12 and the second well 14 in the joint surface between the covering member 16 and the substrate 10, The biochip 100 is rotated around the rotation axis A in a state where the biochip 100 is arranged such that the distance from the two wells 14 to the rotation axis A is longer than the distance from the first well 12 to the rotation axis A. Thus, using the centrifugal force, the test solution 20 is moved from the first well 12 to the second through the space 17 provided between the covering member 16 and the substrate 10 in the region inside the loop-shaped region 18. The test supplied to the first well 12 includes the step of moving to the well 14 and the step of bringing the covering member 16 into close contact with the biochip 100 and sealing the first well 12 and the second well 14. The liquid 20 can be filled in the second well 14 by a simple method called centrifugation. At this time, since the covering member 16 and the substrate 10 are in close contact with each other in the loop-shaped region 18 surrounding the first well 12 and the second well 14, when the test solution 20 is filled in the second well 14, the outside is externally applied. Foreign matter is not mixed. Furthermore, since the test solution 20 can be moved from the first well 12 to the second well 14 via the space 17 between the covering member 16 and the substrate 10, the first well 12 and the second well 14 are connected to each other. There is no need to manufacture the flow path to be connected to the substrate 10, and the test liquid 20 can be dispensed by a simple method with low cost and accuracy.

  In addition, according to the test liquid inspection method according to the present embodiment, for example, a small amount of test liquid can be dispensed, which is difficult when the test liquid is manually dispensed using a pipette. is there.

  Furthermore, according to the test liquid test method according to the present embodiment, the first well 12 and the second well 14 are sealed in a state where the plurality of second wells 14 of the biochip 100 are separated from the first well 12, respectively. Therefore, the backflow of the test solution 20 from the second well 14 to the first well 12 can be prevented. Thereby, an accurate measurement of the test liquid becomes possible.

  In addition, according to the test liquid inspection method according to the present embodiment, the reagent preparation and the test liquid dispensing process can be greatly reduced. For example, expensive equipment such as an automatic dispensing device can be provided. Since it is not necessary to use, the test liquid can be dispensed at low cost.

  In addition, when both the substrate 10 and the covering member 16 are made of a transparent and low autofluorescent material, the biochip in which the second well 14 is filled with the test liquid 20 by the test liquid inspection method according to the present embodiment. 100 can be used for fluorescence measurement. For this reason, simple measurement is possible.

  In the step of moving the test solution 20 from the first well 12 to the second well 14, when the biochip 100 is rotated, the first surface 10a faces the rotation axis as shown in FIG. In addition, the biochip is 100 so that the distance in the direction perpendicular to the rotation axis from the second well 14 to the rotation axis is longer than the distance in the direction perpendicular to the rotation axis from the first well 12 to the rotation axis. May be arranged.

  Further, the covering member 16 is provided with an adhesive, and in the step of bringing the covering member 16 and the substrate 10 into close contact with each other in the loop-shaped region 18, the loop-shaped region 18 is pressurized and the substrate 10 in the loop-shaped region 18 is pressed. And the covering member 16 may be bonded together. According to this method, since the substrate 10 and the covering member 16 are bonded to each other with the adhesive disposed on the covering member 16 by pressurizing the loop-shaped region 18, the substrate 10 and the covering member can be simply and at low cost. 16 can be brought into close contact with each other. In addition, since the loop-shaped region 18 is only pressurized in the close-contacting process, no heat is generated, the temperature rise of the biochip 200 can be suppressed, and damage to the test solution 20 is reduced. can do.

  The covering member 16 preferably has a property of elastic deformation. According to this method, the covering member 16 is elastically deformed by the hydraulic pressure of the test solution 20 and the centrifugal force applied to the covering member 16, and the covering member 16 is distorted. The space 17 can be easily formed. Then, the test solution 20 can be moved from the first well 12 to the second well 14 through the space 17.

  In the present embodiment, the case where the biochip 100 is used for PCR has been described. However, the biochip 100 obtained by the test method for a test liquid according to the present embodiment may be, for example, a virus, a bacterium, a protein, a low molecule to a high molecule. It can be used for the inspection of molecular compounds, cells, particles, colloids such as allergens such as pollen, poisonous substances, harmful substances, and environmental pollutants. In the present embodiment, the case where the second well 14 of the biochip 100 includes a reagent has been described. However, depending on the examination content, the second well 14 may not include the reagent.

2. Second Embodiment FIG. 10, FIG. 11 and FIG. 13 are diagrams for explaining one process of a test method for a test liquid according to a second embodiment of the present invention (the upper diagram in FIG. 10, FIG. 11 and FIG. 13). Is a plan view, and the lower figure is a sectional view corresponding to the upper figure). 12 is a view for explaining a process of welding the biochip 200 and the covering member 26 shown in FIG. 10 using the ultrasonic welding apparatus 300, and FIG. 14 is a view illustrating the biochip 200 and the covering shown in FIG. It is a figure explaining the process of closely_contact | adhering the member 26 using the ultrasonic welding apparatus 300 (welding).

  In the test method for a test liquid according to the present embodiment, a biochip 200 shown in FIG. 10 is used. That is, the biochip 200 is different from the biochip 100 of the first embodiment in which the convex portions 11 are not provided in that the upper ends 24a of the plurality of second wells 24 are each configured by the convex portions 11. The biochip 200 may be used in the test liquid inspection method according to the first embodiment, or the biochip 100 used in the test liquid inspection method according to the first embodiment is used in this embodiment. You may use with the inspection method of the test liquid which concerns. The first well 22 and the second well 24 of the biochip 200 have the same configuration and function as the first well 12 and the second well 14 of the biochip 100 of the first embodiment.

  In the test liquid test method according to the present embodiment, the same components as those of the test liquid test method according to the first embodiment are denoted by the same reference numerals, and detailed description thereof is omitted. Accordingly, in the constituent components of the test liquid inspection method according to the present embodiment, the constituent components denoted by the same reference numerals as those of the test liquid inspection method according to the first embodiment described above have the same configuration and function.

  In the test method for a test liquid according to the present embodiment, the first embodiment is a method in which the substrate 10 and the covering member 16 are brought into close contact with each other in that the means for bringing the substrate 110 and the covering member 26 into contact is welding by ultrasonic irradiation. This is different from the test method for the test liquid according to the embodiment. Therefore, in the test liquid test method according to the present embodiment, the description of the steps common to the test liquid test method according to the first embodiment is omitted, and the test liquid test method according to the first embodiment is omitted. Processes different from those will be mainly described.

  The covering member 26 is preferably made of a transparent and low autofluorescent material, like the covering member 16 in the first embodiment described above. Furthermore, in the biochip 200, both the substrate 110 and the covering member 26 have a property of melting by heat. In this case, the substrate 110 and the covering member 26 are more preferably made of the same material in that the substrate 110 and the covering member 26 can be reliably welded. Further, when the biochip 200 is used for PCR, the substrate 110 and the covering member 26 are preferably made of materials that can withstand the heating in the PCR. As such materials, transparent and low autofluorescent resin (for example, polycarbonate) Is mentioned.

  First, the test solution 20 is supplied to the first well 22 by the same method as the test method for the test solution according to the first embodiment (see 1.1 above).

  Next, as shown in FIG. 11, the covering member 26 is disposed on the substrate 110 so that the first well 22 and the second well 24 are covered with the covering member 26, as shown in FIG. In the region 28, an ultrasonic wave is irradiated to a loop-shaped region (hereinafter also simply referred to as “region”) 28 surrounding the first well 22 and the second well 24 in the bonding surface between the covering member 26 and the substrate 110. The substrate 110 and the covering member 26 are welded. As a result, the substrate 110 and the covering member 26 are in close contact with each other in the region 28, but the substrate 110 and the covering member 26 are simply in contact with each other in the region inside and outside the region 28. For this reason, in the region inside the region 28, there is a gap (not shown) through which the test liquid 20 can move between the substrate 110 and the covering member 26.

  Here, for example, ultrasonic welding apparatus 300 shown in FIG. 12 can be used for ultrasonic irradiation. In the ultrasonic welding apparatus 300, electrical energy is converted into mechanical vibration energy (ultrasonic waves) by the ultrasonic vibrator 304, and ultrasonic waves are emitted from the horn 302. Here, the irradiated ultrasonic wave is, for example, 20 kHz.

  As shown in FIG. 12, the ultrasonic welding apparatus 300 includes an ultrasonic transducer 304 and a horn 302 attached to the ultrasonic transducer 304. The horn 302 has a hollow portion 305 as shown in FIG. The horn 302 has the same shape as the pressure member 40 shown in FIG. That is, the horn 302 has a hollow portion 305 and an end surface 306, and the hollow portion 305 and the peripheral portion 306 have the same structure as the hollow portion 42 and the end surface 44 of the pressing member 40 shown in FIG.

  In a state where the end surface 306 of the horn 302 is pressed against the covering member 26 on the biochip 200, the biochip 200 is pressed in the direction of the arrow in FIG. 12, and ultrasonic waves are concentrated and emitted from the end surface 306. . As a result, ultrasonic waves are intensively applied to the region 28 (see FIG. 11) in contact with the end surface 306 to generate frictional heat, and the substrate 110 and the covering member 26 are melted in the region 28, so that the substrate 110 and the covering member 26 And adhere to each other (welding).

  Next, in the same manner as the test liquid inspection method according to the first embodiment (see 1.3. Above), the coating member 26 and the covering member 26 are formed in the region inside the loop-shaped region 28 using centrifugal force. The test solution 20 is moved from the first well 22 to the second well 24 through a space (not shown) formed between the substrate 110 and the substrate 110.

  Subsequently, by irradiating the entire covering member 26 with ultrasonic waves, as shown in FIG. 13, the entire bonding surface of the substrate 110 and the covering member 26 is brought into close contact (welding). Thereby, the first well 22 and the second well 24 are sealed.

  Here, for example, ultrasonic welding apparatus 300 shown in FIG. 14 can be used for ultrasonic irradiation. As shown in FIG. 14, the ultrasonic welding apparatus 300 includes an ultrasonic transducer 304 and a horn 303 attached to the ultrasonic transducer 304. The horn 303 has the same configuration as the horn 302 shown in FIG. 12 except that the hollow portion 305 is not provided therein.

  As shown in FIG. 14, the ultrasonic welding apparatus 300 irradiates the entire covering member 26 with ultrasonic waves from above the covering member 26 laminated on the biochip 200. While pressing the end face 307 of the horn 303 against the covering member 26, the biochip 200 is pressed in the direction of the arrow in FIG. 14, and the joining surface between the end face 307 of the horn 303 and the covering member 26 is irradiated with ultrasound. To do. Thereby, the joint surface of the board | substrate 110 and the coating | coated member 26 adheres (welds). Thereby, the first well 22 and the second well 24 are sealed.

  The test liquid inspection method according to the present embodiment has the same effects as the test liquid inspection method according to the first embodiment. Furthermore, according to the test liquid inspection method according to the present embodiment, the substrate 110 and the covering member 26 are brought into close contact (welding) with ultrasonic irradiation, so that the application of heat to the test liquid 20 can be suppressed. Therefore, the damage given to the test solution 20 is small. For this reason, the activity of the reagent contained in the second well 24 can be maintained. Furthermore, since the bonding force between the substrate 110 and the covering member 26 by welding is strong, liquid leakage from the second well 24 can be reliably prevented.

  In addition, the biochip 200 used in the test liquid inspection method according to the present embodiment has the upper end 24 a of the second well 24 formed of the convex portion 11, and thus exceeds the convex portion 11 and the covering member 26. When welding is performed by sonication, since the ultrasonic waves are likely to concentrate on the joint surface between the convex portion 11 and the covering member 26, the convex portion 11 and the covering member 26 can be more reliably welded. In addition, welding by ultrasonic irradiation can suppress an increase in the temperature of the biochip 200, so that damage to the test liquid 20 is small.

  This is the end of the description of the embodiment according to the present invention. The present invention includes configurations that are substantially the same as the configurations described in the embodiments (for example, configurations that have the same functions, methods, and results, or configurations that have the same purposes and results). In addition, the invention includes a configuration in which a non-essential part of the configuration described in the embodiment is replaced. In addition, the present invention includes a configuration that exhibits the same operational effects as the configuration described in the embodiment or a configuration that can achieve the same object. Further, the invention includes a configuration in which a known technique is added to the configuration described in the embodiment.

  DESCRIPTION OF SYMBOLS 10,110 ... Board | substrate, 10a ... 1st surface, 10b ... 2nd surface, 11 ... Convex part, 12, 22 ... 1st well, 14, 24 ... 2nd well, 24a ... Upper end part, 16, 26 ... Cover member, 16a ... surface, 17 ... space, 18, 28 ... area, 20 ... test solution, 30 ... roller, 40 ... pressure member, 42, 305 ... cavity, 44, 306 ... end face, 100, 200 ... Biochip, 300 ... ultrasonic welding apparatus, 302, 303 ... horn, 304 ... ultrasonic transducer, 307 ... end face, A ... rotating shaft

Claims (7)

Supplying a test solution to the first well of the biochip comprising a first well and a plurality of second wells containing reagents separated from the first well on a first surface of the substrate;
With the covering member disposed on the substrate such that the first well and the second well are covered, the first well and the second well of the joint surface between the covering member and the substrate are A step of bringing the covering member and the substrate into close contact with each other about a surrounding loop-shaped region;
The biochip is configured such that a distance in a direction perpendicular to the rotation axis from the second well to the rotation axis is longer than a distance in a direction perpendicular to the rotation axis from the first well to the rotation axis. By rotating the biochip around the rotation axis in the disposed state, the test solution is transferred from the first well to the second well through the space between the covering member and the substrate. A process of moving;
Sealing the first well and the second well by bringing the covering member into close contact with the substrate;
A method for filling a test liquid, comprising: In claim 1,
In the step of moving the test solution from the first well to the second well, when the biochip is rotated, the biochip is disposed so that the first surface faces the rotation axis. Method for filling the test liquid. In claim 2,
In the step of moving the test solution from the first well to the second well, when rotating the biochip, a distance perpendicular to the rotation axis from the first surface to the rotation axis A method for filling a test liquid, wherein the biochip is arranged so that the distance from the second surface facing the first surface to the rotation axis is shorter than the distance in the direction perpendicular to the rotation axis. In any of claims 1 to 3,
The covering member is provided with an adhesive,
In the step of bringing the covering member and the substrate into close contact with each other in the loop-shaped region, pressurizing the loop-shaped region to adhere the substrate and the covering member to the loop-shaped region. Filling method. In any of claims 1 to 3,
The substrate and the covering member have a property of melting by heat,
In the step of bringing the covering member and the substrate into close contact with each other in the loop-shaped region, an ultrasonic wave is applied to the loop-shaped region to weld the substrate and the covering member in the loop-shaped region. How to fill the test solution. In any of claims 1 to 5,
The surface of the substrate has a convex portion,
A method of filling a test liquid, wherein in the step of sealing the first well and the second well, the convex portion and the covering member are in close contact. In any one of Claims 1 thru | or 6.
The method for filling a test liquid, wherein the covering member has a property of elastic deformation.