Surface Functionality of Nanoparticles Determines Cellular Uptake Mechanisms in Mammalian Cells

被引:174
作者
Saha, Krishnendu [1 ]
Kim, Sung Tae [1 ]
Yan, Bo [1 ]
Miranda, Oscar R. [1 ]
Alfonso, Felix S. [1 ]
Shlosman, Denis [1 ]
Rotello, Vincent M. [1 ]
机构
[1] Univ Massachusetts, Dept Chem, Amherst, MA 01003 USA
基金
美国国家卫生研究院;
关键词
gold nanoparticles; surface monolayers; uptake mechanisms; caveolae; dynamin-dependent endocytosis; RECEPTOR-MEDIATED ENDOCYTOSIS; CLATHRIN-INDEPENDENT ENDOCYTOSIS; COATED GOLD NANOPARTICLES; TARGETED DRUG-DELIVERY; SCAVENGER RECEPTORS; LIVING CELLS; SIZE; INTERNALIZATION; PATHWAYS; MACROPHAGES;
D O I
10.1002/smll.201201129
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:300 / 305
页数:6
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