Tattersall M H, Sodergren J E, Dengupta S K, Trites D H, Modest E J, Frei E
Clin Pharmacol Ther. 1975 Jun;17(6):701-8. doi: 10.1002/cpt1975176701.
The distribution and excretion of tritiated actinomycin D have been determined in 3 adult patients with disseminated malignant melanoma. In the blood, the drug was preferentially taken up into nucleated cells. The urinary and fecal excretion was prolonged and only about 30 per cent of the dose of actinomycin was recovered in 9 days. There was evidence that the drug was concentrated in bone marrow and tumor cells, but did not readily cross the blood-brain barrier. The long tissue half-lige of actinomycin D suggeststhat an intermittenr schedule of administration would be the most effective.
已对3例播散性恶性黑色素瘤成年患者体内的氚标记放线菌素D的分布和排泄情况进行了测定。在血液中,该药物优先被有核细胞摄取。尿液和粪便排泄时间延长,9天内仅回收了约30%的放线菌素剂量。有证据表明该药物在骨髓和肿瘤细胞中浓缩,但不易穿过血脑屏障。放线菌素D较长的组织半衰期表明间歇给药方案可能最为有效。