期刊
EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES
卷 33, 期 3, 页码 282-293出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejps.2007.12.008
关键词
hot-melt co-extrusion; controlled release; dissolution mathematical model; oral drug delivery
Aim of this work was to develop a cylindrical co-extrudate characterised by an in vivo sustained release profile by means of a hot-melt extrusion process. Co-extrudate was made up of two concentric extruded matrices: an inner one having a hydrophilic character, based on polyethylene glycol, and an outer one with lipophilic character, based on microcrystalline wax. Both segments contained theophylline as a model drug. A screening between several devices differing for dimensions (diameter and length) and relative proportions of the inner and outer part was carried out on the basis of their in vitro drug release and the release mechanism was studied by means of a mathematical model. The co-extrudate exhibiting the desired sustained release was selected for in vivo bioavailability studies. in vivo studies confirmed the achievement of the purpose of the research, demonstrating the desired release of theophylline on four healthy volunteers. Accordingly, hot-melt extrusion process is a viable method to produce in a single step co-extrudates showing a sustained release. In addition, the developed mathematical model proved to be a reliable descriptor of the both in vitro and in vivo experimental data. (C) 2008 Elsevier B.V. All rights reserved.
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