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
  • B01L3/502715—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 interfacing components, e.g. fluidic, electrical, optical or mechanical interfaces
• • 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
  • B01L3/502769—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 multiphase flow arrangements
  • B01L3/502776—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 multiphase flow arrangements specially adapted for focusing or laminating flows
• • 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
  • B01L2300/0829—Multi-well plates; Microtitration plates
• • 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
  • 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
  • B01L2300/0867—Multiple inlets and one sample wells, e.g. mixing, dilution
• • 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
  • B01L2300/089—Virtual walls for guiding liquids

Definitions

• the invention relates to a microfluidic device.
• Microfluidic devices allow the analysis of small sample volumes with high sensitivity, automation, miniaturization and parallelization. Manual processing steps can be avoided by microfluidic systems. Sample analysis becomes more accurate, more reproducible, and less error-prone. Sample analysis becomes cheaper and faster.
• a very important problem in microfluidic systems is to move small amounts of sample as automated as possible to given locations in order to make them react, to analyze and to carry out other further process steps. This should be done as far as possible without manual steps, so that on the one hand the cost of processing the samples is reduced and on the other hand error causes are minimized, which often occur by manual steps.
• microfluidic device and a method for operating a microfluidic device are described, which allow an accurate and automated placement of samples and which are very useful in the context of automated processing of microfluidic samples.
• a microfluidic device with a chamber, in which two opposite sides in a first direction to produce a laminar flow in the first direction is provided in each case a first distributor, each of the first distributor each having at least one branch point at which a channel is divided into at least two channels, wherein the at least one branch point of the first distributor is arranged such that a first Connection channel is connected via the first manifold to a plurality of first terminals of the chamber.
• the microfluidic device serves to create within the chamber a very accurate and precise laminar and parallel flow.
• the fluid flow provided at the first port is evenly distributed to the first ports.
• the first connections are particularly preferably distributed uniformly over the cross section of the chamber or over the first side and the second side.
• the branches are designed so that flow differences do not occur at the first ports.
• Each first port on the first page can be assigned an exactly opposite first port on the second side.
• the flow inside the chamber is generated exactly uniformly over all the first connections and flows through the chamber in parallel.
• the flow rate of the flow is set so that the flow conditions are laminar at all times. Vibrations or any other disturbances which may influence the laminar flow are avoided by suitable measures (for example a corresponding mounting of the device) in order to maintain the laminar flow conditions at all times.
• the flow in the chamber is adjusted so that the maximum possible disturbances of the flow do not lead to a resolution of the laminarity of the flow.
• branches there are a plurality of branches between the first connection channel and the first connections.
• the connection channel branches in each branch into exactly two subchannels.
• branches preferably exist in three levels. First, a first branch on two channels, then a second branch with two branches on four connecting channels and then a third branch level with four branches on the eight said connections. For 16 first connections exist Accordingly, four branch levels with a total of 15 individual branches, which are divided according to the individual branch levels. By this type of branching can be ensured that the fluid flow is divided exactly at its junction in each case and so a particularly uniform laminar flow is generated within the chamber.
• the construction of branches on two channels can be designed so that the distribution of the liquid on both channels is exactly equal.
• the described microfluidic device allows a special form of parallelization. Due to the very exact laminar flow, samples in the chamber can be moved very precisely. For this purpose, a fluid pressure is applied to one of the first connection channels or a pressure difference is generated between the two first connection channels. This pressure difference drives the fluid flow in the chamber, which runs exactly parallel in the chamber. If the liquid flow is maintained for a certain period of time and at a certain level, the sample continues to move exactly a predetermined distance.
• the procedure for moving samples with the device differs drastically from known mechanical robotic arms in order to move samples.
• Such known devices for moving samples always require a mechanism.
• microfluidic device for transporting samples it has hitherto always been possible to convey all the samples simultaneously in a region which is not discreetly separated by walls.
• the microfluidic device described makes it possible to carry out an individual control of samples which are freely movable in a non-walled space or the chamber described here.
• the microfluidic device is particularly advantageous when a second distributor is provided in each case at two sides opposite to each other in a second direction from the first direction for generating a laminar flow in the second direction, wherein each of the second distributor each has at least one Branching point at which a channel is divided into at least two channels, wherein the at least one branch point of the second manifold is arranged such that a second connection channel is connected via the second manifold to a plurality of second terminals of the chamber.
• the arrangement of second ports of the chamber makes it possible to move samples in a different direction than is possible via the first ports.
• the first direction and the second direction are perpendicular to each other (at an angle of 90 °).
• At least one pump is provided which is connected via a first valve to one of the first distributor and via a second valve to one of the second distributor or can be connected.
• the pump is preferably designed to generate a defined pressure gradient, which (with an open valve) leads to a defined flow within the chamber.
• both the first connection channels or the first distributor and the second connection channels or the second Distributor are controlled. Then only one pump is necessary to provide the necessary liquid pressures for the laminar flows in the chamber in two different directions.
• the device is advantageous if at least one respective shut-off valve is provided on at least one of the distributors.
• shut-off valve With a shut-off valve, the liquid flow can be started and stopped very abruptly (in particular abruptly) via the first distributor or via the second distributor, so that the respective associated laminar flow likewise starts or stops very suddenly.
• the shut-off valves are preferably also designed so that they have no valve volumes or no dead volumes, with the terms “valve volumes” or “dead volumes” here in each case volumes within the valves are meant, which are undefined when opening or closing the valve enter the valve or exit from the valve.
• valve volumes or “dead volumes” here in each case volumes within the valves are meant, which are undefined when opening or closing the valve enter the valve or exit from the valve.
• the first terminals and the second terminals each have a distance of between 5 and 100 pm to each other.
• the first connections and the second connections form a grid with a screen width.
• the grid width is for example from 5 pm to 400 pm, preferably 10 pm to 100 pm (depending on the dimensions of the respective first and second terminals).
• the raster width is preferably associated with a time interval and a fluid pressure with which a sample can be transported from a raster plane to a next raster plane. Operation of the first connection channels / first distributor for X milliseconds, for example, then leads to the sample being transported from one raster plane to the next raster plane.
• the sample When the first connection channels / first manifolds are operated for 5X milliseconds, the sample is transported on 5 raster planes. Subsequently, the sample can be transported by means of a pressure difference or a pressure at the second connection channels / second distributor accordingly.
• the provided screen widths in the first direction and in the second direction respectively correspond.
• a grid of the chamber has preferably in both directions (first Direction and second direction or X direction and Y direction) in each case between 4 and 256 screen rulings in the specified range between 5 mhh and 400 mhh, but preferably at least 8 screen widths.
• the distributors and the terminals are each implemented by means of lithography.
• the distributors and the terminals are implemented by means of photolithography and / or silicon lithography.
• Photolithography or silicon lithography are semiconductor techniques that are commonly used to fabricate integrated circuits but can also be used to fabricate microfluidic devices. Exposure transfers the image of a photomask onto a photosensitive photoresist. Subsequently, the exposed areas of the photoresist are dissolved (alternatively, the resolution of the unexposed areas is also possible if the photoresist cures under light).
• the result is a lithographic mask that allows further processing by chemical and physical processes, such as the introduction of material into the open window or the etching of wells under the open windows. This easily enables the precise production of the manifolds and connectors.
• the microfluidic device is advantageous if the chamber has a plurality of depressions, which are arranged as an array.
• this consists of the array corresponding to the grid of 8 x 8 to 256 x 256 wells., It being particularly preferred if the grid corresponds to a power of two (8, 16, 32, 64 ). This allows the use of particularly effective splitters, each comprising (exclusively) branching with a split into two channels.
• the wells may also be referred to as potty or as a sample container.
• the wells are arranged evenly distributed in the manner of a two-dimensional grid within the chamber.
• Samples can be accurately transported to the designated well by adjusting the liquid pressures at the respective ports for specific time intervals (according to the grid).
• the recesses preferably each have positions at which samples can be subjected to specific process steps. For example, an analysis of the samples can be carried out on the wells. The method described allows precise placement of samples for a variety of parallel analyzes.
• microfluidic device on, when the chamber and the manifolds are provided in a (common) silicon section of the microfluidic device.
• the chamber as well as the manifolds were preferably made together in a silicon material by means of a lithography process (photolithography and / or silicon lithography). Due to the joint production in a silicon section, an exact matching of the chamber and the distributor can be achieved.
• Such a detection unit makes it possible to determine the position of a sample currently.
• the time periods and the pressures applied to the terminals to control the position of the sample can be determined using the information provided by a optical detection unit is dispensed with respect to the position of the sample to be accurately controlled.
• Also to be described herein is a method of operating a microfluidic device having a chamber comprising the steps of: a) providing a sample in the chamber;
• the method is particularly advantageous if it comprises the following method step: b2) generating a laminar flow through the chamber in a second direction different from the first direction, so that the sample reaches a predeterminable position in the second direction.
• This method can be carried out in particular with a microfluidic device described further above. However, it is also possible that this method be carried out with other microfluidic devices, in particular with other microfluidic devices.
• Such (other) microfluidic devices for example, do not have the described manifolds. Instead, such (other) microfluidic devices optionally also have laminar flow generating elements. The method is intended to describe the basic principle of positioning samples by laminar flow in two directions.
• the method step b1) and the method step b2) are preferably carried out successively in time (in particular not simultaneously).
• the sample is particularly preferably after the execution of process step b1) first stopped before process step b2) is started.
• Very particular preference is given (temporally) between the process steps b1) and b2) a process step b1a) in which the sample is carried out for a fixed time interval (for example between 1 ms and 5 ms). is in order to avoid mutual interference of the process steps bl) and b2).
• an actual position of the sample within the chamber is detected by an optical detection unit and wherein the laminar flow is adjusted on the basis of the position of the sample detected by the optical detection unit such that the sample enters the predetermined position arrives.
• the array of wells described above is an array of reaction volumes for performing sample analyzes.
• This array is particularly similar to a so-called multiwell plate in the macroscopic application, which is a common arrangement for analyzing a large number of samples.
• the array allows so-called multiplex approaches of quantitative PCR or partitioning of a sample.
• the individual wells within the array or within the chamber respectively form pots that are independent of each other.
• an oil layer can be applied to the samples, which causes separation of the individual samples from one another. Due to the oil layer, the fluids within the chamber are no longer fluidically modifiable. Additional reagents in the single chamber must be added before applying the oil layer. After application of the oil layer, the chambers are completed.
• the size of the individual wells or the accuracy with which the grid is provided with the device described herein within the chamber in particular allows the analysis of individual cells (biological cells, for example, human, animal or plant cells) in the individual wells of the chamber.
• the individual chambers are filled so that a cell suspension is presented with many cells on the array.
• functionalized beads are small polmeric microspheres coated, for example, with an antibody or RNA / DNA sequence.
• a first deterministic filling of a depression corresponding to a well of one of the multiwell plates
• a cell a cell
• the interaction of the steps b1) and b2) is used to occupy the individual pots or depressions in such an array individually (in each case specifically with a cell).
• a problem that occurs in conventional methods for distributing cells onto a plurality of arrayed pits is that pots normally remain empty and others are manned multiple times. This problem occurs because cells have different sizes and the pure distribution prevents accurate distribution to the individual wells of the array without precise control of the individual cell locations.
• the microfluidic device and the microfluidic method are based on the particular properties of laminar flow in microfluidic systems.
• the pumps used to generate the laminar flow in the chamber with the microfluidic device or in the microfluidic method are particularly preferably microfluidic peristaltic pumps.
• Microfluidic peristaltic pumps make it possible to convey fluid evenly (depending on the angle of rotation of an eccentric of such pumps).
• a device in an arrangement with a peristaltic pump can be adjusted so that a rotation angle of the eccentric of the peristaltic pump (for example, 1 angle degree) corresponds to a further movement of the sample in the chamber by a grid width.
• the method and the device are particularly suitable for the analysis of tumor cells, as already described above, but also if appropriate for an analysis of rare stem cells in a special way.
• a so-called index sorting is part of the experiment (especially in the case of rare cells).
• a cell suspension is searched by means of a flow cytometer. If a positive cell is found, it is sorted for the array and the array is indexed.
• a "positive cell” in this context is a cell that fulfills protein expression patterns for a desired cell type. This index preserves cell identity. Now it is necessary to move this cell to a specific location where it can be determined exactly what the results of the investigation of this cell are. For this purpose, the precise positioning of samples, as is possible with the device described here and the method described, is advantageous. The measurement at the individual cells in the array can then be linked to further information (in particular to the cytometer measurement).
• FIG. 7 shows an arrangement with a described device, 8a to c: a sample transport with a described device,
• FIG. 9a to e the operation of a pump in the described method
• Fig. 10 an arrangement with a device described.
• FIG. 1 shows a described microfluidic device 1.
• the basic design of such a microfluidic device 1 is described in order to show how a particle in a plane can be moved in a controlled manner with the microfluidic device 1 described.
• Fig. 1 is a sketch of a variant of the described microfluidic device which enables a precise positioning of a sample in only one direction.
• the microfluidic device 1 has a chamber 2 which has a first direction 5 and two sides (a first side 7 and a second side 8) opposite to each other along the first direction 5.
• first connections 14 which are distributed uniformly over the first side 7 and the second side 8, respectively.
• the first connections 14 are supplied with fluid via first connection channels 12.
• the liquid path branches at branching points 11 to the first connections 14 through so-called first distributors 3.
• first distributors 3 Preferably, there is a doubling of the number of subchannels at each branching point 11. In this way, 11 multi-stage first distributor 3 are formed by the branching points. With the help of the manifold 3 and the first terminals 14, a precisely parallel flow is generated in the chamber 2.
• a particle or a sample which is located in the chamber 2, can be moved very precisely in a first direction 5.
• the laminar flow is generated in this principle in particular by the fact that the first terminals are each divided into partial circuits. If the channel dimensions at each branch point 11 remain the same as in the input channel of the respective branching point 11, the flow rate per split is halved, and thus also the speed of the flow.
• the split channels at each branching point 11 are directed into the volume of the plane in the chamber 2.
• the resulting laminar flow in the chamber 2 is preferably absolutely homogeneous or absolutely parallel.
• the constructed as described first distributor 3 are very advantageous for this.
• the first distributor 3 has the advantage that the expansion of the flow is absolutely controlled in all planes and no turbulence can arise.
• the flow only flows freely back into the chamber 2.
• the flow through the expansion in the first distributors 3 is already slowed down to such an extent that no turbulences can likewise occur any more.
• a simple widening of the flow towards the chamber would accordingly cause much inhomogeneous velocity profile in the chamber 2 than the described first distributor 3.
• the first connection channels 12, the branching points 11 and the first connections 14 are each performed symmetrically on the first side 7 and the second side 8, so exactly opposite each first port 14 on the first page 7, a first port 14 on the second side 8.
• the liquid flow from the first port 12 on the first side 7 towards the first port 12 on the second side 8 is first fanned out by the first distributor 3 on the first side 7 and then brought together again by the first distributor 3 on the second side 8.
• the liquid may flow in the first direction 5 either to the first side 7 or to the second side 8. This is possible by reversing a conveying direction of a pump connected to the first connection channel 12.
• FIG. 2 shows a variant of the microfluidic device 1 which, compared to the variant of the microfluidic device 1 in FIG. 1, has been expanded to two-dimensional operation.
• the one-dimensionally explained with reference to FIG. 1 principle is extended in Fig. 2 in two dimensions.
• second connection channels 13 and second connections 15 each have corresponding second distributors 4 on the third side 9 and the fourth side 10
• the chamber 2 is executed at right angles.
• the chamber 2 is even made square.
• FIG. 2 shows in the chamber 2 as particles in a flow level in the chamber 2 controlled in a first direction 5 (possibly also called the X direction) and in a second direction 6 (possibly also called Y direction) can be moved.
• a peristaltic pump also called peristaltic pump
• a peristaltic pump is used, which can be operated forward and backward.
• each shut-off valves 19 are provided with which a liquid flow in the chamber 2 can be brought to a sudden halt.
• a particle or sample may be introduced into the chamber 2 through any of the port channels 12, 13. Once in chamber 2, a particle or sample within chamber 2 can then be positioned deterministically (accurately).
• Fig. 3 shows a flowchart of the described method.
• the chamber 2 is shown schematically here in the microfluidic device 1.
• Step A comprises the placement of a sample 23 in the chamber 2.
• the method steps Bl and B2 are carried out, with which the sample 23 can be positioned in a first direction 5 and in a second direction 6, here with arrows within the chamber 2 is shown.
• FIG. 4 a and FIG. 4 b show how particles or samples are moved on the basis of sketches of the microfluidic device 1.
• valves are closed at second connection channels 13 and second manifolds 4.
• At first connection channels 12 and first manifolds 3 is a liquid flow.
• the sample 23 is moved in the first direction 5 accordingly.
• no movement takes place.
• Fig. 4a To move the sample in the second direction 6 become first Connection channels 12 and first distributor 3, or valves arranged there closed.
• a liquid flow takes place via second distributor 4 or via second connection channels 13.
• the sample then no longer moves in the first direction 5.
• Fig. 4b is outlined how the sample 23 moves accordingly.
• FIGS. 5a and 5b illustrate how different pump sequences (corresponding to steps B1 and B2) are carried out in the context of the described method.
• FIG. 5a the movement of the sample 23 in the chamber 2 in the first direction 5 and in the second direction 6 is sketched.
• FIG. 5 b shows a sequence of individual pumping operations according to method steps B 1 and B 2 (first pump 24, second pump 25, third pump 26 and fourth pump 27) over time t (illustrated here on a time beam), which corresponds to that shown in FIG 5a corresponds to movement 23.
• FIG. 6 shows an arrangement 21 comprising a microfluidic device 1.
• the arrangement 21 shown in FIG. 6 comprises only one peristaltic pump 16.
• first distributor 3 or second distributor 4 can be arranged on the chamber 2, with only one pump 16 via a control of the first valves 17 and the second valves 18, which mecaniclungen a flow path starting from the pump 16 can open or close, can be controlled.
• the sample 23 can be moved in the chamber 2 correspondingly in the first direction 5 or the second direction 6.
• FIG. 7 shows a microfluidic device 1 in an arrangement 21, in which case means for further process steps are shown.
• the microfluidic device 1 has the chamber 2.
• the chamber 2 can be monitored with an optical detection unit 22 to detect where a sample (not shown here) within the chamber 2 is currently located.
• the optical detection unit 22 is part of an optical sensor system. Particles or samples in the chamber 2 can be detected, for example, via fluorescence markers, phase contrast or bright field recordings which are carried out with the optical detection unit 22.
• By means of image evaluation with the optical detection unit 22, for example in a dedicated position detection 29, which may include a control unit, can then be determined determine whether a particular particle or sample is in the chamber and where it is located.
• the desired position of a particle or a sample in the chamber 2 is defined.
• the corresponding X and Y components in the first direction and the second direction can then be calculated and accordingly in the respective direction can be pumped with the (not shown pump).
• the pump not shown, is part of a flow generation 30, with which the flows are generated in the chamber 2.
• a control panel 28 preferably exists.
• the control panel 28 which includes, for example, a joystick or keyboard crosses, can actively control the flow generation 30.
• FIG. 8 demonstrates how a sample or a particle is transported into a depression 20 (possibly also called a cavity, potty or cell) and then fills the depression 20.)
• FIG. 8 a shows the microfluidic device 1 with the first manifolds 3 and represented the second manifolds 4 and the chamber 2, wherein arranged in the chamber in each case in the manner of an array, the recesses 20 are located. Also shown is a sample 23 on its way into one of the recesses 20, the sample being controlled in this way with the laminar flows through the first distributor 3 and the second distributor 4. In the respective recess 20, the sample 23 preferably passes through gravity.
• the transport speed of the sample 23 in the chamber 2 in the first direction 5 and in the second direction 6 is so great that the sample 23 takes a certain time until it sinks into the recess 20 provided.
• the sample 23 can be transported successfully over depressions 20.
• FIG 8b shows the chamber 2 with the recess 20 in a section, wherein the sample 23 is here above the recess 20.
• FIGS. 9a to 9e show a method wherein a pump system with a microfluidic device in a two-phase system is used.
• the depressions 20 are initially filled with an aqueous phase or water 33 (see FIG. 9b).
• Fig. 9c the transport of the sample 23 in oil 32, which prevents contamination of the sample 23, shown in the chamber 2.
• Fig. 9d is shown how the sample 23 sinks into the water 33 in the recess 20 from the oil 32 addition.
• FIG. 9e shows how the sample 23 is transported by the flowing oil 32 via the chamber 2 or via the water 33 present in the chamber 2.
• FIG. 9a shows this again in the plan view of the microfluidic device 1 with the chamber 2, the excavator 5, the second direction 6, the first distributors 3 and the second distributors 4.
• FIG. 10 shows a variant of the microfluidic device 1 according to which the manufacture of the microfluidic device 1 is to be explained.
• the first distributor 3, the second distributor 4, the points 16 with the first valves 17 and the second valves 18 and the chamber 2 can also be seen here.
• the chamber can be located with the therein, not shown array of wells of a silicon chip, which can be made in a lap and a chip cartridge and be made for example an injection mold. Since very small channel sizes and structures can be produced efficiently on a silicon chip, the first distributor 3 and the second distributor 4 are also arranged on the silicon chip.
• the silicon chip thus forms the chamber 2 and the first distributor 3 and the second distributor 4.
• the silicon chip is a splash guard housing, on which liquid paths from the pump 16 and from the first valves 17 and the second valves 18 to the first connection channel 12 and extend the second connection channel 13.

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• Chemical & Material Sciences (AREA)
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• 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)

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• 2018
  • 2018-03-01 DE DE102018203047.2A patent/DE102018203047A1/de active Pending
• 2019
  • 2019-02-19 WO PCT/EP2019/054084 patent/WO2019166279A1/de active Application Filing
  • 2019-02-19 CN CN201980016344.2A patent/CN111757780B/zh active Active
  • 2019-02-19 US US16/976,700 patent/US20210046481A1/en not_active Abandoned
  • 2019-02-19 EP EP19706951.1A patent/EP3758845A1/de not_active Withdrawn

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