Kaojarern S, Feldman M, Richardson C T, Brater D C
Clin Pharmacol Ther. 1981 Feb;29(2):198-202. doi: 10.1038/clpt.1981.31.
Tiotidine and cimetidine kinetics and dynamics were compared to assess mechanisms of the longer duration of effect of tiotidine in man. Both drugs has similar lag times for absorption. Tiotidine with a meal was more slowly absorbed than when fasting and was also more slowly absorbed than cimetidine with a meal. The elimination rates for both drugs did not differ; they were both approximately 2 to 3 hr. Oral doses of cimetidine achieved areas under the plasma concentration curve approximately three times that of tiotidine but these concentrations were only 1/10 as potent. The cimetidine concentration inducing 50% inhibition of food-stimulated gastric acid secretion was 0.41 +/- 0.04 whereas it was 0.04 +/- 0.003 microgram/ml for tiotidine. The effect of tiotidine lasted longer than that of cimetidine because the doses recommended for use in man resulted in higher concentrations in plasma relative to effective concentration than clinical doses of cimetidine.
比较了替奥替丁和西咪替丁的动力学及药效学,以评估替奥替丁在人体内作用持续时间更长的机制。两种药物的吸收滞后时间相似。替奥替丁与食物同服时的吸收速度比空腹时慢,且比与食物同服的西咪替丁吸收更慢。两种药物的消除速率无差异,均约为2至3小时。口服西咪替丁后的血浆浓度曲线下面积约为替奥替丁的三倍,但这些浓度的效力仅为替奥替丁的1/10。诱导食物刺激的胃酸分泌抑制50%时的西咪替丁浓度为0.41±0.04,而替奥替丁为0.04±0.003微克/毫升。替奥替丁的作用持续时间比西咪替丁长,因为推荐用于人体的剂量相对于有效浓度而言,在血浆中产生的浓度高于西咪替丁的临床剂量。