Poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide)/poly(ε-caprolactone) (PCL) amphiphilic block copolymeric nanospheres -: II.: Thermo-responsive drug release behaviors

被引:135
作者
Kim, SY [1 ]
Ha, JC [1 ]
Lee, YM [1 ]
机构
[1] Hanyang Univ, Coll Engn, Dept Ind Chem, Seoul 133791, South Korea
关键词
pluronic; poly(epsilon-caprolactone); block copolymer; nanospheres; drug delivery system;
D O I
10.1016/S0168-3659(99)00207-2
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Amphiphilic block copolymers composed of relatively hydrophilic PEO-PPO-PEO block copolymer (Pluronic) and poly(epsilon-caprolactone) with hydrophobic character were synthesized by ring-opening polymerization of epsilon-caprolactone in the presence of PEO-PPO-PEO block copolymer using stannous octoate as a catalyst. Pluronic/PCL block copolymeric nanospheres with core-shell structure were prepared by dialysis method. They showed the average diameter of 116-196 nm depending on the type of copolymer. All the nanosphere samples exhibited a narrow size distribution. The critical micelle concentrations of Pluronic/PCL amphiphilic block copolymers determined by fluorescence spectroscopy were lower than that of the common low molecular weight surfactant. Their core-shell structure was confirmed by H-1 NMR spectroscopy. Pluronic/PCL block copolymeric nanospheres exhibited the reversible change of size depending on the temperature. Release behaviors of indomethacin from Pluronic/PCL block copolymeric nanospheres also showed temperature dependence and a sustained release pattern. In addition, cytotoxicity test using an MTT assay method revealed that these indomethacin-loaded Pluronic/PCL nanospheres could remarkably reduce the cell damage compared with the unloaded free indomethacin. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:345 / 358
页数:14
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