Dual-vectors of anti-cancer drugs and genes based on pH-sensitive micelles self-assembled from hybrid polypeptide copolymers

被引:40
作者
Li, Yong-Yong [1 ,2 ,3 ]
Hua, Shou-Hu [1 ,2 ]
Xiao, Wang [1 ,2 ]
Wang, Hui-Yuan [1 ,2 ]
Luo, Xiao-Hua [1 ,2 ]
Li, Cao [1 ,2 ]
Cheng, Si-Xue [1 ,2 ]
Zhang, Xian-Zheng [1 ,2 ]
Zhuo, Ren-Xi [1 ,2 ]
机构
[1] Wuhan Univ, Key Lab Biomed Polymers, Minist Educ, Wuhan 430072, Peoples R China
[2] Wuhan Univ, Dept Chem, Wuhan 430072, Peoples R China
[3] Tongji Univ, Inst Adv Mat & Nano Biomed iNANO, Shanghai 200092, Peoples R China
关键词
POLY-L-LYSINE; BLOCK-COPOLYMER; TRANSFECTION EFFICIENCY; BIOLOGICAL SIGNIFICANCE; MULTIBLOCK COPOLYMERS; POLY(ETHYLENE OXIDE); AQUEOUS-SOLUTION; DELIVERY; DNA; ACID);
D O I
10.1039/c0jm03385e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A series of amphiphilic pH-sensitive hybrid polypeptide copolymers, poly(ethylene glycol)-b-poly-(L-lysine)-b-poly(L-phenylalanine) (PEG-PLL-PLP) were synthesized. The copolymers could self-assemble into micelles with PLP as the hydrophobic core and PEG-PLL as the hydrophilic shell, as evidenced by (HNMR)-H-1 and TEM. These micelles exhibited obvious pH response in hydrodynamic diameter and pH-dependent drug release behavior, attributed to the protonation/deprotonation of amino groups in PLL segments. The copolymers could further condense plasmid DNA efficiently. Importantly, the polymer/DNA complexes showed high transfection efficiency in 293T cells under optimized conditions. This study suggested the copolymers may have great potential in both drug and gene delivery.
引用
收藏
页码:3100 / 3106
页数:7
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