Self-Assembly of Polyurethane Phosphate Ester with Phospholipid-Like Structures: Spherical, Worm-Like Micelles, Vesicles, and Large Compound Vesicles

被引:39
作者
Cheng, Xinfeng [1 ,2 ]
Jin, Yong [3 ,4 ]
Fan, Baozhu [1 ,2 ]
Qi, Rui [1 ,2 ]
Li, Hanping [3 ,4 ]
Fan, Wuhou [3 ,4 ]
机构
[1] Chinese Acad Sci, Ctr Polymer Sci & Technol, Chengdu Inst Organ Chem, Chengdu 610041, Peoples R China
[2] Univ Chinese Acad Sci, 19A Yuquan Rd, Beijing 100049, Peoples R China
[3] Sichuan Univ, Natl Engn Lab Clean Technol Leather Mfg, Chengdu 610065, Peoples R China
[4] Sichuan Univ, Key Lab Leather Chem & Engn, Minist Educ, Chengdu 610065, Peoples R China
基金
中国国家自然科学基金;
关键词
BLOCK-COPOLYMER SURFACTANTS; TRIBLOCK COPOLYMER; DELIVERY; GEMINI; NANOPARTICLES; MORPHOLOGIES; TRANSITION; HYDROGELS; POLYMERS; BEHAVIOR;
D O I
10.1021/acsmacrolett.5b00789
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 [高分子化学与物理];
摘要
Here, we report the preparation and self-assembly of amphiphilic polyurethane phosphate ester (PUP) polymers with phospholipid-like structures. The polymers, designed to have a hydrophilic phosphate head and two amphiphilic PPG-IPDI-MPEG (PU) tails were synthesized via coupling and phosphorylation reactions in sequence. These amphiphilic polymers could self assemble into various interesting nanostructures in aqueous solution, such as spherical, worm-like micelles, vesicles, and large compound vesicles, depending on the hydrophobic chain length of PU tails and the initial polymer concentrations. It was found that the morphology transition is not only caused by the unique molecular structure of amphiphilic polyurethanes, but also influenced by the additional hydrophilic phosphate groups incorporated, which disturb the force balance governing the aggregation structures. This research supplies a new clue for the fabrication of well-defined nanostructures.
引用
收藏
页码:238 / 243
页数:6
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