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The cell uptake properties and hyperthermia performance of Zn(0.5)Fe(2.5)O(4)/SiO(2) nanoparticles as magnetic hyperthermia agents

Zn(0.5)Fe(2.5)O(4) nanoparticles (NPs) of 22 nm are synthesized by a one-pot approach and coated with silica for magnetic hyperthermia agents. The NPs exhibit superparamagnetic characteristics, high-specific absorption rate (SAR) (1083 wg(−1), f = 430 kHz, H = 27 kAm(−1)), large saturation magnetiza...

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Detalles Bibliográficos
Autores principales: Wang, Runsheng, Liu, Jianheng, Liu, Yihao, Zhong, Rui, Yu, Xiang, Liu, Qingzu, Zhang, Li, Lv, Chenhui, Mao, Keya, Tang, Peifu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029910/
https://www.ncbi.nlm.nih.gov/pubmed/32218945
http://dx.doi.org/10.1098/rsos.191139
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author Wang, Runsheng
Liu, Jianheng
Liu, Yihao
Zhong, Rui
Yu, Xiang
Liu, Qingzu
Zhang, Li
Lv, Chenhui
Mao, Keya
Tang, Peifu
author_facet Wang, Runsheng
Liu, Jianheng
Liu, Yihao
Zhong, Rui
Yu, Xiang
Liu, Qingzu
Zhang, Li
Lv, Chenhui
Mao, Keya
Tang, Peifu
author_sort Wang, Runsheng
collection PubMed
description Zn(0.5)Fe(2.5)O(4) nanoparticles (NPs) of 22 nm are synthesized by a one-pot approach and coated with silica for magnetic hyperthermia agents. The NPs exhibit superparamagnetic characteristics, high-specific absorption rate (SAR) (1083 wg(−1), f = 430 kHz, H = 27 kAm(−1)), large saturation magnetization (M(s) = 85 emu g(−1)), excellent colloidal stability and low cytotoxicity. The cell uptake properties have been investigated by Prussian blue staining, transmission electron microscopy and the inductively coupled plasma-mass spectrometer, which resulted in time-dependent and concentration-dependent internalization. The internalization appeared between 0.5 and 2 h, the NPs were mainly located in the lysosomes and kept in good dispersion after incubation with human osteosarcoma MG-63 cells. Then, the relationship between cell uptake and magnetic hyperthermia performance was studied. Our results show that the hyperthermia efficiency was related to the amount of internalized NPs in the tumour cells, which was dependent on the concentration and incubation time. Interestingly, the NPs could still induce tumour cells to apoptosis/necrosis when extracellular NPs were rinsed, but the cell kill efficiency was lower than that of any rinse group, which indicated that local temperature rise was the main factor that induced tumour cells to death. Our findings suggest that this high SAR and biocompatible silica-coated Zn(0.5)Fe(2.)O(4) NPs could serve as new agents for magnetic hyperthermia.
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spelling pubmed-70299102020-03-26 The cell uptake properties and hyperthermia performance of Zn(0.5)Fe(2.5)O(4)/SiO(2) nanoparticles as magnetic hyperthermia agents Wang, Runsheng Liu, Jianheng Liu, Yihao Zhong, Rui Yu, Xiang Liu, Qingzu Zhang, Li Lv, Chenhui Mao, Keya Tang, Peifu R Soc Open Sci Physics and Biophysics Zn(0.5)Fe(2.5)O(4) nanoparticles (NPs) of 22 nm are synthesized by a one-pot approach and coated with silica for magnetic hyperthermia agents. The NPs exhibit superparamagnetic characteristics, high-specific absorption rate (SAR) (1083 wg(−1), f = 430 kHz, H = 27 kAm(−1)), large saturation magnetization (M(s) = 85 emu g(−1)), excellent colloidal stability and low cytotoxicity. The cell uptake properties have been investigated by Prussian blue staining, transmission electron microscopy and the inductively coupled plasma-mass spectrometer, which resulted in time-dependent and concentration-dependent internalization. The internalization appeared between 0.5 and 2 h, the NPs were mainly located in the lysosomes and kept in good dispersion after incubation with human osteosarcoma MG-63 cells. Then, the relationship between cell uptake and magnetic hyperthermia performance was studied. Our results show that the hyperthermia efficiency was related to the amount of internalized NPs in the tumour cells, which was dependent on the concentration and incubation time. Interestingly, the NPs could still induce tumour cells to apoptosis/necrosis when extracellular NPs were rinsed, but the cell kill efficiency was lower than that of any rinse group, which indicated that local temperature rise was the main factor that induced tumour cells to death. Our findings suggest that this high SAR and biocompatible silica-coated Zn(0.5)Fe(2.)O(4) NPs could serve as new agents for magnetic hyperthermia. The Royal Society 2020-01-15 /pmc/articles/PMC7029910/ /pubmed/32218945 http://dx.doi.org/10.1098/rsos.191139 Text en © 2020 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Physics and Biophysics
Wang, Runsheng
Liu, Jianheng
Liu, Yihao
Zhong, Rui
Yu, Xiang
Liu, Qingzu
Zhang, Li
Lv, Chenhui
Mao, Keya
Tang, Peifu
The cell uptake properties and hyperthermia performance of Zn(0.5)Fe(2.5)O(4)/SiO(2) nanoparticles as magnetic hyperthermia agents
title The cell uptake properties and hyperthermia performance of Zn(0.5)Fe(2.5)O(4)/SiO(2) nanoparticles as magnetic hyperthermia agents
title_full The cell uptake properties and hyperthermia performance of Zn(0.5)Fe(2.5)O(4)/SiO(2) nanoparticles as magnetic hyperthermia agents
title_fullStr The cell uptake properties and hyperthermia performance of Zn(0.5)Fe(2.5)O(4)/SiO(2) nanoparticles as magnetic hyperthermia agents
title_full_unstemmed The cell uptake properties and hyperthermia performance of Zn(0.5)Fe(2.5)O(4)/SiO(2) nanoparticles as magnetic hyperthermia agents
title_short The cell uptake properties and hyperthermia performance of Zn(0.5)Fe(2.5)O(4)/SiO(2) nanoparticles as magnetic hyperthermia agents
title_sort cell uptake properties and hyperthermia performance of zn(0.5)fe(2.5)o(4)/sio(2) nanoparticles as magnetic hyperthermia agents
topic Physics and Biophysics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029910/
https://www.ncbi.nlm.nih.gov/pubmed/32218945
http://dx.doi.org/10.1098/rsos.191139
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