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A Nanomedicine Fabricated from Gold Nanoparticles‐Decorated Metal–Organic Framework for Cascade Chemo/Chemodynamic Cancer Therapy

The incorporation of new modalities into chemotherapy greatly enhances the anticancer efficacy combining the merits of each treatment, showing promising potentials in clinical translations. Herein, a hybrid nanomedicine (Au/FeMOF@CPT NPs) is fabricated using metal–organic framework (MOF) nanoparticl...

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Autores principales: Ding, Yuan, Xu, Hao, Xu, Chang, Tong, Zongrui, Zhang, Sitong, Bai, Yang, Chen, Yining, Xu, Qianhui, Zhou, Liuzhi, Ding, Hao, Sun, Zhongquan, Yan, Sheng, Mao, Zhengwei, Wang, Weilin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507500/
https://www.ncbi.nlm.nih.gov/pubmed/32995124
http://dx.doi.org/10.1002/advs.202001060
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author Ding, Yuan
Xu, Hao
Xu, Chang
Tong, Zongrui
Zhang, Sitong
Bai, Yang
Chen, Yining
Xu, Qianhui
Zhou, Liuzhi
Ding, Hao
Sun, Zhongquan
Yan, Sheng
Mao, Zhengwei
Wang, Weilin
author_facet Ding, Yuan
Xu, Hao
Xu, Chang
Tong, Zongrui
Zhang, Sitong
Bai, Yang
Chen, Yining
Xu, Qianhui
Zhou, Liuzhi
Ding, Hao
Sun, Zhongquan
Yan, Sheng
Mao, Zhengwei
Wang, Weilin
author_sort Ding, Yuan
collection PubMed
description The incorporation of new modalities into chemotherapy greatly enhances the anticancer efficacy combining the merits of each treatment, showing promising potentials in clinical translations. Herein, a hybrid nanomedicine (Au/FeMOF@CPT NPs) is fabricated using metal–organic framework (MOF) nanoparticles and gold nanoparticles (Au NPs) as building blocks for cancer chemo/chemodynamic therapy. MOF NPs are used as vehicles to encapsulate camptothecin (CPT), and the hybridization by Au NPs greatly improves the stability of the nanomedicine in a physiological environment. Triggered by the high concentration of phosphate inside the cancer cells, Au/FeMOF@CPT NPs effectively collapse after internalization, resulting in the complete drug release and activation of the cascade catalytic reactions. The intracellular glucose can be oxidized by Au NPs to produce hydrogen dioxide, which is further utilized as chemical fuel for the Fenton reaction, thus realizing the synergistic anticancer efficacy. Benefitting from the enhanced permeability and retention effect and sophisticated fabrications, the blood circulation time and tumor accumulation of Au/FeMOF@CPT NPs are significantly increased. In vivo results demonstrate that the combination of chemotherapy and chemodynamic therapy effectively suppresses the tumor growth, meantime the systemic toxicity of this nanomedicine is greatly avoided.
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spelling pubmed-75075002020-09-28 A Nanomedicine Fabricated from Gold Nanoparticles‐Decorated Metal–Organic Framework for Cascade Chemo/Chemodynamic Cancer Therapy Ding, Yuan Xu, Hao Xu, Chang Tong, Zongrui Zhang, Sitong Bai, Yang Chen, Yining Xu, Qianhui Zhou, Liuzhi Ding, Hao Sun, Zhongquan Yan, Sheng Mao, Zhengwei Wang, Weilin Adv Sci (Weinh) Communications The incorporation of new modalities into chemotherapy greatly enhances the anticancer efficacy combining the merits of each treatment, showing promising potentials in clinical translations. Herein, a hybrid nanomedicine (Au/FeMOF@CPT NPs) is fabricated using metal–organic framework (MOF) nanoparticles and gold nanoparticles (Au NPs) as building blocks for cancer chemo/chemodynamic therapy. MOF NPs are used as vehicles to encapsulate camptothecin (CPT), and the hybridization by Au NPs greatly improves the stability of the nanomedicine in a physiological environment. Triggered by the high concentration of phosphate inside the cancer cells, Au/FeMOF@CPT NPs effectively collapse after internalization, resulting in the complete drug release and activation of the cascade catalytic reactions. The intracellular glucose can be oxidized by Au NPs to produce hydrogen dioxide, which is further utilized as chemical fuel for the Fenton reaction, thus realizing the synergistic anticancer efficacy. Benefitting from the enhanced permeability and retention effect and sophisticated fabrications, the blood circulation time and tumor accumulation of Au/FeMOF@CPT NPs are significantly increased. In vivo results demonstrate that the combination of chemotherapy and chemodynamic therapy effectively suppresses the tumor growth, meantime the systemic toxicity of this nanomedicine is greatly avoided. John Wiley and Sons Inc. 2020-06-14 /pmc/articles/PMC7507500/ /pubmed/32995124 http://dx.doi.org/10.1002/advs.202001060 Text en © 2020 The Authors. Published by WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Communications
Ding, Yuan
Xu, Hao
Xu, Chang
Tong, Zongrui
Zhang, Sitong
Bai, Yang
Chen, Yining
Xu, Qianhui
Zhou, Liuzhi
Ding, Hao
Sun, Zhongquan
Yan, Sheng
Mao, Zhengwei
Wang, Weilin
A Nanomedicine Fabricated from Gold Nanoparticles‐Decorated Metal–Organic Framework for Cascade Chemo/Chemodynamic Cancer Therapy
title A Nanomedicine Fabricated from Gold Nanoparticles‐Decorated Metal–Organic Framework for Cascade Chemo/Chemodynamic Cancer Therapy
title_full A Nanomedicine Fabricated from Gold Nanoparticles‐Decorated Metal–Organic Framework for Cascade Chemo/Chemodynamic Cancer Therapy
title_fullStr A Nanomedicine Fabricated from Gold Nanoparticles‐Decorated Metal–Organic Framework for Cascade Chemo/Chemodynamic Cancer Therapy
title_full_unstemmed A Nanomedicine Fabricated from Gold Nanoparticles‐Decorated Metal–Organic Framework for Cascade Chemo/Chemodynamic Cancer Therapy
title_short A Nanomedicine Fabricated from Gold Nanoparticles‐Decorated Metal–Organic Framework for Cascade Chemo/Chemodynamic Cancer Therapy
title_sort nanomedicine fabricated from gold nanoparticles‐decorated metal–organic framework for cascade chemo/chemodynamic cancer therapy
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7507500/
https://www.ncbi.nlm.nih.gov/pubmed/32995124
http://dx.doi.org/10.1002/advs.202001060
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