In Vivo Evaluation of Nose-to-Brain Delivery of Liposomal Donepezil, Memantine, and BACE-1 siRNA for Alzheimer’s Disease Therapy

Our study took an innovative approach by evaluating, in vivo, the efficacy of intranasal (IN) administration of liposomal formulations of donepezil, memantine, and beta-site amyloid precursor protein-cleaving enzyme (BACE-1) siRNA, and their combination as a "triple-drug therapy" in treating Alzheimer's disease (AD). Female APP/PS1 homozygous, transgenic mice were used as an AD model. The spatial short-term memory of the APP/PS1 mice was evaluated by a Y-maze behavioral test. IN-administered formulations demonstrated better short-term memory recovery than oral administration. Triple-drug therapy induced short-term memory recovery and lowered beta-amyloid (Aβ) 40 and 42 peptide levels and BACE-1 mRNA expression. Additionally, inflammatory cytokine mRNA expression was downregulated. This innovative approach opens new possibilities for Alzheimer's disease treatment and nose-to-brain delivery.

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Publication Details

Journal
International Journal of Molecular Sciences
Published
2024-09-26
DOI
https://doi.org/10.3390/ijms251910357
Citations
8
Primary Topic
Advanced Drug Delivery Systems
Type
article
Field-Weighted Citation Impact
1.66
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article

In Vivo Evaluation of Nose-to-Brain Delivery of Liposomal Donepezil, Memantine, and BACE-1 siRNA for Alzheimer’s Disease Therapy

Milinkumar T. Shah, Andrew M. Shen, Olga B. Garbuzenko, Tamara Minko et al.
8 citations
International Journal of Molecular Sciences
Advanced Drug Delivery Systems
1.66
article

In Vivo Evaluation of Nose-to-Brain Delivery of Liposomal Donepezil, Memantine, and BACE-1 siRNA for Alzheimer’s Disease Therapy

Milinkumar T. Shah, Andrew M. Shen, Olga B. Garbuzenko, Tamara Minko, David Lee
article en
8 citations

Abstract

Our study took an innovative approach by evaluating, in vivo, the efficacy of intranasal (IN) administration of liposomal formulations of donepezil, memantine, and beta-site amyloid precursor protein-cleaving enzyme (BACE-1) siRNA, and their combination as a "triple-drug therapy" in treating Alzheimer's disease (AD). Female APP/PS1 homozygous, transgenic mice were used as an AD model. The spatial short-term memory of the APP/PS1 mice was evaluated by a Y-maze behavioral test. IN-administered formulations demonstrated better short-term memory recovery than oral administration. Triple-drug therapy induced short-term memory recovery and lowered beta-amyloid (Aβ) 40 and 42 peptide levels and BACE-1 mRNA expression. Additionally, inflammatory cytokine mRNA expression was downregulated. This innovative approach opens new possibilities for Alzheimer's disease treatment and nose-to-brain delivery.

International Journal of Molecular SciencesVol. 25(19)
Rutgers, The State University of New Jersey (US), Environmental and Occupational Health Sciences Institute (US), Rutgers Cancer Institute (US)
Good health and well-being
Openalex Percentile: Top 18%
Advanced Drug Delivery Systems
1.66
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In Vivo Evaluation of Nose-to-Brain Delivery of Liposomal Donepezil, Memantine, and BACE-1 siRNA for Alzheimer’s Disease Therapy — Milinkumar T. Shah, Andrew M. Shen, et al. · International Journal of Molecular Sciences (2024) | TGRS Research Map | TGRS