EP2074341A2 - Clapets de non-retour microfluidiques - Google Patents

Clapets de non-retour microfluidiques

Info

Publication number
EP2074341A2
EP2074341A2 EP07843872A EP07843872A EP2074341A2 EP 2074341 A2 EP2074341 A2 EP 2074341A2 EP 07843872 A EP07843872 A EP 07843872A EP 07843872 A EP07843872 A EP 07843872A EP 2074341 A2 EP2074341 A2 EP 2074341A2
Authority
EP
European Patent Office
Prior art keywords
channel
microfluidic device
less
chamber
outlet
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP07843872A
Other languages
German (de)
English (en)
Other versions
EP2074341A4 (fr
Inventor
Jing Wang
Hany R. Nassef
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Standard Biotools Corp
Original Assignee
Fluidigm Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Fluidigm Corp filed Critical Fluidigm Corp
Publication of EP2074341A2 publication Critical patent/EP2074341A2/fr
Publication of EP2074341A4 publication Critical patent/EP2074341A4/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16KVALVES; TAPS; COCKS; ACTUATING-FLOATS; DEVICES FOR VENTING OR AERATING
    • F16K99/00Subject matter not provided for in other groups of this subclass
    • F16K99/0001Microvalves
    • F16K99/0003Constructional types of microvalves; Details of the cutting-off member
    • F16K99/0026Valves using channel deformation
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L3/00Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
    • B01L3/50Containers for the purpose of retaining a material to be analysed, e.g. test tubes
    • B01L3/502Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
    • B01L3/5027Containers 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
    • B01L3/502738Containers 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
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16KVALVES; TAPS; COCKS; ACTUATING-FLOATS; DEVICES FOR VENTING OR AERATING
    • F16K99/00Subject matter not provided for in other groups of this subclass
    • F16K99/0001Microvalves
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16KVALVES; TAPS; COCKS; ACTUATING-FLOATS; DEVICES FOR VENTING OR AERATING
    • F16K99/00Subject matter not provided for in other groups of this subclass
    • F16K99/0001Microvalves
    • F16K99/0034Operating means specially adapted for microvalves
    • F16K99/0055Operating means specially adapted for microvalves actuated by fluids
    • F16K99/0057Operating means specially adapted for microvalves actuated by fluids the fluid being the circulating fluid itself, e.g. check valves
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/12Specific details about manufacturing devices
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2300/00Additional constructional details
    • B01L2300/08Geometry, shape and general structure
    • B01L2300/0887Laminated structure
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2400/00Moving or stopping fluids
    • B01L2400/06Valves, specific forms thereof
    • B01L2400/0605Valves, specific forms thereof check valves
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01LCHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2400/00Moving or stopping fluids
    • B01L2400/06Valves, specific forms thereof
    • B01L2400/0633Valves, specific forms thereof with moving parts
    • B01L2400/0638Valves, specific forms thereof with moving parts membrane valves, flap valves
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16KVALVES; TAPS; COCKS; ACTUATING-FLOATS; DEVICES FOR VENTING OR AERATING
    • F16K99/00Subject matter not provided for in other groups of this subclass
    • F16K2099/0073Fabrication methods specifically adapted for microvalves
    • F16K2099/0078Fabrication methods specifically adapted for microvalves using moulding or stamping
    • FMECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
    • F16ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
    • F16KVALVES; TAPS; COCKS; ACTUATING-FLOATS; DEVICES FOR VENTING OR AERATING
    • F16K99/00Subject matter not provided for in other groups of this subclass
    • F16K2099/0073Fabrication methods specifically adapted for microvalves
    • F16K2099/008Multi-layer fabrications

Definitions

  • Microfluidic devices can be used for analytical, preparative, metering, and other manipulative functions on a scale not imagined until recently.
  • the advantages of microfluidic devices include conservation of precious reagents and samples, high density and throughput of sample analysis or synthesis, fluidic precision and accuracy at a level scarcely visible to the unaided eye, and a space reduction accompanying the replacement of counterpart equipment operating at the macrofluidic scale.
  • Associated with the reduction in size and the increased density of microfluidic devices is increased complexity and higher engineering and fabrication costs associated with increasingly intricate device architecture.
  • the present invention a microfluidic check valve and it method of use, can reduce the complexity of microfluidic chips and simplify their operation.
  • the present invention is a robust, microfluidic check valve and a method of using the check valve in microfluidic devices.
  • the check valve is comprised two stacked chambers that are separated by a pore-containing membrane.
  • the membrane is composed of an elastomeric material and can be configured in normally open or normally closed state.
  • the normally open check valve can be implemented so that the degree of back pressure necessary to close the valve can be set.
  • the normally closed embodiment can maintain a closed state with essentially no back pressure. Both the normally open and the normally closed version can be readily produced by multilayer soft lithographic techniques and may retain effective functioning through many thousands of opening and closing cycles without failure.
  • FIG. 1 provides an illustration of a microfluidic check valve in an embodiment
  • FIG. 2 illustrates a method for fabrication of a microfluidic check valve in an embodiment
  • FIG. 3 illustrates the flow rate through a microfluidic check valve as a function of applied pressure in one embodiment
  • Fig. 4 is a micrograph of check valves fabricated in series using the methods illustrated in Fig. 2.
  • Fig. 5 is a diagram of a microfluidic check valve.
  • the invention provides a microfluidic check valve that is easily manufactured and incorporated into microfluidic devices.
  • the check valve is characterized as having exceptionally low activation pressure to open or close, minimal dead volume, and essentially no back flow.
  • the valves of the present invention can withstand thousands of opening and closing cycles and survive the high end of pressures that are encountered in microfluidic devices.
  • the invention provides for a microfluidic device comprising, an inlet channel, a check valve, and an outlet channel wherein, in the absence of outlet channel flow restrictions, an inlet channel pressure of less than 5 psi (pounds per square inch) is required to produce flow to the outlet channel and wherein substantially no flow occurs from the outlet channel to the inlet channel when an outlet pressure exceeds the inlet channel pressure by about 3 psi.
  • the check valve will allow flow to occur from the inlet channel to the outlet channel with an inlet channel pressure of less than 3 psi, 2 psi, 1 psi, 0.5 psi or 0.2 PSI.
  • the initial inlet pressure required to open the check valve will, in some cases, exceed the pressure required to open the check valve in subsequent opening.
  • the opening pressures recited above represent the average opening pressures of 10 repeated openings and closings within a 30 minutes period.
  • the check valve will close when the pressure in the outlet channel exceeds the pressure in the inlet channel by 2 psi, 1 psi, 0.5 psi, 0.25 psi, 0.1 psi, or 0.05 psi.
  • the check valve will close when the pressure in the outlet channel exceeds the pressure in the inlet channel by 0.005 psi.
  • the check valves of the present invention are further characterized by a very low dead volume.
  • the check valves my have a dead volume of 100 nL (nanoliters) or less, 50 nL or less, 25 nL or less, 15 nL or less, 10 nL, or less, 5 nL or less, 4 nL or less, 2.5 nL or less, or, in a further embodiment, about 1 nL.
  • the invention further relates to a check valve having a dead volume of less than 100 nL, the check valve comprising, an outlet chamber in fluidic communication with an outlet channel, an inlet chamber in fluidic communication with an inlet channel, and a deflectable membrane between the outlet chamber from the inlet chamber, the membrane having a fluidic channel that places the inlet chamber in fluidic communication with the outlet chamber.
  • the check valve may be further defined in this embodiment wherein the inlet and outlet chambers of the check valve have a columnar shape and the footprint of the columns defining either the inlet or outlet chamber that is selected from the group consisting of a polygon, a quadrangle, a square, an oval, a circle, or a partially rounded polygon.
  • circular footprints are preferred.
  • polygonal footprints are preferred, hi particular, quadrilateral or square footprints may be preferred for some applications.
  • Polygonal footprints can also be used for the chambers, and, in some instances, a rounded polygon or an oval footprint may be desired.
  • the footprint of the inlet chamber has a shortest internal width, A
  • the inlet chamber has a height, B
  • the footprint of the outlet chamber has a shortest internal width, C
  • the outlet chamber has a height, D.
  • the membrane channel has a width, E, and a membrane thickness, F (Fig. 5).
  • the check valves of the invention will typically have a ratio of C to A is greater than or equal to aboutl .2, a ratio of D to B is greater than or equal to about 1.4, and a ratio of A to E is greater than or equal to about 1.9.
  • the ratio of C to A is equal to or less than about 1.5, equal to or less than about 1.75, equal to or less than about 2, equal to or less that about 2.5, equal to or less than about 3, or greater than 3.
  • the ratio of D to B can be equal to about 1.6 or less, equal to or less than about 1.8, equal to or less than about 2, equal to or less than about 2.5, or equal to or less than about 3, or greater than 3.
  • the ratio of A to E can be equal to or less than about 2.2, equal to or less than about 2.5, equal to or less than about 2.8, equal to or less than about 3, or greater than 3.
  • the membrane thickness, F can be from about 2 to about 100 urn, preferably from about 2 to about 75 urn, preferably from about 2 to about 50 um, more preferably from about 2 to about 25 urn. In some embodiments, it is preferred that F is less than about 25 um. In some embodiments it is preferred that F is equal to or less than about 10 um. In other embodiments, it is preferred that F is equal to or less than 5 um in thickness.
  • the membrane (503) should have a Young's modulus of about 100 MPA (megapascals) or less, hi other embodiments, the Young's modulus of the membrane is about 75 MPA or less, about 50 MPa or less, about 25 MPa or less, about 10 MPa or less, about 8 MPa or less, about 5 MPa or less, or about 2 MPa or less.
  • the check valves of the invention may be constructed wherein the fluidic channel of the membrane defines an axis and the inlet chamber and the outlet chamber are substantially axially aligned. This may result in a configuration, for example where the output chamber and the inlet chamber are arranged so as to appear as concentric circles around a central axis that is the membrane fluid channel, hi other embodiments, the chambers may be offset from each other.
  • the geometrical shapes of the chamber footprints may be the same or different with, for example, the input chamber having a quadrilateral footprint, such as a square, and the outlet chamber having a substantially circular footprint.
  • the check valves of the invention are generally constructed of three layers; an upper layer defining the outlet chamber and, optionally, an outlet channel; a bottom layer defining the inlet chamber, and, optionally, an inlet channel; and a middle layer that, minimally, defines the membrane layer, hi a preferred embodiment, the middle membrane layer is integral to the bottom layer that defines the input chamber.
  • the bottom layer might be prepared from an elastomeric material that is cast such that the top of the input chamber defines the membrane.
  • the microfluidic devices of the invention may be conveniently constructed out of elastomer materials in their entirety, but this is not required or, in some cases, preferred.
  • Non-elastomeric materials such as glass, steel, brass, copper, silicon, quartz, and hard plastics may be used to form the upper and/or lower layers. These layers may be prepared by machining, etching, casting, molding, embossing, vacuum forming, or similar methodologies. Elastomeric layers may also be prepared and used as described below. Elastomers used in the present invention may have a Young's modulus of from about 1 kilopascal (KPa) to about 2.5 gigapascals (GPa).
  • Ranges of Young's moduli used for elastomeric materials for the present invention include from about 1 KPa to about 2 GPa, from about 50 KPa to about 500 MPa, from about 50 KPa to about 100 MPa, from about 50 KPa, to about 100 MPa, from about 100 KPa to about 10 MPa, from about 100 KPa to about 1 MPa, from about 200 KPa to about 500 MPa, from about 200 KPa to about 100 MPa, and from about 200 KPa to about 10 MPa.
  • Microfabricated refers to the size of features of an elastomeric structure fabricated in accordance with an embodiment of the present invention.
  • variation in at least one dimension of microfabricated structures is controlled to the micron level, with at least one dimension being microscopic (i.e. below 1000 ⁇ m).
  • Microfabrication typically involves semiconductor or MEMS fabrication techniques such as photolithography and spincoating that are designed for to produce feature dimensions on the microscopic level, with at least some of the dimension of the microfabricated structure requiring a microscope to reasonably resolve/image the structure.
  • flow channels preferably have width-to-depth ratios of about 10:1.
  • a non-exclusive list of other ranges of width-to-depth ratios in accordance with embodiments of the present invention is 0.1:1 to 100:1, more preferably 1:1 to 50:1, more preferably 2:1 to 20:1, and most preferably 3:1 to 15:1.
  • flow channels have widths of about 1 to 1000 microns.
  • a non-exclusive list of other ranges of widths of flow channels in accordance with embodiments of the present invention is 0.01 to 1000 microns, more preferably 0.05 to 1000 microns, more preferably 0.2 to 500 microns, more preferably 1 to 250 microns, and most preferably 10 to 200 microns.
  • Exemplary channel widths include 0.1 ⁇ m, 1 ⁇ m, 2 ⁇ m, 5 ⁇ m, 10 ⁇ m, 20 ⁇ m, 30 ⁇ m, 40 ⁇ m, 50 ⁇ m, 60 ⁇ m, 70 ⁇ m, 80 ⁇ m, 90 ⁇ m, 100 ⁇ m, 110 ⁇ m, 120 ⁇ m, 130 ⁇ m, 140 ⁇ m, 150 ⁇ m, 160 ⁇ m, 170 ⁇ m, 180 ⁇ m, 190 ⁇ m, 200 ⁇ m, 210 ⁇ m, 220 ⁇ m, 230 ⁇ m, 240 ⁇ m, and 250 ⁇ m.
  • Flow channels have depths of about 1 to 100 microns.
  • a non-exclusive list of other ranges of depths of flow channels in accordance with embodiments of the present invention is 0.01 to 1000 microns, more preferably 0.05 to 500 microns, more preferably 0.2 to 250 microns, and more preferably 1 to 100 microns, more preferably 2 to 20 microns, and most preferably 5 to 10 microns.
  • Exemplary channel depths include including 0.01 ⁇ m, 0.02 ⁇ m, 0.05 ⁇ m, 0.1 ⁇ m, 0.2 ⁇ m, 0.5 ⁇ m, 1 ⁇ m, 2 ⁇ m, 3 ⁇ m, 4 ⁇ m, 5 ⁇ m, 7.5 ⁇ m, 10 ⁇ m, 12.5 ⁇ m, 15 ⁇ m, 17.5 ⁇ m, 20 ⁇ m, 22.5 ⁇ m, 25 ⁇ m, 30 ⁇ m, 40 ⁇ m, 50 ⁇ m, 75 ⁇ m, 100 ⁇ m, 150 ⁇ m, 200 ⁇ m, and 250 ⁇ m.
  • Elastomeric layers may be cast thick for mechanical stability.
  • a layer is 50 microns to over a centimeter thick, and more preferably approximately 4 mm thick.
  • a non-exclusive list of ranges of thickness of the elastomer layer in accordance with other embodiments of the present invention is between about 0.1 micron to 1 cm, 1 micron to 1 cm, 10 microns to 0.5 cm, 100 microns to 10 mm.
  • membranes separating flow channels have a typical thickness of between about 0.01 and 1000 microns, more preferably 0.05 to 500 microns, more preferably 0.2 to 250, more preferably 1 to 100 microns, more preferably 2 to 50 microns, and most preferably 5 to 40 microns.
  • Exemplary membrane thicknesses include 0.01 ⁇ m, 0.02 ⁇ m, 0.03 ⁇ m, 0.05 ⁇ m, 0.1 ⁇ m, 0.2 ⁇ m, 0.3 ⁇ m, 0.5 ⁇ m, 1 ⁇ m, 2 ⁇ m, 3 ⁇ m, 5 ⁇ m, 7.5 ⁇ m, 10 ⁇ m, 12.5 ⁇ m, 15 ⁇ m, 17.5 ⁇ m, 20 ⁇ m, 22.5 ⁇ m, 25 ⁇ m, 30 ⁇ m, 40 ⁇ m, 50 ⁇ m, 75 ⁇ m, 100 ⁇ m, 150 ⁇ m, 200 ⁇ m, 250 ⁇ m, 300 ⁇ m, 400 ⁇ m, 500 ⁇ m, 750 ⁇ m, and 1000 ⁇ m.
  • FIG. 5 illustrates an embodiment of a microfluidic check valve of the present invention.
  • An upper layer (507) defines an outlet chamber (501) that is in fluidic communication with and outlet channel (506).
  • the outlet chamber has a height, D, and a chamber width, C.
  • the upper layer is adhered to, pressed onto, or bonded to the membrane (503) with its flow channel (504) opening into the outlet chamber.
  • the membrane has a thickness, F, and a flow channel width (or diameter), E.
  • the membrane layer is adhered to, pressed onto, bonded to, or integral with the bottom layer (508) which defines the input chamber (502) and the input flow channel (505).
  • the input chamber has a width (or diameter), A, and a height, B.
  • the layer 508 is adhered to, pressed onto, or bonded to a substrate (either hard or elastomeric) (509) that forms the inlet channel (505).
  • microfluidic devices disclosed herein are typically constructed at least in part from elastomeric materials and constructed by single and multilayer soft lithography (MSL) techniques and/or sacrificial-layer encapsulation methods (see, e.g., Unger et al. (2000) Science 288:113-116, and PCT Publication WO 01/01025, both of which are incorporated by reference herein in their entirety for all purposes).
  • MSL soft lithography
  • sacrificial-layer encapsulation methods see, e.g., Unger et al. (2000) Science 288:113-116, and PCT Publication WO 01/01025, both of which are incorporated by reference herein in their entirety for all purposes.
  • microfluidic devices can be designed in which solution flow through flow channels of the device is controlled, at least in part, with one or more control channels that are separated from the flow channel by an elastomeric membrane or segment.
  • This membrane or segment can be deflected into or retracted from the flow channel with which a control channel is associated by applying an actuation force to the control channels.
  • solution flow can be slowed or entirely blocked through the flow channel.
  • control and flow channels of this type one can prepare a variety of different types of valves and pumps for regulating solution flow as described in extensive detail in Unger et al. (2000) Science 288:113-116, and PCT Publication WO/02/43615 and WO 01/01025.
  • the present invention provides an advancement of microfluidic architecture by providing a device that can be integrated into known types of microfluidic devices and facilitate one way flow into and through critical regions of such devices.
  • the invention also provides a method of flowing a fluid in a microfluidic device in a single direction along a flow path.
  • the method comprises providing (a) providing a check valve having a dead volume of less than 100 nL, the check valve comprising, an outlet chamber in fluidic communication with an outlet channel, an inlet chamber in fluidic communication with an inlet channel, a deflectable membrane between the outlet chamber from the inlet chamber, the membrane having a fluidic channel that places the inlet chamber in fluidic communication with the outlet chamber, (b) flowing a fluid in the inlet channel to form an inlet channel fluidic pressure such that the fluid appears in the outlet channel and forms an outlet channel fluidic pressure, (c) raising the fluidic pressure in the outlet channel or lowering the fluidic pressure in the inlet channel such that the fluidic pressure in the outlet channel exceeds the fluidic pressure of the inlet channel, and (d) deflecting the membrane to close the check valve to seal off a flow of fluid from the outlet channel to the inlet channel.
  • the check valve may be further defined in this embodiment wherein the inlet and outlet chambers of the check valve have a columnar shape and the footprint of the columns defining either the inlet or outlet chamber that is selected from the group consisting of a polygon, a quadrangle, a square, an oval, a circle, or a partially rounded polygon.
  • a polygon a quadrangle, a square, an oval, a circle, or a partially rounded polygon.
  • circular footprints are preferred.
  • polygonal footprints are preferred.
  • quadrilateral or square footprints may be preferred for some applications.
  • Polygonal footprints can also be used for the chambers, and, in some instances, a rounded polygon or an oval footprint may be desired.
  • the footprint of the inlet chamber has a shortest internal width, A
  • the inlet chamber has a height, B
  • the footprint of the outlet chamber has a shortest internal width, C
  • the outlet chamber has a height, D.
  • the membrane channel has a width, E, and a membrane thickness, F (Fig. 5).
  • the check valves of the invention will typically have a ratio of C to A is greater than or equal to aboutl.2, a ratio of D to B is greater than or equal to about 1.4, and a ratio of A to E is greater than or equal to about 1.9.
  • the ratio of C to A is equal to or less than about 1.5, equal to or less than about 1.75, equal to or less than about 2, equal to or less that about 2.5, equal to or less than about 3, or greater than 3.
  • the ratio of D to B can be equal to about 1.6 or less, equal to or less than about 1.8, equal to or less than about 2, equal to or less than about 2.5, or equal to or less than about 3, or greater than 3.
  • the ratio of A to E can be equal to or less than about 2.2, equal to or less than about 2.5, equal to or less than about 2.8, equal to or less than about 3, or greater than 3.
  • the membrane thickness, F can be from about 2 to about 100 um, preferably from about 2 to about 75 urn, preferably from about 2 to about 50 um, more preferably from about 2 to about 25 um. In some embodiments, it is preferred that F is less than about 25 um. In some embodiments it is preferred that F is equal to or less than about 10 um. In other embodiments, it is preferred that F is equal to or less than 5 um in thickness.
  • the membrane (503) should have a Young's modulus of about 100 MPA (megapascals) or less, hi other embodiments, the Young's modulus of the membrane is about 75 MPA or less, about 50 MPa or less, about 25 MPa or less, about 10 MPa or less, about 8 MPa or less, about 5 MPa or less, or about 2 MPa or less.
  • elastomeric layers are bonded together chemically, using chemistry that is intrinsic to the polymers comprising the patterned elastomer layers.
  • the bonding comprises two component "addition cure" bonding.
  • the various layers of elastomer are bound together in a heterogeneous bonding in which the layers have a different chemistry.
  • a homogenous bonding may be used in which all layers would be of the same chemistry.
  • the respective elastomer layers may optionally be glued together by an adhesive instead.
  • the elastomeric layers may be thermoset elastomers bonded together by heating.
  • the elastomeric layers are composed of the same elastomer material, with the same chemical entity in one layer reacting with the same chemical entity in the other layer to bond the layers together.
  • bonding between polymer chains of like elastomer layers may result from activation of a crosslinking agent due to light, heat, or chemical reaction with a separate chemical species.
  • the elastomeric layers are composed of different elastomeric materials, with a first chemical entity in one layer reacting with a second chemical entity in another layer,
  • the bonding process used to bind respective elastomeric layers together may comprise bonding together two layers of RTV 615 silicone.
  • RTV 615 silicone is a two-part addition-cure silicone rubber. Part A contains vinyl groups and catalyst; part B contains silicon hydride (Si-H) groups. The conventional ratio for RTV 615 is 10A:lB.
  • one layer may be made with 3OA: IB (i.e. excess vinyl groups) and the other with 3A:1B (i.e. excess Si-H groups). Each layer is cured separately. When the two layers are brought into contact and heated at elevated temperature, they bond irreversibly forming a monolithic elastomeric substrate.
  • bonding methods including activating the elastomer surface, for example by plasma exposure, so that the elastomer layers/substrate will bond when placed in contact.
  • activating the elastomer surface for example by plasma exposure
  • elastomer layers/substrate will bond when placed in contact.
  • one possible approach to bonding together elastomer layers composed of the same material is set forth by Duffy et al, "Rapid Prototyping of Microfluidic Systems in Poly (dimethylsiloxane)", Analytical Chemistry (1998), 70, 4974-4984, incorporated herein by reference. This paper discusses that exposing polydimethylsiloxane (PDMS) layers to oxygen plasma causes oxidation of the surface, with irreversible bonding occurring when the two oxidized layers are placed into contact.
  • PDMS polydimethylsiloxane
  • Yet another approach to bonding together successive layers of elastomer is to utilize the adhesive properties of uncured elastomer. Specifically, a thin layer of uncured elastomer such as RTV 615 is applied on top of a first cured elastomeric layer. Next, a second cured elastomeric layer is placed on top of the uncured elastomeric layer. The thin middle layer of uncured elastomer is then cured to produce a monolithic elastomeric structure. Alternatively, uncured elastomer can be applied to the bottom of a first cured elastomer layer, with the first cured elastomer layer placed on top of a second cured elastomer layer. Curing the middle thin elastomer layer again results in formation of a monolithic elastomeric structure.
  • a thin layer of uncured elastomer such as RTV 615 is applied on top of a first cured elastomeric layer.
  • Elastomeric layers may be created by spin-coating an RTV mixture on microfabricated mold at 2000 rpm for 30 seconds yielding a thickness of approximately 40 microns. Additional elastomeric layers may be created by spin-coating an RTV mixture on microfabricated mold. Both layers maybe separately baked or cured at about 80 0 C. for 1.5 hours. The additional elastomeric layer may be bonded onto first elastomeric layer at about 80°C for about 1.5 hours.
  • elastomers in general as polymers existing at a temperature between their glass transition temperature and liquefaction temperature.
  • Elastomeric materials exhibit elastic properties because the polymer chains readily undergo torsional motion to permit uncoiling of the backbone chains in response to a force, with the backbone chains recoiling to assume the prior shape in the absence of the force.
  • elastomers deform when force is applied, but then return to their original shape when the force is removed.
  • the elasticity exhibited by elastomeric materials may be characterized by a Young's modulus.
  • the systems of the present invention may be fabricated from a wide variety of elastomers, hi an exemplary aspect, elastomeric layers may preferably be fabricated from silicone rubber. However, other suitable elastomers may also be used.
  • the present systems are fabricated from an elastomeric polymer such as GE RTV 615 (formulation), a vinyl-silane crosslinked (type) silicone elastomer (family).
  • an elastomeric polymer such as GE RTV 615 (formulation), a vinyl-silane crosslinked (type) silicone elastomer (family).
  • the present systems are not limited to this one formulation, type or even this family of polymer; rather, nearly any elastomeric polymer is suitable.
  • An important requirement for the preferred method of fabrication of the present microvalves is the ability to bond multiple layers of elastomers together, hi the case of multilayer soft lithography, layers of elastomer are cured separately and then bonded together. This scheme requires that cured layers possess sufficient reactivity to bond together. Either the layers may be of the same type, and are capable of bonding to themselves, or they may be of two different types, and are capable of bonding to each other. Other possibilities include the use an adhesive between layers and the use
  • elastomeric polymers There are many, many types of elastomeric polymers. A brief description of the most common classes of elastomers is presented here, with the intent of showing that even with relatively “standard” polymers, many possibilities for bonding exist. Common elastomeric polymers include polyisoprene, polybutadiene, polychloroprene, polyisobutylene, poly(styrene-butadiene-styrene), the polyurethanes, and silicones.
  • Polyisoprene, polybutadiene, and polychloroprene are all polymerized from diene monomers, and therefore have one double bond per monomer when polymerized.
  • This double bond allows the polymers to be converted to elastomers by vulcanization (essentially, sulfur is used to form crosslinks between the double bonds by heating). This would easily allow homogeneous multilayer soft lithography by incomplete vulcanization of the layers to be bonded; photoresist encapsulation would be possible by a similar mechanism.
  • the isoprene monomers give pendant double bonds on the polyisobutylene backbone, which may then be vulcanized as above.
  • Poly(styrene-butadiene-styrene) is produced by living anionic polymerization (that is, there is no natural chain-terminating step in the reaction), so "live” polymer ends can exist in the cured polymer. This makes it a natural candidate for the present photoresist encapsulation system (where there will be plenty of unreacted monomer in the liquid layer poured on top of the cured layer). Incomplete curing would allow homogeneous multilayer soft lithography (A to A bonding). The chemistry also facilitates making one layer with extra butadiene (“A”) and coupling agent and the other layer (“B”) with a butadiene deficit (for heterogeneous multilayer soft lithography). SBS is a "thermoset elastomer", meaning that above a certain temperature it melts and becomes plastic (as opposed to elastic); reducing the temperature yields the elastomer again. Thus, layers can be bonded together by heating.
  • Polyurethanes are produced from di-isocyanates (A-A) and di-alcohols or diamines (B-B); since there are a large variety of di-isocyanates and di-alcohols/amines, the number of different types of polyurethanes is huge.
  • the A vs. B nature of the polymers would make them useful for heterogeneous multilayer soft lithography just as RTV 615 is: by using excess A-A in one layer and excess B-B in the other layer.
  • Silicone polymers probably have the greatest structural variety, and almost certainly have the greatest number of commercially available formulations.
  • the vinyl-to-(Si— H) crosslinking of RTV 615 (which allows both heterogeneous multilayer soft lithography and photoresist encapsulation) has already been discussed, but this is only one of several crosslinking methods used in silicone polymer chemistry.
  • crosslinking agents may be added. Some agents (like the monomers bearing pendant double bonds for vulcanization) are suitable for allowing homogeneous (A to A) multilayer soft lithography or photoresist encapsulation; in such an approach the same agent is incorporated into both elastomer layers. Complementary agents (i.e. one monomer bearing a pendant double bond, and another bearing a pendant Si-H group) are suitable for heterogeneous (A to B) multilayer soft lithography. In this approach complementary agents are added to adjacent layers. [0051] Other Materials:
  • polymers incorporating materials such as chlorosilanes or methyl-, ethyl-, and phenylsilanes, and polydimethylsiloxane (PDMS) such as Dow Chemical Corp. Sylgard 182, 184 or 186, or aliphatic urethane diacrylates such as (but not limited to) Ebecryl 270 or Irr 245 from UCB Chemical may also be used.
  • PDMS polydimethylsiloxane
  • elastomeric materials which may be utilized in connection with the present invention: polyisoprene, polybutadiene, polychloroprene, polyisobutylene, poly(styrene-butadiene-styrene), the polyurethanes, and silicone polymers; or poly(bis(fluoroaLkoxy)phosphazene) (PNF, Eypel-F), poly(carborane-siloxanes) (Dexsil), poly(acrylonitrile-butadiene) (nitrile rubber), poly(l-butene), poly(chlorotrifluoroethylene- vinylidene fluoride) copolymers (KeI-F), poly(ethyl vinyl ether), poly(vinylidene fluoride), poly(vinylidene fluoride-hexafluoropropylene) copolymer (Viton), elastomeric compositions of polyvin
  • Elastomers may also be "doped" with uncrosslinkable polymer chains of the same class.
  • RTV 615 may be diluted with GE SF96-50 Silicone Fluid. This serves to reduce the viscosity of the uncured elastomer and reduces the Young's modulus of the cured elastomer.
  • the crosslink-capable polymer chains are spread further apart by the addition of "inert” polymer chains, so this is called “dilution”.
  • RTV 615 cures at up to 90% dilution, with a dramatic reduction in Young's modulus.
  • doping of elastomer material may include the introduction of electrically conducting or magnetic species, as described in detail below in conjunction with alternative methods of actuating the membrane of the device.
  • doping with fine particles of material having an index of refraction different than the elastomeric material is also contemplated as a system for altering the refractive index of the material. Strongly absorbing or opaque particles may be added to render the elastomer colored or opaque to incident radiation. This may conceivably be beneficial in an optically addressable system.
  • these doped chemical species may be presented at the elastomer surface, thus serving as anchors or starting points for further chemical derivitization.
  • micro fluidic check valves of the present invention can be incorporated into devices in which fluids must be contained under various levels of pressurization. Such applications may include loading reactant solutions into a sealed reaction chamber, moving biological entities, such as cells, into a detection region of a device while preventing the backwards flow of the solution (and biological entities contained therein), or providing for the semi-permanent activation of control channels and associated structures, such as valves.
  • FIG. 1 depicts the functional process for a normally closed check valve.
  • the membrane (103) with a pore (flow channel) (104) is relaxed and the portion of the membrane containing the pore rests on the floor (109) of the bottom chamber (102).
  • the valve is closed do to the portion of the membrane surrounding the pore touching the substrate and thereby sealing the bottom chamber.
  • a forward pressure is applied, (b), the membrane is raised by the flowing liquid which then passes through the membrane pore.
  • the membrane returns to the normally close state (c).
  • reverse pressure is applied, the liquid in the top chamber (101) exerts a pressure on the membrane and the channel is closed (d). There is substantially no back flow under this condition.
  • Figure 2 depicts a fabrication process for a microfluidic check valve, hi this
  • Example, the microfluidic check valve utilized two elastomeric layers bonded to each other and attached to a substrate.
  • the substrate could be elastomeric or made of a rigid material.
  • Column A shows the fabrication of the bottom (inlet) chamber (201) and the membrane (203) with a pore (flow channel) (204).
  • Column B shows the fabrication of the top (outlet) chamber (201).
  • the fabrication of the bottom chamber begins with a photoresist lithographic process that produces a mold (220 and 225) defining a chamber with a thin membrane roof and an inlet channel (Column A (I)).
  • An uncured, liquid elastomeric compound such as polydimethylsiloxane (PDMS) is spin-layered onto the mold to evenly distribute the elastomeric liquid on the surface of the mold (Column A (2)) and the elastomeric liquid is cured or is allowed to cure.
  • the elastomer is pealed off the mold, and the mold (Column A (3)) and a hole (204) is punched in the membrane roof (203) of the bottom chamber (Column A (4)).
  • the top chamber is fabricated by a similar process, i.e.
  • the two elastomeric layers are assembled by bonding the layer defining the top chamber onto the elastomeric layer defining the bottom chamber, membrane, and pore. The layers are aligned such that the cavity defining the top chamber is aligned with the membrane roof of the bottom chamber so that sufficient membrane remains unbonded and pliable to allow actuation (5).
  • Assembly of the microfluidic check valve is completed by attachment of the bonded elastomeric structure to a substrate (carrier) by gluing or bonding the side of the elastomeric structure with the cavity defining the bottom chamber to the substrate (209) so that connections to liquid flow channels are obtained (6).
  • a flow channel defined in the carrier to make direct connection to the bottom chamber of connection to a recess in the elastomeric structure that defines an input flow channel leading to the bottom chamber.
  • Figure 3 shows the flow rates (nL/s) through the microfluidic check valves and through an open channel with no check valve.
  • forward pressure positive values
  • the flow rates increase linearly as a function of pressure.
  • Very little fluidic resistance is imposed on the flow channels by the inclusion of the check valve.
  • the check valves were prepared from PDMS with circular footprint chambers. The widths (chamber diameters) are given in Table 1. The heights of the outlet chambers were 100 urn. The heights of the inlet chambers were 15 urn.
  • Example 2 The check valves were placed in series through the use of a via that connects the upper outlet flow channel of a first check valve with the lower inlet flow channel of a second check valve. A micrograph of the two check valves connected in series is shown in Figure 4.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • General Engineering & Computer Science (AREA)
  • Dispersion Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Health & Medical Sciences (AREA)
  • Analytical Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Hematology (AREA)
  • Clinical Laboratory Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Micromachines (AREA)

Abstract

La présente invention concerne un clapet de non-retour microfluidique robuste ainsi qu'un procédé d'utilisation dudit clapet dans des dispositifs microfluidiques. Le clapet de non-retour est composé de deux chambres disposées l'une au-dessus de l'autre et séparées par une membrane contenant des pores. La membrane est composée d'un matériau élastomère et peut être configurée dans un état normalement ouvert ou normalement fermé. Le clapet de non-retour normalement ouvert peut être mise en œuvre de manière à pouvoir fixer le degré de contre-pression nécessaire pour fermer le clapet. Le mode de réalisation normalement fermé peut maintenir l'état fermé quasiment sans contre-pression. Les deux versions, normalement ouverte ou normalement fermée, sont faciles à fabriquer par des techniques de lithographie molle multicouche et peuvent conserver un fonctionnement efficace après de nombreux milliers de cycles d'ouverture et de fermeture, sans défaillance. De tels clapets de non-retour peuvent remplacer des structures de clapet actives dans des dispositifs microfluidiques et, correctement mis en œuvre, sont susceptibles de simplifier la conception, la fabrication et/ou l'utilisation de dispositifs les contenant.
EP07843872.8A 2006-10-04 2007-10-04 Clapets de non-retour microfluidiques Withdrawn EP2074341A4 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US84922306P 2006-10-04 2006-10-04
PCT/US2007/080489 WO2008043046A2 (fr) 2006-10-04 2007-10-04 Clapets de non-retour microfluidiques

Publications (2)

Publication Number Publication Date
EP2074341A2 true EP2074341A2 (fr) 2009-07-01
EP2074341A4 EP2074341A4 (fr) 2013-04-10

Family

ID=39269233

Family Applications (1)

Application Number Title Priority Date Filing Date
EP07843872.8A Withdrawn EP2074341A4 (fr) 2006-10-04 2007-10-04 Clapets de non-retour microfluidiques

Country Status (2)

Country Link
EP (1) EP2074341A4 (fr)
WO (1) WO2008043046A2 (fr)

Families Citing this family (54)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6221654B1 (en) 1996-09-25 2001-04-24 California Institute Of Technology Method and apparatus for analysis and sorting of polynucleotides based on size
US8709153B2 (en) 1999-06-28 2014-04-29 California Institute Of Technology Microfludic protein crystallography techniques
US7306672B2 (en) 2001-04-06 2007-12-11 California Institute Of Technology Microfluidic free interface diffusion techniques
US8052792B2 (en) 2001-04-06 2011-11-08 California Institute Of Technology Microfluidic protein crystallography techniques
EP2309130B1 (fr) 1999-06-28 2016-08-10 California Institute of Technology Obturateur élastomère micro-usiné et systèmes de pompe
US7459022B2 (en) 2001-04-06 2008-12-02 California Institute Of Technology Microfluidic protein crystallography
US7144616B1 (en) 1999-06-28 2006-12-05 California Institute Of Technology Microfabricated elastomeric valve and pump systems
US20050118073A1 (en) 2003-11-26 2005-06-02 Fluidigm Corporation Devices and methods for holding microfluidic devices
US7867763B2 (en) 2004-01-25 2011-01-11 Fluidigm Corporation Integrated chip carriers with thermocycler interfaces and methods of using the same
US7351376B1 (en) 2000-06-05 2008-04-01 California Institute Of Technology Integrated active flux microfluidic devices and methods
EP2299256A3 (fr) 2000-09-15 2012-10-10 California Institute Of Technology Dispositifs de flux transversal microfabriqués et procédés
EP1343973B2 (fr) 2000-11-16 2020-09-16 California Institute Of Technology Appareil et procedes pour effectuer des dosages et des criblages a haut rendement
US7691333B2 (en) 2001-11-30 2010-04-06 Fluidigm Corporation Microfluidic device and methods of using same
WO2003085379A2 (fr) 2002-04-01 2003-10-16 Fluidigm Corporation Systemes d'analyse de particules microfluidiques
EP2298448A3 (fr) 2002-09-25 2012-05-30 California Institute of Technology Intégration microfluidique à large échelle
US8220494B2 (en) 2002-09-25 2012-07-17 California Institute Of Technology Microfluidic large scale integration
US8871446B2 (en) 2002-10-02 2014-10-28 California Institute Of Technology Microfluidic nucleic acid analysis
US8828663B2 (en) 2005-03-18 2014-09-09 Fluidigm Corporation Thermal reaction device and method for using the same
US7604965B2 (en) 2003-04-03 2009-10-20 Fluidigm Corporation Thermal reaction device and method for using the same
CA2526368A1 (fr) 2003-05-20 2004-12-02 Fluidigm Corporation Procede et systeme pour dispositif microfluidique et son imagerie
US7407799B2 (en) 2004-01-16 2008-08-05 California Institute Of Technology Microfluidic chemostat
CN102680440A (zh) 2004-06-07 2012-09-19 先锋生物科技股份有限公司 用于微流体器件的光学透镜系统和方法
WO2006060748A2 (fr) 2004-12-03 2006-06-08 California Institute Of Technology Soupapes a tamis microfluidiques
EP1838431A4 (fr) 2004-12-03 2012-08-22 California Inst Of Techn Dispositifs microfluidiques a circuits de reactions chimiques
US7883669B2 (en) 2005-04-20 2011-02-08 Fluidigm Corporation Analysis engine and database for manipulating parameters for fluidic systems on a chip
WO2007033385A2 (fr) 2005-09-13 2007-03-22 Fluidigm Corporation Dispositifs et procedes de dosage microfluidique
US7815868B1 (en) 2006-02-28 2010-10-19 Fluidigm Corporation Microfluidic reaction apparatus for high throughput screening
US8055034B2 (en) 2006-09-13 2011-11-08 Fluidigm Corporation Methods and systems for image processing of microfluidic devices
US8473216B2 (en) 2006-11-30 2013-06-25 Fluidigm Corporation Method and program for performing baseline correction of amplification curves in a PCR experiment
WO2008089493A2 (fr) 2007-01-19 2008-07-24 Fluidigm Corporation Dispositifs microfluidiques d'efficacité élevée et de précision élevée et procédés
US7974380B2 (en) 2007-05-09 2011-07-05 Fluidigm Corporation Method and system for crystallization and X-ray diffraction screening
EP2280905B1 (fr) 2008-04-11 2016-07-06 Fluidigm Corporation Systèmes et procédés microfluidiques à plusieurs niveaux
WO2010011852A1 (fr) 2008-07-25 2010-01-28 Fluidigm Corporation Procédé et système de fabrication de puces fluidiques intégrées
US8617488B2 (en) 2008-08-07 2013-12-31 Fluidigm Corporation Microfluidic mixing and reaction systems for high efficiency screening
US8058630B2 (en) 2009-01-16 2011-11-15 Fluidigm Corporation Microfluidic devices and methods
US8551787B2 (en) 2009-07-23 2013-10-08 Fluidigm Corporation Microfluidic devices and methods for binary mixing
SG169918A1 (en) 2009-10-02 2011-04-29 Fluidigm Corp Microfluidic devices with removable cover and methods of fabrication and application
US9855735B2 (en) 2009-11-23 2018-01-02 Cyvek, Inc. Portable microfluidic assay devices and methods of manufacture and use
WO2013134742A2 (fr) 2012-03-08 2013-09-12 Cyvek, Inc Particules micro-tubulaires pour analyses microfluidiques et procédés de fabrication
US9759718B2 (en) 2009-11-23 2017-09-12 Cyvek, Inc. PDMS membrane-confined nucleic acid and antibody/antigen-functionalized microlength tube capture elements, and systems employing them, and methods of their use
JP5701894B2 (ja) 2009-11-23 2015-04-15 サイヴェク・インコーポレイテッド アッセイを行う方法及び装置
US10065403B2 (en) 2009-11-23 2018-09-04 Cyvek, Inc. Microfluidic assay assemblies and methods of manufacture
US10022696B2 (en) 2009-11-23 2018-07-17 Cyvek, Inc. Microfluidic assay systems employing micro-particles and methods of manufacture
US9700889B2 (en) 2009-11-23 2017-07-11 Cyvek, Inc. Methods and systems for manufacture of microarray assay systems, conducting microfluidic assays, and monitoring and scanning to obtain microfluidic assay results
US9500645B2 (en) 2009-11-23 2016-11-22 Cyvek, Inc. Micro-tube particles for microfluidic assays and methods of manufacture
WO2012054933A2 (fr) 2010-10-22 2012-04-26 Fluidigm Corporation Méthodes de dosage par sondes universelles
CN106552682B (zh) 2011-03-22 2020-06-19 西维克公司 微流体装置以及制造方法和用途
US9168531B2 (en) 2011-03-24 2015-10-27 Fluidigm Corporation Method for thermal cycling of microfluidic samples
CN108342453A (zh) 2011-05-09 2018-07-31 富鲁达公司 基于探针的核酸检测
US9644231B2 (en) 2011-05-09 2017-05-09 Fluidigm Corporation Nucleic acid detection using probes
DE102013201342A1 (de) * 2013-01-29 2014-07-31 Robert Bosch Gmbh Verfahren zum Herstellen eines normal-geschlossenen Rückschlagventils für mikrofluidische Bauteile aus einem polymeren Schichtsystem und Rückschlagventil
JP5866470B1 (ja) * 2015-05-01 2016-02-17 株式会社朝日Fr研究所 チェックバルブ及びこれを用いたマイクロ化学チップ
US10228367B2 (en) 2015-12-01 2019-03-12 ProteinSimple Segmented multi-use automated assay cartridge
ES2775876T3 (es) 2016-04-11 2020-07-28 Nat Res Council Canada Película estampada para formar blíster lleno de fluido, blíster microfluídico, y kit y método para formarla

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0587912A1 (fr) * 1992-04-02 1994-03-23 Seiko Epson Corporation Microdispositif de regulation de debit de fluide, et procede de fabrication dudit dispositif
WO2001021988A1 (fr) * 1999-09-24 2001-03-29 California Institute Of Technology Micro-clapet de non-retour normalement ferme place dans le canal
US6767194B2 (en) * 2001-01-08 2004-07-27 President And Fellows Of Harvard College Valves and pumps for microfluidic systems and method for making microfluidic systems
US20060030796A1 (en) * 2004-08-03 2006-02-09 Agency For Science, Technology And Research Method and device for the treatment of biological samples

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0587912A1 (fr) * 1992-04-02 1994-03-23 Seiko Epson Corporation Microdispositif de regulation de debit de fluide, et procede de fabrication dudit dispositif
WO2001021988A1 (fr) * 1999-09-24 2001-03-29 California Institute Of Technology Micro-clapet de non-retour normalement ferme place dans le canal
US6767194B2 (en) * 2001-01-08 2004-07-27 President And Fellows Of Harvard College Valves and pumps for microfluidic systems and method for making microfluidic systems
US20060030796A1 (en) * 2004-08-03 2006-02-09 Agency For Science, Technology And Research Method and device for the treatment of biological samples

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
See also references of WO2008043046A2 *
SHOJI S ET AL: "Microflow devices and systems", JOURNAL OF MICROMECHANICS & MICROENGINEERING, INSTITUTE OF PHYSICS PUBLISHING, BRISTOL, GB, vol. 4, no. 4, 1 December 1994 (1994-12-01), pages 157-171, XP020069428, ISSN: 0960-1317, DOI: 10.1088/0960-1317/4/4/001 *
XUAN-QI WANG ET AL.: "A Parylene Micro Check Valve", IEEE, CALIFORNIA INSTITUTE OF TECHNOLOGY, PASADENA [US], 17 January 1999 (1999-01-17), pages 177-182, XP000830743, *

Also Published As

Publication number Publication date
WO2008043046A3 (fr) 2008-08-07
EP2074341A4 (fr) 2013-04-10
WO2008043046A2 (fr) 2008-04-10

Similar Documents

Publication Publication Date Title
EP2074341A2 (fr) Clapets de non-retour microfluidiques
EP1065378B1 (fr) Systemes de micropompes et microsoupapes elastomeriques
US7144616B1 (en) Microfabricated elastomeric valve and pump systems
US7216671B2 (en) Microfabricated elastomeric valve and pump systems
US6929030B2 (en) Microfabricated elastomeric valve and pump systems
US20080277007A1 (en) Microfabricated elastomeric valve and pump systems
EP1557565B1 (fr) Système de micropompes ou soupapes flexibles
CA2767084C (fr) Obturateur elastomere micro-usine et systemes de pompe

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20090428

AK Designated contracting states

Kind code of ref document: A2

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR

AX Request for extension of the european patent

Extension state: AL BA HR MK RS

DAX Request for extension of the european patent (deleted)
A4 Supplementary search report drawn up and despatched

Effective date: 20130313

RIC1 Information provided on ipc code assigned before grant

Ipc: F16K 15/00 20060101ALI20130307BHEP

Ipc: F16K 1/00 20060101AFI20130307BHEP

17Q First examination report despatched

Effective date: 20160215

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20160628