Multiparametric LC-MS/MS method for simultaneous determination of eleven antifungal drugs and metabolites in human plasma

IF 3.1 3区 医学 Q2 CHEMISTRY, ANALYTICAL
Jean-Joseph Bendjilali-Sabiani , Céline Constans , Olivier Mathieu , Yoann Cazaubon
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Abstract

A multiparametric liquid chromatography-tandem mass spectrometry method has been developed for the simultaneous quantification of 11 antifungal drugs and their metabolites in human plasma. This method addresses the critical need for therapeutic drug monitoring in the treatment of invasive fungal infections, which are increasingly prevalent among immunocompromised patients and those in intensive care units. The method quantifies flucytosin, fluconazole, itraconazole, hydroxy-itraconazole, posaconazole, isavuconazole, voriconazole, voriconazole-N-oxide, anidulafungin, caspofungin, and micafungin. Key challenges in method development included optimising mass spectrometer settings, chromatographic conditions, and sample preparation techniques to ensure accurate, sensitive, and specific detection. Validation of this method was conducted in accordance with the guidelines set by the USA Food and drug administration and the European Medicines Agency covering linearity, precision, accuracy, selectivity, matrix effect, and stability. The method exhibited robust performance with intra- and inter-assay precision under 10 % and average accuracy for intra- and inter-assay comparison of −2.35 % and 0.80 %, respectively. Limits of detection (0.002 to 0.110 mg/L) and a quantification range between 0.005 and 200 mg/L make this method suitable for clinical TDM applications. The ability to simultaneously analyse eleven antifungals and their metabolites within a single 5-minute run enhances its utility in clinical settings, particularly for critically ill patients who may experience significant pharmacokinetic variations. The method requires only 100 µL of plasma, demonstrating good analytical performances rendering it a valuable tool for optimising antifungal therapy and improving patient outcomes in ICU management.
同时测定人体血浆中 11 种抗真菌药物及其代谢物的多参数 LC-MS/MS 方法
本研究开发了一种多参数液相色谱-串联质谱法,用于同时定量检测人体血浆中的 11 种抗真菌药物及其代谢物。该方法满足了治疗侵袭性真菌感染的治疗药物监测的关键需求,这种感染在免疫力低下的患者和重症监护室患者中越来越普遍。该方法可定量检测氟唑醇、氟康唑、伊曲康唑、羟基伊曲康唑、泊沙康唑、异武康唑、伏立康唑、伏立康唑-N-氧化物、阿尼芬净、卡泊芬净和米卡芬净。方法开发的主要挑战包括优化质谱仪设置、色谱条件和样品制备技术,以确保准确、灵敏和特异的检测。根据美国食品药品管理局和欧洲药品管理局的指导方针,对该方法进行了验证,包括线性、精密度、准确度、选择性、基质效应和稳定性。该方法性能稳定,测定内和测定间精密度均低于 10%,测定内和测定间比较的平均准确度分别为-2.35%和 0.80%。检测限(0.002 至 0.110 mg/L)和定量范围(0.005 至 200 mg/L)使该方法适用于临床 TDM 应用。该方法能在 5 分钟的单次运行中同时分析 11 种抗真菌药物及其代谢物,这增强了它在临床环境中的实用性,尤其适用于可能出现显著药代动力学变化的重症患者。该方法只需要 100 µL 的血浆,具有良好的分析性能,因此是优化抗真菌治疗和改善重症监护室病人治疗效果的重要工具。
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来源期刊
CiteScore
6.70
自引率
5.90%
发文量
588
审稿时长
37 days
期刊介绍: This journal is an international medium directed towards the needs of academic, clinical, government and industrial analysis by publishing original research reports and critical reviews on pharmaceutical and biomedical analysis. It covers the interdisciplinary aspects of analysis in the pharmaceutical, biomedical and clinical sciences, including developments in analytical methodology, instrumentation, computation and interpretation. Submissions on novel applications focusing on drug purity and stability studies, pharmacokinetics, therapeutic monitoring, metabolic profiling; drug-related aspects of analytical biochemistry and forensic toxicology; quality assurance in the pharmaceutical industry are also welcome. Studies from areas of well established and poorly selective methods, such as UV-VIS spectrophotometry (including derivative and multi-wavelength measurements), basic electroanalytical (potentiometric, polarographic and voltammetric) methods, fluorimetry, flow-injection analysis, etc. are accepted for publication in exceptional cases only, if a unique and substantial advantage over presently known systems is demonstrated. The same applies to the assay of simple drug formulations by any kind of methods and the determination of drugs in biological samples based merely on spiked samples. Drug purity/stability studies should contain information on the structure elucidation of the impurities/degradants.
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