SciELO - Scientific Electronic Library Online

 
vol.26 issue5Evaluation of Cementitious Repair Mortars for Corrosion ResistanceElectrochemical Studies on the Corrosion Behavior of Carbon Steel in Presence of Cu and Ni author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • Have no similar articlesSimilars in SciELO

Share


Portugaliae Electrochimica Acta

Print version ISSN 0872-1904

Abstract

GUPTA, Hanuman P.; SAINI, Kalawati; DHINGRA, Priyanka  and  PANDEY, R.. Study of Acid Catalyzed Reactions of Proton Pump Inhibitors at D.M.E.. Port. Electrochim. Acta [online]. 2008, vol.26, n.5, pp.433-448. ISSN 0872-1904.

Acid catalyzed reactions of three proton pump inhibitors (PPIs), namely omeprazole, lansoprazole and pantoprazole, have been investigated and monitored by direct current polarography at dropping mercury electrode (D.M.E) in phosphate buffer (0.1 M) of pH 3-7.5. This gives well defined current-time profiles of individual electroactive degradation products along with their starting materials. The investigation shows that the order of stability of three PPIs can be written as: pantoprazole > omeprazole > lansoprazole. The rate of degradation of PPIs decreases with decreasing the basicity of the corresponding benzimidazole nitrogen of PPIs, as predicted by the effect of individual substituents on each of the benzimidazole rings. At pH 7.5 all three PPIs are almost stable and the observed half wave potentials (E1/2 ) are -1.07 V for omeprazole, -1.25 V for lansoprazole and -1.32 V for pantoprazole. On decreasing the pH from 7.5 to 3.0 the anodic shift in E1/2 values were observed along with degradation of the PPIs and simultaneous appearance of degradation products. The present study may provide an insight for designing more potent new proton pump inhibitors.

Keywords : polarography; stability; proton pump inhibitors (PPIs); half wave potential.

        · text in English     · English ( pdf )

 

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License