Magnetite/Ceria Nanoparticle Assemblies for Extracorporeal Cleansing of Amyloid-β in Alzheimer's Disease.
Dokyoon KimHyek Jin KwonTaeghwan HyeonPublished in: Advanced materials (Deerfield Beach, Fla.) (2019)
Accumulation of amyloid-β (Aβ) peptides in the brain is regarded as a major contributor to the pathogenesis and progression of Alzheimer's disease (AD). However, development of clinically relevant techniques to reduce Aβ levels in AD patients is hindered by low efficiency and/or side effects. Here, an extracorporeal Aβ cleansing system, where multifunctional magnetite/ceria nanoparticle assemblies are used to remove Aβ peptides from flowing blood by specific capture and magnetic separation, is reported. The magnetite nanoparticles in the nanoassembly core enable the magnetic isolation of the captured Aβ peptides by generating a large attraction force under an external magnetic field. The ceria nanoparticles in the nanoassembly shell relieve oxidative stress by scavenging reactive oxygen species that are produced by immune response during the process. Blood Aβ cleansing treatment of 5XFAD transgenic mice not only demonstrates the decreased Aβ levels both in the blood and in the brain but also prevents the spatial working memory deficits, suggesting the potential of the method for AD prevention and therapy.
Keyphrases
- working memory
- immune response
- oxidative stress
- reactive oxygen species
- end stage renal disease
- white matter
- ejection fraction
- newly diagnosed
- chronic kidney disease
- amino acid
- resting state
- cognitive decline
- traumatic brain injury
- molecularly imprinted
- transcranial direct current stimulation
- prognostic factors
- peritoneal dialysis
- attention deficit hyperactivity disorder
- stem cells
- cerebral ischemia
- mouse model
- single molecule
- multiple sclerosis
- liquid chromatography
- combination therapy
- simultaneous determination
- oxide nanoparticles