| Literature DB >> 33484777 |
Smrithi Padmakumar1, Gregory Jones1, Grishma Pawar1, Olga Khorkova2, Jane Hsiao2, Jonghan Kim1, Mansoor M Amiji1, Benjamin S Bleier3.
Abstract
The limitations of central nervous system (CNS) drug delivery conferred by the blood-brain barrier (BBB) have been a significant obstacle in the development of large molecule therapeutics for CNS disease. Though significantly safer than direct CNS administration via intrathecal (IT) or intracerebroventricular (ICV) injection, the topical intranasal delivery of CNS therapeutics has failed to become clinically useful due to a variety of practical and physiologic drawbacks leading to high dose variability and poor bioavailability. This study describes the minimally invasive nasal depot (MIND) technique, a novel method of direct trans-nasal CNS drug delivery which overcomes the dosing variability and efficiency challenges of traditional topical trans-nasal, trans-olfactory strategies by delivering the entire therapeutic dose directly to the olfactory submucosal space. We found that the implantation of a depot containing an AntagoNAT (AT) capable of de-repressing brain derived neurotrophic factor (BDNF) expression enabled CNS distribution of ATs with significant and sustained upregulation of BDNF with efficiencies approaching 40% of ICV delivery. As the MIND technique is derived from common outpatient rhinological procedures routinely performed in Ear, Nose and Throat (ENT) clinics, our findings support the significant translational potential of this novel minimally invasive strategy as a reliable therapeutic delivery approach for the treatment of CNS diseases.Entities:
Keywords: AntagoNAT; BDNF; CNS delivery; Neurodegenerative diseases; Neurotrophic factor; Trans-nasal delivery
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Year: 2021 PMID: 33484777 PMCID: PMC7946770 DOI: 10.1016/j.jconrel.2021.01.027
Source DB: PubMed Journal: J Control Release ISSN: 0168-3659 Impact factor: 9.776