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Modeling microcapsules that communicate through nanoparticles to undergo self-propelled motion

机译:模拟通过纳米粒子进行自我驱动运动的微胶囊

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摘要

Using simulation and theory, we demonstrate how nanoparticles can be harnessed to regulate the interaction between two initially stationary microcapsules on a surface and promote the self-propelled motion of these capsules along the substrate. The first microcapsule, the "signaling" capsule, encases nanoparticles, which diffuse from the interior of this carrier and into the surrounding solution; the second capsule is the "target" capsule, which is initially devoid of particles. Nanoparticles released from the signaling capsule modify the underlying substrate and thereby initiate the motion of the target capsule. The latter motion activates hydrodynamic interactions, which trigger the signaling capsule to follow the target. The continued release of the nanoparticles sustains the motion of both capsules. In effect, the system constitutes a synthetic analogue of biological cell signaling and our findings can shed light on fundamental physical forces that control interactions between cells. Our findings can also yield guidelines for manipulating the interactions of synthetic microcapsules in microfluidic devices.
机译:使用模拟和理论,我们演示了如何利用纳米粒子来调节表面上两个最初固定的微胶囊之间的相互作用,并促进这些胶囊沿基材的自推进运动。第一个微胶囊是“信号”胶囊,包裹着纳米颗粒,这些纳米颗粒从载体内部扩散到周围的溶液中。第二个胶囊是“目标”胶囊,最初没有颗粒。从信号胶囊释放的纳米粒子会修饰下面的底物,从而启动目标胶囊的运动。后一个动作激活了流体动力相互作用,从而触发信号胶囊跟随目标。纳米颗粒的持续释放维持了两个胶囊的运动。实际上,该系统构成了生物细胞信号传导的合成类似物,我们的发现可以揭示控制细胞之间相互作用的基本物理力。我们的发现还可以为在微流控设备中操纵合成微胶囊的相互作用提供指导。

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