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ApoE-2 Brain-Targeted Gene Therapy Through Transferrin and Penetratin Tagged Liposomal Nanoparticles.

Authors :
dos Santos Rodrigues, Bruna
Kanekiyo, Takahisa
Singh, Jagdish
Source :
Pharmaceutical Research; Nov2019, Vol. 36 Issue 11, p1-11, 11p, 2 Diagrams, 1 Chart, 5 Graphs
Publication Year :
2019

Abstract

Purpose: Apolipoprotein E2 (ApoE2) gene therapy is a potential disease-modifying therapy for Alzheimer's disease (AD). We investigated the potential of plasmid encoding ApoE2 loaded brain-targeted functionalized-liposomes for treatment of AD. This was achieved via systemic administration of liposomes entrapping therapeutic gene targeting the brain of mice. Methods: Targeting and transfection efficiency of designed liposomes were determined in bEnd.3, primary glial and primary neuronal cells. The ability of liposomal formulations to translocate across in vitro blood-brain barrier (BBB) and, thereafter, transfect primary neuronal cells was investigated using in vitro triple co-culture BBB model. We quantified ApoE expression in the brain of mice after single intravenous injection of brain-targeted liposomes loaded with plasmid ApoE2. Results: Dual surface modification enhanced the in vitro transfection efficiency of designed liposomes. Successful delivery of therapeutic gene overcoming BBB by Transferrin-Penetratin- modified liposomes was demonstrated both in vitro and in vivo. Significant (p < 0.05) increase in ApoE levels in the brain of mice was observed after intravenous administration of Tf-Pen-liposomes encasing plasmid ApoE2. Conclusion: The results indicate that dual-ligand based liposomal gene delivery systems had both enhanced brain targeting and gene delivery efficiencies. Transferrin-Penetratin modified liposomes for delivery of plasmid ApoE2 has great potential for AD treatment. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
07248741
Volume :
36
Issue :
11
Database :
Complementary Index
Journal :
Pharmaceutical Research
Publication Type :
Academic Journal
Accession number :
139095529
Full Text :
https://doi.org/10.1007/s11095-019-2691-7