Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.biomaterials.2004.07.026
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dc.titleSurface engineering of electrospun polyethylene terephthalate (PET) nanofibers towards development of a new material for blood vessel engineering
dc.contributor.authorMa, Z.
dc.contributor.authorKotaki, M.
dc.contributor.authorYong, T.
dc.contributor.authorHe, W.
dc.contributor.authorRamakrishna, S.
dc.date.accessioned2014-06-17T06:34:58Z
dc.date.available2014-06-17T06:34:58Z
dc.date.issued2005-05
dc.identifier.citationMa, Z., Kotaki, M., Yong, T., He, W., Ramakrishna, S. (2005-05). Surface engineering of electrospun polyethylene terephthalate (PET) nanofibers towards development of a new material for blood vessel engineering. Biomaterials 26 (15) : 2527-2536. ScholarBank@NUS Repository. https://doi.org/10.1016/j.biomaterials.2004.07.026
dc.identifier.issn01429612
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/61425
dc.description.abstractNon-woven polyethylene terephthalate nanofiber mats (PET NFM) were prepared by electrospinning technology and were surface modified to mimic the fibrous proteins in native extracellular matrix towards constructing a biocompatible surface for endothelial cells (ECs). The electrospun PET NFM was first treated in formaldehyde to yield hydroxyl groups on the surface, followed by the grafting polymerization of methacrylic acid (MAA) initiated by Ce(IV). Finally, the PMAA-grafted PET NFM was grafted with gelatin using water-soluble carbodiimide as coupling agent. Plane PET film was also surface modified and characterized for basic understanding of the surface modification process. The grafting of PMAA and gelatin on PET surface was confirmed by XPS spectroscopy and quantitatively analyzed by colorimetric methods. ECs were cultured on the original and gelatin-modified PET NFM and the cell morphology, proliferation and viability were studied. Three characteristic surface makers expressed by ECs were studied using immuno-florescent microscopy. The gelatin grafting method can obviously improve the spreading and proliferation of the ECs on the PET NFM, and moreover, can preserve the EC's phenotype. © 2004 Elsevier Ltd. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.biomaterials.2004.07.026
dc.sourceScopus
dc.subjectBlood vessel
dc.subjectElectrospinning
dc.subjectNanofiber
dc.subjectPET
dc.subjectSurface modification
dc.subjectTissue engineering
dc.subjectVascular graft
dc.typeArticle
dc.contributor.departmentNUS NANOSCIENCE & NANOTECH INITIATIVE
dc.contributor.departmentBIOENGINEERING
dc.contributor.departmentMECHANICAL ENGINEERING
dc.description.doi10.1016/j.biomaterials.2004.07.026
dc.description.sourcetitleBiomaterials
dc.description.volume26
dc.description.issue15
dc.description.page2527-2536
dc.description.codenBIMAD
dc.identifier.isiut000226698400035
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