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Issue 3, 2018

In vivo formation of protein corona on gold nanoparticles. The effect of their size and shape

Author affiliations

Abstract

The efficacy of drug delivery and other nanomedicine-related therapies largely relies on the ability of nanoparticles to reach the target organ. However, when nanoparticles are injected into the bloodstream, their surface is instantly modified upon interaction with blood components, principally with proteins. It is well known that a dynamic and multi-layered protein structure is formed spontaneously on the nanoparticle upon contact with physiological media, which has been termed protein corona. Although several determinant factors involved in protein corona formation have been identified from in vitro studies, specific relationships between the nanomaterial synthetic identity and its ensuing biological identity under realistic in vivo conditions remain elusive. We present here a detailed study of in vivo protein corona formation after blood circulation of anisotropic gold nanoparticles (nanorods and nanostars). Plasmonic gold nanoparticles of different shapes and sizes were coated with polyethyleneglycol, intravenously administered in CD-1 mice and subsequently recovered. The results from gel electrophoresis and mass spectrometry analysis revealed the formation of complex protein coronas, as early as 10 minutes post-injection. The total amount of protein adsorbed onto the particle surface and the protein corona composition were found to be affected by both the particle size and shape.

Graphical abstract: In vivo formation of protein corona on gold nanoparticles. The effect of their size and shape

Supplementary files

Article information


Submitted
08 Nov 2017
Accepted
04 Dec 2017
First published
07 Dec 2017

Nanoscale, 2018,10, 1256-1264
Article type
Paper

In vivo formation of protein corona on gold nanoparticles. The effect of their size and shape

R. García-Álvarez, M. Hadjidemetriou, A. Sánchez-Iglesias, L. M. Liz-Marzán and K. Kostarelos, Nanoscale, 2018, 10, 1256 DOI: 10.1039/C7NR08322J

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