Magnetite nanoparticles for cancer diagnosis, treatment, and treatment monitoring: recent advances.

Mater Today (Kidlington)

Department of Materials Science and Engineering, University of Washington, Seattle, WA 98195, USA.

Published: April 2016

AI Article Synopsis

  • Nanoparticles (NPs) have made significant advancements in cancer detection and treatment over the last 20 years, being used for imaging enhancements, drug delivery, and therapies that directly target tumor cells.
  • Iron oxide (magnetite) nanoparticles, in particular, have been extensively studied due to their favorable properties like superparamagnetism, biocompatibility, and biodegradability.
  • The review discusses recent uses of magnetite NPs in cancer diagnosis and treatment, along with concerns about their toxicity and potential for clinical application, while also exploring future developments for integrating multiple cancer therapies into one formulation.

Article Abstract

The development of nanoparticles (NPs) for use in all facets of oncological disease detection and therapy has shown great progress over the past two decades. NPs have been tailored for use as contrast enhancement agents for imaging, drug delivery vehicles, and most recently as a therapeutic component in initiating tumor cell death in magnetic and photonic ablation therapies. Of the many possible core constituents of NPs, such as gold, silver, carbon nanotubes, fullerenes, manganese oxide, lipids, micelles, etc., iron oxide (or magnetite) based NPs have been extensively investigated due to their excellent superparamagnetic, biocompatible, and biodegradable properties. This review addresses recent applications of magnetite NPs in diagnosis, treatment, and treatment monitoring of cancer. Finally, some views will be discussed concerning the toxicity and clinical translation of iron oxide NPs and the future outlook of NP development to facilitate multiple therapies in a single formulation for cancer theranostics.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4981486PMC
http://dx.doi.org/10.1016/j.mattod.2015.08.022DOI Listing

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