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枸橼酸雷尼替丁铋:一种新型抗溃疡药物,具有与枸橼酸铋 - 雷尼替丁混合物不同的物理化学特性和更高的生物活性。

Ranitidine bismuth citrate: a novel anti-ulcer agent with different physico-chemical characteristics and improved biological activity to a bismuth citrate-ranitidine admixture.

作者信息

McColm A A, McLaren A, Klinkert G, Francis M R, Connolly P C, Grinham C J, Campbell C J, Selway S, Williamson R

机构信息

Glaxo Wellcome Research and Development Ltd, Hertfordshire, UK.

出版信息

Aliment Pharmacol Ther. 1996 Jun;10(3):241-50. doi: 10.1111/j.0953-0673.1996.00241.x.

Abstract

BACKGROUND

Ranitidine bismuth citrate (RBC) is a new chemical entity for the treatment of peptic ulcer disease.

RESULTS

RBC is freely soluble in water (more than 600 mg/mL at pH 4.6), whereas an equimolar admixture of its component molecules, bismuth citrate and ranitidine, formed an almost totally insoluble suspension. Even at very low pH values (around 2.0), the solubility of bismuth in ranitidine bismuth citrate was at least two-fold better than in the admixture. Comparison of several physico-chemical characteristics indicated that RBC possessed significantly different melting point properties, X-ray powder diffraction patterns, infra-red spectra and 13C-NMR solid-state spectra to the admixture. Ranitidine bismuth citrate inhibited human pepsin isoenzymes 1, 2, 3 and 5 but the admixture was inactive. RBC showed approximately two-fold greater anti-Helicobacter pylori activity in vitro than the admixture (geometric mean minimum inhibitory concentrations of 12.5 and 25.7 mg/L, respectively) and was more rapidly bactericidal. In a mouse model of gastric H. pylori colonization, 200 mg/kg of bismuth, given as RBC, eradicated the organism from all mice while only 10% of infections were eradicated by equivalent levels of bismuth in admixture form.

CONCLUSION

It is believed that the significantly greater solubility of RBC, especially at lower pH values, is highly relevant to its better antipepsin and anti-H. pylori action compared to the insoluble admixture of bismuth citrate and ranitidine.

摘要

背景

枸橼酸雷尼替丁(RBC)是一种用于治疗消化性溃疡疾病的新型化学实体。

结果

RBC可自由溶于水(在pH 4.6时溶解度超过600 mg/mL),而其组成分子枸橼酸铋和雷尼替丁的等摩尔混合物形成了几乎完全不溶的混悬液。即使在非常低的pH值(约2.0)下,枸橼酸铋在枸橼酸雷尼替丁中的溶解度也比在混合物中的溶解度至少高两倍。几种物理化学特性的比较表明,RBC与混合物相比具有显著不同的熔点特性、X射线粉末衍射图谱、红外光谱和13C-NMR固态光谱。枸橼酸雷尼替丁可抑制人胃蛋白酶同工酶1、2、3和5,而混合物则无活性。RBC在体外的抗幽门螺杆菌活性比混合物高约两倍(几何平均最低抑菌浓度分别为12.5和25.7 mg/L),且杀菌速度更快。在小鼠胃幽门螺杆菌定植模型中,以RBC形式给予200 mg/kg铋可使所有小鼠体内的该菌被根除,而以混合物形式给予等量铋仅能根除10%的感染。

结论

据信,RBC显著更高的溶解度,尤其是在较低pH值下,与其比枸橼酸铋和雷尼替丁的不溶混合物具有更好的抗胃蛋白酶和抗幽门螺杆菌作用高度相关。

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