Aman W, Thoma Karl
Department of Pharmaceutical Technology, Ludwig-Maximilians-Universität München, Butenandtstr. 5, 81377 Munich, Germany.
Int J Pharm. 2002 Aug 28;243(1-2):33-41. doi: 10.1016/s0378-5173(02)00110-2.
The formulation and the manufacturing process can significantly influence the photostability of tablets. Investigations of various formulation and manufacturing parameters were done with tablets containing nifedipine and molsidomine as highly light sensitive drugs. The effect of relevant formulation factors are stated. Whereas the particle size of the drug substance and the choice of the lubricant had no effect, the drug content, the compression diluent and geometric alterations significantly affected the photoinstability. Depending on the formulation drug losses varied between 30 and 55% after 12 h irradiation in a light testing cabinet (Suntest CPS+). Manufacturing parameters like compression force and direct compression versus granulation showed less serious influences. Nevertheless, photostability changes up to 10% were registered.
制剂配方和制造工艺会显著影响片剂的光稳定性。以硝苯地平和莫西赛利为对光高度敏感药物的片剂,对各种制剂配方和制造参数进行了研究。阐述了相关制剂因素的影响。原料药的粒径和润滑剂的选择没有影响,而药物含量、压缩稀释剂和几何形状改变对光不稳定性有显著影响。根据制剂配方不同,在光照试验箱(Suntest CPS+)中照射12小时后,药物损失在30%至55%之间。压片力以及直接压片与制粒等制造参数的影响较小。然而,仍记录到光稳定性变化高达10%。