Amphiphilic Block Copolymer Micelles for Gene Delivery

被引:6
作者
Li Qin [1 ]
Jin Bixin [1 ]
Luo Yunjun [1 ,2 ]
Li Xiaoyu [1 ,2 ,3 ]
机构
[1] Beijing Inst Technol, Sch Mat Sci & Engn, Beijing 100081, Peoples R China
[2] Beijing Inst Technol, Key Lab High Energy Dens Mat, Minist Educ, Beijing 100081, Peoples R China
[3] Beijing Inst Technol, Expt Ctr Adv Mat, Beijing 100081, Peoples R China
基金
中国国家自然科学基金;
关键词
Polymeric micelle; Block copolymer; Gene delivery; MONODISPERSE CYLINDRICAL MICELLES; PCL-G-PEI; CO-DELIVERY; SIRNA DELIVERY; TRANSFECTION EFFICIENCY; POLYMERIC NANOPARTICLES; TRIBLOCK COPOLYMERS; FOLATE RECEPTOR; IN-VIVO; POLYETHYLENIMINE-GRAFT-POLYCAPROLACTONE-BLOCK-POLY(ETHYLENE GLYCOL)-FOLATE;
D O I
10.1007/s40242-022-2005-1
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Gene therapy is a promising method to treat acquired and inherited diseases by introducing exogenous genes into specific recipient cells. Polymeric micelles with different nanoscopic morphologies and properties hold great promise for gene delivery system. Conventional cationic polymers, poly(ethyleneimine)(PEI), poly(L-lysine)(PLL), poly(2-dimethylaminoethyl methacrylate)(PDMAEMA) and novel cationic polymers poly(2-oxazoline)s(POxs), have been incorporated into block copolymers and decorated with targeting moieties to enhance transfection efficiency. In order to minimize cytotoxicity, nonionic block copolymer micelles are utilized to load gene through hydrophilic and hydrophobic interactions or covalent conjugations, recently. From our perspective, properties(shape, size, and mechanical stiffness, etc.) of block copolymer micelles may significantly affect cytotoxicity, transfection efficiency, circulation time, and load capacity of gene vectors in vivo and in vitro. This review briefly sums up recent efforts in cationic and nonionic amphiphilic polymeric micelles for gene delivery.
引用
收藏
页码:1368 / 1379
页数:12
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