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首页> 外文期刊>Quimica nova >Multi-component quantitation of loratadine, pseudoephedrine and paracetamol in plasma and pharmaceutical formulations with liquid chromatography-tandem mass spectrometry utilizing a monolithic column
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Multi-component quantitation of loratadine, pseudoephedrine and paracetamol in plasma and pharmaceutical formulations with liquid chromatography-tandem mass spectrometry utilizing a monolithic column

机译:液相色谱-串联质谱法利用整体式色谱柱对血浆和药物制剂中的氯雷他定,伪麻黄碱和扑热息痛进行多组分定量

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摘要

The purpose of this study was to develop a rapid, simple and sensitive quantitation method for pseudoephedrine (PSE), paracetamol (PAR) and loratadine (LOR) in plasma and pharmaceuticals using liquid chromatography-tandem mass spectrometry with a monolithic column. Separation was achieved using a gradient composition of methanol-0.1% formic acid at a flow rate of 1.0 mL min~ (-1). Mass spectral transitions were recorded in SRM mode. System validation was evaluated for precision, specificity and linearity. Limit of detection for pseudoephedrine, paracetamol, and loratadine were determined to be 3.14, 1.86 and 1.44 ng mL~(-1), respectively, allowing easy determination in plasma with % recovery of 93.12 to 101.56%.
机译:这项研究的目的是使用液相色谱-串联质谱联用整体色谱柱建立血浆,药物中伪麻黄碱(PSE),扑热息痛(PAR)和氯雷他定(LOR)的快速,简单和灵敏的定量方法。使用甲醇-0.1%甲酸的梯度组合物以1.0 mL min-1(-1)的流速进行分离。质谱跃迁以SRM模式记录。对系统验证的准确性,特异性和线性进行了评估。伪麻黄碱,扑热息痛和氯雷他定的检出限分别为3.14、1.86和1.44 ng mL〜(-1),在血浆中的测定简便,回收率93.12%至101.56%。

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