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1.
Dig Dis Sci ; 55(12): 3423-9, 2010 Dec.
Article in English | MEDLINE | ID: mdl-20238247

ABSTRACT

AIM: The aim of this study was to compare acid control with a once-daily (od) modified-release (MR) formulation of esomeprazole vs. the conventional formulation (CF) dosed twice-daily (bid). METHODS: In a randomized, five-way crossover study, 55 healthy volunteers underwent 24-h intragastric pH monitoring after 5-day treatment with MR esomeprazole (40, 60 or 80 mg od) and CF esomeprazole (20 or 40 mg bid). RESULTS: Modified-release 60 and 80 mg od resulted in a significantly longer time with intragastric pH > 4 than MR 40 mg od (77.1 and 79.0% vs. 66.4%, respectively; both p < 0.05). At equivalent total daily doses, CF 20 mg bid led to a significantly longer time with intragastric pH > 4 than MR 40 mg od (72.3 vs. 66.4%; p < 0.05), and CF 40 mg bid led to a significantly longer time with pH > 4 than MR 80 mg od (85.5 vs. 79.0%; p < 0.05). CONCLUSIONS: At equivalent total daily doses, the MR formulation of esomeprazole provides less 24-h acid control than the conventional formulation dosed twice-daily.


Subject(s)
Esomeprazole/administration & dosage , Gastric Acid/metabolism , Gastroesophageal Reflux/drug therapy , Proton Pump Inhibitors/administration & dosage , Adult , Cross-Over Studies , Delayed-Action Preparations , Esomeprazole/pharmacokinetics , Female , Humans , Male , Middle Aged , Proton Pump Inhibitors/pharmacokinetics
2.
Basic Clin Pharmacol Toxicol ; 95(3): 112-9, 2004 Sep.
Article in English | MEDLINE | ID: mdl-15447734

ABSTRACT

This study aimed to investigate the effect of omeprazole on intragastric pH and gastrin release as well as the plasma concentration of omeprazole in relation to CYP2C19 genotypes after repeated doses in Korean patients. Twenty-six Korean patients with acid related disease were genotyped for CYP2C19 by allele specific PCR (wt/wt, CYP2C19*1/*1; wt/mut, CYP2C19*1/*2 or *1/*3; mut/mut, CYP2C19*2/*2, *2/*3 or *3/*3). Intragastric pH was monitored during 24 hr, and the plasma concentrations of omeprazole, hydroxyomeprazole, omeprazole sulfone and meal-stimulated gastrin were measured during 4 hr before and after 8 consecutive daily doses of 20 mg omeprazole. Unexpectedly the AUCs of omeprazole in the three genotypes were similarly high on Day 8. The mean 24 hr pH increased significantly in all three genotypes (paired t-test; P<0.0001), and the AUCs (4 hr) of gastrin in all patients increased markedly from 129+/-73 to 298+/-142 pMhr (P<0.0001). However, there was no statistically significant difference between the three genotypes in the mean pH and gastrin AUCs on Day 8. After 8 consecutive doses of 20 mg omeprazole, the gastric pH and the plasma gastrin were increased significantly in all three CYP2C19 genotypes, which were confirmed by high plasma concentrations of omeprazole in all three genotype groups. We suggest that the reason why the wt/wt had high concentrations of omeprazole similar to those in the other two genotype groups is that some of them were old with low CYP2C19 activity. In these patients omeprazole accumulated from the first to the eighth dose similar to that in the heterozygotes.


Subject(s)
Anti-Ulcer Agents/therapeutic use , Aryl Hydrocarbon Hydroxylases/genetics , Gastrins/metabolism , Mixed Function Oxygenases/genetics , Omeprazole/analogs & derivatives , Omeprazole/therapeutic use , Stomach Diseases/drug therapy , 2-Pyridinylmethylsulfinylbenzimidazoles , Adult , Aged , Anti-Ulcer Agents/blood , Anti-Ulcer Agents/pharmacokinetics , Area Under Curve , Cytochrome P-450 CYP2C19 , Female , Gastric Acidity Determination , Gastrins/blood , Genotype , Humans , Hydrogen-Ion Concentration/drug effects , Korea , Male , Middle Aged , Omeprazole/blood , Omeprazole/pharmacokinetics , Phenotype , Stomach Diseases/genetics , Stomach Diseases/metabolism
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