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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/116798
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dc.contributor.authorBertanha, Matheus-
dc.contributor.authorMoroz, Andrei-
dc.contributor.authorJaldin, Rodrigo G.-
dc.contributor.authorSilva, Regina A. M.-
dc.contributor.authorRinaldi, Jaqueline C.-
dc.contributor.authorGolim, Márjorie de Assis-
dc.contributor.authorFelisbino, Sergio L.-
dc.contributor.authorDomingues, Maria Aparecida Custódio-
dc.contributor.authorSobreira, Marcone Lima-
dc.contributor.authorReis, Patricia Pintor dos-
dc.contributor.authorDeffune, Elenice-
dc.date.accessioned2015-03-18T15:54:10Z-
dc.date.accessioned2016-10-25T20:28:05Z-
dc.date.available2015-03-18T15:54:10Z-
dc.date.available2016-10-25T20:28:05Z-
dc.date.issued2014-08-01-
dc.identifierhttp://dx.doi.org/10.1016/j.yexcr.2014.05.023-
dc.identifier.citationExperimental Cell Research. San Diego: Elsevier Inc, v. 326, n. 1, p. 103-111, 2014.-
dc.identifier.issn0014-4827-
dc.identifier.urihttp://hdl.handle.net/11449/116798-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/116798-
dc.description.abstractClinical experience for peripheral arterial disease treatment shows poor results when synthetic grafts are used to approach infrapopliteal arterial segments. However, tissue engineering may be an option to yield surrogate biocompatible neovessels. Thus, biological decellularized scaffolds could provide natural tissue architecture to use in tissue engineering, when the absence of ideal autologous veins reduces surgical options. The goal of this study was to evaluate different chemical induced decellularization protocols of the inferior vena cava of rabbits. They were decellularized with Triton X100 (TX100), sodium dodecyl sulfate (SDS) or sodium deoxycholate (DS). Afterwards, we assessed the remaining extracellular matrix (ECM) integrity, residual toxicity and the biomechanical resistance of the scaffolds. Our results showed that TX100 was not effective to remove the cells, while protocols using SDS 1% for 2 h and DS 2% for 1 h, efficiently removed the cells and were better characterized. These scaffolds preserved the original organization of ECM. In addition, the residual toxicity assessment did not reveal statistically significant changes while decellularized scaffolds retained the equivalent biomechanical properties when compared with the control. Our results concluded that protocols using SDS and DS were effective at obtaining decellularized scaffolds, which may be useful for blood vessel tissue engineering. (C) 2014 Published by Elsevier Inc.en
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)-
dc.format.extent103-111-
dc.language.isoeng-
dc.publisherElsevier B.V.-
dc.sourceWeb of Science-
dc.subjectPeripheral arterial diseaseen
dc.subjectBlood vesselsen
dc.subjectTissue engineeringen
dc.subjectBiomechanicsen
dc.subjectExtracellular matrixen
dc.titleMorphofunctional characterization of decellularized vena cava as tissue engineering scaffoldsen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationSao Paulo State Univ UNESP, Botucatu Med Sch, Dept Surg & Orthoped, Vasc Lab, BR-18618970 Botucatu, SP, Brazil-
dc.description.affiliationSao Paulo State Univ UNESP, Botucatu Med Sch, Cell Engn Lab, Blood Transfus Ctr, Botucatu, SP, Brazil-
dc.description.affiliationSao Paulo State Univ, Sch Pharmaceut Sci, Dept Bioproc & Biotechnol, Araraquara, SP, Brazil-
dc.description.affiliationSao Paulo State Univ, Botucatu Biosci Inst, Extracellular Matrix Lab, Dept Morphol, Botucatu, SP, Brazil-
dc.description.affiliationSao Paulo State Univ UNESP, Botucatu Med Sch, Flow Cytometry Lab, Ctr Blood Transfus, Botucatu, SP, Brazil-
dc.description.affiliationSao Paulo State Univ, Botucatu Med Sch, Immunohistochem Lab, Dept Pathol, Botucatu, SP, Brazil-
dc.description.affiliationScio Paulo State Univ UNESP, Botucatu Med Sch, Dept Urol, Botucatu, SP, Brazil-
dc.description.affiliationUnespSao Paulo State Univ UNESP, Botucatu Med Sch, Dept Surg & Orthoped, Vasc Lab, BR-18618970 Botucatu, SP, Brazil-
dc.description.affiliationUnespSao Paulo State Univ UNESP, Botucatu Med Sch, Cell Engn Lab, Blood Transfus Ctr, Botucatu, SP, Brazil-
dc.description.affiliationUnespSao Paulo State Univ, Sch Pharmaceut Sci, Dept Bioproc & Biotechnol, Araraquara, SP, Brazil-
dc.description.affiliationUnespSao Paulo State Univ, Botucatu Biosci Inst, Extracellular Matrix Lab, Dept Morphol, Botucatu, SP, Brazil-
dc.description.affiliationUnespSao Paulo State Univ UNESP, Botucatu Med Sch, Flow Cytometry Lab, Ctr Blood Transfus, Botucatu, SP, Brazil-
dc.description.affiliationUnespSao Paulo State Univ, Botucatu Med Sch, Immunohistochem Lab, Dept Pathol, Botucatu, SP, Brazil-
dc.description.affiliationUnespScio Paulo State Univ UNESP, Botucatu Med Sch, Dept Urol, Botucatu, SP, Brazil-
dc.description.sponsorshipIdFAPESP: 10/52549-8-
dc.identifier.doi10.1016/j.yexcr.2014.05.023-
dc.identifier.wosWOS:000339704600010-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileWOS000339704600010.pdf-
dc.relation.ispartofExperimental Cell Research-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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