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Updated: Feb 15, 2026

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Cell Labeling and Targeting with Superparamagnetic Iron Oxide Nanoparticles
Published on: October 19, 2015
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Comprehensive cytotoxicity studies of superparamagnetic iron oxide nanoparticles
Rakesh M Patil1,2, Nanasaheb D Thorat3, Prajkta B Shete2
1Directorate of Forensic Science Laboratory, Govt. of Maharashtra Kalina, Mumbai, India.
Biochemistry and Biophysics Reports
|January 20, 2018
Summary
Superparamagnetic iron oxide nanoparticles (SPIONs) show promise in medicine, but their toxicity requires careful study. This review details SPIONs
Area of Science:
- Biomedical Engineering
- Nanotechnology
- Toxicology
Background:
- Superparamagnetic iron oxide nanoparticles (SPIONs) are increasingly developed for biomedical applications.
- Understanding the potential toxicity of SPIONs is crucial for their safe clinical translation.
Purpose of the Study:
- To comprehensively review the toxicity associated with SPIONs.
- To elucidate the mechanisms of SPIONs toxicity at cellular and organismal levels.
- To inform the design of safer SPION-based therapeutics.
Main Methods:
- Review of existing literature on SPIONs toxicity.
- Analysis of studies focusing on cellular alterations, oxidative stress, and nucleic acid damage.
- Evaluation of in vitro and in vivo toxicity data.
- Discussion of time-dependent toxicity and nanoparticle fate in biological systems.
Main Results:
- SPIONs can induce cellular alterations, including damage to nucleic acids via oxidative stress.
- Both in vitro and in vivo studies reveal significant toxicity profiles for SPIONs.
- The toxicity of SPIONs is dependent on factors such as dose, size, and surface modifications.
- The long-term fate and potential accumulation of SPIONs in the body contribute to their toxicity.
Conclusions:
- A thorough understanding of SPIONs toxicity is essential for their safe application in medicine.
- Further research is needed to mitigate SPIONs-induced toxicity and optimize their therapeutic potential.
- Future studies should focus on developing biocompatible SPIONs with predictable clearance mechanisms.
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