TY - JOUR
T1 - Paramagnetic lipid-coated silica nanoparticles with a fluorescent quantum dot core: a new contrast agent platform for multimodality imaging
AU - Koole, Rolf
AU - van Schooneveld, Matti M.
AU - Hilhorst, Jan
AU - Castermans, Karolien
AU - Cormode, David P.
AU - Strijkers, Gustav J.
AU - de Mello Donegá, Celso
AU - Vanmaekelbergh, Daniel
AU - Griffioen, Arjan W.
AU - Nicolay, Klaas
AU - Fayad, Zahi A.
AU - Meijerink, Andries
AU - Mulder, Willem J. M.
PY - 2008
Y1 - 2008
N2 - 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
AB - 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
U2 - https://doi.org/10.1021/bc800368x
DO - https://doi.org/10.1021/bc800368x
M3 - Article
C2 - 19035793
SN - 1043-1802
VL - 19
SP - 2471
EP - 2479
JO - Bioconjugate chemistry
JF - Bioconjugate chemistry
IS - 12
ER -