Synthesis and Characterization of Amphiphilic Pluronic (F68)-1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine Copolymers and Their Micelles as a Drug Carrier

被引:16
作者
Wang, Tiewei [1 ,2 ]
Wu, Yan [1 ]
Zeng, Ai Jun [2 ]
机构
[1] Natl Ctr Nanosci & Technol, Dept Manomed & Nanobiol, Beijing 100190, Peoples R China
[2] China Agr Univ, Dept Chem, Beijing 100083, Peoples R China
关键词
Pluronic (F68); 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine; copolymeric micelles; amphotericin B; drug delivery; POLYMERIC MICELLES; BLOCK-COPOLYMERS; IN-VITRO; DOXORUBICIN; RELEASE; DELIVERY; MICROPARTICLES; CYCLODEXTRINS; NANOCARRIERS; PERMEABILITY;
D O I
10.1002/app.31231
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A new Pluronic (F68)-1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine (DPPE) (Pluronic (F68)DPPE) copolymer was synthesized with Pluronic (F68) and DPPE. The chemical structure and physical properties of copolymers were determined by FTIR, H-1. NMR, C-13 NMR, P-31 NMR, and TGA. Environmental scanning electron microscopy, fluorescence spectroscopy, and dynamic light scattering method confirmed the formation of copolymeric micelles of Pluronic (F68)-DPPE. To estimate the feasibility as novel drug carriers, the copolymer micelles were prepared by the phase separation dialysis method. Amphotericin B as a lipophilic model drug was incorporated into copolymeric micelles and the drug release behavior was investigated. It was found that the chemical composition of the micelle was a key factor in controlling micelles size, drug-loading content, and drug release behavior. As DPPE segment weight ratio increased, the micelle size and drug-loading content increased, and the drug release rate decreased. (C) 2010 Wiley Periodicals, Inc. J Appl Polym Sci 117: 604-613, 2010
引用
收藏
页码:604 / 613
页数:10
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