Validation of a quick and simple chromatographic method for simultaneous quantification of sertraline, escitalopram, risperidone and paliperidone levels in the human plasma

Q4 Pharmacology, Toxicology and Pharmaceutics Arhiv za Farmaciju Pub Date : 2021-01-01 DOI:10.5937/arhfarm71-31163
A. Jeremić, F. Milosavljević, S. Vladimirov, B. Batinić, B. Marković, M. Jukic
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Abstract

Simultaneous quantification of multiple psychiatric drugs is important for the therapeutic drug monitoring of psychiatric patients. In addition, it would be highly advantageous if the method could be simple, straightforward, and not time-consuming. A 200 µl plasma sample was deproteinized, drugs were separated by a ZORBAX Eclipse XDB-Phenyl column with the mobile phase composed of acetonitrile and 0.1 % formic acid in water (60:40, v/v), and recorded in the MRM mode by using a positive electrospray source with tandem mass spectrometry detection. The dynamic range was 2-256 ng/ml for all the analyzed drugs, except escitalopram (8-256 ng/ml). Quality control samples were prepared in quintuplicates in three relevant concentrations for each drug. Coefficients of determination (R2 ) were higher than 0.99, while the relative difference between nominal and measured concentrations (RE) and CV were lower than 15% for all targets. High performance liquid chromatography coupled with the mass detector (HPLC-MS/MS) method for simultaneous determination of sertraline, escitalopram, risperidone and paliperidone in human plasma was validated with respect to selectivity, linearity, accuracy, precision, matrix effect and stability. This method has significant advantages in terms of low sample volume (200 µl), short preparation time (3 hours) and short runtime per sample (4 minutes).
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同时定量人血浆中舍曲林、艾司西酞普兰、利培酮和帕利培酮含量的快速简便色谱方法的验证
多种精神科药物的同时定量对精神科患者的治疗药物监测具有重要意义。此外,如果该方法简单、直接且不耗时,那将是非常有利的。取200µl血浆样品脱蛋白,用ZORBAX Eclipse XDB-Phenyl色谱柱分离药物,流动相为乙腈和0.1%甲酸水溶液(60:40,v/v),采用正电喷雾源,串联质谱检测,MRM模式记录。除艾司西酞普兰(8 ~ 256 ng/ml)外,所有分析药物的动态范围均为2 ~ 256 ng/ml。每种药物以三种相关浓度制备五份质控样品。测定系数(R2)均大于0.99,标称浓度与实测值(RE)和CV之间的相对差异均小于15%。建立了高效液相色谱-质谱联用(HPLC-MS/MS)同时测定人血浆中舍曲林、艾司西酞普兰、利培酮和帕利培酮的选择性、线性度、准确度、精密度、基质效应和稳定性的方法。该方法具有样品体积小(200µl)、制备时间短(3小时)、每个样品运行时间短(4分钟)等显著优势。
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来源期刊
Arhiv za Farmaciju
Arhiv za Farmaciju Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
自引率
0.00%
发文量
19
审稿时长
12 weeks
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