Abstract
A major computational challenge for a multiscale modeling is the coupling of disparate length and timescales between molecular mechanics and macroscopic transport, spanning the spatial and temporal scales characterizing the complex processes taking place in flow-induced blood clotting. Flow and pressure effects on a cell-like platelet can be well represented by a continuum mechanics model down to the order of the micrometer level. However, the molecular effects of adhesion/aggregation bonds are on the order of nanometer. A successful multiscale model of platelet response to flow stresses in devices and the ensuing clotting responses should be able to characterize the clotting reactions and their interactions with the flow. This paper attempts to describe a few of the computational methods that were developed in recent years and became available to researchers in the field. They differ from traditional approaches that dominate the field by expanding on prevailing continuum-based approaches, or by completely departing from them, yielding an expanding toolkit that may facilitate further elucidation of the underlying mechanisms of blood flow and the cellular response to it. We offer a paradigm shift by adopting a multidisciplinary approach with fluid dynamics simulations coupled to biophysical and biochemical transport.
Original language | English (US) |
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Pages (from-to) | 1225-1235 |
Number of pages | 11 |
Journal | Annals of Biomedical Engineering |
Volume | 38 |
Issue number | 3 |
DOIs | |
State | Published - Mar 2010 |
Keywords
- Blood flow
- Clotting
- DPD
- Devices
- Multiscale modeling
- Numerical methods
- Particle dynamics
- Platelets
ASJC Scopus subject areas
- Biomedical Engineering