Sousa J J, Sousa A, Moura M J, Podczeck F, Newton J M
Laboratório de Galénica e Tecnologia Farmacêutica, Faculdade de Farmácia, Rua do Norte, 3000 Coimbra, Portugal.
Int J Pharm. 2002 Feb 21;233(1-2):111-22. doi: 10.1016/s0378-5173(01)00921-8.
The objective of this study was to analyse the influence of the composition of the core of the pellets on the in vitro drug release profile. The different materials (drugs and fillers) were chosen according to their relative solubility. Pellets were prepared by a standardised process of extrusion/spheronisation. A selected fraction size (1-1.4 mm diameter) of pellets of each preparation was coated with Surelease (an aqueous dispersion of ethyl cellulose) to give 5% weight gain. The dissolution studies were performed and data analysed in terms of the Area under the Curve (AUC) of the % dissolved as function of time and Mean Dissolution Time (MDT). ANOVA was applied in order to identify the influence factors and the relationship of cross effects. Canonical analysis and multiple regression were employed to quantify these relationships. The film coat was found to be the major factor controlling the drug release. The results however, show that both drug and filler solubility influenced the drug release profile. Some of the unusual results could only be explained if consideration was given to the physical characteristics of both powder and pellets. In particular, the specific surface area of calcium phosphate compared with other fillers played an important role on the release profile of the model drug.
本研究的目的是分析微丸核心组成对体外药物释放曲线的影响。根据不同材料(药物和填充剂)的相对溶解度进行选择。微丸通过标准化的挤出/滚圆工艺制备。每种制剂选择特定粒径范围(直径1 - 1.4毫米)的微丸,用Surelease(乙基纤维素水分散体)包衣,增重5%。进行溶出度研究,并根据溶解百分数随时间变化的曲线下面积(AUC)和平均溶出时间(MDT)对数据进行分析。应用方差分析以确定影响因素及交叉效应的关系。采用典型分析和多元回归对这些关系进行量化。发现薄膜包衣是控制药物释放的主要因素。然而,结果表明药物和填充剂的溶解度均会影响药物释放曲线。只有考虑到粉末和微丸的物理特性,才能解释一些异常结果。特别是,与其他填充剂相比,磷酸钙的比表面积对模型药物的释放曲线起着重要作用。