On-line preconcentration of pharmaceutical residues from large volume water samples using short reversed-phase monolithic cartridges coupled to LC-UV-ESI-MS

被引:86
作者
Bones, Jonathan
Thomas, Kevin
Nesterenko, Pavel N.
Paull, Brett [1 ]
机构
[1] Dublin City Univ, Sch Chem Sci, Natl Ctr Sensor Res, Dublin 9, Ireland
[2] Norwegian Inst Water Res, NIVA, NO-0411 Oslo, Norway
关键词
pharmaceuticals; LC-UV-ESI-MS; on-line SPE; preconcentration; monolithic reversed-phase silica;
D O I
10.1016/j.talanta.2006.02.026
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A simplified preconcentration method for a range of ultra-trace level pharmaceuticals in natural waters has been developed. Solid phase extraction was performed on-line using a micro-reversed-phase monolithic silica column, allowing for very rapid trace enrichment front large Volume (500 ml) samples with minimal sample handling. Acceptable recoveries of > 70% were obtained for the majority of compounds investigated and the monolithic columns could be washed and conditioned on-line with no sample carryover and used reproducibly for up to eight extractions each. The on-line SPE-LC-UV method was coupled to electrospray ionisation ion trap mass spectrometry (ESI-MS) to increase both selectivity and specificity. Detection limits were determined in spiked river and tap water samples and found to lie in the low ng/l region using sample volumes of 500 ml., loaded at a flow rate of 10 ml/min, and therefore, were suitable for ultra trace analysis. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:1117 / 1128
页数:12
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