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Validation of a liquid chromatography coupled with tandem mass spectrometry method for the determination of drugs in wastewater using a three-phase solvent system.
Pascale, Raffaella; Bianco, Giuliana; Coviello, Donatella; Cristina Lafiosca, Maria; Masi, Salvatore; Mancini, Ignazio M; Bufo, Sabino A; Scrano, Laura; Caniani, Donatella.
Afiliação
  • Pascale R; Scuola di Ingegneria, Università degli Studi della Basilicata, Potenza, Italy.
  • Bianco G; Dipartimento di Scienze, Università degli Studi della Basilicata, Potenza, Italy.
  • Coviello D; Dipartimento di Scienze, Università degli Studi della Basilicata, Potenza, Italy.
  • Cristina Lafiosca M; Dipartimento di Scienze, Università degli Studi della Basilicata, Potenza, Italy.
  • Masi S; Scuola di Ingegneria, Università degli Studi della Basilicata, Potenza, Italy.
  • Mancini IM; Scuola di Ingegneria, Università degli Studi della Basilicata, Potenza, Italy.
  • Bufo SA; Dipartimento di Scienze, Università degli Studi della Basilicata, Potenza, Italy.
  • Scrano L; Department of Geography, Environmental Management & Energy Studies, University of Johannesburg, South Africa.
  • Caniani D; Dipartimento delle Culture Europee e del Mediterraneo, Arch., Ambiente, Patrimoni Culturali, Università degli Studi della Basilicata, Matera, Italy.
J Sep Sci ; 43(5): 886-895, 2020 Mar.
Article em En | MEDLINE | ID: mdl-31849166
Pharmaceuticals constitute one of the most important emerging classes of environmental pollutants. A three-phase solvent system of water, water containing 0.1% of formic acid and acetonitrile was successfully used to separate, by liquid chromatography with mass spectrometry (LC-MS), polarity-matched pharmaceuticals, that is, carbamazepine, clarithromycin, and erythromycin, as well as amoxicillin and metformin. Despite of polarity similarities, these pharmaceuticals were completely resolved in the analytical run time of 15 min. The optimized three-phase solvent system based-method was validated for the simultaneous analysis of six matched-polarity pharmaceuticals in wastewater samples. Good linearity (coefficient of determination more than 0.993) and precision (relative standard deviation less than 15.66%) were achieved. Recovery of analytes from the wastewater was between 0.70 and 1.18. Limits of detections ranged from 0.0001 to 0.5114 µg/L. No significant matrix effect, evaluated by post extraction addition, was observed in the electrospray ionization (ESI) source. Then, this methodology has been successfully applied to environmental study of pharmaceutical residues occurring in influent and effluent wastewater samples, from the main wastewater treatment plant in Potenza (Basilicata, Southern Italy).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Poluentes Químicos da Água / Carbamazepina / Eritromicina / Claritromicina / Amoxicilina / Metformina Idioma: En Revista: J Sep Sci Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália País de publicação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Poluentes Químicos da Água / Carbamazepina / Eritromicina / Claritromicina / Amoxicilina / Metformina Idioma: En Revista: J Sep Sci Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Itália País de publicação: Alemanha