Heating Capacity and Biocompatibility of Hybrid Nanoparticles for Magnetic Hyperthermia Treatment

Int J Mol Sci. 2023 Dec 29;25(1):493. doi: 10.3390/ijms25010493.

Abstract

Cancer is one of the deadliest diseases worldwide and has been responsible for millions of deaths. However, developing a satisfactory smart multifunctional material combining different strategies to kill cancer cells poses a challenge. This work aims at filling this gap by developing a composite material for cancer treatment through hyperthermia and drug release. With this purpose, magnetic nanoparticles were coated with a polymer matrix consisting of poly (L-co-D,L lactic acid-co-trimethylene carbonate) and a poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) triblock copolymer. High-resolution transmission electron microscopy and selected area electron diffraction confirmed magnetite to be the only iron oxide in the sample. Cytotoxicity and heat release assays on the hybrid nanoparticles were performed here for the first time. The heat induction results indicate that these new magnetic hybrid nanoparticles are capable of increasing the temperature by more than 5 °C, the minimal temperature rise required for being effectively used in hyperthermia treatments. The biocompatibility assays conducted under different concentrations, in the presence and in the absence of an external alternating current magnetic field, did not reveal any cytotoxicity. Therefore, the overall results indicate that the investigated hybrid nanoparticles have a great potential to be used as carrier systems for cancer treatment by hyperthermia.

Keywords: cytotoxicity; hybrid nanoparticles; hyperthermia.

MeSH terms

  • Electricity
  • Heating*
  • Humans
  • Hyperthermia
  • Hyperthermia, Induced*

Grants and funding

This work was supported by the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Grant/Award Number 404938/2016-7, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) and Fundação de Amparo à Pesquisa do Estado de Minas Gerais (FAPEMIG) Grant/Award Number APQ-03585-16, Instituto Nacional de Ciência e Tecnologia em Medicina Regenerativa (INCT-Regenera) Grant/Award Number 4465656/2014-5, Rede Mineira de Nanomedicina Teranóstica/FAPEMIG Grant/Award Number RED00079-22, and Rede Mineira de Engenharia de Tecidos e Terapia Celular (REMETTEC/FAPEMIG) Grant/Award Number RED-00570-16. We thank them for their financial support and promotion of scholarships for some of the authors. This work was also developed within the scope of the project CICECO-Aveiro Institute of Materials, UIDB/50011/2020, UIDP/50011/2020, and LA/P/0006/2020, financed by national funds through the FCT/MCTES (PIDDAC).