Sinchaipanid Nuttanan, Chitropas Padungkwan, Mitrevej Ampol
Department of Industrial Pharmacy, Faculty of Pharmacy, Mahidol University, Bangkok, Thailand.
Pharm Dev Technol. 2004;9(2):163-70. doi: 10.1081/pdt-120030246.
This study evaluated and compared theophylline pellets prepared by both suspension and powder layering processes using the bottom spray coater and the tangential rotary granulator, respectively. Hydroxypropyl methylcellulose (HPMC) and hydroxypropyl cellulose (HPC) were employed as binders at various concentrations. The pellets were coated with Eudragit RS and RL to various levels. It was found that pellet sizes, true densities, and drug contents were comparable and independent of processes and binder levels. However, the increase in binder resulted in lower porosity and pore size, as well as smoother pellet surface. The powder layered pellets possessed higher pellet density and smoother surface than did the suspension layered pellets due to the greater consolidation resulted from tumbling and colliding of pellets. Powder x-ray diffraction pattern revealed that theophylline present in the suspension layered pellets was a mixture of anhydrous form II and hydrate, indicating that transformation could occur in aqueous medium. Drug release from uncoated pellets was found to be complete within 20 min. For coated pellets, the release was markedly decreased with the increase in Eudragit level. Both film thickness and anhydrous/hydrate form influenced the release of drug from the pellets. In general, two methods of layering produced the pellets of slightly differences in pellet properties; however, changes of drug characteristics could occur in suspension.
本研究分别使用底喷包衣机和切向旋转制粒机,对通过悬浮法和粉末层积法制备的茶碱微丸进行了评估和比较。羟丙基甲基纤维素(HPMC)和羟丙基纤维素(HPC)被用作不同浓度的粘合剂。微丸用不同水平的Eudragit RS和RL进行包衣。结果发现,微丸尺寸、真密度和药物含量具有可比性,且与制备工艺和粘合剂水平无关。然而,粘合剂用量增加会导致孔隙率和孔径降低,以及微丸表面更光滑。由于微丸翻滚和碰撞导致的固结作用更强,粉末层积微丸比悬浮层积微丸具有更高的微丸密度和更光滑的表面。粉末X射线衍射图谱显示,悬浮层积微丸中的茶碱是无水II型和水合物的混合物,表明在水性介质中可能发生转变。未包衣微丸在20分钟内药物释放完全。对于包衣微丸,随着Eudragit用量的增加,释放明显减少。膜厚度和无水/水合形式均影响微丸中药物的释放。总体而言,两种层积方法制备的微丸在性质上略有差异;然而,悬浮过程中药物特性可能会发生变化。