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采用液相色谱-串联质谱法同时定量测定大鼠血浆中的咖啡因及其三种主要代谢物。

Simultaneous quantification of caffeine and its three primary metabolites in rat plasma by liquid chromatography-tandem mass spectrometry.

机构信息

College of Pharmacy, The Catholic University of Korea, Bucheon, Gyeonggi-do 420-743, Republic of Korea.

出版信息

Food Chem. 2013 Dec 1;141(3):2735-42. doi: 10.1016/j.foodchem.2013.05.069. Epub 2013 May 24.

Abstract

A rapid, sensitive, simple and accurate LC-MS/MS method for the simultaneous quantitation of caffeine, and its three primary metabolites, theobromine, paraxanthine, and theophylline, in rat plasma was developed and validated. Chromatographic separation was performed on an Agilent Poroshell 120 EC-C18 column using 1 μg/mL acetaminophen as an internal standard. Each sample was run at 0.5 mL/min for a total run time of 7 min/sample. Detection and quantification were performed using a mass spectrometer in selected reaction-monitoring mode with positive electrospray ionization. The lower limit of quantification was 5 ng/mL for all analytes with linear ranges up to 5000 ng/mL for caffeine and 1000 ng/mL for its metabolites. The coefficient of variation for assay precision was less than 12.6%, with an accuracy of 93.5-114%. The assay was successfully applied to determine plasma concentrations of caffeine, theobromine, paraxanthine, and theophylline in rat administered various energy drinks containing the same caffeine content. Various energy drinks exhibited considerable variability in the pharmacokinetic profiles of caffeine and its three primary metabolites, even containing the same caffeine. Different additives of energy drinks might contribute to these results.

摘要

建立并验证了一种灵敏、准确、简单、快速的 LC-MS/MS 法,用于同时定量测定大鼠血浆中的咖啡因及其三种主要代谢物:可可碱、尿嘧啶和茶碱。采用 Agilent Poroshell 120 EC-C18 柱进行色谱分离,以 1μg/mL 对乙酰氨基酚为内标。每个样品以 0.5 mL/min 的流速运行,总运行时间为 7 min/样品。采用质谱仪在选择反应监测模式下进行检测和定量,正电喷雾电离。所有分析物的定量下限均为 5 ng/mL,咖啡因及其代谢物的线性范围高达 5000 ng/mL 和 1000 ng/mL。测定精密度的变异系数小于 12.6%,准确度为 93.5-114%。该方法成功应用于测定大鼠给予含有相同咖啡因含量的各种能量饮料后咖啡因、可可碱、尿嘧啶和茶碱的血浆浓度。即使含有相同的咖啡因,各种能量饮料的咖啡因及其三种主要代谢物的药代动力学特征也存在很大差异。不同的能量饮料添加剂可能导致这些结果。

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