Mistry B, Leslie J, Eddington N E
Department of Pharmaceutical Sciences, University of Maryland at Baltimore 21201-1082, USA.
J Pharm Biomed Anal. 1998 Feb;16(6):1041-9. doi: 10.1016/s0731-7085(97)00115-5.
A reverse-phase High Performance Liquid Chromatographic (HPLC) method was developed for the analysis of metoprolol in the large number of human plasma samples obtained in in vitro-in vivo correlations (IVIVC) and bioavailability studies of extended release formulations of metoprolol tartrate. The metabolite, alpha-hydroxy metoprolol (OH-met), could also be quantified. The analytes were extracted from the plasma using solid phase columns, separated on a C-4 analytical column followed by fluorimetric detection. The linearity, precision, accuracy, stability, selectivity and ruggedness were validated for the concentration ranges of 1-400 ng ml-1 for metoprolol and 0.5-200 ng ml-1 for OH-met. The same chromatographic conditions were slightly modified to quantify dextromethorphan and its metabolite dextrorphan in urine in the concentration range 0.052-0.05 microgram ml-1 as a method for screening for fast metabolizers.
开发了一种反相高效液相色谱(HPLC)方法,用于分析在酒石酸美托洛尔缓释制剂的体外-体内相关性(IVIVC)和生物利用度研究中获得的大量人体血浆样本中的美托洛尔。代谢物α-羟基美托洛尔(OH-美托洛尔)也可以进行定量分析。使用固相柱从血浆中提取分析物,在C-4分析柱上进行分离,然后进行荧光检测。对美托洛尔浓度范围为1-400 ng/ml以及OH-美托洛尔浓度范围为0.5-200 ng/ml时的线性、精密度、准确度、稳定性、选择性和耐用性进行了验证。对相同的色谱条件进行了轻微修改,以定量尿液中右美沙芬及其代谢物右啡烷,浓度范围为0.052-0.05 μg/ml,作为一种筛选快速代谢者的方法。