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Prolonged Drug-Releasing Fibers Attenuate Alzheimer's Disease-like Pathogenesis.

ACS Appl Mater Interfaces · 2018

Last updated 2026-05-28

Researchers created a biodegradable implant that slowly releases a GLP-1 drug called liraglutide for 14 days in mice. After 4 weeks, the implant reduced brain plaques linked to Alzheimer’s disease and lowered brain inflammation, while also boosting new brain cell growth in a specific brain region.

AI summary of the abstract below.

JournalACS Appl Mater Interfaces, 2018
Citations17
Relative citation ratio0.87
NIH percentile46
Molecules
Conditions studied Alzheimers

Abstract

Delivering drugs and agents to the brain is a huge challenge, especially for chronic neurodegenerative disorders, such as Alzheimer's disease (AD). For this, prolonged and sustained release methods to increase brain uptake represent an impacting concept. The bioresorbable polymer poly-lactic acid (PLA) has high potential for medical implants; at the same time, glucagon-like peptide-1 (GLP-1) analogues have considerable neuroprotective attributes and represent a therapeutic strategy for AD. Here, a biodevice is produced by electrospinning PLA with a GLP-1 analogue (liraglutide, LG), coated with a thin layer of gelatin. The biodevice is subcutaneously implanted in a transgenic mouse model of AD and LG is released for 14 days in mice serum. After 4 weeks of implantation, crucial hallmarks of the AD are highly diminished: hippocampal senile amyloid β plaque load and neuroinflammatory markers. Furthermore, neurogenesis is enhanced in the subventricular zone, an important neurogenic niche in the brain. The designed biodevice holds great promise for being an affordable candidate to act as a prolonged drug provider, promoting LG mission through increasing its lifetime, constituting a relevant approach for old and impaired brain.

Verbatim abstract via PubMed 30298718 ↗