The controlled production of biocompatible microparticles with tailored size and transport properties is crucial for biomedical applications such as drug delivery and blood analogues. This study explores a hybrid milli-microfluidic approach for microparticle fabrication, combining flow-focusing with passive arrays of obstacles to enhance droplet breakup and size control. Two relevant systems were investigated: perfluorodecalin droplets in sodium alginate and sodium alginate droplets in mineral oil. Monodisperse droplets were initially generated using a 3D-printed millifluidic flow-focusing device featuring a herringbone array of obstacles, then further processed in a polydimethylsiloxane microchannel containing transverse rectangular obstacles. Droplet breakup was characterized at the millifluidic outlet and at the microchannel inlet and outlet. At the milliscale, experiments covered viscosity ratios ( X ) from 10 -2 to 10 2 and Capillary numbers of the dispersed phase ( C a d ) from 10 -4 to 10 0 . Results revealed that droplet area distributions at the millifluidic outlet were weakly influenced by flow rates and X , highlighting the dominant role of geometric confinement. However, droplet area decreased with increasing C a d for all values of X . Within the microchannel, successive breakup events reduced droplet diameters from ∼60 µm to ∼10 µm. The results demonstrate that arrays of obstacles provide a simple, efficient, and scalable method for producing uniform micrometric droplets.
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Cerdeira et al. (2026) studied this question.
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