Anti-Alzheimer's effect of memantine/donepezil/metformin-loaded PVA/PEO composite nanofibers produced by pressurized gyration: Production, characterization, and in vitro evaluation

View/ Open
Date
2024Author
Güler, EceKopuz, Ayşen
Ertaş, Büşra
Yılmaz Göler, Ayşe Mine
Yazır, Yusufhan
Kalaskar, Deepak M.
Çam, Muhammet Emin
Metadata
Show full item recordCitation
Güler, E.; Kopuz, A.; Ertaş, B.; Yılmaz Göler, A. M.; Yazır, Y.; M. Kalaskar, D.; Çam, M. E. (2024). Anti-Alzheimer's effect of memantine/donepezil/metformin-loaded PVA/PEO composite nanofibers produced by pressurized gyration: Production, characterization, and in vitro evaluation. Journal of Drug Delivery Science and Technology, v.97,105795.Abstract
In this study, memantine (MM) and donepezil (DO) were combined with metformin (MF) as a new approach to
Alzheimer’s disease (AD) treatment sublingually. MM, DO, and MF were loaded in polyvinyl alcohol (PVA)/
polyethylene oxide (PEO) composite nanofibers (NFs), which were produced in three different ratios (9/1, 8/2,
and 7/3) by pressurized gyration. The diameter of fibers was decreased by reducing the PEO ratios and adding
the drugs in polymer solutions. MM, DO, and MF were successfully loaded and distributed in NFs by the results of
FTIR, XRD, and DSC tests. The drug release percentages were enhanced with an increasing ratio of PVA in fibers
by the dissolution test results. All fibers at various ratios were found suitable for the sublingual route by dis integrating quickly. No significant toxicity of nanofibers at 24 and 48 h was observed on SH-SY5Y cells. The
highest neuroprotection activity was observed in the cells treated with MM/DO/MF-loaded NFs at 7/3. The
mRNAs of APP and BACE-1 of the MM/DO/MF-loaded NF group were lower than those of the Aβ1-42 group.
While, ADAM-10 mRNA expression increased in the MM/DO/MF-loaded NFs treatment group via PCR results.
The morphological structure of the cells treated with the MM/DO/MF-loaded NFs was protected from Aβ1-42-
induced neurotoxicity according to confocal laser scanning microscopy images.
Source
Journal of Drug Delivery Science and TechnologyVolume
97URI
https://www.sciencedirect.com/science/article/pii/S1773224724004647?via%3Dihubhttps://doi.org/10.1016/j.jddst.2024.105795
https://hdl.handle.net/20.500.12780/932