Edsbäcker S, Larsson P, Bergstrand M
Experimental Medicine, AstraZeneca, Wayne, PA, USA.
Aliment Pharmacol Ther. 2003 Feb;17(3):403-8. doi: 10.1046/j.1365-2036.2003.01431.x.
To investigate whether omeprazole affects the pharmacokinetics and systemic effects of budesonide controlled-release capsules when the two medications are taken together.
Thirteen healthy volunteers were enrolled into a randomized, double-blind, placebo-controlled, cross-over study. Participants received omeprazole, 20 mg/day, or placebo every morning for 5 days, with three 3-mg budesonide controlled-release capsules being given with omeprazole or placebo on day 5. After a 12-day washout period, participants were switched from omeprazole to placebo, or vice versa, and the trial was repeated. Blood samples for pharmacokinetic evaluation and urine samples for cortisol assessments were collected before and after the budesonide doses.
No statistically significant differences were seen between omeprazole and placebo treatment with regard to any of the parameters analysed, including the maximum budesonide plasma concentration, time to concentration maximum, area under the concentration-time curve, mean residence time and urinary excretion of cortisol. Very few adverse events were reported during the trial, and the majority were of mild to moderate severity.
Omeprazole treatment does not affect the pharmacokinetics or systemic effects of budesonide controlled-release capsules when the two medications are taken simultaneously.
研究当两种药物同时服用时,奥美拉唑是否会影响布地奈德控释胶囊的药代动力学及全身效应。
13名健康志愿者参与了一项随机、双盲、安慰剂对照的交叉研究。参与者每天早晨服用20毫克奥美拉唑或安慰剂,持续5天,在第5天与奥美拉唑或安慰剂一起服用3粒3毫克的布地奈德控释胶囊。经过12天的洗脱期后,参与者从奥美拉唑换为安慰剂,或反之,试验重复进行。在服用布地奈德剂量前后采集血样进行药代动力学评估,采集尿样进行皮质醇评估。
在分析的任何参数方面,包括布地奈德的最大血浆浓度、达峰时间、浓度-时间曲线下面积、平均驻留时间和皮质醇尿排泄量,奥美拉唑和安慰剂治疗之间均未观察到统计学上的显著差异。试验期间报告的不良事件很少,且大多数为轻度至中度严重程度。
当两种药物同时服用时,奥美拉唑治疗不会影响布地奈德控释胶囊的药代动力学或全身效应。