Application of a novel solid-phase-extraction sampler and ultra-performance liquid chromatography quadrupole-time-of-flight mass spectrometry for determination of pharmaceutical residues in surface sea water

被引:65
作者
Magner, Jorgen [1 ]
Filipovic, Marko [1 ]
Alsberg, Tomas [1 ]
机构
[1] Stockholm Univ, Dept Appl Environm Sci, SE-10691 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Bag-solid phase extraction; Pharmaceuticals; Sea water; Ultra-performance liquid chromatography; Quadrupole time-of-flight mass-spectrometry; WASTE-WATER; ACTIVE COMPOUNDS; PRECONCENTRATION; CONTAMINANTS; ANTIBIOTICS; ENVIRONMENT; PRODUCTS; DRUGS; FATE;
D O I
10.1016/j.chemosphere.2010.06.065
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In the present study, a multi-residue method based on a bag-solid phase extraction (bag-SPE) technique was evaluated for determination of 10 pharmaceuticals in surface water close to the effluent of a sewage treatment plant (STP) and along a coastal gradient from a STP effluent. The 10 compounds selected were caffeine, atenolol, metoprolol, oxazepam, carbamazepine, ketoprofen, naproxen, ibuprofen, diclofenac and gemfibrozil. All analyses were performed using ultra-performance liquid chromatography (UPLC) combined with quadrupole time-of-flight (QTOF) mass spectrometry. The detection limits (LOD) ranged from 1.0 to 13 ng L-1. The method showed linear concentration ranges from 25 to 800 ng L-1 with regression coefficients (R-2) better than 0.9801. The recoveries of the selected analytes ranged from 11 to 65% with relative standard deviations (RSD) of <16% and inter-day variations of less than 18%. Isotopically labeled surrogate standards were used to compensate for sampling losses and matrix effects. Four of the selected 10 pharmaceuticals (caffeine, metoprolol, oxazepam and carbamazepine) were quantified, at concentrations ranging from 4 to 210 ng L-1 (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1255 / 1260
页数:6
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