Modified cyclodextrin-based nanoparticles mediated delivery of siRNA for huntingtin gene silencing across an in vitro BBB model
Loading...
Files
Accepted version
Supplementary material
Date
2021-11-15
Authors
Mendonça, Monique C. P.
Cronin, Michael F.
Cryan, John F.
O'Driscoll, Caitríona M.
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier
Published Version
Abstract
Huntington's disease (HD) is a neurodegenerative disorder caused by a mutation in the huntingtin (HTT) gene, leading to a toxic version of the HTT protein. There are currently no disease-modifying therapies available. In this scenario, gene-based treatments for HD aimed at lowering HTT levels have become one of the most promising emerging therapeutic options. To date, however, promising results have only been achieved following direct intrathecal or intracranial injections designed to circumvent the blood-brain barrier (BBB). Consequently, efforts to develop less invasive delivery platforms are highly desirable. Here, we described a novel delivery system based on modified cyclodextrin nanoparticles (CDs) loaded with small interfering RNAs (siRNAs) targeting HTT and complexed with the rabies virus glycoprotein (RVG), a BBB-shuttle peptide. Results using an in vitro BBB model, indicate the formulation successfully crosses the brain endothelial cells, releases the encapsulated siRNAs into the cytoplasm of neuronal cells, and mediates downregulation of HTT. In conclusion, the CD platform is a promising option for delivery of siRNA-based therapeutics for HD with wider potential to treat other diseases with a genetically validated target in the central nervous system.
Description
Keywords
Huntington's disease , Nanocarriers , Non-viral gene therapy , RVG , Targeted cyclodextrins
Citation
Mendonça, M., Cronin, M., Cryan, J. and O'Driscoll, C., (2021) ‘Modified cyclodextrin-based nanoparticles mediated delivery of siRNA for huntingtin gene silencing across an in vitro BBB model’, European Journal of Pharmaceutics and Biopharmaceutics, 169, pp. 309-318. doi: 10.1016/j.ejpb.2021.11.003