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Oil-in-water lecithin-based microemulsions as a potential delivery system for amphotericin B

dc.contributor.authorPestana, K. C. [UNESP]
dc.contributor.authorFormariz, T. P. [UNESP]
dc.contributor.authorFranzini, C. M. [UNESP]
dc.contributor.authorSarmento, V. H. V. [UNESP]
dc.contributor.authorChiavacci, L. A. [UNESP]
dc.contributor.authorScarpa, M. V. [UNESP]
dc.contributor.authorEgito, E. S. T.
dc.contributor.authorOliveira, Anselmo Gomes de [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Federal do Rio Grande do Norte (UFRN)
dc.date.accessioned2014-05-20T14:18:31Z
dc.date.available2014-05-20T14:18:31Z
dc.date.issued2008-10-15
dc.description.abstractIn this work the structural features of microemulsions (MEs) containing the pharmaceutical biocompatible Soya phosphatidylcholine/Tween 20 (1:1) as surfactant (S), Captex(TM) 200 as oil phase (0), and phosphate buffer 10mM, pH 7.2 as aqueous phase (W) were Studied. Systems obtained with different proportions of the components were described by pseudo-ternary phase diagrams in order to characterize the microemulsions studied here. MEs were prepared with and without the polyene antifungal drug amphotericin B (AmB). The maximum AmB incorporation into the ME system was dependent on both the oil phase and surfactant proportions with 6.80 and 5.7 mg/mL in high contents, respectively. The incorporation of AmB into the ME systems significantly increased the profile of the droplet size of the ME for all ranges of surfactant proportions used in the formulations. The microstructures of the system were characterized by dynamic light scattering (DLS) and theological behavior. The DLS results showed that the size of the oil droplets increases 4.6-fold when AmB is incorporated into the ME system. In all cases the increase in the proportion of the oil phase of the ME leads to a slight increase in the diameter of the oil droplets of the system. Furthermore, for both the AmB-loaded and AmB-unloaded MEs, the size of the oil droplets decrease significantly with the increase of the S proportion in the formulations, demonstrating the efficiency of the surfactant in stabilizing the ME. Depending on the ME composition, an anti-thixotropic behavior was found. The maximum increases of the consistency index caused by the increase of the oil phase of the ME were of 17- and 25-times for the drug-loaded and drug-unloaded MEs, respectively. However, the observed effect for the drug-loaded ME was about 4.6 times higher than that for the drug-unloaded one, demonstrating the strong effect of the drug on the theological characteristics of the ME system. Therefore, it is possible to conclude that the investigated ME can be used as a very promising vehicle for AmB. (C) 2008 Elsevier B.V. All rights reserved.en
dc.description.affiliationUNESP, Dept Farm & Medicamentos, Fac Ciencias Farmaceut, BR-14801902 Araraquara, SP, Brazil
dc.description.affiliationUNESP, Inst Quim, Dept Fisicoquim, BR-14800900 Araraquara, SP, Brazil
dc.description.affiliationUniversidade Federal do Rio Grande do Norte (UFRN), Ctr Ciencias Saude, Dept Farm, BR-59010180 Natal, RN, Brazil
dc.description.affiliationUnespUNESP, Dept Farm & Medicamentos, Fac Ciencias Farmaceut, BR-14801902 Araraquara, SP, Brazil
dc.description.affiliationUnespUNESP, Inst Quim, Dept Fisicoquim, BR-14800900 Araraquara, SP, Brazil
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)
dc.description.sponsorshipCoordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
dc.format.extent253-259
dc.identifierhttp://dx.doi.org/10.1016/j.colsurfb.2008.06.016
dc.identifier.citationColloids and Surfaces B-biointerfaces. Amsterdam: Elsevier B.V., v. 66, n. 2, p. 253-259, 2008.
dc.identifier.doi10.1016/j.colsurfb.2008.06.016
dc.identifier.issn0927-7765
dc.identifier.urihttp://hdl.handle.net/11449/25579
dc.identifier.wosWOS:000259792900015
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofColloids and Surfaces B: Biointerfaces
dc.relation.ispartofjcr3.997
dc.relation.ispartofsjr1,071
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectmicroemulsionen
dc.subjectamphotericin Ben
dc.subjectdrug deliveryen
dc.subjectrheologyen
dc.subjectphase diagramen
dc.titleOil-in-water lecithin-based microemulsions as a potential delivery system for amphotericin Ben
dc.typeArtigopt
dcterms.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dcterms.rightsHolderElsevier B.V.
dspace.entity.typePublication
relation.isDepartmentOfPublicatione214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isDepartmentOfPublication.latestForDiscoverye214da1b-9929-4ae9-b8fd-655e9bfeda4b
relation.isOrgUnitOfPublication95697b0b-8977-4af6-88d5-c29c80b5ee92
relation.isOrgUnitOfPublication.latestForDiscovery95697b0b-8977-4af6-88d5-c29c80b5ee92
unesp.author.lattes9114495952533044[8]
unesp.author.orcid0000-0002-0107-9940[8]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.campusUniversidade Estadual Paulista (UNESP), Faculdade de Ciências Farmacêuticas, Araraquarapt
unesp.departmentFármacos e Medicamentos - FCFpt
unesp.departmentFísico-Química - IQARpt

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