Sauvage F L, Gaulier J M, Lachâtre G, Marquet P
Department of Pharmacology-Toxicology, University Hospital, Limoges, France.
Ther Drug Monit. 2006 Feb;28(1):123-30. doi: 10.1097/01.ftd.0000194026.04483.c3.
Antidepressants belong to a variety of chemical and pharmacologic classes. Most require therapeutic drug monitoring, at least in certain circumstances, such as unexplained inefficacy or suspected toxicity. Several types of chromatographic methods have generally been used. This paper presents a fully automated, sensitive, and specific method for the therapeutic drug monitoring of 13 antidepressants of all classes (amoxapine, amitriptyline, citalopram, clomipramine, dothiepin, doxepin, fluoxetine, imipramine, maprotiline, mianserin, paroxetine, sertraline, trimipramine) and some of their respective active metabolites (nortriptyline, monodesmethylcitalopram, desmethylclomipramine, desipramine, norfluoxetine, desmethylmianserin, N-desmethylsertraline), based on the innovative turbulent-flow liquid chromatography (TFC) technology, coupled to tandem-mass spectrometry (MS/MS). The antidepressants were divided in two groups depending on their chromatographic properties, so that two injections would be necessary to screen all compounds (which is infrequent for therapeutic drug monitoring). Calibration curves ranged from 10 to 500 ng/mL. No significant memory effect was observed after the injection of a blank serum sample spiked at 500 ng/mL. The intra-assay and inter-assay precision CVs ranged from 0.4% to 12% and from 1% to 16%, respectively. The method was further validated by blindly analyzing Heathcontrol-Therapeutic Drugs Scheme samples (Cardiff Bioanalytical Services Ltd.) containing several antidepressants.
抗抑郁药属于多种化学和药理类别。大多数抗抑郁药至少在某些情况下需要进行治疗药物监测,例如出现无法解释的无效情况或怀疑有中毒现象时。一般使用了几种类型的色谱方法。本文基于创新的湍流液相色谱(TFC)技术与串联质谱(MS/MS)联用,提出了一种用于治疗药物监测的全自动、灵敏且特异的方法,可同时检测所有类别的13种抗抑郁药(阿莫沙平、阿米替林、西酞普兰、氯米帕明、多塞平、多塞平、氟西汀、丙咪嗪、马普替林、米安色林、帕罗西汀、舍曲林、曲米帕明)及其一些各自的活性代谢物(去甲替林、去甲基西酞普兰、去甲氯米帕明、地昔帕明、去甲氟西汀、去甲基米安色林、N-去甲基舍曲林)。根据抗抑郁药的色谱特性将其分为两组,因此需要进样两次才能筛查所有化合物(这在治疗药物监测中并不常见)。校准曲线范围为10至500 ng/mL。注射加样至500 ng/mL的空白血清样品后未观察到明显的记忆效应。批内和批间精密度CV分别为0.4%至12%和1%至16%。通过对含有几种抗抑郁药的Heathcontrol - 治疗药物方案样品(加的夫生物分析服务有限公司)进行盲法分析,进一步验证了该方法。