Nanoparticle diffusion in sheared cellular blood flow
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Publication:5378185
DOI10.1017/JFM.2019.320zbMATH Open1419.76732arXiv1904.06452OpenAlexW3098653969WikidataQ127812744 ScholiaQ127812744MaRDI QIDQ5378185FDOQ5378185
Authors: Jonathan R. Clausen, Rekha R. Rao, Cyrus K. Aidun, Zi-Xiang Liu 
Publication date: 12 June 2019
Published in: Journal of Fluid Mechanics (Search for Journal in Brave)
Abstract: Using a multiscale blood flow solver, the complete diffusion tensor of nanoparticle (NP) in sheared cellular blood flow is calculated over a wide range of shear rate and haematocrit. In the short-time regime, NPs exhibit anomalous dispersive behaviors under high shear and high haematocrit due to the transient elongation and alignment of the red blood cells (RBCs). In the long-time regime, the NP diffusion tensor features high anisotropy. Particularly, there exists a critical shear rate (100 ) around which the shear-rate dependence of the diffusivity tensor changes from linear to nonlinear scale. Above the critical shear rate, the cross-stream diffusivity terms vary sublinearly with shear rate, while the longitudinal term varies superlinearly. The dependence on haematocrit is linear in general except at high shear rates, where a sublinear scale is found for the vorticity term and a quadratic scale for the longitudinal term. Through analysis of the suspension microstructure and numerical experiments, the nonlinear hemorheological dependence of the NP diffusion tensor is attributed to the streamwise elongation and cross-stream contraction of RBCs under high shear, quantified by a Capillary number. The RBC size is shown to be the characteristic length scale affecting the RBC-enhanced shear-induced diffusion (RESID), while the NP size at submicron exhibits negligible influence on the RESID. Based on the observed scaling behaviors, empirical correlations are proposed to bridge the NP diffusion tensor to specific shear rate and haematocrit. The characterized NP diffusion tensor provides a constitutive relation that can lead to more effective continuum models to tackle large-scale NP biotransport applications.
Full work available at URL: https://arxiv.org/abs/1904.06452
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