Tumor targeting based on the effect of enhanced permeability and retention (EPR) and the mechanism of receptor-mediated endocytosis (RME)

被引:170
作者
Tanaka, T [1 ]
Shiramoto, S [1 ]
Miyashita, M [1 ]
Fujishima, Y [1 ]
Kaneo, Y [1 ]
机构
[1] Fukuyama Univ, Fac Pharm & Pharmaceut Sci, Dept Biopharmaceut, Fukuyama, Hiroshima 7290292, Japan
关键词
drug delivery system; tumor targeting; mitomycin c; macromolecular conjugate; serum albumin; transferrin; enhanced permeability and retention; receptor-mediated endocytosis; intracellular disposition; antitumor activity;
D O I
10.1016/j.ijpharm.2003.09.050
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This review is focused on the macromolecular drug carrier systems by the effect of enhanced permeability and retention (EPR) and the mechanism of receptor-mediated endocytosis (RME). The effect of EPR is thought to be useful for the targeting of the macromolecular drugs to the tumor tissues on a vasculolymphatic level. The RME reveals the selective recognition, high affinity binding, and immediate internalization for the ligand on a cellular level. In the receptor, recognizing transferrin, a level of expression on the tumor cells is higher than that on the normal cells. We have used serum albumin and transferrin as drug carriers to deliver mitomycin C (MMC) to the tumor tissues and into the tumor cells. The properties of the conjugates of MMC to serum albumin and transferrin were examined in vitro and in vivo. We concluded that MMC could be delivered to the tumor tissue and cells by the use of albumin and transferrin as drug carriers. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:39 / 61
页数:23
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