Kocoshis S A, Ghent C N, Gryboski J D
Dig Dis Sci. 1984 Dec;29(12):1148-52. doi: 10.1007/BF01317091.
We investigated the capability of Pepto-Bismol and its components (Veegum and bismuth subsalicylate) to sequester bile acids from aqueous solution in vitro and compared it to that of cholestyramine. Through a pH range of 3-9, all substances tested sequestered free and conjugated bile acids in quantities directly related to the concentration of the sequestering agent within the incubation mixture. Veegum was more effective gram for gram than bismuth subsalicylate. Pepto-Bismol, whose sequestering capacity approximated cholestyramine's, absorbed more than either of its components alone. The relationship between Pepto-Bismol's in vitro bile acid binding and its in vivo antidiarrheal properties is unknown.
我们研究了必奇及其成分(硅酸镁铝和碱式水杨酸铋)在体外从水溶液中螯合胆汁酸的能力,并将其与消胆胺进行了比较。在pH值为3至9的范围内,所有测试物质都能螯合游离和结合胆汁酸,其螯合量与孵育混合物中螯合剂的浓度直接相关。每克硅酸镁铝比碱式水杨酸铋更有效。必奇的螯合能力接近消胆胺,其吸收的胆汁酸比单独的任何一种成分都多。必奇在体外的胆汁酸结合能力与其体内止泻特性之间的关系尚不清楚。