EP2729251A1 - Microfluidic structure having recesses - Google Patents
Microfluidic structure having recessesInfo
- Publication number
- EP2729251A1 EP2729251A1 EP12732642.9A EP12732642A EP2729251A1 EP 2729251 A1 EP2729251 A1 EP 2729251A1 EP 12732642 A EP12732642 A EP 12732642A EP 2729251 A1 EP2729251 A1 EP 2729251A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- cavity
- liquid
- region
- microfluidic structure
- depression
- 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.)
- Granted
Links
- 239000007788 liquid Substances 0.000 claims abstract description 70
- 230000007704 transition Effects 0.000 claims description 12
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 239000000523 sample Substances 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 7
- 239000008280 blood Substances 0.000 description 4
- 210000004369 blood Anatomy 0.000 description 4
- 238000001514 detection method Methods 0.000 description 3
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000005429 filling process Methods 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 239000013060 biological fluid Substances 0.000 description 1
- 239000012472 biological sample Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 239000011888 foil Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 210000003296 saliva Anatomy 0.000 description 1
- 210000002700 urine Anatomy 0.000 description 1
- 238000009423 ventilation Methods 0.000 description 1
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
- B01L3/502746—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by the means for controlling flow resistance, e.g. flow controllers, baffles
-
- 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
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
- B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
- B01L3/502738—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by integrated valves
-
- 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
- B01L2200/0642—Filling fluids into wells by specific techniques
-
- 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
- B01L2300/08—Geometry, shape and general structure
- B01L2300/0809—Geometry, shape and general structure rectangular shaped
-
- 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
- B01L2300/0848—Specific forms of parts of containers
- B01L2300/0858—Side walls
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/08—Geometry, shape and general structure
- B01L2300/0861—Configuration of multiple channels and/or chambers in a single devices
- B01L2300/0864—Configuration of multiple channels and/or chambers in a single devices comprising only one inlet and multiple receiving wells, e.g. for separation, splitting
-
- 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
- B01L2400/04—Moving fluids with specific forces or mechanical means
- B01L2400/0403—Moving fluids with specific forces or mechanical means specific forces
- B01L2400/0406—Moving fluids with specific forces or mechanical means specific forces capillary forces
-
- 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
- B01L2400/08—Regulating or influencing the flow resistance
- B01L2400/084—Passive control of flow resistance
-
- 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
- B01L2400/08—Regulating or influencing the flow resistance
- B01L2400/084—Passive control of flow resistance
- B01L2400/086—Passive control of flow resistance using baffles or other fixed flow obstructions
-
- 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
- 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
- B01L3/502753—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 bulk separation arrangements on lab-on-a-chip devices, e.g. for filtration or centrifugation
Definitions
- the invention relates to a microfluidic structure, comprising at least one cavity with at least one inlet opening and at least one outlet opening, wherein the cavity can be filled with a liquid or flowed through by a liquid and within the cavity at least one element is provided which the liquid in the flow within the cavity stops at least temporarily and / or at least partially deflects.
- Microfluidic structures are components of microfluidic platforms or
- microfluidic components and essentially comprise cavities and / or channels in which sample liquids to be examined or manipulated are taken up and by suitable means (for example capillary forces, generated pressure differences)
- the present invention encompasses microfluidic platforms such as, for example, sample carriers, test strips, biosensors, or the like, which may serve to perform individual tests or measurements.
- biological fluids eg blood, urine or saliva
- pathogens eg blood, urine or saliva
- cholesterol blood fat
- microfluidic platforms corresponding detection reactions or whole
- the biological sample liquid is transported to the appropriate reaction site or the reaction sites by suitable means.
- a transport of the sample liquid can take place, for example, by means of passive capillary forces (by means of appropriate capillary systems or microchannels) or else by means of an active actuator.
- active actuators syringe or diaphragm pumps are used, for example, which can be located outside of the microfluidic platform or even on this and build up a corresponding pressure within a microfluidic structure consisting in particular of microchannels and microcavities.
- microfluidic platforms have a sample task in the order of a few millimeters to give up a sample liquid amount on the order of a few microliters, the sample liquid (for example, blood) must be transported via a microchannel or via a microchannel system to corresponding cavities, in which, for example chemical reactants in
- Air bubbles or bubbles can form in the cavity.
- the entire volume of the cavity for the sample liquid is not available.
- stored dry substances are not sufficiently dissolved and it can lead to lump formation, whereby a desired
- Detection reaction can be affected.
- a disadvantage of this structure is that volume actually consumed within the cavity is consumed by the web-like elements.
- From DE 103 60 220 A1 is a microfluidic structure or a microfluidic
- Platform for bubble-free filling known. Concretely, there is provided a cavity, with an inlet opening and an outlet opening. In the area of the inlet opening, the Cavity microstructure elements in the form of columns on. This area forms a site with increased capillary force. Due to the increased capillary force, first a complete and air bubble-free wetting of the entrance area of the cavity with sample liquid takes place. Only then is a wetting of the outlet opening facing part of the cavity.
- a ramp is provided in the cavity, which raises the level of the cavity floor to the level of the outlet opening.
- the invention is therefore based on the object to improve a microfluidic structure according to the preamble of claim 1 such that an improved, in particular substantially air bubble-free filling, in particular of large cavities is made possible.
- the invention is therefore based on a microfluidic structure, comprising at least one cavity with at least one inlet opening and at least one outlet opening, wherein the cavity can be filled with a liquid or flowed through by a liquid and within the cavity at least one element is provided, which at the liquid whose flow within the cavity at least temporarily stops and / or at least partially deflects.
- the at least one element is formed by a depression formed in a wall of the cavity, which has at least one first region at which the liquid is stopped and / or at least partially deflected at least temporarily and at least one second region at which the liquid preferably flows into the depression.
- the liquid runs immediately upon reaching the second region, that is, without a significant stop into the depression and pulls from a certain filling level the well also in the first region of the well first stopped liquid into the recess.
- the liquid in the cavity can be controlled so that the cavity is filled evenly and substantially free of air bubbles. This is also possible with large, in particular wide and irregularly shaped cavities, which
- a filling volume in the order of about 10 ⁇ to 10 ml.
- said wall of the cavity may be, for example, a bottom of the cavity. But there are also any other walls of the cavity conceivable.
- the second region is formed by a ramp-like transition, which, starting from a bottom level of the cavity, passes over to a bottom level of the depression.
- This ramp-like transition ensures in a simple manner that the sample liquid at this point runs into the depression without a stop and fills it.
- the ramp-like transition starting from a boundary edge of the recess with a bottom plane of the cavity forms an angle of about 10 degrees to 60 degrees, more preferably of about 45 degrees.
- the second region could also be formed by a "soft" transition, for example by a convex or concave fillet, and also a notch-like structure (seen in plan view of the depression) is conceivable.
- the first region is expediently formed by a boundary edge of the depression on which the converging, forming the boundary edge Walls occupy an angle which is less than 120 degrees, preferably approximately between 95 degrees and 70 degrees, more preferably at about 90 degrees.
- the first region forms a capillary stop in a very reliable manner, at which the inflowing liquid is first stopped or deflected.
- the inflowing liquid can be controlled such that it initially reaches the first area, is stopped there, deflected and preferably reaches the second area (without a noteworthy stop) into the depression and fills it.
- the desired liquid control of the specific length of a cavity can be adjusted.
- the recess may be formed in plan view, for example, approximately rectangular. But it can also be different in plan view, for example, be arcuate. This may be expedient, for example, if the cavity to be filled is likewise curved in its longitudinal extension.
- a further advantageous embodiment of the inventive idea provides that a plurality of depressions are provided, which are arranged starting from side walls of the cavity, mutually.
- the at least one first region extends approximately over the entire length of one longitudinal side of the at least one depression and the at least one second region only over a portion of the length of another longitudinal face.
- the invention also relates to a microfluidic platform with at least one microfluidic structure according to at least one of claims 1 to 7.
- a microfluidic platform can be produced inexpensively and meets high demands on a process-reliable, in particular air bubble-free filling of the existing cavities.
- FIG. 1 shows a microfluidic structure according to a first, preferred
- FIG. 2 is a sectional view of the microfluidic structure according to section line II in Fig. 1,
- FIG. 3 is a detailed view III of Fig. 2,
- Fig. 5 shows a microfluidic structure in a plan view according to a second
- Fig. 6 shows a microfluidic structure in a plan view according to a third
- Fig. 7 shows a microfluidic structure according to the prior art
- FIG. 8 is a sectional view according to section line VIII of FIG. 7. First, reference is made to Figs. 1 to 3.
- the microfluidic structure 1 comprises a cavity 10, which has a filling volume of about 15 ⁇ .
- the cavity 10 is unevenly shaped and provided with an inlet opening 1 1, which connects the cavity 10 with a filling channel 16.
- the filling channel 16 itself may be connected to an unspecified numbering filling opening (for example, a sample task area).
- the cavity 10 is provided with an outlet opening 12 which, for example, releases the fluidic connection to a ventilation channel 17.
- a capillary stop 24 is also provided in the usual way.
- the cavity 10 may be connected via an outlet opening to a further microchannel 18 (indicated by dashed lines) if a liquid is to be transported through the cavity 10, for example into a further cavity (not shown).
- the cavity 10 is a comparatively large cavity having dimensions of about 12 mm in width, 36 mm in length and about 1.5 mm in depth.
- Each recess 13 has in plan view approximately a rectangular appearance with a length L and a width B. In this case, the recesses 13, starting from
- each depression 13 has a first region 14 which faces an inflowing liquid F (cf. FIG. 4) and at which the inflowing liquid F is at least temporarily stopped and / or at least partially deflected.
- each depression 13 is provided with a second region 15, at which an incoming liquid F runs into the depression 13 without stopping.
- the cavity 10 is closed by a cover 21 (for example, a glued foil) and has a bottom 19.
- Each recess 13 has a bottom 20. 3
- the first region 14 (capillary stop) is formed by a boundary edge 22 of the depression 13, at which the converging walls forming the boundary edge 22 occupy an angle ⁇ which is 90 degrees. Deviating from the embodiment, of course, other angles are conceivable, which may be greater or less than 90 degrees.
- the second region 15 is formed by a ramp-like transition R, which, starting from the bottom level 19 of the cavity 10, to a bottom level 20 of the recess 13 passes.
- the ramp-like transition R starting from a boundary edge 23 of the recess 13 with the bottom plane 19 of the cavity 10 forms an angle ⁇ of approximately 45 degrees. Again, angles greater or less than 45 degrees are conceivable.
- the second area 15 does not necessarily have to be formed by a ramp-like transition, but other configurations are also conceivable.
- the second region can also be formed, for example, by a "smooth" transition, for example by a concave (15 ") or convex (15" ') rounding.
- the inflowing liquid F first flows toward the first of the cavities 13 with a flow direction S (FIG. 4a).
- the liquid F is first stopped at the first region 14 or the boundary edge 22 and deflected (FIG. 4b).
- the liquid F continues to the first region 14 of the second recess 13 and thereby also to the second region 15 of the first recess 13, whereby the liquid F via the second region 15, the first recess 13 fills (see dashed lines indicated arrow in Fig. 4c ).
- the liquid F is then stopped and deflected again at the first region 14 of the second depression 13, and the cavity 10 is completely filled initially, leaving the second depression 13 (see FIG. 4d).
- the second depression 13 is also filled via the second region 15 (ramp-like transition R).
- the liquid front of the liquid F now extends to the first region 14 of the last depression 13 (FIG. 4e).
- the liquid F is again initially stopped and deflected until it subsequently reaches the second region 15 of the last depression 13 and, starting there, fills it.
- the filling process extends to the capillary stop 24 in the region of the outlet opening 12 and essentially takes place without air inclusions (air bubbles) (compare FIG. 4f).
- the second region 15 does not extend over the entire length L of a depression 13, but only constitutes part of this length. Furthermore, the region 15 also assumes a width which is significantly smaller than the width B of the entire depression 13. In particular, the width of the region 15 is preferably less than half the width B of the depression 13. This makes it possible, with sufficient filling function Area 15 well exploit the volume of the recess 13.
- FIG. 5 shows a second exemplary embodiment 3 for a microfluidic structure of a microfluidic component 4.
- the microfluidic structure 3 comprises a cavity 30, with Each recess 31 is in turn equipped with a first region 32 in the form of a stop edge (capillary stop), which faces the flow direction S of an inflowing liquid.
- a second region 33 in the form of a ramp is again provided on the longitudinal side of the depression 31 facing away from an inflowing liquid, the region 33 extending over an entire length L of the depression 31.
- the width of the region 33 is in turn only about a maximum of half a width B of the recess 31. Also in this
- Embodiment is mimicked by the mutual arrangement of the recesses 31, a meandering flow of an incoming liquid.
- a microfluidic structure 5 can be seen on a microfluidic component 6, which (in contrast to the preceding exemplary embodiments) has a curved cavity 40 viewed in the inflow direction S of a liquid.
- each recess 41 has a longitudinal extent L and extends over this length L curved. Furthermore, it can be seen that each depression 41 is in turn provided with a first region 42 in the form of a stop edge (comparable to region 14 of the first embodiment) and on the longitudinal side facing away from an inflowing liquid, each having two regions 43 in the form of a ramp (comparable to FIG the area 15 in the first embodiment).
- a microfluidic structure 7 of a microfluidic component 8 can be seen, in which, within a cavity 50 unlike the embodiments according to the invention, no depressions, but webs 51 are attached.
- the webs 51 starting from longitudinal sides of the cavity 50, are mutually arranged and intended to meander a flow of an inflowing liquid (not shown) and thus enable a largely bubble-free filling of the cavity 50.
- the webs 51 extend from a bottom 53 of the cavity 50 starting up to a cavity 50 upwards final cover 52 zoom.
Landscapes
- 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)
- Physical Or Chemical Processes And Apparatus (AREA)
- Micromachines (AREA)
Abstract
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP12732642.9A EP2729251B1 (en) | 2011-07-05 | 2012-07-02 | Microfluid structure with cavities |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP11172775 | 2011-07-05 | ||
PCT/EP2012/062863 WO2013004673A1 (en) | 2011-07-05 | 2012-07-02 | Microfluidic structure having recesses |
EP12732642.9A EP2729251B1 (en) | 2011-07-05 | 2012-07-02 | Microfluid structure with cavities |
Publications (2)
Publication Number | Publication Date |
---|---|
EP2729251A1 true EP2729251A1 (en) | 2014-05-14 |
EP2729251B1 EP2729251B1 (en) | 2018-11-14 |
Family
ID=44773214
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP12732642.9A Not-in-force EP2729251B1 (en) | 2011-07-05 | 2012-07-02 | Microfluid structure with cavities |
Country Status (4)
Country | Link |
---|---|
US (2) | US20140227148A1 (en) |
EP (1) | EP2729251B1 (en) |
JP (1) | JP6098020B2 (en) |
WO (1) | WO2013004673A1 (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP3083054A2 (en) | 2013-12-20 | 2016-10-26 | 3M Innovative Properties Company | Systems and methods for sample concentration and detection |
WO2015184343A1 (en) * | 2014-05-30 | 2015-12-03 | Absolute Exhibits, Inc. | Thermoset in-mold finishing film |
TWI499637B (en) * | 2014-06-20 | 2015-09-11 | Ind Tech Res Inst | Foam body and light emitting device with thereof |
GB201617869D0 (en) | 2016-10-21 | 2016-12-07 | Blacktrace Holdings Limited | A microfluidic device |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4271119A (en) * | 1979-07-23 | 1981-06-02 | Eastman Kodak Company | Capillary transport device having connected transport zones |
US4618476A (en) * | 1984-02-10 | 1986-10-21 | Eastman Kodak Company | Capillary transport device having speed and meniscus control means |
DE10313201A1 (en) * | 2003-03-21 | 2004-10-07 | Steag Microparts Gmbh | Microstructured separator and microfluidic process for separating liquid components from a liquid containing particles |
DE10360220A1 (en) | 2003-12-20 | 2005-07-21 | Steag Microparts Gmbh | Fine structure arrangement in fluid ejection system, has predetermined region in transitional zone between inlet and discharge ports, at which capillary force is maximum |
DE102004027422A1 (en) * | 2004-06-04 | 2005-12-29 | Boehringer Ingelheim Microparts Gmbh | Device for receiving blood and separating blood components |
EP1616619A1 (en) * | 2004-07-17 | 2006-01-18 | Tecan Trading AG | Device and method to influence air bubbles in a hybridizaion chamber |
ATE503578T1 (en) * | 2005-01-27 | 2011-04-15 | Boehringer Ingelheim Micropart | USE OF A DEVICE FOR EXAMINING SAMPLE FLUID |
DE102005017653A1 (en) * | 2005-04-15 | 2006-10-19 | Boehringer Ingelheim Microparts Gmbh | Device and method to control liquid flow has two sections of channel whereby liquid flows from one to the other and can be held at first section using capillary stop and said stop can be bypassed if wished by moving sections |
JP4685611B2 (en) * | 2005-12-02 | 2011-05-18 | 株式会社エンプラス | Microfluidic device |
-
2012
- 2012-07-02 JP JP2014517765A patent/JP6098020B2/en active Active
- 2012-07-02 US US14/127,341 patent/US20140227148A1/en not_active Abandoned
- 2012-07-02 WO PCT/EP2012/062863 patent/WO2013004673A1/en active Application Filing
- 2012-07-02 EP EP12732642.9A patent/EP2729251B1/en not_active Not-in-force
-
2015
- 2015-05-22 US US14/719,503 patent/US9409171B2/en not_active Expired - Fee Related
Non-Patent Citations (1)
Title |
---|
See references of WO2013004673A1 * |
Also Published As
Publication number | Publication date |
---|---|
US20140227148A1 (en) | 2014-08-14 |
JP6098020B2 (en) | 2017-03-22 |
US9409171B2 (en) | 2016-08-09 |
JP2014521056A (en) | 2014-08-25 |
EP2729251B1 (en) | 2018-11-14 |
US20150251182A1 (en) | 2015-09-10 |
WO2013004673A1 (en) | 2013-01-10 |
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