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Effective heating of magnetic nanoparticle aggregates for in vivo nano-theranostic hyperthermia
Magnetic resonance (MR) nano-theranostic hyperthermia uses magnetic nanoparticles to target and accumulate at the lesions and generate heat to kill lesion cells directly through hyperthermia or indirectly through thermal activation and control releasing of drugs. Preclinical and translational applic...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584909/ https://www.ncbi.nlm.nih.gov/pubmed/28894366 http://dx.doi.org/10.2147/IJN.S141072 |
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author | Wang, Chencai Hsu, Chao-Hsiung Li, Zhao Hwang, Lian-Pin Lin, Ying-Chih Chou, Pi-Tai Lin, Yung-Ya |
author_facet | Wang, Chencai Hsu, Chao-Hsiung Li, Zhao Hwang, Lian-Pin Lin, Ying-Chih Chou, Pi-Tai Lin, Yung-Ya |
author_sort | Wang, Chencai |
collection | PubMed |
description | Magnetic resonance (MR) nano-theranostic hyperthermia uses magnetic nanoparticles to target and accumulate at the lesions and generate heat to kill lesion cells directly through hyperthermia or indirectly through thermal activation and control releasing of drugs. Preclinical and translational applications of MR nano-theranostic hyperthermia are currently limited by a few major theoretical difficulties and experimental challenges in in vivo conditions. For example, conventional models for estimating the heat generated and the optimal magnetic nanoparticle sizes for hyperthermia do not accurately reproduce reported in vivo experimental results. In this work, a revised cluster-based model was proposed to predict the specific loss power (SLP) by explicitly considering magnetic nanoparticle aggregation in in vivo conditions. By comparing with the reported experimental results of magnetite Fe(3)O(4) and cobalt ferrite CoFe(2)O(4) magnetic nanoparticles, it is shown that the revised cluster-based model provides a more accurate prediction of the experimental values than the conventional models that assume magnetic nanoparticles act as single units. It also provides a clear physical picture: the aggregation of magnetic nanoparticles increases the cluster magnetic anisotropy while reducing both the cluster domain magnetization and the average magnetic moment, which, in turn, shift the predicted SLP toward a smaller magnetic nanoparticle diameter with lower peak values. As a result, the heating efficiency and the SLP values are decreased. The improvement in the prediction accuracy in in vivo conditions is particularly pronounced when the magnetic nanoparticle diameter is in the range of ~10–20 nm. This happens to be an important size range for MR cancer nano-theranostics, as it exhibits the highest efficacy against both primary and metastatic tumors in vivo. Our studies show that a relatively 20%–25% smaller magnetic nanoparticle diameter should be chosen to reach the maximal heating efficiency in comparison with the optimal size predicted by previous models. |
format | Online Article Text |
id | pubmed-5584909 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55849092017-09-11 Effective heating of magnetic nanoparticle aggregates for in vivo nano-theranostic hyperthermia Wang, Chencai Hsu, Chao-Hsiung Li, Zhao Hwang, Lian-Pin Lin, Ying-Chih Chou, Pi-Tai Lin, Yung-Ya Int J Nanomedicine Original Research Magnetic resonance (MR) nano-theranostic hyperthermia uses magnetic nanoparticles to target and accumulate at the lesions and generate heat to kill lesion cells directly through hyperthermia or indirectly through thermal activation and control releasing of drugs. Preclinical and translational applications of MR nano-theranostic hyperthermia are currently limited by a few major theoretical difficulties and experimental challenges in in vivo conditions. For example, conventional models for estimating the heat generated and the optimal magnetic nanoparticle sizes for hyperthermia do not accurately reproduce reported in vivo experimental results. In this work, a revised cluster-based model was proposed to predict the specific loss power (SLP) by explicitly considering magnetic nanoparticle aggregation in in vivo conditions. By comparing with the reported experimental results of magnetite Fe(3)O(4) and cobalt ferrite CoFe(2)O(4) magnetic nanoparticles, it is shown that the revised cluster-based model provides a more accurate prediction of the experimental values than the conventional models that assume magnetic nanoparticles act as single units. It also provides a clear physical picture: the aggregation of magnetic nanoparticles increases the cluster magnetic anisotropy while reducing both the cluster domain magnetization and the average magnetic moment, which, in turn, shift the predicted SLP toward a smaller magnetic nanoparticle diameter with lower peak values. As a result, the heating efficiency and the SLP values are decreased. The improvement in the prediction accuracy in in vivo conditions is particularly pronounced when the magnetic nanoparticle diameter is in the range of ~10–20 nm. This happens to be an important size range for MR cancer nano-theranostics, as it exhibits the highest efficacy against both primary and metastatic tumors in vivo. Our studies show that a relatively 20%–25% smaller magnetic nanoparticle diameter should be chosen to reach the maximal heating efficiency in comparison with the optimal size predicted by previous models. Dove Medical Press 2017-08-28 /pmc/articles/PMC5584909/ /pubmed/28894366 http://dx.doi.org/10.2147/IJN.S141072 Text en © 2017 Wang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Wang, Chencai Hsu, Chao-Hsiung Li, Zhao Hwang, Lian-Pin Lin, Ying-Chih Chou, Pi-Tai Lin, Yung-Ya Effective heating of magnetic nanoparticle aggregates for in vivo nano-theranostic hyperthermia |
title | Effective heating of magnetic nanoparticle aggregates for in vivo nano-theranostic hyperthermia |
title_full | Effective heating of magnetic nanoparticle aggregates for in vivo nano-theranostic hyperthermia |
title_fullStr | Effective heating of magnetic nanoparticle aggregates for in vivo nano-theranostic hyperthermia |
title_full_unstemmed | Effective heating of magnetic nanoparticle aggregates for in vivo nano-theranostic hyperthermia |
title_short | Effective heating of magnetic nanoparticle aggregates for in vivo nano-theranostic hyperthermia |
title_sort | effective heating of magnetic nanoparticle aggregates for in vivo nano-theranostic hyperthermia |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5584909/ https://www.ncbi.nlm.nih.gov/pubmed/28894366 http://dx.doi.org/10.2147/IJN.S141072 |
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