Emery M, Kowtko J
J Pharm Sci. 1979 Sep;68(9):1185-7. doi: 10.1002/jps.2600680937.
A high-performance liquid chromatographic procedure was developed for diazepam tablet analysis. This procedure separates the manufacturing intermediate, 7-chloro-1,3-dihydro-5-phenyl-2H-1,4-benzodiazepin-2-one, and the decomposition products, 3-amino-6-chloro-1-methyl-4-phenylcarbostyril and 2-methylamino-5-chlorobenzophenone, from diazepam. The liquid chromatographic procedure is superior to the USP UV assay because it is stability indicating. The method is simple, accurate, and fast, involving only one extraction step. A reversed-phase column and a methanol-water mobile phase were used. Under these conditions, 0.1% of the decomposition products was detectable. Typical samples of diazepam tablets showed no degradation.
开发了一种用于地西泮片剂分析的高效液相色谱法。该方法可将生产中间体7-氯-1,3-二氢-5-苯基-2H-1,4-苯并二氮杂卓-2-酮以及分解产物3-氨基-6-氯-1-甲基-4-苯基咔唑和2-甲基氨基-5-氯二苯甲酮与地西泮分离。该液相色谱法优于美国药典紫外测定法,因为它具有稳定性指示作用。该方法简单、准确且快速,仅涉及一步萃取。使用了反相柱和甲醇-水流动相。在这些条件下,可检测到0.1%的分解产物。地西泮片剂的典型样品未显示出降解。