“…Thus, particles that are relatively denser and stiffer than the surrounding medium are trapped at the acoustic pressure nodes, whereas other particles are trapped at acoustic pressure antinodes created by the acoustic standing wave. − Therefore, in general, acoustic trapping method is noninvasive and just tuning of the acoustic standing wavelength can lead to spatial manipulation of particles, regardless of their optical, electrical, or magnetic properties. , As a result, acoustic standing waves have been exploited in the field of tissue engineering, point-of-care diagnostics, and biophysical studies by spatial patterning and manipulation of micron-sized particles, living cells, bacteria, blood constituents, synthetic cells (protocells), aqueous droplets dispersed in oil, and so forth. ,− For example, a combination of acoustic standing wave pressure field and in situ complex coacervation has been used to design and build microarrays of coacervate microdroplets with controllable spatial geometry, lattice dimensions, and physical and chemical properties. ,− Acoustic-mediated in situ assembly of coacervate droplets exhibits variable surface-attachment properties and dynamic behavior and shows spontaneous uptake of dye molecules, proteins, enzymes, nanoparticles, and microparticles, thus producing spatial and time-dependent fluorescent output when exposed to a reactant diffusion gradient. Further, these spatially positioned coacervate droplets containing enzymes have been explored to understand the chemical signaling pathway between the protocell communities via enzymatic cascade reactions and to understand higher-order collective behavior. ,− Further, contactless nature of the acoustic force simplifies the fabrication of the chip and combining acoustic technology with microfluidics (acoustofluidic) enables a greater degree of control over the spatial localization of different constituents dispersed in the fluid. ,− …”