Thibeault D, Pagé M
Department of Biochemistry, Faculty of Medicine, Université Laval, Sainte-Foy, Québec, Canada.
Int J Immunopharmacol. 1990;12(5):503-7. doi: 10.1016/0192-0561(90)90113-2.
We report the synthesis of daunorubicin antialphafoetoprotein conjugates, using a new coupling method. At equimolar concentrations on AFP producing cells in vitro, these conjugates were found three times as cytotoxic as the free drug.
我们报告了使用一种新的偶联方法合成柔红霉素抗甲胎蛋白缀合物。在体外对产生甲胎蛋白的细胞采用等摩尔浓度时,发现这些缀合物的细胞毒性是游离药物的三倍。