Brater D C, Peters M N, Eshelman F N, Richardson C T
Clin Pharmacol Ther. 1982 Oct;32(4):484-9. doi: 10.1038/clpt.1982.192.
Ranitidine is a histamine H2-receptor antagonist that differs structurally from cimetidine. We assessed its kinetics, potency, and duration of effect in patients with chronic duodenal ulcers. Ranitidine had an absorption lag time of approximately 30 min, an absorption half-life (t 1/2) of approximately 40 min, and an elimination t 1/2 of 3 hr, all differing from those of cimetidine. It is five times as potent, so that equal doses of ranitidine induce considerably longer suppression of both basal and food-stimulated gastric acid secretion than cimetidine.
雷尼替丁是一种组胺H2受体拮抗剂,在结构上与西咪替丁不同。我们评估了其在慢性十二指肠溃疡患者中的动力学、效力和作用持续时间。雷尼替丁的吸收延迟时间约为30分钟,吸收半衰期(t 1/2)约为40分钟,消除t 1/2为3小时,所有这些均与西咪替丁不同。其效力是西咪替丁的五倍,因此相同剂量的雷尼替丁比西咪替丁能更显著地延长对基础胃酸分泌和食物刺激胃酸分泌的抑制时间。