Hisaoka M, Tsukada K, Morioka T
J Pharmacobiodyn. 1982 Jan;5(1):18-26. doi: 10.1248/bpb1978.5.18.
The effects of encapsulation of carboquone (CQ) in the liposomes were investigated on the plasma clearance and tissue distribution of CQ in rabbit and rat. CQ-Liposome, the liposomes in which CQ was encapsulated, was prepared by the method described in a previous report. By intravenous administration at the same dose. CQ-liposome showed approximately three times higher plasma concentration than free CQ in rabbit and rat. However, prolonged release from liposomes or stabilization of CQ in plasma was not observed by encapsulation. The distribution to lung and reticuloendothelial-rich organs such as liver and spleen was enhanced, but on the contrary the distribution to the peripheral tissues such as muscle and skin was decreased. In rats pretreated with drug free liposomes, high plasma CQ concentration was obtained after intravenous administration of CQ-liposome. From these results, it is considered that the large parts of CQ-liposome is distributed into reticuloendothelial system (RES) and RES is saturable with liposomes. And it is also presumed that the high plasma concentration obtained after intravenous administration of CQ-liposome, would be caused by altering the tissue distribution of CQ by encapsulation.
研究了脂质体包裹卡波醌(CQ)对其在兔和大鼠体内的血浆清除率及组织分布的影响。CQ脂质体(即包裹了CQ的脂质体)采用先前报告中所述方法制备。以相同剂量静脉给药后,CQ脂质体在兔和大鼠体内的血浆浓度比游离CQ高约三倍。然而,未观察到脂质体对CQ有缓释作用或使其在血浆中稳定。CQ脂质体在肺以及肝脏和脾脏等富含网状内皮系统的器官中的分布增加,但相反,在肌肉和皮肤等外周组织中的分布减少。在用不含药物的脂质体预处理的大鼠中,静脉注射CQ脂质体后可获得较高的血浆CQ浓度。根据这些结果,认为大部分CQ脂质体分布到网状内皮系统(RES)中,且RES会被脂质体饱和。还推测静脉注射CQ脂质体后获得的高血浆浓度是由于包裹改变了CQ的组织分布所致。