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Extractionless and sensitive method for high-throughput quantitation of cetirizine in human plasma samples by liquid chromatography-tandem mass spectrometry

机译:液相色谱-串联质谱法高灵敏度定量测定人血浆样品中西替利嗪的无萃取方法

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摘要

Following a single 10-mg oral dose of cetirizine dihydrochloride to 24 healthy volunteers, the analyte was quantified in human plasma. Protein precipitation using acetonitrile (ACN) was followed by reversed-phase liquid chromatography and tandem mass spectrometry. The MS/MS method was optimised using a PE Sciex API 2000 triple quadrupole mass spectrometer in selected reaction monitoring (SRM) node, using electrospray with positive ionisation. Oxybutynin was used as the internal standard. The assay method represents a robust, high-throughput, highly specific and sensitive quantitative assay procedure, with 0.5 ng/ml being the lowest plasma concentration that could be reliably quantified. The procedure involves minimal sample preparation, and is well suited to clinical studies of the drug involving large numbers of generated samples. Pre-dose as well as post-dose samples up to and including 48 h were quantified, and the data generated were used to determine the pharmacokinetic profile of the drug.
机译:在向24位健康志愿者单次口服10 mg盐酸西替利嗪后,在人血浆中对分析物进行定量。使用乙腈(ACN)沉淀蛋白质,然后进行反相液相色谱和串联质谱分析。 MS / MS方法使用PE Sciex API 2000三重四极杆质谱仪在选定的反应监测(SRM)节点中进行了优化,并使用了具有正电离的电喷雾技术。奥昔布宁用作内标。该测定方法代表了可靠,高通量,高度特异性和灵敏的定量测定程序,其中0.5 ng / ml是可以可靠定量的最低血浆浓度。该程序涉及最少的样品制备,非常适合涉及大量生成样品的药物临床研究。量化直至和包括48小时的给药前和给药后样品,并将产生的数据用于确定药物的药代动力学特征。

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