TY - JOUR
T1 - Intranasal delivery of chitosan decorated PLGA core /shell nanoparticles containing flavonoid to reduce oxidative stress in the treatment of Alzheimer's disease
AU - Dhas, Namdev
AU - Mehta, Tejal
N1 - Funding Information:
Authors would like to thank Council of Scientific and Industrial Research (CSIR) and Institute of Pharmacy, Nirma University for providing financial assistance in the form of CSIR-Senior Research Fellowship (SRF) (09/1048(007)/2018-EMR-I) and Nirma University-Junior Research Fellowship (JRF) ( NU/IP/stipend/Ph.D./2016 ) to Namdev Dhas. The authors are again thankful to Institute of Pharmacy, Nirma University for providing the necessary facilities to carry out the research work.
Funding Information:
Authors would like to thank Council of Scientific and Industrial Research (CSIR) and Institute of Pharmacy, Nirma University for providing financial assistance in the form of CSIR-Senior Research Fellowship (SRF) (09/1048(007)/2018-EMR-I) and Nirma University-Junior Research Fellowship (JRF) (NU/IP/stipend/Ph.D./2016) to Namdev Dhas. The authors are again thankful to Institute of Pharmacy, Nirma University for providing the necessary facilities to carry out the research work.
Publisher Copyright:
© 2020 Elsevier B.V.
PY - 2021/2
Y1 - 2021/2
N2 - 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.
AB - 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.
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U2 - 10.1016/j.jddst.2020.102242
DO - 10.1016/j.jddst.2020.102242
M3 - Article
AN - SCOPUS:85096967089
VL - 61
JO - Journal of Drug Delivery Science and Technology
JF - Journal of Drug Delivery Science and Technology
SN - 1773-2247
M1 - 102242
ER -