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Megan A. Jamiolkowski

Publications and source records attributed to Megan A. Jamiolkowski.

3 recordsLinked to original sources

Synergistic effect of shear and ADP on platelet growth on ZTA and Ti6Al4V surfaces

Continuous-flow ventricular assist devices (VADs) have been an increasingly common, life-saving therapy for advanced heart-failure patients, but elevate the risk of thrombosis due to a combination of non-physiological hemodynamics and synthetic biomaterials. Limited work has been done to address platelet adhesion and aggregation on artificial surfaces under flow with sub-threshold concentrations of weak agonists. We perfused a blood analog containing hemoglobin-depleted red blood cells and fluorescently labeled platelets across a titanium alloy (Ti6Al4V) and zirconia-toughened alumina (ZTA) surface at shear rates of 400 and 1000 s-1. Upstream of the specimen, sub-threshold concentrations of ADP were uniformly introduced at concentrations of 0, 5, and 10 nM. Time-lapse videos of depositing platelets were recorded, and the percentage of the surface covered was quantified. Surface coverage percentages at 400 s-1and 1000 s-1were compared for each concentration of ADP and material surface combination. We observed a threshold concentration of ADP that expedites platelet deposition that is dependent on both shear and material surface chemistry. Additionally, we observed embolization when thrombus areas exceeded 300μm2, which was dependent on the combination of shear, ADP concentration, and material surface. This work is the first to simultaneously examine the three key contributing factors leading to thrombotic events. Our findings assist in considering alternative material choices constituting VADs and the need to address material reactivity in assessing antiplatelet agent tests.

q-bio.TO

Influence of shear rate and surface chemistry on thrombus formation in micro-crevice

Thromboembolic complications remain a central issue in management of patients on mechanical circulatory support. Despite the best practices employed in design and manufacturing of modern ventricular assist devices, complexity and modular nature of these systems often introduces internal steps and crevices in the flow path which can serve as nidus for thrombus formation. Thrombotic potential is influenced by multiple factors including the characteristics of the flow and surface chemistry of the biomaterial. This study explored these elements in the setting of blood flow over a micro-crevice using a multi-constituent numerical model of thrombosis. The simulations reproduced the platelet deposition patterns observed experimentally and elucidated the role of flow, shear rate, and surface chemistry in shaping the deposition. The results offer insights for design and operation of blood-contacting devices.

q-bio.TO

Multi-Constituent Simulation of Thrombus Deposition

In this paper, we present a spatio-temporal mathematical model for simulating the formation and growth of a thrombus. Blood is treated as a multi-constituent mixture comprised of a linear fluid phase and a thrombus (solid) phase. The transport and reactions of 10 chemical and biological species are incorporated using a system of coupled convection-reaction-diffusion (CRD) equations to represent three processes in thrombus formation: initiation, propagation and stabilization. Computational fluid dynamic (CFD) simulations using the libraries of OpenFOAM were performed for two illustrative benchmark problems: in vivo thrombus growth in an injured blood vessel and in vitro thrombus deposition in micro-channels (1.5mm x 1.6mm x 0.1mm) with small crevices (125μm x 75μm and 125μm x 137μm). For both problems, the simulated thrombus deposition agreed very well with experimental observations, both spatially and temporally. Based on the success with these two benchmark problems, which have very different flow conditions and biological environments, we believe that the current model will provide useful insight into the genesis of thrombosis in blood-wetted devices, and provide a tool for the design of less thrombogenic devices.

physics.bio-ph