This work reports the use of metallo tetra-amino phthalocyanines (MTAPc, M = Co and Mn) polymer thin films on gold and glassy carbon electrode surfaces for the detection and monitoring of hydrogen peroxide (H 2 O 2 ). The polymer-modified electrodes were characterized using electrochemical and microscopic-based methods. Atomic force microscopy (AFM) was used to study the bare and polymermodified ITO surfaces. The electrocatalytic reduction of H 2 O 2 with glassy carbon polymer-modified electrodes gave higher current densities compared to their gold counterparts. The electroanalytical properties of H 2 O 2 were obtained using a real-time calibration curve of the amperometric determination in pH 7.4 aqueous solution. The limits of detection (LoD) of the polymer-modified electrodes towards electroreduction of H 2 O 2 were of the order of 10 -7 M, with high sensitivity ranging from 6.0-15.4 mA.mM -1 .cm -2 .APPlICAtIOnS Of POlymerIzeD metAl tetrA-AmInO PhthAlOCyA nIneS 253MPc-modified electrodes are their ability to form stable polymers on electrode surfaces [6-13, 24] and long shelflife. We have previously reported [4] on the use of CoPc derivative-modified gold electrodes using self-assembly monolayer method (SAM) for the detection and monitoring of H 2 O 2 with detection limits of 1 × 10 -7 M and a reduction potential of -0.2 V vs. Ag|AgCl. SAMs on gold electrodes desorbs from the electrode at high pH, allowing only narrow potential range to be used [21]. CoPc-, MnPc-and FePc-modified screen-printed carbon electrodes (SPCE) have been employed for the detection of hydrogen peroxide with electrochemical reduction potential of -0.35 V vs. Ag|AgCl [20]. There is a need to lower both the detection limit and reduction potential for hydrogen peroxide without the use of unstable enzyme electrodes. The MPc complexes studied in this work contain cobalt and manganese as metal ion centers and these complexes are known to exhibit excellent electrocatalytic activity [25][26][27][28][29][30]. The amino functionalities on the phthalocyanine macrocycle were chosen due to their known ease of forming polymers on electrode surfaces [12,13,24], which are more stable for analysis compared to SAMs. The electrocatalytic and electroanalytical properties of gold and glassy carbon electrodes modified with thin polymeric films of CoTAPc and MnTAPc are compared for electroreduction of H 2 O 2 .