Cederberg C, Lind T, Röhss K, Olbe L
Clinical Pharmacology, Astra Hässle AB, Mölndal, Sweden.
Digestion. 1992;53(3-4):171-8. doi: 10.1159/000200992.
The effect of 5 days of once-daily dosing with 20 mg p.o. and 40 mg i.v. omeprazole on pentagastrin-stimulated acid secretion was studied in 8 patients with duodenal ulcer. In addition they also received a 10-mg i.v. dose on day 6 during the oral treatment period. The antisecretory effect was measured 6-7 h after dose at a time point when maximal inhibition during the dosing interval is anticipated. The median percent inhibition of peak acid output (PAO) markedly increased from 43% on day 1 to 100% on day 5 during treatment with 20 mg p.o. The first 40-mg i.v. dose produced a median inhibition of 98% of PAO already on day 1. After 5 days of dosing, the inhibition had increased to 100%. On the other hand, a 10-mg i.v. dose could essentially maintain the degree of PAO reduction reached after 5 days of oral treatment. Plasma omeprazole concentrations increased during repeated dosing both with 20 mg p.o. and 40 mg i.v.
在8例十二指肠溃疡患者中研究了口服20 mg和静脉注射40 mg奥美拉唑每日1次、连续给药5天对五肽胃泌素刺激的胃酸分泌的影响。此外,在口服治疗期间的第6天,他们还接受了10 mg的静脉注射剂量。在预计给药间隔期间最大抑制作用出现的时间点,于给药后6 - 7小时测量抗分泌作用。口服20 mg治疗期间,峰值胃酸分泌量(PAO)的抑制率中位数从第1天的43%显著增加至第5天的100%。首次静脉注射40 mg剂量在第1天就使PAO的抑制率中位数达到了98%。给药5天后,抑制率增加到了100%。另一方面,10 mg静脉注射剂量基本可以维持口服治疗5天后所达到的PAO降低程度。重复给药期间,口服20 mg和静脉注射40 mg时血浆奥美拉唑浓度均升高。