Determination of a broad spectrum of pharmaceuticals and endocrine disruptors in biofilm from a waste water treatment plant-impacted river

Wastewater treatment plants (WWTPs) are one of the main sources of pharmaceuticals and endocrine disrupting compounds in freshwater ecosystems, and several studies have reported bioaccumulation of these compounds in different organisms in those ecosystems. River biofilms are exceptional indicators o...

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Detalles Bibliográficos
Autores: Huerta Buitrago, Belinda, Rodríguez Mozaz, Sara, Nannou, Christina, Nakis, L., Ruhí i Vidal, Albert, Acuña, Vicenç, Sabater, Sergi, Barceló i Cullerés, Damià
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2016
País:España
Institución:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositorio:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:10256/12577
Acceso en línea:http://hdl.handle.net/10256/12577
Access Level:acceso abierto
Palabra clave:Aigua -- Contaminació
Water -- Pollution
Disruptors endocrins
Endocrine disrupting chemicals
Contaminants emergents en l'aigua
Emerging contaminants in water
Biofilms
Descripción
Sumario:Wastewater treatment plants (WWTPs) are one of the main sources of pharmaceuticals and endocrine disrupting compounds in freshwater ecosystems, and several studies have reported bioaccumulation of these compounds in different organisms in those ecosystems. River biofilms are exceptional indicators of pollution, but very few studies have focused on the accumulation of these emerging contaminants. The objectives of this study were first to develop an efficient analytical methodology for the simultaneous analysis of 44 pharmaceuticals and 13 endocrine disrupting compounds in biofilm, and second, to assess persistence, distribution, and bioaccumulation of these contaminants in natural biofilms inhabiting a WWTP-impacted river. The method is based on pressurized liquid extraction, purification by solid-phase extraction, and analysis by ultra performance liquid chromatography coupled to a mass spectrometer (UPLC-MS/MS) in tandem. Recoveries for pharmaceuticals were 31-137%, and for endocrine disruptors 32-93%. Method detection limits for endocrine disruptors were in the range of 0.2-2.4ng g-1, and for pharmaceuticals, 0.07-6.7ng g-1. A total of five endocrine disruptors and seven pharmaceuticals were detected in field samples at concentrations up to 100ng g-1