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Biodegradable 2D Fe–Al Hydroxide for Nanocatalytic Tumor‐Dynamic Therapy with Tumor Specificity
Therapeutic nanocatalysis has emerged as an intriguing strategy for efficient cancer‐specific therapy, but the traditional inorganic nanocatalysts suffer from low catalytic efficiency and difficulty in biodegradation, hindering their further clinical translation. Herein, a tumor microenvironment‐tri...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6247031/ https://www.ncbi.nlm.nih.gov/pubmed/30479938 http://dx.doi.org/10.1002/advs.201801155 |
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author | Cao, Zhenbang Zhang, Liang Liang, Kang Cheong, Soshan Boyer, Cyrille Gooding, J. Justin Chen, Yu Gu, Zi |
author_facet | Cao, Zhenbang Zhang, Liang Liang, Kang Cheong, Soshan Boyer, Cyrille Gooding, J. Justin Chen, Yu Gu, Zi |
author_sort | Cao, Zhenbang |
collection | PubMed |
description | Therapeutic nanocatalysis has emerged as an intriguing strategy for efficient cancer‐specific therapy, but the traditional inorganic nanocatalysts suffer from low catalytic efficiency and difficulty in biodegradation, hindering their further clinical translation. Herein, a tumor microenvironment‐triggered, biodegradable and biocompatible nanocatalyst employing 2D hydroxide nanosheet is presented, and is shown to have high catalytic capacity to efficiently produce abundant hydroxyl radicals under the tumor microenvironment and consequently kill tumor cells selectively. A polyethylene glycol (PEG)‐conjugated Fe(2+)‐containing hydroxide nanosheet is successfully constructed via a facile but efficient bottom‐up approach that concurrently realizes nanosheet synthesis and PEGylation. Importantly, the nanosheets are featured with high catalytic activity to disproportionate H(2)O(2) in tumors, and consequently generate abundant hydroxyl radicals at a high reaction rate under tumorous acidic condition; the highly toxic hydroxyl radicals, as a result, cause the death of tumor cells in vitro and suppress the tumor growth in vivo without the use of any supplementary toxic agent, only with the biocompatible nanocatalysts. Meanwhile, the desirable biodegradation and biocompatibility of the hydroxide nanosheet render a high degree of safety to the organism. Therefore, this work provides the first paradigm of biodegradable 2D nanocatalytic platform with concurrently high catalytic‐therapeutic performance and biosafety for efficient tumor‐specific treatment. |
format | Online Article Text |
id | pubmed-6247031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62470312018-11-26 Biodegradable 2D Fe–Al Hydroxide for Nanocatalytic Tumor‐Dynamic Therapy with Tumor Specificity Cao, Zhenbang Zhang, Liang Liang, Kang Cheong, Soshan Boyer, Cyrille Gooding, J. Justin Chen, Yu Gu, Zi Adv Sci (Weinh) Communications Therapeutic nanocatalysis has emerged as an intriguing strategy for efficient cancer‐specific therapy, but the traditional inorganic nanocatalysts suffer from low catalytic efficiency and difficulty in biodegradation, hindering their further clinical translation. Herein, a tumor microenvironment‐triggered, biodegradable and biocompatible nanocatalyst employing 2D hydroxide nanosheet is presented, and is shown to have high catalytic capacity to efficiently produce abundant hydroxyl radicals under the tumor microenvironment and consequently kill tumor cells selectively. A polyethylene glycol (PEG)‐conjugated Fe(2+)‐containing hydroxide nanosheet is successfully constructed via a facile but efficient bottom‐up approach that concurrently realizes nanosheet synthesis and PEGylation. Importantly, the nanosheets are featured with high catalytic activity to disproportionate H(2)O(2) in tumors, and consequently generate abundant hydroxyl radicals at a high reaction rate under tumorous acidic condition; the highly toxic hydroxyl radicals, as a result, cause the death of tumor cells in vitro and suppress the tumor growth in vivo without the use of any supplementary toxic agent, only with the biocompatible nanocatalysts. Meanwhile, the desirable biodegradation and biocompatibility of the hydroxide nanosheet render a high degree of safety to the organism. Therefore, this work provides the first paradigm of biodegradable 2D nanocatalytic platform with concurrently high catalytic‐therapeutic performance and biosafety for efficient tumor‐specific treatment. John Wiley and Sons Inc. 2018-10-09 /pmc/articles/PMC6247031/ /pubmed/30479938 http://dx.doi.org/10.1002/advs.201801155 Text en © 2018 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 Cao, Zhenbang Zhang, Liang Liang, Kang Cheong, Soshan Boyer, Cyrille Gooding, J. Justin Chen, Yu Gu, Zi Biodegradable 2D Fe–Al Hydroxide for Nanocatalytic Tumor‐Dynamic Therapy with Tumor Specificity |
title | Biodegradable 2D Fe–Al Hydroxide for Nanocatalytic Tumor‐Dynamic Therapy with Tumor Specificity |
title_full | Biodegradable 2D Fe–Al Hydroxide for Nanocatalytic Tumor‐Dynamic Therapy with Tumor Specificity |
title_fullStr | Biodegradable 2D Fe–Al Hydroxide for Nanocatalytic Tumor‐Dynamic Therapy with Tumor Specificity |
title_full_unstemmed | Biodegradable 2D Fe–Al Hydroxide for Nanocatalytic Tumor‐Dynamic Therapy with Tumor Specificity |
title_short | Biodegradable 2D Fe–Al Hydroxide for Nanocatalytic Tumor‐Dynamic Therapy with Tumor Specificity |
title_sort | biodegradable 2d fe–al hydroxide for nanocatalytic tumor‐dynamic therapy with tumor specificity |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6247031/ https://www.ncbi.nlm.nih.gov/pubmed/30479938 http://dx.doi.org/10.1002/advs.201801155 |
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