首页> 外文期刊>European journal of pharmaceutical sciences >Preparation of sustained release co-extrudates by hot-melt extrusion and mathematical modelling of in vitro/in vivo drug release profiles.
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Preparation of sustained release co-extrudates by hot-melt extrusion and mathematical modelling of in vitro/in vivo drug release profiles.

机译:通过热熔挤出和体外/体内药物释放曲线的数学模型制备缓释共挤出物。

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摘要

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.
机译:这项工作的目的是通过热熔挤出工艺开发一种以体内持续释放曲线为特征的圆柱形共挤出物。共挤出物由两种同心挤出的基质组成:一种内部具有基于聚乙二醇的亲水特性,另一种外部具有基于微晶蜡的亲脂特性。两个部分均包含茶碱作为模型药物。根据其体外药物释放,对几种尺寸(直径和长度)以及内部和外部的相对比例不同的装置进行了筛选,并通过数学模型研究了释放机理。选择具有所需持续释放的共挤出物用于体内生物利用度研究。体内研究证实了该研究目的的实现,证明了四名健康志愿者所需的茶碱释放量。因此,热熔挤出工艺是在一步中生产显示出持续释放的共挤出物的可行方法。此外,开发的数学模型被证明是体外和体内实验数据的可靠描述。

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