Kaniwa N, Katori N, Aoyagi N, Kojima S, Ishigame N, Seta Y, Shinba T, Fujiwara K, Nakai T, Oda Y
Kokuritsu Iyakuhin Shokuhin Eisei Kenkyusho Hokoku. 1998(116):189-91.
The collaborative study participated by seven laboratories was carried out to develop a dissolution standard for evaluating vibration levels of dissolution apparatuses using enteric-coated granules of cefalexin (EG). Dissolution apparatuses could be divided into two groups according to their vibration levels and the dissolution test results of EG by the rotating basket method at 50 rpm. The critical value of acceleration was about 0.05 m/s2. The upper limit of normal dissolution rates of EG was calculated from the results of the rotating basket method at 50 rpm obtained from low vibration apparatuses. All high vibration apparatuses used in this study were distinguished by the limit from low vibration apparatuses, although most of them were not distinguished by current USP calibrators. These results suggest that EG would be useful as a calibrator for detection of apparatuses on high vibration levels.
由七个实验室参与的合作研究开展了,目的是制定一个溶出度标准,用于评估使用头孢氨苄肠溶颗粒(EG)的溶出度仪的振动水平。根据振动水平以及通过50转/分钟的旋转篮法对EG进行的溶出度测试结果,溶出度仪可分为两组。加速度的临界值约为0.05米/秒²。EG正常溶出速率的上限是根据从低振动水平的仪器在50转/分钟下通过旋转篮法获得的结果计算得出的。本研究中使用的所有高振动水平的仪器都与低振动水平的仪器在限值上有所区分,尽管它们中的大多数无法通过现行的美国药典校准仪区分开来。这些结果表明,EG作为检测高振动水平仪器的校准剂将是有用的。