| Literature DB >> 31666200 |
Vasyl Sava1, Oksana Fihurka1, Anastasia Khvorova2, Juan Sanchez-Ramos3.
Abstract
Therapies to lower gene expression in brain disease currently require chronic administration into the cerebrospinal fluid (CSF) by intrathecal infusions or direct intracerebral injections. Though well-tolerated in the short-term, this approach is not tenable for a life-time of administration. Nose-to-brain delivery of enriched chitosan-based nanoparticles loaded with anti-HTT siRNA was studied in a transgenic YAC128 mouse model of Huntington's Disease (HD). A series of chitosan-based nanoparticle (NP) formulations encapsulating anti-HTT small interfering RNA (siRNA) was designed to protect the payload from degradation "en route" to the target. Factors to improve production of effective nanocarriers of anti-HTT siRNA were identified and tested in a YAC128 mouse model of Huntington's disease. Four formulations of nanocarriers were identified to be effective in lowering HTT mRNA expression by at least 50%. Intranasal administration of nanoparticles carrying siRNA is a promising therapeutic alternative for safe and effective lowering of mutant HTT expression.Entities:
Keywords: Gene-therapy; Huntington's disease; Intranasal administration; Nanocarriers; YAC128 mouse model
Mesh:
Substances:
Year: 2019 PMID: 31666200 PMCID: PMC7098382 DOI: 10.1016/j.nano.2019.102119
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307