Horseradish peroxidase and toluidine blue covalently immobilized leak-free sol-gel composite biosensor for hydrogen peroxide

The enzyme horseradish peroxidase and the water-soluble mediator toluidine blue were covalently immobilized to 3-aminopropyl trimethoxy silane precursor through glutaraldehyde crosslinker. A rigid ceramic composite electrode was fabricated from this modified silane along with graphite powder, which resulted in an amperometric biosensor for H2O2. The electrochemical behaviour of the modified biosensor was monitored using cyclic voltammetry in the potential range of 0.2 V to - 0.4 V vs SCE. The biosensor exhibited a stable voltammogram with cathodic peak at - 0.234 V and anodic peak at - 0.172 V, with a formal potential of - 0.203 V. Various factors influencing the performance of the biosensor such as buffer solution, pH, temperature and potential were examined for optimizing the working conditions. The modified biosensor exhibited a good catalytic behaviour for the reduction of H2O2 at a lower potential of - 0.25 V without any barrier from possible interferents. The analytical working range was found to be 0.429 mu M to 0.455 mM of H2O2 with a detection limit of 0.171 mu M. The fabricated biosensor is robust for long-term usage in addition to the high sensitivity, rapid response and having an advantage of surface renewability by simple mechanical polishing. (C) 2016 Elsevier B.V. All rights reserved.