Folic acid-conjugated liposomal vincristine for multidrug resistant cancer therapy

被引:32
|
作者
Wang, Chenyu [1 ]
Feng, Linglin [3 ]
Yang, Xiangkun [1 ]
Wang, Fei [1 ]
Lu, Weiyue [1 ,2 ]
机构
[1] Fudan Univ, Sch Pharm, Dept Pharmaceut, Minist Educ & PLA, Shanghai 201203, Peoples R China
[2] Fudan Univ, State Key Lab Mol Engn Polymers, Shanghai 200433, Peoples R China
[3] Shanghai Inst Planned Parenthood Res, Lab Contracept & Devices Res, NPFC China, Shanghai 200032, Peoples R China
基金
中国国家自然科学基金;
关键词
Multidrug resistance; Folic acid; Liposome; Vincristine; Targeting delivery; Pharmacodynamics;
D O I
10.1016/j.ajps.2013.07.015
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We encapsulated vincristine into folic acid-conjugated PEGylated liposomes to improve the anti-tumor efficacy on multidrug resistant cancers. It was observed that the drug delivery system we constructed exhibited maximum cytotoxicity on KBv200 cells (multidrug resistant variant) compared with any other formulations. The semi-quantitative analysis of region of interest revealed that there was a great increase in area under curve (AUC) of a near-infrared fluorescein in solid tumors due to folic acid-mediated accumulation. Folic acid-conjugated PEGylated liposomes showed a significant tumor growth inhibiting effect in vitro and in vivo. TUNEL assay revealed that folic acid-conjugated PEGylated liposomes could induce cell apoptosis much more greatly than others. This study demonstrated that it had potential application prospective for the treatment of multidrug resistant cancer. (C) 2013 Shenyang Pharmaceutical University. Production and hosting by Elsevier B.V. All rights reserved.
引用
收藏
页码:118 / 127
页数:10
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