Carrera G, Mitjavila S, Lacombe C, Derache R
Toxicology. 1976 Aug-Sep;6(2):191-71. doi: 10.1016/0300-483x(76)90018-4.
The absorption and distribution of Morestan 35S in the organism of the rat were studied after administration by stomach tube. It was shown that Morestan, in vivo and in vitro, forms a complex with plasma proteins and particularly with albumins. Most of the plasma Morestan is distributed like this. After intravenous admininstration, the constant of elimination, K13, and the biological half-life determination show that plasma Morestan 35S is eliminated very slowly. The K12 and K21 constants indicate that there is an equilibrium between the plasma compartment and a peripheral compartment. After intragastric administration, the increase of radioactivity in epididymal adipose tissue, indicate that the peripheral compartment should include the adipose tissue.
通过胃管给药后,研究了莫雷斯汀35S在大鼠体内的吸收和分布情况。结果表明,莫雷斯汀在体内和体外均与血浆蛋白,尤其是白蛋白形成复合物。大部分血浆中的莫雷斯汀都是以这种形式分布的。静脉给药后,消除常数K13和生物半衰期测定表明,血浆中的莫雷斯汀35S消除非常缓慢。K12和K21常数表明,血浆隔室和外周隔室之间存在平衡。胃内给药后,附睾脂肪组织中放射性的增加表明外周隔室应包括脂肪组织。