Novel cisplatin-magnetoliposome complex shows enhanced antitumor activity via Hyperthermia
Metadatos
Mostrar el registro completo del ítemAutor
Jiménez-López, M. Carmen; Moreno-Maldonado, Ana Carolina; Martín Morales, Natividad; O´Valle, Francisco; Ibarra, M. Ricardo; Goya, Gerardo F.; Molina Pineda Infantas, Ignacio JesúsEditorial
Springer Nature
Materia
Magnetoliposomes Magnetic hyperthermia Cis-diamminedichloroplatinum (II) CDDP Lung tumor
Fecha
2025-02-08Referencia bibliográfica
Jiménez-López, M.C., Moreno-Maldonado, A.C., Martín-Morales, N. et al. Novel cisplatin-magnetoliposome complex shows enhanced antitumor activity via Hyperthermia. Sci Rep 15, 4780 (2025). https://doi.org/10.1038/s41598-025-88533-z
Patrocinador
Ministry of Science and Innovation of Spain RTC-2017-6620-1; H2020-MSCA-RISE-2020 101007629-NESTOR, European Commision; University of GranadaResumen
There are several methods to improve cancer patient survival rates by inducing hyperthermia in tumor tissues, which involves raising their temperature above 41 °C. These methods utilize different energy sources to deliver heat to the target region, including light, microwaves or radiofrequency electromagnetic fields. We have developed a new, magnetically responsive nanocarrier, consisting of liposomes loaded with magnetic nanoparticles and cis-diamminedichloroplatinum (II) (CDDP), commonly known as Cisplatin. The resulting magnetoliposome (ML) is rapidly internalized by lung and pancreas tumor cell lines, stored in intracellular vesicles, and capable of inducing hyperthermia under magnetic fields. The ML has no significant toxicity both in vitro and in vivo and, most importantly, enhances cell death by apoptosis after magnetic hyperthermia. Remarkably, mice bearing induced lung tumors, treated with CDDP-loaded nanocarriers and subjected to an applied electromagnetic field, showed an improved survival rate over those treated with either soluble CDDP or hyperthermia alone. Therefore, our approach of magnetic hyperthermia plus CDDP-ML significantly enhances in vitro cell death and in vivo survival of treated animals.





