RESUMO
A miniaturized biosensing platform, based on monoclonal amyloid-beta antibodies (mAßab) that were immobilized on a disc-shaped platinum/iridium (Pt/Ir) microelectrode surface coupled with an impedimetric signal transducer, was developed for the label-free and sensitive detection of amyloid-beta peptide fragment 1-40 (Aß40); a reliable biomarker for early diagnosis of Alzheimer's disease (AD). A Pt/Ir microelectrode was electropolymerized with poly (ortho-phenylenediamine), a conducting free amine-containing aromatic polymer; followed by crosslinking with glutaraldehyde for subsequent coupling of mAßab on the microelectrode surface. This modification strategy efficiently improved the impedimetric detection performance of Aß40 in terms of charge transfer resistance (â¼400-fold difference) and normalized impedance magnitude percentage change (â¼40% increase) compared with a passive adsorption-based immobilization method. The sensitivity of the micro-immunosensing assay was found to be 1056 kΩ/(pg/mL)/cm2 and the limit of detection was found to be 4.81â¯pg/mL with a dynamic range of 1-104â¯pg/mL (R2â¯=â¯0.9932). The overall precision of the assay, as measured by relative standard deviation, ranged from 0.84 to 5.15%, demonstrating its reliability and accuracy; while in respect to assay durability and stability, the immobilized mAßab were able to maintain 80% of their binding activity to Aß40 after incubation for 48â¯hâ¯at ambient temperature (25⯰C). To validate the practical applicability, the assay was tested using brain tissue lysates prepared from AD-induced rats. Results indicate that the proposed impedimetric micro-immunosensing platform is highly versatile and adaptable for the quantitative detection of other disease-related biomarkers.