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The efficiency of magnetic hyperthermia and in vivo histocompatibility for human-like collagen protein-coated magnetic nanoparticles

Magnetic hyperthermia is a promising technique for the minimally invasive elimination of solid tumors. In this study, uniform magnetite nanoparticles (MNPs) with different particle sizes were used as a model system to investigate the size and surface effects of human-like collagen protein-coated MNP...

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Autores principales: Chang, Le, Liu, Xiao Li, Di Fan, Dai, Miao, Yu Qing, Zhang, Huan, Ma, He Ping, Liu, Qiu Ying, Ma, Pei, Xue, Wei Ming, Luo, Yan E, Fan, Hai Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4809344/
https://www.ncbi.nlm.nih.gov/pubmed/27042065
http://dx.doi.org/10.2147/IJN.S101741
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author Chang, Le
Liu, Xiao Li
Di Fan, Dai
Miao, Yu Qing
Zhang, Huan
Ma, He Ping
Liu, Qiu Ying
Ma, Pei
Xue, Wei Ming
Luo, Yan E
Fan, Hai Ming
author_facet Chang, Le
Liu, Xiao Li
Di Fan, Dai
Miao, Yu Qing
Zhang, Huan
Ma, He Ping
Liu, Qiu Ying
Ma, Pei
Xue, Wei Ming
Luo, Yan E
Fan, Hai Ming
author_sort Chang, Le
collection PubMed
description Magnetic hyperthermia is a promising technique for the minimally invasive elimination of solid tumors. In this study, uniform magnetite nanoparticles (MNPs) with different particle sizes were used as a model system to investigate the size and surface effects of human-like collagen protein-coated MNPs (HLC-MNPs) on specific absorption rate and biocompatibility. It was found that these HLC-MNPs possess rapid heating capacity upon alternating magnetic field exposure compared to that of MNPs without HLC coating, irrespective of the size of MNPs. The significant enhancement of specific absorption rate is favorable for larger sized nanoparticles. Such behavior is attributed to the reduced aggregation and increased stability of the HLC-MNPs. By coating HLC on the surface of certain sized MNPs, a significant increase in cell viability (up to 2.5-fold) can be achieved. After subcutaneous injection of HLC-MNPs into the back of Kunming mice, it was observed that the inflammatory reaction hardly occurred in the injection site. However, there was a significant presence of phagocytes and endocytosis after the injection of nonconjugated counterparts. The overall strategy to fabricate HLC-MNPs can serve as a general guideline to address the current challenges in clinical magnetic hyperthermia, improved biocompatibility, and enhanced heating characteristics through protein coating.
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spelling pubmed-48093442016-04-01 The efficiency of magnetic hyperthermia and in vivo histocompatibility for human-like collagen protein-coated magnetic nanoparticles Chang, Le Liu, Xiao Li Di Fan, Dai Miao, Yu Qing Zhang, Huan Ma, He Ping Liu, Qiu Ying Ma, Pei Xue, Wei Ming Luo, Yan E Fan, Hai Ming Int J Nanomedicine Original Research Magnetic hyperthermia is a promising technique for the minimally invasive elimination of solid tumors. In this study, uniform magnetite nanoparticles (MNPs) with different particle sizes were used as a model system to investigate the size and surface effects of human-like collagen protein-coated MNPs (HLC-MNPs) on specific absorption rate and biocompatibility. It was found that these HLC-MNPs possess rapid heating capacity upon alternating magnetic field exposure compared to that of MNPs without HLC coating, irrespective of the size of MNPs. The significant enhancement of specific absorption rate is favorable for larger sized nanoparticles. Such behavior is attributed to the reduced aggregation and increased stability of the HLC-MNPs. By coating HLC on the surface of certain sized MNPs, a significant increase in cell viability (up to 2.5-fold) can be achieved. After subcutaneous injection of HLC-MNPs into the back of Kunming mice, it was observed that the inflammatory reaction hardly occurred in the injection site. However, there was a significant presence of phagocytes and endocytosis after the injection of nonconjugated counterparts. The overall strategy to fabricate HLC-MNPs can serve as a general guideline to address the current challenges in clinical magnetic hyperthermia, improved biocompatibility, and enhanced heating characteristics through protein coating. Dove Medical Press 2016-03-23 /pmc/articles/PMC4809344/ /pubmed/27042065 http://dx.doi.org/10.2147/IJN.S101741 Text en © 2016 Chang 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
Chang, Le
Liu, Xiao Li
Di Fan, Dai
Miao, Yu Qing
Zhang, Huan
Ma, He Ping
Liu, Qiu Ying
Ma, Pei
Xue, Wei Ming
Luo, Yan E
Fan, Hai Ming
The efficiency of magnetic hyperthermia and in vivo histocompatibility for human-like collagen protein-coated magnetic nanoparticles
title The efficiency of magnetic hyperthermia and in vivo histocompatibility for human-like collagen protein-coated magnetic nanoparticles
title_full The efficiency of magnetic hyperthermia and in vivo histocompatibility for human-like collagen protein-coated magnetic nanoparticles
title_fullStr The efficiency of magnetic hyperthermia and in vivo histocompatibility for human-like collagen protein-coated magnetic nanoparticles
title_full_unstemmed The efficiency of magnetic hyperthermia and in vivo histocompatibility for human-like collagen protein-coated magnetic nanoparticles
title_short The efficiency of magnetic hyperthermia and in vivo histocompatibility for human-like collagen protein-coated magnetic nanoparticles
title_sort efficiency of magnetic hyperthermia and in vivo histocompatibility for human-like collagen protein-coated magnetic nanoparticles
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4809344/
https://www.ncbi.nlm.nih.gov/pubmed/27042065
http://dx.doi.org/10.2147/IJN.S101741
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