How can we generate double emulsions using microfluidics? How can we control PDMS surface wettability? What are the new microfluidic-based techniques for generating double emulsions? We address these questions in this review.
Multiple emulsions are complex polydisperse systems where both oil in water and water in oil emulsions exist simultaneously, stabilized by hydrophobic and hydrophilic surfactants respectively. They are promising materials for industrial fields like cosmetics, pharmaceutics, or food. These emulsions in an emulsion can be used to encapsulate fragile compounds (drugs, vitamins, aromas…), protect them during storage, and eventually release them on demand at a suitable time and place.
Typically, double emulsions are made in two steps with two surfactants. For example, to create a water-in-oil-in-water (w/o/w) emulsion, water is first emulsified with an oil phase containing a hydrophobic surfactant, and re-emulsified in a second step with a water phase containing a hydrophilic surfactant. Double emulsion droplets are thus complex to obtain. The second step, in particular, needs to be handled with care to preserve the primary emulsion. In addition, emulsions produced with this technique are polydisperse, which is not desirable for the industry and affects the stability of double emulsions. Microfluidics can address some of these drawbacks and allow the formation of perfectly monodisperse double emulsion droplets in a controlled way.
There are three major geometries to generate droplets with microfluidics: flow-focusing, co-flowing, T-junction (Figure 1), glass capillary, and the potential combination of these geometries. These techniques have been adapted for the formation of double emulsion droplets.
The simplest and most widely studied geometry is the succession of two cross junctions, flow-focusing. This configuration is compatible with soft-lithography techniques and can be easily adapted to the formation of high-order multiple emulsions [1]. At the first junction, internal droplets are formed and they are encapsulated into external droplets at the second junction. Co-flowing configuration is widely used with all fluids flowing coaxially. The fluid that has been dispersed is entirely embraced by the fluid flowing continuously in co-flowing streams which makes surface treatment unnecessary [2, 3].
Two consecutive T-junctions on glass can be used to produce double emulsion drops with a controlled number of inner drops. This number increase with the increasing flow rate of the inner phase [4]. Glass capillaries are optically transparent, electrically insulate, and chemically robust. Two-step microfluidic emulsification methods in a three-phase glass capillary device were developed, allowing the generation of high-order multiple emulsions [5]. In combination with co-flow geometry, the microcapillary device can generate monodisperse emulsions in a single step [6].
To generate droplets in a microfluidic chip, the wettability of the walls is a crucial parameter. The formation of double emulsion droplets in a microfluidic chip seems quite complex.
PDMS, the most widely used material for microfluidics, is intrinsically a hydrophobic material, which has consequences for droplet-based microfluidics. To successfully generate droplets, the continuous phase needs to effectively wet the chip walls. In the case of water-in-oil (w/o) droplets, walls have to be hydrophobic, to minimize the contact between the microchannels and the aqueous phase. Therefore, PDMS is ideally suited for the generation of these droplets. However, to generate oil-in-water (o/w) droplets, the continuous phase should not wet the walls, otherwise, droplets would be broken. Thus, it is not possible to produce o/w droplets with native, untreated PDMS. Moreover, double emulsions (water-in-oil-in-water (w/o/w), and oil-in-water-in-oil (o/w/o)) require more complex, spatially defined control of wettability [8]. Several efforts were done to make PDMS walls hydrophilic and combine PDMS hydrophilic and hydrophobic parts on the same chip [9].
When exposed to oxygen ions generated by plasma cleaner, the PDMS surface is oxidized, and the methyl groups of the surface are replaced by -OH moieties, making it hydrophilic. However, this effect only lasts a couple of hours, because the uncured oligomers contained in the bulk material will migrate to the surface over time. The exposure to plasma is also a way of activating the PDMS surface: the -OH moieties are indeed able to create covalent bonds with various silanes for example [10]. However, it is difficult to coat only a specific part of the microfluidic chip to produce double emulsion droplets.
Hu and colleagues [11], and later on Abate and colleagues [12] tried coating the device’s walls with a hydrophilic polymer. First, they adsorb a photoinitiator on the walls, and then they inject an acrylic acid solution inside the channels and initiate the polymerization by exposure to UV light. Hu and colleagues worked with benzophenone, whereas Abate and colleagues worked with silanes. Only channels that need to become hydrophilic were coated thanks to the use of a mask during UV exposure.
These techniques are very efficient, but also time-consuming. Moreover, the injection of liquids into the chips previously to the formation of double emulsions increases the risk of obstructing the channels. Bauer and colleagues [13] developed a protocol based on the use of layer-by-layer adsorption of hydrophilic polyelectrolytes on the channels, alternating positive and negative charges. The parts that need to be kept hydrophobic are protected by injection of dionized water at a carefully controlled flow rate (Figure 2).
More recently, other techniques were developed without any coating. They are based on precise control of the part of the microfluidic chip exposed to plasma.
Kim and colleagues [14] worked with plasma-bonded chips that have recovered their hydrophobic properties. The chips are exposed to plasma again, and oxygen ions enter into the chips through the inlets and outlets punched in the PDMS. PDMS surface is oxidized and turns hydrophilic. Some inlets or outlets are blocked with tape during the exposure, and diffusion barriers are integrated into the chip to spatially control the ion’s diffusion. The geometry of the chip needs to be optimized to allow the oxidation of the targeted channels only (Figure 3).
Li and colleagues [15] developed easy and quick techniques to pattern the wettability of the chip, by using either epoxy glue or permanent marker In the first case, glue is removed just before bonding, and in the latter, the marker is rinsed by injecting ethanol into the chip after the bonding. In that way, it is possible to combine hydrophilic and hydrophobic parts on the same chip. However, since the effect of the plasma is temporary, these chips can be used to produce double emulsions only for a couple of hours before the hydrophobic recovery of PDMS (Figure 3).
In recent years, the general concept of emulsion formation has been successfully transferred from PDMS-based to 3D-printed microfluidics [8]. 3D-printed droplet-based microfluidics present unique features such as modular design, facile integration, and parallelization [16] and have been demonstrated efficient for the complicated operation of multiple emulsions [17].
Mannel and colleagues demonstrated a fabrication process in which the first hydrophilic material is 3D-printed onto another hydrophobic resin to print the remaining part of the device. They changed photopolymer formulations while printing the single layers. O/w droplets are first formed after traveling through the first hydrophobic region and the second hydrophilic region, then o/w droplets are encapsulated by oil in the third hydrophobic region to form o/w/o double emulsions. This method adopted the planar junction design, though the locally modulated surface wettability led to the stable generation of double emulsion droplets [8, 16].
Ji and colleagues reported pneumatic control of multiple emulsions generation in modular 3D-printed devices, consisting of three modules: the function module, T-junction, and co-flow modules. The function module consists of a single-inlet, pneumatic control unit (PCU), and dual-inlet modules (Figure 4). The T-junction module is used for inner droplet generation, and the co-flow module is used for outer droplet generation. Double emulsions with different numbers and compositions of inner droplets have been successfully generated with easy control of the different phases’ flow rates thanks to a microfluidics pressure-driven flow controller [17].
Recent advances in microfluidics have enabled the controlled production of monodispersed tunable multiple-emulsion droplets. However, double emulsions, water-in-oil-in-water, and oil-in-water-in-oil, require complex spatially defined control of wettability. PDMS surface wettability can be achieved using coating and non-coating techniques. 3D-printed microfluidics integrating a pressure-driven flow controller allow to overcome the issues of these techniques. Furthermore, 3D-printed technologies can be applied in other fields, such as material engineering and bioengineering. In the future, we believe that more complicated devices for microfluidics and more controllable methods for emulsion generation can be developed based on the rapidly developing 3D-printed technologies.
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