Novel cisplatin-magnetoliposome complex shows enhanced antitumor activity via Hyperthermia

Abstract 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 radiofreque...

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Main Authors: M. Carmen Jiménez-López, Ana Carolina Moreno-Maldonado, Natividad Martín-Morales, Francisco O’Valle, M. Ricardo Ibarra, Gerardo F. Goya, Ignacio J. Molina
Format: Article
Language:English
Published: Nature Portfolio 2025-02-01
Series:Scientific Reports
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Online Access:https://doi.org/10.1038/s41598-025-88533-z
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author M. Carmen Jiménez-López
Ana Carolina Moreno-Maldonado
Natividad Martín-Morales
Francisco O’Valle
M. Ricardo Ibarra
Gerardo F. Goya
Ignacio J. Molina
author_facet M. Carmen Jiménez-López
Ana Carolina Moreno-Maldonado
Natividad Martín-Morales
Francisco O’Valle
M. Ricardo Ibarra
Gerardo F. Goya
Ignacio J. Molina
author_sort M. Carmen Jiménez-López
collection DOAJ
description Abstract 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.
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issn 2045-2322
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spelling doaj-art-233bab1b3ad746fb88eb2ff5523e70982025-02-09T12:29:28ZengNature PortfolioScientific Reports2045-23222025-02-0115111410.1038/s41598-025-88533-zNovel cisplatin-magnetoliposome complex shows enhanced antitumor activity via HyperthermiaM. Carmen Jiménez-López0Ana Carolina Moreno-Maldonado1Natividad Martín-Morales2Francisco O’Valle3M. Ricardo Ibarra4Gerardo F. Goya5Ignacio J. Molina6Institute of Biopathology and Regenerative Medicine, Center for Biomedical Research. Health Sciences Technology Park, University of GranadaInstitute of Nanoscience and Materials of Aragón, CSIC-University of ZaragozaInstitute of Biopathology and Regenerative Medicine, Center for Biomedical Research. Health Sciences Technology Park, University of GranadaInstitute of Biopathology and Regenerative Medicine, Center for Biomedical Research. Health Sciences Technology Park, University of GranadaInstitute of Nanoscience and Materials of Aragón, CSIC-University of ZaragozaInstitute of Nanoscience and Materials of Aragón, CSIC-University of ZaragozaInstitute of Biopathology and Regenerative Medicine, Center for Biomedical Research. Health Sciences Technology Park, University of GranadaAbstract 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.https://doi.org/10.1038/s41598-025-88533-zMagnetoliposomesMagnetic hyperthermiaCis-diamminedichloroplatinum (II)CDDPLung tumorPancreas tumor
spellingShingle M. Carmen Jiménez-López
Ana Carolina Moreno-Maldonado
Natividad Martín-Morales
Francisco O’Valle
M. Ricardo Ibarra
Gerardo F. Goya
Ignacio J. Molina
Novel cisplatin-magnetoliposome complex shows enhanced antitumor activity via Hyperthermia
Scientific Reports
Magnetoliposomes
Magnetic hyperthermia
Cis-diamminedichloroplatinum (II)
CDDP
Lung tumor
Pancreas tumor
title Novel cisplatin-magnetoliposome complex shows enhanced antitumor activity via Hyperthermia
title_full Novel cisplatin-magnetoliposome complex shows enhanced antitumor activity via Hyperthermia
title_fullStr Novel cisplatin-magnetoliposome complex shows enhanced antitumor activity via Hyperthermia
title_full_unstemmed Novel cisplatin-magnetoliposome complex shows enhanced antitumor activity via Hyperthermia
title_short Novel cisplatin-magnetoliposome complex shows enhanced antitumor activity via Hyperthermia
title_sort novel cisplatin magnetoliposome complex shows enhanced antitumor activity via hyperthermia
topic Magnetoliposomes
Magnetic hyperthermia
Cis-diamminedichloroplatinum (II)
CDDP
Lung tumor
Pancreas tumor
url https://doi.org/10.1038/s41598-025-88533-z
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