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Title:
Surface Functionality of Nanoparticles Determines Cellular Uptake Mechanisms in Mammalian Cells
Date:
1/2013
Link to Journal Abstract
Abstract:
Nanoparticles (NPs) are versatile scaffolds for numerous biomedical applications including drug delivery and bioimaging. The surface functionality of NPs essentially dictates intracellular NP uptake and controls their therapeutic action. Using several pharmacological inhibitors, it is demonstrated that the cellular uptake mechanisms of cationic gold NPs in both cancer (HeLa) and normal cells (MCF10A) strongly depend on the NP surface monolayer, and mostly involve caveolae and dynamin-dependent pathways as well as specific cell surface receptors (scavenger receptors). Moreover, these NPs show different uptake mechanisms in cancer and normal cells, providing an opportunity to develop NPs with improved selectivity for delivery applications.
Non-technical Summary:
This study uses several pharmacological inhibitors to investigate the cellular uptake mechanisms of cationic gold nanoparticles (NPs) in both cancer (HeLa) and normal cells (MCF10A).
Content Emphasis
Peer Reviewed Journal Article
Exposure Or Hazard Target
Mammalian
Exposure Pathway
Other/Unspecified
Method Of Study
In Vitro
Paper Type
Hazard
Applications
Particle Type
Metal
Production Method
Engineered
Risk Exposure Group
General Population
Target Audience
Technical Research
Citation:
Small, 9(2): 300-305 (January 2013)
Publication:
Small
Author:
Saha K, Kim ST, Yan B, Miranda OR, Alfonso FS, Shlosman D, Rotello FS
Volume:
9
Number:
2
Pages:
300-305
Last updated on March 1, 2013
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This work is supported in part by the Nanoscale Science and Engineering Initiative of the National Science Foundation
under NSF Award Number EEC-0118007.
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