Kim S, Kim D J, Howell S B
Cancer Chemother Pharmacol. 1987;19(4):307-10. doi: 10.1007/BF00261478.
Liposomes containing cytosine arabinoside (ara-C) release drug slowly and can be used to maintain a locally high concentration of ara-C in the peritoneal cavity for intracavitary chemotherapy. However, a significant amount of active drug does reach the systemic circulation and contributes to systemic toxicity. We have devised a novel method of decreasing toxicity and increasing intraperitoneal half-life by pretreatment with "blank" liposomes containing no active drug. This technique has resulted in prolongation of intraperitoneal half-life of the liposomal ara-C from 21 h to 165 h, enabling maintenance of a therapeutic drug concentration even at 11 days after initial injection. One hundred percent cures (60-day survival) were achieved with a single-dose therapy begun 1 day after i.p. implantation of 10(6) L1210 leukemia cells.
含有阿糖胞苷(ara-C)的脂质体可缓慢释放药物,可用于在腔内化疗时维持腹腔内局部高浓度的阿糖胞苷。然而,相当数量的活性药物确实会进入体循环并导致全身毒性。我们设计了一种新方法,通过用不含活性药物的“空白”脂质体进行预处理来降低毒性并延长腹腔内半衰期。该技术已使脂质体阿糖胞苷的腹腔内半衰期从21小时延长至165小时,即使在初次注射后11天也能维持治疗药物浓度。在腹腔内植入10⁶个L1210白血病细胞后1天开始单剂量治疗,实现了100%的治愈(60天存活)。