Gavilán Helena, Avugadda Sahitya Kumar, Fernández-Cabada Tamara, Soni Nisarg, Cassani Marco, Mai Binh T, Chantrell Roy, Pellegrino Teresa
Istituto Italiano di Tecnologia, via Morego 30, 16163 Genoa, Italy.
Department of Physics, University of York, York YO10 5DD, UK.
Chem Soc Rev. 2021 Oct 18;50(20):11614-11667. doi: 10.1039/d1cs00427a.
Magnetic hyperthermia (MHT) is a therapeutic modality for the treatment of solid tumors that has now accumulated more than 30 years of experience. In the ongoing MHT clinical trials for the treatment of brain and prostate tumors, iron oxide nanoparticles are employed as intra-tumoral MHT agents under a patient-safe 100 kHz alternating magnetic field (AMF) applicator. Although iron oxide nanoparticles are currently approved by FDA for imaging purposes and for the treatment of anemia, magnetic nanoparticles (MNPs) designed for the efficient treatment of MHT must respond to specific physical-chemical properties in terms of magneto-energy conversion, heat dose production, surface chemistry and aggregation state. Accordingly, in the past few decades, these requirements have boosted the development of a new generation of MNPs specifically aimed for MHT. In this review, we present an overview on MNPs and their assemblies produced different synthetic routes, focusing on which MNP features have allowed unprecedented heating efficiency levels to be achieved in MHT and highlighting nanoplatforms that prevent magnetic heat loss in the intracellular environment. Moreover, we review the advances on MNP-based nanoplatforms that embrace the concept of multimodal therapy, which aims to combine MHT with chemotherapy, radiotherapy, immunotherapy, photodynamic or phototherapy. Next, for a better control of the therapeutic temperature at the tumor, we focus on the studies that have optimized MNPs to maintain gold-standard MHT performance and are also tackling MNP imaging with the aim to quantitatively assess the amount of nanoparticles accumulated at the tumor site and regulate the MHT field conditions. To conclude, future perspectives with guidance on how to advance MHT therapy will be provided.
Colloids Surf B Biointerfaces. 2024-2
Int J Mol Sci. 2024-9-19
Pharmaceuticals (Basel). 2024-2-26
ChemMedChem. 2022-1-19
J Nanotheranostics. 2024-6
ACS Appl Mater Interfaces. 2025-8-20
ACS Appl Nano Mater. 2025-7-11
Int J Nanomedicine. 2025-6-17
Discov Oncol. 2025-6-21
Mater Today Bio. 2025-5-26