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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:利用整体柱的液相色谱 - 串联质谱法在血浆和药物制剂中的多组分定量血浆和药物制剂中的乙酰氨基酚

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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:本研究的目的是在血浆和药物中使用液相色谱 - 串联质谱法在血浆和药物中发育一种快速,简单,敏感的定量方法,伪麻黄碱(PSE),扑热息痛(PAR)和LorataDine(LOR),用整体柱。使用甲醇-0.1%甲酸的梯度组成以1.0mL MIN-1的流速进行分离。以SRM模式记录质谱转换。评估系统验证以获得精度,特异性和线性。测定伪麻黄碱,扑热息痛和加拉沙汀的检测极限分别为3.14,1.86和1.44ng mL-1,允许差异测定血浆,%回收率为93.12至101.56%。

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