Synthesis of Amphiphilic Comb-Shape Copolymers Via Ring-Opening Polymerization of a Macromonomer

被引:10
|
作者
Zhang, Xiaojin [1 ]
Zhang, Zhenguo [1 ]
Su, Xin [1 ]
Dong, Hui [1 ]
Zhong, Zhenlin [1 ]
Zhuo, Renxi [1 ]
机构
[1] Wuhan Univ, Dept Chem, Key Lab Biomed Polymers, Minist Educ, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
comb-shape copolymers; controlled drug release; macromonomer; ring-opening polymerization; self-assembly; GRAFT-COPOLYMERS; RAFT POLYMERIZATION; RADICAL POLYMERIZATION; POLYMERS; BLOCK; BEHAVIOR; BRUSHES; CHAINS; WATER; ATRP;
D O I
10.1002/macp.201500161
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Amphiphilic comb-shape copolymers PCL-co-P(MTC-mPEG(16)) (where PCL, MTC, and mPEG refer to poly(epsilon-caprolactone), 2-methyltrimethylene carbonate, and methoxy poly(ethylene glycol), respectively) are synthesized by ring-opening polymerization of epsilon-caprolactone and cyclic carbonate-terminated PEG macromonomer (MTC-mPEG(16)) with benzyl alcohol as an initiator and Sn(Oct)(2) as a catalyst. Amphiphilic copolymers PCL-co-P(MTC-mPEG(16)) can form micelles in aqueous solution by self-assembly. The diameters of PCL-co-P(MTC-mPEG(16)) micelles characterized by dynamic light scattering area few dozens of nanometers with a narrow size distribution and the morphology of the micelles observed through transmission electron microscopy are nanosized spheres. The in vitro drug release of comb-shape copolymer PCL-co-P(MTC-mPEG(16)) micelles is more stable and sustained than that of linear block copolymers mPEG-b-PCL.
引用
收藏
页码:1712 / 1717
页数:6
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