2013
DOI: 10.1016/j.biomaterials.2012.12.036
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Surface engineering of cardiovascular stent with endothelial cell selectivity for in vivo re-endothelialisation

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Cited by 172 publications
(144 citation statements)
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“…[3][4][5][6]39 Cell-resistant surface can be generated via hydrophilic macromolecule immobilization or hydrogel-like surface coating. [40][41][42][43][44][45] In this study, we fabricated the zwitterionic PMPC brush onto the hydrophobic IOL surface via SI-RAFT polymerization. Such zwitterionic PMPC brush modification can effectively reduce the initial adhesion of residual LECs or bacteria, and is prospective in reducing the PCO incidence in vivo.…”
mentioning
confidence: 99%
“…[3][4][5][6]39 Cell-resistant surface can be generated via hydrophilic macromolecule immobilization or hydrogel-like surface coating. [40][41][42][43][44][45] In this study, we fabricated the zwitterionic PMPC brush onto the hydrophobic IOL surface via SI-RAFT polymerization. Such zwitterionic PMPC brush modification can effectively reduce the initial adhesion of residual LECs or bacteria, and is prospective in reducing the PCO incidence in vivo.…”
mentioning
confidence: 99%
“…46,47 Those findings were concordant to previous reports, demonstrating that specificity of functionalization can be augmented by targeted bioactive sequence selection and combinatory application thereof. 15,22,25,39,48 Validation in a functional rodent aortic transplantation model under physiological flow conditions and full exposure to the native blood 7 failed to show a significant biological effect despite showing in vivo persistence of the dECM functionalization. Although a trend toward increased in vivo endothelialization of the functionalized dAoGs compared to the nonfunctionalized controls could be observed, it failed to reach statistical significance within the number of animals subjected to our model system and due to observed large biological variability of the early endothelialization process, which was also evident in the control group.…”
Section: Evaluation Of Biological Effects Of Functionalization Of Decmentioning
confidence: 99%
“…21 In particular, a biological blood-graft interface with high endothelial cell (EC) specificity, while suppressing activation of platelet attachment, immune cell recruitment, and smooth muscle cell overproliferation, is crucial in the process of in vivo endothelialization. 22 In this regard, cell-specific surface functionalization can be achieved using short synthetic peptides with defined bioactive sequences. 15,23 Interestingly, custom-made peptides, which are derived from ECM proteins but encompass only defined cell adhesive motifs, offer a series of advantages compared to the use of native proteins: they are chemically defined structures, show higher stability, and are devoid of immunogenicity.…”
Section: Introductionmentioning
confidence: 99%
“…1 Tissue-engineered vascular grafting is a promising solution that would provide patients with an alternative source of vascular replacements, thereby circumventing the shortage of autologous cells and avoiding diseased vessels. 2 To better assist cell engraftment and proliferation, surrogate scaffolds must be bioengineered to be as similar as possible to the native histo-architecture of the damaged vessel.…”
Section: Introductionmentioning
confidence: 99%