Aqueous Self-Assembly of Purely Hydrophilic Block Copolymers into Giant Vesicles

被引:68
作者
Brosnan, Sarah M. [1 ]
Schlaad, Helmut [2 ]
Antonietti, Markus [1 ]
机构
[1] Max Planck Inst Colloids & Interfaces, Dept Colloid Chem, D-14424 Potsdam, Germany
[2] Univ Potsdam, Inst Chem, D-14476 Potsdam, Germany
基金
美国国家科学基金会;
关键词
block copolymers; polymersomes; polysaccharides; self-assembly; vesicles; MULTIPLE MORPHOLOGIES; DIBLOCK COPOLYMERS; POLYMERSOMES; DEPOLYMERIZATION; KINETICS; DEXTRAN;
D O I
10.1002/anie.201502100
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Self-assembly of macromolecules is fundamental to life itself, and historically, these systems have been primitively mimicked by the development of amphiphilic systems, driven by the hydrophobic effect. Herein, we demonstrate that self-assembly of purely hydrophilic systems can be readily achieved with similar ease and success. We have synthesized double hydrophilic block copolymers from polysaccharides and poly(ethylene oxide) or poly(sarcosine) to yield high molar mass diblock copolymers through oxime chemistry. These hydrophilic materials can easily assemble into nanosized (<500nm) and microsized (>5m) polymeric vesicles depending on concentration and diblock composition. Because of the solely hydrophilic nature of these materials, we expect them to be extraordinarily water permeable systems that would be well suited for use as cellular mimics.
引用
收藏
页码:9715 / 9718
页数:4
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