利用 LC-MS/MS 同时测定人体血浆中的三种酪氨酸激酶抑制剂和三种三唑类药物:在治疗药物监测和药物相互作用研究中的应用

IF 2.8 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS
Ninghong Li , Lu Liu , Dong Liu , Hengyi Yu , Guangjie Yang , Lihui Qiu , Yufei Chen , Dong Xiang , Xuepeng Gong
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引用次数: 0

摘要

酪氨酸激酶抑制剂(TKIs)和三唑类抗真菌药物分别是治疗慢性髓性白血病(CML)和真菌感染的一线药物,但这两种药物都存在暴露差异大和治疗窗口狭窄的问题。此外,这两类药物通常同时用于患有真菌感染的 CML 患者。多项研究和指南都提出了对 TKIs 和三唑类药物进行治疗药物监测 (TDM) 的重要性。目前,同时测定这两种药物的方法还很有限。我们开发了一种简单、快速、可靠的液相色谱-串联质谱(LC-MS/MS)方法,用于同时定量检测人体血浆中三种常用的 TKIs(伊马替尼、达沙替尼和尼洛替尼)和三种常用的三唑类药物(伏立康唑、伊曲康唑和泊沙康唑)。采用 Welch XB-C18 分析柱(50 × 2.1 mm,5 µm),以 0.7 mL/min 的速度,使用 10 mM 甲酸铵(A)和含 0.2 % 甲酸的甲醇-乙腈-异丙醇(80:10:10,v/v/v)(B)进行梯度洗脱,总分析时间为 3.5 分钟。伊马替尼和尼洛替尼在 20 至 4000 纳克/毫升、达沙替尼在 2 至 400 纳克/毫升、伏立康唑、伊曲康唑和泊沙康唑在 50 至 10,000 纳克/毫升范围内线性关系良好。选择性、准确性、精密度、回收率、基质效应和稳定性均符合验证要求。该方法成功地用于同时接受TKIs和三唑类药物治疗的CML患者的TDM。TKIs与三唑类药物之间的药物相互作用分析表明,伊马替尼与伏立康唑、达沙替尼与伏立康唑之间存在显著的正相关性。因此,这种方法可以很好地应用于同时接受 TKIs、三唑类药物或两者的患者的临床 TDM。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Simultaneous determination of three tyrosine kinase inhibitors and three triazoles in human plasma by LC-MS/MS: applications to therapeutic drug monitoring and drug-drug interaction studies

Tyrosine kinase inhibitors (TKIs) and triazole antifungals are the first-line drugs for treating chronic myeloid leukemia (CML) and fungal infections, respectively, but both suffer from large exposure differences and narrow therapeutic windows. Moreover, these two types of drugs are commonly used together in CML patients with fungal infections. Multiple studies and guidelines have suggested the importance of therapeutic drug monitoring (TDM) of TKIs and triazoles. Currently, methods for the simultaneous determination of both types of drugs are limited. We developed a simple, rapid, and reliable liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for simultaneous quantification of three commonly used TKIs (imatinib, dasatinib, and nilotinib) and three commonly used triazoles (voriconazole, itraconazole, and posaconazole) in human plasma. The analytes were eluted on a Welch XB-C18 analytical column (50 × 2.1 mm, 5 µm) at 0.7 mL/min, using a gradient elution of 10 mM ammonium formate (A) and methanol–acetonitrile-isopropanol (80:10:10, v/v/v) containing 0.2 % formic acid (B) with a total analysis time of 3.5 min. The calibration curves were linear over the range from 20 to 4000 ng/mL for imatinib and nilotinib, from 2 to 400 ng/mL for dasatinib, and from 50 to 10,000 ng/mL for voriconazole, itraconazole, and posaconazole. Selectivity, accuracy, precision, recovery, matrix effect, and stability all met the validation requirements. The method was successfully used for TDM in CML patients who co-treated with both TKIs and triazoles. Drug-drug interaction analysis between TKIs and triazoles showed that a significant positive correlation was observed between imatinib and voriconazole, as well as dasatinib and voriconazole. Therefore, this method can be well applied in clinical TDM for patients receiving TKIs, triazoles, or both simultaneously.

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来源期刊
Journal of Chromatography B
Journal of Chromatography B 医学-分析化学
CiteScore
5.60
自引率
3.30%
发文量
306
审稿时长
44 days
期刊介绍: The Journal of Chromatography B publishes papers on developments in separation science relevant to biology and biomedical research including both fundamental advances and applications. Analytical techniques which may be considered include the various facets of chromatography, electrophoresis and related methods, affinity and immunoaffinity-based methodologies, hyphenated and other multi-dimensional techniques, and microanalytical approaches. The journal also considers articles reporting developments in sample preparation, detection techniques including mass spectrometry, and data handling and analysis. Developments related to preparative separations for the isolation and purification of components of biological systems may be published, including chromatographic and electrophoretic methods, affinity separations, field flow fractionation and other preparative approaches. Applications to the analysis of biological systems and samples will be considered when the analytical science contains a significant element of novelty, e.g. a new approach to the separation of a compound, novel combination of analytical techniques, or significantly improved analytical performance.
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