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Direct electrochemistry of covalently immobilized hemoglobin on a naphthylimidazolium butyric acid ionic liquid/MWCNT matrix
[Display omitted] •Naphthyl substituted, carboxyl functionalized, imidazolium ionic liquid was synthesized.•The hydrophobic IL was dropcasted on multiwalled carbon nanotube coated GCE.•Hemoglobin was covalently attached to NIBA-IL/MWCNT/GCE platform and DET of Hb was established.•NIBA-IL/MWCNT/GCE o...
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Published in: | Colloids and surfaces, B, Biointerfaces B, Biointerfaces, 2021-03, Vol.199, p.111540-111540, Article 111540 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | [Display omitted]
•Naphthyl substituted, carboxyl functionalized, imidazolium ionic liquid was synthesized.•The hydrophobic IL was dropcasted on multiwalled carbon nanotube coated GCE.•Hemoglobin was covalently attached to NIBA-IL/MWCNT/GCE platform and DET of Hb was established.•NIBA-IL/MWCNT/GCE offered high conductivity and impressive biocompatibility.•NIBA-IL/MWCNT/GCE biosensor demonstrated excellent performance towards H2O2 biosensing.
Monitoring the concentration levels of hydrogen peroxide (H2O2) is significant in both clinical and industrial applications. Herein, we develop a facile biosensor for the detection of H2O2 based on direct electron transfer of hemoglobin (Hb), which was covalently immobilized on a hydrophobic naphthylimidazolium butyric acid ionic liquid (NIBA-IL) over a multiwalled carbon nanotube (MWCNT) modified glassy carbon electrode (GCE) to obtain an Hb/NIBA-IL/MWCNT/GCE. Highly water-soluble Hb protein was firmly immobilized on NIBA-IL via stable amide bonding between the free NH2 groups of Hb and COOH groups of NIBA-IL via EDC/NHS coupling. Thus fabricated biosensor showed a well resolved redox peak with a cathodic peak potential (Epc) at −0.35 V and anodic peak potential (Epa) at −0.29 V with a formal potential (E°’) of −0.32 V, which corresponds to the deeply buried FeIII/FeII redox centre of Hb, thereby direct electrochemistry of Hb was established. Further, the modified electrode demonstrated very good electrocatalytic activity towards H2O2 reduction and showed a wide linear range of detection from 0.01 to 6.3 mM with a limit of detection and sensitivity of 3.2 μM and 111 μA mM−1 cm−2, respectively. Moreover, the developed biosensor displayed high operational stability under dynamic conditions as well as during continuous potential cycles and showed reliable reproducibility. The superior performance of the fabricated biosensor is attributed to the effective covalent immobilization of Hb on the newly developed highly conducting and biocompatible NIBA-IL/MWCNT/GCE platform. |
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ISSN: | 0927-7765 1873-4367 |
DOI: | 10.1016/j.colsurfb.2020.111540 |