Evolving Platinum-Copper Nanostructures for Enhanced Photothermal Therapy and Controlled Copper Release in Cancer Therapy
Metadatos
Afficher la notice complèteAuteur
Garcia-Peiro, Jose I.; Sancho-Albero, María; Miguel, Silvia; Mosseri, Andrea; Hornos, Felipe; Contreras-Montoya, Rafael; Hueso, Jose L.; Santamaria, JesusEditorial
Wiley-VCH
Date
2025-07-09Referencia bibliográfica
J. I. Garcia-Peiro, M. Sancho-Albero, S. Miguel, A. Mosseri, F. Hornos, R. Contreras-Montoya, J. L. Hueso, J. Santamaria, Evolving Platinum-Copper Nanostructures for Enhanced Photothermal Therapy and Controlled Copper Release in Cancer Therapy. Adv. Funct. Mater. 2025, e02999. https://doi.org/10.1002/adfm.202502999
Patrocinador
European Research Council (Grant Number 742684); Agencia Estatal de Investigación - Severo Ochoa (Grant Number: CEX2023-001286-S); Fundación Científica Asociación Española Contra el Cáncer (Grant Number: POSTD234966SANC); Conselleria de Cultura, Educación y Ciencia, Generalitat Valenciana (Grant Number: APOSTD/2021/196)Résumé
Nanotechnology provides a panoply of new tools in cancer therapy, enabling advanced treatments such as chemodyamic therapy (CDT), radiation therapy (RT), photothermal therapy (PTT) or photodynamic therapy (PDT). The therapeutic effect can be increased by combining one or more of these actions and this is usually considered already from the design of the nanoparticles (NPs). Bimetallic NPs are obvious candidates in this respect, being able to trigger a multifunctional response associated to each metal and achieving a synergistic action in combined therapies. In this work, we designed platinum-copper bimetallic NPs (PtCu NPs) capable to evolve during treatment and fulfill a dual role as chemotherapeutic agents, (controlled release of ionic Cu), and as tumor ablation agents under near infrared (NIR) irradiation. Tuning the synthesis conditions demonstrated the influence of metal composition and alloying degree on the Cu release pattern when exposed to physiological media. The Cu ions released disrupt the redox balance in cells by generating reactive hydrogen species (likely hydroxyl radicals •OH through reaction with H2O2 overexpressed in the tumor microenvironment) while simultaneously oxidizing glutathione (GSH). After Cu release, the remaining Pt-rich structures present enhanced photothermal (PT) response. The efficacy of the combined therapy enabled by these NPs has been evaluated in vitro and in vivo.





