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Updated: Apr 22, 2026

Using Magnetometry to Monitor Cellular Incorporation and Subsequent Biodegradation of Chemically Synthetized Iron Oxide Nanoparticles
Published on: February 27, 2021
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.
Abstract:
The use of nanoparticles in medical treatment has prompted the question of their safety. In this study, the pathophysiology and biodistribution of three different concentrations of intravenously-delivered dextran-coated Fe3O4 iron oxide nanoparticles (IONP) were evaluated in mice. Some groups of mice were exposed to an AC magnetic field (AMF) at levels comparable with those proposed for cancer treatments. Iron biodistribution analysis for both AMF and non-AMF treated mice was performed for all three concentrations used (.6 mg Fe/mouse, 1.8 mg Fe/mouse, and 5.6 mg Fe/mouse). Blood urea nitrogen, alanine transaminase, alkaline phosphatase, total serum protein, and creatinine were also assessed at 4 hours, 7 days, and 14 days post-injection. Histological analysis of lung, spleen, heart, liver, and kidney tissue was conducted at 7 and 14 days post-injection. Prussian blue and H&E stains were used to histomorphometrically assess iron content in the tissues studied. Preliminary results demonstrate small temporary elevation in liver enzymes and hepatocyte vacuolization at all iron concentrations studied. Liver and spleen were the primary sites of IONP deposition. None of the animals demonstrated systemic or local toxicity or illness, with or without AMF activation.
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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