The FLOW Framework: a panvascular-on-a-chip platform to model systemic disease and guide panvascular interventional device suitcordance
收藏中国科学数据2026-03-31 更新2026-04-25 收录
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https://www.sciengine.com/AA/doi/10.1016/j.scib.2025.12.051
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Panvascular diseases, encompassing systemic vascular disorders driven by atherosclerosis, represent the leading cause of global mortality, posing significant challenges in modeling due to their prolonged, multi-organ nature and complex device–vessel interactions. Current in vitro and in vivo models fall short in recapitulating high-fidelity hemodynamics, long-term monitoring, multi-vascular bed heterogeneity, and three-dimensional (3D) dynamic interactions essential for advancing interventional device development. To address these gaps, we introduce the FLOW framework—a novel panvascular-on-a-chip platform leveraging organ-on-a-chip (OoC) technology. This framework integrates four core modules: Fidelity hemodynamic reconstruction (F) for simulation of physiological/pathological blood flow; Longitudinal physiological surveillance (L) for real-time tracking of chronic processes like endothelialization and inflammation; Omni-vascular bed modeling (O) for simulating coexisting lesions across diverse vascular beds and inter-organ crosstalk; and Whole-space 3D interactive work-flow (W) for evaluating device deployment and biomechanical interactions in 3D vascular microenvironments.Guided by the concept of “suitcordance” (defined here as short-term suitability and long-term concordance between devices and vascular tissues), the FLOW platform enables high-fidelity modeling of panvascular pathologies, such as atherosclerosis-induced downstream diseases (e.g., myocardial infarction, stroke, diabetic foot) and thrombosis, while facilitating optimization of interventional devices like stents, valves, and thrombectomy catheters to achieve post-intervention rebalancing of biomechanical, cellular, and physicochemical–immune ecologies. We review macro-construction foundations, including microfluidic technologies, real-time sensing, cell engineering, and hydrogel-based structural designs, and discuss applications in mechanistic studies and device translation. Future prospects include multi-organ integration, AI-driven analytics, long-term culture, and gene editing for personalized medicine, positioning panvascular-on-a-chip as a paradigm-shifting tool to bridge clinical outcomes, enhancing device–vessel harmony and combating humanity’s “number one killer”.
创建时间:
2026-03-31



