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      Hemodynamic analysis for stenosis microfluidic model of thrombosis with refined computational fluid dynamics simulation

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          Abstract

          Disturbed blood flow has been increasingly recognized for its critical role in platelet aggregation and thrombosis. Microfluidics with hump shaped contractions have been developed to mimic microvascular stenosis and recapitulate the prothrombotic effect of flow disturbance. However the physical determinants of microfluidic hemodynamics are not completely defined. Here, we report a refined computational fluid dynamics (CFD) simulation approach to map the shear rate ( γ) and wall shear stress ( τ) distribution in the stenotic region at high accuracy. Using ultra-fine meshing with sensitivity verification, our CFD results show that the stenosis level ( S) is dominant over the bulk shear rate ( γ 0) and contraction angle ( α) in determining γ and τ distribution at stenosis. In contrast, α plays a significant role in governing the shear rate gradient ( γ ) distribution while it exhibits subtle effects on the peak γ. To investigate the viscosity effect, we employ a Generalized Power-Law model to simulate blood flow as a non-Newtonian fluid, showing negligible difference in the γ distribution when compared with Newtonian simulation with water medium. Together, our refined CFD method represents a comprehensive approach to examine microfluidic hemodynamics in three dimensions and guide microfabrication designs. Combining this with hematological experiments promises to advance understandings of the rheological effect in thrombosis and platelet mechanobiology.

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          Most cited references62

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          Heart Disease and Stroke Statistics—2020 Update

          Circulation
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            Arterial thrombosis--insidious, unpredictable and deadly.

            The formation of blood clots--thrombosis--at sites of atherosclerotic plaque rupture is a major clinical problem despite ongoing improvements in antithrombotic therapy. Progress in identifying the pathogenic mechanisms regulating arterial thrombosis has led to the development of newer therapeutics, and there is general anticipation that these treatments will have greater efficacy and improved safety. However, major advances in this field require the identification of specific risk factors for arterial thrombosis in affected individuals and a rethink of the 'one size fits all' approach to antithrombotic therapy.
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              Platelets and shear stress.

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                Author and article information

                Contributors
                arnold.ju@sydney.edu.au
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                25 March 2021
                25 March 2021
                2021
                : 11
                : 6875
                Affiliations
                [1 ]GRID grid.1013.3, ISNI 0000 0004 1936 834X, School of Biomedical Engineering, Faculty of Engineering, , The University of Sydney, ; Darlington, NSW 2008 Australia
                [2 ]GRID grid.1013.3, ISNI 0000 0004 1936 834X, Charles Perkins Centre, , The University of Sydney, ; Camperdown, NSW 2006 Australia
                [3 ]GRID grid.1076.0, ISNI 0000 0004 0626 1885, Heart Research Institute, ; Newtown, NSW 2042 Australia
                [4 ]GRID grid.1013.3, ISNI 0000 0004 1936 834X, School of Chemical and Biomolecular Engineering, Faculty of Engineering, , The University of Sydney, ; Darlington, NSW 2008 Australia
                [5 ]GRID grid.1024.7, ISNI 0000000089150953, School of Mechanical, Medical and Process Engineering, , Queensland University of Technology, ; Brisbane, 4000 Australia
                Article
                86310
                10.1038/s41598-021-86310-2
                7994556
                33767279
                41eb7922-a7af-43e3-8500-cb5cf5b0e354
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 26 July 2020
                : 11 March 2021
                Funding
                Funded by: USYD Core Research Facilities User Access Scheme
                Award ID: RPF – L.A.J., Y.C.Z., Y.Z.
                Award ID: RPF – L.A.J., Y.C.Z., Y.Z.
                Award ID: RPF – L.A.J., Y.C.Z., Y.Z.
                Award Recipient :
                Funded by: Australian Research Council Discovery Project
                Award ID: DP200101970
                Award Recipient :
                Funded by: NSW Cardiovascular Capacity Building Program
                Award ID: Early-Mid Career Researcher Grant – L.A.J
                Award Recipient :
                Funded by: Sydney Research Accelerator prize
                Award ID: SOAR – L.A.J.
                Award Recipient :
                Funded by: The University of Sydney Faculty of Engineering Startup Fund and Major Equipment Scheme
                Award ID: L.A.J.
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100009860, Ramaciotti Foundations;
                Award ID: 2020HIG76 – L.A.J.
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100000925, National Health and Medical Research Council;
                Award ID: APP2003904 – L.A.J.
                Award Recipient :
                Categories
                Article
                Custom metadata
                © The Author(s) 2021

                Uncategorized
                biomedical engineering,lab-on-a-chip
                Uncategorized
                biomedical engineering, lab-on-a-chip

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