“…For example, transmitting the low‐intensity vibration associated with the SAW or SRBW through a fluid coupling layer [ 179,262 ] into cells or organisms within a petri dish, agar plate, or cell culture chamber was not only observed to facilitate cell–cell interactions, [ 133 ] activate mechanosensitive ion channels, [ 134,135 ] stimulate exosome production in the internal cell machinery, [ 136 ] drive cell migration along acoustotactic gradients, [ 137 ] promote tissue oxygenation for wound healing, [ 138 ] or trigger neuronal stimulation in nematodes, [ 139,140 ] but also to enhance cellular uptake of nanoparticles, molecules, and nucleic acids by several‐fold, while retaining very high viabilities (>97%). [ 142 ] Unlike cavitation‐induced pore formation in sonoporation processes, which can often lead to some irreversible cell damage and apoptosis (with cellular viabilities as low as 60% having being commonly reported), [ 263–265 ] the high‐frequency SAW or SRBW excitation does not induce pore formation but rather temporarily disrupts the membrane lipid structure [ 141 ] or cytoskeletal structure, [ 266 ] thus increasing its permeability sufficiently to allow efficient transmembrane molecular transport. [ 142,267 ] We note that such rapid healing of the membrane leading to the retention of high cellular viabilities has also been reported following GHz frequency excitation, although in that case, nanopore formation in the cell membrane was claimed as a consequence of the larger localized acoustic pressures that can be generated at higher frequencies.…”