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Host-guest system of 4-nerolidylcatechol in 2-hydroxypropyl-beta-cyclodextrin: preparation, characterization and molecular modeling

dc.contributor.authorSoares, Lillian Amelia
dc.contributor.authorVasconcelos Borges Leal, Ana Flavia
dc.contributor.authorFraceto, Leonardo Fernandes [UNESP]
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.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.date.accessioned2014-05-20T13:12:12Z
dc.date.available2014-05-20T13:12:12Z
dc.date.issued2009-06-01
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.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.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipSECTEC-GO
dc.format.extent23-35
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.doi10.1007/s10847-009-9532-y
dc.identifier.issn0923-0750
dc.identifier.urihttp://hdl.handle.net/11449/184
dc.identifier.wosWOS:000266009000003
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofJournal of Inclusion Phenomena and Macrocyclic Chemistry
dc.rights.accessRightsAcesso restrito
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.typeArtigo
dcterms.licensehttp://www.springer.com/open+access/authors+rights?SGWID=0-176704-12-683201-0
dcterms.rightsHolderSpringer
dspace.entity.typePublication
unesp.author.orcid0000-0002-3315-2129[6]
unesp.author.orcid0000-0001-9161-0127[7]
unesp.author.orcid0000-0002-3813-8545[10]
unesp.author.orcid0000-0002-2827-2038[3]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Ciência e Tecnologia, Sorocabapt
unesp.departmentEngenharia Ambiental - ICTSpt

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