2011
DOI: 10.1016/j.biomaterials.2011.04.067
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Platelet inhibition and endothelial cell adhesion on elastin-like polypeptide surface modified materials

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Cited by 61 publications
(49 citation statements)
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“…75 In addition to the favorable cell morphology and increased expression of endothelial nitric oxide synthase, platelet adhesion and activation were reduced compared to control PU surfaces. ECs and EPCs were shown to have adhered well to L-selectin and VE-cadherin chimera proteins that were coated on titanium surfaces.…”
mentioning
confidence: 97%
“…75 In addition to the favorable cell morphology and increased expression of endothelial nitric oxide synthase, platelet adhesion and activation were reduced compared to control PU surfaces. ECs and EPCs were shown to have adhered well to L-selectin and VE-cadherin chimera proteins that were coated on titanium surfaces.…”
mentioning
confidence: 97%
“…[19] However, such modifications have been realized mostly through lengthy processes involving chemical reactions. For example, modification with elastin-like peptide could improve the biocompatibility of PU, [20] but involved a chemical cross-linking step that took more than two days.…”
Section: Introductionmentioning
confidence: 99%
“…The need to unravel these clinical concerns, besides the unresorbability of such metallic stents, which remain permanently in situ , has fostered numerous research groups to explore new biodegradable and bioactive polymers being able to be gradually resorbed by the body, reducing thrombosis and neointimal hyperplasia [2]. Some novel stent coating strategies have already been proposed [2, 3, 68]; however, these approaches are still at the preliminary stage and their long-term behavior is still unknown [3].…”
Section: Introductionmentioning
confidence: 99%
“…Some novel stent coating strategies have already been proposed [2, 3, 68]; however, these approaches are still at the preliminary stage and their long-term behavior is still unknown [3]. …”
Section: Introductionmentioning
confidence: 99%
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