Young C R, Koleng J J, McGinity J W
Drug Dynamics Institute, College of Pharmacy, The University of Texas at Austin, 78712, USA.
J Microencapsul. 2003 Sep-Oct;20(5):613-25. doi: 10.1080/0265204031000148004.
The objectives of this study were to investigate the particle size distribution, morphology and dissolution properties of spherical pellets produced by hot-melt extrusion and spheronization and to compare the properties of hot-melt extruded pellets with beads manufactured by a traditional wet-mass extrusion and spheronization method. Spherical pellets were produced by hot-melt extrusion without the use of water or other solvents. A powder blend of theophylline, Eudragit Preparation 4135 F, microcrystalline cellulose and polyethylene glycol 8000 was hot melt-extruded and the resulting composite rod was cut into cylindrical pellets. The pellets were then spheronized in a traditional spheronizer at an elevated temperature. The same powder blend was processed using conventional wet-mass techniques. Unlike wet-mass extruded pellets, pellets prepared from hot-melt extrusion displayed both a narrow particle size distribution and controlled drug release in dissolution media less than pH 7.4. Scanning electron microscopy, X-ray diffraction and porosity measurements were employed to explain the differences in drug release rates of theophylline from pellets produced by the two processing techniques. Theophylline release from the hot-melt extruded pellets was described using the Higuchi diffusion model, and drug release rates from wet-granulated and melt-extruded pellets did not change after post-processing thermal treatment.
本研究的目的是研究通过热熔挤出和滚圆法制备的球形微丸的粒度分布、形态和溶出特性,并比较热熔挤出微丸与通过传统湿法制粒挤出和滚圆法制备的微丸的性能。通过热熔挤出法在不使用水或其他溶剂的情况下制备球形微丸。将茶碱、尤特奇4135F、微晶纤维素和聚乙二醇8000的粉末混合物进行热熔挤出,然后将所得复合棒切成圆柱形微丸。接着将微丸在传统的滚圆机中于高温下滚圆。使用常规湿法制粒技术对相同的粉末混合物进行加工。与湿法制粒挤出的微丸不同,热熔挤出制备的微丸在pH值小于7.4的溶出介质中显示出较窄的粒度分布和可控的药物释放。采用扫描电子显微镜、X射线衍射和孔隙率测量来解释两种加工技术制备的微丸中茶碱药物释放速率的差异。使用Higuchi扩散模型描述了热熔挤出微丸中茶碱的释放情况,后处理热处理后,湿法制粒和热熔挤出微丸的药物释放速率没有变化。