首页> 外文期刊>Nanoscale >Modeling and self-assembly behavior of PEG-PLA-PEG triblock copolymers in aqueous solution
【24h】

Modeling and self-assembly behavior of PEG-PLA-PEG triblock copolymers in aqueous solution

机译:PEG-PLA-PEG的建模和自组装行为triblock共聚物在水溶液中

获取原文
获取原文并翻译 | 示例
           

摘要

A series of poly(ethylene glycol)-polylactide-poly(ethylene glycol) (PEG-PLA-PEG) triblock copolymers with symmetric or asymmetric chain structures were synthesized by combination of ring-opening polymerization and copper-catalyzed click chemistry. The resulting copolymers were used to prepare self-assembled aggregates by dialysis. Various architectures such as nanotubes, polymersomes and spherical micelles were observed from transmission electron microscopy (TEM), cryo-TEM and atomic force microscopy (AFM) measurements. The formation of diverse aggregates is explained by modeling from the angle of both geometry and thermodynamics. From the angle of geometry, a "blob" model based on the Daoud-Cotton model for star polymers is proposed to describe the aggregate structures and structural changes with copolymer composition and molar mass. In fact, the copolymer chains extend in aqueous medium to form single layer polymersomes to minimize the system's free energy if one of the two PEG blocks is short enough. The curvature of polymersomes is dependent on the chain structure of copolymers, especially on the length of PLA blocks. A constant branch number of aggregates (f) is thus required to preserve the morphology of polymersomes. Meanwhile, the aggregation number (N_(agg)) determined from the thermodynamics of self-assembly is roughly proportional to the total length of polymer chains. Comparing f to N_(agg), the aggregates take the form of polymersomes if N_(agg) ≈ f, and change to nanotubes if N_(agg) >f to conform to the limits from both curvature and aggregation number. The length of nanotubes is mainly determined by the difference between N_(agg) and f. However, the hollow structure becomes unstable when both PEG segments are too long, and the aggregates eventually collapse to yield spherical micelles. Therefore, this work gives new insights into the self-assembly behavior of PEG-PLA-PEG triblock copolymers in aqueous solution which present great interest for biomedical and pharmaceutical applications.
机译:一系列的聚(乙烯乙二醇)-polylactide-poly(乙二醇)(PEG-PLA-PEG) triblock共聚物与对称的或不对称合成链结构通过开环聚合和组合copper-catalyzed点击化学。共聚物被用来准备自组装通过透析总量。多聚体,如碳纳米管和球形从透射电子胶束被观察到显微镜(TEM)、cryo-TEM和原子力显微镜(AFM)测量。不同骨料是由建模几何和热力学的角度。从几何的角度,基于“blob”模型星形聚合物Daoud-Cotton模型提出了描述和总体结构与共聚物组成和结构变化摩尔质量。水介质中形成一层系统的自由能最小化多聚体如果其中一个两个挂钩块足够短。依赖于多聚体的曲率共聚物的链结构,特别是在解放军块的长度。总量(f)因此需要保护多聚体的形态。聚合数量(N_ (gg))的决定自组装是大致的热力学与聚合物的总长度成正比链。多聚体的形式如果N_ (gg)≈f改变纳米管如果N_ (gg) > f符合极限曲率和聚合号码。之间的区别取决于N_ (gg)和f。然而,空心结构变得不稳定当两个挂钩部分太长,聚集最终崩溃产生球形胶束。PEG-PLA-PEG的自组装行为triblock共聚物在水溶液中目前对生物医学和极大的兴趣制药应用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号