Recent advances in tumor vasculature targeting using liposomal drug delivery systems

被引:30
作者
Abu Lila, Amr S. [1 ]
Ishida, Tatsuhiro [1 ]
Kiwada, Hiroshi [1 ]
机构
[1] Univ Tokushima, Inst Hlth Biosci, Dept Pharmacokinet & Biopharmaceut, Tokushima 7708505, Japan
关键词
angiogenesis; anti-angiogenic therapy; anticancer drugs; dual targeting; immunoliposomes; PEG-coated cationic liposome; vascular targeting; ANTI-NEOVASCULAR THERAPY; STERICALLY STABILIZED IMMUNOLIPOSOMES; TYPE-1; MATRIX-METALLOPROTEINASE; PROLONGED CIRCULATION TIME; GLYCOL-COATED LIPOSOMES; CATIONIC LIPOSOMES; ENDOTHELIAL-CELLS; SURFACE-CHARGE; IN-VIVO; ANGIOGENIC THERAPY;
D O I
10.1517/17425240903289928
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Tumor vessels possess unique physiological features that might be exploited for improved drug delivery. The targeting of liposomal anticancer drugs to tumor vasculature is increasingly recognized as an effective strategy to obtain superior therapeutic efficacy with limited host toxicity compared with conventional treatments. This review introduces recent advances in the field of liposomal targeting of tumor vasculature, along with new approaches that can be used in the design and optimization of liposomal delivery systems. In addition, cationic liposome is focused on as a promising carrier for achieving efficient vascular targeting. The clinical implications are discussed of several approaches using a single liposomal anticancer drug formulation: dual targeting, vascular targeting (targeting tumor endothelial cells) and tumor targeting (targeting tumor cells).
引用
收藏
页码:1297 / 1309
页数:13
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