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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/184
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dc.contributor.authorSoares, Lillian Amelia-
dc.contributor.authorVasconcelos Borges Leal, Ana Flavia-
dc.contributor.authorFraceto, Leonardo Fernandes-
dc.contributor.authorMaia, Elaine Rose-
dc.contributor.authorResck, Ines Sabioni-
dc.contributor.authorKato, Massuo Jorge-
dc.contributor.authorGil, Eric de Sousa-
dc.contributor.authorde Sousa, Aparecido Ribeiro-
dc.contributor.authorda Cunha, Luiz Carlos-
dc.contributor.authorRezende, Kennia Rocha-
dc.date.accessioned2014-05-20T13:12:12Z-
dc.date.accessioned2016-10-25T16:32:33Z-
dc.date.available2014-05-20T13:12:12Z-
dc.date.available2016-10-25T16:32:33Z-
dc.date.issued2009-06-01-
dc.identifierhttp://dx.doi.org/10.1007/s10847-009-9532-y-
dc.identifier.citationJournal of Inclusion Phenomena and Macrocyclic Chemistry. Dordrecht: Springer, v. 64, n. 1-2, p. 23-35, 2009.-
dc.identifier.issn0923-0750-
dc.identifier.urihttp://hdl.handle.net/11449/184-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/184-
dc.description.abstractThe interaction of 4-nerolidylcatechol (4-NRC), a potent antioxidant agent, and 2-hydroxypropyl-beta-cyclodextrin (HP-beta-CD) was investigated by the solubility method using Fourier transform infrared (FTIR) methods in addition to UV-Vis, (1)H-nuclear magnetic resonance (NMR) spectroscopy and molecular modeling. The inclusion complexes were prepared using grinding, kneading and freeze-drying methods. According to phase solubility studies in water a B(S)-type diagram was found, displaying a stoichiometry complexation of 2:1 (drug:host) and stability constant of 6494 +/- A 837 M(-1). Stoichiometry was established by the UV spectrophotometer using Job's plot method and, also confirmed by molecular modeling. Data from (1)H-NMR, and FTIR, experiments also provided formation evidence of an inclusion complex between 4-NRC and HP-beta-CD. 4-NRC complexation indeed led to higher drug solubility and stability which could probably be useful to improve its biological properties and make it available to oral administration and topical formulations.en
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)-
dc.description.sponsorshipSECTEC-GO-
dc.format.extent23-35-
dc.language.isoeng-
dc.publisherSpringer-
dc.sourceWeb of Science-
dc.subject4-Nerolidylcatecholen
dc.subject2-Hydroxypropyl-beta-cyclodextrinen
dc.subjectInclusion complexen
dc.subject(1)H-NMR and molecular dynamicsen
dc.titleHost-guest system of 4-nerolidylcatechol in 2-hydroxypropyl-beta-cyclodextrin: preparation, characterization and molecular modelingen
dc.typeoutro-
dc.contributor.institutionUniversidade Federal de Goiás (UFG)-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionUniversidade de Brasília (UnB)-
dc.contributor.institutionUniversidade de São Paulo (USP)-
dc.description.affiliationUniversidade Federal de Goiás (UFG), Fac Farm, Lab Biofarm & Farmacocinet, BR-74605220 Goiania, Go, Brazil-
dc.description.affiliationUniv Estadual Paulista, Dept Engn Ambiental, Sorocaba, SP, Brazil-
dc.description.affiliationUniversidade de Brasilia (UnB), Inst Quim, Brasilia, DF, Brazil-
dc.description.affiliationUniv São Paulo, Inst Quim, Dept Quim Fundamental, São Paulo, Brazil-
dc.description.affiliationUniversidade Federal de Goiás (UFG), Inst Quim, BR-74605220 Goiania, Go, Brazil-
dc.description.affiliationUnespUniv Estadual Paulista, Dept Engn Ambiental, Sorocaba, SP, Brazil-
dc.identifier.doi10.1007/s10847-009-9532-y-
dc.identifier.wosWOS:000266009000003-
dc.rights.accessRightsAcesso restrito-
dc.relation.ispartofJournal of Inclusion Phenomena and Macrocyclic Chemistry-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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