Aqueous Self-Assembly of Y-Shaped Amphiphilic Block Copolymers into Giant Vesicles

被引:6
|
作者
Li, Hanping [1 ,2 ]
Jin, Yong [1 ,2 ]
Fan, Baozhu [3 ,4 ]
Lai, Shuangquan [1 ,2 ]
Sun, Xiaopeng [1 ,2 ]
Qi, Rui [3 ,4 ]
机构
[1] Sichuan Univ, Minist Educ, Key Lab Leather Chem & Engn, Chengdu 610065, Peoples R China
[2] Sichuan Univ, Natl Engn Lab Clean Technol Leather Mfg, Chengdu 610065, Peoples R China
[3] Chinese Acad Sci, Chengdu Inst Organ Chem, Ctr Polymer Sci & Technol, Chengdu 610041, Peoples R China
[4] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
aqueous solution self-assembly; giant unilamellar vesicles; morphology; Y-shaped amphiphilic block copolymers; TRIGGERED DISSOCIATION; AGGREGATION BEHAVIOR; DIBLOCK COPOLYMERS; PORE FORMATION; NANOPARTICLES; POLYMERSOMES; MICELLES; ETHER; SURFACTANTS; FABRICATION;
D O I
10.1002/marc.201600646
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The preparation and aqueous self-assembly of newly Y-shaped amphiphilic block polyurethane (PUG) copolymers are reported here. These amphiphilic copolymers, designed to have two hydrophilic poly(ethylene oxide) (PEO) tails and one hydrophobic alkyl tail via a two-step coupling reaction, can self-assemble into giant unilamellar vesicles (GUVs) (diameter >= 1000 nm) with a direct dissolution method in aqueous solution, depending on their Y-shaped structures and initial concentrations. More interesting, the copolymers can self-assemble into various distinct nano(-)/microstructures, such as spherical micelles, small vesicles, and GUVs, with the increase of their concentrations. The traditional preparation methods of GUVs generally need conventional amphiphilic molecules and additional complicated conditions, such as alternating electrical field, buffer solution, or organic solvent. Therefore, the self-assembly of Y-shaped PUGs with a direct dissolution method in aqueous solution demonstrated in this study supplies a new clue to fabricate GUVs based on the geometric design of amphiphilic polymers.
引用
收藏
页数:8
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