Use este identificador para citar ou linkar para este item: https://repositorio.ufba.br/handle/ri/14862
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dc.contributor.authorLisboa, Normando S.-
dc.contributor.authorFahning, Cristiane S.-
dc.contributor.authorCotrim, Gabriel-
dc.contributor.authorAnjos, Jeancarlo Pereira dos-
dc.contributor.authorAndrade, Jailson Bittencourt de-
dc.contributor.authorHatje, Vanessa-
dc.contributor.authorRocha, Gisele Olímpio da-
dc.creatorLisboa, Normando S.-
dc.creatorFahning, Cristiane S.-
dc.creatorCotrim, Gabriel-
dc.creatorAnjos, Jeancarlo Pereira dos-
dc.creatorAndrade, Jailson Bittencourt de-
dc.creatorHatje, Vanessa-
dc.creatorRocha, Gisele Olímpio da-
dc.date.accessioned2014-04-24T11:32:39Z-
dc.date.issued2013-
dc.identifier.issn0039-9140-
dc.identifier.urihttp://repositorio.ufba.br/ri/handle/ri/14862-
dc.descriptionTexto completo: acesso restrito. p. 168–175pt_BR
dc.description.abstractThe present study proposes a fast and simple analytical methodology employing C18 SPE cartridges (for preconcentration and clean-up), and a ultra-fast liquid chromatography coupled to fluorescence detector (UFLC-FLD) for determination of the following endocrine disrupters (ED): bisphenol A (BPA), 4-n-nonylphenol (4NNP), 4-n-octylphenol (4NOP), 4-t-octylphenol (4TOP), estriol (E3), estrone (E1), 17β-estradiol (E2) and 17α-ethynylestradiol (EE2) in seawater. The proposed method was developed, optimized and validated. Separation was done by a total running time of 10 min in a Shim-pack XR-ODS C-18 (2.0 mm ID × 50 mm) chromatographic column, mobile phases were acetonitrile/ultra-pure water under gradient programming; eluent flow rate at 0.120 mL min−1; column temperature set at 60 °C; emission wavelength of 306 nm and excitation wavelength of 280 nm. The method was validated through assessment of the following parameters: linear range, linearity, selectiveness, precision, recovery test, limit of detection (LOD), and limit of quantification (LOQ). Recoveries ranged from 91% (for EE2) to 104% (for 4NNP) and also was found a suitable repeatability (RSD <4.5%) for all considered compounds. LOD and LOQ ranged from 2.0 ng L−1 (EE2) to 23 ng L−1 (E1) and 9.3 ng L−1 (EE2) to 96 ng L−1 (E1), respectively. The analytical method using SPE UFLC-FLD was applied to seawater samples collected from Todos os Santos Bay (BTS), Brazil to determine the concentration of eight ED.pt_BR
dc.language.isoenpt_BR
dc.rightsAcesso Abertopt_BR
dc.sourcehttp://dx.doi.org/10.1016/j.talanta.2013.08.006pt_BR
dc.subjectEndocrine disrupterspt_BR
dc.subjectSeawaterpt_BR
dc.subjectLiquid chromatography with fluorescence detectionpt_BR
dc.subjectTodos os Santos Baypt_BR
dc.subjectContaminants of emerging concernpt_BR
dc.titleA simple and sensitive UFLC-fluorescence method for endocrine disrupters determination in marine waterspt_BR
dc.title.alternativeTalantapt_BR
dc.typeArtigo de Periódicopt_BR
dc.identifier.numberv. 117pt_BR
dc.embargo.liftdate10000-01-01-
Aparece nas coleções:Artigo Publicado em Periódico (Química)

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