Source abstract
Abstract
Abstract Nanoparticles are commonly administered through systemic injection, which exposes them to the dynamic environment of the bloodstream. Injected nanoparticles travel within the blood and experience a wide range of flow velocities that induce varying shear rates to the blood vessels. Endothelial cells line these vessels, and have been shown to uptake nanoparticles during circulation, but it is difficult to characterize the flow‐dependence of this interaction in vivo. Here, a microfluidic system is developed to control the flow rates of nanoparticles as they interact with endothelial cells. Gold nanoparticle uptake into endothelial cells is quantified at varying flow rates, and it is found that increased flow rates lead to decreased nanoparticle uptake. Endothelial cells respond to increased flow shear with decreased ability to uptake the nanoparticles. If cells are sheared the same way, nanoparticle uptake decreases as their flow velocity increases. Modifying nanoparticle surfaces with endothelial‐cell‐binding ligands partially restores uptake to nonflow levels, suggesting that functionalizing nanoparticles to bind to endothelial cells enables nanoparticles to resist flow effects. In the future, this microfluidic system can be used to test other nanoparticle–endothelial cell interactions under flow. The results of these studies can guide the engineering of nanoparticles for in vivo medical applications.
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Affiliations
Institute of Biomaterials and Biomedical Engineering University of Toronto Toronto Ontario M5S 3G9 Canada
Terrence Donnelly Centre for Cellular and Biomolecular Research University of Toronto Toronto Ontario M5S 3E1 Canada
Department of Chemistry University of Toronto Toronto Ontario M5S 3H6 Canada
Department of Physiology University of Toronto Toronto Ontario M5S 1A8 Canada
Toronto General Research Institute University Health Network Toronto Ontario M5G 2M9 Canada
Department of Chemical Engineering and Applied Chemistry University of Toronto Toronto Ontario M5S 3E5 Canada
Department of Material Science and Engineering University of Toronto Toronto Ontario M5S 1A1 Canada
Funding
Natural Sciences and Engineering Research Council of Canada · Canadian Cancer Society