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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...

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Detalles Bibliográficos
Autores principales: Kuang, Ying, Zhang, Jingwen, Xiong, Mogao, Zeng, Weijia, Lin, Xiaofeng, Yi, Xiaoqing, Luo, Yan, Yang, Min, Li, Feng, Huang, Qitong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
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
Descripción
Sumario: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.