Targeting Anticancer Drugs to Tumor Vasculature Using Cationic Liposomes

被引:90
作者
Abu Lila, Amr S. [1 ]
Ishida, Tatsuhiro [1 ]
Kiwada, Hiroshi [1 ]
机构
[1] Univ Tokushima, Dept Pharmacokinet & Biopharmaceut, Subdiv Biopharmaceut Sci, Inst Hlth Biosci, Tokushima 7708505, Japan
关键词
angiogenesis; anti-angiogenic therapy; anticancer drugs; dosing schedule; dual targeting; PEG-coated cationic liposome; vascular targeting; MEDIATED DNA-TRANSFECTION; STERICALLY STABILIZED LIPOSOMES; IMPROVES ANTITUMORAL EFFICACY; POSITIVELY-CHARGED LIPOSOMES; ENDOTHELIAL GROWTH-FACTOR; IN-VIVO; THERAPEUTIC-EFFICACY; MACROMOLECULAR THERAPEUTICS; PHYSICOCHEMICAL PROPERTIES; ANTIANGIOGENIC AGENTS;
D O I
10.1007/s11095-010-0110-1
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Liposomal drug delivery systems improve the therapeutic index of chemotherapeutic agents, and the use of cationic liposomes to deliver anticancer drugs to solid tumors has recently been recognized as a promising therapeutic strategy to improve the effectiveness of conventional chemotherapeutics. This review summarizes the selective targeting of cationic liposomes to tumor vasculature, the merits of incorporating the polymer polyethylene-glycol (PEG), and the impact of the molar percent of the cationic lipid included in cationic liposomes on liposomal targeting efficacy. In addition, the discussion herein includes the therapeutic benefit of a dual targeting approach, using PEG-coated cationic liposomes in vascular targeting (of tumor endothelial cells), and tumor targeting (of tumor cells) of anticancer drugs. Cationic liposomes have shown considerable promise in preclinical xenograft models and are poised for clinical development.
引用
收藏
页码:1171 / 1183
页数:13
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