Clonazepam release from core-shell type nanoparticles in vitro

被引:203
作者
Jeong, YI
Cheon, JB
Kim, SH
Nah, JW
Lee, YM
Sung, YK
Akaike, T
Cho, CS [1 ]
机构
[1] Chonnam Natl Univ, Dept Polymer Engn, Kwangju 500757, South Korea
[2] Chosun Univ, Coll Pharm, Kwangju 501759, South Korea
[3] Sunchon Natl Univ, Dept Polymer Sci & Engn, Sunchon 540742, South Korea
[4] Hanyang Univ, Dept Ind Chem, Seoul 133791, South Korea
[5] Dongguk Univ, Dept Chem, Seoul 100715, South Korea
[6] Tokyo Inst Technol, Fac Biosci & Biotechnol, Yokohama, Kanagawa 227, Japan
关键词
clonazepam release; core/shell nanoparticles; in vitro studies;
D O I
10.1016/S0168-3659(97)00163-6
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Block copolymers consisting of poly(gamma-benzyl L-glutamate) (PBLG) as the hydrophobic block and poly(ethylene oxide) (PEG) as the hydrophilic block were synthesized and characterized. Core-shell type nanoparticles of the block copolymers (abbreviated as GE) were prepared by the diafiltration method. The particle size diameter obtained by dynamic light scattering of GE-1 (PBLG content: 60.5 mol %), GE-2 (PBLG content: 40.0 mol %), GE-3 (PBLG content: 12.4 mol %) copolymer was 309.9+/-160.9, 251.9+/-220.6 and 200.5+/-177.1 nm, respectively. The shape of the nanoparticles by SEM or TEM was almost spherical. The critical micelle concentration of the block copolymers obtained by fluorescence spectroscopy was dependent on the chain length of hydrophobic PBLG. The micelle structure of the copolymer nanoparticle was very stable against sodium dodecyl sulfate. Clonazepam (CZ) was loaded onto the core part of the nanoparticle as the crystalline state. Release of CZ from the nanoparticles in vitro was dependent on the drug loading contents and PBLG chain length. (C) 1998 Elsevier Science B.V.
引用
收藏
页码:169 / 178
页数:10
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