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采用带紫外检测的高效液相色谱法同时定量测定微量人血浆中的左氧氟沙星、培氟沙星、环丙沙星和莫西沙星。

Simultaneous quantification of levofloxacin, pefloxacin, ciprofloxacin and moxifloxacin in microvolumes of human plasma using high-performance liquid chromatography with ultraviolet detection.

作者信息

Zheng Yi, Wang Ziqing, Lui Gabrielle, Hirt Déborah, Treluyer Jean-Marc, Benaboud Sihem, Aboura Radia, Gana Inès

机构信息

Service de Pharmacologie Clinique, Hôpital Cochin, Assistance Publique des Hôpitaux de Paris, Groupe Hospitalier Paris Centre, Paris, France.

EA 7323, Université Paris Descartes, Paris, France.

出版信息

Biomed Chromatogr. 2019 May;33(5):e4506. doi: 10.1002/bmc.4506. Epub 2019 Feb 28.

DOI:10.1002/bmc.4506
PMID:30743308
Abstract

Levofloxacin, pefloxacin, ciprofloxacin and moxifloxacin are four fluoroquinolones used in the treatment of serious bacterial infections. The antibacterial activity of fluoroquinolones is concentration dependent. Therefore, therapeutic drug monitoring in daily clinical practice is warranted to ensure the therapy's efficacy and prevent bacterial resistance. The purpose of the present study was to develop a method using high-pressure liquid chromatography with an ultraviolet detector for simultaneous quantification of these four fluoroquinolones in human plasma. A 50 μL aliquot of plasma was precipitated by 200 μL of methanol using gatifloxacin as internal standard. The chromatographic separation was performed on a Kinetex XB-C column using a mobile phase composed of a mixture of orthophosphoric acid 0.4% (v/v), acetonitrile and methanol at a flow rate of 1.2 mL/min. Dual UV wavelength mode was used, with levofloxacin and moxifloxacin monitored at 293 nm, and pefloxacin and ciprofloxacin monitored at 280 nm. The calibration was linear over the ranges of 0.125-25 mg/L for levofloxacin, 0.1-20mg/L for moxifloxacin and 0.05-10 mg/L for both pefloxacin and ciprofloxacin. Inter- and intra-day trueness and precision were <13% for all the compounds under study. The proposed method was simple, reliable, cost-effective and suitable for therapeutic drug monitoring or pharmacokinetics studies.

摘要

左氧氟沙星、培氟沙星、环丙沙星和莫西沙星是四种用于治疗严重细菌感染的氟喹诺酮类药物。氟喹诺酮类药物的抗菌活性呈浓度依赖性。因此,在日常临床实践中进行治疗药物监测以确保治疗效果并预防细菌耐药性是必要的。本研究的目的是开发一种使用带紫外检测器的高压液相色谱法同时定量测定人血浆中这四种氟喹诺酮类药物的方法。以加替沙星为内标,用200μL甲醇沉淀50μL血浆样品。色谱分离在Kinetex XB-C柱上进行,流动相由0.4%(v/v)的正磷酸、乙腈和甲醇的混合物组成,流速为1.2 mL/min。采用双紫外波长模式,左氧氟沙星和莫西沙星在293nm处监测,培氟沙星和环丙沙星在280nm处监测。左氧氟沙星在0.125 - 25mg/L范围内、莫西沙星在0.1 - 20mg/L范围内以及培氟沙星和环丙沙星在0.05 - 10mg/L范围内校准曲线呈线性。所研究的所有化合物的日间和日内准确性及精密度均<13%。所提出的方法简单、可靠、经济高效,适用于治疗药物监测或药代动力学研究。

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