Abdou H M, Ast T M, Cioffi F J
J Pharm Sci. 1978 Oct;67(10):1397-9. doi: 10.1002/jps.2600671017.
A new semiautomated high-pressure liquid chromatographic (HPLC) system is described to determine the dissolution rate of fludrocortisone acetate tablets. The system uses a miniaturized dissolution basket and shaft assembly having the same geometry as that given in USP XIX. This reduced size permits use of smaller volumes of dissolution medium, allowing most very low dose oral solid dosage forms to be handled. The USP dissolution kettle was also replaced with a new miniaturized vessel that continuously filters the sample solution before it enters the flow system. Volumes of dissolution medium as small as 15 ml can be accommodated, depending on the sensitivity of the assay employed and the solubility of the drug substance under study. The concentration of fludrocortisone acetate in solution was monitored by a new HPLC system employing a reversed-phase column compatible with the aqueous dissolution medium used. A comparative dissolution study of different lots was made using different basket rotation speeds.
本文介绍了一种用于测定醋酸氟氢可的松片溶出速率的新型半自动高压液相色谱(HPLC)系统。该系统使用了一个小型化的溶出篮和轴组件,其几何形状与美国药典第十九版中规定的相同。这种减小的尺寸允许使用更少量的溶出介质,从而能够处理大多数极低剂量的口服固体剂型。美国药典溶出釜也被一个新的小型化容器所取代,该容器在样品溶液进入流动系统之前对其进行连续过滤。根据所采用分析方法的灵敏度和所研究药物的溶解度,溶出介质的体积可小至15毫升。溶液中醋酸氟氢可的松的浓度通过一种新型HPLC系统进行监测,该系统采用与所用含水溶出介质兼容的反相柱。使用不同的篮旋转速度对不同批次进行了比较溶出度研究。