Irradiated PVAl membrane swelled with chitosan solution as dermal equivalent

dc.contributor.authorRODAS, A.C.D.pt_BR
dc.contributor.authorOHNUKI, T.pt_BR
dc.contributor.authorMATHOR, M.B.pt_BR
dc.contributor.authorLUGAO, A.B.pt_BR
dc.coverageInternacionalpt_BR
dc.date.accessioned2014-07-15T13:49:20Zpt_BR
dc.date.accessioned2014-07-30T11:51:04Z
dc.date.available2014-07-15T13:49:20Zpt_BR
dc.date.available2014-07-30T11:51:04Z
dc.date.issued2005pt_BR
dc.description.abstractSynthetic membranes as dermal equivalent can be applied at in vitro studies for developing new transdermal drugs or cosmetics. These membranes could be composed to mimic the dermis and seed cultivated keratinocytes as epidermal layer on it. The endothelial cells ingrowth to promote neovascularization and fibroblasts ingrowth to promote the substitution of this scaffold by natural components of the dermis. As, they can mimic the scaffold function of dermis; the membranes with biological interaction could be used for in vivo studies as dermal equivalent. For this application, poly(vinyl alcohol) (PVAl) membranes crosslinked by gamma radiation were swelled with chitosan solution. PVAl do not interact with the organism when implanted and is intended to mimic the mechanical characteristics of the dermal scaffold. The chitosan as a biocompatible biosynthetic polysaccharide were incorporated into PVAl membranes to improve the organism response. Degradation of chitosan by the organism occurs preferably by hydrolysis or enzymatic action, for example, by lysozyme. For this purpose the swelling kinetic of PVAl membranes with chitosan solution were performed and it was verified their degradation in vitro. The results showed that the swelling equilibrium of the PVAl membranes with chitosan membranes was reached in 120 h with average swelling of 1730%. After swelling, PVAl and chitosan/PVAl membranes were dried and immersed in phosphate buffer solution pH 5.7 and pH 7.4, with and without lysozyme, as those pH values are the specific physiologic pH for external skin and the general physiological pH for the organism, respectively. It was verified that the pure PVAl membrane did not showed change in their mass during 14 days. PVAl membranes swelled with chitosan solution showed mass decrease from 1 to 14 days inside these solutions. The highest mass decrease was verified at pH 5.7 in phosphate buffer solution without lysozyme. The smallest mass decrease was verified at pH 7.4 in phosphate buffer solution without lysozyme. In general, PVAl membranes swelled with chitosan solution showed a clear mass decrease at pH 5.7.
dc.format.extent536-539pt_BR
dc.identifier.citationRODAS, A.C.D.; OHNUKI, T.; MATHOR, M.B.; LUGAO, A.B. Irradiated PVAl membrane swelled with chitosan solution as dermal equivalent. <b>Nuclear Instruments and Methods in Physics Research</b>, v. 236, n. 1-4, p. 536-539, 2005. Section B. DOI: <a href="https://dx.doi.org/10.1016/j.nimb.2005.04.036">10.1016/j.nimb.2005.04.036</a>. Disponível em: http://repositorio.ipen.br/handle/123456789/5549.
dc.identifier.doi10.1016/j.nimb.2005.04.036
dc.identifier.fasciculo1-4pt_BR
dc.identifier.issn0168-583Xpt_BR
dc.identifier.orcidhttps://orcid.org/0000-0002-1737-3191
dc.identifier.orcidhttp://orcid.org/0000-0002-7294-9106
dc.identifier.suplementoSection Bpt_BR
dc.identifier.urihttp://repositorio.ipen.br/handle/123456789/5549pt_BR
dc.identifier.vol236pt_BR
dc.relation.ispartofNuclear Instruments and Methods in Physics Researchpt_BR
dc.rightsopenAccessen
dc.sourceApresentado tambem em: International Symposium on Ionizing Radiation and Polymers, 6th, 25-30 Sept., 2004, Houffalize, Belgiumpt_BR
dc.subjectalcoholspt_BR
dc.subjectamino acidspt_BR
dc.subjectcross-linkingpt_BR
dc.subjectfibroblastspt_BR
dc.subjectgamma radiationpt_BR
dc.subjecthydrolysispt_BR
dc.subjectin vitropt_BR
dc.subjectin vivopt_BR
dc.subjectirradiationpt_BR
dc.subjectlysozymept_BR
dc.subjectmathematical solutionspt_BR
dc.subjectmembranespt_BR
dc.subjectpolysaccharidespt_BR
dc.subjectskinpt_BR
dc.subjectswellingpt_BR
dc.titleIrradiated PVAl membrane swelled with chitosan solution as dermal equivalentpt_BR
dc.typeArtigo de periódicopt_BR
dspace.entity.typePublication
ipen.autorADEMAR BENEVOLO LUGAO
ipen.autorMONICA BEATRIZ MATHOR
ipen.autorTHIANA OHNUKI
ipen.autorANDREA CECILIA DORION RODAS
ipen.codigoautor339
ipen.codigoautor209
ipen.codigoautor3284
ipen.codigoautor1703
ipen.contributor.ipenauthorADEMAR BENEVOLO LUGAO
ipen.contributor.ipenauthorMONICA BEATRIZ MATHOR
ipen.contributor.ipenauthorTHIANA OHNUKI
ipen.contributor.ipenauthorANDREA CECILIA DORION RODAS
ipen.date.recebimento05-10pt_BR
ipen.identifier.fi1.181pt_BR
ipen.identifier.ipendoc10848pt_BR
ipen.identifier.iwosWoSpt_BR
ipen.range.fi0.001 - 1.499
ipen.type.genreArtigo
relation.isAuthorOfPublication99ac24c5-2ae1-465a-a6f2-40b4d9af6af7
relation.isAuthorOfPublication742b424f-9dfb-4e4a-993b-000052bb1313
relation.isAuthorOfPublicationf4c4232a-ca27-4ce4-abb2-7b4bde4db366
relation.isAuthorOfPublication0b208ad2-c765-4c4d-ae39-7c24fd6a8d55
relation.isAuthorOfPublication.latestForDiscovery0b208ad2-c765-4c4d-ae39-7c24fd6a8d55
sigepi.autor.atividadeRODAS, A.C.D.:1703:-1:Spt_BR
sigepi.autor.atividadeOHNUKI, T.:3284:-1:Npt_BR
sigepi.autor.atividadeMATHOR, M.B.:209:2:Npt_BR
sigepi.autor.atividadeLUGAO, A.B.:339:37:Npt_BR

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