Rapid-clearance iron nanoparticles for inflammation imaging of atherosclerotic plaque: initial experience in animal model

Radiology. 2009 Aug;252(2):401-9. doi: 10.1148/radiol.2522081484.


Purpose: To evaluate the use of a recently developed fast-clearing ultrasmall superparamagnetic iron oxide (USPIO) for detection of vascular inflammation in atherosclerotic plaque.

Materials and methods: The study protocol was approved by the animal experimentation ethics committee. A recently introduced USPIO, P904, and a reference-standard USPIO, ferumoxtran-10, were tested in a rabbit model of induced aortic atherosclerosis. In vivo magnetic resonance (MR) angiography and T2*-weighted plaque MR imaging were performed at baseline and after administration of P904 and ferumoxtran-10 (administered dose for both, 1000 micromol of iron per kilogram of body weight) in 26 hyperlipidemic New Zealand white rabbits. The variation in vessel wall area over time was evaluated with nonparametric testing. Ex vivo MR imaging findings were compared with iron content at linear regression analysis.

Results: With in vivo MR imaging, plaque analysis was possible as early as 24 hours after P904 injection. The authors observed a 27.75% increase in vessel wall area due to susceptibility artifacts on day 2 (P = .04) and a 38.81% increase on day 3 (P = .04) after P904 administration compared with a 44.5% increase in vessel wall area on day 7 (P = .04) and a 34.8% increase on day 10 (P = .22) after ferumoxtran-10 administration. These susceptibility artifacts were correlated with intraplaque iron uptake in the corresponding histologic slices. The number of pixels with signal loss on the ex vivo MR images was linearly correlated with the logarithm of the iron concentration (P = .0001; R(2) = 0.93).

Conclusion: Plaque inflammation in rabbits can be detected earlier with P904 than with ferumoxtran-10 owing to the faster blood pharmacokinetics and the early uptake of P904 in the reticuloendothelial system.

Supplemental material: http://radiology.rsnajnls.org/cgi/content/full/252/2/401/DC1.

Publication types

  • Comparative Study
  • Evaluation Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Aortitis / metabolism*
  • Aortitis / pathology*
  • Atherosclerosis / metabolism*
  • Atherosclerosis / pathology*
  • Contrast Media / pharmacokinetics
  • Dextrans
  • Disease Models, Animal
  • Ferrosoferric Oxide
  • Humans
  • Iron / pharmacokinetics*
  • Magnetic Resonance Angiography / methods*
  • Magnetite Nanoparticles
  • Metabolic Clearance Rate
  • Oxides / pharmacokinetics*
  • Pilot Projects
  • Rabbits
  • Reproducibility of Results
  • Sensitivity and Specificity


  • Contrast Media
  • Dextrans
  • Magnetite Nanoparticles
  • Oxides
  • ferumoxtran-10
  • Iron
  • Ferrosoferric Oxide