Direct electrochemistry of hemoglobin/peptide-carbon nanotube modified electrode for hydrogen peroxide biosensing

被引:7
|
作者
Sheikholeslam, Mohammadali [1 ,2 ,3 ]
Nanda, Piyush
Sanati, Alireza [1 ]
Pritzker, Mark [3 ]
Chen, P. [3 ,4 ]
机构
[1] Isfahan Univ Med Sci, Biosensor Res Ctr, Esfahan, Iran
[2] Isfahan Univ Med Sci, Sch Adv Technol Med, Dept Biomat Tissue Engn & Nanotechnol, Esfahan 8174673461, Iran
[3] Univ Waterloo, Dept Chem Engn, 200 Univ Ave West, Waterloo, ON N2L 3G1, Canada
[4] Univ Waterloo, Waterloo Inst Nanotechnol, 200 Univ Ave West, Waterloo, ON N2L 3G1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Self-assembling peptide; Single-wall carbon nanotubes (SWNTs); Mediatorless biosensor; Direct electron transfer; Hemoglobin;
D O I
10.1016/j.matlet.2022.133799
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
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 mu M and a detection limit of 7.54 mu M (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.
引用
收藏
页数:4
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