School of Pharmacy, University of East Anglia, Norwich, Norfolk NR47TJ, UK.
Pharm Res. 2011 Sep;28(9):2311-26. doi: 10.1007/s11095-011-0461-2. Epub 2011 May 24.
To characterise phase separations in aged hot-melt-extruded solid dispersions at a micron to submicron scale.
Hot-melt-extruded felodipine and Eudragit® E PO systems at a range of compositions were studied after a standard period of aging to allow phase separation to occur. The samples were characterised using combined nano-thermal analysis, photothermal FTIR microspectroscopy coupled with pulsed force mode AFM as a novel characterisation approach.
Crystalline felodipine presents in all formulations with drug loadings from 10-70% (w/w). In formulations with high drug loadings (50 and 70%), amorphous felodipine co-exists with crystalline forms, and higher drug concentration is observed in the centre compared to the outer surface of the extrudates. Drug crystal dimensions in extrudates with low drug loadings (10-30%) are small, in the micron to submicron range. We propose that uneven drug distribution is principally caused by processing-associated factors such as expansion of extrudates during extrusion.
We have demonstrated that the novel combined approach allows site-specific characterisation of the extruded systems and that drug distribution may be uneven across the extrudates, with concomitant implications for understanding stability and drug release behaviour.
在微米到亚微米尺度上描述老化热熔挤出固体分散体中的相分离。
研究了一系列组成的菲洛地平与 Eudragit® E PO 的热熔挤出系统,经过标准的老化期以允许相分离发生。使用组合纳米热分析、光热傅里叶变换红外微光谱学结合脉冲力模式原子力显微镜对样品进行了表征,这是一种新颖的表征方法。
所有制剂中均存在载药量为 10-70%(w/w)的结晶菲洛地平。在高载药量(50%和 70%)的制剂中,无定形菲洛地平与结晶形式共存,并且在挤出物的中心观察到比外表面更高的药物浓度。低载药量(10-30%)的挤出物中药物晶体尺寸较小,处于微米到亚微米范围。我们提出,不均匀的药物分布主要是由加工相关因素引起的,例如挤出过程中挤出物的膨胀。
我们已经证明,新的组合方法允许对挤出系统进行特定部位的表征,并且药物分布可能在挤出物中不均匀,这对理解稳定性和药物释放行为具有重要意义。