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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/75595
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dc.contributor.authorCaetano, Josiane-
dc.contributor.authorDragunski, Douglas C.-
dc.contributor.authorPedrosa, Valber A.-
dc.contributor.authorMachado, Sergio A.S.-
dc.date.accessioned2014-05-27T11:29:38Z-
dc.date.accessioned2016-10-25T18:49:36Z-
dc.date.available2014-05-27T11:29:38Z-
dc.date.available2016-10-25T18:49:36Z-
dc.date.issued2013-06-01-
dc.identifierhttp://www.electrochemsci.org/papers/vol8/80607795.pdf-
dc.identifier.citationInternational Journal of Electrochemical Science, v. 8, n. 6, p. 7795-7805, 2013.-
dc.identifier.issn1452-3981-
dc.identifier.urihttp://hdl.handle.net/11449/75595-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/75595-
dc.description.abstractAn enzymatic biosensor based on inhibition of acetylcholinesterase activity was developed to analyze methomyl contamination in different matrices. The detection limits under optimal working conditions were found to be 30.4 μg L-1 methomyl using the biosensor and 0.15 μg L-1 using HPLC. The biosensor was then applied to analysis of methomyl in fruit and vegetable samples at concentrations in the ppb range in the absence of sample pretreatment. Recovery levels using the biosensor were effective, ranging from 78.0 to 96.5%, while the HPLC method yielded 57.0 to 99.5% recovery. Results for total carbamate concentrations obtained using the acetylcholinesterase biosensor were compared to those obtained using HPLC. © 2013 by ESG.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.format.extent7795-7805-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectBiosensor-
dc.subjectFood analysis-
dc.subjectMethomyl-
dc.subjectPesticides-
dc.titleQuantification of methomyl levels in cabbage, tomato, and soya milk using a renewable amperometric biosensoren
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual do Oeste do Parań-
dc.contributor.institutionUNIPAR-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.description.affiliationUniversidade Estadual do Oeste do Parań, 85903-000 - Toledo - Paraná-
dc.description.affiliationUniversidade Paranaense UNIPAR, Umuarama- PR-
dc.description.affiliationInstitute of Bioscience Department of Chemistry and Biochemistry UNESP, Botucatu, SP-
dc.description.affiliationInstituto de Química de São Carlos Universidade de São Paulo, 13560-970 São Carlos - SP-
dc.description.affiliationUnespInstitute of Bioscience Department of Chemistry and Biochemistry UNESP, Botucatu, SP-
dc.description.sponsorshipIdFAPESP: 03/07653-8-
dc.description.sponsorshipIdFAPESP: 06/51625-7-
dc.identifier.wosWOS:000323546100026-
dc.rights.accessRightsAcesso aberto-
dc.identifier.file2-s2.0-84878993001.pdf-
dc.relation.ispartofInternational Journal of Electrochemical Science-
dc.identifier.scopus2-s2.0-84878993001-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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