Recent advances in droplet manipulation methods by electric fields and signals require a deeper understanding of water droplet charge. In this paper, we have investigated the electrophoretic motion of individual water microdroplets injected into non-polar silicone and paraffin oil by video optical microscopy on an individual droplet basis to determine droplet charge. It was found that the initial surface charge density of surfactant free droplets directly after injection from a micropipette is positive and of the order of 10−6 C/m2, regardless of pH and ion concentration in the range from pH 4 to pH 10 and from 0.01 mmol/l to 1.5 mol/l, respectively. The experimental results together with molecular dynamics simulations show that the nature and polarity of the charge can be explained by anisotropic orientation of water molecules at the interface rather than selective adsorption of ions. Furthermore, we showed that slip at the liquid-liquid boundary must be taken into account when interpreting electrophoretic measurements of droplets.

The primary goal of bioprocess cell line development is to obtain high product yields from robustly growing and well-defined clonal cell lines in timelines measured in weeks rather than months. Likewise, high-throughput screening of B cells and hybridomas is required for most cell line engineering workflows. A substantial bottleneck in these processes is detecting and isolating rare clonal cells with the required characteristics. Traditionally, this was achieved by the resource-intensive method of limiting dilution cloning, and more recently aided by semiautomated technologies such as cell sorting (e.g., fluorescence-activated cell sorting) and colony picking. In this paper we report on our novel Cyto-Mine Single Cell Analysis and Monoclonality Assurance System, which overcomes the limitations of current technologies by screening hundreds of thousands of individual cells for secreted target proteins, and then isolating and dispensing the highest producers into microtiter plate wells (MTP). The Cyto-Mine system performs this workflow using a fully integrated, microfluidic Cyto-Cartridge. Critically, all reagents and Cyto-Cartridges used are animal component-free (ACF) and sterile, thus allowing fast, robust, and safe isolation of desired cells.

We present a facile approach for producing large and monodisperse core-shell drops with ultrathin shells using a single-step process. A biphasic compound jet is introduced into a quiescent third (outer) phase that ruptures to form core-shell drops. Ultrathin shelled drops could only be produced within a certain range of surfactant concentrations and flow rates, highlighting the effect of interfacial tension in engulfing the core in a thin shell. An increase in surfactant concentrations initially resulted in drops with thinner shells. However, the drops with thinnest shells were obtained at an optimum surfactant concentration, and a further increase in the surfactant concentrations increased the shell thickness. Highly monodisperse (coefficient of variation smaller than 3 %) core-shell drops with diameter of ∼200 μm-2 mm with shell thickness as small as ∼2 μm were produced. The resulting drops were stable enough to undergo polymerisation and produce ultrathin shelled capsules.

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