The present invention relates to the general field of microfluidics and, more particularly, the formation of microfluidic arrays comprising channels of half-round section.
In numerous fields, it is sought to manipulate and analyse liquid samples of small volume the least intrusively and as simply as possible. This may be the case, for example, to establish biological and/or chemical interactions between solutions for chemical analysis, biological or medical diagnosis, or instead in the field of genetic engineering or food processing.
In these fields, in general a flow of liquids is manipulated in microfluidic components comprising channels and chambers, using actuators external to the components, of pump, pressure controller or syringe driver type.
This type of component generally implements a technology of MEMS type. The channels are formed by assembly of two plates, with at least one of the two etched and structured for example by photolithography to form the desired grooves.
According to another technology, less relevant because of the much lower resolution, the channels are formed by micro-machining on a PMMA type plastic card then covered with a cover.
The channels may also be formed by pouring cross-linking materials of PDMS type onto moulds machined beforehand by the aforementioned methods.
In all of these known devices, the geometry of the fluidic array is defined at conception. Moreover, their manufacture requires white room type equipment involving important means and manufacturing times. For a new geometry of components, it is thus necessary to carry out a new long and costly cycle of conception and formation.
Patent application WO2009/130274 of the applicant resolves this problem by proposing a method of manufacturing microfluidic channels, in a programmable and reconfigurable manner, using EWOD (ElectroWetting On Dielectric) displacement techniques or by LDEP (Liquid DiElectroPhoresis). More particularly, two non-miscible fluids, one of which could be solidified, are introduced between two plates provided with electrodes. One of the fluids is displaced according to the EWOD or LDEP technique and when the desired channels are formed, the phenomenon of hardening is activated to congeal the formation of these fluidic channels. The section of the channels manufactured by this method is rectangular.
Nevertheless, channels with rounded or semi-circular section are particularly useful for example in the manufacture of microfluidic pumps as described for example in the article of Unger et al., “Monolithic microfabricated valves and pumps by multilayer soft lithography”, Science vol. 288:113-116 (2000).
However, it is difficult to implement a controlled and reproducible method to form hemispherical structures. To form channels of rounded section, a technique exists described for example by Unger et al., in the document entitled “Monolithic Microfabricated Valves and Pumps by Multilayer Soft Lithography”, Science 288: 113-116 (2000). This technique consists in using firstly the photolithography method for etching grooves on a resin substrate. Then, an additional step known as “resin creep” is used to soften the resin and deform it at the level of the edges of the desired channels, so as to obtain more rounded channels.
Nevertheless, resin creep is a step difficult to control, long, and requires an optimisation for each thickness of resin and for each type of resin. The thickness of resin is often limited to several tens of μm (often 10 μm) because it is a micro-manufacturing step, not developed as the basis for this application and for these orders of magnitude. In addition, it is difficult to control exactly the heights of the channels formed from this technique, and even more difficult to intentionally vary the height of the channels on a same substrate. The desired dimensions (height and width) of the channels are also very limited through this technique. Thus, the creep technique is difficult to control and is not reproducible at all the desired channel dimensions. Moreover, the resins are viscous and thus the shape of the channels is more patatoid than semi-circular section.
The aim of the present invention is to overcome the aforementioned drawbacks by proposing a simple and precise method for the manufacture of microfluidic channels of semi-circular section, in a programmable and reconfigurable manner.
The subject matter of the invention is a method of forming a microfluidic array comprising at least one channel of semi-circular section, comprising the following steps:
bringing into contact a first liquid with an array of electrodes of a microfluidic chip comprising at least one pair of substantially parallel and coplanar electrodes arranged on a substrate,
activating said array of electrodes so as to actuate by liquid dielectrophoresis LDEP said first liquid to form a fluidic structure comprising at least one fluidic finger, and
using said fluidic structure as a mould to form said microfluidic array by solidification or hardening of a second liquid deposited on the microfluidic chip and hugging the shape of said fluidic structure.
Thus, the method uses the technique of liquid dielectrophoresis LDEP in an open configuration to generate in a rapid manner fluidic fingers of semi-circular section. In fact, the sections of the fluidic fingers are naturally semi-circular because the electric field constrains the first liquid to go towards the gap separating the two electrodes. In addition, the dimensions (height and width) of these fluidic fingers can vary over a very wide range extending from several hundreds of nanometres to several hundreds of micrometres. The fluidic fingers are then used to form by moulding, in a simple, reproducible, programmable and reconfigurable manner, microfluidic arrays comprising channels of hemispherical section.
According to a first embodiment, said first liquid has a property of hardening and said method comprises the following steps:
hardening said first liquid materialising said fluidic structure while maintaining the array of electrodes in activation during the step of hardening in order to congeal said fluidic structure, and
flowing the second liquid onto said congealed fluidic structure.
According to this first embodiment, the fluidic structure is congealed before the introduction of the second liquid thereby avoiding any interaction between the two liquids and forming a structural mould of high precision making it possible for example to form in a simple manner a plurality of identical microfluidic arrays without the necessity of restarting the process of actuation of the first liquid.
Advantageously, the first liquid is a liquid-solid phase change material selected from the following materials: epoxy, silicone or resin based adhesive, UV adhesive, gel, cross-linking polymer, paraffin, agarose, gelatine, beeswax, and wax.
Thus, the first liquid may be selected from a wide choice of phase change materials at a temperature comprised for example between 0° C. and 150° C.
Advantageously, the first liquid is a UV adhesive and the hardening of said first liquid is carried out by exposure to UV radiation at a wavelength adapted to the cross-linking wavelength of said UV adhesive.
Thus, the fluidic structure may be congealed at a distance and in a simple and rapid manner without resorting to a heat source.
Advantageously, the method comprises a step of melting the hardened or solidified material of said first liquid in order to reconfigure the fluidic structure.
Thus, by inversing the hardening process the method may be restarted by re-using the microfluidic chip to form a fluidic structure having a different geometry.
According to a second embodiment, the second liquid is non-miscible with the first liquid such that the interface between the two liquids takes the shape of said fluidic structure under the effect of the activation of said array of electrodes, the first liquid being covered with the second liquid.
According to this second embodiment, the interface between the two non-miscible liquids is advantageously used as an impression which is materialised by the hardening of the second liquid thereby forming in a simple manner the microfluidic array.
Advantageously, the first liquid is deionised water, water, an organic liquid, a solvent, or an aqueous solution.
Thus, a liquid is used for which the actuation by the LDEP technique does not require an activation at high frequency and which can then be easily evacuated after the hardening of the second liquid.
Advantageously, the second liquid is a liquid-solid phase change material selected from the following materials : cross-linking polymers, paraffin, agarose, gelatine, beeswax, wax, epoxy, silicone or resin based adhesive, UV adhesive, and gel.
Thus, the second liquid may be selected from a wide choice of phase change materials to form microfluidic arrays of high quality.
Advantageously, the geometry of the microfluidic array is programmable by the activation of the electrodes in an independent manner. Thus, from a single microfluidic chip, it is possible to form a plurality of fluidic arrays having different geometries.
Advantageously, the shape and/or the dimensions of said at least one fluidic finger of the microfluidic array is configurable depending on the shape and/or the width and/or the number of electrodes. Thus, fluidic channels of any shape, width, or height may be formed.
Advantageously, in the course of a same actuation by liquid dielectrophoresis, said at least one fluidic finger may be formed with variable dimensions. Thus, with a same LDEP actuation, it is possible to form fluidic channels comprising different zones having different lengths and/or depths and/or widths.
Advantageously, said microfluidic array is used as a model plate to form other microfluidic arrays.
Thus, the microfluidic array may be used for the manufacture of a mould in order to form in a simple manner a plurality of identical fluidic arrays.
The invention targets a method of forming a microfluidic array comprising at least one channel of semi-circular section, comprising the following steps:
The invention also relates to a method of forming a microfluidic array comprising at least one channel of semi-circular section, comprising the following steps:
Advantageously, the method comprises the following steps:
The invention also relates to a microfluidic device comprising a microfluidic array formed according to any of the preceding characteristics.
Other advantages and characteristics of the invention will become clear from the detailed non-limiting description given below.
Embodiments of the invention will now be described, by way of non-limiting examples, while referring to the appended drawings, in which:
The principle of the invention is to take advantage of the actuation of a liquid by dielectrophoresis LDEP in an open configuration to mould microfluidic arrays comprising channels of semi-circular section.
More particularly,
Pair of electrodes is taken to mean either a pair of continuous electrodes, extending along a given path (see
The array of electrodes 3 is moreover connected to an electrical interface 5 making it possible to apply potential differences between the electrodes 3a, 3b. The array of electrodes 3 is thereby configured to form by liquid dielectrophoresis LDEP, under the effect of an electrical activation, at least one fluidic finger along the activated electrodes.
Liquid dielectrophoresis LDEP is taken to mean the application of an electrical force, generated by an oscillating non uniform electric field, on a liquid. The formation of a fluidic finger by liquid dielectrophoresis is especially described in the article of Jones entitled “Liquid dielectrophoresis on the microscale”, J. Electrostat, 51-52 (2001), 290-299. When the liquid is situated in an electric field, the molecules of the liquid acquire a non-zero dipole and are polarised. In so far as the field is non uniform, a Coulomb force appears and induces the displacement of the molecules of the liquid, and thus all of the liquid, towards a field maximum. The liquid is then naturally constrained by the electric field to have a semi-circular section.
Thus, under the effect of the electric field, the first liquid 7 is stretched by liquid dielectrophoresis to form a fluidic structure 9 comprising at least one fluidic finger 9a (see also
Thus, the solidification (or hardening) of the second liquid 11 that forms the surrounding enclosure of the fluidic structure 9 generates a solid three-dimensional structure, the shape of which hugs the fluidic finger. In other words, the fluidic finger constitutes an impression or a mould, defining the shape of the second hardened liquid. At this stage, the electrical activation is stopped, which leads to the removal of the liquid finger whereas the solidified structure of the second liquid remains integrated. The latter then forms a microfluidic array 13 comprising at least one fluidic channel 13a of substantially semi-circular section, as illustrated in
It will be noted that the microfluidic array 13 can also be used as a model plate to form other microfluidic arrays.
The example of
Furthermore,
The example of
Thus, the present invention makes it possible to re-use the same microfluidic chip 1 to create moulds materialised by fluidic structures 9 of different geometric shapes.
It is also possible to control the heights of a fluidic finger 9a on a same microfluidic chip 1 by varying the number of activated electrodes 3i. In fact, the example of
Thus, the geometric shape and/or the dimensions of a fluidic finger 9a may be configurable as a function of the shape and/or the number of electrodes 3i activated and/or the width of the electrodes 3a, 3b (see also
Furthermore,
In
The array of electrodes 3 in continuous configuration may have complex shapes comprising for example coil shaped electrodes 33, electrodes having bends at right angles or cross-shaped 35, and electrodes of variable width 37.
The fluidic fingers derived from the mother drop extend along different paths determined by the pairs of activated electrodes. Then, it is possible to form in a simple manner and in a single operation channels of different dimensions and different shapes for practically all microfluidic applications. For example, it is possible to form a microfluidic array comprising a channel with a stage and/or a chamber and/or a convergent section and/or a divergent section and/or a constriction and/or a coil-shaped channel.
The example of
It is then possible to envisage different shapes and dimensions of fluidic fingers 9a by varying the number and the geometry of the electrodes 3i, 3a, 3b. In particular, it is possible to vary the dimensions (lengths, heights, widths) of the fluidic fingers 9a in the course of a same LDEP actuation by activating electrodes 3a, 3b of variable widths (
It will be noted that, in the prior art, the heights of channels are defined by the methods and the associated etching times. Thus, to vary the height of a channel, the sole means was to go through several steps of photolithography requiring several masks, followed by several etching steps. In other words, a number N of different heights of channels required the manufacture of N photolithography masks, N photolithography steps and as many etching steps.
In
The microfluidic chip 1 comprises a substrate 4 having a free surface 4a. The material of the substrate 4 may be selected from the following materials: silicon, monocrystalline silicon, polycrystalline silicon, silicon nitride, silicon oxide, glass, Pyrex or an organic material such as polycarbonate or PEEK, plastic, paper, nickel, tungsten, platinum, etc. The thickness of the substrate 4 may be any thickness, comprised for example between several tens of microns and several millimetres.
The substrate 4 comprises a metal level for the definition of an array of electrodes 3 adapted to form by liquid dielectrophoresis fluidic fingers on the free surface 4a of the substrate. These electrodes 3a, 3b are impressions obtained by deposition then etching of a fine layer of a semi-conductor or of a metal which may be selected from aluminium, copper, gold, platinum, ITO (Indium Tin Oxide). The thickness of the electrodes 3a, 3b is from several tens of nm to several hundreds of nm, for example of the order of 200 nm.
The array of electrodes 3 comprises at least one pair of displacement electrodes 3a, 3b parallel and coplanar with each other, arranged at the level of the free surface 4a of the substrate 4. The structure of the electrodes makes it possible to define the zones where the electrophoresis forces are going to act. The example of
The inner edges of a pair of electrodes are spaced apart by a distance g, for example of the order of 4 μm to 10 μm. Each electrode has a width noted w of the order of 8 μm to 20 μm and consequently, by noting 2R the distance separating the outer edges of the electrodes 3a, 3b, the radius R given by R=w+g/2 of the semi-circular section of the fluidic finger is then of the order of 10 μm to 25 μm. In fact, when the width w of the electrodes is of the same order of magnitude as their spacing g, the fluidic finger at all points of the path covers a zone inscribed between the two lateral ends of the electrodes. Thus, the dimensions of the channels formed by the fluidic fingers are of the order of 10 μm to 25 μm in terms of width and depth. It may also be envisaged to form channels, the dimensions (width, depth) of which are comprised between 1 μm (or even less than a micrometre) up to several hundreds of micrometres, for example 500 μm.
Moreover, the lengths of the fluidic fingers and consequently those of the channels can be very consequent. In fact, it is possible to form fluidic fingers by LDEP over lengths of several tens of millimetres. It is even possible to envisage forming fluidic fingers (and thus channels) of several tens of centimetres, as long as the input of liquid of the mother drop is conserved.
It should be noted that the formation of a fluidic finger is very rapid, with a displacement speed of the liquid of the order of 0.1 to 10 cm/s; only 50 to 500 ms suffices to form a fluidic finger of 5 mm.
After structuring the array of electrodes 3, the substrate 4 may advantageously be covered with at least one passivation dielectric layer 17 in order to guard against risks of electrolysis of the first liquid if the latter is electrically conducting.
The passivation layer 17 may be an insulating layer for example, an oxide SiO2, a nitride (SiN, Si3N4), resins, dry films, SiOC, Teflon type hydrophobic polymers (registered trademark—tetra-fluoroethylene) or other fluoropolymers, a polymer of poly-p-xylylene (parylene), a high-k oxide deposited by a method known as ALD (HfO2, Al2O3, ZrO2, SrTiO3, BaTiO3, Ba(1-x)SrxTiO3 (BST) . . . ), and have a thickness comprised between several nm (for example 10 nm or 25 nm) and several microns (for example 5 μm). High-k oxides have a high dielectric permittivity, which makes it possible to increase the efficiency of the transduction. It makes it possible to avoid the electrolysis of the liquid if this was in direct contact with the array of electrodes 3.
Preferably, the substrate 4 is covered with a double passivation layer: a first dielectric layer 17a for example silicon nitride SiN (from 100 nm to 1 μm) and a second layer 17b for example SiOC or Teflon (of 100 nm to 1 μm) for its hydrophobic properties forming the free surface 4a of the substrate 4. It will be noted that the hydrophobic layer enables the liquid to have a high contact angle in particular, greater than 90°.
Moreover, the array of electrodes 3 is connected to an electrical interface 5 comprising switching means 5a and voltage generating means 5b to activate the electrode array 3 according to the desired configuration.
According to this first embodiment, the first liquid 7 has a property of hardening making it possible to congeal the fluidic structure 9 during the activation of the electrodes 3a, 3b.
As an example, the first liquid 7 is composed of a liquid-solid phase change material selected from the following materials: epoxy, silicone or resin based adhesive, UV adhesive, gel (especially alginate or agarose), cross-linking polymer for example of PDMS type, paraffin of CnH2n+2 type, gelatine, beeswax, wax.
According to a first step (
Then, the array of electrodes 3 is activated by applying to it a voltage adapted to generate an oscillating and non-uniform electric field so as to actuate by LDEP the first liquid 7. Thus, a fluidic structure 9 (
In fact, the example of
Then, after the formation of the fluidic structure 9, a process of hardening or solidification of the first liquid 7 is carried out materialising the fluidic structure 9 while maintaining the array of electrodes 3 in activation in order to congeal the fluidic structure 9. The process of hardening or solidification of the first liquid 7 may be carried out by a change of temperature, or by exposure to a specific radiation range depending on the material used for the first liquid 7.
In fact, the example of
In fact, as soon as the fluidic structure 9 is formed and hardened, the second liquid 11 for example PDMS is poured (
Then, a process of hardening or solidification of the second liquid 11 is carried out by change of temperature, drying, or radiation (according to the material used) to form the microfluidic array.
The example of
The example of
Then,
The example of
Advantageously, the moulds can be reconfigured an unlimited number of times as long as the fluidic actuations can be carried out, in other words, as long as the array of electrodes 3 and the potential passivation layer 17 are not damaged. In fact, the phenomena of hardening (for, for example, the UV adhesive) or solidification (for, for example, paraffin) are reversible. It is possible for example to liquefy the paraffin by heating it and the UV adhesive may be dissolved with a stripping solution (for example, acetone or piranha) and thereby reconfigure the microfluidic array 13, creating a new array different from the first.
The example of
According to this second embodiment, the second liquid 11 is non-miscible with the first liquid 7 such that the interface between the two liquids takes the shape of the fluidic structure 9 during the actuation of the first liquid 7 by LDEP.
As an example, the first liquid 7 is water, deionised water DIW, an organic liquid (for example oil), an aqueous solution or a solvent of ethanol, acetone, or glycerol type. The second liquid 11 is made of material having a property of hardening or solidification and preferably, a second liquid is chosen with a dielectric permittivity quite different to that of the first liquid in order that the actuation of the first liquid 7 by LDEP is optimal.
According to a first step, the first and second non-miscible liquids 7, 11 are placed on the free surface 4a of the substrate 4. As an example, firstly a bath of the second liquid 11 (for example, paraffin) is formed on the microfluidic chip 1 (
Then, the array of electrodes 3 is activated by applying thereto a voltage adapted to generate an oscillating and non-uniform electric field so as to actuate by LDEP the first liquid 7. More specifically, the interface between the two liquids is shaped by the liquid dielectrophoresis forces actuating the displacement of the first liquid 7 on the path defined by the activated electrodes 3a, 3b. Thus, the interface between the first and second liquids 7, 11 takes the shape of the fluidic structure 9 formed by the first liquid 7.
When the geometry of the desired fluidic structure 9 has been formed, the second liquid 11 covering the fluidic structure 9 is congealed by a process of hardening, solidification or phase change while maintaining the array of electrodes 3 in activation. The material of the second liquid 11 is thus going to memorise the shape of the fluidic structure 9 or, in other words, the impression of the fluidic structure 9 is going to be replicated in the material of the second hardened liquid 11 thereby forming the fluidic array 13 (
Then, the solidified or hardened microfluidic array 13 is disbonded from the microfluidic chip 1 (
The method according to the invention thus makes it possible to manufacture microfluidic devices for all applications that use microfluidics. Among these applications, may particularly be cited the manufacture of “Quake” peristaltic pumps or valves because channels with semi-circular section are practically indispensable for addressing this type of application.
Moreover, it will be noted that the invention may be used to conduct rapid prototyping with microfluidic chips made of PDMS, to address for example all biological and chemical applications.
Obviously, various modifications may be made by those skilled in the art to the invention that has been described, uniquely by way on non-limiting examples.
Number | Date | Country | Kind |
---|---|---|---|
12 62930 | Dec 2012 | FR | national |