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dc.contributor.authorJurney, Patrick
dc.contributor.authorAgarwal, Rachit
dc.contributor.authorRoy, Krishnendu
dc.contributor.authorSreenivasan, S. V.
dc.contributor.authorShi, Li
dc.date.accessioned2017-05-09T01:22:11Z
dc.date.available2017-05-09T01:22:11Z
dc.date.issued2015
dc.identifier.issn1949-2944
dc.identifier.othernano_006_01_011007.pdf
dc.identifier.urihttp://yetl.yabesh.ir/yetl/handle/yetl/159255
dc.description.abstractAn in vitro cell culture system is developed for studying the uptake characteristics of nanoparticles (NPs) by endothelial cells under shear stress. Results show that the smaller polystyrene nanospheres are uptaken more than larger nanospheres for sizes ranging from 100 nm to 500 nm for 12, 24, and 48 hrs delivery times. While the result is similar to that found in static cultures, the observed trend is different from NP delivery behaviors to a simple glass surface in a flow, where no clear size dependence was observed because of repulsive electrostatic force on marginating NPs. The trend is also opposite to the behavior found in another study of the adhesion of labeled particles onto endothelial cells in whole blood flow. The comparison shows that the reduced zeta potential of NPs in a serumcontaining cell medium and particle removal by cells results in reduced repulsive electrostatic force on marginating NPs. Consequently, the uptake behaviors are dominated by Brownian diffusion and cell membrane deformation process, which favor the uptake of NPs with reduced sizes.
dc.publisherThe American Society of Mechanical Engineers (ASME)
dc.titleSize Dependent Nanoparticle Uptake by Endothelial Cells in a Capillary Flow System
dc.typeJournal Paper
dc.journal.volume6
dc.journal.issue1
dc.journal.titleJournal of Nanotechnology in Engineering and Medicine
dc.identifier.doi10.1115/1.4031856
dc.journal.fristpage11007
dc.journal.lastpage11007
dc.identifier.eissn1949-2952
dc.treeJournal of Nanotechnology in Engineering and Medicine:;2015:;volume( 006 ):;issue: 001
dc.contenttypeFulltext


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