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A Novel Nanosystem Realizing Curcumin Delivery Based on Fe(3)O(4)@Carbon Dots Nanocomposite for Alzheimer’s Disease Therapy
Alzheimer’s disease (AD) is the most common neurodegenerative disease, which seriously affects human health but lacks effective treatment methods. Amyloid β (Aβ) aggregates are considered a possible target for AD treatment. Evidence is increasingly showing that curcumin (CUR) can partly protect cell...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744485/ https://www.ncbi.nlm.nih.gov/pubmed/33344438 http://dx.doi.org/10.3389/fbioe.2020.614906 |
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author | Kuang, Ying Zhang, Jingwen Xiong, Mogao Zeng, Weijia Lin, Xiaofeng Yi, Xiaoqing Luo, Yan Yang, Min Li, Feng Huang, Qitong |
author_facet | Kuang, Ying Zhang, Jingwen Xiong, Mogao Zeng, Weijia Lin, Xiaofeng Yi, Xiaoqing Luo, Yan Yang, Min Li, Feng Huang, Qitong |
author_sort | Kuang, Ying |
collection | PubMed |
description | Alzheimer’s disease (AD) is the most common neurodegenerative disease, which seriously affects human health but lacks effective treatment methods. Amyloid β (Aβ) aggregates are considered a possible target for AD treatment. Evidence is increasingly showing that curcumin (CUR) can partly protect cells from Aβ-mediated neurotoxicity by inhibiting Aβ aggregation. However, the efficiency of targeted cellular uptake and bioavailability of CUR is very low due to its poor stability and water-solubility. In order to better improve the cell uptake efficiency and bioavailability of CUR and reduce the cytotoxicity of high-dose CUR, a novel CUR delivery system for AD therapy has been constructed based on the employment of the Fe(3)O(4)@carbon dots nanocomposite (Fe(3)O(4)@CDs) as the carrier. CUR-Fe(3)O(4)@CDs have a strong affinity toward Aβ and effectively inhibit extracellular Aβ fibrillation. In addition, CUR-Fe(3)O(4)@CDs can inhibit the production of reactive oxygen species (ROS) mediated by Aβ fibrils and the corresponding neurotoxicity in PC12 cells. More importantly, it can restore nerve damage and maintained neuronal morphology. These results indicate that the application of CUR-Fe(3)O(4)@CDs provides a promising platform for the treatment of AD. |
format | Online Article Text |
id | pubmed-7744485 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-77444852020-12-18 A Novel Nanosystem Realizing Curcumin Delivery Based on Fe(3)O(4)@Carbon Dots Nanocomposite for Alzheimer’s Disease Therapy Kuang, Ying Zhang, Jingwen Xiong, Mogao Zeng, Weijia Lin, Xiaofeng Yi, Xiaoqing Luo, Yan Yang, Min Li, Feng Huang, Qitong Front Bioeng Biotechnol Bioengineering and Biotechnology Alzheimer’s disease (AD) is the most common neurodegenerative disease, which seriously affects human health but lacks effective treatment methods. Amyloid β (Aβ) aggregates are considered a possible target for AD treatment. Evidence is increasingly showing that curcumin (CUR) can partly protect cells from Aβ-mediated neurotoxicity by inhibiting Aβ aggregation. However, the efficiency of targeted cellular uptake and bioavailability of CUR is very low due to its poor stability and water-solubility. In order to better improve the cell uptake efficiency and bioavailability of CUR and reduce the cytotoxicity of high-dose CUR, a novel CUR delivery system for AD therapy has been constructed based on the employment of the Fe(3)O(4)@carbon dots nanocomposite (Fe(3)O(4)@CDs) as the carrier. CUR-Fe(3)O(4)@CDs have a strong affinity toward Aβ and effectively inhibit extracellular Aβ fibrillation. In addition, CUR-Fe(3)O(4)@CDs can inhibit the production of reactive oxygen species (ROS) mediated by Aβ fibrils and the corresponding neurotoxicity in PC12 cells. More importantly, it can restore nerve damage and maintained neuronal morphology. These results indicate that the application of CUR-Fe(3)O(4)@CDs provides a promising platform for the treatment of AD. Frontiers Media S.A. 2020-12-03 /pmc/articles/PMC7744485/ /pubmed/33344438 http://dx.doi.org/10.3389/fbioe.2020.614906 Text en Copyright © 2020 Kuang, Zhang, Xiong, Zeng, Lin, Yi, Luo, Yang, Li and Huang. http://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 | Bioengineering and Biotechnology Kuang, Ying Zhang, Jingwen Xiong, Mogao Zeng, Weijia Lin, Xiaofeng Yi, Xiaoqing Luo, Yan Yang, Min Li, Feng Huang, Qitong A Novel Nanosystem Realizing Curcumin Delivery Based on Fe(3)O(4)@Carbon Dots Nanocomposite for Alzheimer’s Disease Therapy |
title | A Novel Nanosystem Realizing Curcumin Delivery Based on Fe(3)O(4)@Carbon Dots Nanocomposite for Alzheimer’s Disease Therapy |
title_full | A Novel Nanosystem Realizing Curcumin Delivery Based on Fe(3)O(4)@Carbon Dots Nanocomposite for Alzheimer’s Disease Therapy |
title_fullStr | A Novel Nanosystem Realizing Curcumin Delivery Based on Fe(3)O(4)@Carbon Dots Nanocomposite for Alzheimer’s Disease Therapy |
title_full_unstemmed | A Novel Nanosystem Realizing Curcumin Delivery Based on Fe(3)O(4)@Carbon Dots Nanocomposite for Alzheimer’s Disease Therapy |
title_short | A Novel Nanosystem Realizing Curcumin Delivery Based on Fe(3)O(4)@Carbon Dots Nanocomposite for Alzheimer’s Disease Therapy |
title_sort | novel nanosystem realizing curcumin delivery based on fe(3)o(4)@carbon dots nanocomposite for alzheimer’s disease therapy |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7744485/ https://www.ncbi.nlm.nih.gov/pubmed/33344438 http://dx.doi.org/10.3389/fbioe.2020.614906 |
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