Formelli F, Casazza A M, Di Marco A, Mariani A, Pollini C
Cancer Chemother Pharmacol. 1979;3(4):261-9. doi: 10.1007/BF00254742.
The tissue distribution of 4-demethoxydaunorubicin and 4-demethoxydoxorubicin was studied in comparison with that of their patient compounds, daunorubicin and doxorubicin, in mice bearing transplanted tumors. The doses administered were equal or equitoxic to those of their parent compounds. The levels of total fluorescence due to initial drugs and metabolites were determined on tissue extracts by fluorometry. After administration of equal doses of daunorubicin and 4-demethoxydaunorubicin, the calculated Cxt values of 4-demethoxydaunorubicin equivalents were higher than those for daunorubicin in all the organs tested except the heart. In animals treated with equitoxic doses, lower 4-demethoxydaunorubicin levels were found in all the organs tested. In mice treated with equitoxic doses of doxorubicin and 4-demethoxydoxorubicin, 4-demethoxydoxorubicin reached higher drug concentrations than doxorubicin in spleen and liver, whereas in all the other organs tested lower drug levels were found. The rate of drug disappearance from organs was slower in animals treated with 4-demethoxyderivatives than in those treated with their parent drugs.
在荷移植瘤小鼠中,研究了4-去甲氧基柔红霉素和4-去甲氧基阿霉素与其母体化合物柔红霉素和阿霉素相比的组织分布情况。给药剂量与其母体化合物相等或等效。通过荧光法测定组织提取物中初始药物和代谢产物产生的总荧光水平。给予等量的柔红霉素和4-去甲氧基柔红霉素后,除心脏外,在所有测试器官中,计算得出的4-去甲氧基柔红霉素当量的Cxt值均高于柔红霉素。在用等效剂量治疗的动物中,在所有测试器官中发现4-去甲氧基柔红霉素水平较低。在用等效剂量的阿霉素和4-去甲氧基阿霉素治疗的小鼠中,4-去甲氧基阿霉素在脾脏和肝脏中的药物浓度高于阿霉素,而在所有其他测试器官中发现药物水平较低。用4-去甲氧基衍生物治疗的动物器官中药物消失的速度比用其母体药物治疗的动物慢。