UV filters, contained in sunscreens and other cosmetic products, as well as in some plastics and industrial products, are nowadays considered contaminants of emerging concern because their widespread and increasing use has lead to their presence in the environment. Furthermore, some UV filters are suspected to have endocrine disruption activity. In the present work, we developed an analytical method based on liquid chromatography with tandem mass spectrometry for the determination of UV filters in tap and lake waters. Sixteen UV filters were extracted from water samples by solid-phase extraction employing graphitized carbon black as adsorbent material. Handling 200 mL of water sample, satisfactory recoveries were obtained for almost all the analytes. The limits of detection and quantification of the method were comparable to those reported in other works, and ranged between 0.7-3.5 and 1.9-11.8 ng/L, respectively; however in our case the number of investigated compounds was larger. The major encountered problem in method development was to identify the background contamination sources and reduce their contribution. UV filters were not detected in tap water samples, whereas the analyses conducted on samples collected from three different lakes showed that the swimming areas are most subject to UV filter contamination. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Multiresidue determination of UV filters in water samples by solid-phase extraction and liquid chromatography with tandem mass spectrometry analysis / Capriotti, ANNA LAURA; Cavaliere, Chiara; Piovesana, Susy; Samperi, Roberto; Stampachiacchiere, Serena; Ventura, Salvatore; Lagana', Aldo. - In: JOURNAL OF SEPARATION SCIENCE. - ISSN 1615-9314. - STAMPA. - 37:20(2014), pp. 2882-2891. [10.1002/jssc.201400708]

Multiresidue determination of UV filters in water samples by solid-phase extraction and liquid chromatography with tandem mass spectrometry analysis

CAPRIOTTI, ANNA LAURA;CAVALIERE, CHIARA
;
PIOVESANA, SUSY;SAMPERI, Roberto;STAMPACHIACCHIERE, SERENA;VENTURA, SALVATORE;LAGANA', Aldo
2014

Abstract

UV filters, contained in sunscreens and other cosmetic products, as well as in some plastics and industrial products, are nowadays considered contaminants of emerging concern because their widespread and increasing use has lead to their presence in the environment. Furthermore, some UV filters are suspected to have endocrine disruption activity. In the present work, we developed an analytical method based on liquid chromatography with tandem mass spectrometry for the determination of UV filters in tap and lake waters. Sixteen UV filters were extracted from water samples by solid-phase extraction employing graphitized carbon black as adsorbent material. Handling 200 mL of water sample, satisfactory recoveries were obtained for almost all the analytes. The limits of detection and quantification of the method were comparable to those reported in other works, and ranged between 0.7-3.5 and 1.9-11.8 ng/L, respectively; however in our case the number of investigated compounds was larger. The major encountered problem in method development was to identify the background contamination sources and reduce their contribution. UV filters were not detected in tap water samples, whereas the analyses conducted on samples collected from three different lakes showed that the swimming areas are most subject to UV filter contamination. © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
2014
emerging contaminants; lake waters; liquid chromatography with mass spectrometry; solid-phase extraction; uv filters
01 Pubblicazione su rivista::01a Articolo in rivista
Multiresidue determination of UV filters in water samples by solid-phase extraction and liquid chromatography with tandem mass spectrometry analysis / Capriotti, ANNA LAURA; Cavaliere, Chiara; Piovesana, Susy; Samperi, Roberto; Stampachiacchiere, Serena; Ventura, Salvatore; Lagana', Aldo. - In: JOURNAL OF SEPARATION SCIENCE. - ISSN 1615-9314. - STAMPA. - 37:20(2014), pp. 2882-2891. [10.1002/jssc.201400708]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/592800
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