Hui Yue, Yang Guangze, Fu Changkui, Liu Yun, Zhao Chun-Xia
Australian Institute for Bioengineering and Nanotechnology, University of Queensland, St. Lucia, Queensland 4072, Australia.
Australian Institute for Bioengineering and Nanotechnology, University of Queensland, St. Lucia, Queensland 4072, Australia.
J Colloid Interface Sci. 2021 Jan 1;581(Pt A):185-194. doi: 10.1016/j.jcis.2020.07.107. Epub 2020 Jul 26.
Biomimetic nanomaterials have attracted tremendous research interest in the past decade. We recently developed biomimetic core-shell nanoparticles - silica nanocapsules, using a designer dual-functional peptide SurSi under room temperature, neutral pH and without use of any toxic reagents or chemicals. The SurSi peptide is designed capable of not only stabilizing nanoemulsions because of its excellent surface activity, but also inducing the formation of silica through biosilicification at an oil-water interface. However, it remains challenging to precisely control the peptide-induced nucleation and biosilicification specifically at the oil-water interface, thus forming oil-core silica-shell nanocapsules with uniform size and monodispersity. In this study, the fundamental mechanism of silica formation through a peptide catalyzed biosilicification was systematically investigated, so that the formation of oil-core silica-shell nanocapsules can be precisely controlled. The SurSi peptide induced hydrolysis and nucleation of biomineralized silica particles were monitored to study the biosilicification kinetics. Effects of pH, SurSi peptide concentration and pre-hydrolysis of silica precursors were also studied to optimize the formation of biomimetic silica nanocapsules. The fundamental understanding achieved through these systematic studies provides valuable insights for making core-shell nanoparticles via controlling nucleation and reaction at interfaces.
在过去十年中,仿生纳米材料引起了极大的研究兴趣。我们最近在室温、中性pH条件下,不使用任何有毒试剂或化学品,利用一种设计的双功能肽SurSi开发了仿生核壳纳米粒子——二氧化硅纳米胶囊。SurSi肽不仅因其出色的表面活性能够稳定纳米乳液,还能通过在油水界面的生物矿化作用诱导二氧化硅的形成。然而,要精确控制肽诱导的成核和生物矿化作用,特别是在油水界面,从而形成尺寸均匀且单分散的油核二氧化硅壳纳米胶囊,仍然具有挑战性。在本研究中,系统地研究了通过肽催化生物矿化形成二氧化硅的基本机制,以便能够精确控制油核二氧化硅壳纳米胶囊的形成。监测了SurSi肽诱导生物矿化二氧化硅颗粒的水解和成核过程,以研究生物矿化动力学。还研究了pH值、SurSi肽浓度和二氧化硅前体的预水解的影响,以优化仿生二氧化硅纳米胶囊的形成。通过这些系统研究获得的基本认识为通过控制界面成核和反应制备核壳纳米粒子提供了有价值的见解。