Toxicity and Biodistribution of Activated and Non-activated Intravenous Iron Oxide Nanoparticles

Ja Tate1, Ja Ogden1, Rr Strawbridge2

  • 1Thayer School of Engineering, Dartmouth College, Hanover, NH 03755 USA.

Insights

Dextran-coated iron oxide nanoparticles (IONP) showed no systemic toxicity in mice, even with AC magnetic field exposure. The liver and spleen were primary deposition sites, with minor, temporary liver enzyme elevations observed.

Area of Science:

  • Biomedical Engineering
  • Nanotechnology
  • Toxicology

Background:

  • Nanoparticles are increasingly used in medical treatments, necessitating safety evaluations.
  • Iron oxide nanoparticles (IONP) are candidates for various biomedical applications.
  • Understanding IONP behavior in vivo is crucial for clinical translation.

Purpose of the Study:

  • To assess the safety and biodistribution of dextran-coated IONP in mice.
  • To investigate the influence of alternating current magnetic fields (AMF) on IONP effects.
  • To evaluate IONP toxicity at different concentrations and time points.

Main Methods:

  • Intravenous administration of three concentrations of dextran-coated IONP to mice.
  • Exposure of some groups to AMF at clinically relevant levels.
  • Analysis of iron biodistribution, serum biochemistry, and histology (Prussian blue, H&E) in various organs.
  • Assessment at 4 hours, 7 days, and 14 days post-injection.

Main Results:

  • IONP primarily accumulated in the liver and spleen.
  • Minor, transient elevations in liver enzymes and hepatocyte vacuolization were observed at all concentrations.
  • No systemic or local toxicity, or adverse health effects were detected in any group, with or without AMF exposure.
  • Histological analysis confirmed iron deposition in the liver and spleen.

Conclusions:

  • Dextran-coated IONP demonstrate a favorable safety profile in mice at the tested concentrations.
  • AMF exposure did not induce additional toxicity.
  • The liver and spleen are the main organs for IONP clearance.
  • Further research may support the clinical application of these IONP.

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