Prewett E J, Nwokolo C U, Hudson M, Sawyerr A M, Fraser A, Pounder R E
University Department of Medicine, Royal Free Hospital School of Medicine, London, UK.
Aliment Pharmacol Ther. 1991 Oct;5(5):481-90. doi: 10.1111/j.1365-2036.1991.tb00517.x.
GR122311X (ranitidine bismuth citrate Glaxo Group Research Ltd) is a bismuth compound with histamine H2-receptor antagonist activity. The gastric acid antisecretory activity of three oral dosage regimens of GR122311X was compared with placebo and 150 mg ranitidine b.d. The median 24-h integrated intragastric acidity was 38, 26 and 18% of the median placebo value during dosing with GR122311X 196, 391 and 782 mg b.d., respectively. The 24-h acid suppression with GR122311X 391 mg b.d. was not significantly different to that produced by 150 mg ranitidine b.d. (24% of placebo acidity). The median 24-h urinary bismuth excretion increased with rising dosage of GR122311X from 19.2 micrograms with 196 mg b.d., to 36.4 micrograms with 391 mg b.d., to 68.7 micrograms with 782 mg b.d. In conclusion, GR122311X is an effective antisecretory agent with modest systemic bismuth absorption.
GR122311X(雷尼替丁枸橼酸铋,葛兰素集团研究有限公司)是一种具有组胺H2受体拮抗剂活性的铋化合物。将GR122311X的三种口服给药方案的胃酸分泌抑制活性与安慰剂和每日两次150毫克雷尼替丁进行了比较。在分别给予GR122311X每日两次196、391和782毫克期间,24小时胃内酸度积分中位数分别为安慰剂中位数的38%、26%和18%。GR122311X每日两次391毫克的24小时胃酸抑制作用与每日两次150毫克雷尼替丁产生的胃酸抑制作用(安慰剂酸度的24%)无显著差异。随着GR122311X剂量的增加,24小时尿铋排泄中位数从每日两次196毫克时的19.2微克增加到每日两次391毫克时的36.4微克,再增加到每日两次782毫克时的68.7微克。总之,GR122311X是一种有效的胃酸分泌抑制剂,全身铋吸收量适中。