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Nanoscale ; 16(23): 11069-11080, 2024 Jun 13.
Article in English | MEDLINE | ID: mdl-38745454

ABSTRACT

Microwave ablation (MWA) is recognized as a novel treatment modality that can kill tumor cells by heating the ions and polar molecules in these cells through high-speed rotation and friction. However, the size and location of the tumor affect the effective ablation range of microwave hyperthermia, resulting in residual tumor tissue and a high recurrence rate. Due to their tunable porous structure and high specific surface area, metal-organic frameworks (MOFs) can serve as microwave sensitizers, promoting microwave energy conversion owing to ion collisions in the porous structure of the MOFs. Moreover, iron-based compounds are known to possess peroxidase-like catalytic activity. Therefore, Fe-doped Cu bimetallic MOFs (FCMs) were prepared through a hydrothermal process. These FCM nanoparticles not only increased the efficiency of microwave-thermal energy conversion as microwave sensitizers but also promoted the generation of reactive oxygen species (ROS) by consuming glutathione (GSH) and promoted the Fenton reaction to enhance microwave dynamic therapy (MDT). The in vitro and in vivo results showed that the combination of MWA and MDT treatment effectively destroyed tumor tissues via microwave irradiation without inducing significant side effects on normal tissues. This study provides a new approach for the combined application of MOFs and microwave ablation, demonstrating excellent potential for future applications.


Subject(s)
Carcinoma, Hepatocellular , Copper , Iron , Liver Neoplasms , Metal-Organic Frameworks , Microwaves , Reactive Oxygen Species , Metal-Organic Frameworks/chemistry , Metal-Organic Frameworks/pharmacology , Copper/chemistry , Copper/pharmacology , Carcinoma, Hepatocellular/pathology , Carcinoma, Hepatocellular/therapy , Carcinoma, Hepatocellular/drug therapy , Carcinoma, Hepatocellular/metabolism , Animals , Iron/chemistry , Humans , Liver Neoplasms/pathology , Liver Neoplasms/drug therapy , Liver Neoplasms/therapy , Reactive Oxygen Species/metabolism , Mice , Hyperthermia, Induced , Hep G2 Cells , Cell Line, Tumor , Glutathione/chemistry , Glutathione/metabolism
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