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使用氘代内标对血浆和尿液中的美托洛尔及其两种代谢物进行选择离子监测。

Selected ion monitoring of metoprolol and two metabolites in plasma and urine using deuterated internal standards.

作者信息

Ervik M, Hoffmann K J, Kylberg-Hanssen K

出版信息

Biomed Mass Spectrom. 1981 Jul;8(7):322-6. doi: 10.1002/bms.1200080708.

Abstract

A highly sensitive and specific quantitative assay for metoprolol and two of its metabolites, containing an unchanged 2-hydroxy-4-isopropylaminopropoxy sidechain, has been developed. The compounds are isolated from the alkalized sample (plasma or urine) by extraction with dichloromethane, and converted to trifluoroacetyl derivatives by reaction with methyl-bis-(trifluoroacetamide). The reaction mixture is gas chromatographed on an OV-17 column and each substance is assayed by electron impact mass spectrometry using selected ion monitoring, and quantified by comparing the intensity of fragment ion m/z 266 with the intensities of corresponding fragment ions from the deuterated internal standards (m/z 270 and 271). It is possible to determine concentrations as low as 1 nmol l-1 (0.3 ng ml-1) in 1 ml of sample with relative standard deviation of less than 10%.

摘要

已开发出一种高灵敏度和特异性的定量测定方法,用于测定美托洛尔及其两种代谢物,这些代谢物含有未改变的2-羟基-4-异丙氨基丙氧基侧链。通过用二氯甲烷萃取从碱化样品(血浆或尿液)中分离出这些化合物,并通过与甲基双(三氟乙酰胺)反应将其转化为三氟乙酰衍生物。反应混合物在OV-17柱上进行气相色谱分析,每种物质通过选择离子监测的电子轰击质谱法进行测定,并通过将碎片离子m/z 266的强度与来自氘代内标(m/z 270和271)的相应碎片离子的强度进行比较来定量。在1 ml样品中能够测定低至1 nmol l-1(0.3 ng ml-1)的浓度,相对标准偏差小于10%。

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