Construction of ROS-responsive cascade-targeted liposomes and investigation of their anti-AD effects
- Junjie Yu 1, Dejin Ma 1, Shutong Li 1, Suyu Yang 1, Tianhua Li 1, Liang Kong 1, Yang Liu 1, Juan Zang 1, Yang Yu 1, Xuetao Li 1
- Junjie Yu 1, Dejin Ma 1, Shutong Li 1
- 1School of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian 116600, People's Republic of China.
- 0School of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian 116600, People's Republic of China.
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View abstract on PubMed
Summary
This summary is machine-generated.This study developed novel liposomes that target Alzheimer's disease pathology. These liposomes enhance drug delivery to the brain, reducing oxidative stress and neuroinflammation for improved Alzheimer's treatment.
Area Of Science
- Neuroscience
- Biomedical Engineering
- Pharmacology
Background
- Oxidative stress and neuroinflammation are key drivers in Alzheimer's disease (AD) pathogenesis, linked to beta-amyloid production.
- Current AD treatments face challenges due to poor drug water solubility and limited blood-brain barrier (BBB) penetration.
Purpose Of The Study
- To develop a drug delivery system that overcomes BBB limitations and targets neuroinflammation in Alzheimer's disease.
- To enhance the therapeutic efficacy of resveratrol (Res) for Alzheimer's disease treatment.
Main Methods
- Constructed reactive oxygen species (ROS)-responsive cascade-targeting liposomes (ROS@Res-Lip) using DSPE-PEG2000-MG1 and DSPE-TK-PEG2000-Bor.
- Incorporated ROS-responsive thioketal (TK) bonds and borneol (Bor) to reduce ROS and enhance BBB penetration.
- Utilized MG1 peptide for targeted delivery of resveratrol to M1-type microglia.
Main Results
- Significantly increased drug concentration within the brain.
- Demonstrated enhanced therapeutic efficacy for Alzheimer's disease treatment.
- Achieved anti-inflammatory, antioxidant, and neuroprotective effects.
Conclusions
- ROS@Res-Lip effectively targets M1-type microglia and promotes their conversion to M2-type microglia.
- The developed liposomes show potential for improved Alzheimer's disease therapy by addressing oxidative stress and neuroinflammation.
- This targeted drug delivery approach offers a promising strategy for overcoming BBB challenges in AD treatment.
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