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Identifying the start of a platelet aggregate by the shear rate and the cell-depleted layer

Computer simulations were performed to study the transport of red blood cells and platelets in high shear flows, mimicking earlier published in vitro experiments in microfluidic devices with high affinity for platelet aggregate formation. The goal is to understand and predict where thrombus formatio...

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Detalles Bibliográficos
Autores principales: van Rooij, B. J. M., Závodszky, G., Azizi Tarksalooyeh, V. W., Hoekstra, A. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6833312/
https://www.ncbi.nlm.nih.gov/pubmed/31575344
http://dx.doi.org/10.1098/rsif.2019.0148
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author van Rooij, B. J. M.
Závodszky, G.
Azizi Tarksalooyeh, V. W.
Hoekstra, A. G.
author_facet van Rooij, B. J. M.
Závodszky, G.
Azizi Tarksalooyeh, V. W.
Hoekstra, A. G.
author_sort van Rooij, B. J. M.
collection PubMed
description Computer simulations were performed to study the transport of red blood cells and platelets in high shear flows, mimicking earlier published in vitro experiments in microfluidic devices with high affinity for platelet aggregate formation. The goal is to understand and predict where thrombus formation starts. Additionally, the need of cell-based modelling in these microfluidic devices is demonstrated by comparing our results with macroscopic models, wherein blood is modelled as a continuous fluid. Hemocell, a cell-based blood flow simulation framework is used to investigate the transport physics in the microfluidic devices. The simulations show an enlarged cell-depleted layer at the site where a platelet aggregate forms in the experiments. In this enlarged cell-depleted layer, the probability to find a platelet is higher than in the rest of the microfluidic device. In addition, the shear rates are sufficiently high to allow for the von Willebrand factor to elongate in this region. We hypothesize that the enlarged cell-depleted layer combined with a sufficiently large platelet flux and sufficiently high shear rates result in an haemodynamic environment that is a preferred location for initial platelet aggregation.
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spelling pubmed-68333122019-11-13 Identifying the start of a platelet aggregate by the shear rate and the cell-depleted layer van Rooij, B. J. M. Závodszky, G. Azizi Tarksalooyeh, V. W. Hoekstra, A. G. J R Soc Interface Life Sciences–Physics interface Computer simulations were performed to study the transport of red blood cells and platelets in high shear flows, mimicking earlier published in vitro experiments in microfluidic devices with high affinity for platelet aggregate formation. The goal is to understand and predict where thrombus formation starts. Additionally, the need of cell-based modelling in these microfluidic devices is demonstrated by comparing our results with macroscopic models, wherein blood is modelled as a continuous fluid. Hemocell, a cell-based blood flow simulation framework is used to investigate the transport physics in the microfluidic devices. The simulations show an enlarged cell-depleted layer at the site where a platelet aggregate forms in the experiments. In this enlarged cell-depleted layer, the probability to find a platelet is higher than in the rest of the microfluidic device. In addition, the shear rates are sufficiently high to allow for the von Willebrand factor to elongate in this region. We hypothesize that the enlarged cell-depleted layer combined with a sufficiently large platelet flux and sufficiently high shear rates result in an haemodynamic environment that is a preferred location for initial platelet aggregation. The Royal Society 2019-10 2019-10-02 /pmc/articles/PMC6833312/ /pubmed/31575344 http://dx.doi.org/10.1098/rsif.2019.0148 Text en © 2019 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Life Sciences–Physics interface
van Rooij, B. J. M.
Závodszky, G.
Azizi Tarksalooyeh, V. W.
Hoekstra, A. G.
Identifying the start of a platelet aggregate by the shear rate and the cell-depleted layer
title Identifying the start of a platelet aggregate by the shear rate and the cell-depleted layer
title_full Identifying the start of a platelet aggregate by the shear rate and the cell-depleted layer
title_fullStr Identifying the start of a platelet aggregate by the shear rate and the cell-depleted layer
title_full_unstemmed Identifying the start of a platelet aggregate by the shear rate and the cell-depleted layer
title_short Identifying the start of a platelet aggregate by the shear rate and the cell-depleted layer
title_sort identifying the start of a platelet aggregate by the shear rate and the cell-depleted layer
topic Life Sciences–Physics interface
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6833312/
https://www.ncbi.nlm.nih.gov/pubmed/31575344
http://dx.doi.org/10.1098/rsif.2019.0148
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