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首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Determination of memantine in human plasma by liquid chromatography-electrospray tandem mass spectrometry: Application to a bioequivalence study
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Determination of memantine in human plasma by liquid chromatography-electrospray tandem mass spectrometry: Application to a bioequivalence study

机译:液相色谱-电喷雾串联质谱法测定人血浆中的美金刚:在生物等效性研究中的应用

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A simple, sensitive and specific liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the quantification of memantine (1) in human plasma is presented. Sample preparation consisted of the addition of amantadine (11) as internal standard (IS), liquid-liquid extraction in basic conditions using a mixture of diethyl ether-chloroform (7:3, v/v) as extracting solvent, followed by centrifugation, solvent evaporation and sample reconstitution in methanol. Both I and 11 (internal standard) were analyzed using a C18 column and a mobile phase composed of methanol-water-formic acid (80:20:0.1, v/v/v). Eluted compounds were monitored using positive mode electrospray (ES) tandem mass spectrometry. The analyses were carried out by selected reaction monitoring (SRM) using the parent to daughter combinations of m/z 180 > 163 (memantine) and m/z 152 > 135 (amantadine). The peak areas from the analyte and IS were used for quantification of I. The achieved limit of quantification (LOQ) was 0.1 ng/mL; the assay exhibited a linear dynamic range of 0.1-50.0 ng/mL with a determination coefficient (r(2)) of at least 0.98. Validation results on linearity, specificity, accuracy, precision and stability, as well as on application to the analysis of samples taken up to 320 h after oral administration of 20 mg (two 10 mg capsules) of I in healthy volunteers demonstrated the applicability to bioequivalence studies. (c) 2006 Elsevier B.V. All rights reserved.
机译:提出了一种简单,灵敏,特异的液相色谱-串联质谱(LC-MS / MS)方法,用于定量测定人血浆中的美金刚(1)。样品制备包括添加金刚烷胺(11)作为内标(IS),在碱性条件下使用乙醚-氯仿(7:3,v / v)的混合物作为萃取溶剂进行液-液萃取,然后离心,蒸发溶剂并在甲醇中进行样品重建。使用C18色谱柱和由甲醇-水-甲酸(80:20:0.1,v / v / v)组成的流动相分析I和11(内标)。使用正模式电喷雾(ES)串联质谱监测洗脱的化合物。使用m / z 180> 163(美金刚)和m / z 152> 135(金刚烷胺)的父子结合,通过选择的反应监测(SRM)进行分析。来自分析物和IS的峰面积用于I的定量。达到的定量限(LOQ)为0.1 ng / mL;该测定法的线性动态范围为0.1-50.0 ng / mL,测定系数(r(2))至少为0.98。线性,特异性,准确性,精密度和稳定性的验证结果,以及在健康志愿者中口服20 mg(两个10 mg胶囊)I后长达320 h所采集样品的分析结果均证明了其对生物等效性的适用性学习。 (c)2006 Elsevier B.V.保留所有权利。

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