TY - JOUR
T1 - Enhanced endothelialization of a new stent polymer through surface enhancement and incorporation of growth factor-delivering microparticles
AU - Xu, Hao
AU - Nguyen, Kytai T.
AU - Brilakis, Emmanouil S.
AU - Yang, Jian
AU - Fuh, Eric
AU - Banerjee, Subhash
N1 - Funding Information:
Acknowledgments We acknowledge the support from the NIH (HL082644: K.N.) and UTA Research Area Enhancement grant.
PY - 2012/8
Y1 - 2012/8
N2 - In this study, we sought to develop strategies for improved endothelialization of a new polymer coating for vascular stents. Surface enhancement of the new poly-1,8- octanediol-co-citric acid (POC) polymer was achieved through conjugation of anti-CD34 antibody and incorporation of vascular endothelial growth factor and basic fibroblast growth factor-containing poly-lactic-co-glycolic acid microparticles to improve capture and proliferation of endothelial progenitor cells (EPC) and compared to untreated POC and poly-L-lactic acid (PLLA) polymer. Our results indicate that compared to PLLA, POC coating was more hemocompatible, with less platelet activation (p=0.01), thrombogenicity (p<0.05 for 20 and 30 min clot formation), and inflammatory response (IL-1β release, p=0.0009; TNF-α release, p=0.004). EPC adhesion and proliferation on POC were significantly improved with surface enhancement and microparticle incorporation compared to untreated POC (p=0.006) and PLLA (p=0.003). These results suggest a new strategy for enhancing endothelialization of polymeric coatings of vascular prostheses.
AB - In this study, we sought to develop strategies for improved endothelialization of a new polymer coating for vascular stents. Surface enhancement of the new poly-1,8- octanediol-co-citric acid (POC) polymer was achieved through conjugation of anti-CD34 antibody and incorporation of vascular endothelial growth factor and basic fibroblast growth factor-containing poly-lactic-co-glycolic acid microparticles to improve capture and proliferation of endothelial progenitor cells (EPC) and compared to untreated POC and poly-L-lactic acid (PLLA) polymer. Our results indicate that compared to PLLA, POC coating was more hemocompatible, with less platelet activation (p=0.01), thrombogenicity (p<0.05 for 20 and 30 min clot formation), and inflammatory response (IL-1β release, p=0.0009; TNF-α release, p=0.004). EPC adhesion and proliferation on POC were significantly improved with surface enhancement and microparticle incorporation compared to untreated POC (p=0.006) and PLLA (p=0.003). These results suggest a new strategy for enhancing endothelialization of polymeric coatings of vascular prostheses.
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U2 - 10.1007/s12265-012-9381-8
DO - 10.1007/s12265-012-9381-8
M3 - Article
C2 - 22639344
AN - SCOPUS:84866133421
SN - 1937-5387
VL - 5
SP - 519
EP - 527
JO - Journal of cardiovascular translational research
JF - Journal of cardiovascular translational research
IS - 4
ER -