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Acta Pharmacol. Sin. · Jun 2003
Pharmacokinetics and tissue distribution of iv injection of polyphase liposome-encapsulated cisplatin (KM-1) in rats.
- Shan Wang, Jie-Bo Mi, Yuan-Zong Li, Wen-Bao Chang, Yun-Xiang Ci, Min-Zheng Zhao, Yun-Kun Zhao, Li-Ya Zhu, and Guang Xu.
- College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China. wangshan420@163.net
- Acta Pharmacol. Sin. 2003 Jun 1; 24 (6): 589-92.
AimThe pharmacokinetics and biodistribution of cisplatin encapsulated in polyphase liposome (KM-1) were compared with those of free drug in rats.MethodsThe platinum levels in serum and normal organs, after a single dose of iv injection of free or encapsulated cisplatin to rats, were determined by induced coupled plasma atomic emission spectrometry.ResultsSerum platinum concentration-time curve after a single iv dose of KM-1 4.5 mg/kg in rats was fitted with an open three-compartment model. The pharmacokinetic parameters were as follows: Vc=0.10 L/kg, T1/2pai=0.3 h, T1/2alpha=3.5 h, T1/2beta=2.7 h, AUC=265 mg.h.L(-1), and CL(s) =0.02 g.L.h(-1). KM-1 was cleared from the circulation much more slowly than free cisplatin. Liver and spleen had the highest concentration of platinum after KM-1 treatment.ConclusionKM-1 remained in the bloodstream longer than its free drug, and was taken mainly by the reticuloendothelial system.
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