Physiological pH-triggered morphological transition of amphiphilic block copolymer self-assembly

被引:18
|
作者
Wu, Wei [1 ]
Wang, Weigang [1 ]
Li, Shuai [1 ]
Wang, Jiantao [1 ]
Zhang, Qiujing [1 ]
Li, Xiuhua [2 ]
Luo, Xianglin [1 ]
Li, Jianshu [1 ]
机构
[1] Sichuan Univ, Coll Polymer Sci & Engn, Chengdu 610065, Peoples R China
[2] Changzhou Inst Engn Technol, Changzhou 213164, Peoples R China
基金
中国国家自然科学基金;
关键词
Physiological pH-triggered; Morphological transition; Self-assembly; Functional polymer; DIBLOCK COPOLYMERS; DRUG-DELIVERY; MULTIPLE MORPHOLOGIES; SOLVENT; POLYMERIZATION; MICELLES; NANOPARTICLES; POLYMERSOMES; ARCHITECTURE; LIPOSOMES;
D O I
10.1007/s10965-014-0494-4
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In order to develop polymeric self-assembly with an intelligent morphological transition property under appropriate stimuli, a series of pH-sensitive amphiphilic block copolymers have been prepared via atom transfer radical polymerization (ATRP). Due to the delicately designed macromolecular structure, poly(ethylene glycol)(44)-b-poly(2-diisopropylaminoethyl methacrylate)(15) (PEG(44)-b-PDPA(15)) could form self-assemblies with a controllable morphological transition in response to the physiological pH changes. As demonstrated by the results of dynamic light scattering (DLS) records and transmission electron microscopy (TEM) micrographs, PEG(44)-b-PDPA(15) could self-assemble into toruloid aggregates arranged by several single micelles at pH 7.4, but the morphology changed into uniform single micelles at pH 6.5. With a further decrease of pH value to 5.5, PEG-b-PDPA became double hydrophilic and could not self-assemble into any nanostructure. Therefore, this block copolymer provides a feasible approach to construct a nanoscale smart self-assembly with adjustable morphologies, which exhibits its potential for biomedical applications with specific physiological pH stimuli, such as intracellular delivery and tumor therapy.
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页数:8
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