| Literature DB >> 34252799 |
Smrithi Padmakumar1, Gregory Jones1, Olga Khorkova2, Jane Hsiao2, Jonghan Kim3, Benjamin S Bleier4, Mansoor M Amiji5.
Abstract
The development of drug delivery strategies for efficacious therapeutic administration directly into the central nervous system (CNS) in a minimally invasive manner remains a major obstacle hindering the clinical translation of biological disease-modifying therapeutics. A novel direct trans-nasal delivery method, termed 'Minimally-Invasive Nasal Depot' (MIND), has proved to be successful in providing high CNS uptake and brain distribution of blood-brain barrier (BBB) impermeant therapeutics via direct administration to the olfactory submucosal space in a rodent model. The present study describes the engineering of custom-made implants with a unique architecture of an "osmotically-active core" entrapping the therapeutic and a "biodegradable polymeric shell" to enable long-acting delivery using the MIND procedure. The MIND-administered implant provided sustained CNS delivery of brain derived neurotrophic factor (BDNF) AntagoNATs for up to 4 weeks in Sprague Dawley rats resulting in significant endogenous BDNF protein upregulation in several brain tissues. The biocompatibility of such core-shell implants coupled with their substantial pharmacokinetic advantages and safety of the MIND procedure highlights the practical utility and translational potential of this synergistic approach for treatment of chronic age-related neurodegenerative diseases.Entities:
Keywords: AntagoNAT; Brain-derived neurotrophic factor; CNS Delivery; Minimially-invasive nasal depot (MIND); Neurodegenerative diseases; Osmotic implant
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Year: 2021 PMID: 34252799 PMCID: PMC8607190 DOI: 10.1016/j.biomaterials.2021.120989
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479