| Literature DB >> 29785179 |
Yuhang Jiang1, James M Fay2, Chi-Duen Poon3, Natasha Vinod2, Yuling Zhao1, Kristin Bullock4, Si Qin1, Devika S Manickam1, Xiang Yi1, William A Banks4, Alexander V Kabanov1.
Abstract
Brain-derived neurotrophic factor (BDNF) is identified as a potent neuroprotective and neuroregenerative agent for many neurological diseases. Regrettably, its delivery to the brain is hampered by poor serum stability and rapid brain clearance. Here, a novel nanoformulation is reported composed of a bio-compatible polymer, poly(ethylene glycol)-b-poly(L-glutamic acid) (PEG-PLE), that hosts the BDNF molecule in a nanoscale complex, termed here Nano-BDNF. Upon simple mixture, Nano-BDNF spontaneously forms uniform spherical particles with a core-shell structure. Molecular dynamics simulations suggest that binding between BDNF and PEG-PLE is mediated through electrostatic coupling as well as transient hydrogen bonding. The formation of Nano-BDNF complex stabilizes BDNF and protects it from nonspecific binding with common proteins in the body fluid, while allowing it to associate with its receptors. Following intranasal administration, the nanoformulation improves BDNF delivery throughout the brain and displays a more preferable regional distribution pattern than the native protein. Furthermore, intranasally delivered Nano-BDNF results in superior neuroprotective effects in the mouse brain with lipopolysaccharides-induced inflammation, indicating promise for further evaluation of this agent for the therapy of neurologic diseases.Entities:
Keywords: central nervous system; drug delivery; intranasal delivery; neurotrophic factors; polyion complexes
Year: 2017 PMID: 29785179 PMCID: PMC5958903 DOI: 10.1002/adfm.201703982
Source DB: PubMed Journal: Adv Funct Mater ISSN: 1616-301X Impact factor: 18.808