Document Type
Article
Publication Date
4-21-2026
Abstract
Iron-based nanoparticles, particularly iron oxide nanostructures (IONPs), have emerged as versatile and clinically relevant platforms for drug delivery and theranostic applications. Among these, superparamagnetic iron oxide nanoparticles (SPIONs), including magnetite (Fe3O4) and maghemite (γ-Fe2O3), are the most extensively investigated due to their biocompatibility, magnetic responsiveness, and established safety profiles. Their unique superparamagnetic behavior enables external magnetic-field-guided targeting, magnetic resonance imaging (MRI) contrast enhancement, and magnetically triggered hyperthermia, enabling simultaneous diagnosis and therapy. Surface functionalization with polymers, silica, lipids, peptides, and biomolecules further improves colloidal stability, circulation time, targeting specificity, and controlled drug release. Core–shell architectures and multifunctional hybrid systems have expanded the therapeutic scope of iron nanoparticles, integrating chemotherapy, gene delivery, photothermal therapy, and Fenton reaction–mediated catalytic therapy. Despite promising preclinical outcomes, challenges remain regarding long-term biosafety, oxidative stress induction, biodistribution, large-scale reproducibility, and regulatory translation. This review summarizes the physicochemical properties, synthesis strategies, surface-engineering approaches, drug-loading mechanisms, and biomedical applications of iron-based nanoparticles, highlighting recent advances in multifunctional and peptide-functionalized systems. Critical considerations for clinical translation and future perspectives in precision nanomedicine are also discussed.
Recommended Citation
Parang, K.; Vadlapatla, R.; Koomer, A.; Moran, V.; Jackson, L.; Shirazi, A.N. Iron-Based Nanoparticles as Delivery Tools. Pharmaceuticals 2026, 19, 654. https://doi.org/10.3390/ph19050654
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The authors
Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 License.
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Medicinal and Pharmaceutical Chemistry Commons, Nanomedicine Commons, Pharmaceutics and Drug Design Commons
Comments
This article was originally published in Pharmaceuticals, volume 19, issue 5, in 2026. https://doi.org/10.3390/ph19050654