Open Access

ARTICLE

Computational Fluid Dynamics Simulations at Micro-Scale Stenosis for Microfluidic Thrombosis Model Characterization

Yunduo Charles Zhao^1,2,#, Parham Vatankhah^1,#, Tiffany Goh^1,2,3, Jiaqiu Wang⁴, Xuanyi Valeria Chen¹, Moein Navvab Kashani^5,6, Keke Zheng⁷, Zhiyong Li⁴, Lining Arnold Ju^1,2,3,*

1 School of Biomedical Engineering, Faculty of Engineering, The University of Sydney, Darlington, NSW 2008, Australia
2 Charles Perkins Centre, The University of Sydney, Camperdown, NSW 2006, Australia
3 Heart Research Institute, Newtown, NSW 2042, Australia
4 School of Mechanical, Medical and Process Engineering, Queensland University of Technology, Brisbane, 4000, Australia
5 Future Industries Institute, University of South Australia, Mawson Lakes, SA 5095, Australia
6 South Australian Node, Australian National Fabrication Facility, University of South Australia, Mawson Lakes, SA 5095, Australia
7 School of Aerospace, Mechanical and Mechatronic Engineering, Faculty of Engineering, The University of Sydney, Darlington, NSW 2008, Australia

* Corresponding Author: Lining Arnold Ju. Email:
# These authors contributed equally

Molecular & Cellular Biomechanics 2021, 18(1), 1-10. https://doi.org/10.32604/mcb.2021.012598

Received 12 July 2020; Accepted 27 October 2020; Issue published 26 January 2021

Abstract

Platelet aggregation plays a central role in pathological thrombosis, preventing healthy physiological blood flow within the circulatory system. For decades, it was believed that platelet aggregation was primarily driven by soluble agonists such as thrombin, adenosine diphosphate and thromboxane A2. However, recent experimental findings have unveiled an intriguing but complementary biomechanical mechanism—the shear rate gradients generated from flow disturbance occurring at sites of blood vessel narrowing, otherwise known as stenosis, may rapidly trigger platelet recruitment and subsequent aggregation. In our Nature Materials 2019 paper [1], we employed microfluidic devices which incorporated micro-scale stenoses to elucidate the molecular insights underlying the prothrombotic effect of blood flow disturbance. Nevertheless, the rheological mechanisms associated with this stenotic microfluidic device are poorly characterized. To this end, we developed a computational fluid dynamics (CFD) simulation approach to systematically analyze the hemodynamic influence of bulk flow mechanics and flow medium. Grid sensitivity studies were performed to ensure accurate and reliable results. Interestingly, the peak shear rate was significantly reduced with the device thickness, suggesting that fabrication of microfluidic devices should retain thicknesses greater than 50 µm to avoid unexpected hemodynamic aberration, despite thicker devices raising the cost of materials and processing time of photolithography. Overall, as many groups in the field have designed microfluidic devices to recapitulate the effect of shear rate gradients and investigate platelet aggregation, our numerical simulation study serves as a guideline for rigorous design and fabrication of microfluidic thrombosis models.

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