Experimental study demonstrates soft microgel networks extend acoustic water jet lengths by up to 44%, highlighting a biocompatible approach for needle-free drug delivery.
The stability of high-speed liquid jets is crucial for applications ranging from precision printing to needle-free drug delivery, yet it is fundamentally limited by capillary-driven breakup. We find that tuning the nanoscale softness of Poly( N -Isopropylacrylamide) (PNIPAM) microgels provides a robust, biocompatible strategy to overcome this limitation. Soft, low-cross-linker-density microgels form elastic interfacial networks at the air–water interface that suppress surface tension recovery, delay Rayleigh–Plateau instabilities, and extend Surface Acoustic Wave (SAW)-driven jet lengths by up to 44%. In contrast, stiffer microgels lose network cohesion under strain, leading to rapid jet breakup. To gain molecular-level insights, we perform dissipative particle dynamics simulations, which reveal that polymer bridges in soft microgels remain entangled during elongation, maintaining a reduced effective surface tension. Finally, a simple scaling analysis, balancing the SAW-driven kinetic energy imparted to the droplet against the surface energy required to form a jet, quantitatively predicts the observed length enhancement.
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Razavi et al. (2026) studied this question.
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