Determination of antihypertensive and anti-ulcer agents from surface water with solid-phase extraction-liquid chromatography-electrospray ionization tandem mass spectrometry

被引:32
|
作者
Varga, Renata [1 ]
Somogyvari, Ivan [1 ]
Eke, Zsuzsanna [1 ]
Torkos, Kornel [1 ]
机构
[1] Eotvos Lorand Univ, Joint Res & Training Lab Separat Tech, H-1117 Budapest, Hungary
关键词
Anti-ulcer agents; Antihypertensive drugs; Water analysis; Liquid chromatography-tandem mass spectrometry; Solid-phase extraction; Post-extraction spike method; SEWAGE-TREATMENT PLANTS; 9 BASIC PHARMACEUTICALS; RAY CONTRAST-MEDIA; ENVIRONMENTAL-SAMPLES; WASTE-WATER; AQUEOUS SAMPLES; ANALYTICAL METHODOLOGIES; LC/MS/MS ANALYSES; ION SUPPRESSION; ILLICIT DRUGS;
D O I
10.1016/j.talanta.2010.11.030
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Pharmaceuticals are emerging contaminants in surface water and they must be measured to follow their effects on the aquatic environment. We developed a solid-phase extraction and liquid chromatography-electrospray ionization tandem mass spectrometry (SPE-LC-ESI-MS/MS) method for the determination of twenty-six pharmaceutical compounds - which belong to antihypertensive and anti-ulcer agents - from surface water samples. The selection of pharmaceuticals was based on usage frequency in Hungary. During method development Oasis HLB, SampliQ Polymer SCX and Si-SCX SPE cartridges were tested. As LC eluent ammonium formate. ammonium acetate buffers at pH 3 and 5 were investigated and for quantitation both matrix-matched and internal standard calibration was used. For matrix effect assessment post-extraction spike method was applied which can separate the extraction efficiency from ion suppression for better determination of recovery. Method detection limits (MDLs) varied between 0.2 and 10 ng/L. Precision of the method, calculated as relative standard deviation (RSD), ranged from 0.2 to 14.6% and from 1.2 to 22.4% for intra- and inter-day analysis, respectively. The method was applied to analyze Danube water samples. Measured average concentrations varied between 2 and 39 ng/L for eleven compounds and another one could be detected under LOQ (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:1447 / 1454
页数:8
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