a b s t r a c tA voltammetric microsensor has been developed for the simultaneous assay of ascorbic (AA) and uric (UA) acids in aqueous solution. The electrode surface has been modified by means of electropolymerized conductive poly(3,4-ethylenedioxythiophene) PEDOT organic films. The electrocatalytic activity of the interface was dependent on the electropolymerization parameters inducing change in the structure and the morphology of the resulting polymer. The PEDOT thickness was optimized in order to maximize the peak potential separation between both acids oxidation to more than 400 mV. By using differential pulse voltammetry (DPV), the sensitivity of the microsensor was 0.87 lA lM À1 cm À2 and 4.05 lA lM À1 cm À2 for AA and UA respectively. The later was sensible to the presence of AA in the mixture, making evidence of the catalytic mechanism of UA regeneration. The calibration curves were linear in the concentration range 5.0-300 lmol L À1 for AA and 2.0-600 lmol L À1 for UA. The detection limits were 2.5 lmol L À1 and 1.5 lmol L À1 respectively. The sensor response was unmodified in the presence of the major electroactive biomarkers. The application of the PEDOT modified microsensor to the analysis of human blood serum was evaluated.

International audienceIntegrated (Pt/PEDOT–Pt–Ag/AgCl) and (Au/PEDOT–Pt–Ag/AgCl) electrochemical microcells (ElecCell) were elaborated for the detection of ascorbic acid, dopamine and uric acid by differential pulse voltam-metry. Specific attention was brought to the integration of poly(3,4-ethylenedioxythiophene) (PEDOT) film by electropolymerization. Gold and platinum working microelectrodes were investigated while using ethylenedioxythiophene (EDOT) electrodeposition processes in water or acetonitrile solvents. For the three antioxidant species, best (multi-)detection properties were obtained for acetonitrile-based PEDOT films deposited on gold working electrode. Thus, using integrated (Au/PEDOT–Pt–Ag/AgCl) Elec-Cell microdevices, analytical performances were determined for ascorbic acid, dopamine and uric acid, exhibiting high selectivity (oxidation potential: −40, 150 and 280 mV, respectively), linear concentration range from 0.1 to 300 ␮M, high sensitivities (0.85, 1.65 and 3.06 ␮A/␮M cm 2 , respectively) and low detection limit (0.2 ␮M, 0.1 ␮M and 0.05 ␮M, respectively)