Synthesis of a carbon dioxide-based amphiphilic block copolymer and its evaluation as a nanodrug carrier

被引:9
|
作者
Li, Hongchun [1 ]
Sui, Lulu [1 ]
Niu, Yongsheng [1 ]
机构
[1] Qingdao Agr Univ, Coll Chem & Pharm, Qingdao 266109, Peoples R China
基金
中国国家自然科学基金;
关键词
ONE-POT SYNTHESIS; RING-OPENING POLYMERIZATION; PROPYLENE-OXIDE; POLY(PROPYLENE CARBONATE); TRIBLOCK COPOLYMERS; TERPOLYMERIZATION; PEG; CO2; EPOXIDES; ANHYDRIDE;
D O I
10.1007/s10853-018-2594-8
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
A series of novel amphiphilic block copolymers poly(propylene carbonate)-block-mono-methoxy poly(ethylene oxide) (PPC-b-MPEG) composed of hydrophobic PPC segments and various lengths of hydrophilic MPEG segments was synthesized via "Click Chemistry" between azido-terminated PPC and alkynyl-terminated MPEG. The structure of the copolymers was characterized by FTIR, H-1 NMR and C-13 NHR techniques. Chlorpyrifos (CHP) was encapsulated within micelles through diffusion dialysis method, leading to the formation of CHP-loaded PPC-b-MPEG micelles. The resulting micelles were characterized further by dynamic light scattering (DLS) and scanning electron microscope. The results indicated that PPC-b-MPEG could self-assemble into nanosized micelles with PPC cores and PEG shells in aqueous solution. And the size, zeta potential, morphology, critical micelle concentration of PPC-b-MPEG micelles can be altered by changing the lengths of the PEG segments. CHP was encapsulated into PPC-b-MPEG(2k) micelles with loading capacity of 9.02% and entrapment efficiency of 77.28%. These results suggested that PPC-b-MPEG micelles would be a potential carrier for controlled release.
引用
收藏
页码:12718 / 12730
页数:13
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