“…These include potentiometry (Shamsipur, Jalali, Ershad, 2005;Santini, Pezza, Pezza, 2006;Hassan et al, 2005), capillary zone electrophoresis (Jin, Zhang, 2000), high performance liquid chromatography (HPLC) (González, Yuln, Volonté, 1999;Kasperek, 2008;Arcelloni et al, 2001), highperformance liquid chromatography-mass spectrometry (HPLC-MS) (Abdel-Hamid, Novotny, Hamza, 1990), spectrophotometry (Botello, Perez-Caballero, 1995), spectrofluorometry (Arancibia, Boldrini, Escandar, 2000;Damiani et al, 1999;Carreira et al, 1995), thin layer chromatography (Sun, Fabre, 1994), gas chromatography (Siou, Pommier, Godbillon, 1991;Yilmaz, 2010), polarographic analysis (Xu, Chen, Song, 2004), spectrophotometry (De Souza, Tubino, 2005;AgatonovicKustrin et al, 1997;Matin, Farajzadeh, Joyuban, 2005;Sastry, Prasad-Tipirneni, Suryanarayana, 1989;Sena et al, 2004) and electrochemistry methods (Blanco-Lopez et al, 2003;Goyal, Chatterjee, Agrawal, 2010;Manea et al, 2010). In all electrochemical methods, modified electrodes were used due to the gradual passivation or contamination of unmodified solid working electrodes occurred during the diclofenac oxidation.…”