Sibhghatulla Shaikh, Nazia Nazam, Syed Mohd Danish Rizvi, Talib Hussain, Aisha Farhana and Inho Choi* Pages 1 - 9 ( 9 )
Alzheimer’s disease (AD) is characterized by deposition of amyloid-β protein aggregates and an appropriate treatment strategy is urgently needed, as the number of diagnosed cases continues to increase. The management of AD and of the other brain-associated diseases are limited by the blood brain barrier and its selective control of drug passage. In fact, most of the promising drugs have restricted curative effects on AD owing to their lower bioavailability. Gold nanoparticles (AuNPs) have emerged as attractive therapeutic agents and have distinctive properties that could contribute to the development of a novel treatment strategy for neurodegenerative disorders. In this review article, we attempt to identify promising ways of developing competent AD therapeutic agents from anti-amyloid aggregating AuNPs. Initially, we discuss the current status of anti-amyloid inhibitors, the abilities of AuNPs to inhibit amyloid aggregation, and mechanistic aspects, and then describe plausible modifications that could aid the translation of AuNP-based therapeutics into neuromedicines. The review highlights some interesting characteristics that might effectively bridge the gap between laboratory and bedside treatments.
Alzheimer’s disease, Amyloid-β, Blood-brain barrier, Nanoparticles, Neurodegenerative disorders
Department of Medical Biotechnology, Yeungnam University, Gyeongsan 38541, Amity Institute of Molecular Medicine and Stem Cell Research, Amity University, Noida 201313, Department of Pharmaceutics, University of Hail, Hail 2440, Department of Pharmacology and Toxicology, College of Pharmacy, University of Hail, Hail, Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Jouf University, Department of Medical Biotechnology, Yeungnam University, Gyeongsan 38541