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Harnessing reactive oxygen/nitrogen species and inflammation: Nanodrugs for liver injury
Overall, 12% of the global population (800 million) suffers from liver disease, which causes 2 million deaths every year. Liver injury involving characteristic reactive oxygen/nitrogen species (RONS) and inflammation plays a key role in progression of liver disease. As a key metabolic organ of the h...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8850330/ https://www.ncbi.nlm.nih.gov/pubmed/35198963 http://dx.doi.org/10.1016/j.mtbio.2022.100215 |
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author | Liu, Min Huang, Qiong Zhu, Yan Chen, Li Li, Yumei Gong, Zhicheng Ai, Kelong |
author_facet | Liu, Min Huang, Qiong Zhu, Yan Chen, Li Li, Yumei Gong, Zhicheng Ai, Kelong |
author_sort | Liu, Min |
collection | PubMed |
description | Overall, 12% of the global population (800 million) suffers from liver disease, which causes 2 million deaths every year. Liver injury involving characteristic reactive oxygen/nitrogen species (RONS) and inflammation plays a key role in progression of liver disease. As a key metabolic organ of the human body, the liver is susceptible to injury from various sources, including COVID-19 infection. Owing to unique structural features and functions of the liver, most current antioxidants and anti-inflammatory drugs are limited against liver injury. However, the characteristics of the liver could be utilized in the development of nanodrugs to achieve specific enrichment in the liver and consequently targeted treatment. Nanodrugs have shown significant potential in eliminating RONS and regulating inflammation, presenting an attractive therapeutic tool for liver disease through controlling liver injury. Therefore, the main aim of the current review is to provide a comprehensive summary of the latest developments contributing to our understanding of the mechanisms underlying nanodrugs in the treatment of liver injury via harnessing RONS and inflammation. Meanwhile, the prospects of nanodrugs for liver injury therapy are systematically discussed, which provides a sound platform for novel therapeutic insights and inspiration for design of nanodrugs to treat liver disease. |
format | Online Article Text |
id | pubmed-8850330 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-88503302022-02-22 Harnessing reactive oxygen/nitrogen species and inflammation: Nanodrugs for liver injury Liu, Min Huang, Qiong Zhu, Yan Chen, Li Li, Yumei Gong, Zhicheng Ai, Kelong Mater Today Bio Full Length Article Overall, 12% of the global population (800 million) suffers from liver disease, which causes 2 million deaths every year. Liver injury involving characteristic reactive oxygen/nitrogen species (RONS) and inflammation plays a key role in progression of liver disease. As a key metabolic organ of the human body, the liver is susceptible to injury from various sources, including COVID-19 infection. Owing to unique structural features and functions of the liver, most current antioxidants and anti-inflammatory drugs are limited against liver injury. However, the characteristics of the liver could be utilized in the development of nanodrugs to achieve specific enrichment in the liver and consequently targeted treatment. Nanodrugs have shown significant potential in eliminating RONS and regulating inflammation, presenting an attractive therapeutic tool for liver disease through controlling liver injury. Therefore, the main aim of the current review is to provide a comprehensive summary of the latest developments contributing to our understanding of the mechanisms underlying nanodrugs in the treatment of liver injury via harnessing RONS and inflammation. Meanwhile, the prospects of nanodrugs for liver injury therapy are systematically discussed, which provides a sound platform for novel therapeutic insights and inspiration for design of nanodrugs to treat liver disease. Elsevier 2022-02-08 /pmc/articles/PMC8850330/ /pubmed/35198963 http://dx.doi.org/10.1016/j.mtbio.2022.100215 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Full Length Article Liu, Min Huang, Qiong Zhu, Yan Chen, Li Li, Yumei Gong, Zhicheng Ai, Kelong Harnessing reactive oxygen/nitrogen species and inflammation: Nanodrugs for liver injury |
title | Harnessing reactive oxygen/nitrogen species and inflammation: Nanodrugs for liver injury |
title_full | Harnessing reactive oxygen/nitrogen species and inflammation: Nanodrugs for liver injury |
title_fullStr | Harnessing reactive oxygen/nitrogen species and inflammation: Nanodrugs for liver injury |
title_full_unstemmed | Harnessing reactive oxygen/nitrogen species and inflammation: Nanodrugs for liver injury |
title_short | Harnessing reactive oxygen/nitrogen species and inflammation: Nanodrugs for liver injury |
title_sort | harnessing reactive oxygen/nitrogen species and inflammation: nanodrugs for liver injury |
topic | Full Length Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8850330/ https://www.ncbi.nlm.nih.gov/pubmed/35198963 http://dx.doi.org/10.1016/j.mtbio.2022.100215 |
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