Surface Hydrophilicity of Spherical Micelle from Self-Assembly of Random Copolymer: A Dissipative Particle Dynamics Simulation

被引:1
|
作者
Chen Mei-Ling [1 ]
Wang Li-Xiang [1 ]
Chen Shan-Shan [1 ]
Liu Xiao-Ya [1 ]
机构
[1] Jiangnan Univ, Sch Chem & Mat Engn, Minist Educ, Key Lab Food Colloids & Biotechnol, Wuxi 214122, Jiangsu Provinc, Peoples R China
基金
中国国家自然科学基金;
关键词
Amphiphilic random copolymer; Self-assembly; Dissipative particle dynamics; Spherical micelle; Hydrophilicity; AMPHIPHILIC RANDOM COPOLYMER; MULTICOMPARTMENT MICELLES; TRIBLOCK COPOLYMERS; MULTIPLE MORPHOLOGIES; BLOCK-COPOLYMERS; STAR; SOLVENTS; ACID);
D O I
10.3866/PKU.WHXB201303202
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Coarse-grained models with different ratios of numbers of hydrophilic particles to hydrophobic particles were built for amphiphilic random copolymers. The surface hydrophilicity of spherical micelles formed from self-assembly of amphiphilic random copolymers in solution was investigated via dissipative particle dynamics (DPD) simulations. The simulations showed that solid spherical micelles are formed from self-assembly of amphiphilic random copolymers in selective solvents. The surface hydrophilicity of spherical micelles is related to the content of hydrophilic particles and selectivity of the solvent. The surface hydrophilicity of spherical micelles increases with increasing content of hydrophilic particles. In addition, the surface hydrophilicity of spherical micelles increases with the increase of the repulsion parameters between hydrophobic particles and solvent, which is in good agreement with the experimental results. These findings can provide theoretical guidance for molecular design and experimental studies on self-assembly of amphiphilic random copolymers in solution.
引用
收藏
页码:1201 / 1208
页数:8
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