Hirasawa Noriyuki, Ishise Sayoko, Miyata Hitomi
Research and Development Center, Nichi-iko Pharmaceutical Co., Ltd., 205-1 Shimoumezawa, Namerikawa 936-0857, Japan.
Yakugaku Zasshi. 2004 Jan;124(1):19-23. doi: 10.1248/yakushi.124.19.
Nilvadipine (NIL) solid-dispersion tablets were stored counter to packaging instructions by exposing them to 40 degrees C, 25 degrees C, 75% relative humidity, and light. The dissolution, stability assay, and tablet properties (weight, thickness and hardness) were then examined. NIL dissolved more than 85% after all storage periods with exposure to high temperature and humidity. Powder X-ray diffraction analysis indicated that NIL was present in an amorphous state as in the initial state. The stability assay of NIL showed that it was more than 99% stable during all storage periods when exposed to temperature, humidity, and light, indicating good stability. Tablet properties were influenced by humidity more than by temperature, and the hardness of tablets decreased with time to 42.9 N after storage of 3 months.
尼伐地平(NIL)固体分散体片未按照包装说明储存,而是将其暴露于40摄氏度、25摄氏度、75%相对湿度和光照条件下。然后检测其溶出度、稳定性以及片剂性质(重量、厚度和硬度)。在所有暴露于高温和高湿度的储存期后,NIL的溶出度超过85%。粉末X射线衍射分析表明,NIL与初始状态一样呈无定形状态。NIL的稳定性检测表明,在所有暴露于温度、湿度和光照的储存期内,其稳定性超过99%,表明稳定性良好。片剂性质受湿度的影响大于温度,储存3个月后片剂硬度随时间下降至42.9 N。