León-Urrea F, Girard-Cuesy M E, Cervantes-Campos C, Delgadillo-Valencia M P, Montoya-Cabrera M A
Laboratorio de Farmacología y Desarrollo de Metodología Analítica, Jefatura de Control de Calidad, Instituto Mexicano del Seguro Social.
Arch Invest Med (Mex). 1989 Oct-Dec;20(4):309-13.
An improved HPLC method for the measurement of cimetidine and its major metabolite-cimetidine sulfoxide-is described. The mobile phase was a mixture of methanol-ammonium phosphate (20:80), and methanol was used to elute the drug avoiding the use of acetonitrile, a very hazardous solvent. A device has been developed to wash simultaneously ten or more cartridges and to reduce the time of analysis. With this procedure a plasma sample could be analyzed in less than 30 min. The limit of detection was 0.125 micrograms/ml for cimetidine and 1.00 micrograms/ml for cimetidine sulfoxide. The absolute recovery for cimetidine was 83% and 40% for its major metabolite; is greater than that reported by previous studies. The proposed method is rapid, accurate and precise, and it should be useful for clinical, bioavailability and pharmacokinetic studies of cimetidine.
本文描述了一种改进的高效液相色谱法,用于测定西咪替丁及其主要代谢产物——西咪替丁亚砜。流动相为甲醇 - 磷酸铵(20:80)的混合物,使用甲醇洗脱药物,避免使用乙腈这种极具危险性的溶剂。已开发出一种装置,可同时清洗十个或更多的柱管,并减少分析时间。采用此方法,血浆样品可在30分钟内完成分析。西咪替丁的检测限为0.125微克/毫升,西咪替丁亚砜的检测限为1.00微克/毫升。西咪替丁的绝对回收率为83%,其主要代谢产物的绝对回收率为40%;高于先前研究报道的值。所提出的方法快速、准确且精密,应可用于西咪替丁的临床、生物利用度和药代动力学研究。