Hydroxymethylnitrofurazone:Dimethyl-beta-cyclodextrin Inclusion Complex: A Physical-Chemistry Characterization

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dc.contributor.authorGrillo, Renato [UNESP]
dc.contributor.authorSilva Melo, Nathalie Ferreira [UNESP]
dc.contributor.authorMoraes, Carolina Morales
dc.contributor.authorRosa, Andre Henrique [UNESP]
dc.contributor.authorFrutuoso Roveda, Jose Arnaldo [UNESP]
dc.contributor.authorMenezes, Carla M. S.
dc.contributor.authorFerreira, Elizabeth Igne
dc.contributor.authorFraceto, Leonardo Fernandes [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Estadual de Campinas (UNICAMP)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2014-05-20T15:19:31Z
dc.date.available2014-05-20T15:19:31Z
dc.date.issued2007-12-01
dc.description.abstractHydroxymethylnitrofurazone (NFOH) is active against Trypanosoma cruzi; however, its low solubility and high toxicity precludes its current use in treatment of parasitosis. Cyclodextrin can be used as a drug carrier system, as it is able to form inclusion (host-guest) complexes with a wide variety of organic (guest) molecules. Several reports have shown the interesting use of modified beta-cyclodextrins in pharmaceutical formulation, to improve the bioavailability of drugs and to decrease their toxicity. The aim of this work was to characterize inclusion complexes formed between NFOH and dimethyl-beta-cyclodextrin (DM-beta-CD) by complexation/release kinetics and solubility isotherm experiments using ultraviolet (UV)-visible spectrophotometry and by the measurement of the dynamics information obtained from T (1) relaxation times and diffusion (DOSY) experiments using nuclear magnetic resonance (NMR) spectroscopy. The complex was prepared at different NFOH and DM-beta-CD molar ratios. The UV-visible measurements were recorded in a spectrophotometer, and NMR experiments were recorded at 20 degrees C on a NMR spectrometer (Varian Inova) operating at 500 MHz. Longitudinal relaxation times were obtained by the conventional inversion-recovery method and the DOSY experiments were carried out using the BPPSTE sequence. The kinetics of complexation revealed that 30 h is enough for stabilization of the NFOH absorbance in presence of cyclodextrin. Solubility isotherm studies show a favorable complexation and increase in solubility when NFOH interacts with cyclodextrin. The analysis of the NMR-derived diffusion coefficients and T (1) relaxation times shows that in the presence of DM-beta-CD, NFOH decreases its mobility in solution, indicating that this antichagasic compound interacts with the cyclodextrin cavity. The release kinetics assays showed that NFOH changes its release profile when in the presence of cyclodextrin due to complexation. This study was focused on the physicochemical characterization of drug-delivery formulations that may serve as potentially new therapeutic options for the treatment of Chagas' disease.en
dc.description.affiliationState Univ São Paulo, Dept Environm Engn, BR-18087180 Sorocaba, SP, Brazil
dc.description.affiliationUniv Estadual Campinas, Inst Biol, Dept Biochem, Campinas, SP, Brazil
dc.description.affiliationUniv São Paulo, Fac Pharmaceut Sci, LAPEN, São Paulo, Brazil
dc.description.affiliationUnespState Univ São Paulo, Dept Environm Engn, BR-18087180 Sorocaba, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 05/03045-9
dc.description.sponsorshipIdFAPESP: 06/00787-7
dc.description.sponsorshipIdFAPESP: 04/02091-4
dc.format.extent445-453
dc.identifierhttp://dx.doi.org/10.1007/s10867-008-9054-7
dc.identifier.citationJournal of Biological Physics. Dordrecht: Springer, v. 33, n. 5-6, p. 445-453, 2007.
dc.identifier.doi10.1007/s10867-008-9054-7
dc.identifier.issn0092-0606
dc.identifier.lattes2188736885721242
dc.identifier.orcid0000-0002-2042-018X
dc.identifier.orcid0000-0002-0284-5782
dc.identifier.urihttp://hdl.handle.net/11449/30969
dc.identifier.wosWOS:000259961000009
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofJournal of Biological Physics
dc.relation.ispartofjcr1.000
dc.relation.ispartofsjr0,353
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.subjectHydroxymethylnitrofurazonept
dc.subjectDimethyl-beta-cyclodextrinpt
dc.subjectSolubility isothermpt
dc.subjectNuclear magnetic resonancept
dc.titleHydroxymethylnitrofurazone:Dimethyl-beta-cyclodextrin Inclusion Complex: A Physical-Chemistry Characterizationen
dc.typeArtigo
dcterms.licensehttp://www.springer.com/open+access/authors+rights?SGWID=0-176704-12-683201-0
dcterms.rightsHolderSpringer
unesp.author.lattes5228846314663888[4]
unesp.author.lattes2188736885721242[1]
unesp.author.orcid0000-0002-2042-018X[4]
unesp.author.orcid0000-0002-0284-5782[1]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Ciência e Tecnologia, Sorocabapt

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