State Key Laboratory of Polymer Physics and Chemistry, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022, People's Republic of China.
Soft Matter. 2017 Apr 5;13(14):2634-2642. doi: 10.1039/c7sm00255f.
Asymmetric vesicles with different inner and outer corona compositions are applicable in microreactors, drug delivery, and biomimics because of their unique functions in membrane permeability and protein localization. In this study, we develop a novel approach to construct asymmetric vesicles and demonstrate the first structural transformation of polymeric vesicles from symmetric to asymmetric membranes. Experimental results and Monte Carlo simulation results clearly reveal that increased intercorona repulsion and enhanced hydrophobic chain mobility are essential to realize this transformation. Moreover, similar transformation processes are observed where either HCl or NaOH is added to change the intercorona interaction. This finding indicates that the observed structural transformation is dominated by physical interactions rather than chemical environment. The constructed asymmetric vesicles can be selectively decorated with gold nanoparticles on the outer corona. This study introduces a novel approach to prepare asymmetric vesicles and provides insights into the mechanism underlying the structural transformation of polymeric vesicles from symmetric to asymmetric membranes.
具有不同内外冠组成的不对称囊泡因其在膜通透性和蛋白质定位方面的独特功能,在微反应器、药物传递和仿生学中具有广泛的应用。在本研究中,我们开发了一种构建不对称囊泡的新方法,并首次展示了聚合物囊泡从对称膜到不对称膜的结构转变。实验结果和蒙特卡罗模拟结果清楚地表明,增加冠间斥力和增强疏水性链的流动性对于实现这种转变至关重要。此外,在添加 HCl 或 NaOH 以改变冠间相互作用的情况下,也观察到类似的转变过程。这一发现表明,观察到的结构转变主要由物理相互作用而非化学环境决定。构建的不对称囊泡可以在外冠上选择性地修饰金纳米粒子。本研究介绍了一种制备不对称囊泡的新方法,并深入了解了聚合物囊泡从对称膜到不对称膜的结构转变的机制。