Interlaboratory validation of an environmental monitoring method for trace analysis of endocrine disrupting compounds

Detalhes bibliográficos
Autor(a) principal: Mansilha, Catarina
Data de Publicação: 2012
Outros Autores: Rocha, Sónia, Gameiro, P., Pinho, Carina, Ferreira, Isabel M. P. L. V. O., Silva, Poliana, Domingues, Valentina F.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.22/2182
Resumo: Environmental pollution continues to be an emerging study field, as there are thousands of anthropogenic compounds mixed in the environment whose possible mechanisms of toxicity and physiological outcomes are of great concern. Developing methods to access and prioritize the screening of these compounds at trace levels in order to support regulatory efforts is, therefore, very important. A methodology based on solid phase extraction followed by derivatization and gas chromatography-mass spectrometry analysis was developed for the assessment of four endocrine disrupting compounds (EDCs) in water matrices: bisphenol A, estrone, 17b-estradiol and 17a-ethinylestradiol. The study was performed, simultaneously, by two different laboratories in order to evaluate the robustness of the method and to increase the quality control over its application in routine analysis. Validation was done according to the International Conference on Harmonisation recommendations and other international guidelines with specifications for the GC-MS methodology. Matrix-induced chromatographic response enhancement was avoided by using matrix-standard calibration solutions and heteroscedasticity has been overtaken by a weighted least squares linear regression model application. Consistent evaluation of key analytical parameters such as extraction efficiency, sensitivity, specificity, linearity, limits of detection and quantification, precision, accuracy and robustness was done in accordance with standards established for acceptance. Finally, the application of the optimized method in the assessment of the selected analytes in environmental samples suggested that it is an expedite methodology for routine analysis of EDC residues in water matrices.
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spelling Interlaboratory validation of an environmental monitoring method for trace analysis of endocrine disrupting compoundsEnvironmental pollution continues to be an emerging study field, as there are thousands of anthropogenic compounds mixed in the environment whose possible mechanisms of toxicity and physiological outcomes are of great concern. Developing methods to access and prioritize the screening of these compounds at trace levels in order to support regulatory efforts is, therefore, very important. A methodology based on solid phase extraction followed by derivatization and gas chromatography-mass spectrometry analysis was developed for the assessment of four endocrine disrupting compounds (EDCs) in water matrices: bisphenol A, estrone, 17b-estradiol and 17a-ethinylestradiol. The study was performed, simultaneously, by two different laboratories in order to evaluate the robustness of the method and to increase the quality control over its application in routine analysis. Validation was done according to the International Conference on Harmonisation recommendations and other international guidelines with specifications for the GC-MS methodology. Matrix-induced chromatographic response enhancement was avoided by using matrix-standard calibration solutions and heteroscedasticity has been overtaken by a weighted least squares linear regression model application. Consistent evaluation of key analytical parameters such as extraction efficiency, sensitivity, specificity, linearity, limits of detection and quantification, precision, accuracy and robustness was done in accordance with standards established for acceptance. Finally, the application of the optimized method in the assessment of the selected analytes in environmental samples suggested that it is an expedite methodology for routine analysis of EDC residues in water matrices.Royal Society of ChemistryRepositório Científico do Instituto Politécnico do PortoMansilha, CatarinaRocha, SóniaGameiro, P.Pinho, CarinaFerreira, Isabel M. P. L. V. O.Silva, PolianaDomingues, Valentina F.2013-10-04T11:30:11Z20122012-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.22/2182eng1759-966010.1039/C2AY25450Fmetadata only accessinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-03-13T12:41:39Zoai:recipp.ipp.pt:10400.22/2182Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T17:23:11.852645Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Interlaboratory validation of an environmental monitoring method for trace analysis of endocrine disrupting compounds
title Interlaboratory validation of an environmental monitoring method for trace analysis of endocrine disrupting compounds
spellingShingle Interlaboratory validation of an environmental monitoring method for trace analysis of endocrine disrupting compounds
Mansilha, Catarina
title_short Interlaboratory validation of an environmental monitoring method for trace analysis of endocrine disrupting compounds
title_full Interlaboratory validation of an environmental monitoring method for trace analysis of endocrine disrupting compounds
title_fullStr Interlaboratory validation of an environmental monitoring method for trace analysis of endocrine disrupting compounds
title_full_unstemmed Interlaboratory validation of an environmental monitoring method for trace analysis of endocrine disrupting compounds
title_sort Interlaboratory validation of an environmental monitoring method for trace analysis of endocrine disrupting compounds
author Mansilha, Catarina
author_facet Mansilha, Catarina
Rocha, Sónia
Gameiro, P.
Pinho, Carina
Ferreira, Isabel M. P. L. V. O.
Silva, Poliana
Domingues, Valentina F.
author_role author
author2 Rocha, Sónia
Gameiro, P.
Pinho, Carina
Ferreira, Isabel M. P. L. V. O.
Silva, Poliana
Domingues, Valentina F.
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Instituto Politécnico do Porto
dc.contributor.author.fl_str_mv Mansilha, Catarina
Rocha, Sónia
Gameiro, P.
Pinho, Carina
Ferreira, Isabel M. P. L. V. O.
Silva, Poliana
Domingues, Valentina F.
description Environmental pollution continues to be an emerging study field, as there are thousands of anthropogenic compounds mixed in the environment whose possible mechanisms of toxicity and physiological outcomes are of great concern. Developing methods to access and prioritize the screening of these compounds at trace levels in order to support regulatory efforts is, therefore, very important. A methodology based on solid phase extraction followed by derivatization and gas chromatography-mass spectrometry analysis was developed for the assessment of four endocrine disrupting compounds (EDCs) in water matrices: bisphenol A, estrone, 17b-estradiol and 17a-ethinylestradiol. The study was performed, simultaneously, by two different laboratories in order to evaluate the robustness of the method and to increase the quality control over its application in routine analysis. Validation was done according to the International Conference on Harmonisation recommendations and other international guidelines with specifications for the GC-MS methodology. Matrix-induced chromatographic response enhancement was avoided by using matrix-standard calibration solutions and heteroscedasticity has been overtaken by a weighted least squares linear regression model application. Consistent evaluation of key analytical parameters such as extraction efficiency, sensitivity, specificity, linearity, limits of detection and quantification, precision, accuracy and robustness was done in accordance with standards established for acceptance. Finally, the application of the optimized method in the assessment of the selected analytes in environmental samples suggested that it is an expedite methodology for routine analysis of EDC residues in water matrices.
publishDate 2012
dc.date.none.fl_str_mv 2012
2012-01-01T00:00:00Z
2013-10-04T11:30:11Z
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dc.publisher.none.fl_str_mv Royal Society of Chemistry
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