Mechanical and physio-biological properties of peptide-coated stent for re-endothelialization

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dc.contributor.authorI H Bae-
dc.contributor.authorM H Jeong-
dc.contributor.authorD S Park-
dc.contributor.authorKyungseob Lim-
dc.contributor.authorJ W Shim-
dc.contributor.authorM K Kim-
dc.contributor.authorJ K Park-
dc.date.accessioned2020-04-24T16:30:05Z-
dc.date.available2020-04-24T16:30:05Z-
dc.date.issued2020-
dc.identifier.issn1226-1226-
dc.identifier.uri10.1186/s40824-020-0182-xko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/19320-
dc.description.abstractBackground: The aim of this study was to characterize the mechanical and physio-biological properties of peptide-coated stent (PCS) compared to commercialized drug-eluting stents (DESs). Methods: WKYMVm (Trp-Lys-Tyr-Met-Val-D-Met), a stimulating peptide for homing endothelial colony-forming cell was specially synthesized and coated to bare metal stent (BMS) by dopamine-derived coordinated bond. Biological effects of PCS were investigated by endothelial cell proliferation assay and pre-clinical animal study. And mechanical properties were examined by various experiment. Results: The peptide was well-coated to BMS and was maintained and delivered to 21 and 7 days in vitro and in vivo, respectively. Moreover, the proliferation of endothelial cell in PCS group was increased (approximately 36.4±5.77%) in PCS group at 7 day of culture compare to BMS. Although, the radial force of PCS was moderated among study group. The flexibility of PCS was (0.49±0.082?N) was greatest among study group. PCS did not show the outstanding performance in recoil and foreshortening test (3.1±0.22% and 2.1±0.06%, respectively), which was the reasonable result under the guide line of FDA (less than 7.0%). The nominal pressure (3.0 mm in a diameter) of PCS established by compliance analysis was 9 atm. The changing of PCS diameter by expansion was similar to other DESs, which is less than 10 atm of pressure for the nominal pressure. Conclusions: These results suggest that the PCS is not inferior to commercialized DES. In addition, since the PCS was fabricated as polymer-free process, secondary coating with polymer-based immunosuppressive drugs such as -limus derivatives may possible.-
dc.publisherSpringer-Nature Pub Group-
dc.titleMechanical and physio-biological properties of peptide-coated stent for re-endothelialization-
dc.title.alternativeMechanical and physio-biological properties of peptide-coated stent for re-endothelialization-
dc.typeArticle-
dc.citation.titleBiomaterials Research-
dc.citation.number0-
dc.citation.endPage4-
dc.citation.startPage4-
dc.citation.volume24-
dc.contributor.affiliatedAuthorKyungseob Lim-
dc.contributor.alternativeName배인호-
dc.contributor.alternativeName정명호-
dc.contributor.alternativeName박대성-
dc.contributor.alternativeName임경섭-
dc.contributor.alternativeName심재원-
dc.contributor.alternativeName김문기-
dc.contributor.alternativeName박준규-
dc.identifier.bibliographicCitationBiomaterials Research, vol. 24, pp. 4-4-
dc.identifier.doi10.1186/s40824-020-0182-x-
dc.subject.keywordDrug-eluting stent-
dc.subject.keywordMechanical properties-
dc.subject.keywordPeptide delivery-
dc.subject.keywordPeptide-coated stent-
dc.subject.keywordRe-endothelialization-
dc.subject.localDrug-Eluting Stents-
dc.subject.localdrug-eluting stents-
dc.subject.localDrug-eluting stent-
dc.subject.localMechanical property-
dc.subject.localMechanical properties-
dc.subject.localmechanical properties-
dc.subject.localPeptide delivery-
dc.subject.localPeptide-coated stent-
dc.subject.localRe-endothelialization-
dc.description.journalClassY-
Appears in Collections:
Ochang Branch Institute > Division of National Bio-Infrastructure > Futuristic Animal Resource & Research Center > 1. Journal Articles
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