Droplet-Based MicrofluidicsDroplet Transport and Spatiotemporal Dynamics in Microfluidic Networks Currently, microfluidic devices can produce millions of nanoliter-scale droplets in an hourallowing high throughput encapsulation of single biomolecules and cells. Given the complexity ofbiological analysis, these droplets often need to be shuttled through a network of fluidic channelsso that they can be merged with other reagent-loaded droplets, then sorted and eventuallyanalyzed. Realizing this vision of an ultrafast fluidic bioprocessor in the laboratory is quite adaunting task because akin to car traffic on congested highways, collective hydrodynamicinteractions between drops in interconnected networks precludes full control over the positionand timing of droplets. For example, as shown in the figure below, decision making of thedroplets arriving at the junction can be quite complex. We are pursuing a combined experimental and computational approach to understand droplettraffic in fluidic networks. We are currently quantifying the hydrodynamic resistance of drops inmicrochannels and incorporating that knowledge to understand and model the spatiotemporaldynamics of drops in simple fluidic networks. In the long term, we aim to develop a rationalframework for the design of large-scale droplet-based fluidic processors. Nanoliter-Scale Droplet Arrays for Biological Analysis Multi-well plates combined with robotics are currently the gold standard for conducting highthroughput screening assays in biology and medicine. This approach uses microliter volumes ofreagents and limits the throughput and the level of combinatorial screening that can be achievedin applications such as drug discovery. Droplet-based microfluidics has the potential to reducethe volumes down to nanoliters. However an engineering challenge is to develop ways to eitherarray or store droplets on a chip. We are currently engineering fluidic networks on a chip that can generate two-dimensionalarrays of drops. The advantage of 2D arrays lies in alleviating the need for indexing since dropsare stored at predefined locations. We are pursuing scientific studies to understand the factorsthat regulate the production of 2D drop arrays that will enable us to robustly generate dropletarrays not only with homogeneous composition but also with varying compositional gradients ofreagents. Crystallization and Partial Coalescence in Oil-in-Water Emulsions A relatively unexplored and poorly understood route to designing soft materials is forcingemulsions containing crystallizable oils to undergo a process known as partial coalescence.Partial coalescence occurs when the interfacial crystals of one fat droplet penetrate a seconddroplet. The mechanical strength of the crystalline network linking the droplets is capable ofovercoming the Laplace pressure and maintains the aggregate shape as shown in Figure 1.From a practical perspective, this mechanism has been exploited in ice cream manufacture fornearly three centuries and has found additional applications in cosmetics, pharmaceuticalcreams, and phase change materials. Technological control of partial coalescence in theseapplications requires scientific understanding of crystallization transitions and the kinetics ofpartial coalescence in oil-in-water emulsions. Direct experimental characterization of out-of-equilibrium phenomena such as crystallization andpartial coalescence requires investigating statistically large ensembles of well-controlled dropletsizes. Our principal approach is to deploy microfluidic technology to create organized arrayscontaining several hundred monodisperse single droplets and doublets for probing nucleationand kinetics of partial coalescence under quiescent conditions. In addition, we are designingmicrofluidic devices to probe shear-induced kinetics of partial coalescence. This microfluidic-based bottom-up approaches and direct visualization methods are expected to fill fundamentalgaps in the current understanding of partial coalescence in emulsions.