Dual-energy CT imaging of atherosclerotic plaque using novel ultrasmall superparamagnetic iron oxide in

Hideyuki Sato1,2, Shinichiro Fujimoto1, Yuko O Kawaguchi1

  • 1Department of Cardiovascular Biology and Medicine, Juntendo University Graduate School of Medicine, Tokyo, Japan.

Abstract

Insights

Dual-energy computed tomography (DECT) effectively visualizes carboxymethyl-diethylaminoethyl dextran magnetite ultra-small superparamagnetic iron oxide (CMEADM-U) accumulation in arteriosclerotic lesions, aiding macrophage assessment in rabbits.

Area of Science:

  • Biomedical Imaging
  • Nanotechnology
  • Cardiovascular Research

Background:

  • Magnetic resonance imaging (MRI) shows ultra-small superparamagnetic iron oxide (USPIO) uptake by macrophages.
  • MRI has limitations in spatial and temporal resolution for imaging USPIO accumulation.

Purpose of the Study:

  • To evaluate dual-energy computed tomography (DECT) for visualizing carboxymethyl-diethylaminoethyl dextran magnetite ultra-small superparamagnetic iron oxide (CMEADM-U) in arteriosclerotic lesions.
  • To assess CMEADM-U accumulation in hyperlipidemic rabbit models of atherosclerosis.

Main Methods:

  • CMEADM-U was administered to Watanabe hereditary atherosclerotic (WHHL) and New Zealand white (NZW) rabbits.
  • DECT imaging was performed, generating virtual monochromatic images (35 keV, 70 keV) and an iron-based map.
  • Aorta analysis included hematoxylin and eosin, Berlin blue, and RAM11 immunostaining.

Main Results:

  • CMEADM-U accumulation was visualized at 35 keV and on the iron-based map in WHHL rabbits, correlating with arteriosclerotic lesions.
  • No CMEADM-U accumulation was detected in NZW rabbits.
  • Iron-based map values showed significant differences based on macrophage marker expression and correlated with 35 keV imaging.

Conclusions:

  • DECT imaging effectively visualizes CMEADM-U accumulation in atherosclerotic lesions.
  • DECT facilitates assessment of macrophage accumulation in an in vivo rabbit atherosclerosis model.
  • This technique offers improved imaging of nanoparticle-based contrast agents in atherosclerosis research.

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