Electrochemical assay of proteolytically active prostate specific antigen based on anodic stripping voltammetry of silver enhanced gold nanoparticle labels

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Author listParnsubsakul A., Safitri R.E., Rijiravanich P., Surareungchai W.

PublisherElsevier

Publication year2017

JournalJournal of Electroanalytical Chemistry (1572-6657)

Volume number785

Start page125

End page130

Number of pages6

ISSN1572-6657

URLhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85007246673&doi=10.1016%2fj.jelechem.2016.12.010&partnerID=40&md5=752c04826f6dcd060d72db2f805e38e2

LanguagesEnglish-Great Britain (EN-GB)


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Abstract

This work demonstrated the determination of proteolytically active prostate specific antigen (paPSA), a potential biomarker for prostate cancer diagnosis, in human serum using a sensitive and low-cost electrochemical sensor. A specifically designed peptide probe was immobilized on the surface of a 96-well plate. The probe could be recognized by paPSA causing cleavage of the peptide, resulting in a decrease in the thiols group remaining on the probe. Gold nanoparticles (AuNPs) were attached to the peptide thiol groups by self-assembly. Hence the amount of AuNPs relates to the length of peptide probe. After cleavage and binding of AuNPs, an amplification step was performed using a silver enhancer solution. The quantity of deposited silver was then measured by differential pulse anodic stripping voltammetry (DPASV) using a disposable screen-printed carbon electrode (SPCE). The signal for paPSA detection was the linear range from 0.1 to 100 ng mL− 1, with a detection limit of 27 pg mL− 1. We also showed that the assay was reliable and has potential for clinical applications. © 2016 Elsevier B.V.


Keywords

paPSAScreen-printed carbon electrodeSilver enhancement


Last updated on 2023-27-09 at 07:36