pH-sensitive cationic polymer gene delivery vehicle:: N-Ac-poly(L-histidine)-graft-poly(L-lysine) comb shaped polymer

被引:338
作者
Benns, JM
Choi, JS
Mahato, RI
Park, JS
Kim, SW
机构
[1] Univ Utah, Dept Pharmaceut & Pharmaceut Chem, Ctr Controlled Chem Delivery, Salt Lake City, UT 84112 USA
[2] Seoul Natl Univ, Dept Chem, Seoul 151742, South Korea
关键词
D O I
10.1021/bc0000177
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Advancing biotechnology spurs the development of new pharmaceutically engineered gene delivery vehicles. Poly(L-histidine) {PLH} has been shown to induce membrane fusion at endosomal pH values, whereas PLL has a well documented efficacy in polyplex formation. Therefore, N-Ac-poly(L-histidine)graft-poly(L-lysine) {PLH-g-PLL} was synthesized by grafting poly(L-histidine) to poly(L-lysine) {PLL}. PLH-g-PLL formed polyplex particles by electrostatic interactions with plasmid DNA {pDNA}. The mean particle size of the polyplexes was in the range of 117 +/- 6 nm to 306 +/- 77 nm. PLH-g-PLL gene carrier demonstrated higher transfection efficacy in 293T cells than PLL at all equivalent weight ratios with pDNA. The inclusion of chloroquine as an endosomolytic agent enhanced transfection for both PLL and PLH-g-PLL gene carriers. PLH-g-PLL enhanced beta-galactosidase expression compared to PLL, but still increased in efficacy when chloroquine was included.
引用
收藏
页码:637 / 645
页数:9
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