WO2017069256A1 - ナノ流体デバイス及び化学分析装置 - Google Patents
ナノ流体デバイス及び化学分析装置 Download PDFInfo
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- WO2017069256A1 WO2017069256A1 PCT/JP2016/081315 JP2016081315W WO2017069256A1 WO 2017069256 A1 WO2017069256 A1 WO 2017069256A1 JP 2016081315 W JP2016081315 W JP 2016081315W WO 2017069256 A1 WO2017069256 A1 WO 2017069256A1
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
- B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
- B01L3/502738—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by integrated valves
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
- B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
- B01L3/502715—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by interfacing components, e.g. fluidic, electrical, optical or mechanical interfaces
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B81—MICROSTRUCTURAL TECHNOLOGY
- B81B—MICROSTRUCTURAL DEVICES OR SYSTEMS, e.g. MICROMECHANICAL DEVICES
- B81B1/00—Devices without movable or flexible elements, e.g. microcapillary devices
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82B—NANOSTRUCTURES FORMED BY MANIPULATION OF INDIVIDUAL ATOMS, MOLECULES, OR LIMITED COLLECTIONS OF ATOMS OR MOLECULES AS DISCRETE UNITS; MANUFACTURE OR TREATMENT THEREOF
- B82B1/00—Nanostructures formed by manipulation of individual atoms or molecules, or limited collections of atoms or molecules as discrete units
- B82B1/001—Devices without movable or flexible elements
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B82—NANOTECHNOLOGY
- B82B—NANOSTRUCTURES FORMED BY MANIPULATION OF INDIVIDUAL ATOMS, MOLECULES, OR LIMITED COLLECTIONS OF ATOMS OR MOLECULES AS DISCRETE UNITS; MANUFACTURE OR TREATMENT THEREOF
- B82B3/00—Manufacture or treatment of nanostructures by manipulation of individual atoms or molecules, or limited collections of atoms or molecules as discrete units
- B82B3/0009—Forming specific nanostructures
- B82B3/0019—Forming specific nanostructures without movable or flexible elements
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16K—VALVES; TAPS; COCKS; ACTUATING-FLOATS; DEVICES FOR VENTING OR AERATING
- F16K99/00—Subject matter not provided for in other groups of this subclass
- F16K99/0001—Microvalves
- F16K99/0003—Constructional types of microvalves; Details of the cutting-off member
- F16K99/0015—Diaphragm or membrane valves
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/08—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor using a stream of discrete samples flowing along a tube system, e.g. flow injection analysis
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N37/00—Details not covered by any other group of this subclass
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
- B01L2200/06—Fluid handling related problems
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/08—Geometry, shape and general structure
- B01L2300/0887—Laminated structure
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/08—Geometry, shape and general structure
- B01L2300/0896—Nanoscaled
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/12—Specific details about materials
- B01L2300/123—Flexible; Elastomeric
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2400/00—Moving or stopping fluids
- B01L2400/06—Valves, specific forms thereof
- B01L2400/0633—Valves, specific forms thereof with moving parts
- B01L2400/0655—Valves, specific forms thereof with moving parts pinch valves
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
- B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
- B01L3/502707—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by the manufacture of the container or its components
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16K—VALVES; TAPS; COCKS; ACTUATING-FLOATS; DEVICES FOR VENTING OR AERATING
- F16K99/00—Subject matter not provided for in other groups of this subclass
- F16K2099/0082—Microvalves adapted for a particular use
- F16K2099/0084—Chemistry or biology, e.g. "lab-on-a-chip" technology
Definitions
- the present invention relates to a nanofluidic device and a chemical analysis apparatus.
- micro-scale micro-spaces are expected to be used in fields such as diagnosis and analysis as a means of shortening mixing and reaction times, greatly reducing the amount of samples and reagents, and making smaller devices.
- a device in which a chemical system is integrated by forming a microchannel (microchannel) composed of a groove with a depth of several hundred ⁇ m or less on a glass substrate (microchip) of several centimeters square is known. .
- valve that can control a fluid as one element device for integrating a chemical system.
- the flow direction of the fluid flowing through the microchannel can be defined, or the fluid flow itself can be controlled.
- Non-Patent Document 1 describes a device that opens and closes a micro-channel using a shape change of dimethylpolysiloxane (PDMS), which is a soft polymer substance.
- PDMS dimethylpolysiloxane
- Patent Document 1 describes a fluid control device provided with a microscale valve capable of controlling a fluid by changing the volume of a hollow portion using a glass substrate provided with a hollow portion. ing.
- the nanoscale fine space is overwhelmingly smaller than a single cell, so it is expected to be used as a single cell analysis device. For example, by analyzing proteins in a cell of several tens of ⁇ m in an extended nanospace of tens to hundreds of nanometers, which is overwhelmingly smaller than that, the average of many cells so far This makes it possible to analyze the functions unique to each cell. In addition, for example, it is expected that a cancer diagnosis or the like is performed with a single cancer cell that has occurred early.
- devices using nanoscale fine spaces are expected to become ultra-sensitive analytical tools.
- the extended nanospace it is possible to realize high sensitivity, high speed chromatography, immunoassay of single molecules or countable molecules (numerable molecules), and the like.
- Non-Patent Document 2 describes a stop valve in which a hydrophobic portion and a hydrophilic portion are provided in a nanochannel and a Laplace pressure at the interface between them is used.
- a soft PDMS or the like can hardly function as a valve that can freely open and close the channel even if a nano-sized channel can be produced.
- the nano-sized channel is narrower than the micro-sized channel. Therefore, the internal pressure applied to the flow path is high, and it is necessary to increase the pressure when opening and closing the flow path.
- soft PDMS or the like is used as a material constituting the flow path, the PDMS is deformed by being pressed by the internal pressure, and the designed nano-flow path shape cannot be maintained.
- deformation at the time of pressing is too strong, PDMS may be adsorbed, and the nanochannel cannot be maintained. That is, even if a soft member such as PDMS is used as a nanofluidic device for opening and closing the nanochannel, a sufficient effect cannot be obtained.
- a nanofluidic device using PDMS or the like as a material constituting the flow path has a problem that it cannot be used in an organic chemical process.
- the diaphragm type valve structure used in the fluid control device described in Patent Document 1 cannot be scaled down to the nanoscale.
- the diaphragm type valve of Patent Document 1 controls the flow of fluid by forming a hollow portion in glass and changing the volume of the hollow portion.
- the hole diameter of the hollow portion that can be controlled and provided in the glass is about several tens ⁇ m to several hundreds ⁇ m. That is, when trying to apply a hollow portion to a nanoscale channel, the hole diameter is too large to function properly as a valve.
- FIB focused ion beam
- the FIB process cannot form a hole that penetrates the glass. .
- the stop valve using the Laplace pressure described in Non-Patent Document 1 can control the flow of the nano-sized flow path.
- the stop valve using the Laplace pressure controls the fluid using the Laplace pressure generated by the surface tension of the liquid as a threshold value. Therefore, the flow of fluid can be controlled only once, and it is difficult to freely control the flow of fluid multiple times.
- the present invention has been made in view of the above circumstances, and an object thereof is to provide a nanofluidic device provided with a valve capable of opening and closing a nanochannel. It is another object of the present invention to provide a chemical analyzer using these nanofluidic devices.
- a nanofluidic device is provided integrally with a first substrate having a nanoscale groove on one surface, and the first substrate and one surface bonded to each other. And a second substrate that forms a nanochannel together with the groove, wherein either one of the first substrate and the second substrate overlaps the nanochannel in plan view. At least a thin part is provided in part, and the thin part is deformed by pressing to open and close the nanochannel.
- the thickness of the thin portion may be 10 mm or less.
- a width in a direction in which the nanochannel of the thin portion extends may be 2 ⁇ m to 100 ⁇ m.
- the nanochannel configured by the first substrate and the second substrate is a channel extending in one direction. And a valve operation region that is provided at a position overlapping the thin portion in plan view and wider than the nanochannel.
- the substrate that does not include the thin portion of the first substrate or the second substrate is the thin portion.
- the substrate that does not include the thin portion of the first substrate or the second substrate is the thin portion.
- a concave portion that matches the shape of the deformed thin wall portion may be provided at a position in the nanochannel opposite to.
- a pressing mechanism that performs the pressing may be provided.
- a chemical analysis apparatus includes the nanofluidic device according to any one of (1) to (7) above.
- a chemical analysis apparatus includes a nanofluidic device according to any one of (1) to (7) above, and a microscale device disposed so as to sandwich the nanofluidic device.
- the nanochannel can be freely opened and closed, and the fluid flowing through the nanochannel can be controlled.
- FIG. 2 is a diagram schematically showing a cross-section (AA plane in FIG. 1) of the nanofluidic device according to one embodiment of the present invention.
- 1 is a schematic plan view of a nanofluidic device according to one embodiment of the present invention. It is a cross-sectional schematic diagram for demonstrating the function of the nanofluidic device which concerns on 1 aspect of this invention. It is the figure which showed typically the modification of the cross section which cut
- 1 is a schematic plan view of a nanofluidic device according to one embodiment of the present invention. It is a cross-sectional schematic diagram for demonstrating the function of the nanofluidic device which concerns on 1 aspect of this invention. 1 is a schematic perspective view of a chemical analyzer according to one embodiment of the present invention. 2 is a microscopic image before and after opening and closing a nanochannel by injecting a fluorescent solution into the fluid device of Example 1, operating an actuator, and FIG.
- FIG. 1 is a schematic perspective view of a nanofluidic device according to one embodiment of the present invention.
- the nanofluidic device 10 includes a first substrate 1 having a groove 1 a and a second substrate 2 bonded to the first substrate 1.
- the nanofluid device 10 is provided with an actuator (pressing mechanism) 3 that presses a predetermined portion of the nanofluid device 10.
- the nanofluidic device 10 has a nanochannel C formed by joining the first substrate 1 and the second substrate 2.
- the nanochannel C is formed by the groove 1 a of the first substrate 1 and one surface of the second substrate 2.
- FIG. 2 is a diagram schematically showing a cross section (AA plane in FIG. 1) of the nanofluidic device according to one embodiment of the present invention.
- a thin portion 2 ⁇ / b> A is provided on the second substrate 2 on the side pressed by the actuator 3.
- the entire second substrate 2 is thinned to form a thin portion 2A.
- the thin portion 2A is a portion that is deformed by the pressing of the actuator 3, and is an operating portion of the valve.
- a protrusion 1A is provided at a position facing the thin portion 2A of the first substrate 1 where the thin portion 2A is not provided.
- the nanochannel C is closed. That is, in the nanofluidic device 10, the nanochannel C can be opened and closed by pressing the actuator 3.
- the thickness of the thin portion 2 ⁇ / b> A varies depending on the pressing pressure, the hardness of the second substrate 2, and the like. If the amount of operation necessary for the thin portion 2A and the projection 1A to be brought into close contact with each other by pressing of the actuator 3 is sufficiently small, the thickness of the thin portion 2A may be about 10 mm, but the thickness of the thin portion 2A may be 100 ⁇ m or less. Preferably, it is 10 ⁇ m or less. Moreover, it is preferable that the thickness of 2 A of thin parts is 100 nm or more. If the thin portion 2A is within this thickness range, the thin portion 2A can be deformed without being broken by pressing.
- the pressure for pressing the actuator 3 against the thin portion 2A varies depending on the Young's modulus, thickness, area of the pressed portion, and the like of the material constituting the nanofluidic device. However, it must be pressed with a pressure equal to or higher than the internal pressure in the nanochannel, and is preferably 10 6 Pa or higher, more preferably 10 7 Pa or higher, and even more preferably 10 9 Pa or higher.
- FIG. 3 is a schematic plan view of a nanofluidic device according to one embodiment of the present invention.
- the nanochannel C provided in the nanofluidic device 10 shown in FIG. 3 has a channel portion C1 and a storage portion C2.
- the channel portion C1 is a passage through which fluid flows from the supply side toward the discharge side.
- the reservoir C2 stores the fluid when the fluid is blocked by the press of the actuator 3.
- the storage part C2 is also an operation region in which the thin part 2A that is the operation part of the valve can operate. By having the storage part C2, when the fluid is dammed up, it is possible to avoid the flow path resistance from changing drastically.
- the nanochannel C has an extended nanosize at least one of depth and width.
- the extended nanosize means a size from 10 nm to 1000 nm.
- the expanded nanosize is small compared to a protein in one cell having a size of several tens of ⁇ m. Therefore, each cell can be separated and distributed.
- the space volume of the nanochannel C becomes extremely small from femtoliter to attoliter, and the amount of liquid supplied to the nanochannel C can be made extremely small.
- the depth D c of the channel portion C1 is preferably 10 nm to 1000 nm, more preferably 100 nm to 600 nm, and even more preferably 300 nm to 500 nm.
- the width W c of the flow path portion C1 is preferably 10 nm ⁇ 1000 nm, more preferably 500 nm ⁇ 1000 nm, more preferably from 700 nm ⁇ 900 nm. If the flow path part C1 is within the range, the flow path part C1 can be processed with high processing accuracy, and a large number of cells can be prevented from flowing into the flow path part C1 at one time.
- the volume of the reservoir C2 of the nanochannel C is preferably picoliter or less, and preferably satisfies the following relational expression (1).
- the volume of the reservoir C2 is extremely large relative to the volume of the fluid supplied from the expanded nano-sized nanochannel C1, the solution flowing into the reservoir C2 cannot fill the reservoir C2 and a dead space occurs. As a result, there is a case where fluid does not flow to the discharge side of the nanochannel C even though the nanochannel C is not blocked, and the fluid controllability of the nanofluidic device 10 is deteriorated.
- the nanochannel C is an expanded nanosize. That is, the volume of the fluid flowing in the flow path is from femtoliter to attoliter. If the volume of the storage part C2 is picoliter or less, a dead space will arise in the storage part C2, and it can prevent that a fluid retains in the storage part C2.
- Formula (1) has shown the conditions from which a dead space becomes difficult to produce.
- the numerator of the formula (1) indicates the volume of the reservoir C2.
- the denominator of Equation (1) shows the volume of the flow path portion C1 of the width W v min apart area of the storage portion C2 from the boundary of the reservoir C2 and the channel section C1 to the flow path portion C1 side Yes. That is, the denominator indicates the approximate volume of the liquid that will flow into the reservoir C2 when fluid flows through the nanochannel C. If the volume of the reservoir C2 is too large for this inflow amount, a dead space is likely to occur.
- the left side of the formula (1) is preferably smaller than 10, more preferably smaller than 5, more preferably smaller than 3. preferable.
- the depth Dv and the width Wv of the storage part C2 can be appropriately set so that the volume of the storage part C2 satisfies the above relationship.
- the depth of the reservoir C2 is preferably 10 nm to 1000 nm, more preferably 20 nm to 300 nm, and even more preferably 50 nm to 200 nm.
- the depth of the storage part C2 is deep, the shape displacement amount of the thin part 2A becomes large. In this case, it is necessary to increase the pressing of the thin portion 2A, and the thin portion 2A is easily broken.
- the depth of the storage part C2 is too shallow, it will be influenced by the surface roughness of glass. Depending on the surface state of the glass, the controllability of the fluid is reduced.
- the width Wv of the storage part C2 can be calculated back from the condition of the depth Dv of the storage part C2 and the volume of the storage part C2.
- the width W v of the reservoir C2 is preferably 2 [mu] m ⁇ 100 [mu] m, more preferably 10 [mu] m ⁇ 50 [mu] m, more preferably 20 ⁇ 40 [mu] m. If the width W v of the reservoir C2 a is within this range, it is possible to avoid a dead space is formed in the reservoir C2.
- variety of the storage part C2 corresponds with the width
- the volume of storing part C2 is above defined preferred range of the depth D v and the width W v of the reservoir C2.
- it can be a reservoir C2 in view of the operating area on the operating section of the valve, also determine the preferable range of the depth D v and the width W v of the reservoir (operation area) C2.
- the width W v of the reservoir (operation area) C2 is wider is preferable.
- the width W v of the reservoir (operation area) C2 is preferably preferably at 2 ⁇ m or more and 10 ⁇ m or more.
- the depth D v of the reservoir (operation area) C2 is shallow it is preferable.
- the depth D v of the reservoir (operation area) C2 is preferably preferably at 10nm or more and 1 ⁇ m or less.
- substrate 2 will not ask
- the rigidity capable of forming the nanochannel C and maintaining the shape for example, the Young's modulus is preferably 10 7 Pa or more, the Young's modulus is more preferably 10 9 Pa or more, and the Young's modulus is 10 10. More preferably, it is the above.
- glass, silicon, ceramics, acrylic, polycarbonate (PC), polyphenylene sulfide (PPS), polyether ether ketone (PEEK), polyacetal (POM), polyethylene terephthalate (PET), polybutylene terephthalate (PET) And the like can be used for the first substrate 1 and the second substrate 2.
- glass, silicon, and ceramics have a Young's modulus of 10 10 to 10 11 Pa
- acrylic and polycarbonate have a Young's modulus of 10 6 Pa
- PDMS has a soft Young's modulus of 10 6 Pa. It is conceivable that the soft material is deformed by the internal pressure of the fluid flowing in the flow path, and is not preferable.
- an inorganic material such as glass, silicon, or ceramic.
- glass, silicon, or the like are preferable to use glass, silicon, or the like. These can form the nanochannel C by low-temperature bonding described later.
- FIG. 4 is a schematic cross-sectional view for explaining the function of the nanofluidic device according to one embodiment of the present invention. As shown in the diagram on the left side of FIG. 4, when the actuator 3 is not pressed against the second substrate 2, the fluid flows through the nanochannel C because the nanochannel C is open.
- the change rate of the channel resistance before and after opening / closing of the nanochannel C is preferably 10 times or more, more preferably 30 times or more, and further preferably 50 times or more.
- a large channel resistance means that the fluid hardly flows in the nanochannel C, and conversely a small channel resistance means that the fluid easily flows in the nanochannel C.
- the large change rate of the channel resistance indicates that the fluid does not easily flow when the nanochannel C is closed, and the fluid easily flows when the nanochannel C is open. If the rate of change of the channel resistance is within the above range, the fluid can be flowed to the discharge side at the same time as the nanochannel C is opened, and the response characteristics of the nanofluidic device 10 can be enhanced.
- the nanofluidic device 10 can freely open and close the nanochannel C by pressing or stopping the pressing with the actuator 3.
- the nanochannel C in order to form the nanochannel C, a substrate having high rigidity is required from the viewpoint of processing accuracy. That is, there was no report of mechanical channel opening and closing.
- the nanochannel C itself is an extremely small channel with an expanded nanosize, and a sufficient amount of displacement can be obtained even when a highly rigid substrate is used. .
- the nanofluidic device 10 according to one embodiment of the present invention can freely open and close the nanochannel C by mechanical force.
- the first substrate 1 may not be provided with a protrusion, and the depth of the nanochannel C may be constant. Moreover, it is good also as a structure which does not provide the storage part C2 of the nanochannel C in FIG. That is, the actuator 3 may be disposed on the nanochannel C extending in one direction and pressed. According to such a configuration, it is possible to easily process the nanochannel C.
- the thin-walled portion 2A of the second substrate 2 may be provided only in a portion where the actuator 3 is pressed.
- the nanofluidic device 12 may be damaged. Can be avoided.
- the width (width in the direction in which the nanochannel extends) in which the thin portion 2A is provided in the second substrate 2 is preferably 2 to 100 ⁇ m.
- the width of the thin portion 2A is within the range, the thin portion 2A can be provided only in the portion pressed by the actuator 3, and the nanofluid device 12 can be further prevented from being damaged.
- the groove 1a is provided only in the first substrate 1, but the second substrate 2 is provided with the groove 2a corresponding to the groove 1a as in the nanofluidic device 13 shown in FIG. May be.
- the nanochannel C is formed by the groove 1 a of the first substrate 1 and the groove 2 a of the second substrate 2.
- the actuator 3 presses the first substrate 1. Also good. In this case, since the portion pressed by the actuator 3 of the first substrate 1 needs to be deformed, the thin portion 1B is formed. The portions other than the thin portion 1B of the first substrate 1 may be thinner or thicker than the thin portion 1B.
- the shape of the reservoir (operation region) C2 of the nanochannel C is not limited to a square as shown in FIG. 3, and can take any shape.
- the shape of the storage part (operation region) C2 may be circular in plan view. If the shape of the reservoir C2 is circular in plan view, the pressure of the actuator 3 is uniformly distributed in the reservoir C2.
- the width of the storage part C2 means the diameter of the storage part C2.
- the relational expression of the volume of the storage part C2 of the nanochannel C preferably satisfies the following relational expression (2).
- FIG. 10 is a schematic cross-sectional view for explaining the function of the nanofluidic device 17 according to one embodiment of the present invention.
- the connection path C3 is a groove provided in the protruding portion 1A of the first substrate 1 that connects the flow path portion C1 and the storage portion (operation region) C2.
- a chemical analysis apparatus includes the nanofluidic device described above.
- FIG. 11 is a schematic perspective view of a chemical analyzer 100 according to one aspect of the present invention.
- the chemical analysis apparatus 100 includes the above-described nanofluidic device 10 and two or more microchannel devices 20 each having a microscale microchannel disposed so as to sandwich the nanofluidic device 10.
- the nanofluidic device 10 and each of the two or more microchannel devices 20 are connected by communication between the nanochannel and the microchannel.
- the chemical analyzer 100 includes a microscale region ⁇ formed by the microchannel device 20 and a nanoscale region n including the nanofluidic device 10.
- a known configuration can be used for the configuration of the microchannel device 20.
- a temporary storage area 22 for temporarily storing a sample injected from the injection port 21 and a decomposition processing area 23 for decomposing cells carried from the temporary storage area 22 may be provided.
- the cell decomposition means by the decomposition treatment region 23 is not particularly limited. It is good also as a structure which installs a pillar etc. in a flow path and decomposes
- a microscale region ⁇ serves to connect a macroscale region where a human works and a nanoscale region n.
- a sample such as a cell separated by a human with a test tube or the like on a macro scale is injected from the injection port 21.
- the injected sample flows through the microchannel and is stored in the temporary storage area 22.
- one cell is selected from the temporary storage area 22 with optical tweezers or the like, and is carried to the decomposition processing area 23.
- the carried cells are decomposed in the decomposition region 23 and supplied in the nanoscale region n.
- the microscale region ⁇ can connect the macroscale and the nanoscale.
- the sample supplied to the nanoscale region n including the nanofluidic device 10 in the above procedure is subjected to various measurements in the nanoscale region.
- the nanoscale region n has an overwhelmingly small spatial volume compared to a protein in a cell having a size of several tens of ⁇ m, and it is possible to analyze each cell-specific function that was not understood by the average of many cells. .
- the nanochannel is a controlled space and has a very high specific surface area, it can be counted as a single molecule or countable individual molecules (e.g., highly efficient separation using chromatography or immunoassay). (Degree of molecules) can also be detected.
- a predetermined functional device 15 is installed in a predetermined portion of the nanoscale region n.
- an immunoassay or a chromatography can be installed as required.
- the fluid containing the sample supplied from the microscale region ⁇ to the nanoscale region n reaches the functional device 15 while flowing through the nanochannel.
- a plurality of nanofluidic devices 10 according to one embodiment of the present invention are installed before reaching the functional device 15.
- the nanofluidic device 10 according to one embodiment of the present invention functions as a valve. Therefore, by opening and closing the nanofluidic device 10, the flow path through which the fluid flows can be limited. Moreover, the timing which supplies the fluid to the functional device 15 can also be controlled.
- FIG. 11 only one functional device 15 is installed. However, a plurality of functional devices 15 are installed, the flow path is restricted by the nanofluidic device 10 according to the application, and various analyzes are performed with one element. It is possible to realize a chemical analysis apparatus 100 that can perform such a process.
- the sample that has been subjected to various measurements in the nanoscale region n is sent again to the microscale region ⁇ and discharged from the discharge port 24 to the macroscale.
- the chemical analysis apparatus when used, it is possible to realize an apparatus capable of performing various analyzes at once according to the application.
- the timing of supplying the sample to a predetermined functional device can be controlled, and a more precise analysis can be performed.
- the method for manufacturing a chemical analyzer includes a step of forming a groove on one surface of the first substrate and / or the second substrate, and a step of imparting a predetermined function to a part of the formed groove.
- a step of thinning a predetermined position of the second substrate 2 a step of adjusting the hydrophilicity by subjecting the bonding surface of the first substrate and / or the second substrate to be bonded to fluorine, and the first substrate; Bonding a second substrate to form a nanochannel.
- the first substrate 1 and the second substrate 2 are prepared.
- a groove 1 a is formed in the prepared first substrate 1.
- the manufacturing method of the groove 1a is not particularly limited, but the groove 1a is formed on the surface of the substrate while appropriately adjusting the size thereof using an appropriate means such as laser processing or etching processing.
- grooves are also formed in a portion that becomes the functional device 15 and other nanochannels. For example, when a Mach-Zehnder element or the like is used as the functional device, a groove branched into two is formed.
- a predetermined function is imparted to a part of the formed groove.
- a chemical analyzer is used as an immunoassay
- an antibody is installed in a portion that becomes the functional device 15.
- necessary things are installed in the groove according to the function to be provided.
- the second substrate 2 is thinned.
- FIG. 1 when the 2nd board
- FIG. 6 when only a predetermined position is thinned, it can be thinned by laser processing, etching processing, or the like in the same manner as the method of forming the groove 1a.
- the bonding surface of at least one of the substrates is treated with fluorine to adjust the hydrophilicity.
- the bonding surface of the substrate is treated with fluorine.
- the fluorination treatment can be realized by supplying fluorine (for example, tetrafluoromethane: CF 4 ) simultaneously with the oxygen plasma irradiation.
- oxygen plasma conditions at this time for example, oxygen pressure of 60 Pa, 250 W, irradiation for 40 seconds, or the like can be used.
- the degree of hydrophilization can be regarded as sufficiently hydrophilized if the contact angle of water on the surface subjected to fluorination treatment is 10 ° to 50 °. If it has the contact angle of the said range, the joining strength after joining can be 0.5 J / m ⁇ 2 > or more, and sufficient joining strength can be obtained.
- first substrate 1 and the second substrate 2 are bonded so that the fluorine-treated surface becomes the bonding surface.
- the first substrate 1 and the second substrate 2 can be bonded at a low temperature, and damage from heat can be avoided.
- the heating temperature at the time of joining is preferably 25 ° C. to 400 ° C., and more preferably at or near room temperature (25 ° C. to 100 ° C.). If it is in the said temperature range, the damage which damages the antibody etc. which were installed for the functional device 15 can be made small, for example. In substrate bonding by a method such as the thermal fusion method, the temperature becomes 1000 ° C. or higher, and therefore, when the surface modification is performed inside the device, damage to the surface-modified antibody or the like increases.
- the pressurizing pressure at the time of joining is preferably 1000 N to 5000 N, and more preferably 4000 N to 5000 N. If it is less than 1000 N, sufficient bonding strength cannot be maintained. If sufficient bonding strength cannot be obtained, a part of the sample passing through the bonding surface may leak. On the other hand, if it exceeds 5000 N, the substrate may be damaged.
- the pressurization time is preferably 1 hour to 10 hours, more preferably 9 hours to 10 hours. If it is the said range, joining strength can be made high.
- a chemical analysis apparatus including a nanofluidic device and a nanofluidic device or a functional device can be easily obtained. At this time, it is possible to avoid damaging an antibody or the like that exhibits a predetermined function.
- Example 1 A nanofluidic device having the same configuration as that shown in FIG. 1 was produced.
- the configuration of the nanochannel was as follows.
- Channel part depth 400nm, width 900nm
- Reservoir depth 100nm, side width 30 ⁇ m, volume 90fL Length from one end of the circulation part to one end on the storage part side: 400 ⁇ m Dead volume indicated on the left side of Formula (1): 8.3 times
- Flow path resistance change 80 times
- Actuator tip width 10 ⁇ m
- Material of first substrate and second substrate Glass Thickness of second substrate (including thin portion): 10 ⁇ m
- a micro-scale microchannel was formed at both ends of the supply port and the discharge port of the nanofluidic device described above, and the fluorescent solution was supplied at a pressure of 20 kPa by a pressure controller.
- FIG. 12 is a microscopic image before and after opening and closing the nanochannel by injecting the fluorescent solution into the fluid device of Example 1, operating the actuator.
- 12A is a microscopic image in a state where the actuator is not pressed
- FIG. 12B is a microscopic image in a state where the actuator is pressed. The actuator was pressed on the assumption that 680 MPa was applied to the glass surface at the time of 100 nm indentation.
- FIG. 12A shows that the entire flow path of the nanofluidic device is shining, whereas in FIG. 12B, the right side is not shining. That is, it can be seen that the flow of the fluorescent solution can be controlled by changing the pressure of the actuator. That is, it can be seen that the nanofluidic device functions as a valve that controls the flow of fluid flowing through the nanochannel.
- the displacement of the thin glass layer was measured using a thin glass layer having a thickness of 10 ⁇ m manufactured by Nippon Electric Glass. As a measuring method, a thin glass layer was placed on a glass having a hole having a diameter of 30 ⁇ m. And the thin glass installed in the upper part of a hole was pressed using the actuator with a 10-micrometer tip diameter, and the displacement of the thin glass with respect to a press was measured.
- the displacement of the thin glass increased in proportion to the pressure, and the thin glass broke when it was displaced to 2.5 ⁇ m. That is, it can be seen that the use of 10 ⁇ m thin glass can open and close the nanochannels of the extended nanospace without breaking.
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Abstract
Description
このように、拡張ナノ空間を利用することで、高感度、高速のクロマトグラフィ、単一分子や可算個分子(数えられる程度の分子)のイムノアッセイ等が実現可能となる。
(1)本発明の一態様に係るナノ流体デバイスは、一面にナノスケールの溝を有する第1基板と、該第1基板と互いの一面同士を接合して一体に設けられ、前記第1基板の溝とともにナノ流路を形成する第2基板とを備えたナノ流体デバイスであって、前記第1基板または前記第2基板のいずれか一方は、平面視して前記ナノ流路と重なる位置の一部に少なくとも薄肉部を備え、前記薄肉部が押圧によって変形して前記ナノ流路を開閉する。
図1は、本発明の一態様にかかるナノ流体デバイスの斜視模式図である。ナノ流体デバイス10は、溝1aを有する第1基板1と、第1基板1と接合する第2基板2とからなる。ナノ流体デバイス10の使用態様時においては、ナノ流体デバイス10には、ナノ流体デバイス10の所定の箇所を押圧するアクチュエーター(押圧機構)3が設けられる。
薄肉部2Aがこの厚みの範囲内であれば、薄肉部2Aが押圧により破断することなく、変形することができる。
貯留部C2の深さが深いと、薄肉部2Aの形状変位量が大きくなる。この場合、薄肉部2Aの押圧を高くする必要があり、薄肉部2Aが破断しやすくなる。一方で、貯留部C2の深さが浅すぎると、ガラスの表面粗さの影響を受けてしまう。ガラスの表面状態によっては、流体の制御性が低下してしまう。
本発明の一態様に係る化学分析装置は、上述のナノ流体デバイスを備える。図11は、本発明の一態様に係る化学分析装置100の斜視模式図である。化学分析装置100は、上述のナノ流体デバイス10と、該ナノ流体デバイス10を挟むように配置されたマイクロスケールのマイクロ流路を有する2つ以上のマイクロ流路デバイス20とを備える。ナノ流体デバイス10と2つ以上のマイクロ流路デバイス20のそれぞれとは、ナノ流路とマイクロ流路との連通によって連結されている。
本発明の一態様に係る化学分析装置の製造方法は、第1基板及び/又は第2基板の一面に溝を形成する工程と、形成した溝内の一部に所定の機能を付与する工程と、第2基板2の所定の位置を薄肉化する工程と、接合される第1の基板及び/又は第2の基板の接合面をフッ素処理して親水性を調整する工程と、第1基板と第2基板を接合し、ナノ流路を形成する工程とを有する。以下、図1~図11を利用して、化学分析装置及びナノ流体デバイスの製造方法について具体的に説明する。
親水性を調整する工程として、基板の接合面をフッ素処理する。フッ素化処理は、種々の方法を用いることができ、例えば、酸素プラズマの照射と同時にフッ素(例えば、四フッ化メタン:CF4)を供給することで行うことで実現することができる。このときの酸素プラズマ条件としては、例えば酸素圧力60Pa、250W、40秒照射等を用いることができる。また親水化の程度としては、フッ素化処理を行った表面における水の接触角が10°~50°になっていれば、十分親水化されているとみなすことができる。当該範囲の接触角を有していれば、接合後の接合強度を0.5J/m2以上とすることができ、十分な接合強度を得ることができる。
図1に示す構成と同一の構成のナノ流体デバイスを作製した。ナノ流路の構成は以下のようにした。
流路部:深さ400nm、幅900nm
貯留部:深さ100nm、一辺の幅30μm、体積90fL
流通部の一端から貯留部側の一端までの長さ:400μm
式(1)の左辺で表記されるデッドボリューム:8.3倍
流路抵抗変化:80倍
アクチュエーターの先端幅:10μm
第1基板及び第2基板の材質:ガラス
第2基板の厚み(薄肉部を含む):10μm
日本電気硝子社製の厚み10μmの薄層ガラスを用いて、薄層ガラスの変位を測定した。測定方法は、直径30μmの穴を有するガラス上に薄層ガラスを設置した。そして、穴の上部に設置された薄層ガラスを、先端径10μmのアクチュエーターを用いて押し付け、押圧に対する薄層ガラスの変位を測定した。
Claims (9)
- 一面にナノスケールの溝を有する第1基板と、該第1基板と互いの一面同士を接合して一体に設けられ、前記第1基板の溝とともにナノ流路を形成する第2基板とを備えたナノ流体デバイスであって、
前記第1基板または前記第2基板のいずれか一方は、平面視して前記ナノ流路と重なる位置の一部に少なくとも薄肉部を備え、
前記薄肉部が押圧によって変形して前記ナノ流路を開閉するナノ流体デバイス。 - 前記薄肉部の厚みが10mm以下である請求項1に記載のナノ流体デバイス。
- 前記薄肉部のナノ流路が延在する方向の幅が2~100μmである請求項1または2のいずれかに記載のナノ流体デバイス。
- 前記第1基板及び前記第2基板により構成される前記ナノ流路は、一方向に延在する流路部と、平面視で前記薄肉部と重なる位置に設けられ、前記ナノ流路より幅が広い動作領域と、を備える請求項1~3のいずれか一項に記載のナノ流体デバイス。
- 前記第1基板または前記第2基板のうち、前記薄肉部を備えない方の基板が、前記薄肉部に相対する前記ナノ流路内の位置に、変形した薄肉部が当たる突起部を有する請求項1~4のいずれか一項に記載のナノ流体デバイス。
- 前記第1基板または前記第2基板のうち、前記薄肉部を備えない方の基板が、前記薄肉部に相対する前記ナノ流路内の位置に、変形した薄肉部の形状に合わせた凹部を有する請求項1~5のいずれか一項に記載のナノ流体デバイス。
- 前記押圧を行う押圧機構を備えた請求項1~6のいずれか一項に記載のナノ流体デバイス。
- 請求項1~7のいずれか一項に記載のナノ流体デバイスを備えた化学分析装置。
- 請求項1~7のいずれか一項に記載のナノ流体デバイスと、該ナノ流体デバイスを挟むように配置されたマイクロスケールのマイクロ流路を有する2つ以上のマイクロ流路デバイスとを備え、
前記ナノ流体デバイスと前記2つ以上のマイクロ流路デバイスのそれぞれとは、前記ナノ流路と前記マイクロ流路との連通によって連結され、
前記ナノ流体デバイスで化学分析を行うことができる化学分析装置。
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US11565253B2 (en) | 2023-01-31 |
EP3367105A1 (en) | 2018-08-29 |
EP3367105A4 (en) | 2019-05-15 |
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