Cationic Amphiphilic Star and Linear Block Copolymers: Synthesis, Self-Assembly, and in Vitro Gene Transfection

被引:57
|
作者
Alhoranta, Anu M. [1 ]
Lehtinen, Julia K. [2 ,3 ]
Urtti, Arto O. [2 ]
Butcher, Sarah J. [4 ]
Aseyev, Vladimir O. [1 ]
Tenhu, Heikki J. [1 ]
机构
[1] Univ Helsinki, Dept Chem, Polymer Chem Lab, FIN-00014 Helsinki, Finland
[2] Univ Helsinki, Ctr Drug Res, FIN-00014 Helsinki, Finland
[3] Univ Helsinki, Div Biopharm & Pharmacokinet, Fac Pharm, FIN-00014 Helsinki, Finland
[4] Univ Helsinki, Inst Biotechnol, FIN-00014 Helsinki, Finland
关键词
TRANSFER RADICAL POLYMERIZATION; WELL-DEFINED POLYSTYRENE; DRUG-DELIVERY; METHACRYLATE); POLYMERS; NANOCONTAINERS; MICELLIZATION; CHEMISTRY; MICELLES; THERAPY;
D O I
10.1021/bm2006906
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A series of amphiphilic star and linear block copolymers were synthesized using ATRP. The core consisted of either polystyrene (PS) or poly(n-butyl acrylate) (PBuA), having different glass-transition (T-g) values. These polymers were used as macro-initiators in the polymerization of the cationic 2-(dimethylamino)ethyl methacrylate (DMAEMA). The polymers were used to study the effects of polymer architecture and flexibility on the self-assembling properties, DNA complexation, and transfection. All polymers formed core-shell micelles in aqueous solutions and condensed plasmid DNA. Linear PDMAEMA-PBuA-PDMAEMA has transfection efficiency comparable to PEI25K in ARPE19 cell line. Glassy state of the micellar core and star-shaped architecture decreased the DNA transfection compared with the rubbery and linear polymer structures. The polymers showed low cellular toxicity at low nitrogen/phosphate (n/p) ratios.
引用
收藏
页码:3213 / 3222
页数:10
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