Journal
MICROCHIMICA ACTA
Volume 186, Issue 12, Pages -Publisher
SPRINGER WIEN
DOI: 10.1007/s00604-019-3903-x
Keywords
beta-Amyloid((1-42)); Peptisensor; Beta-amyloid; Neurodegenerative disease; Pathophysiology; Nanoparticles; Blood; Clinical diagnosis
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Funding
- Iran National Science Foundation [96005985]
- Research Councils of Shiraz University of Medical Sciences
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Alzheimer's disease (AD) is connected to aggregation of amyloid-beta (A beta) peptide and formation of insoluble plaques in the brain. A beta level can be monitored as an AD early diagnosis route. In this study, an irregular shaped microporous gold nanostructure with a typical size of 150x250 nm was electrodeposited on a polycrystalline gold surface at 0 mV (vs. AgCl) using sodium alendronate. The nanostructure was then characterized by field-emission scanning electron microscopy. An electrochemical peptide-based biosensor was fabricated by immobilizing an A beta((1-42))-binding peptide on the gold nanostructure. Binding of A beta((1-42)) by the peptide was followed electrochemically using ferro/ferricyanide as a redox probe. Differential pulse voltammograms in a potential range of 0-500 mV (vs. AgCl) with typical peak potentials at 224 mV are linear in the 3-7000 pg mL(-1) A beta((1-42)) concentration range, with a 0.2 pg mL(-1) detection limit. The biosensor is free of interferences and was applied to the quantitation of A beta((1-42)) in artificial cerebrospinal fluid and spiked serum samples.
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