Publicação:
Comparison of different clean-up procedures for the determination of N-methylcarbamate insecticides in vegetable matrices by high-performance liquid chromatography with UV detection

dc.contributor.authorNunes, G. S S
dc.contributor.authorRibeiro, M. L.
dc.contributor.authorPolese, L.
dc.contributor.authorBarcelo, D.
dc.contributor.institutionCSIC
dc.contributor.institutionUniversidade Federal do Maranhão (UFMA)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T15:24:42Z
dc.date.available2014-05-20T15:24:42Z
dc.date.issued1998-01-30
dc.description.abstractSeveral clean-up procedures which included the use of glass chromatography columns (silica gel, alumina, Florisil, silanized Celite-charcoal), Sep-Pak cartridges and standard solutions were compared for the determination of the following N-methylcarbamate (NMC) insecticides: aldicarb, carbaryl, carbofuran, methomyl and propoxur. According to recovery results of the compounds after elution in a glass column, the most efficient systems employed 4.6% deactivated alumina and a silanized Celite-charcoal (4:1) as adsorbents, using dichloromethane-methanol (99:1) and toluene-acetonitrile (75:25) mixtures, respectively, as binary eluents. The recoveries of the compounds studied varied from 84 to 120%. Comparable recoveries (75-100%) for Sep-Pak cartridges in normal phase (NH2, CN) and reversed phase (C-8) were observed. Different temperatures were tested during the concentration step in a rotary evaporator, and we verified a strong influence of this parameter on the stability of some compounds, such as carbofuran and carbaryl. Recovery studies employing the best clean up procedures were performed at the Brazilian agricultural level in potato and carrot samples; Validation methodology of the US Food and Drug Administration was adapted for the N-methylcarbamate analysis. Their recoveries ranged between 79 and 93% with coefficients of variation of 2.3-8%. (C) 1998 Elsevier B.V. B.V.en
dc.description.affiliationCSIC, Cid, Dept Environm Chem, ES-08034 Barcelona, Spain
dc.description.affiliationFed Univ Maranhao, Dept Chem Technol, BR-65080040 Sao Luis Ma, Brazil
dc.description.affiliationUNESP, Inst Chem, BR-14800900 Araraquara, SP, Brazil
dc.description.affiliationUnespUNESP, Inst Chem, BR-14800900 Araraquara, SP, Brazil
dc.format.extent43-51
dc.identifierhttp://dx.doi.org/10.1016/S0021-9673(97)01176-X
dc.identifier.citationJournal of Chromatography A. Amsterdam: Elsevier B.V., v. 795, n. 1, p. 43-51, 1998.
dc.identifier.doi10.1016/S0021-9673(97)01176-X
dc.identifier.issn0021-9673
dc.identifier.urihttp://hdl.handle.net/11449/35261
dc.identifier.wosWOS:000072036500005
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofJournal of Chromatography A
dc.relation.ispartofjcr3.716
dc.relation.ispartofsjr1,378
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectsample preparationpt
dc.subjectvegetablespt
dc.subjectfood analysispt
dc.subjectpesticidespt
dc.subjectcarbamatespt
dc.titleComparison of different clean-up procedures for the determination of N-methylcarbamate insecticides in vegetable matrices by high-performance liquid chromatography with UV detectionen
dc.typeArtigo
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
unesp.author.orcid0000-0002-8873-0491[4]

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