The present disclosure relates to a test appartus for measurement by injection of a test solution into a microchannel, an injection method, and a microchannel device.
In order to test sensitivity or the like of bacteria to an antimicrobial, a test method using a microchannel device as in Japanese Patent Laying-Open No. 2017-67620 has been known. For example, in Japanese Patent Laying-Open No. 2017-67620, in a microchannel device including an introduction port and a discharge port that communicate with the outside and a channel through which a test solution supplied from the introduction port flows toward the discharge port, by injecting air into the channel from the introduction port, the test solution introduced previously is pressed into small channels. The channel is provided with a reaction portion where the test solution supplied from the introduction port is stored and an agent arranged in the reaction portion acts on bacteria.
In filling a microchannel with a test solution, a method using a capillary action or a pressure application has been known. A method of injecting air as in Japanese Patent Laying-Open No. 2017-67620 is effective for reliably and quickly fill the microchannel with the test solution. When the test solution is injected from one introduction port into a microchannel device in which branching into a plurality of channels is made, however, there may be a difference in height of a fluid level (a fluid head) between channels or in a portion from the introduction port to a channel, and the difference may cause a flow of the test solution in each channel. When a flow of the test solution is produced in the reaction portion, a correct result may not be observed.
The present disclosure was made to solve such a problem, and the present disclosure provides a test apparatus, an injection method, and a microchannel device that can suppress a flow of a test solution produced in a channel and can allow observation of a correct result.
A test apparatus in the present disclosure is a test apparatus for a test using a test solution containing a sample with a microchannel device. The microchannel device includes a first opening where the test solution is received, a plurality of branch channels that communicate with the first opening, a plurality of microchannels that communicate with each of the branch channels, a collection portion where some of the test solution is collected, the collection portion being provided at an end of each of the branch channels located opposite to a side where communication with the first opening is established, and a second opening provided in the collection portion. The test apparatus includes a pressure application unit that is connected to the first opening and applies an air pressure to inject the test solution into the microchannels, an opening and closing unit that switches between opening and closing of the second opening, and a controller that controls the pressure application unit and the opening and closing unit. The controller controls the opening and closing unit to close the second opening and controls the pressure application unit to inject the test solution into the microchannels, and the controller controls the opening and closing unit to open the second opening after the test solution is injected into the microchannels and controls the pressure application unit to apply an air pressure to collect in the collection portion, the test solution in each of the branch channels.
An injection method in the present disclosure is an injection method of injecting a test solution containing a sample into a microchannel device. The microchannel device includes a first opening where the test solution is received, a plurality of branch channels that communicate with the first opening, a plurality of microchannels that communicate with each of the branch channels, a collection portion where some of the test solution is collected, the collection portion being provided at an end of each of the branch channels located opposite to a side where communication with the first opening is established, and a second opening provided in the collection portion. The injection method includes closing the second opening, connecting a pipet that has suctioned the test solution to the first opening, injecting the test solution into the microchannels by discharging the suctioned test solution to the first opening, opening the second opening, and applying an air pressure with the pipet to collect in the collection portion, the test solution in each of the branch channels.
A microchannel device in the present disclosure is used in a test using a test solution containing a sample, and includes a first opening where the test solution is received, a plurality of branch channels that communicate with the first opening, a plurality of microchannels that communicate with each of the branch channels, a collection portion where some of the test solution is collected, the collection portion being provided at an end of each of the branch channels located opposite to a side where communication with the first opening is established, and a second opening provided in the collection portion.
The foregoing and other objects, features, aspects and advantages of the present invention will become more apparent from the following detailed description of the present invention when taken in conjunction with the accompanying drawings.
An embodiment of the present disclosure will be described below in detail with reference to the drawings. The same or corresponding elements in the drawings have the same reference characters allotted and description thereof will not be repeated.
[Apparatus Construction]
Referring to
Test solution placement portion 10 is a rack where a plurality of test solution containers 5 each containing a test solution can be arranged. In test solution placement portion 10, a plurality of test solution containers 5 can be set on test apparatus 100, in a unit of a rack.
Pipet nozzle 15 having a removable pipet chip 1 attached thereto suctions or discharges a test solution from test solution container 5 through a tip end of pipet chip 1. Pipet nozzle driver 12 horizontally and vertically moves pipet nozzle 15 and pump 14 connected to pipet nozzle 15. Pipet nozzle driver 12 can freely move pipet nozzle 15, for example, by means of a solenoid actuator or a stepping motor.
Table 16 is a support member on which a microchannel device is carried. Table 16 is in a shape of a flat plate and a microchannel device is fixed to an upper surface thereof. Table driver 13 can horizontally move table 16. Table driver 13 can freely move table 16, for example, by means of a solenoid actuator or a stepping motor. Naturally, table driver 13 may vertically move table 16 so that pipet nozzle 15 is not vertically moved. At least pipet nozzle driver 12 and table driver 13 are each a movement mechanism for changing a position of pipet nozzle 15 and a position of a microchannel device relative to each other.
Though not shown, pump 14 includes, to example, a syringe, a plunger capable of carrying out reciprocating motion within the syringe, and a drive motor that drives the plunger. Pump 14 can regulate an air pressure in pipet chip 1 by causing the plunger to carry out reciprocating motion while the plunger is connected to pipet nozzle 15 through a pipe to suction the test solution into pipet chip 1 or discharge the test solution in pipet chip 1 to the outside. Pump 14 can deliver air to the outside of pipet chip 1 by moving the plunger further into the syringe with the test solution in pipet chip 1 having been discharged to the outside.
Opening and closing unit 30 is a mechanism that opens or closes an opening (a second opening) in the microchannel device which will be described later. Specifically, opening and closing unit 30 is a mechanism for closing the opening with an elastic member, and it is provided, for example, with a silicone resin 30a at a tip end of a rod-shaped support portion. Since opening and closing unit 30 is attached to pipet nozzle 15 at a predetermined position, it is moved to a position of the second opening by moving pipet nozzle 15 to an opening (a first opening) in the microchannel device. Opening and closing driver 31 drives opening and closing unit 30 that has moved to the position of the second opening to vertically move silicone resin 30a to press silicone resin 30a against the second opening to close the second opening, and thus controls the second opening to a closed state. Though
Applicator 32 applies a sealing material to an opening in the microchannel device in order to suppress volatilization of the injected test solution from the opening. Specifically, applicator 32 is implemented, for example, by a nozzle that discharges the sealing material such as silicone oil to the opening or the like, and applies the sealing material to the opening or the like from the nozzle by means of pump 33. The construction of applicator 32 is not limited as such, and a mechanism that applies the sealing material to the opening or the like with a brush may be applicable. Application driver 34 moves applicator 32 to a position of the opening in the microchannel device to which the sealing material is to be applied and drives pump 33. Though
Controller 50 controls an operation of test apparatus 100. Controller 50 includes a processor such as a central processing unit (CPU) and a memory such as a read only memory (ROM) and a random access memory (RAM). A control program is stored in the memory. The processor controls the operation of test apparatus 100 by execution of the control program. The memory of controller 50 may include a hard disk drive (HDD).
Controller 50 controls a motor of table driver 13 to move table 16 such that the microchannel device is located at a prescribed position. Controller 50 controls a motor of pipet nozzle driver 12 to move pipet nozzle 15 in order to discharge the test solution to the opening of the microchannel in the microchannel device after the microchannel device is moved to the prescribed position. Furthermore, controller 50 controls opening and closing driver 31 to switch between opening and closing of the opening (second opening) in the microchannel device. Controller 50 controls application driver 34 to apply the sealing material to the opening or the like in the microchannel device.
Specifically, controller 50 drives the motor of pipet nozzle driver 12 to move pipet nozzle 15 to a position of prescribed test solution container 5, and controls pump 14 to suction the test solution in test solution container 5 from the tip end of pipet chip 1. Thereafter, controller 50 controls the motor of pipet nozzle driver 12 to move pipet nozzle 15 to the position of the opening in the microchannel device, and controls pump 14 to discharge the test solution from the tip end of pipet chip 1.
Controller 50 can be connected to a computing processor 200 implemented by a personal computer (PC) or a dedicated computer. A user can manage test apparatus 100 by means of computing processor 200. For example, with computing processor 200, an amount of movement of table 16 by table driver 13, an amount of movement of pipet nozzle 15 by pipet nozzle driver 12, and an amount of the test solution suctioned or discharged from the tip end of pipet chip 1 by pump 14 can be set. Computing processor 200 may electrically be connected to another apparatus arranged adjacently to test apparatus 100 to configure a test system.
[Construction of Microchannel Device]
As shown in
Opening 22 is a portion provided in aperture 21 and allows communication between aperture 21 and branch channel 23a. In other words, opening 22 is connected to one end of branch channel 23a. The test solution is injected into branch channel 23a from opening 22 by using a fluid pressure. The test solution injected into branch channel 23a is further injected into microchannel 23b. In the present embodiment, an air pressure is used as a fluid pressure. Opening 22 has a cross-section, for example, in an annular shape. Opening 22 has a diameter, for example, from 5 μm to 5 mm. In the present embodiment, four branch channels 23a are connected to opening 22. Four branch channels 23a are arranged radially around opening 22.
Though four branch channels 23a are connected to opening 22 in the present embodiment, contents of the embodiment of the present invention are not limited as such. At least one branch channel 23a should only be connected to opening 22. Two or three branch channels 23a may be connected to opening 22. Furthermore, five or more branch channels 23a may be connected to opening 22.
Branch channel 23a that extends from opening 22 is further branched into a plurality of microchannels 23b. Branch channel 23a is connected to the plurality of microchannels 23b such that the test solution can flow thereto. The test solution that flows in from opening 22 flows to the plurality of branched microchannels 23b through branch channel 23a. Branch channel 23a and microchannel 23b each have a rectangular cross-section, and branch channel 23a and microchannel 23b each have a width, for example, from 1 μm to 1 mm. Branch channel 23a and microchannel 23b, however, are different from each other in depth (height). For example, branch channel 23a has a depth of 0.5 mm, whereas microchannel 23b has a smaller depth of 0.025 mm. Therefore, microchannel 23b is higher in channel resistance than branch channel 23a. With microchannel 23b being higher in channel resistance than branch channel 23a, after branch channel 23a is once filled with the test solution that flows in from opening 22 as will be described later. the test solution can flow into the plurality of microchannels 23b substantially at the same time. In the present embodiment, one branch channel 23a is branched into fourteen microchannels 23b.
Branch channel 23a is arranged along a direction of an X axis until it is branched into the plurality of microchannels 23b, and after branching, each microchannel 23b is arranged along a direction of a Y axis. Reservoir 24 is provided at a midpoint in each branched microchannel 23b. The test solution that flows in from opening 22 flows through each microchannel 23b to reservoir 24.
An agent is arranged in reservoir 24, and reservoir 24 is connected to opening 22 through branch channel 23a and microchannel 23b. The test solution that flows in from opening 22 is stored in reservoir 24. In reservoir 24, the test solution reacts with the agent. The agent is, for example, an antimicrobial. The agent may be a solid or a liquid. The agent is placed in advance in reservoir 24. In other words, before the test solution flows into reservoir 24, the agent is placed in reservoir 24. In the present embodiment, the agent is applied to entire reservoir 24.
Reservoir 24 is formed in a shape of a parallelepiped. Reservoir 24 has a side having a length, for example, from 10 μm to 10 mm.
In
Microchannel 23b between reservoir 24 and opening 26 is formed such that the test solution can flow therethrough. Microchannel 23b is arranged along the direction of the Y axis. Microchannel 23b has one end connected to reservoir 24 and has the other end connected to opening 26. The test solution that flows in from reservoir 24 flows through microchannel 23b to opening 26.
Opening 26 is connected to the other end of microchannel 23b. Opening 26 has a cross-section, for example, in an annular shape. Opening 26 has a diameter, for example, from 5 μm to 5 mm.
Opening 26 is covered with gas permeable membrane 27. Specifically, in
Gas permeable membrane 27 performs a function to allow passage of gas and not to allow passage of liquid therethrough. Examples of a material for gas permeable membrane 27 include polytetrafluoroethylene (PTFE). Gas permeable membrane 27 is preferably water-repellent. Gas permeable membrane 27 has a thickness not larger than 1 mm.
Gas permeable membrane 27 is fixed to plate-shaped member 20 by adhesion by an adhesive or ultrasonic welding. Examples of the adhesive include a photocurable resin, a thermosetting resin, and a pressure-sensitive resin.
Collection portion 28 is a portion where some of the test solution is collected, the portion being connected to an end of branch channel 23a opposite to an end connected to opening 22. Collection portion 28 is formed in a shape of a parallelepiped. Collection portion 28 has a side having a length, for example, from 10 μm to 10 mm. Collection portion 28 may be provided with a member (water absorbing member) that absorbs moisture such as a sponge. A backflow from collection portion 28 to branch channel 23a can thus be prevented and volatilization of the test solution from branch channel 23a can be prevented.
Opening 29 is connected to an end of collection portion 28 opposite to an end connected to branch channel 23a. From opening 22 to opening 29, the test solution can flow through branch channel 23a and collection portion 28. Opening 29 is closed by silicone resin 30a of opening and closing unit 30. By closing opening 29, the test solution that flows in branch channel 23a is not discharged to collection portion 28 and opening 29, and by opening opening 29, the test solution that remains in branch channel 23a can be discharged to collection portion 28 and collected therein.
First plate-shaped member 20a and second plate-shaped member 20b are each formed of a transparent material into a shape of a rectangular plate. Examples of the material for first plate-shaped member 20a and second plate-shaped member 20b include an acrylic resin such as poylmethyl methacrylate and glass. A channel structure is formed in first plate-shaped member 20a. Specifically, in first plate-shaped member 20a, opening 22, branch channel 23a, a microchannel 23b, reservoir 24, opening 26, and collection portion 28 (see
In the present embodiment, the test solution suctioned by pipet chip 1 is discharged to aperture 21 in microchannel device 2, and an air pressure is applied to the discharged test solution to inject the test solution from opening 22 into microchannels 23b. In order to inject the test solution into microchannels 23b by application of a pressure, an injection pad (not shown) that covers aperture 21 that communicates with microchannels 23b may be provided. In an example where the injection pad is provided, however, when the injection pad is pressed against aperture 21 and an air pressure is applied to the test solution to inject the test solution into microchannels 23b, the test solution may adhere to the injection pad and the injection pad may be contaminated. Since the injection pad is repeatedly used for another microchannel device, the test solution that has previously been subjected to measurement may be introduced (contamination) in measurement of another test solution, which may affect a result of the test.
Then, in an example where an injection pad attachable to pipet chip 1 is prepared and a pressure is applied to the test solution to inject the test solution into microchannels 23b, an air pressure is delivered from pipet chip 1 while aperture 21 is covered with the injection pad. Thereafter, the injection pad may be disposed of together with pipet chip 1. Therefore, contamination with the test solution is prevented and a highly accurate test result is obtained.
As shown in
In the present embodiment, after the test solution is injected into the plurality of microchannels 23b, the test solution that remains in branch channel 23a is discharged to collection portion 28. By discharging the test solution that remains in branch channel 23a, each channel becomes independent such that the plurality of microchannels 23b and openings 26 are not connected to one another through branch channel 23a and the entirety cannot be regarded as a single channel. The flow caused by the difference in fluid head is thus prevented.
Each microchannel 23b is higher in channel resistance than branch channel 23a. Therefore, when the test solution flows into branch channel 23a, unless branch channel 23a is completely filled with the test solution, the test solution does not flow into each microchannel 23b. In order for each microchannel 23b to be higher in channel resistance than branch channel 23a, branch channel 23a should be larger in cross-sectional area than each microchannel 23b. When branch channel 23a is equal in width to each microchannel 23b, branch channel 23a is made larger in depth than each microchannel 23b. For example, by setting the depth of each microchannel 23b to 0.001 mm with the depth of branch channel 23a being set to 0.5 mm, the cross-sectional area of branch channel 23a can be five hundred times as large as that of each microchannel 23b.
When the test solution flows into branch channel 23a, opening 29 is closed by silicone resin 30a of opening and closing unit 30. Therefore, the test solution that flows into branch channel 23a is not discharged to collection portion 28 at this stage. After branch channel 23a is completely filled with the test solution, the test solution flows into microchannels 23b substantially at the same time as shown in
Thereafter, silicone resin 30a of opening and closing unit 30 that closes opening 29 is removed and air is sent from opening 22 while opening 29 is open, so that the test solution that remains in branch channel 23a is discharged to collection portion 28 as shown in
Whether or not to discharge the test solution in branch channel 23a to collection portion 28 can be controlled by opening and closing of opening 29. The test solution that remains in branch channel 23a is discharged from opening 22 to collection portion 28 by means of air.
In the present embodiment, the test solution is injected into each microchannel 23b and the test solution that remains in branch channel 23a is discharged to collection portion 28. Thereafter, a sealing material such as silicone oil is applied to opening 22, opening 26, and opening 29.
The sealing material to be applied to opening 22, opening 26, and opening 29 is not limited to silicone oil 33a, and any material is applicable so long as the material rests at opening 22, opening 26, and opening 29 and suppresses volatilization of the test solution.
An injection method in the test apparatus according to the present embodiment will now be described with reference to a flowchart.
The position of opening and closing unit 30 with respect to pipet nozzle 15 is determined in advance in accordance with the position of opening 29 with respect to opening 22 in microchannel device 2. Therefore, when pipet nozzle 15 is aligned with the position of opening 22 in microchannel device 2 in step S12, opening and closing unit 30 has moved to a position directly above opening 29. Controller 50 controls opening and closing driver 31 to move an elastic member (silicone resin 30a) to the position where it closes opening 29 (step S13). Controller 50 determines whether or not openings 29 have been closed based on whether or not the elastic members (silicone resins 30a) have been moved to positions where all openings 29 are closed (step S14). When it is determined that all openings 29 have not been closed (NO in step S14), controller 50 has the process return to step S13.
When it is determined that all openings 29 have been closed (YES in step S14), controller 50 controls pump 14 to discharge the test solution from the tip end of pipet chip 1 to inject the test solution into the channel (branch channel 23a and microchannel 23b) in microchannel device 2 (step S15).
Controller 50 determines whether or not the test solution has been injected into all channels in microchannel device 2 (step S16). Controller 50 determines whether or not the test solution has been injected into all channels in microchannel device 2, for example, based on a time period of injection of the test solution into the channels in microchannel device 2 and a remaining amount of the test solution in pipet chip 1. When the test solution has not been injected into all channels in microchannel device 2 (NO in step S16), controller 50 has the process return to step S15.
When the test solution has been injected into all channels in microchannel device 2 (YES in step S16), controller 50 controls opening and closing driver 31 to move the elastic member (silicone resin 30a) from the position where it closes opening 29 to open opening 29 (step S17). Controller 50 controls pump 14 to discharge air from the tip end of pipet chip 1 to discharge the test solution that remains in branch channel 23a to collection portion 28 (step S18).
Controller 50 controls the motor of pipet nozzle driver 12 to move applicator 32 to positions of openings 22, 26 and 29 to apply the sealing material to openings 22, 26, and 29 (step S19).
[Modification]
(1) In test apparatus 100 according to the present embodiment, opening 29 is closed by silicone resin 30a of opening and closing unit 30. Without being limited as such, any construction to switch between opening and closing of opening 29 may be applicable. For example, when an opening and closing mechanism (a shutter etc.) is provided in advance at opening 29 of microchannel device 2, opening and closing unit 30 may be constructed to switch a state of the opening and closing mechanism.
(2) In test apparatus 100 according to the present embodiment, the sealing material is described as being applied to openings 22, 26, and 29. Without being limited as such, any construction may be applicable so long as volatilization of the test solution can be suppressed. For example, volatilization of the test solution may be suppressed by attaching a prepared cover to openings 22, 26, and 29.
(3) In test apparatus 100 according to the present embodiment, for example, opening 29 has an annular cross-section and communicates with collection portion 28. Therefore, when the test solution that remains in branch channel 23a is discharged to collection portion 28 by sending air from opening 22 while opening 29 is open, depending on the pressure of sent air, the test solution is not only discharged to collection portion 28 but also may flow over opening 29. Then, opening 29 is covered with a gas permeable membrane.
By covering opening 29 with gas permeable membrane 27a, in discharging the test solution that remains in branch channel 23a to collection portion 28, a flow of the test solution over opening 29 can be prevented. In order to close opening 29, opening 29 should be closed by silicone resin 30a of opening and closing unit 30 from above gas permeable membrane 27a.
By thus further including gas permeable membrane 27a that covers opening 29 (second opening), in discharging the test solution that remains in branch channel 23a to collection portion 28, possibility that the test solution does not stay in collection portion 28 but is discharged from opening 29 can be lowered.
Though opening 29 is provided at the end of collection portion 28 opposite to the end connected to branch channel 23a in
Gas permeable membrane 27b may be made of a material the same as or different from the material for gas permeable membrane 27 that covers opening 26, and should only perform a function to allow passage of gas and not to allow passage of liquid. Examples of the material for gas permeable membrane 27b include polytetrafluoroethylene (PTFE). Gas permeable membrane 27b is preferably water-repellent. Gas permeable membrane 27b has a thickness not larger than 1 mm.
By covering aperture 28a provided in collection portion 28 with gas permeable membrane 27b, in discharging the test solution that remains in branch channel 23a to collection portion 28, a flow of the test solution over aperture 28a can be prevented. In order to close aperture 28a, entire aperture 28a should be closed by silicone resin 30a of opening and closing unit 30 from above gas permeable membrane 27b.
Thus, collection portion 2828 includes aperture 28a in at least a part thereof and further includes gas permeable membrane 27b that covers aperture 28a, so that all test solution that remains in branch channel 23a can readily be discharged and possibility that the test solution does not stay in collection portion 28 but is discharged from aperture 28a can be lowered.
[Aspects]
The embodiment described above is understood by a person skilled in the art as specific examples of aspects below.
(Clause 1)
A test apparatus according to one aspect is a test apparatus for a test using a test solution containing a sample with a microchannel device, the microchannel device includes a first opening where the test solution is received, a plurality of branch channels that communicate with the first opening, a plurality of microchannels that communicate with each of the branch channels, a collection portion where some of the test solution is collected, the collection portion being provided at an end of each of the branch channels located opposite to a side where communication with the first opening is established, and a second opening provided in the collection portion, the test apparatus includes a pressure application unit that is connected to the first opening and applies an air pressure to inject the test solution into the microchannels, an opening and closing unit that switches between opening and closing of the second opening, and a controller that controls the pressure application unit and the opening and closing unit, the controller controls the opening and closing unit to close the second opening and controls the pressure application unit to inject the test solution into the microchannels, and the controller controls the opening and closing unit to open the second opening after the test solution is injected into the microchannels and controls the pressure application unit to apply an air pressure to collect in the collection portion, the test solution in each of the branch channels.
According to the test apparatus described in Clause 1, the test solution in the branch channel can be discharged to the collection portion and collected therein. Therefore, a flow of the test solution produced in a channel can be suppressed and a correct result can be observed.
(Clause 2)
In the test apparatus described in Clause 1, the opening and closing unit includes a mechanism for closing the second opening with an elastic member.
According to the test apparatus described in Clause 2, the second opening is closed by the elastic member. Therefore, the apparatus construction can be simplified and the second opening can readily be closed.
(Clause 3)
In the test apparatus described in Clause 1, the pressure application unit includes a pipet that suctions or discharges the teat solution and a movement mechanism that changes a position of the pipet and a position of the microchannel device relative to each other, and the test solution is injected into the microchannels as the movement mechanism connects the pipet to the first opening to discharge the suctioned test solution to the first opening.
According to the test apparatus described in Clause 3, the test solution can readily be injected into each microchannel in the microchannel device.
(Clause 4)
The test apparatus described in Clause 1 further includes an applicator that applies a sealing material that suppresses volatilization of the test solution, the microchannel device further includes a third opening provided on a downstream side when viewed from the side where communication with the branch channel is established, and the applicator applies the sealing material at least to the first opening and the third opening of each of the microchannels in which the test solution has been injected.
According to the test apparatus described in Clause 4, since the sealing material is applied to the first opening and the third opening, volatilization of the test solution from the opening can be prevented.
(Clause 5)
In the test apparatus described in Clause 4, the sealing material is silicone oil.
According to the test apparatus described in Clause 5, since the sealing material is silicone oil, the sealing material is readily applied to the opening.
(Clause 6)
An injection method according to one aspect is an injection method of injecting a test solution containing a sample into a microchannel device, the microchannel device includes a first opening where the test solution is received, a plurality of branch channels that communicate with the first opening, a plurality of microchannels that communicate with each of the branch channels, a collection portion where some of the test solution is collected, the collection portion being provided at an end of each of the branch channels located opposite to a side where communication with the first opening is established, and a second opening provided in the collection portion, and the injection method includes closing the second opening, connecting a pipet that has suctioned the test solution to the first opening, injecting the test solution into the microchannels by discharging the suctioned test solution to the first opening, opening the second opening, and applying an air pressure with the pipet to collect in the collection portion, the test solution in each of the branch channels.
According to the injection method described in Clause 6, the test solution in the branch channel can be discharged to the collection portion and collected therein. Therefore, a flow of the test solution produced in a channel can be suppressed and a correct result can be observed.
(Clause 7)
In the injection method described in Clause 6, the microchannel device further includes a third opening provided on a downstream side when viewed from the side where communication with the branch channel is established, and the injection method farther includes applying a sealing material that suppresses volatilization of the test solution at least to the first opening and the third opening of each of the microchannels in which the test solution has been injected.
According to the injection method described in Clause 7, since the sealing material is applied to the first opening and the third opening, volatilization of the test solution from the opening can be prevented.
(Clause 8)
In the injection method described in Clause 7, the sealing material is silicone oil.
According to the injection method described in Clause 8, since the sealing material is silicone oil, the sealing material is readily applied to the opening.
(Clause 9)
A microchannel device according to one aspect is a microchannel device used in a test using test solution containing a sample, and the microchannel device includes a first opening where the test solution is received, a plurality of branch channels that communicate with the first opening, a plurality of microchannels that communicate with each of the branch channels, a collection portion where some of the test solution is collected, the collection portion being provided at an end of each of the branch channels located opposite to a side where communication with the first opening is established, and a second opening provided in the collection portion.
According to the microchannel device described in Clause 9, the test solution in the branch channel can be discharged to the collection portion and collected therein. Therefore, a flow of the test solution produced in a channel can be suppressed and a correct result can be observed.
(Clause 10)
In the microchannel device described in Clause 9, the collection portion is a buffer space that communicates with an end of each of the branch channels and is larger in volume than each of the branch channels.
According to the microchannel device described in Clause 10, the collection portion is a buffer space larger in volume than the branch channel, and hence the test solution that remains in the branch channel can all be collected.
(Clause 11)
In the microchannel device described in Clause 10, the buffer space is provided with a water absorbing member.
According to the microchannel device described in Clause 11, a backflow from the collection portion to the branch channel can be prevented and volatilization of the test solution from the branch channel can be prevented.
(Clause 12)
In the microchannel device described in Clause 9, the microchannels are higher in channel resistance than the branch channels.
According to the microchannel device described in Clause 12, the microchannel is higher in channel resistance than the branch channel, and hence the test solution in the branch channel can flow into the microchannels substantially at the same time.
(Clause 13)
The microchannel device described in Clause 9 further includes a gas permeable membrane that covers the second opening.
According to the microchannel device described in Clause 13, in discharging the test solution that remains in the branch channel to the collection portion, possibility that the test solution does not stay in the collection portion but is discharged from the opening can be lowered.
(Clause 14)
In the microchannel device described in Clause 9, the collection portion includes an aperture in at least a part, and the microchannel device further includes a gas permeable membrane that covers the aperture.
According to the microchannel device described in Clause 14, all test solution that remains in the branch channel can readily be discharged and possibility that the test solution does not stay in the collection portion but is discharged from the aperture can be lowered.
Though an embodiment of the present invention has been described, it should be understood that the embodiment disclosed herein is illustrative and non-restrictive in every respect. The scope of the present invention is defined by the terms of the claims and is intended to include any modifications within the scope and meaning equivalent to the terms of the claims.
Number | Date | Country | Kind |
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2020-149834 | Sep 2020 | JP | national |
2021-139555 | Aug 2021 | JP | national |
Number | Name | Date | Kind |
---|---|---|---|
20100260626 | Fajolle | Oct 2010 | A1 |
20160051985 | Knight | Feb 2016 | A1 |
20190177677 | Jonas | Jun 2019 | A1 |
20200276581 | Imamura et al. | Sep 2020 | A1 |
Number | Date | Country |
---|---|---|
103602578 | Feb 2014 | CN |
107847929 | Mar 2018 | CN |
109475866 | Mar 2019 | CN |
110785373 | Feb 2020 | CN |
2017-67620 | Apr 2017 | JP |
2018198543 | Dec 2018 | JP |
2016195480 | Dec 2016 | WO |
2018007819 | Jan 2018 | WO |
Entry |
---|
Oh et al “Design of Pressure-Driven Microfluidic Networks Using Electric Circuit Analogy” Lab on a Chip 12(3):515-45 (Year: 2011). |
English translation of Chinese document CN 103602578A (Year: 2014). |
English translation of Japanese Document JP2017067620 (Year: 2017). |
ScienceEquip—Benefits of Choosing an Electronic Pipette Controller Jan. 2020 (Year: 2020). |
Le at al “Design and Fabrication of a PDMS-Based Manual Micro-Valve System for Microfluidic Applications” Hindawi Advances in Polymer Technology vol. 2020, Article ID 2460212, 7 pages (Year: 2020). |
Yamada et al Generation of uniform-size droplets by multistep hydrodynamic droplet division in microfluidic circuits Article in Microfluidics and Nanofluidics ⋅ (Year: 2011). |
English translation of Japanese document JP 2009109459 (Year: 2009). |
JP2018198543A English translation (Year: 2018). |
Translated Examination Opening of the State Intelectual Property Office of People's Republic of China for CN 2011028364.7 published Jul. 27, 2023 (Year: 2023). |
U.S. Appl. No. 17/942,296, filed Sep. 12, 2022 in the name of Shimadzu Corporation. |
Number | Date | Country | |
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20220072546 A1 | Mar 2022 | US |