Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/11035
Title: Intranasal Delivery of Chitosan Decorated PLGA Core /Shell Nanoparticles Containing Flavonoid to Reduce Oxidative Stress in the Treatment of Alzheimer’s Disease
Authors: Dhas, Namdev
Mehta, Tejal
Keywords: Curcumin
Curcumin Core/shell nanoparticles Antioxidant activity BBB co-Culture model Systemic toxicity
Antioxidant activity
BBB co-Culture model
Systemic toxicity
Issue Date: 2021
Publisher: Elsevier
Series/Report no.: IPFP0490;
Abstract: Curcumin (Cur), an antioxidant flavonoid has demonstrated high efficiency in attenuating oxidative stress in Alzheimer’s disease (AD). Nevertheless, despite of its therapeutic potential, its clinical applications are hindered due to low solubility and low bioavailability and and first-pass metabolism. Thus, we fabricated Cur encapsulated chitosan functionalized PLGA core/shell NPs (CH@Cur-PLGA C/S NPs) and administered via intranasal route. Research also include comparative study of PLGA NPs (core) and CH@Cur-PLGA C/S NPs (C/S NPs) to investigate effect of CH coating over PLGA NPs on therapeutic efficacy, cellular uptake and stability. Fabricated NPs were extensively characterized and confirmed Cur encapsulation with 75% of entrapment efficiency and particle size in the range of 200 nm. TEM analysis confirmed uniform coating of CH over PLGA NPs. Release and permeation study demonstrated sustained release and enhanced permeation through nasal mucosa. Cellular uptake mechanism showed caveolae-mediated-enhance endocytosis of NPs. In-vitro BBB-co-cufure model exhibited efficient passage for C/SNPs. Antioxidant assay demonstrated significant ROS scavenging activity of C/ SNPs. In-vivo toxicity showed insignificant toxicity. Bio-distribution of C/S NPs was higher in brain following intranasal route. Photo and thermal stability confirmed protection of Cur by C/SNPs. Obtained results demonstrate potential application of C/SNPs for reducing oxidative stress in brain for effective AD treat.
Description: Journal of Drug Delivery Science and Technology 61 (2021) 102242
URI: http://10.1.7.192:80/jspui/handle/123456789/11035
Appears in Collections:Faculty Papers

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