Hsu Ryan M, Szafron Jason M, Carvalho Camila C, Humphrey Jay D, Marsden Alison L
Department of Biomedical Engineering, Yale University, United States of America.
Department of Pediatrics, Stanford University, United States of America; Cardiovascular Institute, Stanford University, United States of America; Department of Biomedical Engineering, Carnegie Mellon University, United States of America.
J Biomech. 2025 Jun;186:112670. doi: 10.1016/j.jbiomech.2025.112670. Epub 2025 Apr 18.
Tissue engineered vascular grafts can offer long-term benefits in matching the geometry, properties, and function of native blood vessels. Yet, choosing appropriate design parameters for biodegradeable scaffolds such that they evolve into neovessels with favorable characteristics is challenging with iterative experimental testing alone. Herein, we present an in silico framework for constrained optimization of scaffold microstructure, mechanical behavior, and degradation kinetics. Our approach combines a biomechanical model of growth and remodeling informed by large animal experiments with numerical optimization to identify design parameters that limit clinically relevant failure modes, including stenosis and dilatation, and improve functional matching to native vessel compliance. Towards this end, constraints on geometry were introduced as a straightforward way to prevent adverse remodeling outcomes and shown to be useful in shaping desired outcomes in graft remodeling. Our simulations of long-term graft evolution suggest the need for a modest initial immune response to ensure graded load transfer from polymer to neotissue and to prevent extreme changes in diameter. Optimized designs showed less sensitivity to simulated variability in their design parameters, which could limit subject-to-subject variability. Together, these findings highlight the utility of computational modeling in identifying candidate designs for improved outcomes in tissue engineered vascular grafts - elimination of stenosis/aneurysm, better compliance matching, and consistent changes in behavior over time.
组织工程血管移植物在匹配天然血管的几何形状、特性和功能方面可带来长期益处。然而,仅通过反复的实验测试来为可生物降解支架选择合适的设计参数,使其演变成具有良好特性的新血管具有挑战性。在此,我们提出了一个用于支架微观结构、力学行为和降解动力学约束优化的计算机模拟框架。我们的方法将基于大型动物实验的生长和重塑生物力学模型与数值优化相结合,以确定限制临床相关失效模式(包括狭窄和扩张)的设计参数,并改善与天然血管顺应性的功能匹配。为此,引入几何约束作为防止不良重塑结果的直接方法,并证明其在塑造移植物重塑的理想结果方面很有用。我们对长期移植物演变的模拟表明,需要适度的初始免疫反应以确保从聚合物到新组织的分级载荷传递,并防止直径发生极端变化。优化设计对其设计参数的模拟变异性表现出较低的敏感性,这可以限制个体间的变异性。总之,这些发现突出了计算建模在确定候选设计以改善组织工程血管移植物结果方面的实用性——消除狭窄/动脉瘤、更好的顺应性匹配以及随时间行为的一致变化。