Recent Advances and Strategies in Tumor Vasculature Targeted Nano-Drug Delivery Systems

被引:18
|
作者
Ying, Man [1 ,2 ]
Chen, Guanyu [1 ,2 ,3 ]
Lu, Weiyue [1 ,2 ,4 ,5 ,6 ,7 ]
机构
[1] Fudan Univ, Sch Pharm, Dept Pharmaceut, Shanghai 201203, Peoples R China
[2] Fudan Univ, Key Lab Smart Drug Delivery, Minist Educ, Shanghai 201203, Peoples R China
[3] Univ Auckland, Sch Pharm, Fac Med & Hlth Sci, Auckland 1042, New Zealand
[4] Fudan Univ, State Key Lab Med Neurobiol, Shanghai 200032, Peoples R China
[5] Fudan Univ, State Key Lab Med Neurobiol, Shanghai 200433, Peoples R China
[6] Fudan Univ, State Key Lab Mol Engn Polymers, Shanghai 200032, Peoples R China
[7] Fudan Univ, State Key Lab Mol Engn Polymers, Shanghai 200433, Peoples R China
基金
中国国家自然科学基金;
关键词
Angiogenesis; drug delivery systems; systematic targeted drug delivery; target; tumor vasculature; vasculogenic mimicry; EPHA2-EXPRESSING CANCER-CELLS; ENDOTHELIAL GROWTH-FACTOR; FACTOR RECEPTOR-BETA; END-RULE PEPTIDES; VASCULOGENIC MIMICRY; IN-VIVO; BLOOD-VESSELS; BREAST-CANCER; HEPATOCELLULAR-CARCINOMA; CHANNEL FORMATION;
D O I
10.2174/1381612821666150531163047
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In recent decades, targeted nano-drug delivery systems have attracted extensive attention in cancer therapy for their efficient drug delivery and tumor site specificity. Tumor vasculature, including angiogenesis and vasculogenic mimicry is associated tightly with tumor growth, progression and metastasis. Therefore, nano-drug delivery systems targeting tumor vasculature are becoming a promising approach for tumor treatment. As complicated mechanisms and various factors are involved in the tumor vasculature, different ligands modified on the surface of nanocarriers acquire active targeting through binding to the receptors over-expressed by cancer cells or angiogenic endothelial cells. In this review, the tumor vasculature characteristics are briefly described and the recent advances and potential strategies in tumor vasculature targeted nano-drug delivery systems are introduced.
引用
收藏
页码:3066 / 3075
页数:10
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