Sol-gel processed porous silica carriers for the controlled release of diclofenac diethylamine

被引:10
作者
Czarnobaj, Katarzyna [1 ]
Czarnobaj, Joanna [2 ]
机构
[1] Med Univ Gdansk, Dept Phys Chem, PL-80416 Gdansk, Poland
[2] Univ Alberta, Fac Med & Dent, Dept Dent, Edmonton, AB, Canada
关键词
drug delivery/release; in vitro study; NSAID-s; microstructure of silica xerogel matrix;
D O I
10.1002/jbm.b.31076
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Silica xerogels doped with diclofenac diethylamine were prepared by the sol-gel method from a hydrolysed tetraethoxysilane (TEOS) solution containing diclofenac diethylamine. Two different catalysts, drying conditions and levels of water content were used to alter the microstructure of the silica xerogels. The aim of this study was to determine the rate of Diclofenac release from the silica xerogels. This in vitro study showed that the sol-gel method is useful for entrapping Diclofenac in the pores of xerogels. It also showed that, in vitro, Diclofenac is released from the silica xerogel, through the pores, by diffusion. Base-catalysed gels proved to be much more effective than acid-catalyzed gels. (c) 2008 Wiley Peiodicals, Inc.
引用
收藏
页码:114 / 120
页数:7
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