Levina Marina, Rajabi-Siahboomi Ali R
Colorcon Limited, Flagship House, Victory Way, Crossways, Dartford, Kent DA2 6QD, UK.
J Pharm Sci. 2004 Nov;93(11):2746-54. doi: 10.1002/jps.20181.
The influence of commonly used excipients, spray-dried lactose (SDL), microcrystalline cellulose (MCC), and partially pregelatinized maize starch (Starch 1500) on drug release from hydroxypropyl methylcellulose (HPMC, hypromellose) matrix system has been investigated. A model formulation contained 30%w/w drug, 20%w/w HPMC, 0.5%w/w fumed silica, 0.25%w/w magnesium stearate, and 49.25%w/w filler. Chlorpheniramine maleate and theophylline were used as freely (1 in 4) and slightly (1 in 120) water-soluble drugs, respectively. It was found that for both drugs, addition of 20 to 49.25%w/w Starch 1500 resulted in a significant reduction in drug release rates compared to when MCC or SDL was used. The study showed that using lactose or microcrystalline cellulose in the formulations resulted in faster drug release profiles. Partially pregelatinized maize starch contributed to retardation of both soluble and slightly soluble drugs. This effect may be imparted through synergistic interactions between Starch 1500 and HPMC and the filler actively forming an integral part within the HPMC gel structure.
已研究了常用辅料喷雾干燥乳糖(SDL)、微晶纤维素(MCC)和部分预胶化玉米淀粉(淀粉1500)对羟丙基甲基纤维素(HPMC,羟丙甲纤维素)基质系统药物释放的影响。一种模型制剂含有30%w/w药物、20%w/w HPMC、0.5%w/w气相二氧化硅、0.25%w/w硬脂酸镁和49.25%w/w填充剂。马来酸氯苯那敏和茶碱分别用作水溶性良好(1/4)和水溶性稍差(1/120)的药物。结果发现,对于这两种药物,与使用MCC或SDL时相比,添加20%至49.25%w/w的淀粉1500会导致药物释放速率显著降低。研究表明,在制剂中使用乳糖或微晶纤维素会导致更快的药物释放曲线。部分预胶化玉米淀粉有助于延缓可溶性和微溶性药物的释放。这种作用可能是通过淀粉1500与HPMC之间的协同相互作用以及填充剂在HPMC凝胶结构中积极形成一个整体部分来实现的。