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Curcumin-loaded PLGA-PEG nanoparticles conjugated with B6 peptide for potential use in Alzheimer’s disease

Alzheimer’s disease is a neurodegenerative disorder mainly characterized by β-amyloid deposit and tau hyperphosphorylation with no curative treatments. Curcumin (Cur) has been proved to have potential use in Alzheimer’s disease with its anti-amyloid, anti-inflammatory, and anti-oxidant properties, e...

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Autores principales: Fan, Shengnuo, Zheng, Yuqiu, Liu, Xuan, Fang, Wenli, Chen, Xiaoyu, Liao, Wang, Jing, Xiuna, Lei, Ming, Tao, Enxiang, Ma, Qiulan, Zhang, Xingmei, Guo, Rui, Liu, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116673/
https://www.ncbi.nlm.nih.gov/pubmed/30107760
http://dx.doi.org/10.1080/10717544.2018.1461955
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author Fan, Shengnuo
Zheng, Yuqiu
Liu, Xuan
Fang, Wenli
Chen, Xiaoyu
Liao, Wang
Jing, Xiuna
Lei, Ming
Tao, Enxiang
Ma, Qiulan
Zhang, Xingmei
Guo, Rui
Liu, Jun
author_facet Fan, Shengnuo
Zheng, Yuqiu
Liu, Xuan
Fang, Wenli
Chen, Xiaoyu
Liao, Wang
Jing, Xiuna
Lei, Ming
Tao, Enxiang
Ma, Qiulan
Zhang, Xingmei
Guo, Rui
Liu, Jun
author_sort Fan, Shengnuo
collection PubMed
description Alzheimer’s disease is a neurodegenerative disorder mainly characterized by β-amyloid deposit and tau hyperphosphorylation with no curative treatments. Curcumin (Cur) has been proved to have potential use in Alzheimer’s disease with its anti-amyloid, anti-inflammatory, and anti-oxidant properties, etc. However, its hydrophobicity and low bioavailability hinder its application. In this paper, we designed a novel brain-target nanoparticle, poly(lactide-co-glycolide)-block-poly(ethylene glycol) (PLGA-PEG) conjugated with B6 peptide and was loaded with Cur (PLGA-PEG-B6/Cur) and administered it into HT22 cells and APP/PS1 Al transgenic mice. The in vitro assays including dynamic light scattering (DLS), flow cytometry (FCM), red blood cell (RBC) lysis, and thromboelastography (TEG) analysis indicated that this nanoparticle could narrow the diameter of Cur, increase its cellular uptake and possess good blood compatibility. The results from Morris water maze proved that PLGA-PEG-B6/Cur could tremendously improve the spatial learning and memory capability of APP/PS1 mice, compared with native Cur. The ex vivo assays including Bielschowsky silver staining, immunostaining, and western blotting demonstrated that PLGA-PEG-B6/Cur could reduce hippocampal β-amyloid formation and deposit and tau hyperphosphorylation. Thus, we suggested that PLGA-PEG-B6/Cur nanoparticles would be of potential and promising use for the treatment of Alzheimer’s disease.
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spelling pubmed-61166732018-09-04 Curcumin-loaded PLGA-PEG nanoparticles conjugated with B6 peptide for potential use in Alzheimer’s disease Fan, Shengnuo Zheng, Yuqiu Liu, Xuan Fang, Wenli Chen, Xiaoyu Liao, Wang Jing, Xiuna Lei, Ming Tao, Enxiang Ma, Qiulan Zhang, Xingmei Guo, Rui Liu, Jun Drug Deliv Research Article Alzheimer’s disease is a neurodegenerative disorder mainly characterized by β-amyloid deposit and tau hyperphosphorylation with no curative treatments. Curcumin (Cur) has been proved to have potential use in Alzheimer’s disease with its anti-amyloid, anti-inflammatory, and anti-oxidant properties, etc. However, its hydrophobicity and low bioavailability hinder its application. In this paper, we designed a novel brain-target nanoparticle, poly(lactide-co-glycolide)-block-poly(ethylene glycol) (PLGA-PEG) conjugated with B6 peptide and was loaded with Cur (PLGA-PEG-B6/Cur) and administered it into HT22 cells and APP/PS1 Al transgenic mice. The in vitro assays including dynamic light scattering (DLS), flow cytometry (FCM), red blood cell (RBC) lysis, and thromboelastography (TEG) analysis indicated that this nanoparticle could narrow the diameter of Cur, increase its cellular uptake and possess good blood compatibility. The results from Morris water maze proved that PLGA-PEG-B6/Cur could tremendously improve the spatial learning and memory capability of APP/PS1 mice, compared with native Cur. The ex vivo assays including Bielschowsky silver staining, immunostaining, and western blotting demonstrated that PLGA-PEG-B6/Cur could reduce hippocampal β-amyloid formation and deposit and tau hyperphosphorylation. Thus, we suggested that PLGA-PEG-B6/Cur nanoparticles would be of potential and promising use for the treatment of Alzheimer’s disease. Taylor & Francis 2018-08-15 /pmc/articles/PMC6116673/ /pubmed/30107760 http://dx.doi.org/10.1080/10717544.2018.1461955 Text en © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Fan, Shengnuo
Zheng, Yuqiu
Liu, Xuan
Fang, Wenli
Chen, Xiaoyu
Liao, Wang
Jing, Xiuna
Lei, Ming
Tao, Enxiang
Ma, Qiulan
Zhang, Xingmei
Guo, Rui
Liu, Jun
Curcumin-loaded PLGA-PEG nanoparticles conjugated with B6 peptide for potential use in Alzheimer’s disease
title Curcumin-loaded PLGA-PEG nanoparticles conjugated with B6 peptide for potential use in Alzheimer’s disease
title_full Curcumin-loaded PLGA-PEG nanoparticles conjugated with B6 peptide for potential use in Alzheimer’s disease
title_fullStr Curcumin-loaded PLGA-PEG nanoparticles conjugated with B6 peptide for potential use in Alzheimer’s disease
title_full_unstemmed Curcumin-loaded PLGA-PEG nanoparticles conjugated with B6 peptide for potential use in Alzheimer’s disease
title_short Curcumin-loaded PLGA-PEG nanoparticles conjugated with B6 peptide for potential use in Alzheimer’s disease
title_sort curcumin-loaded plga-peg nanoparticles conjugated with b6 peptide for potential use in alzheimer’s disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116673/
https://www.ncbi.nlm.nih.gov/pubmed/30107760
http://dx.doi.org/10.1080/10717544.2018.1461955
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