2026-04-13T00:58:35Zhttps://recercat.cat/oai/request
oai:recercat.cat:10256/131302024-06-18T13:51:52Zcom_2072_452955com_2072_2054col_2072_453073
RECERCAT author Valls Cantenys, Carme author Scheurer, Marco author Iglesias Juncà, Mònica author Sacher, Frank author Brauch, Heinz Jürgen author Salvadó Martín, Victòria 2024-06-18T13:51:52Z 2024-06-18T13:51:52Z info:eu-repo/date/embargoEnd/2026-01-01info:eu-repo/date/embargoEnd/2026-01-012016-09-01 http://hdl.handle.net/10256/13130 A sensitive, multi-residue method using solid-phase extraction followed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) was developed to determine a representative group of 35 analytes, including corrosion inhibitors, pesticides and pharmaceuticals such as analgesic and anti-inflammatory drugs, five iodinated contrast media, β-blockers and some of their metabolites and transformation products in water samples. Few other methods are capable of determining such a broad range of contrast media together with other analytes. We studied the parameters affecting the extraction of the target analytes, including sorbent selection and extraction conditions, their chromatographic separation (mobile phase composition and column) and detection conditions using two ionisation sources: electrospray ionisation (ESI) and atmospheric pressure chemical ionisation (APCI). In order to correct matrix effects, a total of 20 surrogate/internal standards were used. ESI was found to have better sensitivity than APCI. Recoveries ranging from 79 to 134 % for tap water and 66 to 144 % for surface water were obtained. Intra-day precision, calculated as relative standard deviation, was below 34 % for tap water and below 21 % for surface water, groundwater and effluent wastewater. Method quantification limits (MQL) were in the low ng L−1 range, except for the contrast agents iomeprol, amidotrizoic acid and iohexol (22, 25.5 and 17.9 ng L−1, respectively). Finally, the method was applied to the analysis of 56 real water samples as part of the validation procedure. All of the compounds were detected in at least some of the water samples analysedThis study was financed by the SpanishMinistry of Science and Innovation through projects CTM2011-28765-C02-02 and CGL2013-48802-C3-2-R, and an FPI grant (Ref. BES-2009-024892) awarded to C. Valls-Cantenys Tots els drets reservats info:eu-repo/semantics/embargoedAccess Cromatografia de líquids Liquid chromatography Contaminants emergents en l'aigua Emerging contaminants in water Aigua -- Contaminació Water -- Pollution A sensitive multi-residue method for the determination of 35 micropollutants including pharmaceuticals, iodinated contrast media and pesticides in water info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion