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通过加压液体萃取和液相色谱-电喷雾电离质谱联用同时测定污水污泥中的氟喹诺酮类、磺胺类和四环素类药物

Simultaneous determination of fluoroquinolones, sulfonamides and tetracyclines in sewage sludge by pressurized liquid extraction and liquid chromatography electrospray ionization-mass spectrometry.

作者信息

Lillenberg Merike, Yurchenko Sergei, Kipper Karin, Herodes Koit, Pihl Viljar, Sepp Kalev, Lõhmus Rünno, Nei Lembit

机构信息

Department of Food Science and Hygiene, Estonian University of Life Sciences, Kreutzwaldi 58A, 51014 Tartu, Estonia.

出版信息

J Chromatogr A. 2009 Aug 7;1216(32):5949-54. doi: 10.1016/j.chroma.2009.06.029. Epub 2009 Jun 13.

Abstract

A new scheme for the quantitative determination of traces of fluoroquinolones (FQs), tetracyclines (TCs) and sulfonamides (SAs) in sewage sludge was developed. The compounds were simultaneously extracted from sewage sludge by pressurized liquid extraction (PLE). A novel and effective method for PLE was developed. Solid-phase extraction was used for cleaning up the extracts. Identification and quantification of the compounds was done using high-performance liquid chromatography with electrospray ionization mass spectrometry in selected reaction monitoring mode. The best recovery of FQs and TCs was obtained by using hydrophilic-lipophilic balance cartridges, recoveries ranged 59% for norfloxacin to 82% for ofloxacin and 95% for doxycycline; for SAs strong cation-exchange cartridges were more efficient, recoveries were 96% for sulfamethoxazole and 43% for sulfadimethoxine. Limit of quantification ranged from 0.1 ng/g for SAs to 160 ng/g for tetracycline. Method precision for TCs was 5.06% and 1.12%, and for SAs 0.43% and 2.01%. FQs precision ranged from 0.77% to 1.89%.

摘要

开发了一种用于定量测定污水污泥中痕量氟喹诺酮类(FQs)、四环素类(TCs)和磺胺类(SAs)的新方案。通过加压液体萃取(PLE)从污水污泥中同时提取这些化合物。开发了一种新颖且有效的PLE方法。采用固相萃取对提取物进行净化。使用高效液相色谱-电喷雾电离质谱联用仪在选择反应监测模式下对化合物进行鉴定和定量。使用亲水亲油平衡柱可获得FQs和TCs的最佳回收率,诺氟沙星的回收率为59%,氧氟沙星为82%,强力霉素为95%;对于SAs,强阳离子交换柱效率更高,磺胺甲恶唑的回收率为96%,磺胺二甲氧嘧啶为43%。定量限范围从SAs的0.1 ng/g到四环素的160 ng/g。TCs的方法精密度为5.06%和1.12%,SAs为0.43%和2.01%。FQs的精密度范围为0.77%至1.89%。

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