Determination of levofloxacin in human serum using liquid chromatography tandem mass spectrometry

S. Ghimire, K. V. Hateren, Natasha Vrubleuskaya, R. Koster, D. Touw, J. Alffenaar
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引用次数: 13

Abstract

A rapid liquid chromatography tandem-mass spectrometry method was developed for the determination of levofloxacin and its metabolite (desmethyl-levofloxacin) in human serum. Sample preparation was done using protein precipitation technique. Our method had a run time of 2.5 min and retention times of 1.6 min for all analytes. The standard curves were linear within the concentration range of 0.10 to 5.00 mg/L for levofloxacin and 0.10 to 4.99 mg/L for desmethyllevofloxacin; a correlation coefficient (R2) of 0.999 and 0.998 respectively. The lower limit of quantification for both analytes was 0.10 mg/L. Within-day precision ranged from 1.4% and 2.4% for levofloxacin, 1.5% to 5% for desmethyl-levofloxacin and between-day precision ranged from 3.6% to 4.1% for levofloxacin and 0.0% to 3.3% for desmethyl-levofloxacin; whereas, accuracy ranged from 0.1% to 12.7% for levofloxacin and 0.2% to 15.6% for desmethyl-levofloxacin. This method could be a useful asset for routine therapeutic drug monitoring of levofloxacin in multi-drug resistant tuberculosis patients.
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液相色谱串联质谱法测定人血清中左氧氟沙星
建立了快速液相色谱串联质谱法测定人血清中左氧氟沙星及其代谢物去甲基左氧氟沙星的含量。采用蛋白沉淀技术制备样品。本方法运行时间为2.5 min,保留时间为1.6 min。左氧氟沙星浓度范围为0.10 ~ 5.00 mg/L,去甲基左氧氟沙星浓度范围为0.10 ~ 4.99 mg/L,标准曲线呈线性;相关系数R2分别为0.999和0.998。两种分析物的定量下限均为0.10 mg/L。左氧氟沙星日内精密度为1.4% ~ 2.4%,去甲基左氧氟沙星日间精密度为1.5% ~ 5%,左氧氟沙星日间精密度为3.6% ~ 4.1%,去甲基左氧氟沙星日间精密度为0.0% ~ 3.3%;而左氧氟沙星的准确度为0.1% ~ 12.7%,去甲基左氧氟沙星的准确度为0.2% ~ 15.6%。该方法可为耐多药结核病患者左氧氟沙星的常规治疗药物监测提供有益的参考。
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