Gustavson L E, Kaiser J F, Edmonds A L, Locke C S, DeBartolo M L, Schneck D W
Abbott Laboratories, North Chicago, Illinois 60064-3500, USA.
Antimicrob Agents Chemother. 1995 Sep;39(9):2078-83. doi: 10.1128/AAC.39.9.2078.
This study was conducted to determine (i) the effect of omeprazole on steady-state concentrations of clarithromycin and 14-(R)-hydroxyclarithromycin in plasma and gastric mucosa, (ii) the effect of clarithromycin on steady-state concentrations of omeprazole in plasma, and (iii) the effect of clarithromycin on the suppression of gastric acid secretion by omeprazole. Twenty healthy, Helicobacter pylori-negative male subjects completed this three-period, double-blind, randomized crossover study. In period 1, all subjects received 40 mg of omeprazole each morning for 6 days. Twenty-four-hour gastric pH monitoring took place on days -1 and 6. Pharmacokinetic sampling took place on day 6. In periods 2 and 3, subjects were randomly assigned to receive either 40 mg of omeprazole or omeprazole placebo daily for 6 days plus clarithromycin (500 mg) every 8 h for 5 days with a single 500-mg dose on day 6. Gastric tissue and mucus samples were obtained via endoscopy on day 5. Gastric pH monitoring and pharmacokinetic sampling took place on day 6. Two-week washout intervals separated the three study periods. Clarithromycin increased mean omeprazole area under the concentration-time curve from 0 to 24 h from 3.3 +/- 2.0 to 6.3 +/- 4.5 micrograms.h/ml (P < 0.05) and harmonic mean half-life from 1.2 to 1.6 h (P < 0.05) but did not significantly alter the effect of omeprazole on gastric pH. Mean clarithromycin area under the concentration-time curve from 0 to 8 h increased from 22.9 +/- 5.5 (placebo) to 26.4 +/- 5.7 micrograms.h/ml (omeprazole) (P < 0.05) when clarithromycin was administered with omeprazole. Analysis of variance revealed that mean concentrations of clarithromycin in tissue and mucus were statistically significantly higher when clarithromycin was given with omeprazole than when clarithromycin was given with placebo (P <0.001). Mean maximum observed concentrations of clarithromycin in the gastric fundus increased from 20.8 +/- 7.6 (placebo) to 24.3 +/- 6.4 micrograms/g (omeprazole), and those in the gastric mucous from 4.2 +/- 7.7 placebo to 39.3 +/- 32.8 micrograms/g (omeprazole). Similar increases were observed for the 14-(R)-hydroxyclarithromycin. These results show that omeprazole increases concentrations of clarithromycin in gastric tissue and mucus and may provide a mechanism for synergy between clarithromycin ad omeprazole that explains the excellent eradication of H. pylori seen in clinical trials.
(i)奥美拉唑对血浆及胃黏膜中克拉霉素和14-(R)-羟基克拉霉素稳态浓度的影响;(ii)克拉霉素对血浆中奥美拉唑稳态浓度的影响;(iii)克拉霉素对奥美拉唑抑制胃酸分泌作用的影响。20名健康的幽门螺杆菌阴性男性受试者完成了这项为期三个阶段的双盲随机交叉研究。在第1阶段,所有受试者每天早晨服用40mg奥美拉唑,共6天。在第-1天和第6天进行24小时胃pH监测。在第6天进行药代动力学采样。在第2和第3阶段,受试者被随机分配,每天服用40mg奥美拉唑或奥美拉唑安慰剂,共6天,外加每8小时服用克拉霉素(500mg),共5天,第6天服用一次500mg剂量。在第5天通过内镜获取胃组织和黏液样本。在第6天进行胃pH监测和药代动力学采样。三个研究阶段之间间隔两周的洗脱期。克拉霉素使奥美拉唑0至24小时浓度-时间曲线下的平均面积从3.3±2.0增加至6.3±4.5μg·h/ml(P<0.05),并使调和平均半衰期从1.2小时延长至1.6小时(P<0.05),但未显著改变奥美拉唑对胃pH的影响。当克拉霉素与奥美拉唑联用时,克拉霉素0至8小时浓度-时间曲线下的平均面积从22.9±5.5(安慰剂)增加至26.4±5.7μg·h/ml(奥美拉唑)(P<0.05)。方差分析显示,与安慰剂联用时相比,克拉霉素与奥美拉唑联用时组织和黏液中克拉霉素的平均浓度在统计学上显著更高(P<0.001)。胃底中克拉霉素的平均最大观察浓度从20.8±7.6(安慰剂)增加至24.3±6.4μg/g(奥美拉唑),胃黏液中从4.2±7.7(安慰剂)增加至39.3±32.8μg/g(奥美拉唑)。14-(R)-羟基克拉霉素也观察到类似的增加。这些结果表明,奥美拉唑可增加胃组织和黏液中克拉霉素的浓度,并可能为克拉霉素与奥美拉唑之间的协同作用提供一种机制,这解释了在临床试验中观察到的幽门螺杆菌的良好根除效果。