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Grant: Project Grant

University of Alberta

$730,576.00

Biodegradable acidic nanoparticles attenuate beta-amyloid aggregation/toxicity: potential implication in the treatment of Alzheimer's disease pathology

FY 2021-22

Summary
Alzheimer's disease (AD), the most common cause of dementia affecting the elderly population, is believed to be caused by clumps of protein called amyloid beta (Ab) peptide. This Ab peptide builds up in the brain and triggers death of brain cells, but how it does so is not clear. Evidence suggests that increased levels of Ab can aggregate with each other, leading to formation of toxic molecules that can trigger brain cell death in AD brains. In this study, we will use one type of biomolecule called PLGA nanoparticles, which are clinically approved for human use, to determine their ability to prevent Ab aggregation and trigger disassembly of preformed Ab aggregates. Additionally, we will test how these nanoparticles enter the cells and if they can able to reduce AD-related pathology in cellular as well as animal models of AD. Finally, we will use samples from AD patients to determine therapeutic potential of these nanoparticles in the treatment of AD.
Program
Project Grant
Location
Alberta, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
443438
Name
Kar Satyabrata
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Aging
Theme2
Biomedical
Prcname2
Biological and Clinical Aspects of Aging
Projecttitle
Biodegradable acidic nanoparticles attenuate beta-amyloid aggregation/toxicity: potential implication in the treatment of Alzheimer's disease pathology
Programtype2
Operating Grants
Orgnameinp2
University of Alberta
Cihramount2
$730,576
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Acidic Nanoparticles; Alzheimer'S Disease; Animal Models Of Alzheimer'S Disease; Beta-Amyloid Peptide; Cognitive Deficits; Induced Pluripotent Stem Cells; Lysosomal Leakage; Neuroprotection; Neurotoxicity; Protein Aggregation
Abstract
Alzheimer's disease (AD), the most common cause of dementia affecting the elderly population, is believed to be caused by clumps of protein called amyloid beta (Ab) peptide. This Ab peptide builds up in the brain and triggers death of brain cells, but how it does so is not clear. Evidence suggests that increased levels of Ab can aggregate with each other, leading to formation of toxic molecules that can trigger brain cell death in AD brains. In this study, we will use one type of biomolecule called PLGA nanoparticles, which are clinically approved for human use, to determine their ability to prevent Ab aggregation and trigger disassembly of preformed Ab aggregates. Additionally, we will test how these nanoparticles enter the cells and if they can able to reduce AD-related pathology in cellular as well as animal models of AD. Finally, we will use samples from AD patients to determine therapeutic potential of these nanoparticles in the treatment of AD.
Competitiondate
202104
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Kar, Satyabrata
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $730,576~ $0~
University of Alberta - $730,576 Grant (2021-22) | Canada Spends