| Literature DB >> 19035793 |
Rolf Koole1, Matti M van Schooneveld, Jan Hilhorst, Karolien Castermans, David P Cormode, Gustav J Strijkers, Celso de Mello Donegá, Daniel Vanmaekelbergh, Arjan W Griffioen, Klaas Nicolay, Zahi A Fayad, Andries Meijerink, Willem J M Mulder.
Abstract
Silica particles as a nanoparticulate carrier material for contrast agents have received considerable attention the past few years, since the material holds great promise for biomedical applications. A key feature for successful application of this material in vivo is biocompatibility, which may be significantly improved by appropriate surface modification. In this study, we report a novel strategy to coat silica particles with a dense monolayer of paramagnetic and PEGylated lipids. The silica nanoparticles carry a quantum dot in their center and are made target-specific by the conjugation of multiple alphavbeta3-integrin-specific RGD-peptides. We demonstrate their specific uptake by endothelial cells in vitro using fluorescence microscopy, quantitative fluorescence imaging, and magnetic resonance imaging. The lipid-coated silica particles introduced here represent a new platform for nanoparticulate multimodality contrast agents.Entities:
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Year: 2008 PMID: 19035793 PMCID: PMC3345202 DOI: 10.1021/bc800368x
Source DB: PubMed Journal: Bioconjug Chem ISSN: 1043-1802 Impact factor: 4.774