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Carbon nanomaterials and amyloid-beta interactions: potentials for the detection and treatment of Alzheimer's disease?
dc.contributor.author | Mohajeri M. | |
dc.contributor.author | Behnam B. | |
dc.contributor.author | Barreto G.E. | |
dc.contributor.author | Sahebkar A. | |
dc.date.accessioned | 2020-09-02T22:23:03Z | |
dc.date.available | 2020-09-02T22:23:03Z | |
dc.date.issued | 2019 | |
dc.identifier | 10.1016/j.phrs.2019.03.023 | |
dc.identifier.citation | 143, , 186-203 | |
dc.identifier.issn | 10436618 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12728/5353 | |
dc.description | Carbon-based nanomaterials have unique physicochemical properties relevant to the diagnosis and treatment of various diseases. There have been many reports indicating that carbon nanomaterials (CNMs) can interact and perturb biomolecules such as proteins and amyloid structures. This review is an attempt to reflect the role of CNMs in the treatment and detection of Alzheimer's disease (AD). The potential of CNMs in the field of neuroscience has also been reviewed. The exposure to CNMs ends up with effective radical and peptide scavenging structures, which, in turn, inhibit further formation and progression of amyloid fibrils. However, the effect of CNMs on initial nucleation and lag phase in this process may promote fibrillation. We have discussed the controversy that whether CNMs promote or inhibit the formation of amyloid beta (Aβ) fibrils to help preventing their toxicity or enhancing their therapeutic effects. © 2019 Elsevier Ltd | |
dc.language.iso | en | |
dc.publisher | Academic Press | |
dc.subject | Alzheimer's disease | |
dc.subject | Amyloid beta fibril | |
dc.subject | Carbon nanomaterials | |
dc.subject | Toxicity | |
dc.subject | amyloid beta protein | |
dc.subject | amyloid precursor protein | |
dc.subject | biological marker | |
dc.subject | carbon nanomaterial | |
dc.subject | cholinesterase inhibitor | |
dc.subject | donepezil | |
dc.subject | fluorodeoxyglucose f 18 | |
dc.subject | flutemetamol f 18 | |
dc.subject | fullerene | |
dc.subject | galantamine | |
dc.subject | graphene | |
dc.subject | nanomaterial | |
dc.subject | rivastigmine | |
dc.subject | tacrine | |
dc.subject | unclassified drug | |
dc.subject | amyloid beta protein | |
dc.subject | carbon | |
dc.subject | nanomaterial | |
dc.subject | Alzheimer disease | |
dc.subject | drug delivery system | |
dc.subject | drug effect | |
dc.subject | drug efficacy | |
dc.subject | drug exposure | |
dc.subject | drug mechanism | |
dc.subject | genetic association | |
dc.subject | human | |
dc.subject | limit of detection | |
dc.subject | limit of quantitation | |
dc.subject | near infrared spectroscopy | |
dc.subject | nonhuman | |
dc.subject | nuclear magnetic resonance imaging | |
dc.subject | physical chemistry | |
dc.subject | positron emission tomography | |
dc.subject | priority journal | |
dc.subject | protein aggregation | |
dc.subject | protein function | |
dc.subject | protein interaction | |
dc.subject | protein secretion | |
dc.subject | protein structure | |
dc.subject | Review | |
dc.subject | animal | |
dc.subject | genetic procedures | |
dc.subject | metabolism | |
dc.subject | Alzheimer Disease | |
dc.subject | Amyloid beta-Peptides | |
dc.subject | Animals | |
dc.subject | Biosensing Techniques | |
dc.subject | Carbon | |
dc.subject | Humans | |
dc.subject | Nanostructures | |
dc.title | Carbon nanomaterials and amyloid-beta interactions: potentials for the detection and treatment of Alzheimer's disease? | |
dc.type | Review |