Li J, Milne R W, Nation R L, Turnidge J D, Coulthard K, Johnson D W
Centre for Pharmaceutical Research, University of South Australia, Adelaide Australia.
J Chromatogr B Biomed Sci Appl. 2001 Sep 25;761(2):167-75. doi: 10.1016/s0378-4347(01)00326-7.
A simple, selective and sensitive high-performance liquid chromatographic (HPLC) method is described for the determination of colistin in human plasma. Derivatization with 9-fluorenylmethyl chloroformate was performed in the same solid-phase extraction C18 cartridge used for sample pre-treatment, followed by reversed-phase HPLC with fluorimetric detection. Quantification was achieved using the ratio of the summed peak areas of colistin A and B derivatives to that of the derivative of netilmicin (internal standard). Linear calibration curves were obtained within the concentrations of colistin sulfate from 0.10 to 4.0 mg/l in plasma. Accuracy was within 10% and reproducibility (RSD) was less than 10%.
描述了一种简单、选择性和灵敏的高效液相色谱(HPLC)方法,用于测定人血浆中的多粘菌素。用9-芴基甲基氯甲酸酯进行衍生化反应,在用于样品预处理的同一固相萃取C18柱中进行,然后进行反相HPLC并采用荧光检测。通过多粘菌素A和B衍生物的总峰面积与奈替米星(内标)衍生物的峰面积之比进行定量。在血浆中硫酸多粘菌素浓度为0.10至4.0mg/l范围内获得线性校准曲线。准确度在10%以内,重现性(相对标准偏差)小于10%。