Tuning of Ultrasmall Gold Nanoparticles Surface Properties Affect Their Biological Fate

Author:

Ferreira Avelino1,Fernandez Alarcon Jennifer2ORCID,Guffanti Federica2ORCID,Morelli Annalisa2,Russo Luca2,Violatto Martina B.2ORCID,Cognet Valentin3,Barrientos Africa3,Soliman Mahmoud G.14ORCID,Dobricic Marko1,Moya Sergio E.5ORCID,Bigini Paolo2ORCID,Monopoli Marco P.1ORCID

Affiliation:

1. Department of Chemistry Royal College of Surgeons of Ireland RCSI St Stephens Green 123 Dublin D02 YN77 Ireland

2. Department of Molecular Biochemistry and Pharmacology Istituto di Ricerche Farmacologiche Mario Negri IRCCS Via Mario Negri 2 Milano 20156 Italy

3. Midatech Pharma Plc 1 Caspian Point, Caspian Way Cardiff CF104DQ UK

4. Physics Department Faculty of Science Al‐Azhar University Cairo 4434103 Egypt

5. Soft Matter Nanotechnology Laboratory CIC Biomagune Paseo Miramon 182 San Sebastian‐Donostia 20014 Spain

Abstract

AbstractUltrasmall nanoparticles of 10 nm or less in size have been shown to have great potential in the biomedical field due to their high surface area and strong tissue penetration. Their easy functionalization and unique behavior at the nanoscale, such as the reduced corona formation and lower liver retention allow them to be a potential tool for precision targeting. In this study, PEGylated ultrasmall gold nanoparticles (GNPs) with a 4 nm core size are developed. They are functionalized with the cyclic RGD (cRGD) targeting peptide, which provides high binding affinity toward αVβ3 integrin receptor, often overexpressed in solid tumors. Further evidence is presented that cRGD functionalized GNPs partially escape lysosomes while penetrating deeper into the liver parenchyma. These particles provide a potential future strategy for specific αVβ3 integrin targeting.

Funder

Science Foundation Ireland

Publisher

Wiley

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