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马尿液中咖啡因及其主要代谢物的气相色谱-质谱联用同时定量分析。

Simultaneous quantification of caffeine and its main metabolites by gas chromatography mass spectrometry in horse urine.

机构信息

Doping Control Laboratory, Istanbul Pendik Veterinary Control Institude, Istanbul, Turkey.

Department of Comparative Biomedical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, USA.

出版信息

Biomed Chromatogr. 2022 Oct;36(10):e5445. doi: 10.1002/bmc.5445. Epub 2022 Jul 15.

Abstract

Caffeine is a naturally occurring alkaloid and it is metabolized to paraxanthine, theophylline and theobromine. Analysis of caffeine and its metabolites is challenging since the metabolites theophylline and paraxanthine generate similar product and precursor ions. In this study, a new method was developed for the simultaneous analysis of caffeine, paraxanthine, theobromine and theophylline in horse urine using gas chromatography-mass spectrometry (GC-MS). Urine samples were treated using solid-phase extraction followed by the elution with dichloromethane-isopropanol (90:10) after the pH was adjusted to 6, and then derivatization with N-methyl-N-trimethylsilyl-trifluoroacetamide-1% trimethylchlorosilane before analysis with GC-MS. Sample preparation and derivatization steps were optimized and the method permitted elution all of these analytes within 13 min. The method was fully validated according to Commission Decision, 2002/657/EC guidelines. The calibration curves were linear with a correlation coefficient of >0.99. Precision and accuracy were well within the 15% acceptance range and the method was robust. The validation results demonstrated that the method is highly reproducible, easily applicable and selective. The method was applied to urine samples collected from racehorses to demonstrate its applicability.

摘要

咖啡因是一种天然存在的生物碱,它会代谢为副黄嘌呤、茶碱和可可碱。由于茶碱和副黄嘌呤生成的产物和前体离子相似,因此分析咖啡因及其代谢物具有一定的挑战性。在这项研究中,我们开发了一种使用气相色谱-质谱联用仪(GC-MS)同时分析马尿中咖啡因、副黄嘌呤、可可碱和茶碱的新方法。尿液样品经过固相萃取处理,然后在 pH 值调整为 6 后用二氯甲烷-异丙醇(90:10)洗脱,再用 N-甲基-N-三甲基硅基三氟乙酰胺-1%三甲基氯硅烷衍生化,最后进行 GC-MS 分析。对样品制备和衍生化步骤进行了优化,该方法允许在 13 分钟内洗脱所有这些分析物。该方法根据委员会决定 2002/657/EC 指南进行了全面验证。校准曲线的线性相关系数大于 0.99。精密度和准确度均在 15%的可接受范围内,方法具有良好的稳健性。验证结果表明,该方法具有高度的重现性、易于应用和选择性。该方法已应用于从赛马中采集的尿液样本,以证明其适用性。

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