依维莫司
冠状动脉疾病
再狭窄
体内
医学
支架
药品
生物信息学
临床试验
药物开发
计算机辅助设计
生物医学工程
气球
药理学
心脏病学
内科学
生物
生物技术
基因
生物化学
作者
Georgia S. Karanasiou,Vasileios S. Loukas,Panagiotis K. Siogkas,Antonis I. Sakellarios,Nikolaos S. Tachos,Christos Katsouras,Anargyros N. Moulas,Konstantinos Ioakimidis,Arsenios Chatzimichailidis,Arsen Semertzioglou,Athanassios Vratimos,Ioannis Spyridonidis,Lambros K. Michalis,Dimitrios I. Fotiadis
标识
DOI:10.1109/embc40787.2023.10340583
摘要
Coronary artery disease (CAD) is a chronic disease associated with high mortality and morbidity. Although treatment with drug-eluting stents is the most frequent interventional approach for coronary artery disease, drug-coated balloons (DCBs) constitute an innovative alternative, especially in the presence of certain anatomical conditions in the local coronary vasculature. DCBs allow the fast and homogenous transfer of drugs into the arterial wall, during the balloon inflation. Their use has been established for treating in-stent restenosis caused by stent implantation, while recent clinical trials have shown a satisfactory efficacy in de novo small-vessel disease. Several factors affect DCBs performance including the catheter design, the drug dose and formulation. Cleverballoon focuses on the design and development of an innovative DCB with everolimus. For the realization of the development of this new DCB, an integrated approach, including in- vivo, in-vitro studies and in-silico modelling towards the DCB optimization, is presented.Clinical Relevance—The proposed study introduces the integration of in- vivo, in-vitro and in silico approaches in the design and development process of a new DCB, following the principles of 3R’s for the replacement, reduction, and refinement of animal and clinical studies.
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