Kabra P M, Bhatnagar P K, Nelson M A
J Anal Toxicol. 1983 Nov-Dec;7(6):283-5. doi: 10.1093/jat/7.6.283.
A simple, accurate, and specific liquid chromatographic procedure is described for the determination of gentamicin in 50 muL of serum. Gentamicin and sisomicin (IS) were converted into their trinitrophenyl derivatives by reaction with a water soluble derivatizing agent at 70 degrees C for 30 minutes. The derivatives were extracted from the crude mixture with chloroform, which was separated, evaporated, and the residue reconstituted in acetonitrile. Gentamicin was separated into three major isomers (C1, C2, and C1a) on a reversed-phase octyl column by eluting with a mobile phase. The eluted compounds were detected at 340 nm and quantified from their peak heights or peak areas. Chromatography was complete in less than 11.0 minutes. The lower limit of detection for gentamicin was less than 0.5 mg/L, analytical recoveries varied from 96.6% to 99.3%, linearity extended to 15.0 mg/L, and day-to-day precision was between 2.2% to 2.9%.
本文描述了一种简单、准确且特异的液相色谱法,用于测定50 μL血清中的庆大霉素。庆大霉素和西索米星(内标)在70℃下与水溶性衍生化试剂反应30分钟,转化为它们的三硝基苯基衍生物。衍生物用氯仿从粗混合物中萃取,分离、蒸发氯仿,残渣用乙腈复溶。庆大霉素在反相辛基柱上通过流动相洗脱分离为三个主要异构体(C1、C2和C1a)。洗脱的化合物在340 nm处检测,根据其峰高或峰面积进行定量。色谱分析在不到11.0分钟内完成。庆大霉素的检测下限低于0.5 mg/L,分析回收率在96.6%至99.3%之间,线性范围扩展至15.0 mg/L,日间精密度在2.2%至2.9%之间。