Creation of amyloid β (Aβ) peptides involved in disease progression is the important pathway in Alzheimer’s disease (AD) progression and that is a crucial target for the treatment of AD. NMDA receptor antagonists have emerged as a promising strategy to lower Aβ levels and slow AD development. However, because the blood-brain barrier (BBB) is so restrictive, their efficacy is restricted when administered systemically. In AD, inflammation, oxidative stress, and the buildup of abnormal proteins like amyloid and tau are common and recent research suggests use of curcumin may help counteract these damaging processes and protect neurons. Unfortunately, both NMDA receptor antagonists and curcumin face challenges crossing the BBB, resulting in poor brain uptake. The nose-to-brain (NtB) delivery route offers a potential solution by bypassing the BBB and allowing direct access to the brain. Liposomal drug delivery systems enhances drug reach by improving efficient transport to the brain as well as greater drug stability. This study used the rotary evaporation method to prepare memantine liposomes and coupled memantine-curcumin liposomes, which were then evaluated In-vitro. The findings indicate that liposomal formulations of memantine and memantine-curcumin can promote effective intracellular drug delivery, potentially cross tight junctions in the BBB, and may help reduce amyloid plaque formation and inflammation, highlighting their promise as an AD treatment via NtB delivery having good physicochemical properties and stability of drug.
How to cite this article: Abhish Jadhav, Mrudula Bele. Formulation, Development and Evaluation of Memantine and Memantine-Curcumin Co-Loaded Liposomes for Intranasal Delivery in Alzheimer's. International Journal of Drug Delivery Technology. 2025;15(3):1205-11. doi: 10.25258/ijddt.15.3.40
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