Abstract
Introduction: : Vascular inflammation, as observed in vasculitis, disrupts normal hemodynamics and can lead to life-threatening outcomes. Conventional laboratory models often fall short in reproducing the complex biomechanical forces acting within inflamed arteries. This research introduces an advanced bioreactor-based simulation aimed at more accurately replicating pathological blood vessel conditions to better understand disease progression and therapeutic targets [1, 2].
Materials and
Methods: : Using Ansys (CFX) software, a cylindrical artery model was created to simulate inflamed vascular regions. The model integrated physiologically relevant flow rates and inflammatory parameters to mirror vasculitis-specific conditions. By incorporating recent data on endothelial responses to mechanical forces, the simulation provided valuable insights into shear stress impact during inflammatory episodes [3, 4, 5].
Results, Conclusions, and Discussions:: • The outcomes of this research may improve diagnostics and treatment strategies in vascular pathology.
A. Cross-sectional visualization of the carotid artery shows narrowing due to inflammatory thickening, reducing blood flow.
B. Streamline analysis reveals maximum flow velocity at the narrowest central point in a blood vessel.
The simulation indicates an increase in shear stress, peaking at just above 0.25 psi in the occluded region—consistent with stress-induced endothelial dysfunction in vasculitis.
Our bioreactor system successfully models vascular dynamics and enables measurement of velocity shifts and shear force distribution.
• Continued optimization of the bioreactor is underway.
• These models are essential tools for studying disease mechanisms in vascular inflammation.
Materials and
Methods: : Using Ansys (CFX) software, a cylindrical artery model was created to simulate inflamed vascular regions. The model integrated physiologically relevant flow rates and inflammatory parameters to mirror vasculitis-specific conditions. By incorporating recent data on endothelial responses to mechanical forces, the simulation provided valuable insights into shear stress impact during inflammatory episodes [3, 4, 5].
Results, Conclusions, and Discussions:: • The outcomes of this research may improve diagnostics and treatment strategies in vascular pathology.
A. Cross-sectional visualization of the carotid artery shows narrowing due to inflammatory thickening, reducing blood flow.
B. Streamline analysis reveals maximum flow velocity at the narrowest central point in a blood vessel.
The simulation indicates an increase in shear stress, peaking at just above 0.25 psi in the occluded region—consistent with stress-induced endothelial dysfunction in vasculitis.
Our bioreactor system successfully models vascular dynamics and enables measurement of velocity shifts and shear force distribution.
• Continued optimization of the bioreactor is underway.
• These models are essential tools for studying disease mechanisms in vascular inflammation.
| Original language | American English |
|---|---|
| State | Published - Oct 8 2025 |
| Event | Biomedical Engineering Society (BMES) Annual Meeting - San Diego, United States Duration: Oct 8 2025 → Oct 12 2025 |
Conference
| Conference | Biomedical Engineering Society (BMES) Annual Meeting |
|---|---|
| Country/Territory | United States |
| City | San Diego |
| Period | 10/8/25 → 10/12/25 |
Funding
Florida Heart Research Foundation This work has been partially supported by NSU President’s Research Grant 334949
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Dive into the research topics of 'Bioengineered Vascular Reactor for Vasculitis Research Applications'. Together they form a unique fingerprint.Prizes
-
2025 Early Career Stop Heart Disease Researcher of the Year Award
Salinas, M. (Recipient), Aug 2 2025
Prize: Prize (including medals and awards)
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