Abstract
Horseradish peroxidase (HRP) and thionine (TN) were co-adsorbed onto a porous carbon felt (CF), and the resulting HRP and TN-adsorbed CF (HRP-TN-CF) was successfully used as a working electrode unit of a novel bioelectrocatalytic flow detector for a highly sensitive amperometric determination of hydrogen peroxide (H2O2). Co-adsorbed TN was essential to enhance the cathodic peak current of H2O2, and the current responses of the HRP-TN-CF-based detector were much larger than those of the HRP-CF-based detector (without TN). When air-saturated 0.1 M phosphate buffer (pH 7.0) was used as a carrier at a flow rate of 3.9 ml/min, cathodic peak currents of H2O2 (sample injection volume, 200 µl) obtained at an applied potential of 0 V (vs. Ag/AgCl) increased linearly up to 50 µM with a detection limit of 0.1 µM. Repetitive 100 sample injection of 100 µM H2O2 induced no serious current decrease, and RSD was 0.41 to 1.21% (n = 100). The HRP-TN-CF retained 42% of its original activity after 8 days of storage in 0.1 M phosphate buffer at 4°C.
