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Direct Electrochemistry of Hemoglobin/Peptide-Carbon Nanotube Modified Electrode for Hydrogen Peroxide Biosensing Publisher



Sheikholeslam M1, 2, 3, 4 ; Nanda P3 ; Sanati A1 ; Pritzker M3 ; Chen P3, 4
Authors
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Authors Affiliations
  1. 1. Biosensor Research Center, Isfahan University of Medical Sciences, Isfahan, Iran
  2. 2. Department of Biomaterials, Tissue Engineering and Nanotechnology, School of Advanced Technologies in Medicine, Isfahan University of Medical Sciences, Isfahan, 81746 73461, Iran
  3. 3. Department of Chemical Engineering, University of Waterloo, 200 University Avenue West, Waterloo, N2L 3G1, ON, Canada
  4. 4. Waterloo Institute for Nanotechnology, University of Waterloo, 200 University Avenue West, Waterloo, N2L 3G1, ON, Canada

Source: Materials Letters Published:2023


Abstract

Mediatorless enzymatic biosensors based on direct electron transfer show promise due to their high stability and remarkable electrocatalytical performance. In this study, the direct electrochemistry of a glassy carbon electrode modified with hemoglobin (Hb) embedded in a hybrid layer of self-assembling EFK8 peptide and single-walled carbon nanotubes (SWNTs) was investigated. Electrochemical studies in 0.1 M phosphate buffer (PB) revealed that the immobilized Hb did not denature and retained its bio-catalytic activity. The resulting biosensor was used to detect and measure the hydrogen peroxide (H2O2) concentration in 0.1 M PB (pH 7.0), yielding a linear detection range from 20 to 960 µM and a detection limit of 7.54 µM (S/N = 3). The EFK8-SWNT hybrid layer shows promise as a biocompatible layer for simple non-covalent enzyme immobilization as the basis for future mediatorless enzymatic biosensors. © 2022