EP2559488A1 - Contrôle de l'écoulement d'un fluide dans un système microfluidique - Google Patents

Contrôle de l'écoulement d'un fluide dans un système microfluidique Download PDF

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Publication number
EP2559488A1
EP2559488A1 EP11191919A EP11191919A EP2559488A1 EP 2559488 A1 EP2559488 A1 EP 2559488A1 EP 11191919 A EP11191919 A EP 11191919A EP 11191919 A EP11191919 A EP 11191919A EP 2559488 A1 EP2559488 A1 EP 2559488A1
Authority
EP
European Patent Office
Prior art keywords
microfluidic system
sample fluid
cartridge
port
venting
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
EP11191919A
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German (de)
English (en)
Inventor
designation of the inventor has not yet been filed The
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.)
Koninklijke Philips NV
Original Assignee
Koninklijke Philips Electronics NV
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 Koninklijke Philips Electronics NV filed Critical Koninklijke Philips Electronics NV
Priority to PCT/IB2012/053788 priority Critical patent/WO2013024381A1/fr
Publication of EP2559488A1 publication Critical patent/EP2559488A1/fr
Ceased legal-status Critical Current

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Classifications

    • 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
    • B01L3/502723—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 venting arrangements
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/06—Fluid handling related problems
    • B01L2200/0621—Control of the sequence of chambers filled or emptied
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
    • B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
    • B01L2200/06—Fluid handling related problems
    • B01L2200/0684—Venting, avoiding backpressure, avoid gas bubbles
    • 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
    • B01L2300/04—Closures and closing means
    • B01L2300/041—Connecting closures to device or container
    • B01L2300/044—Connecting closures to device or container pierceable, e.g. films, membranes
    • 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
    • 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
    • B01L2400/0688—Valves, specific forms thereof surface tension valves, capillary stop, capillary break

Definitions

  • the invention relates to a method, a cartridge, an apparatus, and a sample processing system with means for controlling the flow of a sample fluid.
  • the WO 2010/070521 A1 discloses a sensing device which comprises an inlet port, a channel leading to a measurement chamber, and a venting hole. As the venting hole is initially closed by a foil, capillary flow of sample fluid stops in the channel before the measurement chamber is reached. Only after the foil is punctured, fluid flow can proceed and the sample reaches the measurement chamber.
  • the invention relates to a cartridge that comprises a microfluidic system for processing a sample fluid.
  • microfluidic system shall denote a system or set of connected cavities or chambers housed within some substrate, wherein the dimensions (diameters) of these cavities or chambers are typically in the range of 0.1 ⁇ m to 1000 ⁇ m. Due to the small dimensions, the movement of fluids inside a microfluidic system is usually dominated by capillary forces.
  • the sample fluid that is processed may be any fluid of interest, particularly a fluid of biological origin like blood, saliva or urine in which certain target components shall be detected.
  • the cartridge is typically a separate component of its own, though it may optionally also be firmly integrated into some apparatus, for example a sensor apparatus.
  • the cartridge will be a low-cost disposable component made for example from plastic by injection molding, and it is used only once for the processing of a single sample.
  • the cartridge comprises the following components:
  • venting port shall denote a connection of the microfluidic system to the outside that is initially closed (usually in an airtight manner). Moreover, the venting port is arranged at a position remote from the inlet port such that it is connected to the compartment of the microfluidic system in which trapped air resides. Accordingly, this air - but not sample fluid - will pass through the venting port after its opening.
  • the opening of the venting port may be complete or optionally be graded. Moreover, it may optionally be possible to close the venting port again after the opening.
  • the microfluidic system may have several branches, i.e. interior compartments with associated venting ports such that the selective opening of a venting port affects only the associated interior compartment.
  • the invention relates to a cartridge that comprises a microfluidic system for processing a sample fluid, particularly a cartridge of the kind described above.
  • the second cartridge shall comprise the following components:
  • the invention relates to an apparatus for processing a sample fluid in a cartridge of the kind described above, said apparatus comprising an opening actuator that can open the venting control element of the cartridge.
  • the invention further relates to a sample processing system comprising a cartridge of the kind described above and an apparatus of the kind described above, wherein the opening actuator of the apparatus can open the venting control element of the cartridge.
  • the cartridge and the apparatus may be combined into one integrated device, though they will typically be components of their own that can temporarily be put together for the processing of a sample.
  • the invention relates to a method for processing a sample fluid in a microfluidic system.
  • the method comprises the following steps:
  • the method, the cartridge, the apparatus, and the sample processing system are related embodiments of the present invention. Explanations given for one of these embodiments therefore hold analogously for the other embodiments, too.
  • a microfluidic system which can be filled in two steps, namely (i) by the provision of a sample fluid at (at least) one inlet port, and (ii) by the opening of a venting port.
  • This combination of two independent steps allows for a better control of the filling process and hence the assay that is executed in the microfluidic system.
  • the filling of the interior compartment of the microfluidic system can be started at a well defined point in time.
  • the provision of a fluidic stop unit in front of the venting port has the advantage that sample fluid cannot reach the venting port. Hence it cannot be spilled out of the venting port or contact instruments in the venting port (e.g. a needle puncturing a sealing foil). This is a considerable advantage as it safeguards the reader instruments in which the cartridge is processed from a contamination with sample.
  • the optional inlet closure of the inlet port has the advantage that the microfluidic system is protected during the storage of the cartridge. In particular, sensitive (e.g. hygroscopic) reagents are thus protected from humidity. Hence there is no need to store the complete cartridge in a sealed container and/or a dried atmosphere.
  • the microfluidic system comprises a sample chamber in which the sample fluid can be processed and a channel that connects said sample chamber to the inlet port.
  • the channel will typically have dimensions that are as small as possible in order to minimize its (dead) volume; it must however be long enough to connect the inlet port to the sample chamber and have a diameter that allows a sufficient fluid flow (by capillary forces).
  • the dimensions of the sample chamber are usually larger (and more compact) according to the requirements of the intended processing of the sample fluid.
  • a typical volume of the sample chamber ranges from about 0.1 ⁇ l to about 1 ⁇ l.
  • the microfluidic system is designed such that the sample fluid introduced at the inlet port will not reach the sample chamber while the venting port is closed. Driven by capillary forces, sample fluid introduced at the inlet port will advance along the channel until the counter-pressure that is built up by the compression of the captured air will balance the driving force. While the magnitude of the capillary forces is primarily determined by the dimensions of the channel and by its surface material, the buildup of air pressure is mainly controlled by the size of the air volume in the microfluidic system. Hence there are two separate sets of parameters that can independently be adjusted to achieve the desired design of the microfluidic system. It should be noted that the capillary forces are determined by the interaction between the interior surface of the microfluidic system and the sample fluid at hand. Accordingly, different designs may be found for the processing of different given sample fluids. To give an example, the design process may be executed with an aqueous fluid (e.g. pure water) as given sample fluid.
  • an aqueous fluid e.g. pure water
  • venting control element and the inlet closure can be realized in many different ways, including the designs of microfluidic valves that are known in the state of the art (cf. J. C. T. Eijkel, "The use of capillarity for passive flow handling in lab on chip devices", Lab on Chip (2006), 6, 1405-1408 ; Kwang, W Oh and Chong H Ahn, "A review of microvalves", J. Micromech. Microeng., 16 (2006), R13-R39 ).
  • the venting control element or the inlet closure comprises an element that can be moved between a position in which it closes the port and a position in which it opens the respective port.
  • Said element may for example be a cap that is glued to or snapped into the port and that can completely be removed, or by a slider that is attached to the cartridge such that it is linearly or rotationally movable.
  • the venting control element and/or the inlet closure comprises a layer or sheet of material, called “foil” in the following, that (initially) closes the venting or inlet port and that can be disrupted or moved to open the port.
  • foil a layer or sheet of material, called “foil” in the following, that (initially) closes the venting or inlet port and that can be disrupted or moved to open the port.
  • a foil that can be disrupted can be realized very cost-effectively and is particularly suited for a disposable cartridge that shall be used only once.
  • the foil can be disrupted or moved by a mechanical, chemical, thermal, optical, and/or electromagnetic operation.
  • a mechanical operation may for instance comprise piercing of the foil by some tip or blade, or pushing of the foil by some plunger.
  • a chemical operation may comprise the dissolution of the foil by a chemical reagent.
  • a thermal operation and an optical operation may comprise the melting of the foil by heat or irradiation.
  • An electromagnetic operation may comprise the movement of the foil (from a closed to an open position) by electrical and/or magnetic forces.
  • the above-mentioned foil may optionally comprise magnetic or magnetizable components, for example ferromagnetic particles. Integration of such components into the foil allows to move the whole foil controllably by magnetic forces.
  • the foil may comprise an integrated electrical wire that can externally be contacted by an electrical circuit. A current can then for example be passed through the wire by said circuit, leading to a heating and finally a melting of the foil.
  • the fluidic stop unit can be realized in many different ways. According to one embodiment, it comprises a channel structure constituting an obstacle or barrier that stops the (capillary) flow of the sample fluid.
  • the obstacle or barrier may for example comprise a sharp edge or a sudden enlargement of the channel (i.e. a chamber) where fluid flow is interrupted.
  • the fluidic stop unit comprises a surface coating on the interior wall of the microfluidic system that repels the sample fluid.
  • the surface coating may for example be hydrophobic.
  • the fluidic stop unit may comprise a gas-permeable but liquid-tight element that allows the passage of air but not of a liquid sample.
  • the opening actuator comprises an instrument for piercing a foil, i.e. for mechanically disrupting it.
  • the opening actuator may comprise a heating unit for melting a foil, thus thermally disrupting it.
  • the opening actuator may comprise a light source for irradiating a foil, which will typically also lead to the destruction of the foil (e.g. by melting).
  • the opening actuator may comprise a magnet, for instance an electromagnet, for exerting magnetic forces on a venting control element. These forces may for example move a foil and/or disrupt it.
  • the processing of a sample fluid in the microfluidic system may comprise any manipulation that is of interest in an application at hand, for example a physical or chemical transformation of the sample material.
  • the processing of the sample fluid may comprise the carrying out of a measurement with the sample fluid in the microfluidic system. This measurement may for example comprise the qualitative or quantitative detection of target components in the sample fluid.
  • the apparatus may particularly comprise an appropriate sensor unit for such measurements.
  • the sample fluid may advance into the microfluidic system and fill it, typically driven by capillary forces.
  • This provides a definite starting point for processing steps with a critical timing. Accordingly, the processing of the sample fluid is preferably started with respect to this definite point in time, i.e. immediately after or a definite time interval after the opening of the venting port.
  • the method of the invention may particularly comprise that the sample fluid is first introduced into the microfluidic system of the cartridge (step a), that the cartridge is then inserted into an apparatus, and that the venting port is thereafter opened (step b). The sample fluid may then be processed, particularly while the cartridge is still in the apparatus.
  • the venting port may be opened just once, for example if the venting control element is realized by a foil that has to be disrupted to open the venting port.
  • the venting port may be opened and closed at least once, for example if the venting control element is realized by a controllable microvalve.
  • the opening may have just two states, i.e. "open” and “closed”, or it may have a plurality or continuum of opening degrees, for example "closed", “half open”, and “completely open”.
  • the opening and closing and/or the degree of opening of the venting port (or of the venting control element, respectively) may preferably be controlled to achieve a desired flow in the cartridge.
  • the venting control element may for example be partially opened to allow a slow progression of the sample fluid into a first sample chamber, then be closed to allow the processing of the sample in said first sample chamber, then be fully reopened to allow a fast progression of the sample fluid into a next sample chamber etc.
  • the detection of disease markers based on immuno-chemistry and using (para)magnetic beads is based on kinetic readout of the biochemical assay signal.
  • the detection happens in a kinetic regime of the assay, not in a saturated or steady state regime. Therefore, timing/start of the assay is crucial for the process of (quantitative) detection.
  • the start and timing of the assay may be installed as follows: a) an empty cartridge is inserted in the detection unit, b) calibration is performed, c) fluid is administered manually by the user to the cartridge, i.e. cartridge is sticking out of detection unit, d) visual detection with a CMOS camera is used to see/determine the moment of fluid filling of reaction chambers. This is the actual start of the assay.
  • FIG. 1 depicts a top view of a microfluidic cartridge 100 showing an injection molded part 101.
  • a microfluidic system 110 is formed in the molded part 101.
  • This microfluidic system 110 comprises a fluid inlet port 111 which is initially sealed by an inlet closure (foil) 140 and from which a fluid capillary channel 112 leads to two sample chambers 113. Downstream of the reaction chambers, air venting channels 114 are visible that terminate in an air venting port 115.
  • a sample fluid is transported inside the cartridge 100 using capillary flow.
  • the air present in the fluid channels has to be able to exit the channels, i.e. air venting. If the air is not able to exit, air pressure will build up counteracting the capillary forces transporting the fluid inwards.
  • the cartridges are used in a bench top instrument and cartridges are handled not by the user but by the instrument.
  • the cartridges need to have small dimensions, and they are completely inserted into the detection unit. Therefore, fluid has to be administered to the cartridge before the moment of inserting into the detection unit. This makes determining the start of the assay less controlled.
  • Cartridges are usually provided with sensitive reagents, for example with hygroscopic chemicals that have to be shielded from humidity. This requires elaborate means for storing cartridges before use.
  • FIG. 2 schematically shows a side view of the cartridge 100 according to the present invention in a cross section along line II-II of Figure 1 .
  • a single sided adhesive foil 102 is attached to the bottom side of the injection molded plastic part 101 of the cartridge 100.
  • the microfluidic system 110 is formed with the following components:
  • the microfluidic system 110 is closed in an airtight manner from the bottom side by the foil 102.
  • a region of this foil that closes the venting port 115 constitutes a "venting control element" 120 as will be explained in more detail below.
  • FIG. 2 shows the cartridge 100 in a first stage of sample processing, in which the inlet closure foil 140 has been partially torn open such that a sample fluid S can be introduced into the inlet port 111.
  • the sample fluid advances into the adjacent channel 112 driven by capillary forces.
  • the air that initially fills the microfluidic system is trapped in the sample chamber 113, the venting channels 114, and the (rest of the) channel 112.
  • this captured air is compressed, resulting in the buildup of a counter-pressure p.
  • Figure 3 shows the stage when the aforementioned counter-pressure p is large enough to balance the capillary forces. Accordingly, the advancement of the sample fluid S has comes to a rest.
  • FIG 4 shows the next stage in which the cartridge 100 has been inserted into an associated (sensor) apparatus 150 for processing of the sample fluid.
  • the apparatus 150 comprises a means 151 for processing the sample fluid in the sample chamber 113 when the latter is disposed above it.
  • This processing may particularly comprise the detection of target components in the sample fluid, for example of target molecules labeled with magnetic particles.
  • a sensor unit 151 for this detection may for example comprise a magnetic sensor according to the WO 2005/010543 A1 or WO 2005/010542 A2 , or it may comprise optical elements for detecting target components by frustrated total internal reflection (FTIR) as described in the WO 2008/155716 .
  • FTIR frustrated total internal reflection
  • the apparatus 150 further comprises an "opening actuator", here realized by a needle 152, that can controllably be moved up and down, for example with the help of an electromagnet (not shown).
  • the needle 152 is disposed in an outlet channel 153 that leads to the atmosphere or into some gas reservoir (not shown). In the shown stage of the process, the needle 152 has just been lifted up and punctured the "venting control unit" 120 of the foil 102 to open the venting port 115.
  • Figure 5 shows the next step of the procedure, in which the needle 152 has been retracted.
  • the captured air in the microfluidic system can now escape through the venting channel 114, the venting port 115, the hole in the foil 102, and the outlet channel 153.
  • the sample fluid S can therefore advance and fill the sample chamber 113. After this, the measurements in the sample chamber 113 can start.
  • the Figures further show a fluidic stop unit 130 that is disposed (in the venting channels 114) between the sample chambers 113 and the venting port 115.
  • This fluidic stop unit 130 may for example be realized by a hydrophobic coating of the interior walls of the microfluidic system, or by a waterproof but air-permeable material (e.g. Gore-Tex®) that fills the channel.
  • the Figures illustrate a simple, exemplary embodiment of the invention, in which the air vent is closed by a foil at the bottom of the cartridge.
  • the air pressure build up during fluid filling will ensure not filling the reaction chambers.
  • simply piercing the foil enables air venting and thus reduction of air pressure and renewed liquid propagation.
  • mechanical piercing of the foil can be done using a needle actuated by the processing system (instrument) while the cartridge is situated in the detection apparatus.
  • a typical process flow may contain the following steps:
  • foil, inlet port opening and air vent opening could be:
  • the inlet port (111) on the same side as the venting port 115 (e.g. the bottom side with respect to Figures 2-5 ).
  • the same foil (102) can be used to cover both the inlet and the venting port. This foil could be precut between the inlet port and the venting port in order to allow separate removal of the foil from the inlet port without affecting it at the venting port.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Analytical Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Hematology (AREA)
  • Clinical Laboratory Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Automatic Analysis And Handling Materials Therefor (AREA)
EP11191919A 2011-08-18 2011-12-05 Contrôle de l'écoulement d'un fluide dans un système microfluidique Ceased EP2559488A1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PCT/IB2012/053788 WO2013024381A1 (fr) 2011-08-18 2012-07-25 Régulation de l'écoulement d'un fluide dans un système microfluidique

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201161524896P 2011-08-18 2011-08-18

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EP2559488A1 true EP2559488A1 (fr) 2013-02-20

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9739714B2 (en) * 2012-10-29 2017-08-22 Mbio Diagnostics, Inc. Particle identification system, cartridge and associated methods
EP3089823A4 (fr) * 2013-12-31 2017-12-20 Canon U.S. Life Sciences, Inc. Système microfluidique à premiers résultats rapides de petit format pouvant être déployé sur le terrain
JP2018036209A (ja) * 2016-09-01 2018-03-08 山梨県 マイクロ流体デバイス
US10114020B2 (en) 2010-10-11 2018-10-30 Mbio Diagnostics, Inc. System and device for analyzing a fluidic sample
CN114700127A (zh) * 2022-06-07 2022-07-05 至美时代生物智能科技(北京)有限公司 一种芯片

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10258984B2 (en) 2014-06-16 2019-04-16 Koninklijke Philips N.V. Cartridge for fast sample intake

Citations (8)

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US5230866A (en) * 1991-03-01 1993-07-27 Biotrack, Inc. Capillary stop-flow junction having improved stability against accidental fluid flow
WO2005010543A1 (fr) 2003-07-30 2005-02-03 Koninklijke Philips Electronics N.V. Dispositif du type capteur magnetique monte sur puce et caracterise par une suppression de la diaphonie
WO2005010542A2 (fr) 2003-07-30 2005-02-03 Koninklijke Philips Electronics N.V. Detecteur de particules magnetiques monte sur puce et caracterise par un rsb ameliore
US7316802B2 (en) * 2002-11-14 2008-01-08 Boehringer Ingelheim Microparts Gmbh Device for the stepwise transport of liquid utilizing capillary forces
US20080190220A1 (en) * 2004-12-23 2008-08-14 Oktavia Backes Novel Microfluidic Sample Holder
US20080257754A1 (en) * 2003-06-27 2008-10-23 Pugia Michael J Method and apparatus for entry of specimens into a microfluidic device
WO2008155716A1 (fr) 2007-06-21 2008-12-24 Koninklijke Philips Electronics N. V. Dispositif de détecteur microélectronique pour détecter des particules de marqueur
WO2010070521A1 (fr) 2008-12-18 2010-06-24 Koninklijke Philips Electronics N.V. Dispositif de mesure pour mesurer un fluide

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US5230866A (en) * 1991-03-01 1993-07-27 Biotrack, Inc. Capillary stop-flow junction having improved stability against accidental fluid flow
US7316802B2 (en) * 2002-11-14 2008-01-08 Boehringer Ingelheim Microparts Gmbh Device for the stepwise transport of liquid utilizing capillary forces
US20080257754A1 (en) * 2003-06-27 2008-10-23 Pugia Michael J Method and apparatus for entry of specimens into a microfluidic device
WO2005010543A1 (fr) 2003-07-30 2005-02-03 Koninklijke Philips Electronics N.V. Dispositif du type capteur magnetique monte sur puce et caracterise par une suppression de la diaphonie
WO2005010542A2 (fr) 2003-07-30 2005-02-03 Koninklijke Philips Electronics N.V. Detecteur de particules magnetiques monte sur puce et caracterise par un rsb ameliore
US20080190220A1 (en) * 2004-12-23 2008-08-14 Oktavia Backes Novel Microfluidic Sample Holder
WO2008155716A1 (fr) 2007-06-21 2008-12-24 Koninklijke Philips Electronics N. V. Dispositif de détecteur microélectronique pour détecter des particules de marqueur
WO2010070521A1 (fr) 2008-12-18 2010-06-24 Koninklijke Philips Electronics N.V. Dispositif de mesure pour mesurer un fluide

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Title
J. C. T. EIJKEL: "The use of capillarity for passive flow handling in lab on chip devices", LAB ON CHIP, vol. 6, 2006, pages 1405 - 1408
KWANG, W OH; CHONG H AHN: "A review of microvalves", J. MICROMECH. MICROENG., vol. 16, 2006, pages R13 - R39, XP020105009, DOI: doi:10.1088/0960-1317/16/5/R01

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10114020B2 (en) 2010-10-11 2018-10-30 Mbio Diagnostics, Inc. System and device for analyzing a fluidic sample
US9739714B2 (en) * 2012-10-29 2017-08-22 Mbio Diagnostics, Inc. Particle identification system, cartridge and associated methods
EP3089823A4 (fr) * 2013-12-31 2017-12-20 Canon U.S. Life Sciences, Inc. Système microfluidique à premiers résultats rapides de petit format pouvant être déployé sur le terrain
JP2018036209A (ja) * 2016-09-01 2018-03-08 山梨県 マイクロ流体デバイス
CN114700127A (zh) * 2022-06-07 2022-07-05 至美时代生物智能科技(北京)有限公司 一种芯片
CN114700127B (zh) * 2022-06-07 2022-08-05 至美时代生物智能科技(北京)有限公司 一种芯片

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