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Tumor-targeted Gd-doped mesoporous Fe(3)O(4) nanoparticles for T(1)/T(2) MR imaging guided synergistic cancer therapy

In this study, a novel intelligent nanoplatform to integrate multiple imaging and therapeutic functions for targeted cancer theranostics. The nanoplatform, DOX@Gd-MFe(3)O(4) NPs, was constructed Gd-doped mesoporous Fe(3)O(4) nanoparticles following with the doxorubicin (DOX) loading in the mesopores...

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Autores principales: Zheng, Shaohui, Jin, Shang, Jiao, Min, Wang, Wenjun, Zhou, Xiaoyu, Xu, Jie, Wang, Yong, Dou, Peipei, Jin, Zhen, Wu, Changyu, Li, Jingjing, Ge, Xinting, Xu, Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079076/
https://www.ncbi.nlm.nih.gov/pubmed/33866915
http://dx.doi.org/10.1080/10717544.2021.1909177
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author Zheng, Shaohui
Jin, Shang
Jiao, Min
Wang, Wenjun
Zhou, Xiaoyu
Xu, Jie
Wang, Yong
Dou, Peipei
Jin, Zhen
Wu, Changyu
Li, Jingjing
Ge, Xinting
Xu, Kai
author_facet Zheng, Shaohui
Jin, Shang
Jiao, Min
Wang, Wenjun
Zhou, Xiaoyu
Xu, Jie
Wang, Yong
Dou, Peipei
Jin, Zhen
Wu, Changyu
Li, Jingjing
Ge, Xinting
Xu, Kai
author_sort Zheng, Shaohui
collection PubMed
description In this study, a novel intelligent nanoplatform to integrate multiple imaging and therapeutic functions for targeted cancer theranostics. The nanoplatform, DOX@Gd-MFe(3)O(4) NPs, was constructed Gd-doped mesoporous Fe(3)O(4) nanoparticles following with the doxorubicin (DOX) loading in the mesopores of the NPs. The DOX@Gd-MFe(3)O(4) NPs exhibited good properties in colloidal dispersity, photothermal conversion, NIR triggered drug release, and high T(1)/T(2) relaxicity rate (r(1)=9.64 mM(−1)s(−1), r(2)= 177.71 mM(−1)s(−1)). Benefiting from the high MR contrast, DOX@Gd-MFe(3)O(4) NPs enabled simultaneous T(1)/T(2) dual-modal MR imagining on 4T1 bearing mice in vivo and the MR contrast effect was further strengthened by external magnetic field. In addition, the DOX@Gd-MFe(3)O(4) NPs revealed the strongest inhibition to the growth of 4T1 in vitro and in vivo under NIR irradiation and guidance of external magnetic field. Moreover, biosafety was also validated by in vitro and in vivo tests. Thus, the prepared DOX@Gd-MFe(3)O(4) NPs would provide a promising intelligent nanoplatform for dual-modal MR imagining guided synergistic therapy in cancer theranostics.
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spelling pubmed-80790762021-05-06 Tumor-targeted Gd-doped mesoporous Fe(3)O(4) nanoparticles for T(1)/T(2) MR imaging guided synergistic cancer therapy Zheng, Shaohui Jin, Shang Jiao, Min Wang, Wenjun Zhou, Xiaoyu Xu, Jie Wang, Yong Dou, Peipei Jin, Zhen Wu, Changyu Li, Jingjing Ge, Xinting Xu, Kai Drug Deliv Research Article In this study, a novel intelligent nanoplatform to integrate multiple imaging and therapeutic functions for targeted cancer theranostics. The nanoplatform, DOX@Gd-MFe(3)O(4) NPs, was constructed Gd-doped mesoporous Fe(3)O(4) nanoparticles following with the doxorubicin (DOX) loading in the mesopores of the NPs. The DOX@Gd-MFe(3)O(4) NPs exhibited good properties in colloidal dispersity, photothermal conversion, NIR triggered drug release, and high T(1)/T(2) relaxicity rate (r(1)=9.64 mM(−1)s(−1), r(2)= 177.71 mM(−1)s(−1)). Benefiting from the high MR contrast, DOX@Gd-MFe(3)O(4) NPs enabled simultaneous T(1)/T(2) dual-modal MR imagining on 4T1 bearing mice in vivo and the MR contrast effect was further strengthened by external magnetic field. In addition, the DOX@Gd-MFe(3)O(4) NPs revealed the strongest inhibition to the growth of 4T1 in vitro and in vivo under NIR irradiation and guidance of external magnetic field. Moreover, biosafety was also validated by in vitro and in vivo tests. Thus, the prepared DOX@Gd-MFe(3)O(4) NPs would provide a promising intelligent nanoplatform for dual-modal MR imagining guided synergistic therapy in cancer theranostics. Taylor & Francis 2021-04-19 /pmc/articles/PMC8079076/ /pubmed/33866915 http://dx.doi.org/10.1080/10717544.2021.1909177 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zheng, Shaohui
Jin, Shang
Jiao, Min
Wang, Wenjun
Zhou, Xiaoyu
Xu, Jie
Wang, Yong
Dou, Peipei
Jin, Zhen
Wu, Changyu
Li, Jingjing
Ge, Xinting
Xu, Kai
Tumor-targeted Gd-doped mesoporous Fe(3)O(4) nanoparticles for T(1)/T(2) MR imaging guided synergistic cancer therapy
title Tumor-targeted Gd-doped mesoporous Fe(3)O(4) nanoparticles for T(1)/T(2) MR imaging guided synergistic cancer therapy
title_full Tumor-targeted Gd-doped mesoporous Fe(3)O(4) nanoparticles for T(1)/T(2) MR imaging guided synergistic cancer therapy
title_fullStr Tumor-targeted Gd-doped mesoporous Fe(3)O(4) nanoparticles for T(1)/T(2) MR imaging guided synergistic cancer therapy
title_full_unstemmed Tumor-targeted Gd-doped mesoporous Fe(3)O(4) nanoparticles for T(1)/T(2) MR imaging guided synergistic cancer therapy
title_short Tumor-targeted Gd-doped mesoporous Fe(3)O(4) nanoparticles for T(1)/T(2) MR imaging guided synergistic cancer therapy
title_sort tumor-targeted gd-doped mesoporous fe(3)o(4) nanoparticles for t(1)/t(2) mr imaging guided synergistic cancer therapy
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8079076/
https://www.ncbi.nlm.nih.gov/pubmed/33866915
http://dx.doi.org/10.1080/10717544.2021.1909177
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