Transferrin-functionalized nanoparticles lose their targeting capabilities when a biomolecule corona adsorbs on the surface

Nanoparticles have been proposed as carriers for drugs, genes and therapies to treat various diseases 1 , 2 . Many strategies have been developed to target nanomaterials to specific or over-expressed receptors in diseased cells, and these typically involve functionalizing the surface of nanoparticle...

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Veröffentlicht in:Nature nanotechnology 2013-02, Vol.8 (2), p.137-143
Hauptverfasser: Salvati, Anna, Pitek, Andrzej S., Monopoli, Marco P., Prapainop, Kanlaya, Bombelli, Francesca Baldelli, Hristov, Delyan R., Kelly, Philip M., Åberg, Christoffer, Mahon, Eugene, Dawson, Kenneth A.
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Sprache:eng
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Zusammenfassung:Nanoparticles have been proposed as carriers for drugs, genes and therapies to treat various diseases 1 , 2 . Many strategies have been developed to target nanomaterials to specific or over-expressed receptors in diseased cells, and these typically involve functionalizing the surface of nanoparticles with proteins, antibodies or other biomolecules. Here, we show that the targeting ability of such functionalized nanoparticles may disappear when they are placed in a biological environment. Using transferrin-conjugated nanoparticles, we found that proteins in the media can shield transferrin from binding to both its targeted receptors on cells and soluble transferrin receptors. Although nanoparticles continue to enter cells, the targeting specificity of transferrin is lost. Our results suggest that when nanoparticles are placed in a complex biological environment, interaction with other proteins in the medium and the formation of a protein corona 3 , 4 can ‘screen’ the targeting molecules on the surface of nanoparticles and cause loss of specificity in targeting. When placed in a complex biological environment, targeting molecules on the surface of nanoparticles are shielded by surrounding biomolecules and their ability to bind to the targeted receptors on cells is lost.
ISSN:1748-3387
1748-3395
DOI:10.1038/nnano.2012.237