Modified graphitized carbon black as transducing material for reagentless H2O2 and enzyme sensors

Julija Razumiene; Jurgis Barkauskas; Virgaudas Kubilius; Rolandas Meskys; Valdas Laurinavicius

doi:10.1016/j.talanta.2005.04.004

Modified graphitized carbon black as transducing material for reagentless H2O2 and enzyme sensors

Talanta. 2005 Oct 15;67(4):783-90. doi: 10.1016/j.talanta.2005.04.004. Epub 2005 Apr 21.

Authors

Julija Razumiene¹, Jurgis Barkauskas, Virgaudas Kubilius, Rolandas Meskys, Valdas Laurinavicius

Affiliation

¹ Institute of Biochemistry, Mokslininku 12, Vilnius, Lithuania. julija.R@bchi.lt

PMID: 18970240
DOI: 10.1016/j.talanta.2005.04.004

Abstract

Direct electron transfer between redox enzymes and electrodes is the basis for the third generation biosensors. We established direct electron transfer between quinohemoprotein alcohol dehydrogenase (PQQ-ADH) and modified carbon black (CBs) electrodes. Furthermore, for the first time, this phenomenon was observed for pyrroloquinoline quinone (PQQ)-dependent glucose dehydrogenase (PQQ-GDH). Reagentless enzyme biosensors suitable for the determination of ethanol, glucose and sensors for hydrogen peroxide were designed using CB electrodes and screen-printing technique. Aiming to create an optimal transducing material for biosensors, a set of CB batches was synthesized using the matrix of Plackett-Burman experimental design. Depending on the obtained surface functional groups as well as the nano-scale carbon structures in CBs batches, the maximal direct electron transfer current of glucose and ethanol biosensors can vary from 20 to 300 nA and from 30 to 6300 nA for glucose and ethanol, respectively. Using modified CB electrodes, an electrocatalytic oxidation of H(2)O(2) takes place at more negative potentials (0.1-0.4V versus Ag/AgCl). Moreover, H(2)O(2) oxidation efficiency depends on the amount and morphology of fine fraction in the modified CBs.