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Achieving NIR Light-Mediated Tumor-Specific Fenton Reaction-Assisted Oncotherapy by Using Magnetic Nanoclusters

As an emerging strategy for oncotherapy, Fenton chemistry can efficiently improve the conversion from endogenous H(2)O(2) into highly toxic ·OH in the whole high-performance therapeutic process. Although promising, the efficiency of Fenton reaction in tumor regions is highly limited by the inefficie...

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Autores principales: Qin, Shaoyou, Xue, Jinru, Jia, Erna, Ren, Na, Dong, Yongqiang, Zhou, Changyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8573244/
https://www.ncbi.nlm.nih.gov/pubmed/34760710
http://dx.doi.org/10.3389/fonc.2021.777295
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author Qin, Shaoyou
Xue, Jinru
Jia, Erna
Ren, Na
Dong, Yongqiang
Zhou, Changyu
author_facet Qin, Shaoyou
Xue, Jinru
Jia, Erna
Ren, Na
Dong, Yongqiang
Zhou, Changyu
author_sort Qin, Shaoyou
collection PubMed
description As an emerging strategy for oncotherapy, Fenton chemistry can efficiently improve the conversion from endogenous H(2)O(2) into highly toxic ·OH in the whole high-performance therapeutic process. Although promising, the efficiency of Fenton reaction in tumor regions is highly limited by the inefficient delivery of Fenton reagents and the restrictive conditions of tumor microenvironment. One promising strategy against the above limitations is to specifically increase the temperature around the tumor regions. In this study, a novel NIR light-mediated tumor-specific nanoplatform based on magnetic iron oxide nanoclusters (MNCs) was rationally designed and well developed for photothermally enhanced Fenton reaction-assisted oncotherapy. MNCs could accumulate into the tumor regions with the help of an external magnet field to enable T(2)-weighted magnetic resonance (MR) imaging of tumors and MR imaging-guided combined antitumor therapy. Our well-prepared MNCs also revealed excellent photothermal effect upon a NIR light irradiation, promising their further important role as a photothermal therapy (PTT) agent. More importantly, heat induced by the PTT of MNCs could accelerate the release of Fe from MNCs and enhance the efficiency of Fenton reaction under H(2)O(2)-enriched acidic tumor microenvironment. Results based on long-term toxicity investigations demonstrated the overall safety of MNCs after intravenous injection. This work therefore introduced a novel nanoplatform based on MNCs that exerted a great antitumor effect via photothermally enhanced tumor-specific Fenton chemistry.
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spelling pubmed-85732442021-11-09 Achieving NIR Light-Mediated Tumor-Specific Fenton Reaction-Assisted Oncotherapy by Using Magnetic Nanoclusters Qin, Shaoyou Xue, Jinru Jia, Erna Ren, Na Dong, Yongqiang Zhou, Changyu Front Oncol Oncology As an emerging strategy for oncotherapy, Fenton chemistry can efficiently improve the conversion from endogenous H(2)O(2) into highly toxic ·OH in the whole high-performance therapeutic process. Although promising, the efficiency of Fenton reaction in tumor regions is highly limited by the inefficient delivery of Fenton reagents and the restrictive conditions of tumor microenvironment. One promising strategy against the above limitations is to specifically increase the temperature around the tumor regions. In this study, a novel NIR light-mediated tumor-specific nanoplatform based on magnetic iron oxide nanoclusters (MNCs) was rationally designed and well developed for photothermally enhanced Fenton reaction-assisted oncotherapy. MNCs could accumulate into the tumor regions with the help of an external magnet field to enable T(2)-weighted magnetic resonance (MR) imaging of tumors and MR imaging-guided combined antitumor therapy. Our well-prepared MNCs also revealed excellent photothermal effect upon a NIR light irradiation, promising their further important role as a photothermal therapy (PTT) agent. More importantly, heat induced by the PTT of MNCs could accelerate the release of Fe from MNCs and enhance the efficiency of Fenton reaction under H(2)O(2)-enriched acidic tumor microenvironment. Results based on long-term toxicity investigations demonstrated the overall safety of MNCs after intravenous injection. This work therefore introduced a novel nanoplatform based on MNCs that exerted a great antitumor effect via photothermally enhanced tumor-specific Fenton chemistry. Frontiers Media S.A. 2021-10-25 /pmc/articles/PMC8573244/ /pubmed/34760710 http://dx.doi.org/10.3389/fonc.2021.777295 Text en Copyright © 2021 Qin, Xue, Jia, Ren, Dong and Zhou https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Qin, Shaoyou
Xue, Jinru
Jia, Erna
Ren, Na
Dong, Yongqiang
Zhou, Changyu
Achieving NIR Light-Mediated Tumor-Specific Fenton Reaction-Assisted Oncotherapy by Using Magnetic Nanoclusters
title Achieving NIR Light-Mediated Tumor-Specific Fenton Reaction-Assisted Oncotherapy by Using Magnetic Nanoclusters
title_full Achieving NIR Light-Mediated Tumor-Specific Fenton Reaction-Assisted Oncotherapy by Using Magnetic Nanoclusters
title_fullStr Achieving NIR Light-Mediated Tumor-Specific Fenton Reaction-Assisted Oncotherapy by Using Magnetic Nanoclusters
title_full_unstemmed Achieving NIR Light-Mediated Tumor-Specific Fenton Reaction-Assisted Oncotherapy by Using Magnetic Nanoclusters
title_short Achieving NIR Light-Mediated Tumor-Specific Fenton Reaction-Assisted Oncotherapy by Using Magnetic Nanoclusters
title_sort achieving nir light-mediated tumor-specific fenton reaction-assisted oncotherapy by using magnetic nanoclusters
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8573244/
https://www.ncbi.nlm.nih.gov/pubmed/34760710
http://dx.doi.org/10.3389/fonc.2021.777295
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