医学
钙化
碘
钙
胶体金
主动脉
病理
核医学
纳米颗粒
内科学
材料科学
纳米技术
冶金
作者
David P. Cormode,Ewald Roessl,Axel Thran,Torjus Skajaa,Ronald E. Gordon,Jens‐Peter Schlomka,Valentín Fuster,Edward A. Fisher,Willem J. M. Mulder,Roland Proksa,Zahi A. Fayad
出处
期刊:Radiology
[Radiological Society of North America]
日期:2010-09-01
卷期号:256 (3): 774-782
被引量:435
标识
DOI:10.1148/radiol.10092473
摘要
To investigate the potential of spectral computed tomography (CT) (popularly referred to as multicolor CT), used in combination with a gold high-density lipoprotein nanoparticle contrast agent (Au-HDL), for characterization of macrophage burden, calcification, and stenosis of atherosclerotic plaques.The local animal care committee approved all animal experiments. A preclinical spectral CT system in which incident x-rays are divided into six different energy bins was used for multicolor imaging. Au-HDL, an iodine-based contrast agent, and calcium phosphate were imaged in a variety of phantoms. Apolipoprotein E knockout (apo E-KO) mice were used as the model for atherosclerosis. Gold nanoparticles targeted to atherosclerosis (Au-HDL) were intravenously injected at a dose of 500 mg per kilogram of body weight. Iodine-based contrast material was injected 24 hours later, after which the mice were imaged. Wild-type mice were used as controls. Macrophage targeting by Au-HDL was further evaluated by using transmission electron microscopy and confocal microscopy of aorta sections.Multicolor CT enabled differentiation of Au-HDL, iodine-based contrast material, and calcium phosphate in the phantoms. Accumulations of Au-HDL were detected in the aortas of the apo E-KO mice, while the iodine-based contrast agent and the calcium-rich tissue could also be detected and thus facilitated visualization of the vasculature and bones (skeleton), respectively, during a single scanning examination. Microscopy revealed Au-HDL to be primarily localized in the macrophages on the aorta sections; hence, the multicolor CT images provided information about the macrophage burden.Spectral CT used with carefully chosen contrast agents may yield valuable information about atherosclerotic plaque composition.
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