Hisaoka M, Tsukada K, Morioka T, Inomata T, Arakawa M
J Pharmacobiodyn. 1982 Jan;5(1):34-9. doi: 10.1248/bpb1978.5.34.
The antitumor effects of liposome-encapsulated carboquone (CQ-liposome) were studied following intraperitoneal administration into mice bearing Ehrlich ascites carcinoma (EAC). CQ-liposome showed nearly 3 times superior efficiencies to parent CQ (free CQ) in the growth inhibitory effect on EAC cells inoculated in mice, and also showed almost the same toxicity as free CQ in normal mice. CQ-liposome prolonged the life span of EAC bearing mice about 2 times that of free CQ. In the results of electrophoresis, it was found that CQ-liposome and EAC cells had positive and negative surface charges, respectively. These observations suggest that CQ-liposome is a favorite delivery system to enhance the efficiency of CQ to EAC in mice. One of the reasons for its excellent effect may be explained by an easy contact of CQ-liposome with EAC cells because of its opposite surface charges.
对携带艾氏腹水癌(EAC)的小鼠腹腔注射脂质体包裹的卡波醌(CQ-脂质体)后,研究了其抗肿瘤作用。CQ-脂质体对接种于小鼠体内的EAC细胞的生长抑制作用效率比母体CQ(游离CQ)高近3倍,并且在正常小鼠中显示出与游离CQ几乎相同的毒性。CQ-脂质体使荷EAC小鼠的寿命延长至游离CQ的约2倍。在电泳结果中发现,CQ-脂质体和EAC细胞分别具有正表面电荷和负表面电荷。这些观察结果表明,CQ-脂质体是提高CQ对小鼠EAC作用效率的理想递送系统。其优异效果的原因之一可能是由于CQ-脂质体与EAC细胞表面电荷相反,易于接触。