WO2002081934A2 - Pneumatic valve interface for use in microfluidic structures - Google Patents

Pneumatic valve interface for use in microfluidic structures Download PDF

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Publication number
WO2002081934A2
WO2002081934A2 PCT/US2002/010509 US0210509W WO02081934A2 WO 2002081934 A2 WO2002081934 A2 WO 2002081934A2 US 0210509 W US0210509 W US 0210509W WO 02081934 A2 WO02081934 A2 WO 02081934A2
Authority
WO
WIPO (PCT)
Prior art keywords
microfluidic
valve
microfluidic structure
channel
altered
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.)
Ceased
Application number
PCT/US2002/010509
Other languages
English (en)
French (fr)
Other versions
WO2002081934A3 (en
WO2002081934A9 (en
Inventor
Bernard H. Weigl
Patrick Saltsman
Jon W. Hayenga
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.)
Micronics Inc
Original Assignee
Micronics Inc
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 Micronics Inc filed Critical Micronics Inc
Priority to JP2002579674A priority Critical patent/JP2005509113A/ja
Priority to EP02763925A priority patent/EP1377821A2/en
Publication of WO2002081934A2 publication Critical patent/WO2002081934A2/en
Publication of WO2002081934A9 publication Critical patent/WO2002081934A9/en
Publication of WO2002081934A3 publication Critical patent/WO2002081934A3/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • G01N1/4005—Concentrating samples by transferring a selected component through a membrane
    • G01N2001/4016—Concentrating samples by transferring a selected component through a membrane being a selective membrane, e.g. dialysis or osmosis
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N1/00—Sampling; Preparing specimens for investigation
    • G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
    • G01N1/40—Concentrating samples
    • G01N1/4055—Concentrating samples by solubility techniques
    • G01N2001/4061—Solvent extraction
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N1/00—Sampling; Preparing specimens for investigation
    • G01N1/28—Preparing specimens for investigation including physical details of (bio-)chemical methods covered elsewhere, e.g. G01N33/50, C12Q
    • G01N1/40—Concentrating samples
    • G01N1/4077—Concentrating samples by other techniques involving separation of suspended solids
    • G01N2001/4094—Concentrating samples by other techniques involving separation of suspended solids using ultrasound
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
    • G01N15/02—Investigating particle size or size distribution
    • G01N2015/0288—Sorting the particles
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
    • G01N15/10—Investigating individual particles
    • G01N15/14—Optical investigation techniques, e.g. flow cytometry
    • G01N15/1404—Handling flow, e.g. hydrodynamic focusing
    • G01N15/1409—Handling samples, e.g. injecting samples
    • G01N2015/1411—Features of sheath fluids
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
    • G01N15/10—Investigating individual particles
    • G01N15/14—Optical investigation techniques, e.g. flow cytometry
    • G01N15/1404—Handling flow, e.g. hydrodynamic focusing
    • G01N2015/1413—Hydrodynamic focussing
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
    • G01N15/10—Investigating individual particles
    • G01N15/14—Optical investigation techniques, e.g. flow cytometry
    • G01N15/1434—Optical arrangements
    • G01N2015/144—Imaging characterised by its optical setup
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N15/00—Investigating characteristics of particles; Investigating permeability, pore-volume or surface-area of porous materials
    • G01N15/10—Investigating individual particles
    • G01N15/14—Optical investigation techniques, e.g. flow cytometry
    • G01N2015/1486—Counting the particles
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
    • G01N2035/00178—Special arrangements of analysers
    • G01N2035/00237—Handling microquantities of analyte, e.g. microvalves, capillary networks
    • G01N2035/00247—Microvalves
    • 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
    • Y10T436/00—Chemistry: analytical and immunological testing
    • Y10T436/25—Chemistry: analytical and immunological testing including sample preparation
    • Y10T436/25375—Liberation or purification of sample or separation of material from a sample [e.g., filtering, centrifuging, etc.]
    • 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
    • Y10T436/00—Chemistry: analytical and immunological testing
    • Y10T436/25—Chemistry: analytical and immunological testing including sample preparation
    • Y10T436/2575—Volumetric liquid transfer

Definitions

  • This invention relates generally to microscale devices for performing analytical testing and, in particular, to a valve interface for use in laminated microfluidic structures.
  • Microfluidic devices have recently become popular for performing
  • Microfluidic devices may be constructed in a multi-layer laminated structure where each layer has channels and structures fabricated from a laminate material to form microscale voids or channels where fluids flow.
  • a microscale channel is generally defined as a fluid passage which has at least one internal cross-sectional dimension that is less than 500 ⁇ m and typically between about 0.1 ⁇ m and about 500 ⁇ m.
  • the control and pumping of fluids through these channels is affected by either external pressurized fluid forced into the laminate, or by structures located within the laminate.
  • U.S. Patent No. 5,716,852 teaches a method for analyzing the presence and concentration of small particles in a flow ceil using diffusion principles.
  • This patent discloses a channel ceil system for detecting the presence of analyte particles in a sample stream using a laminar flow channel having at least two inlet means which provide an indicator stream and a sample stream, where the laminar flow channel has a depth sufficiently small to allow laminar flow of the streams and length sufficient to allow diffusion of particles of the analyte into the indicator stream to form a detection area, and having an outlet out of the channel to form a single mixed stream.
  • This device which is known at a T-Sensor, may contain an external detecting means for detecting changes in the indicator stream.
  • This detecting means may be provided by any means known in the art, including optical means such as optical spectroscopy, or absorption spectroscopy of fluorescence.
  • optical means such as optical spectroscopy, or absorption spectroscopy of fluorescence.
  • U.S. Patent No. 5,932,100 which patent is also incorporated herein by reference, teaches another method for analyzing particles within microfluidic channels using diffusion principles.
  • a mixture of particles suspended in a sample stream enters an extraction channel from one upper arm of a structure, which comprises microchannels in the shape of an "H".
  • An extraction stream (a dilution stream) enters from the lower arm on the same side of the extraction channel and due to the size of the microfluidic extraction channel, the flow is laminar and the streams do not mix.
  • the sample stream exits as a by-product stream at the upper arm at the end of the extraction channel, while the extraction stream exits as a product stream at the lower arm. While the streams are in parallel laminar flow in the extraction channel, particles having a greater diffusion coefficient (smaller particles such as albumin, sugars, and small ions) have time to diffuse into the extraction stream, while the larger particles (blood cells) remain in the sample stream. Particles in the exiting extraction stream (now called the product stream) may be analyzed without interference from the larger particles.
  • This microfluidic structure commonly known as an "H-Filter," can be used for extracting desired particles from a sample stream containing those particles.
  • valves are commonly used for fluid management in flow systems. Flap valves, ball-in-socket valves, and tapered wedge valves are a few of the valve types existing in the macroscale domain of fluid control.
  • flow channels are often the size of a human hair (approximately 100 microns in diameter)
  • valves which are unique to microscale systems, especially microfluidic devices incorporating fluids with various concentrations of particulates in suspension.
  • Special challenges involve mixing, dilution, fluidic circuit isolation, and anti-
  • valves for use in controlling fluids in microscale
  • Biosensor AB describes a sealing device in a microfluidic channel assembly
  • Pharmacia Biosensor AB describes a valve for use in microfluidic structures in
  • U.S. Patent No. 5,932,799 which issued August 3, 1999 to YSl Incorporated, teaches a microfluidic analyzer module having a plurality of channel forming laminate layers which are directly bonded together without adhesives, with a valve containing layer directly adhesivelessly bonded over the channel containing layers and a flexible valve member integral with the valve layer to open and close communication between feed and sensor channels of the network.
  • microstructures such as valves by combining polymer spin deposition methods with semiconductor manufacturing techniques.
  • U.S. Patent No. 5, 977,355 which issued on October 26, 1999 to Xerox Corporation, describes a valve array system for microdevices based on microelectro-mechanical systems (MEMS) technology consisting of a dielectric material forming a laminate which is embedded within multiple laminate layers.
  • MEMS microelectro-mechanical systems
  • U.S. Patent No. 6,068,751 which issued on May 30, 2000, describes a microfluidic delivery system using elongated capillaries that are enclosed along one surface by a layer of malleable material which is shifted by a valve having a electrically-powered actuator.
  • It is a further object of the present invention is to provide a microfluidic valve which can be integrated into a cartridge constructed of multi-layer laminates.
  • It is a further object of the present invention is to provide an array of microfluidic valves which can be integrated into a cartridge constructed of multi- layer laminates.
  • FIG. 1 is a perspective view of a microfluidic valve according to the present invention
  • FIG. 2 is a fragmentary cross-sectional view of an alternative valve
  • FIG. 3 is a fragmentary cross-sectional view of the valve of FIG. 2 shown
  • FIG. 4 is a fragmentary top view, partly in phantom, of the valve of FIG. 2;
  • FIG. 5 is a fragmentary cross-sectional view of another alternative valve
  • FIG. 6 is a fragmentary cross-sectional view of the valve of FIG. 5 shown
  • FIG. 7 is a perspective view of an array which uses valves according to the present invention.
  • FIG. 1 A basic zero dead volume valve according to the present invention is shown in FIG. 1.
  • a valve generally indicated at 10 consists of a membrane layer 12 which covers a flat surface 13 coupled to an input channel 14, which is connected to a flow channel 16 and also an output channel 18 connected to a flow channel 20.
  • Above layer 12 is an air chamber 22 which is coupled to a pneumatic source 24 by a short air channel 26.
  • zero dead volume valve 10 works as follows: a liquid 30 enters channel 16 and travels into channel 14 where it contacts membrane layer 12. Under atmospheric conditions within air chamber 22, membrane lines flat against surface or seat 13, causing liquid 30 to stop in channel 14.
  • Valve 10 shown in FIG. 1 may operate as a zero volume valve, as it is a normally closed valve in which sufficient fluid pressure moves the membrane away from its sealing position to open with only atmospheric pressure within chamber 22.
  • pneumatic pressure within channel 24 is used to open and close valve 10. If it is desirable to keep valve 0 in its closed position, positive air pressure is applied through source 24 into channel 26, when it fills air chamber 22, which forces membrane 12 against seat 13. It has been found that applying +10 psi air pressure within source 24 will adequately keep valve 10 closed. It is desirable to open valve 10, a negative
  • Pressure from source 24 can also be varied
  • FIGS. 2-4 show an alternate embodiment in which a valve 40 is
  • diaphragm membrane 50 is held between two spacing layers 54 of a laminated
  • Valve 40 is fabricated from a series of laminar sheets 60
  • FIG. 2 is in its relaxed state, which allows liquid to enter a flow inlet
  • the liquid can flow out of valve 40 from chamber 66 through a channel 68 and
  • valve 40 Flow through valve 40 is controlled by pneumatic
  • valve air supply channel 72 which is supplied by a valve air supply channel 72 through a channel 74
  • valve 40 Operation of valve 40 is clearly shown in FIG. 3. Referring now to FIG. 3,
  • FIGS. 5 and 6 show another embodiment of the valve of the present invention.
  • a valve 80 is constructed from a pair of laminar MYLAR ® sheets 82 which are separated by a series of spacing layers 84. Channels are formed in spacing layers 84 by cutout sections which form a flow structure.
  • a flexible membrane 86 is held between two spacing layers 84 in its relaxed state.
  • a fluid input channel 90 is connected to channel 92 and to an upper chamber 94.
  • a fluid output chamber 96 is also coupled to upper chamber 94.
  • a pneumatic supply channel 98 is connected to a lower chamber 100.
  • valve 80 In its normal inactivated state, valve 80 is "on,” allowing liquid to flow from inlet 90 to outlet 96. When it is desirable to turn valve 80 “off,” sufficient air pressure is supplied to supply channel 98, filling lower chamber 100 with pressurized air and forcing membrane 86 upwardly into upper chamber 94, sealing scaling channel 92 such that the flow passage from inlet 90 to outlet 96 is blocked, closing valve 80, as can be seen in FIG. 6.
  • FIG. 7 shows an array 110 in which a plurality of valves 80 can be constructed.
  • Array 110 includes a plurality of input air ports 112 along with a plurality of input fluid ports 114.
  • Each of valves 80 can be selectively operated to control fluid flow through a microfluidic device.
  • Such an array of microfluidic valves can be integrated into a cartridge constructed of multi-layer laminates, and can be used to control multiple parallel fluidic processes, or a single process at multiple locations in a microfluidic circuit.
  • Such a system may have applications in drug discovery processes, or in the analysis of multiple samples. While the present invention has been shown and described in terms of preferred embodiments thereof, it will be understood that this invention is not limited to any particular embodiment and that changes and modifications may be made without departing from the true spirit and scope of the invention as defined in the appended claims.

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  • Chemical Kinetics & Catalysis (AREA)
  • General Engineering & Computer Science (AREA)
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  • Life Sciences & Earth Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Pathology (AREA)
  • Biochemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Fluid Mechanics (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Public Health (AREA)
  • Emergency Medicine (AREA)
  • Vascular Medicine (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Molecular Biology (AREA)
  • Urology & Nephrology (AREA)
  • Veterinary Medicine (AREA)
  • Automatic Analysis And Handling Materials Therefor (AREA)
  • Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
  • Investigating Or Analysing Biological Materials (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)
  • Sampling And Sample Adjustment (AREA)
  • External Artificial Organs (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Check Valves (AREA)
  • Multiple-Way Valves (AREA)
PCT/US2002/010509 2001-04-03 2002-04-03 Pneumatic valve interface for use in microfluidic structures Ceased WO2002081934A2 (en)

Priority Applications (2)

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JP2002579674A JP2005509113A (ja) 2001-04-03 2002-04-03 ミクロ流体構造において使用するための空気バルブ界面
EP02763925A EP1377821A2 (en) 2001-04-03 2002-04-03 Pneumatic valve interface for use in microfluidic structures

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US60/281,114 2001-04-03

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US20050205816A1 (en) 2005-09-22
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US20020148992A1 (en) 2002-10-17
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WO2002081934A9 (en) 2002-11-28
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ATE401566T1 (de) 2008-08-15
EP1377811A2 (en) 2004-01-07
US6674525B2 (en) 2004-01-06
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JP2004528556A (ja) 2004-09-16
US20020149766A1 (en) 2002-10-17
US20020172622A1 (en) 2002-11-21
US20050201903A1 (en) 2005-09-15
US20020160518A1 (en) 2002-10-31
US20020150502A1 (en) 2002-10-17

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