Benson G M, Alston D R, Hickey D M, Jaxa-Chamiec A A, Whittaker C M, Haynes C, Glen A, Blanchard S, Cresswell S R, Suckling K E
SmithKline Beecham Pharmaceuticals, The Frythe, Welwyn, Herts, U.K.
J Pharm Sci. 1997 Jan;86(1):76-81. doi: 10.1021/js960207j.
SK&F 97426-A is a novel bile acid sequestrant that is threefold more potent than cholestyramine at increasing bile acid excretion in the hamster. SK&F 97426-A is a quaternary alkylammonium polymethacrylate that was selected for comparison with cholestyramine in vivo because of its superior in vitro bile acid binding properties. Association, dissociation, affinity, and capacity experiments were performed under physiologically relevant conditions with the most abundant bile acids found in human bile. The bile acids came to equilibrium with SK&F 97426-A and cholestyramine within approximately 30 min and 6 min, respectively. SK&F 97426-A and cholestyramine had similar capacities for all the bile acids (between 2.5 and 4 mmol/g) and both had similar, very high affinities and slow dissociation rates for the dihydroxy bile acids. However, SK&F 97426-A had much higher affinities for the trihydroxy bile acids glycocholic acid and taurocholic acid than did cholestyramine. Dissociation of glycocholic acid and taurocholic acid from SK&F 97426-A was also much slower (27 and 25%, respectively, dissociated after 60 min) than from cholestyramine (89 and 84%, respectively, dissociated after 60 min). The higher affinities and slower dissociation rates of the trihydroxy bile acids for and from SK&F 97426-A probably account for the increased potency of SK&F 97426-A over cholestyramine in vivo.
SK&F 97426 - A是一种新型胆汁酸螯合剂,在增加仓鼠胆汁酸排泄方面的效力是消胆胺的三倍。SK&F 97426 - A是一种季铵化聚甲基丙烯酸酯,因其在体外具有优异的胆汁酸结合特性而被选用于体内与消胆胺进行比较。在生理相关条件下,使用人胆汁中含量最丰富的胆汁酸进行了结合、解离、亲和力和容量实验。胆汁酸分别在约30分钟和6分钟内与SK&F 97426 - A和消胆胺达到平衡。SK&F 97426 - A和消胆胺对所有胆汁酸的容量相似(在2.5至4 mmol/g之间),并且对二羟基胆汁酸都具有相似的、非常高的亲和力和缓慢的解离速率。然而,SK&F 97426 - A对三羟基胆汁酸甘氨胆酸和牛磺胆酸的亲和力比消胆胺高得多。甘氨胆酸和牛磺胆酸从SK&F 97426 - A的解离也比从消胆胺慢得多(60分钟后分别解离27%和25%)(消胆胺在60分钟后分别解离89%和84%)。三羟基胆汁酸对SK&F 97426 - A的较高亲和力和较慢解离速率可能解释了SK&F 97426 - A在体内比消胆胺效力更高的原因。