WO2005036182A1 - キャピラリチップにおける流体の流通方法 - Google Patents
キャピラリチップにおける流体の流通方法 Download PDFInfo
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- WO2005036182A1 WO2005036182A1 PCT/JP2004/015453 JP2004015453W WO2005036182A1 WO 2005036182 A1 WO2005036182 A1 WO 2005036182A1 JP 2004015453 W JP2004015453 W JP 2004015453W WO 2005036182 A1 WO2005036182 A1 WO 2005036182A1
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- Prior art keywords
- opening
- polymer composition
- capillary
- closing
- flow
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Classifications
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/416—Systems
- G01N27/447—Systems using electrophoresis
- G01N27/44756—Apparatus specially adapted therefor
- G01N27/44791—Microapparatus
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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
- B01L3/50273—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 means or forces applied to move the fluids
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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
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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
- F16K99/0017—Capillary or surface tension valves, e.g. using electro-wetting or electro-capillarity effects
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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
- F16K99/0034—Operating means specially adapted for microvalves
- F16K99/0036—Operating means specially adapted for microvalves operated by temperature variations
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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
- B01L2300/0809—Geometry, shape and general structure rectangular shaped
- B01L2300/0816—Cards, e.g. flat sample carriers usually with flow in two horizontal directions
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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
- B01L2300/0861—Configuration of multiple channels and/or chambers in a single devices
- B01L2300/0864—Configuration of multiple channels and/or chambers in a single devices comprising only one inlet and multiple receiving wells, e.g. for separation, splitting
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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
- B01L2400/0661—Valves, specific forms thereof with moving parts shape memory polymer 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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- 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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- 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
- F16K2099/0073—Fabrication methods specifically adapted for microvalves
- F16K2099/0074—Fabrication methods specifically adapted for microvalves using photolithography, e.g. etching
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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
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T137/00—Fluid handling
- Y10T137/0318—Processes
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T137/00—Fluid handling
- Y10T137/206—Flow affected by fluid contact, energy field or coanda effect [e.g., pure fluid device or system]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T137/00—Fluid handling
- Y10T137/206—Flow affected by fluid contact, energy field or coanda effect [e.g., pure fluid device or system]
- Y10T137/218—Means to regulate or vary operation of device
- Y10T137/2191—By non-fluid energy field affecting input [e.g., transducer]
- Y10T137/2196—Acoustical or thermal energy
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T137/00—Fluid handling
- Y10T137/206—Flow affected by fluid contact, energy field or coanda effect [e.g., pure fluid device or system]
- Y10T137/2224—Structure of body of device
Definitions
- the present invention relates to a capillary chip, particularly a capillary chip having a useful capillary for easily analyzing a small amount of sample.
- Micro TAS Micro Total Analysis Systems
- Micro TAS is a system in which cavities, reaction spaces, and detection spaces, which serve as flow paths for liquids, which are samples and reagents, are usually formed on a single cavity chip of about 1 to 2 cm square. This system is expected to be able to save samples, speed up analysis, automate measurement including preprocessing, make equipment portable, disposable equipment, and reduce equipment costs. ing.
- micro TAS which can be used easily even on the patient's bedside, etc., and which can dispose of the cabillary chip touched by the sample are extremely Useful.
- a micro-flow valve such as a microphone port valve that controls the opening and closing of the flow path in the capillary chip and a liquid feed drive element that flows the fluid in the flow path will be required.
- control elements is essential.
- a valve that blocks a flow path with wax is known (for example, see Japanese Patent Application Laid-Open No. 2000-51428).
- a valve using wax has problems such as that it can be used only for a flow path having a certain thickness, that a component in a liquid is adsorbed on the wax, and that it is difficult to control opening and closing quickly.
- a valve using a coupler As another microvalve, a valve using a coupler is known (see, for example, Japanese Patent Application Laid-Open No. 2001-16939). Such a valve stops the flow of liquid that flows into or out of the reservoir by contacting the power coupler with the part of the reservoir that supplies liquid to the flow path that communicates with the atmosphere. Having. Fluid flow can be restored by removing the coupler from close contact ; however, this valve requires that the coupler be in close contact with the reservoir in a gas-tight manner, and its fabrication and operation Is complicated. Furthermore, there is a problem that the open / close portion of the flow channel cannot be arbitrarily selected.
- Tashiro et al, '"A Particles and Biomolecules sorting micro flow system using thermal gelation of methyl cellulose solution contain a solution that gels by laser irradiation.
- a method of closing the flow channel by preparing and gelling the solution in the flow channel is disclosed. However, in this method, a solution that meets specific conditions must be prepared. Also, This method can be used to close the flow path, but it is difficult to use it multiple times as an on-off valve because the open state becomes liquid.
- Japanese Patent Application Publication No. 2003-50370316 discloses that a plug made of a polymer material is provided in a flow path, and the flow path is opened and closed by utilizing a change in volume of the polymer material. A method for doing so is disclosed. However, in this method, it is necessary to provide the plug at an arbitrary position, and there is a problem that opening and closing cannot be performed unless the plug is provided.
- An object of the present invention is to provide a distribution method for distributing a fluid in a capillary by a simple method without changing the composition of a sample or a reagent in a capillary chip, and a distribution control device capable of performing the distribution method.
- the present invention provides a method for manufacturing a chip, comprising: a layer made of a polymer composition; and a capillary chip having a capillary formed on the surface or inside of the layer made of the polymer composition.
- a flow method for flowing a fluid in the container wherein the cabillary includes a flow control unit, the flow control unit includes a plurality of continuous opening / closing units, and the opening / closing unit has a volume of the polymer composition.
- the flow control unit changes the temperature of the polymer composition so that the plurality of opening / closing units are sequentially opened from the open state in the flow direction.
- the fluid in the cavities can be passed by the simple step (a) of merely changing the temperature of the polymer composition.
- step (a) may be repeated a plurality of times.
- the distribution control Is repeatedly extruded.
- the following steps namely, in the flow control section, while keeping one or a plurality of opening / closing sections closed from the downstream end in the flow direction, the temperature of the polymer composition is reduced.
- the next step (a) is started substantially simultaneously with step (c).
- the flow control unit can function as a pump.
- the following steps may be further included: a step of changing the temperature of the polymer composition in the opening / closing section to close the opening / closing section to thereby prevent the flow of the fluid flowing through the capillary.
- the opening / closing section may include a step (e) of changing the temperature of the polymer composition to open the opening / closing section to allow the flow of the fluid flowing through the cabilli.
- the flow of the fluid on the capillary chip can be more complicatedly controlled by combining the circulation in step (a) and the opening and closing in steps (d) and (e).
- the polymer composition for example, a polymer composition whose volume increases with increasing temperature and decreases with decreasing temperature can be used.
- a polymer composition can be used in which the volume decreases with increasing temperature and increases with decreasing temperature. Furthermore, the combination of the two enables simultaneous control of the open state and the closed state in a complicated flow path.
- the polymer composition examples include a side-chain crystalline repeating unit derived from acrylate or methacrylate ester, and a side-chain amorphous repeating unit derived from acrylate or methyl acrylate ester. And a polymer composition containing the same.
- the capillary chip there is a configuration in which the capillary is formed on the surface of the layer, and a lid plate is in close contact with the surface of the layer.
- the capillary tip may further include a fluid inlet and a fluid outlet connected to the capillary.
- Step (a) is preferably a step of heating the opening / closing section of the flow control section sequentially in the flow direction, for example, by irradiating a laser.
- the heating can be performed, for example, by irradiating a laser.
- the opening / closing section may be switched from a closed state to an open state by air-cooling the opening / closing section.
- the polymer composition that changes in volume due to the transition is used. More preferably, the first melt transition of the polymer composition occurs at 80 ° C. or less.
- Cross-sectional area of the Kiyabirari may be, for example, 1 0 0 0 0 xm 2 or more and 2 5 0 0 0 0 m 2 or less.
- the capillary chip may further include a plurality of fluid inlets connected to the capillary, and the capillary may include a plurality of opening / closing portions corresponding to each fluid inlet. .
- the present invention is a distribution control device including a cabillary chip mounting section, a laser irradiating section, and a laser control section, wherein the cabillary chip mounting section can mount a cabillary chip,
- the capillary chip has a layer made of a polymer composition, and a capillary formed on the surface or inside of the layer made of the polymer composition, wherein the capillary has a flow control section, and the flow control section has a plurality of flow control sections.
- the opening / closing section is closed when the volume of the polymer composition increases, and blocks the flow of the fluid flowing through the capillary, and the volume of the polymer composition decreases.
- the laser irradiating section allows the fluid to flow, and the laser irradiating section can irradiate the laser to the capillary chip mounted on the capillary mounting section, and the laser control section can control the laser chip to be mounted on the capillary mounting section by the laser irradiation section.
- the position of the laser irradiation on the opening / closing section can be controlled, and by sequentially irradiating the opening / closing section with the laser in the flow direction, the opening / closing section is sequentially switched from the open state to the closed state in the flow direction, and the fluid flows through the inside of the capillary. It is a distribution control device.
- FIG. 1 is a (a) perspective view, (b) a cross-sectional view showing an Ib-Ib cross-section, and (c) a cross-sectional view showing an Ic-Ic cross-section, schematically showing the appearance of a capillary chip used in the first embodiment. .
- FIG. 2 is a cross-sectional view schematically illustrating a method of controlling the opening and closing of the opening and closing unit.
- FIG. 3 is a cross-sectional view schematically illustrating a flow control method of the flow control unit.
- FIG. 4 is a diagram showing a first method for producing a capillary chip.
- FIG. 5 is a diagram showing a second method for producing a capillary chip.
- FIG. 6 is a diagram showing a third method for producing a capillary chip.
- FIG. 7 is a perspective view schematically showing the appearance of the capillary chip used in the second embodiment.
- FIGS. 8A and 8B are (a) a perspective view, (b) a cross-sectional view showing a Vllb-VIIb cross section, and (c) a cross-sectional view showing a Vnc-VIIc cross section, schematically showing the appearance of a capillary chip used in the third embodiment. .
- FIG. 9 is a block diagram illustrating a configuration of the distribution control device according to the first embodiment.
- FIG. 10 is a block diagram showing a configuration of a distribution control device having a form different from that of FIG. [Best mode for carrying out the invention]
- FIG. 1A is a perspective view schematically illustrating the appearance of the capillary chip 1 used in the present embodiment.
- FIG. 1 (b) is a cross-sectional view showing the Ib-Ib cross section of FIG. 1 (a)
- FIG. 1 (c) is a cross-sectional view showing the Ic-Ic cross section of FIG. 1 (b).
- the capillary chip 1 is composed of a main channel 31, branch channels 32, 33, a sample inlet 21, a reagent inlet 22, 23, and an outlet. It has a substrate 11 having a rectangular planar shape on which an outlet 24 is formed.
- Each of the flow paths 31, 32, and 33 is composed of a capillary.
- the branch channel 32 merges at the junction P 1
- the branch channel 33 merges at the junction P 2.
- the substrate 11 is preferably placed horizontally with respect to the ground. ′
- the sample inlet 21 is constituted by a hole having a circular cross section, and extends from the surface of the substrate 11 to the upstream end of the main channel 31.
- the reagent inlet 22 is formed by a hole having a circular cross section, and extends from the surface of the substrate 11 to the upstream end of the branch channel 32.
- the reagent inlet 23 is formed by a hole having a circular cross section, and extends from the surface of the substrate 11 to the upstream end of the branch channel 33.
- the discharge port 24 is constituted by a hole having a circular cross section, and extends from the surface of the substrate 11 to the downstream end of the main channel 31.
- the sample inlet 21, the reagent inlets 22, 23, and the outlet 24 make each of the channels 31, 32, 33 an open system, allowing the flow of fluid.
- the main flow path 31 is provided with an opening / closing section VI for controlling opening and closing of the main flow path 31 downstream of the junction P2.
- the main flow path 31 has a function of moving the fluid by pushing out the fluid in the flow path to the vicinity of the upstream end, and a function of starting the flow of the fluid by applying a downstream force to the fluid in the flow path.
- a distribution control unit C1 having the following.
- the cross-sectional shape of the flow channels 3 1, 3 2, 3 3 is a polygon such as a square or a triangle.
- the shape, circle, semicircle, semi-ellipse and the like can be used, and there is no particular limitation.
- the fluid circulated in the capillary chip 1 is a liquid.
- Cross-sectional area of the flow path 3 1, 3 2, 3 3 depending on the atmospheric of the particles of the viscosity of the liquid to be circulated and the liquid, there is and in 1 0 0 0 0 0 0 m 2 or less 1 m 2 or more it is preferable, 1 0 0 0 0 xm 2 or more and 2 5 0 0 0 0 m and more preferably 2 or less.
- the size of the substrate 11 is determined by the flow path pattern to be formed.For example, the thickness is 5 mm or more and 50 mm or less, the long side is 5 mm or more and 50 mm or less, and the short side is 3 mm or more. And less than 50 mm.
- the size of the sample inlet 21 and the reagent inlets 22 and 23 is not particularly limited as long as the sample or the reagent can be injected by an injection means such as a pipette or a syringe. Depending on the size, the sample inlet 21 and the reagent inlets 22 and 23 function as sample or reagent reservoirs. When the size of the sample inlet 21 and the reagent inlets 22 and 23 is not sufficient for the liquid reservoir, a liquid reservoir may be formed by connecting, for example, a cylindrical member thereto.
- the cross-sectional shape of the sample inlet 21 and the reagent inlets 22 and 23 is not limited to a circle, but may be a polygon or the like.
- the opening / closing portion V1 is constituted by a peripheral portion 11a of the main channel 31 (hereinafter, referred to as a channel peripheral portion 11a).
- the flow channel peripheral portion 11a is configured by a portion surrounding the main flow channel 31 of the substrate 11 with a predetermined length over the entire circumference.
- the peripheral portion 11a of the flow path is made of a polymer composition.
- the peripheral part 11 a of the flow path constituting the opening / closing part V 1 is a part surrounding the entire circumference of the main flow path 31, but the peripheral part 11 a of the flow path is the entirety of the main flow path 31. JP2004 / 015453
- the opening / closing part VI takes an open state or a closed state according to the volume of the polymer composition.
- the opening / closing section VI changes from an open state to a closed state due to an increase in volume due to a change in temperature of the polymer composition. Further, the opening / closing section VI changes from a closed state to an open state due to a decrease in volume due to a change in temperature of the polymer composition.
- the opening / closing section VI allows the flow of liquid in the open state and blocks the flow of liquid in the closed state.
- the increase in volume and decrease in volume of the polymer composition are irreversible changes. When the volume change of the polymer composition is a reversible change, opening and closing can be controlled not limited to the number of times.
- the polymer composition it is possible to use either a polymer composition that increases in volume due to a rise in temperature and decreases in volume due to a decrease in temperature, or a polymer composition that increases in volume due to a decrease in temperature and decreases in volume due to a rise in temperature. it can.
- a polymer composition such as the former is available as a cool-off type Intellima® from Niyu Corporation.
- a polymer composition such as the latter is available as a warm-off type Intelimer (registered trademark) from Nitta Corporation. Both are plate-shaped polymer compositions.
- a polymer composition that undergoes a first-order melting transition in a specific temperature range is preferably used.
- the change in volume due to the first melting transition is used for opening and closing control.
- the volume change due to the first melting transfer is preferable because the volume change with respect to the temperature change is large and the binary control of opening and closing of the opening and closing section VI is easy.
- a temperature region where the polymer composition undergoes the first melting transition is referred to as a melting temperature region.
- the temperature must be changed from a temperature lower than the melting temperature range to a temperature higher than the melting temperature range, or from a temperature higher than the melting temperature range to a temperature lower than the melting temperature range. Controls the opening and closing of the opening and closing unit V1.
- the narrower the melting temperature range of the polymer composition the better. This is because the temperature change required to control the opening and closing is small, and quick control of the opening and closing is possible.
- the difference between the highest and lowest temperature in the melting temperature range is 15 ° C
- the following polymer composition is used.
- a polymer composition that undergoes a first-order melt transition in a temperature range where the fluid is not denatured is preferable.
- a polymer composition in which the temperature within the melting temperature range is higher than the freezing point of the fluid and lower than the boiling point is used. This is because the temperature of the fluid near the switching unit V1 is affected by the temperature of the switching unit VI.
- the preferred melting temperature range varies depending on the type of fluid to be circulated. For example, a polymer composition having a temperature in the melting temperature range of 30 to 80 ° C. can be used.
- Japanese Patent Application Laid-Open No. 2002-32224 U.S. Patent No. 5,156,911, U.S. Patent No. 5,387,450
- the temperature-sensitive polymer composition described in Japanese Patent Application Laid-Open Publication No. H10-260 can be used.
- a temperature-sensitive polymer composition comprising a side-chain crystalline repeating unit derived from an acrylate or methacrylate ester and a side-chain amorphous repeating unit derived from an acrylate or methacrylate ester Things can be used.
- a temperature-sensitive polymer composition containing hexadecyl acrylate as a side-chain crystalline repeating unit and hexyl acrylate as a side-chain non-crystalline repeating unit is used.
- the polymer composition increases in volume when changed from a temperature lower than the melting temperature region to a temperature higher than the melting temperature region, and decreases in volume when changed from a temperature higher than the melting temperature region to a temperature lower than the melting temperature region.
- a polymer composition having a temperature in the melting temperature range higher than room temperature (25 ° C.) is used.
- the opening / closing portion VI is open at room temperature, is closed by heating, and is left open, that is, opened by air cooling. Normally, switching from the open state to the closed state is required to be quicker than switching from the closed state to the open state. For example, laser heating can quickly achieve local temperature changes and is suitable for controlling from an open state to a closed state.
- a laser When a laser is used as the heating means, it has the necessary heating capacity If this is the case, there is no need to select a type such as a gas laser, solid laser, or semiconductor laser.
- the laser is not limited as long as it emits light having a wavelength suitable for heating the peripheral portion 11a of the flow channel made of the polymer composition to be heated.
- a laser that emits light having a wavelength of 1450 nm to 1490 nm by an IR laser can be used.
- the heating temperature is controlled by the power of the laser and the irradiation time.
- An opening / closing control method of the opening / closing section V1 will be described.
- the opening / closing unit V1 that is open at a temperature lower than T a and closed at a temperature higher than T b will be described.
- a laser is used as a heating unit and air cooling is used as a cooling unit.
- FIG. 2 is a cross-sectional view schematically showing the open state (a) and the closed state (b) of the opening / closing section VI in the same cross section as FIG. 1 (c).
- the opening / closing part VI is open as shown in FIG. 2 (a).
- a beam-shaped laser beam hereinafter, also referred to as “laser beam” L is applied to the opening / closing portion VI.
- the switching unit VI is locally heated, and its temperature rises from room temperature to a temperature higher than Tb.
- the volume of the polymer composition in the peripheral portion 11 a of the flow channel increases, but the volume of the portion other than the peripheral portion 11 a of the substrate 11 does not change.
- the channel expands in a direction to narrow the flow path, whereby the opening / closing portion V1 changes from the open state shown in FIG. 2A to the closed state shown in FIG. 2B.
- the closed state is maintained.
- the switching unit VI is stopped and left, the switching unit V1 is cooled from the temperature higher than Tb to room temperature, which is lower than Ta, and the volume decreases, as shown in Fig. 2 (b). From the closed state, it changes to the open state shown in Fig. 2 (a).
- the volume of the polymer composition in the peripheral portion 11 a of the flow channel increases, but the volume of the portion other than the peripheral portion 11 a of the substrate 11 does not change. Then, the flow path expands in a direction to narrow the flow path, whereby the opening / closing portion V1 changes from the open state shown in FIG. 2A to the closed state shown in FIG. 2B. If the cooling of the switching unit VI is continued and the switching unit V1 is maintained at a temperature lower than Td, the closed state is maintained. On the other hand, when the cooling of the switching unit V1 is stopped and left, the switching unit VI is heated from a temperature lower than Td to room temperature, which is higher than Tc, and its volume decreases. From this state, it will be in the open state as shown in Fig. 2 (a).
- FIGS. 3 (&) to 3 () are partial cross sections schematically showing the control procedure of the flow control section C1 in the same cross section as FIG. 1 (j).
- the flow control unit C1 includes a peripheral portion 1 lb of the main flow channel 31 (hereinafter, referred to as a flow channel peripheral portion 11b).
- the flow path peripheral portion 11b is configured by a portion surrounding the main flow path 31 of the substrate 11 with a predetermined length over the entire circumference.
- the flow path peripheral portion ib is made of a polymer composition, and has a configuration in which a plurality of flow control opening / closing portions V2 capable of performing the same control as the opening / closing control in the opening / closing portion V1 are adjacent to each other.
- the channel peripheral portion 1 1b is a portion surrounding the entire circumference of the main channel 31, but the channel peripheral portion 1 1b is a portion surrounding a part of the entire circumference of the main channel 31. It doesn't matter.
- Preferred materials for the polymer composition forming the flow control section C 1 are the same as those described in the description of the opening / closing section V 1.
- each flow control opening / closing section V 2 of the flow control section C 1 in a state of being filled with liquid is connected to the upstream side in the flow direction (the sample injection port 21 side).
- discharge port 24 To the downstream side in the distribution direction (discharge port 24 (see Fig. 1) side) to irradiate the laser beam L sequentially and heat it to the closed state.
- the liquid can be pushed out from the upstream side to the downstream side, and the liquid can be circulated in the flow path 31.
- each flow control opening / closing unit V2 is assumed to be open at a temperature lower than Ta and closed at a temperature higher than Tb.
- Ta is larger than Tb, and Ta> room temperature (25 ° C.).
- a laser is used as a heating unit and air cooling is used as a cooling unit.
- each of the flow control opening / closing portions V2 in the flow control portion C1 may be independently controlled to open and close to function as an opening / closing portion for switching between blocking and permitting fluid flow.
- the capillary chip 1 can be used, for example, as follows.
- the sample is injected into the sample inlet 21, and the first reagent is injected into the reagent inlet 22.
- the reagent flow flowing through the branch flow path 32 and the sample flow flowing through the main flow path 31 join together to form a mixed flow.
- the sample and the first reagent are mixed, and a reaction occurs.
- the second reagent is injected into the reagent inlet 23 at an appropriate timing.
- the reagent flow flowing through the branch channel 33 joins the mixed flow.
- the sample and the second reagent are mixed, and a reaction occurs.
- An arbitrary analysis is performed at the position P3 of the main channel 31 where the reaction is completed.
- the sample can be analyzed by detecting the reaction solution using an optical detection method such as a photothermal conversion method, a fluorescence method, an absorbance method, and a chemiluminescence method.
- the sample can be analyzed by observing the reaction solution under a microscope.
- the reaction time between the sample and the first and second reagents can be adjusted by closing the opening / closing section V 1. Further, by performing the above-described flow control in the flow control unit C1, the flow of the liquid in the flow path can be promoted.
- Samples used in the present embodiment include biological samples such as blood, cerebrospinal fluid, saliva, and urine.
- biological samples such as blood, cerebrospinal fluid, saliva, and urine.
- biological components contained in blood, cerebrospinal fluid, saliva, and urine biological components derived from organs, tissues, and mucous membranes, and proteins, DNA, RNA, and allergens such as bacteria and viruses that cause infection
- various antigens and the like can be detection target substances.
- the flow path in the capillary chip 1 is mainly used for transferring reagents and samples (from the upstream end of the main flow path 31 to the junction P 1, branch paths 32, 33), and mixing of reagents and samples.
- the main flow path (from the junction P1 to the junction P2 of the main flow path 31), the main flow path for mixing reagents and samples and detecting the reaction solution (the main flow path 31 From the junction P2 to the downstream end).
- the configuration of the flow path is not limited to that shown in the present embodiment, and can be designed according to the application.
- the flow path in the capillary chip 1 may consist of only the flow path portion whose main purpose is one operation (for example, a certain amount of sampling, transfer of a sample or a reagent, etc.). It may be a combination of flow paths mainly for different operations. This makes it possible to construct a device that can perform advanced analysis that involves not only qualitative analysis but also quantitative analysis.
- the configuration of the flow path is, for example, the shape of a flow path mainly for mixing or diluting a sample or a reagent, and the shape where one flow path is combined with another flow path (see Fig. 1). Shape) and a shape in which a plurality of flow paths are merged into one flow path at a single point.
- planar shape of the flow path portion for homogenizing the liquid examples include a linear shape, a meandering shape and a spirally bent shape.
- a reaction part having a larger volume per unit length in the flow direction than the other part in the flow path second embodiment described later
- An easy configuration can be provided.
- it is possible to divide the flow by forming a flow path in which one flow path is divided into many (branch the flow path).
- each of the flow paths 31, 32, and 33 is formed on the substrate 11 is used.
- the capillary chip to which the present invention can be applied is limited to this configuration.
- each flow path 31, 32, 33 may be formed in a columnar base.
- the above-described opening / closing control and flow control can be performed by using a cavity chip having a flow path configured by a groove having an open upper surface. However, as in the present embodiment, the entirety of each flow path is controlled. It is preferable to use a capillary chip whose periphery is formed of a capillary made of a polymer composition, since the above-described opening / closing control and flow control are effectively performed.
- the area around the through hole 21 constituting the sample inlet is heated to reduce the volume of the through hole 21, and the sample consisting of the through hole 21 is formed.
- the fluid may flow so as to be pushed out of the inlet into the main flow path 31.
- the volume of the through hole 21 is naturally reduced by cooling around the through hole 21 constituting the sample inlet.
- FIG. 9 is a block diagram of the distribution control device 51.
- the distribution control device 51 includes a detachable chip mounting portion 52, a laser generator 54, an optical system 55, and a laser control portion 56.
- the laser generator 54 and the optical system 55 together are also referred to as a laser irradiation section.
- the flow control device 51 is used by attaching the capillary chip 1 to the capillary chip mounting section 52.
- the capillary chip mounting portion 52 has a guide member 53 for mounting the capillary chip 1, for example.
- the laser beam L emitted from the laser generator 54 and narrowed down by the optical system 55 is irradiated on the capillary chip 1, the laser controller 56 controls the optical system 55, and the optical system 55.
- the irradiation position of the laser beam L is controlled by deflecting the laser beam L internally.
- the laser controller 56 controls the laser beam L so as to irradiate the opening / closing section V1 and the opening / closing section V2 of the flow control section C1. Also, under the control of the laser control unit 56, it is possible to irradiate the laser beam L while scanning it, and by adjusting the aperture of the laser beam L in the optical system 55, a plurality of open / close units V 2 can be irradiated simultaneously.
- the flow control method of the flow control unit 51 can be implemented by the flow control device 51.
- the flow control device may be configured to include a laser capable of simultaneously irradiating a plurality of laser beams L. Further, the laser beam L may be irradiated at an arbitrary position on the capillary chip 1 so as to have a driving means for driving the capillary chip 1.
- FIG. 10 is a block diagram of a flow control device 57 having a form different from that of FIG. 10, the same components as those in FIG. 9 are denoted by the same reference numerals, and description thereof will be omitted.
- the flow control device 57 shown in FIG. 10 is a flow control device 51 shown in FIG. 9, which is an injection means capable of injecting a sample or a reagent into the sample inlet 21 and the reagent inlets 22, 23. 5 8, Drainage means that can discharge liquid from discharge port 2 4 5 9,
- This configuration is provided with an analysis means 60 such as a microscope capable of performing the above-described analysis. With such a configuration, injection and opening / closing control, flow control, and analysis of a sample and a reagent can be performed by one apparatus.
- the reaction of different capillary chips 1 can be analyzed simply by replacing the capillary chips 1 mounted on the capillary chip mounting section 52.
- the cavity chip 1 is manufactured by bonding a main flat plate (a flat plate for forming a groove) and a lid flat plate.
- Fig. 4 (a) is a top view of the lid flat plate 2a
- Fig. 4 (b) is a top view of the main flat plate 3a
- Fig. 4 (c) is a cross-sectional view of a longitudinal section of the capillary chip 1 manufactured by this manufacturing method. is there.
- the vertical cross section is a cross section that cuts the flow channel 31 in the vertical direction.
- grooves 31a, 32a and 33a serving as flow paths are formed on the surface of the main flat plate 3a.
- Fig. 4 (a) four through holes 21a, 22a, 3a, 24a serving as sample inlet, reagent inlet, and outlet are formed on plate 2a, respectively.
- FIG. 4 (c) the main flat plate 3a and the lid flat plate 2a are connected to the main flat plate 3a with the surfaces on which the grooves 31a, 32a, and 33a are formed inward. Then, the capillary chip 1 is manufactured.
- a main plate in which a layer made of a specific polymer composition (hereinafter, referred to as a polymer composition layer) is formed on the surface of the substrate is used.
- the details of the polymer composition are the same as those described above as the polymer composition forming the opening / closing portion V1.
- the method for forming the polymer composition layer on the substrate is not limited, and can be performed by many methods such as, for example, spray deposition, painting, immersion, gravure printing, and rolling.
- a cool-off type Intellima® which is a temperature-sensitive adhesive tape in which a layer made of a polymer composition that undergoes a first melt transfer is formed on the surface of a substrate made of a PET film, Nitta Corporation
- Cool-off type Intelimer® increases its volume by heating from a temperature lower than the melting temperature range to a higher temperature, and decreases its volume by cooling from a temperature higher than the melting temperature range to a lower temperature.
- an Intellima registered trademark having a melting temperature range of about 30 ° C or more and 40 ° C or less
- -(Registered trademark) is suitable as the material of the main flat plate 3a.
- the grooves 31a, 32a, 33a are formed on the surface of the polymer composition layer.
- the thickness of the polymer composition layer is not particularly limited as long as it is larger than the depths of the grooves 31a, 32a, and 33a, and the entire main plate 3a is formed of a specific polymer composition. There may be.
- an arbitrary part in the flow path can be used as the opening / closing part or the flow control part.
- the above-mentioned polymer composition layer is also formed inside the lid plate 2a.
- the entire circumference of the flow paths 31, 32, 33 formed by laminating the main flat plate 3a and the lid flat plate 2a is formed of the polymer composition.
- the present invention is not limited to this configuration, and the lid plate 2a may have a configuration in which the polymer composition is not formed. In this case, the flow paths 31, 32, and 33 have a part of the entire circumference formed of a polymer composition.
- the substrate of the main plate 3a (that is, the portion other than the polymer composition layer) and the lid plate 2a (the portion other than the polymer composition layer) can be made of an inorganic material such as silicon or glass, or an organic polymer. it can.
- At least one of the substrate of the main flat plate 3a and the lid flat plate 2a uses a material having transparency with respect to the wavelength of light emitted by the heating means. For example, when the opening / closing section V1 or the flow control section C1 is heated by a laser, the laser is irradiated from the outside of the kyabili- ty chip 1, so that the laser is irradiated from the outside to the opening / closing section V1 and the flow control section C1. This is because it is necessary to reach the light, and it is necessary to ensure transparency in the optical path of the laser light.
- the grooves 31a, 32a, and 33a on the surface of the main flat plate 3a are formed by a method such as etching with a cutting laser.
- the through holes 21a, 22a, 23a, 24a of the cover plate 2a are formed by a method such as ultrasonic processing.
- the through holes 21a, 22a, 23a of the lid plate 2a are formed at positions substantially corresponding to the most upstream positions of the grooves 31a, 32a, 33a of the main plate 3a. .
- the through hole 24a is formed at a position substantially corresponding to the most downstream position of the groove 31a.
- the main plate 3a having the grooves 31a, 32a and 33a formed therein, and the cover plate 2a having the through holes 2la, 22a, 23a and 24a formed therein. Are bonded together with the grooves 31 a, 32 a, and 33 a inside, whereby the cavity chip 1 is formed.
- the main flat plate 3a and the lid flat plate 2a are bonded together by, for example, ultrasonic fusion, bonding with an adhesive such as a hot melt adhesive or a UV adhesive, adhesion with an adhesive, double-sided tape, or the like. Method such as pressure welding.
- the grooves 31a, 32a, 33a are the flow paths 31, 33, 33, and the through hole 21a is the sample inlet 21.
- the through holes 22a and 23a become the reagent inlets 22 and 23, and the through hole 24a becomes the outlet 24.
- the capillary chip 1 is manufactured by bonding a main flat plate (a flat plate for forming a groove) and a lid flat plate.
- Fig. 5 (a) is a top view of the lid flat plate 2b
- Fig. 5 (b) is a top view of the main flat plate 3b
- Fig. 5 (c) is a vertical cross section of the capillary chip 1 manufactured by this manufacturing method. It is sectional drawing. The vertical section is a section that cuts the main channel 31 in the vertical direction.
- grooves 31b, 32b, 33b to be flow paths are formed on the surface of the main flat plate 3b. Further, through holes 21b, 22b, 23, 24b are formed in the main plate 3b. The through holes 21b, 22b, and 23b are formed at the most upstream positions of the grooves 31b, 32b, and 33b. The through hole 2 4 b is It is formed at the most downstream position of the groove 31b.
- the main plate 3b and the cover plate 2b are attached with the grooves 31b, 32b, and 33b formed in the main plate 3b inside.
- the capillary chip 1 is formed.
- This manufacturing method is the first manufacturing method except that the grooves 31, 32, 33 and the through holes 21, 22, 23, 24 are formed on the same main plate 3 b. Is the same as Further, as the main plate 3b and the cover plate 2b, those made of the same material as the main plate 3a and the cover plate 2a used in the first manufacturing method can be used. Therefore, also in this method, since the entire groove is formed of the polymer composition, an arbitrary part in the flow path can be used as the opening / closing part or the flow control part.
- the grooves 31b, 32b, and 33b become the flow paths 31, 32, and 33, and the through hole 21b is the sample inlet 21.
- the through holes 22 b and 23 b become the reagent inlets 22 and 23, and the through hole 24 b becomes the outlet 24.
- the capillary chip 1 is manufactured by bonding a main flat plate (a flat plate for forming a slit) and two lid flat plates.
- Fig. 6 (a) is a top view of the first cover plate 2c
- Fig. 6 (b) is a top view of the main cover plate 3c
- Fig. 6 (c) is a top view of the second cover plate 2d.
- FIG. 6D is a cross-sectional view of the longitudinal section of the capillary chip 1 manufactured by the present manufacturing method.
- the longitudinal section is a section that cuts the main channel 31 in the longitudinal direction.
- slits 31c, 32c and 33c to be flow paths are formed in the main flat plate 3c.
- the slits 31c, 32c, and 33c pass through the front and back surfaces of the main flat plate 3c.
- four through-holes 21c, 22c, 23c and 24c, which serve as a sample inlet, reagent inlet and outlet, respectively, are formed in the first lid plate 2c. Form c. Then, as shown in FIG.
- the capillary chip 1 is manufactured.
- a plate made of a polymer composition is used as the main plate 3b.
- the polymer composition is the same as that described above as the polymer composition forming the opening / closing portion V1. Except that the main flat plate 3c and the second lid flat plate 2d are bonded to each other, a flat plate similar to the main flat plate 3a in the first manufacturing method is formed. Same as the method. Therefore, also in this method, since the entire slit is formed of the polymer composition, an arbitrary part in the flow path can be used as the opening / closing part or the flow control part. If the polymer composition layer is formed on the inner surfaces of the two lid plates 2c and 2d, the entire circumference of the flow paths 31, 32, and 33 is preferably made of the polymer composition. It is not limited to this.
- the slits 31 c, 32 c, and 33 c become the flow paths 31, 32, and 33, and the through hole 21 c is the sample inlet 2.
- the through holes 22 c and 23 c become the reagent inlets 22 and 23, and the through hole 24 c becomes the outlet 24.
- FIG. 7 is a perspective view schematically showing the appearance of the capillary chip 1 'used in the present embodiment.
- the capillary tip 1 ′ is provided with an opening / closing section near the upstream end of each of the channels 31, 32, 33 corresponding to the sample inlet 21 and the reagent inlets 22, 23. Opening / closing sections V 2, V 4, V 5 having the same configuration as V 1 are provided. Note that the opening / closing section V2 also functions as the opening / closing section of the flow control section C1.
- the other configuration is the same as that of the capillary chip 1 of the first embodiment. Therefore, the same components are denoted by the same reference numerals and description thereof will be omitted.
- the capillary chip 1 ′ can be used in the same manner as the capillary chip 1 of the first embodiment. And, furthermore, opening and closing part V 2, By controlling the opening and closing of V 4 and V 5, the timing to start, stop and flow the flow of the sample injected into the sample inlet 21 and the reagent injected into the reagent inlets 22 and 23 are controlled. can do.
- the capillaries 1 'of the present embodiment can also perform opening / closing control, flow control, analysis, and the like using the flow control device shown in the first embodiment.
- FIG. 8A is a perspective view schematically showing the appearance of the capillary chip 13 used in the present embodiment.
- FIG. 8 (b) is a cross-sectional view showing a Vllb-VIIb cross section of FIG. 8 (a)
- FIG. 1 (c) is a cross-sectional view showing a VIIc-VIIc cross section of FIG. 1 (b).
- the capillary chip 13 is composed of the main channel 34, branch channels 35, 36, 37, 38, 39, inlet 41, and outlet. It consists of a substrate 14 with a rectangular top surface on which 25, 26, 27, 28, 29 are formed.
- Each of the flow paths 34, 35, 36, 37, 38, 39 is made up of a capillary.
- the main flow path 34 branches into five branch flow paths 35, 36, 37, 38, and 39 at a branch point 34a.
- the configuration and control method of the switching unit V3 are the same as those of the switching unit VI of the first embodiment.
- the configuration and control method of the flow control unit C2 are the same as those of the flow control unit C1 of the first embodiment.
- the cell suspension containing the culture medium is injected from the inlet 41, and the reaction section of each of the branch channels 35, 36, 37, 38, and 39 is made using the pump function of the flow control section C2.
- the suspension is fed up to 35a, 36a, 37a, 38a, and 39a.
- each reaction section 35a, 36a, 37a, 38a, 39a is filled with the suspension, each branch 35, 36, 37, 38, 3
- the opening / closing part V3 provided in 9 is closed.
- the cells are left for 2 days, and the cells are cultured in the reaction layers 35a, 36a, 37a, 38a, and 39a.
- the opening / closing portion V3 of each of the branch channels 35, 36, 37, 38, 39 is opened, and the reagent solution in which the first drug candidate compound is dissolved is injected from the inlet 41.
- the reagent solution is sent to each of the reaction units 35a, 36a, 37a, 38a, and 39a.
- the opening / closing section V3 is closed at the timing when each of the reaction sections 35a, 36a, 37a, 38a, 39a is filled with the reagent.
- the cytotoxicity of the first drug candidate compound and the effect on cells To analyze.
- adherent cells it is preferable to use adherent cells as the cells. Since adherent cells adhere to the reaction layer, most of them can flow out of the reaction layer 35 a, 36 a, 37 a, 37 a, 38 a, or 39 a even if the reagent is sent after culturing. Because there is no.
- an opening / closing section is provided at the upstream end of each of the branched branch channels 35, 36, 37, 38, 39 so that the reaction layers 35a, 36a, 37a, Reagent solutions of different drug candidate compounds may be sent to 38a and 39a to simultaneously analyze the cytotoxicity and the like of a plurality of reagents.
- the capillaries 13 of the present embodiment can also perform opening / closing control, flow control, analysis, and the like using the flow control device described in the first embodiment.
- the flow control and the opening / closing control of the capillaries can be achieved by a simple method of changing the temperature of the opening / closing section in the capillaries. Furthermore, since cavities are formed on the surface or inside of the layer composed of the polymer composition, any part can be selected as the opening / closing part.
- the properties of the sample and the reagent are not affected during the flow control and the opening / closing control.
- the means necessary for performing the above control can be configured with a small device capable of maintaining quietness.
- the distribution method according to the present invention is useful for distributing a liquid such as a reagent or a sample in a microchip for medical diagnosis or a microchip for detecting drug responsiveness.
- the distribution method according to the present invention can be used for micro TAS which performs analysis using a microchip.
- it can be used for micro TAS for analyzing biological samples such as blood, cerebrospinal fluid, saliva, urine and the like.
- desired opening / closing control and distribution control can be performed in a microchip having a simple configuration, and therefore, it is particularly useful as a method applied to disposable cabillary chips.
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Abstract
Description
Claims
Priority Applications (3)
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CN2004800119250A CN1784605B (zh) | 2003-10-15 | 2004-10-13 | 毛细管芯片中流体的流通方法、使用该方法的流通控制装置 |
JP2005514686A JP3798011B2 (ja) | 2003-10-15 | 2004-10-13 | キャピラリチップにおける流体の流通方法 |
US11/195,649 US7055540B2 (en) | 2003-10-15 | 2005-08-03 | Method of moving fluid in capillary chip |
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JP2003354655 | 2003-10-15 |
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US11/195,649 Continuation US7055540B2 (en) | 2003-10-15 | 2005-08-03 | Method of moving fluid in capillary chip |
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WO2005036182A1 true WO2005036182A1 (ja) | 2005-04-21 |
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US (1) | US7055540B2 (ja) |
JP (1) | JP3798011B2 (ja) |
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JP2007024551A (ja) * | 2005-07-12 | 2007-02-01 | Ngk Spark Plug Co Ltd | 中継基板、及びマイクロチップ搭載装置 |
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JP2008045745A (ja) * | 2006-08-16 | 2008-02-28 | Samsung Electronics Co Ltd | バルブユニット、これを備えた反応装置、及びチャンネルにバルブを形成する方法 |
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JP2008121890A (ja) * | 2006-11-09 | 2008-05-29 | Samsung Electronics Co Ltd | 弁ユニット、弁ユニットを備えた微細流動装置、及び微細流動基板 |
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JP2008197097A (ja) * | 2007-02-12 | 2008-08-28 | Samsung Electronics Co Ltd | 希釈のための遠心力基盤の微細流動装置及びそれを備える微細流動システム |
JP2010540905A (ja) * | 2007-09-21 | 2010-12-24 | アプライド バイオシステムズ インコーポレーティッド | 分析カードのチャンバを熱的に隔離するためのデバイスおよび方法 |
JP2015511181A (ja) * | 2012-02-24 | 2015-04-16 | フォンズ エスピシ ジョルジュ シャルパクFonds Espci Georges Charpak | 開放及び/または閉鎖及び/またはポンプ装置を有するマイクロチャネル |
WO2014207857A1 (ja) * | 2013-06-26 | 2014-12-31 | 株式会社日立製作所 | 細胞毒性試験装置、及び細胞毒性試験方法 |
WO2021193281A1 (ja) * | 2020-03-24 | 2021-09-30 | 京セラ株式会社 | 流路デバイス |
JP6991408B1 (ja) * | 2020-03-24 | 2022-01-13 | 京セラ株式会社 | 流路デバイス |
Also Published As
Publication number | Publication date |
---|---|
CN1784605B (zh) | 2011-11-23 |
US7055540B2 (en) | 2006-06-06 |
US20050274423A1 (en) | 2005-12-15 |
JP3798011B2 (ja) | 2006-07-19 |
JPWO2005036182A1 (ja) | 2006-12-21 |
CN1784605A (zh) | 2006-06-07 |
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