2021
DOI: 10.1016/j.bioelechem.2021.107838
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A feasible electrochemical biosensor for determination of glucose based on Prussian blue – Enzyme aggregates cascade catalytic system

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Cited by 24 publications
(9 citation statements)
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“…We have shown that bi-enzymatic cascades layer-by-layer constructed with GOx or GlOx, oxidising their substrates by O 2 with a formation of H 2 O 2 , and either peroxidase or peroxidase mimic -the hemin/PEI complex, electrocatalytically reducing H 2 O 2 at the electrode surface, could be successfully used to sense glucose and glutamate at moderate potentials and compete with the existing enzymatic-cascade-based electrode designs. [32][33][34][35][36][37][38][39][40][41][42] However, the cascade layer-by-layer assembly of enzymes on 5 μm carbon fibre microelectrodes resulted in accelerated mass-transfer of the enzymatically produced H 2 O 2 into solution and not to the sensing layer, disabling the ability of the enzymatic cascades to sense H 2 O 2 produced enzymatically from glucose or glutamate and O 2 . Considering the diffusing layer thickness for H 2 O 2 and the timescale of the experiments, we showed that as the electrode size/radius becomes less than 176 μm, the accelerated radial diffusion of H 2 O 2 from the electrode interferes with electrocatalytic reduction of H 2 O 2 .…”
Section: Discussionmentioning
confidence: 99%
“…We have shown that bi-enzymatic cascades layer-by-layer constructed with GOx or GlOx, oxidising their substrates by O 2 with a formation of H 2 O 2 , and either peroxidase or peroxidase mimic -the hemin/PEI complex, electrocatalytically reducing H 2 O 2 at the electrode surface, could be successfully used to sense glucose and glutamate at moderate potentials and compete with the existing enzymatic-cascade-based electrode designs. [32][33][34][35][36][37][38][39][40][41][42] However, the cascade layer-by-layer assembly of enzymes on 5 μm carbon fibre microelectrodes resulted in accelerated mass-transfer of the enzymatically produced H 2 O 2 into solution and not to the sensing layer, disabling the ability of the enzymatic cascades to sense H 2 O 2 produced enzymatically from glucose or glutamate and O 2 . Considering the diffusing layer thickness for H 2 O 2 and the timescale of the experiments, we showed that as the electrode size/radius becomes less than 176 μm, the accelerated radial diffusion of H 2 O 2 from the electrode interferes with electrocatalytic reduction of H 2 O 2 .…”
Section: Discussionmentioning
confidence: 99%
“…For electrodeposition of PB layers, 0.1 M KCl + 0.01 M HCl supported electrolyte solution (solution 1) and 3.0 mM K 3 Fe(CN) 6 + 3.0 mM FeCl 3 mixture dissolved in solution 1 (solution 2) were prepared. The cleaned Au electrode was electrochemically deposited by applying a potential of 0.4 V for 100 s in the stir-free solution 2, and the PB layer was activated in solution 1 through CV, scanning range of −0.05 to +0.35 V until the presence of a steady CV profile [43]. Finally, the electrode was dried at 65 • C for 30 min to get a steady PB active layer.…”
Section: Electrode Treatmentmentioning
confidence: 99%
“…Then, the PB/AuNS/GR electrode was dried at 50 • C for about 15 min. and characterized by an FE-SEM [16,24].…”
Section: The Preparation Modification and Characterization Of The Gra...mentioning
confidence: 99%
“…PB can be easily synthesized on the electrode surface and can replace the electron-transfer mediator present in the solution [14,15], thereby directly generating an electrochemical signal. This ensures the advancement of reagentless electrochemical glucose biosensors, where all necessary components are integrated, eliminating the need for reagent injection during the analysis process [16,17]. Unfortunately, PB-modified layers exhibit limited operational stability, particularly in neutral and alkaline conditions.…”
Section: Introductionmentioning
confidence: 99%