紫杉醇
动力学
扩散
剂型
材料科学
色散(光学)
化学工程
微球
二氯甲烷
毒品携带者
微粒
沉积(地质)
化学
色谱法
药物输送
溶剂
纳米技术
有机化学
外科
化疗
光学
工程类
生物
古生物学
量子力学
热力学
医学
物理
沉积物
作者
Richard Liggins,Helen M. Burt
标识
DOI:10.1016/j.ijpharm.2004.05.027
摘要
The kinetics of solvent removal in microsphere preparation and their effect on the morphology and release characteristics of paclitaxel-loaded PLLA microspheres were determined. Microspheres were analyzed by SEM and DSC and in vitro paclitaxel release was monitored by HPLC. During manufacture, dichloromethane evaporated at a constant rate, which increased with dispersion stirring speed and decreased with increasing paclitaxel content. Paclitaxel-loaded microspheres had a dimpled surface, due to surface deposition of the drug, while controls were smooth. In the formation of larger microspheres, the deposition of drug in the surface slowed the solidification process resulting in drug-loading dependent thermal properties. Paclitaxel release did not follow diffusion kinetics, rather it was characterized by a large burst followed by a linear phase. We speculate that non-uniform (surface-rich) drug distribution in the microspheres may contribute to the deviation from the theoretical pattern of kinetics for diffusion from a sphere.
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