Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/164919
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dc.creatorMaria Miguel Coelho
dc.creatorAna Rita Ribeiro
dc.creatorJoão C. G. Sousa
dc.creatorCláudia Ribeiro
dc.creatorCarla Fernandes
dc.creatorAdrián M. T. Silva
dc.creatorMaria Elizabeth Tiritan
dc.date.accessioned2025-01-23T00:07:46Z-
dc.date.available2025-01-23T00:07:46Z-
dc.date.issued2019
dc.identifier.issn0731-7085
dc.identifier.othersigarra:363060
dc.identifier.urihttps://hdl.handle.net/10216/164919-
dc.description.abstractThis work presents the development of an enantioselective method to quantify chiral drugs (CDs) in surface water and its application in the Douro River estuary monitoring. Different classes of CDs were targeted, including 23 compounds, namely beta-blockers, antidepressants, one beta(2)-adrenergic agonist, non-steroidal anti-inflammatory drugs, stimulants, and some illicit drugs as cocaine (COC) and its metabolites, and amphetamines. The analytical method was based on an innovative application of solid phase extraction (SPE), followed by liquid chromatography-tandem mass spectrometry (LC-MS/MS) using a triple quadrupole analyzer. The ground-breaking approach of SPE consists in the use of Oasis (R) MCX cartridges to pre-concentrate 500 mL of water samples, allowing the simultaneous extraction of acidic, basic and neutral analytes, rather than the conventional recovery of basic compounds only. Two chiral columns were used for enantiomeric separation in reverse elution mode, a Chirobiotic (TM) V and a Pirkle type Whelk-O (R) 1, for basic and acidic compounds, respectively. The method validation demonstrated good linearity (r(2) > 0.99), selectivity and sensitivity, with method detection limits between 0.01 and 2.66 ng L-1 and method quantification limits between 0.02 and 5.71 ng L-1. The developed method was successfully applied to monitor daily variations along one week in surface waters collected in 5 locations of the Douro River estuary. Tramadol (TRM) and its metabolite N-desmethyltramadol (NDT), presented high concentrations near the affluent of a tributary river, while the second eluted enantiomer of O-desmethyltramadol (ODT) was found at high concentrations at the mouth of the Douro River. The metabolite NDT was quantified at higher concentrations than TRM. Venlafaxine (VNF) was found at high concentrations near the affluent of the same tributary river, but its metabolite, O-desmethylvenlafaxine (ODV), was found at concentrations 3 times higher. COC was found every day at all sampling points along the estuary, with slight variations.
dc.language.isoeng
dc.relationinfo:eu-repo/grantAgreement/FCT - Fundação para a Ciência e a Tecnologia/P2020|COMPETE - Projetos em Todos os Domínios Científicos/POCI-01-0145-FEDER-030521/Novas técnicas miniaturizadas de preparação de amostra para determinação de micropoluentes em matrizes ambientais/SAMPREP
dc.relationinfo:eu-repo/grantAgreement/Comissão de Coordenação e Desenvolvimento Regional do Norte/P2020|Norte2020-Projetos Integrados ICDT/NORTE-01-0145-FEDER-000006/Advanced Industrial Processes and Materials for a Sustainable North Region of Portugal2020/AIProcMat@N2020
dc.rightsopenAccess
dc.titleDual enantioselective LC-MS/MS method to analyse chiral drugs in surface water: Monitoring in Douro River estuary
dc.typeArtigo em Revista Científica Internacional
dc.contributor.uportoFaculdade de Engenharia
dc.contributor.uportoFaculdade de Farmácia
dc.identifier.doi10.1016/j.jpba.2019.03.032
dc.identifier.authenticusP-00Q-BZE
Appears in Collections:FEUP - Artigo em Revista Científica Internacional
FFUP - Artigo em Revista Científica Internacional

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