scholarly journals Beta‐Amyloid Oligomers: Amyloid‐β Oligomer‐Targeted Gadolinium‐Based NIR/MR Dual‐Modal Theranostic Nanoprobe for Alzheimer's Disease (Adv. Funct. Mater. 16/2020)

2020 ◽  
Vol 30 (16) ◽  
pp. 2070101
Author(s):  
Chengke Wang ◽  
Xueli Wang ◽  
Hei‐Nga Chan ◽  
Guifeng Liu ◽  
Zhenxin Wang ◽  
...  
2013 ◽  
Vol 9 ◽  
pp. P502-P502
Author(s):  
Yasuhide Okamoto ◽  
Tatsuki Yokoseki ◽  
Takamatsu Naofumi ◽  
Yukiho Imai ◽  
Shinobu Fujii

2010 ◽  
Vol 24 (1-2) ◽  
pp. 61-66 ◽  
Author(s):  
Emilie Kleiren ◽  
Jean-Marie Ruysschaert ◽  
Erik Goormaghtigh ◽  
Vincent Raussens

Alzheimer's disease (AD) is the most common form of dementia worldwide and represents a growing socio-economical issue. To date, no reliable diagnosis can be obtained at an early-stage of the disease, though it is now recognized that the aggregation of the amyloid β (Aβ) peptide is responsible for the onset of the disease. Recent studies have shown that soluble amyloid oligomers present in the physiological fluids were the most neurotoxic species and correlated best with the first signs of cognitive decline, which makes them good biomarkers in the development of a diagnostic tool.We describe here a new type of biosensor, based on attenuated total reflection Fourier transform infrared (ATR-FTIR) spectroscopy, that would be able to specifically detect and quantify the presence of the different forms of the Aβ peptide in solution. The principle of the detection relies on the recognition of the peptides by specific antibodies that were previously grafted on the surface of an ATR element, consisting of a functionalized germanium crystal. We show that the BIA-ATR technology is able to detect the presence of Aβ if incubated in deuterated water and that this step is crucial in the development of our conformation-sensitive biosensor for AD.


2012 ◽  
Vol 8 (4S_Part_21) ◽  
pp. S783-S783
Author(s):  
Giulio Taglialatela ◽  
Randy Woltjer ◽  
Lindsay Reese ◽  
Nicole Bjorklund ◽  
Anil Mantha

2014 ◽  
Vol 56 ◽  
pp. 99-110 ◽  
Author(s):  
David Allsop ◽  
Jennifer Mayes

One of the hallmarks of AD (Alzheimer's disease) is the formation of senile plaques in the brain, which contain fibrils composed of Aβ (amyloid β-peptide). According to the ‘amyloid cascade’ hypothesis, the aggregation of Aβ initiates a sequence of events leading to the formation of neurofibrillary tangles, neurodegeneration, and on to the main symptom of dementia. However, emphasis has now shifted away from fibrillar forms of Aβ and towards smaller and more soluble ‘oligomers’ as the main culprit in AD. The present chapter commences with a brief introduction to the disease and its current treatment, and then focuses on the formation of Aβ from the APP (amyloid precursor protein), the genetics of early-onset AD, which has provided strong support for the amyloid cascade hypothesis, and then on the development of new drugs aimed at reducing the load of cerebral Aβ, which is still the main hope for providing a more effective treatment for AD in the future.


Author(s):  
Mingeun Kim ◽  
Juhye Kang ◽  
Misun Lee ◽  
Jiyeon Han ◽  
Geewoo Nam ◽  
...  

We report a minimalistic redox-based design strategy for engineering compact molecules based on the simplest aromatic framework, benzene, with multi-reactivity against free radicals, metal-free amyloid-β, and metal-bound amyloid-β, implicated in the most common form of dementia, Alzheimer’s disease.


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