Show simple item record

dc.contributor.authorSabino, Roberta M.
dc.contributor.authorKipper, Matt J.
dc.contributor.authorMartins, Alessandro F.
dc.contributor.authorPopat, Ketul C.
dc.date.accessioned2022-07-11T14:31:45Z
dc.date.available2022-07-11T14:31:45Z
dc.date.issued2022-06-03
dc.identifier.urihttps://hdl.handle.net/1721.1/143637
dc.description.abstractAbstract Purpose Blood compatibility of cardiovascular implants is still a major concern. Rapid endothelialization of these implant surfaces has emerged as a promising strategy to enhance hemocompatibility and prevent complications such as thrombus formation and restenosis. The successful endothelialization of implant surfaces mostly depends on the migration of endothelial cells (ECs), the differentiation of stem cells, and the inhibition of smooth muscle cell (SMC) proliferation. Our previous study demonstrated that nanostructured titania surfaces modified with polyelectrolyte multilayers based on tanfloc (a cationic tannin derivative) and glycosaminoglycans (heparin and hyaluronic acid) have improved antithrombogenic properties. Methods In this work, we used in vitro cell culture of ECs and SMCs to investigate the outcomes of these surface modifications on endothelialization. The cells were seeded on the surfaces, and their viability, adhesion, and proliferation were evaluated after 1, 3, and 5 days. Indirect immunofluorescent staining was used to determine the cellular expression of ECs through the presence of specific marker proteins after 7 and 10 days, and EC migration on the NT surfaces was also investigated. Results The surfaces modified with tanfloc and heparin showed enhanced EC adhesion, proliferation, and migration. However, SMC proliferation is not promoted by the surfaces. Therefore, these surfaces may promote endothelialization without stimulating SMC proliferation, which could improve the hemocompatibility without enhancing the risk of SMC proliferation leading to restenosis. Conclusions The surface modification here proposed is a promising candidate to be used in cardiovascular applications due to enhanced antithrombogenic and endothelialization properties.en_US
dc.publisherSpringer International Publishingen_US
dc.relation.isversionofhttps://doi.org/10.1007/s44164-022-00024-xen_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourceSpringer International Publishingen_US
dc.titleImproved in vitro endothelialization on nanostructured titania with tannin/glycosaminoglycan-based polyelectrolyte multilayersen_US
dc.typeArticleen_US
dc.identifier.citationSabino, Roberta M., Kipper, Matt J., Martins, Alessandro F. and Popat, Ketul C. 2022. "Improved in vitro endothelialization on nanostructured titania with tannin/glycosaminoglycan-based polyelectrolyte multilayers."
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Science
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2022-07-07T03:19:41Z
dc.language.rfc3066en
dc.rights.holderThe Author(s), under exclusive licence to Springer Nature Switzerland AG
dspace.embargo.termsY
dspace.date.submission2022-07-07T03:19:41Z
mit.licensePUBLISHER_POLICY
mit.metadata.statusAuthority Work and Publication Information Neededen_US


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record