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Thermoresponsive Iron Oxide Nanocubes for an Effective Clinical Translation of Magnetic Hyperthermia and Heat-Mediated Chemotherapy
[Image: see text] The use of magnetic nanoparticles in oncothermia has been investigated for decades, but an effective combination of magnetic nanoparticles and localized chemotherapy under clinical magnetic hyperthermia (MH) conditions calls for novel platforms. In this study, we have engineered ma...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American
Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376448/ https://www.ncbi.nlm.nih.gov/pubmed/30624889 http://dx.doi.org/10.1021/acsami.8b16226 |
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author | Mai, Binh T. Balakrishnan, Preethi B. Barthel, Markus J. Piccardi, Federica Niculaes, Dina Marinaro, Federica Fernandes, Soraia Curcio, Alberto Kakwere, Hamilton Autret, Gwennhael Cingolani, Roberto Gazeau, Florence Pellegrino, Teresa |
author_facet | Mai, Binh T. Balakrishnan, Preethi B. Barthel, Markus J. Piccardi, Federica Niculaes, Dina Marinaro, Federica Fernandes, Soraia Curcio, Alberto Kakwere, Hamilton Autret, Gwennhael Cingolani, Roberto Gazeau, Florence Pellegrino, Teresa |
author_sort | Mai, Binh T. |
collection | PubMed |
description | [Image: see text] The use of magnetic nanoparticles in oncothermia has been investigated for decades, but an effective combination of magnetic nanoparticles and localized chemotherapy under clinical magnetic hyperthermia (MH) conditions calls for novel platforms. In this study, we have engineered magnetic thermoresponsive iron oxide nanocubes (TR-cubes) to merge MH treatment with heat-mediated drug delivery, having in mind the clinical translation of the nanoplatform. We have chosen iron oxide based nanoparticles with a cubic shape because of their outstanding heat performance under MH clinical conditions, which makes them benchmark agents for MH. Accomplishing a surface-initiated polymerization of strongly interactive nanoparticles such as our iron oxide nanocubes, however, remains the main challenge to overcome. Here, we demonstrate that it is possible to accelerate the growth of a polymer shell on each nanocube by simple irradiation of a copper-mediated polymerization with a ultraviolet light (UV) light, which both speeds up the polymerization and prevents nanocube aggregation. Moreover, we demonstrate herein that these TR-cubes can carry chemotherapeutic doxorubicin (DOXO-loaded-TR-cubes) without compromising their thermoresponsiveness both in vitro and in vivo. In vivo efficacy studies showed complete tumor suppression and the highest survival rate for animals that had been treated with DOXO-loaded-TR-cubes, only when they were exposed to MH. The biodistribution of intravenously injected TR-cubes showed signs of renal clearance within 1 week and complete clearance after 5 months. This biomedical platform works under clinical MH conditions and at a low iron dosage, which will enable the translation of dual MH/heat-mediated chemotherapy, thus overcoming the clinical limitation of MH: i.e., being able to monitor tumor progression post-MH-treatment by magnetic resonance imaging (MRI). |
format | Online Article Text |
id | pubmed-6376448 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American
Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-63764482019-02-19 Thermoresponsive Iron Oxide Nanocubes for an Effective Clinical Translation of Magnetic Hyperthermia and Heat-Mediated Chemotherapy Mai, Binh T. Balakrishnan, Preethi B. Barthel, Markus J. Piccardi, Federica Niculaes, Dina Marinaro, Federica Fernandes, Soraia Curcio, Alberto Kakwere, Hamilton Autret, Gwennhael Cingolani, Roberto Gazeau, Florence Pellegrino, Teresa ACS Appl Mater Interfaces [Image: see text] The use of magnetic nanoparticles in oncothermia has been investigated for decades, but an effective combination of magnetic nanoparticles and localized chemotherapy under clinical magnetic hyperthermia (MH) conditions calls for novel platforms. In this study, we have engineered magnetic thermoresponsive iron oxide nanocubes (TR-cubes) to merge MH treatment with heat-mediated drug delivery, having in mind the clinical translation of the nanoplatform. We have chosen iron oxide based nanoparticles with a cubic shape because of their outstanding heat performance under MH clinical conditions, which makes them benchmark agents for MH. Accomplishing a surface-initiated polymerization of strongly interactive nanoparticles such as our iron oxide nanocubes, however, remains the main challenge to overcome. Here, we demonstrate that it is possible to accelerate the growth of a polymer shell on each nanocube by simple irradiation of a copper-mediated polymerization with a ultraviolet light (UV) light, which both speeds up the polymerization and prevents nanocube aggregation. Moreover, we demonstrate herein that these TR-cubes can carry chemotherapeutic doxorubicin (DOXO-loaded-TR-cubes) without compromising their thermoresponsiveness both in vitro and in vivo. In vivo efficacy studies showed complete tumor suppression and the highest survival rate for animals that had been treated with DOXO-loaded-TR-cubes, only when they were exposed to MH. The biodistribution of intravenously injected TR-cubes showed signs of renal clearance within 1 week and complete clearance after 5 months. This biomedical platform works under clinical MH conditions and at a low iron dosage, which will enable the translation of dual MH/heat-mediated chemotherapy, thus overcoming the clinical limitation of MH: i.e., being able to monitor tumor progression post-MH-treatment by magnetic resonance imaging (MRI). American Chemical Society 2019-01-09 2019-02-13 /pmc/articles/PMC6376448/ /pubmed/30624889 http://dx.doi.org/10.1021/acsami.8b16226 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Mai, Binh T. Balakrishnan, Preethi B. Barthel, Markus J. Piccardi, Federica Niculaes, Dina Marinaro, Federica Fernandes, Soraia Curcio, Alberto Kakwere, Hamilton Autret, Gwennhael Cingolani, Roberto Gazeau, Florence Pellegrino, Teresa Thermoresponsive Iron Oxide Nanocubes for an Effective Clinical Translation of Magnetic Hyperthermia and Heat-Mediated Chemotherapy |
title | Thermoresponsive
Iron Oxide Nanocubes for an Effective
Clinical Translation of Magnetic Hyperthermia and Heat-Mediated Chemotherapy |
title_full | Thermoresponsive
Iron Oxide Nanocubes for an Effective
Clinical Translation of Magnetic Hyperthermia and Heat-Mediated Chemotherapy |
title_fullStr | Thermoresponsive
Iron Oxide Nanocubes for an Effective
Clinical Translation of Magnetic Hyperthermia and Heat-Mediated Chemotherapy |
title_full_unstemmed | Thermoresponsive
Iron Oxide Nanocubes for an Effective
Clinical Translation of Magnetic Hyperthermia and Heat-Mediated Chemotherapy |
title_short | Thermoresponsive
Iron Oxide Nanocubes for an Effective
Clinical Translation of Magnetic Hyperthermia and Heat-Mediated Chemotherapy |
title_sort | thermoresponsive
iron oxide nanocubes for an effective
clinical translation of magnetic hyperthermia and heat-mediated chemotherapy |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6376448/ https://www.ncbi.nlm.nih.gov/pubmed/30624889 http://dx.doi.org/10.1021/acsami.8b16226 |
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