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Enhanced Visual Wireless Electrochemiluminescence Immunosensing of Prostate-Specific Antigen Based on the Luminol Loaded Into Mil-53(Fe)-Nh 2 Accelerator and Hydrogen Evolution Reaction Mediation Publisher Pubmed



Khoshfetrat SM1 ; Khoshsafar H2 ; Afkhami A3 ; Mehrgardi MA4 ; Bagheri H5
Authors
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Authors Affiliations
  1. 1. Biosensor Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran, 14117-13137, Iran
  2. 2. Research and Development Department, Farin Behbood Tashkhis LTD, Tehran, 15489-13111, Iran
  3. 3. Faculty of Chemistry, Bu-Ali Sina University, Hamedan, 65178-38695, Iran
  4. 4. Department of Chemistry, University of Isfahan, Isfahan, 81746-73441, Iran
  5. 5. Chemical Injuries Research Center, Systems Biology and Poisonings Institute, Baqiyatallah University of Medical Sciences, Tehran, 14359-16471, Iran

Source: Analytical Chemistry Published:2019


Abstract

A sensitive prostate-specific antigen (PSA) detection method using a visual-readout closed bipolar electrode (BPE) system has been introduced by integration of hydrogen evolution reaction (HER) in cathodic pole and electrochemiluminescence (ECL) of luminol loaded within the MIL-53(Fe)-NH 2 (L@MIL-53(Fe)-NH 2 ) in the anodic pole. The cathode of the BPE was electrochemically synthesized by 3D porous copper foam, followed by decorating with nitrogen-doped graphene nanosheet and ruthenium nanoparticles. As an alternative, we employed carboxylate-modified magnetic nanoparticles (MNPs) for immobilization of the primary antibody (Ab1) and utilized the L@MIL-53(Fe)-NH 2 conjugated to secondary antibody (Ab2) as a signaling probe and coreaction accelerator. After sandwiching the target PSA between Ab1 and Ab2, the MNP/Ab1-PSA-Ab2/L@MIL-53(Fe) were introduced to a gold anodic BPE. Finally, the resulting ECL of luminol and H 2 O 2 at the anodic poles was monitored using a photomultiplier tube (PMT) or digital camera. The PMT and visual (camera)-based detections showed linear responses from 1 pg mL -1 to 300 ng mL -1 (limit of detection 0.2 pg mL -1 ) and 5 pg mL -1 to 200 ng mL -1 (limit of detection 0.1 pg mL -1 ), respectively. This strategy provides an effective method for high-performance bioanalysis and opens a new door toward the development of the highly sensitive and user-friendly device. © 2019 American Chemical Society.