Gao Yuan, Zhao Chun-Xia, Sainsbury Frank
Australian Institute for Bioengineering and Nanotechnology, University of Queensland, St Lucia, QLD 4072, Australia.
Australian Institute for Bioengineering and Nanotechnology, University of Queensland, St Lucia, QLD 4072, Australia.
J Colloid Interface Sci. 2021 Feb 15;584:528-538. doi: 10.1016/j.jcis.2020.09.126. Epub 2020 Oct 6.
Many uses of emulsion droplets require precise control over droplet size and shape. Here we report a 'shape-memorable' micro-droplet formulation stabilized by a polyethylene glycol (PEG)-modified protein -surfactant, the droplets are stable against coalescence for months and can maintain non-spherical shapes for hours, depending on the surface coverage of PEGylated protein. Monodisperse droplets with aspect ratios ranging from 1.0 to 3.4 were controllably synthesized with a flow-focusing microfluidic device. Mechanical properties of the interfacial protein network were explored to elucidate the mechanism behind the droplet shape conservation phenomenon. Characterization of the protein film revealed that the presence of a PEG layer at interfaces alters the mechanical responses of the protein film, resulting in interfacial networks with improved strength. Taking advantage of the prolonged stabilization of non-spherical droplets, we demonstrate functionalization of the droplet interface with accessible biotins. The stabilization of micro-droplet shape with surface-active proteins that also serve as an anchor for integrating functional moieties, provides a tailorable interface for diverse biomimetic applications.
乳液微滴的许多应用都需要对微滴的大小和形状进行精确控制。在此,我们报道了一种由聚乙二醇(PEG)修饰的蛋白质表面活性剂稳定的“形状记忆”微滴制剂,这些微滴在数月内抗聚并稳定,并且根据聚乙二醇化蛋白质的表面覆盖率,能够保持非球形形状数小时。使用流动聚焦微流控装置可控地合成了纵横比在1.0至3.4之间的单分散微滴。对界面蛋白质网络的力学性质进行了探索,以阐明微滴形状保持现象背后的机制。蛋白质膜的表征表明,界面处PEG层的存在改变了蛋白质膜的力学响应,从而形成了强度更高的界面网络。利用非球形微滴的长期稳定性,我们展示了用可及生物素对微滴界面进行功能化。用表面活性蛋白质稳定微滴形状,这些蛋白质还作为整合功能部分的锚定物,为各种仿生应用提供了可定制的界面。