JP4962249B2 - Reaction vessel plate and reaction processing method - Google Patents

Description

  INDUSTRIAL APPLICABILITY The present invention relates to a reaction vessel plate suitable for performing various analyzes and analyzes in the field of medical analysis and chemistry in the field of biological analysis, biochemical analysis, or chemical analysis in general, and a method for processing the reaction vessel plate. The present invention relates to a reaction processing method.

  A micro multi-chamber apparatus is used as a small reaction apparatus used for biochemical analysis or normal chemical analysis. As such an apparatus, for example, a microwell reaction vessel plate such as a microtiter plate in which a plurality of wells are formed on a flat substrate surface is used (see, for example, Patent Document 1).

  Moreover, as a trace liquid weighing structure capable of quantitatively handling a trace amount of liquid, a first channel and a second channel, a third channel opening in the channel wall of the first channel, A structure having a fourth channel that opens to the channel walls of the two channels and connects one end of the third channel to the first channel and has a property that capillary attraction is less likely to work than the third channel. Some are provided (see, for example, Patent Documents 2 and 3). According to the trace liquid weighing structure, after the liquid introduced into the first flow path is drawn into the third flow path, the liquid remaining in the first flow path is removed, and then the first flow is performed by gas. By pressurizing the inside of the channel and injecting the liquid in the third channel into the second channel via the fourth channel, a volume of liquid corresponding to the volume of the third channel is supplied to the second channel. Can be weighed.

JP-A-2005-177749 JP 2004-163104 A JP 2005-114430 A Japanese Patent No. 3454717

  In the trace liquid weighing structure disclosed in Patent Documents 2 and 3, the fourth channel has a channel cross-sectional area that is smaller than that of the third channel, so that the capillary attraction is less likely to work than the third channel. Is formed small. Since the fourth channel has a small channel cross-sectional area, the channel resistance is large, and a large pressure and flow rate when the liquid filled in the third channel is injected into the second channel via the fourth channel. Was necessary. There is also a problem that it takes a long time to inject the liquid into the second channel via the fourth channel.

  The present invention includes a main channel, a metering channel branched from the main channel, an injection channel connected to the metering channel and having a smaller channel cross-sectional area than the metering channel, and a reaction vessel connected to the injection channel. In the reaction container plate and the reaction processing method using the reaction container plate, the object is to reduce the injection pressure when injecting the liquid in the measurement channel into the reaction container through the injection channel. .

  The reaction container plate according to the present invention includes a base substrate, a cover substrate having one surface bonded to one surface of the base substrate, the one surface of the base substrate, the one surface of the cover substrate, or both. A reaction vessel comprising a formed recess, and a reaction vessel channel comprising a groove formed on the one surface of the base substrate or the one surface of the cover substrate or both, and connected to the reaction vessel. The reaction vessel channel includes a main channel, a metering channel having a predetermined capacity branched from the main channel, and an injection channel having one end connected to the metering channel and the other end connected to the reaction vessel. The cover substrate is formed of an elastic body at least at a portion forming the injection channel, and at least a part of the injection channel is formed narrower than the metering channel. The injection flow path forming portion of the cover substrate is lifted from the base substrate or returned to the original state by the force acting on the surface of the cover flow passage forming portion opposite to the base substrate. The cross-sectional area is variable, and the liquid is introduced in the liquid introduction pressure state when the liquid is introduced into the main passage and the metering passage, and in the purge pressure state when the liquid in the main passage is purged. The liquid is allowed to pass in a state where the injection channel forming portion of the cover substrate is lifted from the base substrate.

  The reaction processing method according to the present invention is a reaction processing method using the reaction container plate of the present invention, wherein the main channel and the metering channel are filled with liquid at the introduction pressure, and a gas is allowed to flow through the main channel. After removing the liquid in the main channel while leaving the liquid in the metering channel, a force is applied to the surface of the cover substrate on the side opposite to the base substrate of the injection channel forming portion. The injection channel formation portion is lifted from the base substrate to increase the channel cross-sectional area of the injection channel, and the main channel is set to a positive pressure, the reaction vessel is set to a negative pressure, or the positive pressure and By setting both of the negative pressures, the liquid in the metering channel is injected into the reaction vessel through the injection channel.

  In the reaction container plate of the present invention, the injection flow path is formed by the force applied to the surface of the cover substrate on the side opposite to the base substrate of the injection flow path forming portion of the cover substrate. The flow passage cross-sectional area is variable by returning to step (a). The injection channel does not pass the liquid in the liquid introduction pressure state when the liquid is introduced into the main channel and the metering channel and in the purge pressure state when the liquid in the main channel is purged, and the cover substrate The liquid flow path is formed in a state where the injection flow path forming portion is lifted from the base substrate.

  In the reaction container plate and the reaction processing method using the same according to the present invention, when the liquid in the metering channel is injected into the reaction container via the injection channel, the injection channel forming portion of the cover substrate is removed from the base substrate. It is possible to increase the flow passage cross-sectional area of the injection flow path, so that the injection pressure can be reduced. Furthermore, the injection time can be shortened.

As an example of the reaction container plate of the present invention, a convex portion used when the injection flow path forming portion is lifted from the base substrate on the surface of the cover substrate on the side opposite to the base substrate of the injection flow path formation portion. An example can be given.
An example of the reaction processing method of the present invention uses the reaction vessel plate, fills the main flow path and the measurement flow path with the liquid at the introduction pressure, flows gas into the main flow path, and supplies the liquid into the measurement flow path. After removing the liquid in the main flow path while leaving the liquid, the injection flow path forming portion is lifted from the base substrate by grasping and pulling up the convex portion, thereby cross-sectional area of the flow path of the injection flow path And the positive pressure in the main flow channel, the negative pressure in the reaction vessel, or both the positive pressure and the negative pressure, and the above in the measurement flow channel through the injection flow channel. Liquid is poured into the reaction vessel.

As another example of the reaction vessel plate of the present invention, an example in which an air control flow path covering the surface of the cover substrate on the side opposite to the base substrate of the injection flow path forming portion can be given. .
Another example of the reaction processing method of the present invention uses the reaction vessel plate, fills the main channel and the metering channel with the introduction pressure with the introduction pressure, and flows gas into the main channel to allow the inside of the metering channel The liquid in the main flow path is removed while the liquid remains, and then the injection flow path forming portion is lifted from the base substrate by making the inside of the air control flow path have a negative pressure. The flow passage cross-sectional area of the passage is increased, and the main flow passage is set to a positive pressure or the reaction vessel is set to a negative pressure or both the positive pressure and the negative pressure through the injection flow passage. The liquid in the measurement channel is injected into the reaction vessel.

  In the reaction container plate of the present invention, the cover substrate is formed of an elastic body that is integrally formed as a whole, and the thickness of the portion that forms the injection flow channel and the portion that forms the main flow channel and the above An example in which the thickness is smaller than the thickness of the portion forming the metering flow path can be given.

The contact angle of the injection channel with respect to the water droplets is 90 degrees or more, and the area of the boundary between the injection channel and the metering channel is such that the injection channel forming portion of the cover substrate is not lifted from the base substrate 1 to 10000000 μm ² (square micrometer). Here, when the injection flow path is constituted by a plurality of flow paths, the area means an area of a boundary between each of the plurality of flow paths constituting the injection flow path and the measurement flow path.

  Further, a plurality of the reaction vessels may be provided, and the reaction channels may be provided with the metering channel and the injection channel, and the plurality of metering channels may be connected to the main channel.

  Moreover, you may make it further provide the reaction container air vent flow path connected to the said reaction container.

  In addition, a sealing container provided separately from the reaction container, a sealing container channel connected to the sealing container, a syringe for feeding a liquid, and the syringe as the reaction container channel or You may make it further provide the switching valve for connecting to the said sealing container flow path.

  Further, an example in which a plurality of sets of the sealing container and the sealing container channel are provided, and the switching valve can connect the syringe to any of the sealing container channels.

An example in which the switching valve is a rotary valve can be given.
Furthermore, the said rotary type valve | bulb is equipped with the port connected to the said syringe in the rotation center, The example which has arrange | positioned the said syringe on the said rotary type | formula valve can be given.

An example of the sealing container is a sample container for containing a sample liquid.
Furthermore, the sample container may be sealed with an elastic member that can be penetrated by a sharp dispensing device having a sharp tip and that can close the through hole by elasticity when the dispensing device is pulled out after penetration. it can.
Further, a sample pretreatment liquid or reagent may be stored in the sample container in advance.

  In addition to the sample container, one or a plurality of reagent containers including the sealing container may be provided. The reagent container previously contains a reagent used for the reaction of the sample solution and is sealed with a film, or has a cap that can be opened and closed so that the reagent can be injected. An example of the film covering the reagent container and sealing the reagent is one that can be penetrated by a sharp dispensing device having a sharp tip.

  When the reaction container plate of the present invention is intended for gene analysis, it is preferable that the reaction container plate comprises a sealed container and includes a gene amplification container for performing a gene amplification reaction. It is preferable that the gene amplification container has a shape suitable for temperature control at a predetermined temperature cycle. Note that the reaction vessel may be a gene amplification unit.

  The reaction vessel can be used for performing at least one of a color reaction, an enzyme reaction, a reaction that generates fluorescence, chemiluminescence, or bioluminescence.

When the reaction vessel plate of the present invention is used as a reaction vessel plate for measuring a sample containing a gene, a sample subjected to a gene amplification reaction in advance may be introduced into this reaction vessel plate, or this reaction The gene amplification reagent can be stored in advance or dispensed so that the reaction vessel on the container plate can perform the gene amplification reaction.
The gene amplification reaction includes a PCR method and a LAMP method. Focusing on the PCR method for amplifying DNA, a method of directly performing a PCR reaction from a sample such as blood without pretreatment has also been proposed. In the nucleic acid synthesis method for amplifying a target gene in a sample containing a gene, the gene inclusion body in the sample containing the gene or the sample containing the gene itself is added to the gene amplification reaction solution, The target gene in the sample containing the gene is amplified when the pH of the reaction solution is 8.5 to 9.5 (25 ° C.) (see Patent Document 4).

The reaction vessel may be made of a light-transmitting material so that optical measurement can be performed from the bottom or above.
The reaction container may be provided with a probe that reacts with a gene when the liquid introduced into the reaction container channel contains the gene.
Further, the probe may be fluorescently labeled.

  The reaction vessel plate according to the present invention includes a reaction vessel formed by a base substrate and a cover substrate, and a reaction vessel channel connected to the reaction vessel, and the reaction vessel channel is a main channel and a predetermined branched from the main channel A volumetric flow channel, and an injection flow channel having one end connected to the measurement flow channel and the other end connected to the reaction vessel, and at least a portion of the cover substrate forming the injection flow channel is formed of an elastic body It was like that. Further, at least a part of the injection channel is formed to be narrower than the metering channel, and the injection channel is formed on the cover substrate by a force acting on the surface of the injection channel forming part of the cover substrate opposite to the base substrate. The cross-sectional area of the flow path is variable by raising or returning the portion from the base substrate, and the liquid introduction pressure state when the liquid is introduced into the main flow path and the measurement flow path, and the liquid in the main flow path In the purge pressure state when the gas is purged, the liquid is not allowed to pass, and the liquid is allowed to pass in a state where the injection flow path forming portion of the cover substrate is lifted from the base substrate. As a result, when the liquid in the metering channel is injected into the reaction vessel through the injection channel, the injection channel forming portion of the cover substrate is lifted from the base substrate, and the channel cross-sectional area of the injection channel is increased. Therefore, the injection pressure can be reduced. Furthermore, the injection time can be shortened.

  In the reaction processing method according to the present invention, the reaction vessel plate according to the present invention is used, the main channel and the metering channel are filled with the introduction pressure, and the liquid is allowed to flow in the main channel to leave the liquid in the metering channel. While removing the liquid in the main flow path, a force is applied to the surface of the cover substrate on the side opposite to the base substrate of the injection flow path forming portion to lift the injection flow path forming portion from the base substrate. And the liquid in the metering channel through the injection channel by setting the main channel to a positive pressure, the reaction vessel to a negative pressure, or both a positive pressure and a negative pressure. Is injected into the reaction vessel, so that the injection pressure can be reduced. Furthermore, the injection time can be shortened.

  In the reaction container plate of the present invention, the cover substrate is formed of an elastic body that is integrally formed as a whole, and the thickness of the portion that forms the injection flow channel is the portion that forms the main flow channel and the metering flow channel. If it is formed thinner than the thickness of the formed portion, only the portion of the cover substrate forming the injection flow path in the injection pressure state can be lifted from the base substrate. Further, since the entire cover substrate is formed by integral molding, the cover substrate can be easily manufactured as compared with the case where the cover substrate is manufactured by combining a plurality of members.

Further, the contact angle of the injection channel with respect to the water droplets is 90 degrees or more, and the area of the boundary between the injection channel and the metering channel is 1 to 10000000 μm ^{2 in a} state where the injection channel forming portion of the cover substrate is not lifted from the base substrate. As a result, when the liquid is introduced into the main channel and the metering channel, the liquid is less likely to enter the injection channel, and the introduction pressure when introducing the liquid into the main channel and the metering channel is increased. be able to.

  Further, if a plurality of reaction vessels are provided, and each of the reaction vessels is provided with a metering channel and an injection channel, and a plurality of metering channels are connected to the main channel, a liquid is provided in the plurality of metering channels. Can be sequentially introduced, and then liquid can be simultaneously injected into a plurality of reaction vessels via the injection flow path.

  In addition, if a reaction vessel air vent channel connected to the reaction vessel is further provided, the reaction vessel and the reaction vessel air vent flow are supplied when liquid is injected into the reaction vessel through the injection channel. Gas can be circulated between the paths. Thereby, the liquid can be smoothly injected into the reaction vessel. The reaction container air vent channel is an injection method in which when the liquid is injected into the reaction container, the gas in the reaction container is sucked from the reaction container air vent channel to decompress the inside of the reaction container to inject the liquid. It can also be used.

In addition, a sealing container provided separately from the reaction container, a sealing container channel connected to the sealing container, a syringe for feeding liquid, and the syringe into the main channel or the sealing container channel If a switching valve for connection is provided, the liquid in the sealed container can be injected into the main channel using the syringe and the switching valve.
Here, the syringe is subjected to a purge process in which the liquid in the main channel is removed by gas after filling the liquid into the measuring channel, and an injection process in which the inside of the main channel is pressurized to the injection pressure by the gas after the purge process. In the above, it can be used as an air supply mechanism for sending gas into the main flow path. As described above, when the flow channel cross-sectional area of the injection flow channel is not variable, a large injection pressure is required, so it is necessary to increase the size of the syringe as the air supply mechanism, and the size of the entire reaction container plate is also I had to make it bigger. According to the reaction container plate of the present invention, the flow passage cross-sectional area of the injection flow path is variable, and the injection pressure can be reduced as compared with the case where the flow passage cross-sectional area of the injection flow path is not variable. The size of the syringe as a mechanism can be reduced, and the size of the entire reaction container plate can also be reduced.

The switching valve can be a rotary valve. In that case, if a port connected to the syringe is arranged at the rotation center of the rotary valve, the flow path configuration is simplified.
Furthermore, if the rotary valve has a port connected to the syringe at the center of rotation, and the syringe is arranged on the rotary valve, the flow path between the port and the syringe can be shortened or eliminated, The structure becomes simple. Furthermore, the area on the switching valve can be used effectively, and the planar size of the reaction vessel plate can be reduced as compared with the case where the syringe is arranged in an area different from that on the switching valve.

In addition, a sealing container provided separately from the reaction container, a sealing container channel connected to the sealing container, and a switching valve for connecting the syringe to the reaction container channel or the sealing container channel It may be provided.
For example, if the sealing container is a sample container for storing the sample liquid, it is not necessary to separately prepare a container for storing the sample.

Furthermore, if the sample container is sealed by an elastic member that can be penetrated by a sharp dispensing device with a sharp tip and can close the through-hole by elasticity when the dispensing device is pulled out after the penetration, the elastic member It is possible to inject the sample liquid into the sample container via, and then prevent the sample liquid from leaking out of the sample container.
Further, if the sample pretreatment liquid or reagent is previously stored in the sample container, it is not necessary to dispense the sample pretreatment liquid or reagent into the sample container.

  Separately from the sample container, one or more reagent containers comprising a sealed container are provided, and the reagent container contains a reagent used for the reaction of the sample liquid and is sealed with a film, or has an openable / closable cap. If it is prepared and can inject the reagent, it is not necessary to prepare a container for storing the reagent separately.

  If a gene amplification container for conducting a gene amplification reaction is also provided, a sample container containing only a very small amount of the gene to be measured can be obtained by a gene amplification reaction such as PCR or LAMP. The analysis accuracy can be increased by amplifying the gene on the plate.

  In addition, when the reaction vessel plate of the present invention is a reaction vessel plate for measuring a sample containing a gene, if the gene amplification reaction can be performed in the reaction vessel, the gene outside the reaction vessel plate There is no need to prepare a sample that has undergone an amplification reaction.

  In addition, if the reaction vessel is made of a light-transmitting material so that it can be optically measured from the bottom or above, the reaction vessel can be optically moved without moving it to another vessel. Can be measured automatically.

  In addition, if the reaction vessel is equipped with a probe that reacts with the gene when the liquid introduced into the reaction vessel channel contains a gene, the reaction vessel has a base sequence corresponding to the probe in the reaction vessel. Gene detection can be performed.

1A and 1B are diagrams showing an embodiment of a reaction vessel plate. FIG. 1A is a schematic plan view, and FIG. 1B is a sectional view taken along a line AA in FIG. The schematic cross-sectional view which added the cross section of the sample container air vent flow path 19 and 21, the liquid drain space 29, the air drain space 31, and the bellows 53, (C) is the outline which expands and shows the syringe 51 and the bellows 53 vicinity. FIG. FIG. 2 is an exploded sectional view showing this embodiment and a schematic exploded perspective view of the switching valve. FIG. 3 is a schematic view showing the vicinity of one reaction vessel of this embodiment, where (A) is a plan view, (B) is a perspective view, and (C) is a cross-sectional view. 4A and 4B are enlarged views of the sample container. FIG. 4A is a plan view, and FIG. 4B is a cross-sectional view taken along the line BB in FIG. 5A and 5B are enlarged views of the reagent container. FIG. 5A is a plan view, and FIG. 5B is a cross-sectional view taken along the line CC in FIG. 6A and 6B are enlarged views of the air suction container. FIG. 6A is a plan view, and FIG. 6B is a cross-sectional view taken along the DD line in FIG.
An embodiment of the reaction vessel plate will be described with reference to FIGS.

  The reaction vessel plate 1 includes a plurality of reaction vessels 5 having openings on one surface of a vessel base (base substrate) 3. In this embodiment, 6 × 6 reaction vessels 5 are arranged in a staggered manner. A reagent 7 and wax 9 are accommodated in the reaction vessel 5.

  The material of the container base 3 including the reaction container 5 is not particularly limited. However, when the reaction container plate 1 is used as disposable, it is preferable that there is a material available at a low cost. As such a material, for example, a resin material such as polypropylene and polycarbonate is preferable. When the substance in the reaction vessel 5 is detected by absorbance, fluorescence, chemiluminescence, bioluminescence or the like, it must be formed of a light transmissive resin so that optical detection can be performed from the bottom side. Is preferred. In particular, when fluorescence detection is performed, the container base 3 is made of a material such as a resin having a low autofluorescence property (a property of generating less fluorescence from itself) and a light transmitting resin, such as polycarbonate. Is preferred. The thickness of the container base 3 is 0.2 to 4.0 mm (millimeters), preferably 1.0 to 2.0 mm. From the viewpoint of low autofluorescence for fluorescence detection, the container base 3 is preferably thinner.

  Referring to FIGS. 1 and 3, a flow path base (cover substrate) 11 is disposed on the container base 3 so as to cover the arrangement region of the reaction containers 5. The channel base 11 is made of an elastic body such as PDMS (polydimethylsiloxane) or silicone rubber. The thickness of the channel base 11 is, for example, 1.0 to 5.0 mm. The flow path base 11 has a groove on the joint surface with the container base 3. The groove and the surface of the container base 3 form a main channel 13, a metering channel 15, an injection channel 17, reaction vessel air vent channels 19 and 21, and drain space air vent channels 23 and 25. The main channel 13, the metering channel 15 and the injection channel 17 constitute a reaction vessel channel. A concave portion 27 disposed on the reaction vessel 5 is also formed on the joint surface of the flow path base 11 with the vessel base 3. In FIG. 1A and FIGS. 3A and 3B, only the groove and the concave portion of the flow path base 11 are illustrated.

  The main flow path 13 is composed of a single flow path and is formed to be bent so as to pass through the vicinity of all the reaction vessels 5. One end of the main flow path 13 is connected to a flow path 13 a formed of a through hole provided in the container base 3. The flow path 13a is connected to a port of a switching valve 63 described later. The other end of the main channel 13 is connected to a liquid drain space 29 formed in the container base 3. The dimensions of the grooves constituting the main flow path 13 are, for example, a depth of 400 μm (micrometer) and a width of 500 μm. In addition, the main flow path 13 has a predetermined length downstream of the position where the measurement flow path 15 is connected, for example, a 250 μm portion is formed to be narrower than other portions, for example, the width is 250 μm. It is.

  The measuring channel 15 is branched from the main channel 13 and provided for each reaction vessel 5. The end of the measuring channel 15 opposite to the main channel 13 is disposed in the vicinity of the reaction vessel 5. For example, the depth of the groove constituting the measuring flow path 15 is 400 μm at the base end 15 a on the main flow path 13 side and 10 μm at the front end 15 b on the opposite side to the main flow path 13. The measuring channel 15 has an internal capacity of a predetermined capacity, for example, 2.5 μL (microliter). The width dimension of the part connected to the main flow path 13 of the measurement flow path 15 is larger than the narrow part of the main flow path 13 described above, for example, 500 μm. Thereby, the flow resistance of the main flow path 13 is larger than that of the measurement flow path 15 in the portion where the measurement flow path 15 is branched with respect to the liquid flowing from one end of the main flow path 13. The liquid flowing from one end of the main channel 13 first flows into the metering channel 15, and after the metering channel 15 is filled with the liquid, it flows downstream through the narrowed portion of the main channel 13. It has become.

An injection channel 17 is also provided for each reaction vessel 5. In FIG. 1 and FIG. 2, the injection channel 17 is shown in a simplified manner. Referring to FIG. 3, one end 17 a of the injection channel 17 is connected to the tip 15 b of the metering channel 15. The other end 17 b of the injection flow channel 17 is connected to a recess 27 disposed on the reaction vessel 5 and led to the reaction vessel 5. One end 17 a of the injection channel 17 is formed with a dimension that maintains liquid tightness in the reaction vessel 5 in a state where there is no pressure difference between the reaction vessel 5 and the injection channel 17. In this embodiment, one end 17a of the injection channel 17 is constituted by a plurality of grooves, and the dimensions of the grooves are, for example, a depth of 10 μm, a width of 20 μm, a pitch of 20 μm, and 13 in a 500 μm width region. Grooves are formed. Here, the area of the boundary between the groove constituting the one end 17a of the injection channel 17 and the metering channel 15, that is, the cross-sectional area of the groove constituting the one end 17a of the injection channel 17 is 200 μm ² . The other end 17b of the injection channel 17 is constituted by one groove, and the groove has a width of, for example, 500 μm and a depth of 10 μm. The recess 27 has a depth of, for example, 400 μm, and the planar shape is a circle smaller than the reaction vessel 5.

  Referring to FIG. 3, the flow path base 11 includes a recess 18 formed on a surface on one side 17 a of the injection flow path 17 and opposite to the container base 3. In FIG. 1A, the illustration of the recess 18 is omitted. Due to the concave portion 18, the portion forming the one end 17 a of the injection flow channel 17 and the thickness of the surrounding container base 11 are formed thinner than the other portions. The thickness of the container base 11 at the bottom surface of the concave portion 18 is, for example, several tens of μm at the portion where the distal end portion 15b of the measuring flow channel 15 or the other end 17b of the injection flow channel 17 is formed.

  A convex portion 18 a is formed on the bottom surface of the concave portion 18. By grasping the convex portion 18a and pulling it upward or pulling up the concave portion 18a, the portion where the injection flow channel 17 of the flow channel base 11 is formed rises or returns to the original state. Thereby, the channel cross-sectional area of the one end 17a of the injection channel 17 is variable.

  1 and 2, the reaction container air vent channel 19 is provided for each reaction container 5. One end of the reaction container air vent channel 19 is connected to a recess 27 disposed on the reaction container 5 at a position different from the injection channel 17 and disposed on the reaction container 5. The reaction container air vent channel 19 is formed with a dimension that maintains liquid tightness in the reaction container 5 in a state where there is no pressure difference between the reaction container 5 and the reaction container air vent channel 19. The other end of the reaction vessel air vent channel 19 is connected to the reaction vessel air vent channel 21. In this embodiment, the reaction vessel air vent channel 19 is composed of a plurality of grooves, and the dimensions of the grooves are, for example, a depth of 10 μm, a width of 20 μm, a pitch of 20 μm, and 13 in a 500 μm width region. Grooves are formed.

  In this embodiment, a plurality of reaction vessel air vent channels 21 are provided. A plurality of reaction vessel air vent channels 19 are connected to each reaction vessel air vent channel 21. The reaction container air vent channel 21 is for connecting the reaction container air vent channel 19 to an air drain space 31 formed in the container base 3. The dimensions of the grooves constituting the reaction vessel air vent channel 21 are, for example, a depth of 400 μm and a width of 500 μm.

  The drain space air vent channel 23 is for connecting the liquid drain space 29 to a port of a switching valve 63 described later. One end of the drain space air vent channel 23 is disposed on the liquid drain space 29. The other end of the drain space air vent channel 23 is connected to a channel 23 a formed of a through hole provided in the container base 3. The flow path 23a is connected to a port of a switching valve 63 described later. The dimensions of the grooves constituting the drain space air vent channel 23 are, for example, a depth of 400 μm and a width of 500 μm.

  The drain space air vent channel 25 is for connecting the air drain space 31 to a port of a switching valve 63 described later. One end of the drain space air vent channel 25 is disposed on the air drain space 31. The other end of the drain space air vent channel 25 is connected to a channel 25 a formed of a through hole provided in the container base 3. The flow path 25a is connected to a port of a switching valve 63 described later. The dimensions of the grooves constituting the drain space air vent channel 25 are, for example, a depth of 400 μm and a width of 500 μm.

  A flow path cover 33 (not shown in FIG. 1A) is disposed on the flow path base 11. The flow path cover 33 is for fixing the flow path base 11 to the container base 3. A through hole is formed in the flow path cover 33 at a position on the reaction vessel 5.

  Referring to FIGS. 1 and 4, a sample container 35, a reagent container 37, and an air suction container 39 are formed on the container base 3 at positions different from the arrangement region of the reaction container 5 and the drain spaces 29 and 31. Yes. The sample container 35, the reagent container 37, and the air suction container 39 constitute a sealed container for the reaction container plate of the present invention.

  In the container base 3 in the vicinity of the sample container 35, a sample channel 35a penetrating from the bottom of the sample container 35 to the back surface and a sample container air vent channel 35b penetrating from the surface to the back surface are formed. A protrusion 35 c is disposed on the container base 3 around the opening of the sample container 35. A sample container air vent channel 35d made of a through hole is formed in the protrusion 35c on the sample container air vent channel 35b. A sample container air vent channel 35e that connects the sample container 35 and the sample container air vent channel 35d is formed on the surface of the protrusion 35c.

  The sample container air vent channel 35e is formed by, for example, one or a plurality of pores having a width of 5 to 200 μm and a depth of 5 to 200 μm. In the sample container 35 and the sample container air vent channel 35d, This is for maintaining the liquid tightness of the sample container 35 in a state where there is no pressure difference. A septum 41, which is an elastic member, is formed on the projection 35c so as to cover the sample container 35 and the air vent channel 35d. The septum 41 is made of, for example, an elastic material such as silicone rubber or PDMS. The septum 41 can be penetrated by a dispensing device having a sharp tip, and the through-hole can be closed by elasticity when the dispensing device is pulled out after penetration. A septum stopper 43 for fixing the septum 41 is disposed on the septum 41. The septum stopper 43 has an opening on the sample container 35. In this embodiment, the reagent 45 is accommodated in the sample container 35 in advance.

  As shown in FIG. 5, the reagent base 37 in the vicinity of the reagent container 37 has a reagent channel 37 a that penetrates from the bottom to the back of the reagent container 37 and a reagent container air vent channel 37 b that penetrates from the front to the back. Is formed. A protrusion 37 c is arranged on the container base 3 around the opening of the reagent container 37. A reagent container air vent channel 37d made of a through hole is formed in the protrusion 37c on the reagent container air vent channel 37b. A reagent container air vent channel 37e that connects the reagent container 37 and the reagent container air vent channel 37d is formed on the surface of the protrusion 37c.

  The reagent container air vent channel 37e is formed by, for example, one or a plurality of pores having a width of 5 to 200 μm and a depth of 5 to 200 μm. In the reagent container 37 and the reagent container air vent channel 37d, This is for maintaining the liquid tightness of the reagent container 37 in a state where there is no pressure difference. A film 47 made of, for example, aluminum is formed on the protrusion 37c so as to cover the reagent container 37 and the air vent channel 37d. Dilution water 49 is accommodated in the reagent container 37.

  As shown in FIG. 6, the air suction container 39 has the same configuration as the reagent container 37. That is, the air suction flow path 39a penetrating from the bottom to the back surface of the air suction container 39 and the air suction container air venting flow penetrating from the front surface to the back surface are disposed on the container base 3 near the air suction container 39. A path 39b is formed. On the container base 3 around the opening of the air suction container 39, a protrusion 39c having air suction container air vent channels 39d and 39e is disposed. A film 47 made of, for example, aluminum is formed on the protrusion 39c. The air suction container 39 contains no liquid or solid but is filled with air.

  1 and 2, the syringe 51 is provided on the surface of the container base 3 at a position different from the arrangement region of the reaction container 5, the drain spaces 29 and 31, and the containers 35, 37, and 39. Yes. The syringe 51 is formed by a cylinder 51a formed in the container base 3, a plunger 51b disposed in the cylinder 51a, and a cover body 51d. A syringe channel 51c penetrating from the discharge port provided at the bottom of the cylinder 51a to the back surface is formed in the container base 3.

  The cover body 51d has flexibility in the sliding direction of the plunger 51b, and is connected to the cylinder 51a and the plunger 51b. The cover body 51d is for blocking the portion of the inner wall of the cylinder 51a that the plunger 51b contacts with the atmosphere outside the cylinder 51a while maintaining airtightness, and is surrounded by the cylinder 51a, the plunger 51b, and the cover body 51d. A sealing space 51e is formed. The end of the cover body 51d on the side connected to the cylinder 51a is fixed to the upper end of the cylinder 51a with a cylinder cap 51f while ensuring airtightness. The end of the cover body 51d on the side connected to the plunger 51b is connected to the upper surface of the plunger 51b with an adhesive while ensuring airtightness. However, the method and position of connecting the cover body 51d to the cylinder 51a and the plunger 51b are not limited to this.

  Thus, the cover body 51d is connected to the cylinder 51a and the plunger 51b to form a sealed space 51e surrounded by the cylinder 51a, the plunger 51b, and the cover body 51d, so that the space between the cylinder 51a and the plunger 51b is formed. Therefore, it is possible to prevent foreign substances from entering and environmental contamination of the liquid to the outside. Since the cover body 51d is flexible in the sliding direction of the plunger 51b, the sliding operation of the plunger 51b is possible.

  In this embodiment, the plunger 51b and the cover body 51d are formed by separate members, but the plunger and the cover body may be integrally formed. An example of the integrally formed plunger and cover material is silicone rubber.

  The container base 3 is also provided with a bellows 53 at a position different from the arrangement region of the reaction container 5, the drain spaces 29 and 31, the containers 35, 37, and 39 and the syringe 51. The bellows 53 has an internal space sealed, and the internal capacity is passively variable by expanding and contracting. For example, the bellows 53 is disposed in a through hole 53 a provided in the container base 3.

  A container bottom 55 is attached to the back surface of the container base 3 at a position different from the arrangement region of the reaction containers 5. An air vent channel 53 b is provided in the container bottom 55 at a position communicating with the bellows 53. The bellows 53 is in close contact with the surface of the container bottom 55. The container bottom 55 is for guiding the flow paths 13a, 23a, 25a, 35a, 35b, 37a, 37b, 39a, 39b, 51c, 53b to a predetermined port position.

The container base 3 container and the bottom 55 are provided with a syringe air vent channel 53 c having one end connected to the sealed space 51 e and the other end made a bellows 53. Illustration of the syringe air vent channel 53c in FIG. 1 (A) is omitted.
Thus, since the syringe air vent channel 53c having one end connected to the sealed space 51e and the other end bellows 53 is provided, the sealed space 51e is blocked from the atmosphere outside the reaction vessel plate 1. When the plunger 51b slides, the pressure change in the sealed space 51e accompanying the change in the internal capacity of the sealed space 51e can be alleviated, and the plunger 51b can be slid smoothly.

  A rotary switching valve 63 including a disc-shaped seal plate 57, a rotor upper 59, and a rotor base 61 is provided on the surface of the container bottom 55 opposite to the container base 3. The switching valve 63 is attached to the container bottom 55 by a lock 65.

The seal plate 57 is provided in the vicinity of the peripheral edge thereof, and is connected to any of the flow paths 13a, 35a, 37a, 39a, and the flow paths 23a, 25a, 35b, A through groove 57b connected to at least two of 37b, 39b, and 53b and a through hole 57c provided in the center and connected to the syringe flow path 51c are provided.
The rotor upper 59 includes a through hole 59a provided at the same position as the through hole 57a of the seal plate 57, a groove 59b provided on the surface corresponding to the through groove 57b of the seal plate 57, and a through hole provided in the center. A hole 59c is provided.
The rotor base 61 is provided with a groove 61a on its surface for connecting two peripheral holes 59a and 59c disposed at the center and the peripheral portion of the rotor upper 59.

The syringe channel 51c is connected to one of the channels 13a, 35a, 37a, 39a by the rotation of the switching valve 63, and at the same time, the air vent channel 53b is connected to the channels 23a, 25a, 35b, 37b, 39b. Connected to at least one of them.
In the position of the switching valve 63 shown in FIG. 1A, the syringe flow path 51c is not connected to any of the flow paths 13a, 35a, 37a, 39a, and the air vent flow path 53b is also connected to the flow paths 23a, 25a. , 35b, 37b, 39b are not connected to the initial position.

  In the reaction vessel plate 1, the injection channel 17 is formed so as to maintain the liquid tightness of the reaction vessel 5 with no pressure difference between the reaction vessel 5 and the injection channel 17. The reaction vessel air vent channel 19 is also formed so as to maintain the liquid tightness of the reaction vessel 5 in the state where there is no pressure difference between the reaction vessel 5 and the reaction vessel air vent channel 19. The main flow path 13 of the reaction container flow path, the liquid drain space 29 to which the main flow path 13 is connected, and the drain space air vent flow path 23 can be sealed by switching the switching valve 63. The containers 35, 37, and 39 are sealed with a septum 41 or a film 47. The flow paths 35 a, 35 b, 37 a, 37 b, 39 a, 39 b connected to the containers 35, 37, 39 can be sealed by switching the switching valve 63. One end of the air vent channel 53b is connected to the bellows 53 and sealed. Thus, the container and flow path inside the reaction container plate 1 are formed in a closed system. Even when the air vent channel 53b is connected to the atmosphere outside the reaction vessel plate 1 without the bellows 53, the air vent channel 53b is switched to the reaction vessel by switching the switching valve 63. Since it can block | block with the flow paths other than the container inside the plate 1 and the air vent flow path 53b, the container and flow path in which a liquid is accommodated or a liquid flows can be made into a closed system.

FIG. 7 is a cross-sectional view showing a reaction processing apparatus for processing the reaction container plate 1 shown in FIG. Since the structure of the reaction vessel plate 1 is the same as that shown in FIG.
The reaction processing device is switched between a temperature control mechanism 67 for adjusting the temperature of the reaction vessel 5, a syringe drive unit 69 for driving the syringe 51, and a convex pulling mechanism 70 for pulling up the convex 18a. A switching valve drive unit 71 for switching the valve 63 is provided.

  8 to 14 are plan views for explaining the operation of introducing the sample liquid from the sample container 35 into the reaction container 5. FIG. 15 is a cross-sectional view for explaining the operation of the injection channel 17 during the operation. This operation will be described with reference to FIGS. 1 and 8 to 15.

  Using a dispensing device having a sharp point (not shown), for example, 5 μL of sample liquid is dispensed into the sample container 35 through the septum 41 on the sample container 35. After dispensing the sample solution, pull out the dispensing device. The through hole of the septum 41 when the dispensing instrument is pulled out is closed by the elasticity of the septum 41.

The syringe drive unit 69 is connected to the plunger 51 b of the syringe 51, and the switching valve drive unit 71 is connected to the switching valve 63.
As shown in FIG. 8, the switching valve 63 is rotated from the state of the switching valve 63 shown in FIG. 1A to connect the sample flow path 35a and the syringe flow path 51c, and the sample container air vent flow path 35b is aired. It connects with the extraction flow path 53b. At this time, the air vent channels 37b and 39b are also connected to the air vent channel 53b. For example, 45 μL of the reagent 45 is accommodated in the sample container 35.

  The plunger 51b of the syringe 51 is slid to mix the sample liquid and the reagent 45 in the sample container 35. Thereafter, the mixed solution in the sample container 35 is sucked into the flow path in the switching valve 63, the syringe flow path 51c, and the syringe 51 by, for example, 10 μL. At this time, since the sample container 35 is connected to the bellows 53 via the air vent channels 35e, 35d, 35b, the switching valve 63 and the air vent channel 53b, the gas capacity in the sample container 35 is changed. The bellows 53 expands and contracts. Further, the sliding of the plunger 51b deforms the cover body 51d, and the internal capacity of the sealed space 51e (see FIG. 1C) changes. Since the sealed space 51e is connected to the bellows 53 via the syringe air vent channel 53c, the bellows 53 expands and contracts even when the internal capacity of the sealed space 51e changes. Even in the operation process described below, the bellows 53 expands and contracts with the change in the internal capacity of the sealed space 51e due to the sliding of the plunger 51b.

  As shown in FIG. 9, the switching valve 63 is rotated to connect the reagent channel 37a and the syringe channel 51c, and the reagent container air vent channel 37b is connected to the air vent channel 53b. For example, 190 μL of dilution water 49 is accommodated in the reagent container 37. The mixed solution sucked into the flow path in the switching valve 63, the syringe flow path 51 c and the syringe 51 is injected into the reagent container 37, and the syringe 51 is slid to mix the mixed liquid and the dilution water 49. For example, all of the diluted mixed solution is sucked into the flow path in the switching valve 63, the syringe flow path 51c, and the syringe 51, that is, 200 μL. At this time, since the reagent container 37 is connected to the bellows 53 via the air vent channels 37e, 37d, 37b, the switching valve 63 and the air vent channel 53b, the gas capacity in the reagent container 37 is changed. The bellows 53 expands and contracts.

  As illustrated in FIG. 10, the switching valve 63 is rotated to connect the flow path 13 a connected to one end of the main flow path 13 and the syringe flow path 51 c, and the flow connected to the liquid drain space 29 and the air drain space 31. The paths 23a and 25a are connected to the air vent channel 53b. The syringe 51 is driven in the pushing direction to send the diluted mixed solution sucked into the flow path in the switching valve 63, the syringe flow path 51 c, and the syringe 51 to the main flow path 13. The diluted mixed liquid injected from the flow path 13a side into the main flow path 13 fills the metering flow path 15 in order from the flow path 13a side and reaches the liquid drain space 29 as indicated by the embossments and arrows. In the introduction pressure state when the diluted mixture is introduced into the main channel 13 and the metering channel 15, the injection channel 17 allows gas to pass but does not allow the diluted mixture to pass. Therefore, as shown in FIG. 15A, the diluted mixed liquid (see the embossing) filled in the measuring flow path 15 is not injected into the reaction vessel 5. The gas in the metering channel 15 moves into the reaction vessel 5 through the injection channel 17 as the metering channel 15 is filled with the diluted mixed solution. As this gas moves, a part of the gas in the reaction vessel 5 moves to the reaction vessel air vent channels 19 and 21. Furthermore, the gas in the flow path from the reaction container air vent flow path 19 to the bellows 53 sequentially moves to the bellows 53 side (see white arrow). Further, when the diluted mixed liquid is injected into the liquid drain space 29, the gas in the flow path from the liquid drain space 29 to the bellows 53 sequentially moves toward the bellows 53 (see the white arrow). As a result, the bellows 53 expands.

  As shown in FIG. 11, the switching valve 63 is rotated to connect the air suction channel 39a and the syringe channel 51c, and the air suction container air vent channel 39b is connected to the air vent channel 53b. The syringe 51 is driven to the suction side, and the gas in the air suction container 39 is sucked into the flow path in the switching valve 63, the syringe flow path 51 c, and the syringe 51. At this time, since the air suction container 39 is connected to the bellows 53 via the air vent channels 39e, 39d, 39b, the switching valve 63 and the air vent channel 53b, the pressure inside the air suction container 39 is reduced. As a result, the bellows 53 contracts (see the white arrow).

  As shown in FIG. 12, the switching valve 63 is rotated to connect the flow path 13a and the syringe flow path 51c, and connect the flow paths 23a and 25a to the air vent flow path 53b as in the connection state of FIG. The syringe 51 is driven in the pushing direction, and the flow path in the switching valve 63, the syringe flow path 51c, and the gas in the syringe 51 are sent to the main flow path 13 to purge the diluted mixed liquid in the main flow path 13 (open arrow) reference). In the purge pressure state at this time, the dilute mixed solution does not pass through the injection flow channel 17, so that the dilute mixed solution remains in the measuring flow channel 15 (see the embossing in FIGS. 12 and 15A). The purged diluted liquid mixture is accommodated in the liquid drain space 29. Further, when the diluted mixed liquid is injected into the liquid drain space 29, the gas in the flow path from the liquid drain space 29 to the bellows 53 sequentially moves toward the bellows 53 (see the white arrow). As a result, the bellows 53 expands.

  As shown in FIG. 13, the switching valve 63 is rotated to connect the air suction flow path 39a and the syringe flow path 51c as in the connection state of FIG. 11, and the air suction container air vent flow path 39b is vented. Connect to the flow path 53b. The syringe 51 is driven to the suction side, and the gas in the air suction container 39 is sucked into the flow path in the switching valve 63, the syringe flow path 51 c, and the syringe 51. At this time, the bellows 53 contracts as described with reference to FIG. 11 (see the white arrow).

  As shown in FIG. 14, the switching valve 63 is rotated to connect the flow path 13a and the syringe flow path 51c, and connect the flow path 25a to the air vent flow path 53b. This connection state differs from the connection states shown in FIGS. 10 and 12 in that the liquid drain space 29 to which the downstream end of the main flow path 13 is connected is not connected to the flow path in the switching valve 63.

  As shown in FIG. 15B, the convex portion pulling mechanism 70 for pulling up the convex portion 18a is driven to pull up the convex portion 18a. Thereby, the bottom part of the recessed part 18 of the flow path base 11 made of an elastic body is lifted from the container base 3, and the flow path cross-sectional area of the one end 17a of the injection flow path 17 is increased.

  Thereafter, the syringe 51 is driven in the pushing direction to feed gas into the main flow path 13. Since the downstream end of the main channel 13 is not connected to the bellows 53 and is sealed, the inside of the main channel 13 is pressurized with gas. As a result, as shown in FIG. 15B, the diluted mixed solution in the metering channel 15 is injected into the reaction vessel 5 through the injection channel 17. By pulling up the convex portion 18a, the flow path cross-sectional area of the one end 17a of the injection flow path 17 is increased, and the flow path resistance of the injection flow path 17 is decreased. Compared to the case where it is not variable, the injection pressure can be reduced, and the injection time is further shortened.

  After the diluted mixed solution is injected into the reaction vessel 5, a part of the gas in the main channel 13 flows into the reaction vessel 5 through the metering channel 15 and the injection channel 17. At this time, the reaction vessel 5 is connected to the bellows 53 via the reaction vessel air vent channels 19 and 21, the air drain space 31, the drain space air vent channel 25a, and the air vent channel 53b. The gas between the bellows 53 sequentially moves toward the bellows 53 (see the white arrow). As a result, the bellows 53 expands. After the air supply to the main flow path 13 is finished, the convex part pulling-up mechanism 70 releases the convex part 18a, so that the bottom part of the concave part 18 of the flow path base 11 is lifted as shown in FIG. Return to the original.

After the switching valve 63 is connected as shown in FIG. 1 and the container, flow path and drain space inside the reaction container plate 1 are sealed, the reaction container 5 is heated by the temperature control mechanism 67 to melt the wax 9. Thereby, the diluted mixed solution injected into the reaction vessel 5 enters under the wax 9, and the diluted mixed solution and the reagent 7 are mixed and reacted. Thus, according to the reaction container plate 1, the reaction process can be performed in a closed system.
Before injecting the diluted mixed solution into the reaction vessel 5, the reaction vessel 5 is heated by the temperature control mechanism 67 to melt the wax 9, and the wax 9 is injected when the diluted mixed solution is injected into the reaction vessel 5. May be melted. In this case, the diluted mixed solution injected into the reaction vessel 5 immediately enters under the wax 9, and the diluted mixed solution and the reagent 7 are mixed and reacted. Even if the connection state of the switching valve 63 is the state shown in FIG. 14, the sealed system is secured by the bellows 53. If the switching valve 63 is brought into the connection state shown in FIG. 1 after the diluted mixed solution is injected, the container, flow path and drain space inside the reaction container plate 1 can be sealed. Here, the timing for switching the switching valve 63 to the connected state in FIG. 1 may be any timing from immediately after the injection of the diluted mixed solution to the end of the reaction of the diluted mixed solution and the reagent 7, or the diluted mixed solution and the reagent 7. It may be after the completion of the reaction.
Thus, according to the reaction vessel plate 1, the reaction process can be performed in a closed system, and a closed system can be formed before and after the reaction process.

  In this embodiment, the grooves for forming the flow paths 13, 15, 17, 19, 21, and 23 are formed in the flow path base 11, but the present invention is not limited to this, and the flow of these is not limited. A groove for forming all or part of the path may be formed on the surface of the container base 3.

  In this embodiment, the entire flow path base 11 is formed of an elastic body. However, the present invention is not limited to this, and the flow path base (cover substrate) forms at least an injection flow path. Any portion may be used as long as it is formed of an elastic body.

  FIG. 16 is an enlarged schematic cross-sectional view showing the vicinity of the reaction vessel in another embodiment of the reaction vessel plate. This embodiment is the same as the above-described embodiment described with reference to FIGS. 1 to 15 except that a flow path spacer is disposed between the reaction vessel base and the flow path base.

  A flow path spacer 73 is disposed on the container base 3 so as to cover the arrangement region of the reaction containers 5, and a flow path base 11 and a flow path cover 33 are further disposed in that order. The channel spacer 73 is made of, for example, PDMS or silicone rubber. The thickness of the channel spacer 73 is, for example, 0.5 to 5.0 mm. The flow path spacer 73 includes a convex portion 75 protruding into the reaction container 5 for each reaction container 5. The convex portion 75 has a substantially trapezoidal cross section. For example, the base end has a width of 1.0 to 2.8 mm, the tip has a width of 0.2 to 0.5 mm, and the tip has a base end. It is thinner than Further, the surface of the convex portion 75 is subjected to super water repellent treatment. However, the surface of the convex portion 75 may not necessarily be subjected to the water repellent treatment.

Further, the flow path spacer 73 is provided with an injection flow path 77 formed of a through hole penetrating from the tip end portion of the convex portion 75 to the opposite surface for each position where the convex portion 75 is formed. The inner diameter of the injection channel 77 is, for example, 500 μm. The opening on the flow channel base 11 side of the injection flow channel 77 is connected to the injection flow channel 17 of the flow channel base 11. In this embodiment, the channel base 11 is not provided with the recess 27 as compared with the above-described embodiment described with reference to FIGS.
Further, the flow path spacer 73 is also provided with a reaction container air vent flow path 79 including a through hole for communicating the reaction container air vent flow path 19 of the flow path base 11 and the reaction container 5.

  Although not shown, the channel spacer 73 includes both end portions of the main channel 13, end portions of the reaction vessel air vent channel 21 on the air drain space 31 side, and both ends of the drain space air vent channels 23 and 25. The part is provided with a through hole, and the flow paths 13, 21, 23, 25 are connected to the containers 29, 31 or the flow paths 23 a, 25 b provided in the container base 3.

  In this embodiment, the end of the injection flow channel 77 opposite to the injection flow channel 15 (the other end of the injection flow channel) is disposed at the tip of a convex portion 75 formed to protrude from the inner upper surface of the reaction vessel 5. Therefore, the liquid injected into the reaction vessel 5 through the injection flow channels 15 and 77 can be easily dropped into the reaction vessel 5.

  Further, when the liquid is discharged from the tip of the convex portion 75 through the injection channel 77, the tip of the convex portion 75 is adjusted so that the liquid droplet formed at the tip of the convex portion 75 contacts the side wall of the reaction vessel 5. If it arrange | positions in the side wall vicinity of the reaction container 5, a liquid can be inject | poured in the reaction container 5 along the side wall of the reaction container 5, and a liquid can be inject | poured in the reaction container 5 more reliably. However, the formation position of the convex portion 75 may be a position where a droplet formed at the tip of the convex portion 75 does not contact the side wall of the reaction vessel 5.

FIG. 17 is an enlarged schematic cross-sectional view showing the vicinity of a reaction vessel of still another embodiment of the reaction vessel plate.
This embodiment further includes a protrusion 81 inside the reaction vessel 5 as compared to the embodiment described with reference to FIG. The tip of the protrusion 81 is disposed below the tip of the protrusion 75. Thereby, it becomes easy to guide the droplet formed at the tip of the convex portion 75 into the reaction vessel 5. In particular, it is particularly effective if a hydrophilic treatment is applied to at least the tip surface of the protrusion 81.

FIG. 18 is a schematic cross-sectional view showing, in an enlarged manner, the vicinity of the reaction vessel of another embodiment of the reaction vessel plate.
In this embodiment, compared to the embodiment described with reference to FIG. 17, the stepped portion 83 formed on the side wall of the reaction vessel 5 and the upper surface of the reaction vessel 5 are formed on the upper surface of the stepped portion 83 with a gap. Further provided is a convex ridge 85. The step part 83 and the protruding line part 85 are formed in an annular shape when viewed from above. The tip of the ridge 85 is disposed at a distance from the side wall of the reaction vessel 5.
Since the tip of the ridge 85 is disposed at a distance from the upper surface and the side surface of the reaction vessel 5, the liquid stored in the reaction vessel 5 reaches the upper surface of the reaction vessel 5 along the side wall of the reaction vessel 5. Can be prevented. This effect is particularly effective when a water-repellent treatment is performed on at least the tip of the ridge 85.

The configuration provided with the step portion 83 and the convex strip portion 85 shown in FIG. 18 can also be applied to the embodiment shown in FIG.
Moreover, in each Example demonstrated with reference to FIG.16, FIG.17 or FIG. 18, the groove | channel for forming the flow path 13,15,17,19,21,23 is formed in the flow path base 11. FIG. However, the present invention is not limited to this, and the grooves for forming all or part of the flow paths are the surface of the flow path spacer 73 on the flow path base 11 side, the container base 11 of the flow path spacer 73. It may be formed on either the side surface or the surface of the container base 3.

In addition, regarding the syringe 51, a part of the cylinder 51 a may be formed by a part of the switching valve 63.
19A and 19B are views showing still another embodiment of the reaction vessel plate. FIG. 19A is a schematic plan view, and FIG. 19B is a cross-sectional view at the EE position of FIG. Schematic cross-sectional view of the cross section of the passage 17, sample container air vent channels 19, 21, liquid drain space 29, air drain space 31, and bellows 53, (C) is an enlarged view of the vicinity of the syringe 51 and bellows 53 It is a schematic sectional drawing shown. 20A and 20B are schematic exploded views of the switching valve, in which FIG. 20A is a plan view and a cross-sectional view of a seal plate, FIG. 20B is a plan view and a cross-sectional view of a rotor upper, and FIG. A cross-sectional view is shown.

In this embodiment, the cylinder 87 a of the syringe 87 is formed of a resin material such as polypropylene or polycarbonate, and is integrally formed with the rotor upper 91 of the switching valve 95.
The syringe 87 is formed by a cylinder 87a disposed in a through hole formed in the container base 3 and the container bottom 55, a plunger 87b disposed in the cylinder 87a, and a cover body 87d.

  The cover body 87d has flexibility in the sliding direction of the plunger 87b, and is connected to the cylinder 87a and the plunger 87b. The cover body 87d is for shutting off the portion of the inner wall of the cylinder 87a that contacts the plunger 87b while maintaining airtightness from the atmosphere outside the cylinder 87a. The cover body 87d is surrounded by the cylinder 87a, the plunger 87b, and the cover body 87d. A sealing space 87e is formed.

  The end of the cover body 87d on the side connected to the cylinder 87a is fixed to the upper end of the cylinder 87a with a cylinder cap 87f while ensuring airtightness. Further, the end of the cover body 87d on the side connected to the plunger 87b is connected to the upper surface of the plunger 87b with an adhesive while ensuring airtightness. However, the method and position for connecting the cover body 87d to the cylinder 87a and the plunger 87b are not limited thereto. The plunger and the cover body may be integrally formed. An example of the integrally formed plunger and cover material is silicone rubber.

  As described above, the cover body 87d is connected to the cylinder 87a and the plunger 87b to form a sealed space 87e surrounded by the cylinder 87a, the plunger 87b, and the cover body 87d, so that the space between the cylinder 87a and the plunger 87b is formed. Therefore, it is possible to prevent foreign substances from entering and environmental contamination of the liquid to the outside. Since the cover body 87d has flexibility in the sliding direction of the plunger 87b, the sliding operation of the plunger 87b is possible.

The syringe air vent channel 53c and the switching valve 95 will be described with reference to FIG.
The switching valve 95 is formed by a disc-shaped seal plate 89, a rotor upper 91 and a rotor base 93. The switching valve 95 is attached to the container bottom 55 by a lock 65.

  The seal plate 89 is provided in the vicinity of the peripheral edge portion thereof, and is connected to any of the flow paths 13a, 35a, 37a, 39a, and the flow paths 23a, 25a, 35b, A through groove 89b connected to at least two of 37b, 39b, and 53b and a through hole 89c provided at the center and into which the cylinder 87a is inserted are provided. A fluororesin layer (not shown) is formed on the surface of the seal plate 89 facing the container bottom 55.

  The rotor upper 91 corresponds to a cylindrical cylinder 87 a provided at the center of one surface thereof, a through hole 91 a provided at the same position as the through hole 89 a of the seal plate 89, and a through groove 89 b of the seal plate 89. Then, a groove 91b provided on the surface, a through hole 91c provided in the groove 91b, and a through hole 91d provided in the center are provided. The through hole 91d is provided at the bottom of the cylinder 87a and constitutes a discharge port of the cylinder 87a.

  The rotor upper 91 is also formed with a syringe air vent channel 53c formed of a through hole penetrating from the upper end surface of the cylinder 87a to the back surface of the rotor upper 91. A cutout is formed in the upper end surface of the cylinder 87a from the inner wall of the cylinder 87a to the syringe air vent channel 53c. By this notch, as shown in FIG. 19C, the sealing space 87e and the syringe air vent channel 53c communicate with each other with the upper end surface of the cylinder 87a covered with the cover body 87d.

  The rotor base 93 has a groove 93a for connecting the through hole 91a and the through hole 91d formed in the rotor upper 91 on the surface to be bonded to the back surface of the rotor upper 91, and a syringe air vent formed in the rotor upper 91. A groove 93b for connecting the flow paths 53c and 91c is provided.

As shown in FIG. 19, the seal plate 89, the rotor upper 91, and the rotor base 93 are arranged such that a cylinder 87 a is inserted into a through hole 89 c of the seal plate 89 and overlapped to form a switching valve 95.
The through hole 91d of the rotor upper 91 that constitutes the discharge port of the cylinder 87a is connected to the through hole 89a of the seal plate 89 through the groove 93a of the rotor base 93 and the through hole 91a of the rotor upper 91.
The sealing space 87e (see FIG. 19) is connected to the through groove 89b of the seal plate 89 through the syringe air vent channel 53c, the groove 93b of the rotor base 93, the through hole 91c and the through groove 91b of the rotor upper 91. The

The flow path connection will be described with reference to FIGS. 19 and 20.
Through the rotation of the switching valve 95, the through hole 91d of the rotor upper 91 constituting the discharge port of the cylinder 87a is one of the flow paths 13a, 35a, 37a, 39a via the groove 93a, the through hole 91a, and the through hole 89a. Connected to.
At the same time as the through hole 91d is connected to any of the flow paths 13a, 35a, 37a, 39a, the air vent flow path 53b is connected to the flow paths 23a, 25a, 35b, 37b, through the through grooves 89b, 91b. It is connected to at least one of 39b. At this time, the sealing space 87e is connected to the air vent channel 53b via the cylinder air vent channel 53c, the groove 93b, the through hole 91c, and the through grooves 89b and 91b.

According to this embodiment, the flow path between the syringe 87 and the switching valve 95 can be eliminated, and the flow path configuration is simplified.
Further, when there is a seam in the flow path, liquid or gas leakage may occur at the seam part, or a liquid pool may occur at the seam part. In this embodiment, since the cylinder 87a and the rotor upper 91 are integrally formed, there is no joint between the flow path between the syringe 87 and the switching valve 95, and leakage and liquid pool between the syringe 87 and the switching valve 95 are generated. Can be eliminated.
In addition, when a liquid puddle occurs at the joint, there is a concern about the volume reduction of the liquid to be pumped, or liquid carry-over, contamination, or concentration fluctuation due to mixing of the liquid in the puddle with another liquid to be pumped. In this embodiment, these concerns between the syringe 87 and the switching valve 95 can be eliminated.

  Further, when a syringe is arranged on the switching valve, if a flow path 51c is formed between the syringe 51 and the switching valve 63 as shown in FIG. 1, a cylinder is formed in the portion where the flow path 51c is formed. In the embodiment shown in FIG. 19, since there is no flow path between the syringe 87 and the switching valve 95, the capacity of the cylinder 87a can be reduced even if the cylinders 51a and 81a have the same planar size. It can be made larger than the cylinder 51a.

When the cylinder 87a is formed with the same capacity as the cylinder 51a, the height of the cylinder 87a is the same plane size as the cylinder 51a and lower than the cylinder 51a, or the plane size of the cylinder 87a is the same height as the cylinder 51a. It can be made smaller than the cylinder 51a.
For example, even when the upper end surface of the cylinder 51a has to be arranged so as to protrude from the upper surface of the entire reaction container plate 1 due to the limitation of the planar size of the entire reaction container plate 1, the height of the cylinder 87a is the same as that of the cylinder 51a. Further, since the planar size can be lower than that of the cylinder 51a, the upper end surface of the cylinder 87a can be disposed at the same position as the upper surface of the entire reaction vessel plate 1 or at a position lower than that. As a result, there is a problem when the upper end surface of the cylinder protrudes from the upper surface of the entire reaction container plate, for example, a problem when stacking and storing a plurality of reaction container plates, or a problem such as an increase in packaging of the reaction container plate. Can be eliminated.
Further, if the plane size of the cylinder 87a is made smaller than that of the cylinder 51a with the same capacity as the cylinder 51a, the plane size of the entire reaction vessel plate 1 can be reduced.

  In the embodiment described above, the reaction vessel plate 1 includes the convex portion 18a provided in the concave portion 18 formed in the portion where the injection channel 17 of the channel base 11 is formed, and by pulling up the convex portion 18a. The channel cross-sectional area of the one end 17a of the injection channel 17 is variable, but the reaction vessel plate of the present invention is not limited to this. In the reaction container plate of the present invention, the injection flow path forming portion of the cover substrate is formed by the force acting on the surface of the cover substrate (flow path base 11) opposite to the base substrate (container base 3). Any configuration may be used as long as the cross-sectional area of the flow path is variable by lifting or returning from the base substrate.

  FIG. 21 is a schematic cross-sectional view showing, in an enlarged manner, the vicinity of the reaction vessel of another embodiment of the reaction vessel plate. In this embodiment, the configuration other than the configuration in which the channel spacer is arranged between the channel base and the channel cover and the configuration in which the convex portion 18a is not provided are the same as the above-described embodiment described with reference to FIGS. The same.

  A flow path spacer 97 is disposed on the flow path base 11, and a flow path cover 33 is further disposed thereon. The channel spacer 97 is made of, for example, PDMS or silicone rubber. The thickness of the flow path spacer 97 is, for example, 0.5 to 5.0 mm. The flow path spacer 97 includes an air control flow path 99 connected to the recess 18. The air control flow path 99 is formed by a groove formed on the flow path base 11 side surface of the flow path spacer 97. The air control channel 99 has a depth of, for example, 400 μm and a width of 500 μm. The recess 18 and the air control channel 99 constitute an air control channel covering the surface of the reaction vessel plate of the present invention opposite to the base substrate of the injection channel forming part of the cover substrate.

  The end of the air control channel 99 opposite to the recess 18 is connected to a space outside the reaction vessel plate in a region not shown. The air control flow path 99 is connected to all the recesses 18 provided in the container base 11.

  In this embodiment, the air control flow path 99 is formed by a groove provided in the flow path spacer 97, but the air control flow path 99 is provided on the surface of the flow path base 11 on the flow path spacer 97 side. It may be formed by a groove, or may be formed by both a groove provided in the flow path base 11 and a groove provided in the flow path spacer 97.

  FIG. 22 is a cross-sectional view for explaining the operation of the injection channel 17 when the sample liquid is introduced from the sample container 35 (see FIG. 1) into the reaction container 5 in the embodiment shown in FIG.

  Similar to the injection operation described with reference to FIGS. 8 to 10, the sample liquid is dispensed into the sample container 35, the sample liquid and the reagent 45 are mixed in the sample container 35, and the mixed liquid is used as the reagent container. 37 is mixed with dilution water 49 to form a diluted mixed solution, and then the diluted mixed solution is filled into the main flow path and the measurement flow path 15 with the introduction pressure, and the gas is allowed to flow through the main flow path to be diluted in the measurement flow path 15. The diluted mixed solution in the main channel is removed while the mixed solution remains (see FIG. 22A).

  As shown in FIG. 22B, a negative pressure is generated in the air control flow path 99 and the recess 18 by a suction mechanism (not shown). Thereby, the bottom part of the recessed part 18 of the flow path base 11 made of an elastic body is lifted from the container base 3, and the flow path cross-sectional area of the one end 17a of the injection flow path 17 is increased. Thereafter, by sending gas into the main channel and the metering channel 15, the diluted mixed solution in the metering channel 15 is injected into the reaction vessel 5 through the injection channel 17. Since the flow channel cross-sectional area of the one end 17a of the injection flow channel 17 is large and the flow channel resistance of the injection flow channel 17 is small, the flow channel cross-sectional area of the injection flow channel 17 is smaller than that when the flow channel cross-sectional area is not variable. The pressure can be reduced and the injection time is shortened.

  As shown in FIG. 22 (C), after injecting the diluted mixed solution in the measurement flow path 15 into the reaction vessel 5, the negative pressure state in the air control flow path 99 and the recess 18 is released, The bottom portion of the recessed portion 18 of the flow path base 11 that has floated returns to its original state.

  The embodiments of the present invention have been described above, but the present invention is not limited to these, and the shape, material, arrangement, number, dimensions, flow path configuration, etc. are examples, and are described in the claims. Various modifications are possible within the scope of the present invention.

For example, the bellows 53 connected to the air vent channel 53b may have another structure as long as the capacity is a variable capacity member whose internal capacity is passively variable. Examples of such a structure include a bag-like material made of a flexible material and a syringe-like material.
Further, the capacity variable member such as the bellows 53 may not necessarily be provided.
In addition, if the containers 35, 37, and 39 do not contain a liquid such as a reagent in advance, it is not always necessary to provide the flow paths 35e, 37e, and 39e made of pores in a part of the air vent flow path.

Further, in the above embodiment, the air vent channels 35b, 37b, 39b provided in communication with the containers 35, 37, 39 as sealing containers are connected to the air vent channel 53b via the switching valve 63. However, the air vent channel provided in communication with the sealing container may be directly connected to the outside of the reaction container plate or a capacity variable part such as the bellows 53.
Moreover, you may use the cap which can be opened and closed as a sealing method of the containers 35, 37, and 39.

Moreover, in the said Example, although the container base 3 is formed with one component, the container base may be formed with several components.
The reagent in the reaction vessel 5 may be a dry reagent.
In addition, the reagent may not be stored in advance in the sample container 35 or the reaction container 5.
In the above embodiment, the dilution water 49 is stored in the reagent container 37, but the reagent may be stored instead of the dilution water 49.

  Further, the container base 3 may be provided with a gene amplification container for performing a gene amplification reaction. For example, if the reagent container 37 is emptied, it can be used as a gene amplification container.

In addition, if a reagent for performing a gene amplification reaction is accommodated in the reaction container 5, the gene amplification reaction can be performed in the reaction container 5.
Further, when a gene is contained in the liquid introduced into the main flow path 13, a probe that reacts with the gene may be provided in the reaction vessel 5.

Moreover, in the said Example, although the syringe 51 is arrange | positioned on the switching valve 63, the position which arrange | positions the syringe 51 is not limited on the switching valve 63, and may be anywhere.
In the above embodiment, the rotary switching valve 63 is used as the switching valve. However, the switching valve is not limited to this, and various flow path switching valves can be used. A plurality of switching valves may be provided.

  In the above embodiment, when the liquid filled in the metering channel 15 is injected into the reaction vessel 5 through the injection channel 17, the inside of the main channel 13 after air purge is pressurized to supply the liquid to the reaction vessel 5. However, the reaction treatment method of the present invention is not limited to this. For example, by changing the flow path configuration so that the inside of the reaction vessel air vent channel 21 can be made negative pressure using the syringe 51, and by making the inside of the reaction vessel air vent channel 21 and thus the reaction vessel 5 inside negative pressure. You may make it inject | pour into the reaction container 5 through the injection flow path 17 the liquid with which the measurement flow path 15 was filled. Alternatively, a separate syringe may be prepared so that the liquid is injected into the reaction vessel 5 with a positive pressure in the main channel 13 and a negative pressure in the reaction vessel 5.

  Moreover, in the said Example, although the one main flow path 13 was provided and all the measurement flow paths 15 were connected to the main flow path 13, a flow path structure is not limited to this. For example, a plurality of main channels may be provided, and one or a plurality of metering channels may be connected to each main channel.

In the above embodiment, the main flow path can be sealed, but an example in which the main flow path can be sealed by opening and closing both ends of the main flow path can be given. Here, “the both ends of the main channel can be opened and closed” means that other space is connected to the end of the main channel, and the end of the other space opposite to the main channel can be opened and closed This includes cases where For example, in the above embodiment, the flow path 13a, the liquid drain space 29, the drain space air vent flow path 23, and the flow path 23a correspond to the other spaces.
Further, in the above embodiment, the reaction vessel air vent channel can be sealed, but the reaction vessel air vent channel can be opened and closed because the end of the reaction vessel air vent channel opposite to the reaction vessel can be opened and closed. An example in which the extraction channel can be sealed can be given. Here, “the end of the reaction vessel air vent channel opposite to the reaction vessel can be opened and closed” means that the other end of the reaction vessel air vent channel opposite to the reaction vessel This includes a case where a space is connected and the end of the other space opposite to the reaction vessel air vent channel can be opened and closed. For example, in the above embodiment, the air drain space 31, the drain space air vent channel 25, and the channel 25a correspond to the other space.
In such an aspect, after the liquid is introduced into the main channel and the metering channel, the liquid in the main channel is then purged, and the liquid remaining in the metering channel is injected into the reaction vessel, Both ends of the main channel and the end of the reaction vessel air vent channel opposite to the reaction vessel are closed to seal the main channel and the reaction vessel air vent channel.

  The present invention can be used for measurement of various chemical reactions and biochemical reactions.

It is a figure which shows one Example of reaction container plate, (A) is a schematic top view, (B) is a cross section in the AA position of (A), a bellows, drain space, a measurement flow path, an injection flow path FIG. 4C is a schematic cross-sectional view in which a cross section of the sample container air vent channel is added, and FIG. It is sectional drawing which decomposes | disassembles and shows the Example, and a schematic exploded perspective view of a switching valve. It is the schematic which shows the one reaction container vicinity of the Example, (A) is a top view, (B) is a perspective view, (C) is sectional drawing. It is the figure which expanded and showed the sample container of the Example, (A) is a top view, (B) is sectional drawing in the BB position of (A). It is the figure which expanded and showed the reagent container of the Example, (A) is a top view, (B) is sectional drawing in CC position of (A). It is the figure which expanded and showed the container for air suction of the Example, (A) is a top view, (B) is sectional drawing in the DD position of (A). It is the schematic sectional drawing which showed the reaction processing apparatus for processing a reaction container plate with the reaction container plate. It is a top view for demonstrating the operation | movement which introduce | transduces a sample liquid into a reaction container from a sample container. It is a top view for demonstrating the operation | movement following FIG. FIG. 10 is a plan view for explaining the operation following FIG. 9. It is a top view for demonstrating the operation | movement following FIG. It is a top view for demonstrating the operation | movement following FIG. It is a top view for demonstrating the operation | movement following FIG. It is a top view for demonstrating the operation | movement following FIG. It is sectional drawing for demonstrating operation | movement of the injection | pouring flow path at the time of the operation | movement which introduces a sample liquid from a sample container to a reaction container. It is a schematic sectional drawing which expands and shows the reaction container vicinity of the other Example of the reaction container plate. It is a schematic sectional drawing which expands and shows the reaction container vicinity of the further another Example of the reaction container plate. It is a schematic sectional drawing which expands and shows the reaction container vicinity of the further another Example of the reaction container plate. FIG. 10 is a view showing still another embodiment of the reaction vessel plate, (A) is a schematic plan view, (B) is a cross section at the EE position of (A), a metering channel 15, an injection channel 17, Schematic sectional view including sections of the sample container air vent channels 19, 21, the liquid drain space 29, the air drain space 31 and the bellows 53. FIG. It is a schematic exploded view of the switching valve of the embodiment, (A) is a plan view and a sectional view of a seal plate, (B) is a plan view and a sectional view of a rotor upper, (C) is a plan view of a rotor base. And a sectional view is shown. It is a schematic sectional drawing which expands and shows the reaction container vicinity of the further another Example of the reaction container plate. It is sectional drawing for demonstrating operation | movement of the injection | pouring flow path at the time of introduce | transducing a sample liquid from a sample container into a reaction container in the Example.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 Reaction container plate 3 Container base 5 Reaction container 11 Flow path base 13 Main flow path 15 Metering flow path 15a Measuring flow path proximal end 15b Measuring flow path distal end 17 Injection flow path 17a Injection flow path one end 17b Injection flow path The other end 18 Recess 18a Projection 19, 21 Reaction container air vent channel 35 Sample container 35b, 35d, 35e Sample container air vent channel 37 Reagent container 37b, 37d, 37e Reagent container air vent channel 39 Air suction container 39b, 39d, 39e Air suction container air vent channel 51, 87 Syringe 51a, 87a Cylinder 51b, 87b Plunger 51d, 87d Cover body 51e, 87e Sealing space 53 Bellows (capacity variable portion)
53c Syringe air vent channel 63, 95 Switching valve 73 Channel spacer 75 Protrusion 77 Injection channel 79 Reaction vessel air vent channel 97 Channel spacer 99 Air control channel

Claims (22)

A base substrate; a cover substrate having one surface bonded to one surface of the base substrate; and a reaction vessel comprising a recess formed on the one surface of the base substrate, the one surface of the cover substrate, or both A reaction vessel channel formed of a groove formed on the one surface of the base substrate, the one surface of the cover substrate, or both, and connected to the reaction vessel,
The reaction vessel channel includes a main channel, a metering channel having a predetermined capacity branched from the main channel, and an injection channel having one end connected to the metering channel and the other end connected to the reaction vessel.
The cover substrate is formed of an elastic body at least at a portion forming the injection channel,
The injection channel is a groove formed at least partially narrower than the metering channel, and the cover substrate by a force acting on the surface of the cover substrate opposite to the base substrate in the injection channel forming portion. The liquid passage when the flow passage cross-sectional area of the groove is variable because the injection flow passage formation portion of the groove floats up or returns from the base substrate, and the liquid is introduced into the main flow passage and the metering flow passage. In the introduction pressure state and the purge pressure state when the liquid in the main channel is purged, the gas is allowed to pass but the liquid is not allowed to pass, and the injection channel forming portion of the cover substrate is lifted from the base substrate. A reaction vessel plate that is set so that the cross-sectional area of the flow passage becomes larger and allows liquid to pass through.   The cover substrate is formed of an elastic body that is integrally formed as a whole, and the thickness of the portion that forms the injection channel forms the portion that forms the main channel and the metering channel. The reaction container plate according to claim 1, wherein the reaction container plate is formed to be thinner than the thickness of the portion. The contact angle of the injection channel with respect to the water droplets is 90 degrees or more, and the area of the boundary between the injection channel and the metering channel is 1 when the injection channel forming portion of the cover substrate is not lifted from the base substrate. The reaction container plate according to claim 1 or 2, wherein the reaction container plate is -10000000 µm ² .   4. The device according to claim 1, comprising a plurality of the reaction vessels, each of the reaction vessels comprising the metering channel and the injection channel, and the plurality of metering channels connected to the main channel. The reaction container plate according to claim 1.   The reaction container plate according to any one of claims 1 to 4, further comprising a reaction container air vent channel connected to the reaction container. A sealed container provided separately from the reaction container;
A sealed container flow path connected to the sealed container;
A syringe for feeding liquid;
The reaction container plate according to any one of claims 1 to 5, further comprising a switching valve for connecting the syringe to the reaction container flow path or the sealing container flow path. A plurality of sets of the sealing container and the sealing container flow path,
The reaction vessel plate according to claim 6 , wherein the switching valve is capable of connecting the syringe to any of the sealed vessel flow paths.   The reaction vessel plate according to claim 6 or 7, wherein the switching valve is a rotary valve. The rotary valve has a port connected to the syringe at the center of rotation,
The reaction container plate according to claim 8, wherein the syringe is disposed on the rotary valve.   The reaction container plate according to any one of claims 6 to 9, wherein the sealing container is a sample container for containing a sample liquid.   The reaction according to claim 10, wherein the sample container is sealed by an elastic member that can be penetrated by a sharp dispensing device having a sharp tip and can close the through hole by elasticity when the dispensing device is pulled out after penetration. Container plate.   The reaction container plate according to any one of claims 6 to 11, wherein a sample pretreatment liquid or a reagent is previously stored in the sealing container.   The reaction container plate according to any one of claims 6 to 12, further comprising a gene amplification container comprising the sealed container for performing a gene amplification reaction.   The reaction container plate according to any one of claims 1 to 13, wherein the reaction container is for performing at least one of a color reaction, an enzyme reaction, and a reaction that generates fluorescence, chemiluminescence, or bioluminescence. .   The reaction container plate according to any one of claims 1 to 14, which is a reaction container plate for measuring a sample containing a gene and capable of performing a gene amplification reaction in the reaction container.   The reaction vessel plate according to any one of claims 1 to 15, wherein the reaction vessel is made of a light-transmitting material so that optical measurement can be performed from the bottom or from above.   The reaction container plate according to any one of claims 1 to 16, wherein the reaction container includes a probe that reacts with a gene when the liquid injected into the reaction container contains the gene.   The convex part used when raising the said injection flow path formation part from the said base substrate is provided in the surface on the opposite side to the said base substrate of the injection flow path formation part of the said cover substrate. The reaction container plate according to claim 1.   The reaction container plate according to any one of claims 1 to 17, further comprising an air control flow channel covering a surface of the cover substrate on the side opposite to the base substrate of the injection flow channel forming portion. A reaction processing method using the reaction container plate according to any one of claims 1 to 17,
Filling the main channel and the metering channel with the introduction pressure,
After removing the liquid in the main channel while flowing the gas in the main channel and leaving the liquid in the metering channel,
A force is applied to the surface of the cover substrate on which the injection flow path is formed opposite to the base substrate to lift the injection flow path formation portion from the base substrate to increase the flow channel cross-sectional area of the injection flow channel. The liquid in the metering channel is passed through the injection channel by setting the main channel to a positive pressure, the reaction vessel to a negative pressure, or both the positive pressure and the negative pressure. A reaction treatment method characterized by injecting into the reaction vessel. A reaction processing method using the reaction container plate according to claim 18,
Filling the main channel and the metering channel with the introduction pressure,
After removing the liquid in the main channel while flowing the gas in the main channel and leaving the liquid in the metering channel,
The injection flow path forming portion is lifted from the base substrate by grasping and pulling up the convex portion to increase the flow path cross-sectional area of the injection flow path, and the inside of the main flow path is set to a positive pressure or the reaction vessel. A reaction processing method characterized by injecting the liquid in the metering channel into the reaction vessel through the injection channel by setting the inside to a negative pressure or both the positive pressure and the negative pressure. A reaction processing method using the reaction container plate according to claim 19,
Filling the main channel and the metering channel with the introduction pressure,
After removing the liquid in the main channel while flowing the gas in the main channel and leaving the liquid in the metering channel,
By making the inside of the air control channel negative pressure, the injection channel forming portion is lifted from the base substrate to increase the channel cross-sectional area of the injection channel, and the inside of the main channel is set to a positive pressure. Alternatively, the liquid in the metering channel is injected into the reaction vessel through the injection channel by setting the inside of the reaction vessel to a negative pressure or both the positive pressure and the negative pressure. Reaction processing method.

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