Bodemar G, Norlander B, Fransson L, Walan A
Br J Clin Pharmacol. 1979 Jan;7(1):23-31. doi: 10.1111/j.1365-2125.1979.tb00892.x.
1 The absorption of a single oral dose of cimetidine taken on a fasting stomach or together with a meal was studied in 28 patients before and during 12 weeks treatment with cimetidine. 2 No significant changes in bioavailability were seen during treatment measured as the area under the blood concentration curve (AUC). 3 AUC after a single dose of 400 mg cimetidine was 2.05 times the area after a 200 mg dose. 4 There was a good correlation between AUC and the dose of cimetidine given corrected for body weight (r=0.89). 5 There was no difference in bioavailability if 200 mg cimetidine was taken on a fasting stomach or together with a beef steak meal. 6. During fasting conditions there was a peak in blood concentration at about one hour followed by a second unexplained peak during the third to fifth hour after dose administration. 7 With food the initial rise in blood concentrations was slower and there was only one peak occurring about 2 h after dose administration.
在28名患者中,研究了空腹或与餐同服单次口服西咪替丁后的吸收情况,研究时间为西咪替丁治疗前及治疗12周期间。
以血药浓度曲线下面积(AUC)衡量,治疗期间生物利用度未见显著变化。
单次服用400mg西咪替丁后的AUC是服用200mg剂量后面积的2.05倍。
AUC与根据体重校正后的西咪替丁给药剂量之间存在良好相关性(r = 0.89)。
空腹服用200mg西咪替丁或与牛排餐同服时,生物利用度无差异。
在禁食条件下,给药后约1小时血药浓度出现峰值,随后在给药后第三至第五小时出现第二个无法解释的峰值。
进食后血药浓度的初始上升较慢,给药后约2小时仅出现一个峰值。