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Invivo and Invitro Comparative Results for the Hypolipemic Effect of Aminated Dextran Polymers

机译:胺基葡聚糖聚合物的降血脂作用的体内和体外比较结果

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The present paper reports on the derivatization of a polysaccharide (dextran), along with the bile acid binding capacities (invitro) and plasma lipid level lowering capacities (invivo) of the products. The A and B compounds were compared to a commercially hypolipidemic drug, Cholestyramin, with the following results:in vitro study of the values of the binding constants determined for sodium cholate (NaCA) showes that physico-chemical properties of these polymers can influence their binding capacity in the following manner: B A Cholestyramin. in vivo results differ from the in vitro data, which demonstrate the following order of binding efficiencies: Cholestyramin BA. The differences in the efficiency order for the binding of bile acids and the lowering of plasma lipid levels may be due to environmental variations in the digestive tract (pH, electrolytes, fatty acids). Aminated polysaccharides administered in rats did not affect the digestive system, liver or pancreas functions.
机译:本文报道了多糖(葡聚糖)的衍生化,以及产品的胆汁酸结合能力(体外)和血浆脂质水平降低能力(体内)。将A和B化合物与市售降血脂药Cholestyramin进行了比较,结果如下:对胆酸钠(NaCA)测定的结合常数的体外研究表明,这些聚合物的理化性质会影响其结合容量按以下方式:B> A>胆固醇。体内结果与体外数据不同,后者证明了结合效率的以下顺序:胆固醇> B> A。结合胆汁酸的效率顺序和血浆脂质水平降低的效率差异可能是由于消化道(pH,电解质,脂肪酸)的环境变化引起的。在大鼠中施用胺化多糖不会影响消化系统,肝脏或胰腺功能。

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