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Authors Qin J, Peng C, Zhao B, Ye K, Yuan F, Peng Z, Yang X, Huang L, Jiang M, Zhao Q, Tang G, Lu X
Published Date December 2014 Volume 2014:9(1) Pages 5575—5590
DOI http://dx.doi.org/10.2147/IJN.S72819
Received 17 August 2014, Accepted 27 September 2014, Published 2 December 2014
Abstract: Macrophages
are becoming increasingly significant in the progression of atherosclerosis
(AS). Molecular imaging of macrophages may improve the detection and
characterization of AS. In this study, dendrimer-entrapped gold nanoparticles
(Au DENPs) with polyethylene glycol (PEG) and fluorescein isothiocyanate (FI)
coatings were designed, tested, and applied as contrast agents for the enhanced
computed tomography (CT) imaging of macrophages in atherosclerotic lesions.
Cell counting kit-8 assay, fluorescence microscopy, silver staining, and
transmission electron microscopy revealed that the FI-functionalized Au DENPs
are noncytotoxic at high concentrations (3.0 µM) and can be efficiently
taken up by murine macrophages in vitro. These nanoparticles were administered
to apolipoprotein E knockout mice as AS models, which demonstrated that the
macrophage burden in atherosclerotic areas can be tracked noninvasively and
dynamically three-dimensionally in live animals using micro-CT. Our findings
suggest that the designed PEGylated gold nanoparticles are promising
biocompatible nanoprobes for the CT imaging of macrophages in atherosclerotic
lesions and will provide new insights into the pathophysiology of AS and other
concerned inflammatory diseases.
Keywords: atherosclerosis, CT,
in vivo imaging