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Cell-scale hemolysis evaluation of intervenient ventricular assist device based on dissipative particle dynamics

Most of the existing hemolysis mechanism studies are carried out on the macro flow scale. They assume that the erythrocyte membranes with different loads will suffer the same damage, which obviously has limitations. Thus, exploring the hemolysis mechanism through the macroscopic flow field informati...

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Autores principales: Xu, Zhike, Chen, Chenghan, Hao, Pengfei, He, Feng, Zhang, Xiwen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354560/
https://www.ncbi.nlm.nih.gov/pubmed/37476687
http://dx.doi.org/10.3389/fphys.2023.1181423
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author Xu, Zhike
Chen, Chenghan
Hao, Pengfei
He, Feng
Zhang, Xiwen
author_facet Xu, Zhike
Chen, Chenghan
Hao, Pengfei
He, Feng
Zhang, Xiwen
author_sort Xu, Zhike
collection PubMed
description Most of the existing hemolysis mechanism studies are carried out on the macro flow scale. They assume that the erythrocyte membranes with different loads will suffer the same damage, which obviously has limitations. Thus, exploring the hemolysis mechanism through the macroscopic flow field information is a tough challenge. In order to further understand the non-physiological shear hemolysis phenomenon at the cell scale, this study used the coarse-grained erythrocytes damage model at the mesoscopic scale based on the transport dissipative particle dynamics (tDPD) method. Combined with computational fluid dynamics the hemolysis of scalarized shear stress ( [Formula: see text] ) in the clearance of “Impella 5.0” was evaluated under the Lagrange perspective and Euler perspective. The results from the Lagrange perspective showed that the change rate of scaled shear stress ( [Formula: see text] ) was the most critical factor in damaging RBCs in the rotor region of “Impella 5.0”and other transvalvular micro-axial blood pumps. Then, we propose a dimensionless number [Formula: see text] with time integration based on [Formula: see text] to evaluate hemolysis. The Dissipative particle dynamics simulation results are consistent with the [Formula: see text] evaluation results, so [Formula: see text] may be an important factor in the hemolysis of VADs. Finally, we tested the hemolysis of 30% hematocrit whole blood in the “Impella 5.0” shroud clearance from the Euler perspective. Relevant results indicate that because of the wall effect, the RBCs near the impeller side are more prone to damage, and most of the cytoplasm is also gathered at the rotor side.
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spelling pubmed-103545602023-07-20 Cell-scale hemolysis evaluation of intervenient ventricular assist device based on dissipative particle dynamics Xu, Zhike Chen, Chenghan Hao, Pengfei He, Feng Zhang, Xiwen Front Physiol Physiology Most of the existing hemolysis mechanism studies are carried out on the macro flow scale. They assume that the erythrocyte membranes with different loads will suffer the same damage, which obviously has limitations. Thus, exploring the hemolysis mechanism through the macroscopic flow field information is a tough challenge. In order to further understand the non-physiological shear hemolysis phenomenon at the cell scale, this study used the coarse-grained erythrocytes damage model at the mesoscopic scale based on the transport dissipative particle dynamics (tDPD) method. Combined with computational fluid dynamics the hemolysis of scalarized shear stress ( [Formula: see text] ) in the clearance of “Impella 5.0” was evaluated under the Lagrange perspective and Euler perspective. The results from the Lagrange perspective showed that the change rate of scaled shear stress ( [Formula: see text] ) was the most critical factor in damaging RBCs in the rotor region of “Impella 5.0”and other transvalvular micro-axial blood pumps. Then, we propose a dimensionless number [Formula: see text] with time integration based on [Formula: see text] to evaluate hemolysis. The Dissipative particle dynamics simulation results are consistent with the [Formula: see text] evaluation results, so [Formula: see text] may be an important factor in the hemolysis of VADs. Finally, we tested the hemolysis of 30% hematocrit whole blood in the “Impella 5.0” shroud clearance from the Euler perspective. Relevant results indicate that because of the wall effect, the RBCs near the impeller side are more prone to damage, and most of the cytoplasm is also gathered at the rotor side. Frontiers Media S.A. 2023-07-05 /pmc/articles/PMC10354560/ /pubmed/37476687 http://dx.doi.org/10.3389/fphys.2023.1181423 Text en Copyright © 2023 Xu, Chen, Hao, He and Zhang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Xu, Zhike
Chen, Chenghan
Hao, Pengfei
He, Feng
Zhang, Xiwen
Cell-scale hemolysis evaluation of intervenient ventricular assist device based on dissipative particle dynamics
title Cell-scale hemolysis evaluation of intervenient ventricular assist device based on dissipative particle dynamics
title_full Cell-scale hemolysis evaluation of intervenient ventricular assist device based on dissipative particle dynamics
title_fullStr Cell-scale hemolysis evaluation of intervenient ventricular assist device based on dissipative particle dynamics
title_full_unstemmed Cell-scale hemolysis evaluation of intervenient ventricular assist device based on dissipative particle dynamics
title_short Cell-scale hemolysis evaluation of intervenient ventricular assist device based on dissipative particle dynamics
title_sort cell-scale hemolysis evaluation of intervenient ventricular assist device based on dissipative particle dynamics
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10354560/
https://www.ncbi.nlm.nih.gov/pubmed/37476687
http://dx.doi.org/10.3389/fphys.2023.1181423
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