Yu Liu, Ziyu Huang, Runxing Lin, Yuxin Wang, Shizheng Zhou, Zhichao Ma, Yinning Zhou
Introduced the FUS-pen system, a template-free, focused ultrasound platform that enables non-contact, flexible and cross-scale manipulation of microparticles and cells with demonstrated biocompatibility. Achieved a quantified sub-millimeter feature resolution (∼293 μm line width), consistent geometric spot reproducibility, and high cell viability (>94%). Established a compartmentalized tumor-endothelial co-culture layout, demonstrating the platform's utility for constructing complex multicellular models.
Precise spatial organization of cells and microparticles is essential for engineering physiologically relevant tissues and in vitro disease models, yet current bioink-based bioprinting approaches still face limitations regarding cell density dilution and crosslinking-induced cellular stress. Here we introduce the FUS-pen system, a template-free, focused ultrasound platform that enables non-contact, flexible and cross-scale manipulation of microparticles and cells with demonstrated biocompatibility. Mechanistic investigations reveal a cooperative interaction where acoustic streaming drives long-range transport and localized acoustic radiation forces achieve near-focus confinement of microparticles, while boundary reflections establish standing-wave-like fields that yield distinct, frequency-dependent swarm dimensions. By optimizing GelMA hydrogel substrates for reliable cell pattern retention and integrating poly-D-lysine (PDL) modification to facilitate electrostatically driven cell interface interactions, we achieved a quantified sub-millimeter feature resolution (∼293 μm line width), consistent geometric spot reproducibility and high cell viability (>94%). As a proof of concept, a compartmentalized tumor-endothelial co-culture layout was successfully established using breast cancer (MCF-7) cells and endothelial (EA.hy926) cells, where endothelial cells exhibited active proliferation and morphological remodeling into capillary-like networks, demonstrating the platform's utility for constructing complex multicellular models. Together, these results establish the FUS-pen as an agile tool for constructing organized in vitro microenvironments with broad implications for disease modeling and drug screening.