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首页> 外文期刊>International Journal of Pharmaceutics >Evaluation of solid state properties of solid dispersions prepared by hot-melt extrusion and solvent co-precipitation.
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Evaluation of solid state properties of solid dispersions prepared by hot-melt extrusion and solvent co-precipitation.

机译:评估通过热熔挤出和溶剂共沉淀制备的固体分散体的固态性能。

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摘要

The solid state properties of solid dispersions of Compound A in hypromellose acetate succinate (HPMC-AS) prepared by hot-melt extrusion (HME) and solvent co-precipitation (CP) processes were evaluated using powder X-ray diffractometry (PXRD), thermal analysis, optical microscopy, scanning electron microscopy (SEM), FT-IR and Raman spectroscopy, water vapor sorption analyzer, and surface area by BET. PXRD indicated that both processes converted the crystalline drug into amorphous solid dispersions with a glass transition temperature around 104-107 degrees C and both products have similar spectroscopic and hygroscopic properties. The two products have similar true densities; however, the CP product is more porous and has a larger specific surface area than the HME product, as indicated by the BET results and SEM micrographs. Dissolution study using USP apparatus 2 showed that the CP product had a faster dissolution profile, but slower intrinsic dissolution rate than the HME product. The two products have acceptable physical stability after storage in 40 degrees C/75% RH chamber for 3 months. However, the HME product is more stable than the CP product in aqueous suspension formulation.
机译:使用粉末X射线衍射(PXRD),热法评估了通过热熔挤出(HME)和溶剂共沉淀(CP)工艺制备的化合物A在乙酸羟丙甲纤维素琥珀酸酯(HPMC-AS)中的固体分散体的固态性能分析,光学显微镜,扫描电子显微镜(SEM),FT-IR和拉曼光谱,水蒸气吸收分析仪以及BET表面积。 PXRD表明,两种方法均将结晶药物转化为无定形固体分散体,玻璃化转变温度约为104-107摄氏度,并且两种产品均具有相似的光谱和吸湿性能。两种产品的真实密度相似;然而,如BET结果和SEM显微照片所示,CP产品比HME产品更多孔,比表面积更大。使用USP装置2进行的溶出度研究表明,与HME产物相比,CP产物具有更快的溶出曲线,但固有溶出速率较慢。两种产品在40°C / 75%RH的室内存放3个月后具有可接受的物理稳定性。但是,在水性悬浮液配方中,HME产品比CP产品更稳定。

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