Publication:
Electrospun polyurethane/poly (ɛ-caprolactone) nanofibers promoted the attachment and growth of human endothelial cells in static and dynamic culture conditions

dc.contributor.coauthorKarkan, Sonia Fathi
dc.contributor.coauthorRahbarghazi, Reza
dc.contributor.coauthorDavaran, Soodabeh
dc.contributor.coauthorKaleybar, Leila Shafiei
dc.contributor.coauthorKhoshfetrat, Ali Baradar
dc.contributor.coauthorZolali, Elmira
dc.contributor.coauthorAkbarzadeh, Abolfazl
dc.contributor.departmentKUTTAM (Koç University Research Center for Translational Medicine)
dc.contributor.facultymemberNo
dc.contributor.kuauthorHeidarzadeh, Morteza
dc.contributor.schoolcollegeinstituteResearch Center
dc.date.accessioned2024-11-09T23:54:24Z
dc.date.issued2021
dc.description.abstractIn this study, the angiogenic capacity of human endothelial cells was studied after being plated on the surface of polyurethane-poly caprolactone (PU/PCL) scaffolds for 72 h. In this study, cells were designated into five different groups, including PU, PU/PCL (2:1), PU/PCL (1:1); PU/PCL (1:2); and PCL. Data revealed that the PU/PCL (2:1) composition had a higher modulus and breakpoint in comparison with the other groups (p < 0.05). Compared to the other groups, the PU/PCL scaffold with a molar ratio of 2:1 had lower the contact angle theta and higher tensile stress (p < 0.05). The mean size of the PU nanofibers was reduced after the addition of PCL (p 0.05). Based on our data, the culture of endothelial cells on the surface of PU/PCL (2:1) did not cause nitrosative stress and cytotoxic effects under static conditions compared to cells plated on a conventional plastic surface (p 0.05). Based on data from the static condition, we fabricated a tubular PU/PCL (2:1) construct for six-day dynamic cell culture inside loop air-lift bioreactors. Scanning electron microscopy showed the attachment of endothelial cells to the luminal surface of the PU/PCL scaffold. Cells were flattened and aligned under the culture medium flow. Immunofluorescence imaging showed the attachment of cells to the luminal surface indicated by blue nuclei on the luminal surface. These data demonstrated that the application of PU/PCL substrate could stimulate endothelial cells activity under static and dynamic conditions.
dc.description.fulltextNo
dc.description.harvestedfromManual
dc.description.indexedbyWOS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessNO
dc.description.peerreviewstatusN/A
dc.description.publisherscopeInternational
dc.description.readpublishN/A
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipTabriz University of Medical Sciences [IR.TBZMED.VCR.REC.1397.264]
dc.description.studentonlypublicationYes
dc.description.studentpublicationYes
dc.description.versionN/A
dc.identifier.WoSQuartileQ2
dc.identifier.doi10.1016/j.mvr.2020.104073
dc.identifier.eissn1095-9319
dc.identifier.embargoN/A
dc.identifier.grantnoIR.TBZMED.VCR.REC.1397.264
dc.identifier.issn0026-2862
dc.identifier.pubmed32949575
dc.identifier.scopus2-s2.0-85091225429
dc.identifier.urihttps://doi.org/10.1016/j.mvr.2020.104073
dc.identifier.urihttps://hdl.handle.net/20.500.14288/15174
dc.identifier.volume133
dc.identifier.wos000613199900008
dc.keywordsPU/PCL scaffold
dc.keywordsHuman umbilical vein endothelial cells
dc.keywordsEngineered vascular tissue
dc.keywordsAngiogenic capacity
dc.keywordsStatic and dynamic culture
dc.language.isoeng
dc.publisherElsevier
dc.relation.affiliationKoç University
dc.relation.collectionKoç University Institutional Repository
dc.relation.ispartofMicrovascular Research
dc.relation.openaccessN/A
dc.rightsN/A
dc.subjectPeripheral vascular disease
dc.titleElectrospun polyurethane/poly (ɛ-caprolactone) nanofibers promoted the attachment and growth of human endothelial cells in static and dynamic culture conditions
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.kuauthorHeidarzadeh, Morteza
relation.isOrgUnitOfPublication91bbe15d-017f-446b-b102-ce755523d939
relation.isOrgUnitOfPublication.latestForDiscovery91bbe15d-017f-446b-b102-ce755523d939
relation.isParentOrgUnitOfPublicationd437580f-9309-4ecb-864a-4af58309d287
relation.isParentOrgUnitOfPublication.latestForDiscoveryd437580f-9309-4ecb-864a-4af58309d287

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