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用于测定地表水中多种药物混合物的快速液相色谱-串联质谱法

Rapid liquid chromatography-tandem mass spectrometry method for the determination of a broad mixture of pharmaceuticals in surface water.

作者信息

Conley Justin M, Symes Steven J, Kindelberger Scott A, Richards Sean M

机构信息

Department of Biological and Environmental Sciences, University of Tennessee at Chattanooga, 615 McCallie Avenue, Chattanooga, TN 37403, USA.

出版信息

J Chromatogr A. 2008 Mar 28;1185(2):206-15. doi: 10.1016/j.chroma.2008.01.064. Epub 2008 Jan 31.

Abstract

Herein, a new method for the detection of 13 different pharmaceuticals and one metabolite in surface water at low ng/L levels is described. The method utilizes ultra performance liquid chromatography-tandem mass spectrometry and a solid-phase extraction sample preparation. Mean method detection limits were low (4.10 ng/L) and overall solid-phase extraction recovery and reproducibility was adequate (mean recovery, 77.9%; mean RSD, 7.3%). The method allows for quick run times and minimal solvent use as compared with other previously reported high performance liquid chromatography-based methods. Application of this method for the detection of pharmaceuticals in Tennessee River surface water determined that caffeine, sulfamethoxazole, and carbamazepine were frequently detected (100% of samples). Trimethoprim was moderately detected (30% of samples); acetaminophen, atorvastatin, and lovastatin were infrequently detected (10% of samples); and ciprofloxacin, diltiazem, fluoxetine, levofloxacin, norfluoxetine, ranitidine, and sertraline were not detected. This study reports the first detection of lovastatin in surface water.

摘要

本文描述了一种用于检测地表水中低纳克/升水平的13种不同药物和一种代谢物的新方法。该方法采用超高效液相色谱-串联质谱法和固相萃取样品前处理方法。方法的平均检测限较低(4.10纳克/升),固相萃取的总体回收率和重现性良好(平均回收率77.9%;平均相对标准偏差7.3%)。与其他先前报道的基于高效液相色谱的方法相比,该方法分析时间短,溶剂用量少。应用该方法检测田纳西河地表水中的药物,结果表明咖啡因、磺胺甲恶唑和卡马西平频繁检出(100%的样品)。甲氧苄啶中度检出(30%的样品);对乙酰氨基酚、阿托伐他汀和洛伐他汀检出频率较低(10%的样品);而环丙沙星、地尔硫卓、氟西汀、左氧氟沙星、去甲氟西汀、雷尼替丁和舍曲林未检出。本研究首次报道了地表水中洛伐他汀的检测结果。

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