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用于治疗药物监测目的的患者体内选择性5-羟色胺再摄取抑制剂定量测定的分析方法。

Analytical methods for the quantitative determination of selective serotonin reuptake inhibitors for therapeutic drug monitoring purposes in patients.

作者信息

Eap C B, Baumann P

机构信息

Département Universitaire de Psychiatrie Adulte, Prilly-Lausanne, Switzerland.

出版信息

J Chromatogr B Biomed Appl. 1996 Nov 8;686(1):51-63. doi: 10.1016/s0378-4347(96)00338-6.

DOI:10.1016/s0378-4347(96)00338-6
PMID:8953192
Abstract

Five selective serotonin reuptake inhibitors (SSRIs) have been introduced recently: citalopram, fluoxetine, fluvoxamine, paroxetine and sertraline. Although no therapeutic window has been defined for SSRIs, in contrast to tricyclic antidepressants, analytical methods for therapeutic drug monitoring of SSRIs are useful in several instances. SSRIs differ widely in their chemical structure and in their metabolism. The fact that some of them have N-demethylated metabolites, which are also SSRIs, requires that methods be available which allow therapeutic drug monitoring of the parent compounds and of these active metabolites. most procedures are based on prepurification of the SSRIs by liquid-liquid extraction before they are submitted to separation by chromatographic procedures (high-performance liquid chromatography, gas chromatography, thin layer chromatography) and detection by various detectors (UV, fluorescence, electrochemical detector, nitrogen-phosphorus detector, mass spectrometry). This literature review shows that most methods allow quantitative determination of SSRIs in plasma, in the lower ng/ml range, and that they are, therefore, suitable for therapeutic drug monitoring purposes of this category of drugs.

摘要

最近已引入了五种选择性5-羟色胺再摄取抑制剂(SSRI):西酞普兰、氟西汀、氟伏沙明、帕罗西汀和舍曲林。与三环类抗抑郁药不同,尽管尚未确定SSRI的治疗窗,但SSRI治疗药物监测的分析方法在多种情况下都很有用。SSRI的化学结构及其代谢差异很大。其中一些具有N-去甲基代谢物,这些代谢物也是SSRI,这就要求有能对母体化合物及其活性代谢物进行治疗药物监测的方法。大多数程序是基于通过液-液萃取对SSRI进行预纯化,然后通过色谱程序(高效液相色谱、气相色谱、薄层色谱)进行分离,并通过各种检测器(紫外、荧光、电化学检测器、氮磷检测器、质谱)进行检测。这篇文献综述表明,大多数方法能够定量测定血浆中低至纳克/毫升范围内的SSRI,因此适用于此类药物的治疗药物监测目的。

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