Rubio-Retama Jorge, Hernando Jorge, López-Ruiz Beatriz, Härtl Andreas, Steinmüller Doris, Stutzmann Martin, López-Cabarcos Enrique, Garrido José Antonio
Departamento de Química-Física II, Facultad de Farmacia, UCM, Spain.
Langmuir. 2006 Jun 20;22(13):5837-42. doi: 10.1021/la060167r.
Horseradish peroxidase (HRP) has been immobilized on the surface of functionalized nanocrystalline diamond (NCD) thin films. The structure of the modified NCD surface as well as the electrochemical behavior of the whole system was characterized by impedance spectroscopy and cyclic voltammetry. The proximity of HRP heme groups to the NCD surface allowed direct electron transfer between them, resulting in two separated one-electron-transfer peaks at 0.05 V and 0.29 V vs Ag/AgCl, corresponding to the cathodic and anodic process, respectively. The heterogeneous electron-transfer constant for both processes was calculated to be 0.066 s(-1), the charge-transfer coefficient alpha = 0.49, and the immobilized enzymatic layer about 2.10(-10) mol/cm2. The modified NCD electrode was used as a third-generation biosensor for hydrogen peroxide determination showing a linear response in the 0.1-45 mM H2O2 range, at +0.05 V vs Ag/AgCl.
