耗散颗粒动力学模拟
胶束
小泡
共聚物
两亲性
材料科学
化学物理
双层
星团(航天器)
相图
溶剂
分子动力学
层状结构
分子
相(物质)
高分子化学
聚合物
化学工程
化学
复合材料
物理化学
计算化学
有机化学
水溶液
膜
工程类
生物化学
程序设计语言
计算机科学
作者
Man Jung Han,Minhyung Hong,Eunji Sim
摘要
We investigated the formation of various micelle shapes of lipid-like amphiphilic AB2 miktoarm star copolymers in a solution, by performing dissipative particle dynamics simulations. AB2 miktoarm star copolymer molecules are modeled with coarse-grained structures that consist of a relatively hydrophilic head (A) group with a single arm and a hydrophobic tail (B) group with double arms. A decrease in the hydrophilicity of the head group leads to a reduction of the polymer-solvent contact area, causing cluster structure changes from spherical micelles to vesicles. Consequently, a spherical exterior with multi-lamellar or cylindrical phase interior structures forms under poor solvent conditions without the introduction of spherical hard-wall containers. Furthermore we observed that, for small head group lengths, vesicles were formed in much wider range of solvent-head interaction strength than for long head groups, indicating that molecules with short head group offer a superior vesicle forming property. A phase diagram, the structure and kinetics of the cluster formation, a density profile, and a detailed shape analysis are presented to discuss the molecular characteristics of potential candidates for drug carriers that require superior and versatile vesicle forming properties. We also show that, under certain solvent-hydrophilic head group interaction conditions, initially formed cylindrical micelles transform to bilayer fragments through redistribution of copolymers within the cluster.
科研通智能强力驱动
Strongly Powered by AbleSci AI