Use este identificador para citar ou linkar para este item: http://www.alice.cnptia.embrapa.br/alice/handle/doc/1065497
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dc.contributor.authorGONZALEZ, M. H.pt_BR
dc.contributor.authorSILVA, C. S. dapt_BR
dc.contributor.authorAMARAL, C. D. B. dopt_BR
dc.contributor.authorBIANCHI, S. R.pt_BR
dc.contributor.authorOLIVEIRA, L. H. B. dept_BR
dc.contributor.authorCOELHO, J. S.pt_BR
dc.contributor.authorOLIVEIRA, A.pt_BR
dc.contributor.authorNOGUEIRA, A. R. de A.pt_BR
dc.date.accessioned2019-03-30T00:30:34Z-
dc.date.available2019-03-30T00:30:34Z-
dc.date.created2017-02-23
dc.date.issued2017
dc.identifier.citationJournal of the Brazilian Chemical Society, v. 28, n. 1, p. 98-105, 2017.pt_BR
dc.identifier.urihttp://www.alice.cnptia.embrapa.br/alice/handle/doc/1065497-
dc.descriptionInorganic elements present in pharmaceutical products were determined by inductively coupled plasma-mass spectrometer (ICP-MS), employing microwave acid digestion as a sample preparation method. The most abundant isotopes, 75As+ , 65Cu+ , 52Cr+ , 58Ni+ , 208Pb+ , and 51V+ , were determined in acyclovir ointment and its constituents. Elemental impurities in the pharmaceutical samples were determined using an inductively coupled plasma-universal cell technology-mass spectrometer (ICP-UCT-MS) operated in kinetic energy discrimination (KED) and standard mode. The accuracy of the method was assessed by means of addition and recovery experiments. Except for Cr, spiked recoveries of the elements added to the samples before microwave acid digestion (MW-AD) step were between 95.1 and 126%, and after MW-AD step ranged from 85.6 to 132%. Limits of detection (LOD) obtained by proposed method is in agreement to those required by the U.S. Pharmacopeia Convention (USP), showing that the ICP-MS technique is well suited for quantification of these elements. The LOD?s (ng L-1) for 51V+ , 52Cr+ , 58Ni+ , 65Cu+ , 75As+ and 208Pb+ in 1% v v-1 HNO3 medium were: 2.2, 81.3, 91.9, 6.9, 0.2 and 3.1, respectively. The concentration of the analytes in these samples presented a wide range, varying from 2.3 ± 0.8 µg kg-1 for As to 3446 ± 47 µg kg-1 for Cr.pt_BR
dc.language.isoporpt_BR
dc.rightsopenAccesspt_BR
dc.subjectPharmaceutical productpt_BR
dc.subjectElemental impuritypt_BR
dc.subjectAcyclovirpt_BR
dc.titleDetermination of elemental impurities in acyclovir ointment and raw materials using microwave acid digestion (MW-AD) and ICP-MS.pt_BR
dc.typeArtigo de periódicopt_BR
dc.date.updated2019-03-30T00:30:34Z
riaa.ainfo.id1065497pt_BR
riaa.ainfo.lastupdate2019-03-29
dc.identifier.doihttp://dx.doi.org/10.5935/0103-5053.20160151pt_BR
dc.contributor.institutionMario Henrique Gonzalez, UNESP; Caroline Santos da Silva, UFSCar; Clarice Dias Britto do Amaral, UFSCar; SILMARA ROSSANA BIANCHI, CNPS; Luciano Henrique Barca de Oliveira, UNESP; Jessica Silva Coelho, UNESP; Andrea Oliveira, UFPR; ANA RITA DE ARAUJO NOGUEIRA, CPPSE.pt_BR
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