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Comparison of Endothelial Barrier Functional Recovery After Implantation of a Novel Biodegradable-Polymer Sirolimus-Eluting Stent in Comparison to Durable- and Biodegradable-Polymer Everolimus-Eluting Stents
Institution:1. 1st Department of Cardiology, Medical University of Warsaw, Warsaw, Poland;2. Jagiellonian University Medical College, Department of Bioinformatics and Telemedicine, Krakow, Poland;3. Institute of Public Health, Faculty of Health Sciences, Jagiellonian University Medical College, Krakow, Poland;4. KCRI, Krakow, Poland;5. Regional Specialist Hospital in Wroclaw, Research and Development Center, Department of Cardiology, Wroclaw, Poland;6. Department of Cardiology, Cardiology Institute, Bielanski Hospital, Warsaw, Poland
Abstract:AimsThe advantage of biodegradable-polymer drug-eluting stents (BP-DES) versus durable-polymer (DP) DES remains uncertain. We compared neointimal formation and endothelial barrier function of new BP sirolimus-eluting stents (BP-SES, BuMA Supreme®) to other contemporary BP-DES, DP-DES, and bare metal stents (BMS).Methods and resultsLight microscopic assessment in swine coronary arteries showed comparable neointimal formation between BP-SES and DP everolimus-eluting stent (DP-EES). The performance of BP-SES was compared with DP-EES (Xience Xpedition®), BP-EES (Synergy®), and BMS (Multi-Link Vision®) at 45- and 90-days in rabbit ilio-femoral arteries using Evans blue dye (EBD) followed by immunostaining for endothelial barrier proteins (p120/vascular endothelial-cadherin VE-cad]) to evaluate endothelial barrier function and scanning electron microscopy (SEM) to determine strut tissue coverage. BMS followed by BP-SES and BP-EES exhibited smaller EBD positive areas versus that of DP-EES at 45- and 90-days. p120/VE-cad immunostaining and SEM-determined strut coverage was greater at 45- and 90-days for BMS followed by all DESs. Regardless of stent type, the lack of p120/VE-cad co-localization showed greater leukocyte and platelet aggregation.ConclusionThree types of DES showed different endothelial healing pattern regardless their equivalent suppression of neointimal formation.
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