Amyloid -? pathology in Alzheimer?s disease: A nano delivery approach

被引:6
作者
Meghana, G. S. [1 ]
Gowda, D., V [1 ]
Chidambaram, Saravana Babu [2 ,3 ]
Osmani, Riyaz Ali [1 ]
机构
[1] JSS AHER, JSS Coll Pharm, Dept Pharmaceut, Mysuru, India
[2] JSS AHER, JSS Coll Pharm, Dept Pharmacol, Mysuru, India
[3] JSS AHER, Ctr Expt Pharmacol & Toxicol, Cent Anim Facil, Mysuru, India
关键词
Alzheimer?s disease; -amyloid; A? oligomers; Nanotechnology; A? aggregation inhibitors; Neuroprotection; ENDOTHELIN-CONVERTING ENZYME-2; BLOOD-BRAIN-BARRIER; GAMMA-SECRETASE MODULATOR; SOLID LIPID NANOPARTICLES; A-BETA; DRUG-DELIVERY; CEREBROSPINAL-FLUID; IN-VITRO; GOLD NANOPARTICLES; PRECURSOR PROTEIN;
D O I
10.1016/j.vibspec.2023.103510
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The pathology of Alzheimer's disease (AD) is majorly driven by, imbalance between the production and clear-ance and deposition of A beta in brain. Current treatment strategies offer a symptomatic management rather specific targets involved in AD, particularly Amyloid-beta (A beta). Despite mounting evidence demonstrate the role of A beta plaques in AD pathology, the clinical reliability on A beta in diagnosis and treatment is still a matter of debate. Indeed, the oligomeric form of A beta is highly neurotoxic than the soluble forms. The neurotoxic potential of A beta oligomerisation has led to many research works focused to prevent its aggregation. On the other hand, the bioavailability and blood brain barrier (BBB) penetration capability of drugs play a crucial role in AD therapeutic outcome. Nano-technology based delivery systems are emerging as ray of hope as they provide both target specific and increased biodistribution of drugs for many ailments particularly for drugs acting in brain. These nano technologies-based delivery systems are seemed to be promising tools to deliver drugs across BBB through various routes of administration. The present review summarizes research focused on inhibition of A beta oligo-merisation and role of nanotechnologies towards effective management of AD. We also provide update on clinical trials on inhibition of A beta oligomerisation and its clearance and use of nanotechnologies in AD.
引用
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页数:19
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