Pantoprazole: a new and more specific proton pump inhibitor

Abstract

Pantoprazole is the third proton pump inhibitor (PPI) to be launched for the treatment of acid-peptic diseases. Like other drugs in this class, pantoprazole causes long-lasting inhibition of acid secretion by inactivating the parietal cell H+/K+-ATPase. Compared with H2 antagonists, pantoprazole results in faster pain relief, more rapid ulcer healing, healing of resistant ulcers and far greater efficacy in oesophageal reflux disease. The three PPIs currently available display almost identical efficacy in the treatment of acid-peptic diseases and when included as part of Helicobacter pylori eradication regimes. However, pantoprazole shows improvements in selectivity and pharmacokinetic properties compared with omeprazole and lansoprazole. The bioavailability of pantoprazole is considerably higher than omeprazole, remains constant upon repeated dosing, and is unaffected by food. Significantly, pantoprazole does not influence hepatic cytochrome P450 activity and does not therefore interact with co-administered drugs. This is in contrast to omeprazole, which inhibits P450, and lansoprazole, which appears to weakly induce multiple metabolic pathways. Although pantoprazole is entering an antisecretory market dominated by omeprazole and ranitidine, it has a number of potential advantages. In this respect it is worth recalling that enhanced specificity and the absence of drug interactions were decisive factors in determining market share in the H2 antagonist era. Pantoprazole may therefore achieve significant market penetration, particularly at the expense of lansoprazole and the H2 blockers.

• acid-peptic disorders
• amoxycillin
• antisecretory drugs
• cimetidine
• clarithromycin
• cytochrome P450
• development strategy
• drug interactions
• duodenal ulcer
• eradication
• famotidine
• gastric acid
• gastric ulcer
• H+/K+-ATPase
• healing
• Helicobacter pylori
• histamine H2 antagonists
• lansoprazole
• market share
• metronidazole
• nizatidine
• omeprazole
• pantoprazole
• pepsin
• peptic ulcer
• pharmacokinetics
• proton pump inhibitors
• ranitidine
• reflux oesophagitis
• relapse
• resistant ulcer
• safety
• selectivity
• specificity
• Zollinger-Ellison syndrome