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In vivo guiding nitrogen-doped carbon nanozyme for tumor catalytic therapy
Nanomaterials with intrinsic enzyme-like activities (nanozymes), have been widely used as artificial enzymes in biomedicine. However, how to control their in vivo performance in a target cell is still challenging. Here we report a strategy to coordinate nanozymes to target tumor cells and selectivel...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897348/ https://www.ncbi.nlm.nih.gov/pubmed/29650959 http://dx.doi.org/10.1038/s41467-018-03903-8 |
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author | Fan, Kelong Xi, Juqun Fan, Lei Wang, Peixia Zhu, Chunhua Tang, Yan Xu, Xiangdong Liang, Minmin Jiang, Bing Yan, Xiyun Gao, Lizeng |
author_facet | Fan, Kelong Xi, Juqun Fan, Lei Wang, Peixia Zhu, Chunhua Tang, Yan Xu, Xiangdong Liang, Minmin Jiang, Bing Yan, Xiyun Gao, Lizeng |
author_sort | Fan, Kelong |
collection | PubMed |
description | Nanomaterials with intrinsic enzyme-like activities (nanozymes), have been widely used as artificial enzymes in biomedicine. However, how to control their in vivo performance in a target cell is still challenging. Here we report a strategy to coordinate nanozymes to target tumor cells and selectively perform their activity to destruct tumors. We develop a nanozyme using nitrogen-doped porous carbon nanospheres which possess four enzyme-like activities (oxidase, peroxidase, catalase and superoxide dismutase) responsible for reactive oxygen species regulation. We then introduce ferritin to guide nitrogen-doped porous carbon nanospheres into lysosomes and boost reactive oxygen species generation in a tumor-specific manner, resulting in significant tumor regression in human tumor xenograft mice models. Together, our study provides evidence that nitrogen-doped porous carbon nanospheres are powerful nanozymes capable of regulating intracellular reactive oxygen species, and ferritinylation is a promising strategy to render nanozymes to target tumor cells for in vivo tumor catalytic therapy. |
format | Online Article Text |
id | pubmed-5897348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58973482018-04-16 In vivo guiding nitrogen-doped carbon nanozyme for tumor catalytic therapy Fan, Kelong Xi, Juqun Fan, Lei Wang, Peixia Zhu, Chunhua Tang, Yan Xu, Xiangdong Liang, Minmin Jiang, Bing Yan, Xiyun Gao, Lizeng Nat Commun Article Nanomaterials with intrinsic enzyme-like activities (nanozymes), have been widely used as artificial enzymes in biomedicine. However, how to control their in vivo performance in a target cell is still challenging. Here we report a strategy to coordinate nanozymes to target tumor cells and selectively perform their activity to destruct tumors. We develop a nanozyme using nitrogen-doped porous carbon nanospheres which possess four enzyme-like activities (oxidase, peroxidase, catalase and superoxide dismutase) responsible for reactive oxygen species regulation. We then introduce ferritin to guide nitrogen-doped porous carbon nanospheres into lysosomes and boost reactive oxygen species generation in a tumor-specific manner, resulting in significant tumor regression in human tumor xenograft mice models. Together, our study provides evidence that nitrogen-doped porous carbon nanospheres are powerful nanozymes capable of regulating intracellular reactive oxygen species, and ferritinylation is a promising strategy to render nanozymes to target tumor cells for in vivo tumor catalytic therapy. Nature Publishing Group UK 2018-04-12 /pmc/articles/PMC5897348/ /pubmed/29650959 http://dx.doi.org/10.1038/s41467-018-03903-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Fan, Kelong Xi, Juqun Fan, Lei Wang, Peixia Zhu, Chunhua Tang, Yan Xu, Xiangdong Liang, Minmin Jiang, Bing Yan, Xiyun Gao, Lizeng In vivo guiding nitrogen-doped carbon nanozyme for tumor catalytic therapy |
title | In vivo guiding nitrogen-doped carbon nanozyme for tumor catalytic therapy |
title_full | In vivo guiding nitrogen-doped carbon nanozyme for tumor catalytic therapy |
title_fullStr | In vivo guiding nitrogen-doped carbon nanozyme for tumor catalytic therapy |
title_full_unstemmed | In vivo guiding nitrogen-doped carbon nanozyme for tumor catalytic therapy |
title_short | In vivo guiding nitrogen-doped carbon nanozyme for tumor catalytic therapy |
title_sort | in vivo guiding nitrogen-doped carbon nanozyme for tumor catalytic therapy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5897348/ https://www.ncbi.nlm.nih.gov/pubmed/29650959 http://dx.doi.org/10.1038/s41467-018-03903-8 |
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