Date of Award
5-2024
Document Type
Thesis
Degree Name
Master of Science (MS)
Department
Biomedical Engineering and Sciences
First Advisor
Christopher A. Bashur
Second Advisor
Venkat Keshav Chivukula
Third Advisor
James R Brenner
Fourth Advisor
Linxia Gu
Abstract
Large vessel occlusion during acute ischemic strokes requires mechanical thrombectomy (MT) procedures using stent retrievers (SR). However, complete clot removal typically takes several attempts, which can amplify endothelial cell injury (EI). This project aims to characterize the extent of EI during MT using an in vitro vascular platform and a finite-element model (FEM). Impact of SR diameter and characterization of SR mechanical forces are assessed and correlated with human umbilical vein endothelial cell (HUVEC) response. HUVECs were seeded on fibronectin (4 µg/cm2) coated true-scale PDMS arterial phantoms with 2.5 mm luminal diameter. Test groups (n=6) either underwent a simulated MT using two different-sized clinical SRs (Trevo® XP PROVUE 3×20mm and 6×25 mm) or no MT (control). Phantoms were stained and imaged with fluorescence and SEM imaging to evaluate cell viability and function. FEM and mechanical testing found radial forces and shear stresses that were comparable, but exceeded stresses found in native blood flow. Fluorescent images showed significant decreases in cell confluency and area coverage after MT. The large and small SRs applied 220±12.3 and 16.7±5.78 mN forces, respectively, on a testing system with a 2.5 mm gap. SR shear forces were significantly higher for the large (87.8 mN) compared to the small (13.7 mN) SRs. The data showed significant increase in EI caused by MT. Similar EI between SR size was hypothesized as both SRs’ forces exceeding HUVECs survival threshold. Better understanding of the risks of EI after MT has the potential to improve the long-term success of MT surgeries.
Recommended Citation
Lorton, Zackary, "Investigating Endothelial Damage during Ischemic Stroke Treatment using In Vitro and Computational Models" (2024). Theses and Dissertations. 1444.
https://repository.fit.edu/etd/1444
Included in
Biological Engineering Commons, Biomechanics and Biotransport Commons, Molecular, Cellular, and Tissue Engineering Commons