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采用五氟苯基核壳柱 HPLC-FLD-DAD 法测定尿液和血浆中的左氧氟沙星、环丙沙星、莫西沙星和加替沙星:药物监测中的应用。

Determination of levofloxacin, ciprofloxacin, moxifloxacin and gemifloxacin in urine and plasma by HPLC-FLD-DAD using pentafluorophenyl core-shell column: Application to drug monitoring.

机构信息

Department of Analytical Chemistry, Faculty of Pharmacy, Karadeniz Technical University, Trabzon, Turkey.

Department of Infectious Disease, Faculty of Medicine, Karadeniz Technical University, Trabzon, Turkey.

出版信息

Biomed Chromatogr. 2020 Oct;34(10):e4925. doi: 10.1002/bmc.4925. Epub 2020 Jul 29.

DOI:10.1002/bmc.4925
PMID:32557742
Abstract

Concentrations of fluoroquinolones, which are used in the treatment of many bacterial infections, should be monitored in biological fluids as they exhibit concentration-dependent bactericidal activity. In this study, a liquid chromatography method for the determination of levofloxacin, ciprofloxacin, moxifloxacin and gemifloxacin in human urine and plasma was developed for the first time. The efficiency of five different columns for the separation of these fluoroquinolones was compared. Experimental parameters that affect the separation, such as percentage of organic solvent, pH, temperature, gradient shape and detector wavelength, were optimized by a step-by-step approach. Using a pentafluorophenyl core-shell column (100 × 4.6 mm, 2.7 μm), the separation of four analytes was accomplished in <7.5 min. The developed method was validated for the determination of analytes in both urine and plasma with respect to sensitivity, specificity, linearity (r ≥ 0.9989), recovery (79.46-102.69%), accuracy, precision and stability (85.79-111.07%). The intra- and inter-day accuracies were within 89.55-111.94% with relative standard deviations of 0.35-8.05%. The feasibility of method was demonstrated by analyzing urine and plasma samples of patients orally receiving levofloxacin, ciprofloxacin or moxifloxacin. The developed method is suitable for therapeutic drug monitoring of these fluoroquinolones and can be applied to pharmacokinetic and toxicological studies.

摘要

氟喹诺酮类药物被广泛用于治疗多种细菌感染,由于其具有浓度依赖性杀菌活性,因此应在生物体液中监测其浓度。本研究首次建立了一种同时测定人尿液和血浆中左氧氟沙星、环丙沙星、莫西沙星和加替沙星的液相色谱法。比较了五种不同色谱柱对这四种氟喹诺酮类药物分离的效果。采用逐步优化的方法,对影响分离的实验参数,如有机溶剂的比例、pH 值、温度、梯度形状和检测波长等进行了优化。使用五氟苯基核壳柱(100×4.6mm,2.7μm),在<7.5min 内即可完成四种分析物的分离。该方法在尿液和血浆中对分析物的测定均进行了灵敏度、特异性、线性(r≥0.9989)、回收率(79.46-102.69%)、准确度、精密度和稳定性(85.79-111.07%)的验证。日内和日间精密度的准确度在 89.55-111.94%之间,相对标准偏差为 0.35-8.05%。通过分析口服左氧氟沙星、环丙沙星或莫西沙星的患者的尿液和血浆样本,证明了该方法的可行性。该方法适用于这些氟喹诺酮类药物的治疗药物监测,可应用于药代动力学和毒理学研究。

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