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高效液相色谱法用于筛查和定量人血清中的七种选择性5-羟色胺再摄取抑制剂。

High-performance liquid chromatographic method to screen and quantitate seven selective serotonin reuptake inhibitors in human serum.

作者信息

Tournel G, Houdret N, Hédouin V, Deveau M, Gosset D, Lhermitte M

机构信息

Institut de Médecine Légale de Lille, Faculté de Médecine, Université de Lille II, France.

出版信息

J Chromatogr B Biomed Sci Appl. 2001 Sep 25;761(2):147-58. doi: 10.1016/s0378-4347(01)00305-x.

Abstract

A high-performance liquid chromatographic screening method (HPLC) is described for the determination of seven selective serotonin reuptake inhibitors (SSRIs) (fluvoxamine, milnacipran, paroxetine, sertraline, fluoxetine, citalopram, venlafaxine) and for three pharmacologically active N-demethylated metabolites (desmethylcitalopram, didesmethylcitalopram and norfluoxetine). A tricyclic antidepressant, clomipramine, was used as an internal standard. The method consists of liquid extraction of serum after alcalinisation at pH 9.50, followed by chromatography on a Beckman C18 reversed-phase column. Compounds were detected at 200.4 nm. The standard curves were linear over a working range of 50-1,000 ng/ml for fluvoxamine, 15-1,000 ng/ml for fluoxetine, 25-500 ng/ml for norfluoxetine, 50-500 ng/ml for sertraline, 20-500 ng/ml for paroxetine, 25-550 ng/ml for citalopram, 25-750 ng/ml for desmethylcitalopram, 25-800 ng/ml for didesmethylcitalopram, 25-650 ng/ml for milnacipran, and 25-500 ng/ml for venlafaxine. The quantitation limits of the method were 15 ng/ml for fluoxetine, 20 ng/ml for paroxetine, 25 ng/ml for venlafaxine, norfluoxetine and citalopram, and its metabolites, 40 ng/ml for sertraline and 50 ng/ml for fluvoxamine. No interferences were noted with this sensitive and specific method which can be used for therapeutic drug monitoring.

摘要

描述了一种高效液相色谱筛选方法(HPLC),用于测定七种选择性5-羟色胺再摄取抑制剂(SSRI)(氟伏沙明、米那普明、帕罗西汀、舍曲林、氟西汀、西酞普兰、文拉法辛)以及三种具有药理活性的N-去甲基代谢物(去甲基西酞普兰、双去甲基西酞普兰和去甲氟西汀)。使用三环类抗抑郁药氯米帕明作为内标。该方法包括在pH 9.50碱化后对血清进行液液萃取,然后在贝克曼C18反相柱上进行色谱分析。在200.4 nm处检测化合物。氟伏沙明的标准曲线在50 - 1000 ng/ml的工作范围内呈线性,氟西汀为15 - 1000 ng/ml,去甲氟西汀为25 - 500 ng/ml,舍曲林为50 - 500 ng/ml,帕罗西汀为20 - 500 ng/ml,西酞普兰为25 - 550 ng/ml,去甲基西酞普兰为25 - 750 ng/ml,双去甲基西酞普兰为25 - 800 ng/ml,米那普明为25 - 650 ng/ml,文拉法辛为25 - 500 ng/ml。该方法的定量限为:氟西汀15 ng/ml,帕罗西汀20 ng/ml,文拉法辛、去甲氟西汀和西酞普兰及其代谢物25 ng/ml,舍曲林40 ng/ml,氟伏沙明50 ng/ml。该灵敏且特异的方法未观察到干扰,可用于治疗药物监测。

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