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    1,10-Phenanthroline-5,6-dione and 9,10-phenanthrenequinone as redox mediators for amperometric glucose biosensors
    (Springer, 2014) Zor, Erhan; Oztekin, Yasemin; Mikoliunaite, Lina; Voronovic, Jaroslav; Ramanaviciene, Almira; Anusevicius, Zilvinas; Bingol, Haluk
    In this study, two ortho-quinoidal compounds, 1,10-phenanthroline-5,6-dione (PD) and 9,10-phenanthrenequinone (PQ), were examined as electron transfer mediators suitable for amperometric glucose biosensors. The dependences of the electrochemical responses of PD- and PQ-based amperometric glucose biosensors on varied concentrations of glucose were investigated under aerobic and anaerobic conditions. The PD-modified graphite rod (GR) electrode revealed a current response seven times higher than that of the PQ-modified GR electrode. The reactivity indices of ortho-quinoidals assessed by means of B3LYP functional method applying 6-311G(D) basis set showed that the electron-accepting potency for PD was markedly higher as compared with that of PQ. Compared to PQ, considerably higher reactivity of PD has been defined in the reactions with NADP(+)-ferredoxin reductase (FNR, EC 1.18.1.2) as a model single-electron transfer FAD-dependent enzyme, which provided an additional evidence for PD as a more efficient mediator compared to PQ. This study illustrates that PD can be applied as a redox mediator for glucose oxidase and it could be more suitable for a reagent-less biosensor design than PQ.
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    Amperometric Glucose Biosensor Based on Glucose Oxidase, 1,10-Phenanthroline-5,6-dione and Carbon Nanotubes
    (Electrochemical Soc Inc, 2014) Zor, Erhan; Oztekin, Yasemin; Ramanaviciene, Almira; Anusevicius, Zilvinas; Bingol, Haluk; Barkauskas, Jurgis; Ersoz, Mustafa
    A biosensor for glucose determination was fabricated by the immobilization of glucose oxidase (GOx) on carbon nanotubes (CNTs) and/or 1,10-phenanthroline-5,6-dione (PD) modified graphite rod electrodes (GOx/PD/CNTs/GR) and its amperometric response toward glucose was investigated under aerobic and anaerobic conditions. The sensitivity of the GOx/PD/CNTs/GR electrode was found to be higher compared to that of a PD-modified GR electrode without CNTs (GOx/PD/GR), implying that CNTs play an important role in the facilitation of electron transfer between the redox active site of GOx and the electrode surface. The GOx/PD/CNTs/GR biosensor exhibited a linear dependency on substrate concentration in a range from 0.0 until 50.0 mM of glucose with oxygen present and from 0.0 until 62.5 mM of glucose in the absence of oxygen. With oxygen present, the limit of detection (LOD) values were determined to be 5.4 and 8.0 mM, and the limit of quantitation values (LOQ) were calculated as 16.2 and 24 mM for GOx/PD/GR and GOx/PD/CNTs/GR, respectively. In the absence of oxygen, the LOD values were calculated as 4.2 and 10.7 mM, and the LOQ values were calculated as 12.6 and 32.1 mM for GOx/PD/GR and GOx/PD/CNTs/GR, respectively. When examining the interference effect of uric acid for GOx/PD/GR and GOx/PD/CNTs/GR electrodes, no significant changes in the amperometric response of the modified electrodes were observed up to 100.0 mM of uric acid. (C) 2014 The Electrochemical Society. All rights reserved.
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    Evaluation of 1,10-phenanthroline-5,6-dione as redox mediator for glucose oxidase
    (Maik Nauka/Interperiodica/Springer, 2016) Zor, Erhan; Oztekin, Yasemin; Ramanaviciene, Almira; Anusevicius, Zilvinas; Voronovic, Jaroslav; Bingol, Haluk; Barauskas-Memenas, Dana
    A low-cost and simply fabricated amperometric glucose biosensor based on glucose oxidase (GOx) and 1,10-phenanthroline-5,6-dione (PD) modified graphite rod electrode was developed. The electrode exhibited good electrocatalytic activity with a well-defined hyperbolic dependence of amperometric signal upon glucose concentration in the presence and in the absence of oxygen. The electrode showed a good reproducibility and repeatability with relative standard deviation of less than 3 and 5%, respectively. The interaction of GOx with PD mediator was confirmed by means of UV?Vis absorbance spectroscopy.