| Literature DB >> 30369055 |
Timothy M Brenza1, Benjamin W Schlichtmann1, Biju Bhargavan2, Julia E Vela Ramirez1, Rainie D Nelson1, Matthew G Panthani1, JoEllyn M McMillan2, Balaraman Kalyanaraman3, Howard E Gendelman2, Vellareddy Anantharam4,5, Anumantha G Kanthasamy4,5, Surya K Mallapragada1,5, Balaji Narasimhan1,5, Georgette D Kanmogne2.
Abstract
An urgent need to deliver therapeutics across the blood-brain barrier (BBB) underlies a paucity of effective therapies currently available for treatment of degenerative, infectious, traumatic, chemical, and metabolic disorders of the nervous system. With an eye toward achieving this goal, an in vitro BBB model was employed to simulate biodegradable polyanhydride nanoparticle-based drug delivery to the brain. Using a combination of confocal microscopy, flow cytometry, and high performance liquid chromatography, we examined the potential of polyanhydride nanoparticles containing the anti-oxidant, mito-apocynin, to be internalized and then transferred from monocytes to human brain microvascular endothelial cells. The efficacy of this nanoparticle-based delivery platform was demonstrated by neuronal protection against oxidative stress. Taken together, this polyanhydride nanoparticle-based delivery system holds promise for enhancing neuroprotection by facilitating drug transport across the BBB.Entities:
Keywords: blood-brain barrier; cell-mediated transcytosis; mito-apocynin; nanoparticles; polyanhydrides
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Year: 2018 PMID: 30369055 PMCID: PMC6366942 DOI: 10.1002/jbm.a.36477
Source DB: PubMed Journal: J Biomed Mater Res A ISSN: 1549-3296 Impact factor: 4.396