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采用一步法样品制备程序,通过 LC-MS/MS 同时测定人血浆中的氟西汀、文拉法辛、沃替西汀及其活性代谢物。

Simultaneous determination of fluoxetine, venlafaxine, vortioxetine and their active metabolites in human plasma by LC-MS/MS using one-step sample preparation procedure.

机构信息

Department of Pharmacology, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Slovakia; Biomedical Center Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Slovakia.

Department of Pharmacology, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Slovakia.

出版信息

J Pharm Biomed Anal. 2020 Mar 20;181:113098. doi: 10.1016/j.jpba.2020.113098. Epub 2020 Jan 11.

Abstract

The aim of antidepressant therapy is to induce remission and prevent relapses of major depressive disorder with minimum adverse effects during the treatment. Due to high variability in metabolism, therapeutic drug monitoring is recommended as a useful tool for individualisation of the therapy. For this purpose, we have developed simple and sensitive ultra-high performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS) method for quantification of fluoxetine (FLX), venlafaxine (VEN), vortioxetine (VTX) and their active metabolites norfluoxetine (NFLX) and O-desmethylvenlafaxine (ODV). After one-step extraction procedure using OSTRO plate, analytes were separated by gradient elution on Acquity UPLC BEH C18 (50 × 2.1 mm, 1.7 μm) column with runtime 4.2 min. The detection was done on a triple quadrupole tandem mass spectrometer by multiple reaction monitoring (MRM) mode with transitions at m/z 310.23 → 148.20 for FLX, m/z 296.23 → 134.20 for NFLX, m/z 278.31 → 121.13 for VEN, m/z 264.31 → 107.14 for ODV and m/z 299.19 → 150.05 for VTX using a positive electrospray ionisation interface. The method was successfully validated according to the European Medicine Agency guideline for the selectivity, linearity and lower limit of detection, precision and accuracy, matrix effect, extraction recovery, carryover, dilution integrity and stability over a concentration range of 1-300 ng/mL for FLX, NFLX, VEN, ODV and 0.2-100 ng/mL VTX. Extraction recovery for each analyte was > 80 %, and no significant matrix effects were observed. The developed method was employed for quantification of antidepressants in clinical samples from patients treated with either FLX, VEN, or VTX.

摘要

抗抑郁治疗的目的是在治疗过程中诱导并预防重度抑郁障碍的缓解和复发,同时将不良反应最小化。由于代谢的高度变异性,治疗药物监测被推荐作为个体化治疗的有用工具。为此,我们开发了一种简单而灵敏的超高效液相色谱-串联质谱(UHPLC-MS/MS)法,用于定量检测氟西汀(FLX)、文拉法辛(VEN)、沃替西汀(VTX)及其活性代谢物去甲氟西汀(NFLX)和 O-去甲文拉法辛(ODV)。通过 OSTRO 板进行一步提取后,采用梯度洗脱程序在 Acquity UPLC BEH C18(50×2.1mm,1.7μm)柱上进行分离,运行时间为 4.2 分钟。检测通过三重四极杆串联质谱仪以多重反应监测(MRM)模式进行,FLX 的离子对为 m/z 310.23→148.20,NFLX 的离子对为 m/z 296.23→134.20,VEN 的离子对为 m/z 278.31→121.13,ODV 的离子对为 m/z 264.31→107.14,VTX 的离子对为 m/z 299.19→150.05,采用正电喷雾电离接口。该方法按照欧洲药品管理局指南进行了选择性、线性、检测限下限、精密度和准确度、基质效应、提取回收率、交叉污染、稀释完整性和稳定性验证,FLX、NFLX、VEN、ODV 的浓度范围为 1-300ng/mL,VTX 的浓度范围为 0.2-100ng/mL。每个分析物的提取回收率均>80%,且未观察到明显的基质效应。该方法用于定量检测接受 FLX、VEN 或 VTX 治疗的患者的临床样本中的抗抑郁药。

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