| Literature DB >> 32568700 |
Claudia A Razzino1, Verónica Serafín2, Maria Gamella2, María Pedrero2, Ana Montero-Calle3, Rodrigo Barderas3, Miguel Calero4, Anderson O Lobo5, Paloma Yáñez-Sedeño2, Susana Campuzano6, José M Pingarrón7.
Abstract
This work reports a new sensitive strategy for the determination of tau protein, a hallmark of Alzheimer's disease (AD), involving a sandwich immunoassay and amperometric detection at disposable screen-printed carbon electrodes (SPCEs) modified with a gold nanoparticles-poly(amidoamine) (PAMAM) dendrimer nanocomposite (3D-Au-PAMAM) covalently immobilized onto electrografted p-aminobenzoic acid (p-ABA). The capture antibody (CAb) was immobilized by crosslinking with glutaraldehyde (GA) on the amino groups of the 3D-Au-PAMAM-p-ABA-SPCE, where tau protein was sandwiched with a secondary antibody labeled with horseradish peroxidase (HRP-DAb). Amperometry at -200 mV (vs the Ag pseudo-reference electrode) upon the addition of hydroquinone (HQ) as electron transfer mediator and H2O2 as the enzyme substrate was used to detect the immunocomplex formation. The great analytical performance of the immunosensor in terms of selectivity and low limit of detection (LOD) (1.7 pg mL-1) allowed the direct determination of the target protein in raw plasma samples and in brain tissue extracts from healthy individuals and post mortem diagnosed AD patients, using a simple and fast protocol.Entities:
Keywords: Amperometric sandwich immunoassay; Brain tissue; Dendrimer nanocomposite; Raw plasma; Screen-printed electrode; Tau protein
Mesh:
Substances:
Year: 2020 PMID: 32568700 DOI: 10.1016/j.bios.2020.112238
Source DB: PubMed Journal: Biosens Bioelectron ISSN: 0956-5663 Impact factor: 10.618