Juárez-Olguín H, Flores J, Pérez G, Hernández G, Flores C, Guillé A, Camacho A, Toledo A, Carrasco M, Lares I
Department of Pharmacology, National Institute of Pediatrics, Avenue Imán No. 13th Piso, Colony Cuicuilco, CP 04530 Mexico City, Mexico.
Proc West Pharmacol Soc. 2002;45:156-8.
Is well known that food can affect the bioavailability of several drugs, its impact is major for those drugs that have to act near of drug absorption. Documentation about alterations of ranitidine bioavailability by effect of food is poor. The purpose of this work was to evaluate the effect of food over the bioavailability of ranitidine. Twenty healthy Mexican volunteers were included for the study. The study was made in two stages, in the first one the volunteers had 12 hour fast and took a 300 mg of oral dose of ranitidine (without food, WOF) and blood samples were drawn. Two weeks later, the volunteers took a normal diet just before ranitidine intake (with food, WF). The area under the curve (AUC) was 30% greater in WOF, Cmax was 921.5 ng/ml (WF) vs. 1685.2 (WOF), and t1/2 was 2.70 +/- 1.38 (WF) h vs 3.66 +/- 1.34 (WOF). The AUC, Cmax and t1/2 were statistically different. It is evident that there are differences in the drug disposition due to the presence of food, then, it is possible that the efficacy of ranitidine as inhibitor of gastric secretion being limited by food.
众所周知,食物会影响多种药物的生物利用度,对于那些必须在药物吸收部位附近起作用的药物,其影响更为显著。关于食物对雷尼替丁生物利用度影响的文献资料较少。本研究的目的是评估食物对雷尼替丁生物利用度的影响。该研究纳入了20名健康的墨西哥志愿者。研究分两个阶段进行,第一阶段,志愿者禁食12小时后口服300毫克雷尼替丁(空腹,WOF),并采集血样。两周后,志愿者在服用雷尼替丁前正常饮食(进食,WF)。曲线下面积(AUC)在空腹时大30%,Cmax为921.5纳克/毫升(进食)对1685.2(空腹),t1/2为2.70±1.38(进食)小时对3.66±1.34(空腹)。AUC、Cmax和t1/2在统计学上有差异。显然,由于食物的存在,药物处置存在差异,因此,雷尼替丁作为胃酸分泌抑制剂的疗效可能会受到食物的限制。