Ahn Cheol-Hee, Chae Su Young, Bae You Han, Kim Sung Wan
Center for Controlled Chemical Delivery, Department of Pharmaceutics and Pharmaceutical Chemistry, Biomedical Polymers Research Building, University of Utah, RM 205, 84112, Salt Lake City, UT, USA
J Control Release. 2002 Apr 23;80(1-3):273-82. doi: 10.1016/s0168-3659(01)00547-8.
Poly(ethylenimine) (PEI) has been known as an efficient gene carrier with the highest cationic charge potential. High transfection efficiency of PEI, along with its cytotoxicity, strongly depends on the molecular weight. Synthesis of cationic copolymers derived from the low molecular weight of PEI and hydrophilic poly(ethylene glycol) (PEG), which are water soluble and degradable under physiological conditions, was investigated for plasmid delivery. Hydrophilic PEG is expected to reduce the toxicity of the copolymer, improve the poor solubility of the PEI and DNA complexes, and help to introduce degradable bonds by reaction with the primary amines in the PEI. Considering the dependence of transfection efficiency and cytotoxicity on the molecular weight of the PEI, high transfection efficiency is expected from an increased molecular weight of the copolymer and low cytotoxicity from the introduction of PEG and the degradation of the copolymer into low molecular weight PEIs. Reaction conditions were carefully controlled to produce water soluble copolymers. Results from a gel retardation assay and zetapotentiometer indicated that complete neutralization of the complexes was achieved at the charge ratios of copolymer/pSV-beta-gal plasmid from 0.8 to 1.0 with the mean particle size of the polyplexes ranging from 129.8+/-0.9 to 151.8+/-3.4 nm. In vitro transfection efficiency of the synthesized copolymer increased up to three times higher than that of starting low molecular weight PEI, while the cell viability was maintained over 80%.
聚乙烯亚胺(PEI)作为一种具有最高阳离子电荷电位的高效基因载体而闻名。PEI的高转染效率及其细胞毒性在很大程度上取决于分子量。研究了由低分子量PEI和亲水性聚乙二醇(PEG)衍生的阳离子共聚物的合成,这些共聚物在生理条件下是水溶性且可降解的,用于质粒递送。亲水性PEG有望降低共聚物的毒性,改善PEI与DNA复合物的不良溶解性,并通过与PEI中的伯胺反应帮助引入可降解键。考虑到转染效率和细胞毒性对PEI分子量的依赖性,预计共聚物分子量的增加会带来高转染效率,而PEG的引入和共聚物降解为低分子量PEI会带来低细胞毒性。仔细控制反应条件以制备水溶性共聚物。凝胶阻滞试验和zeta电位仪的结果表明,在共聚物/pSV-β-半乳糖苷酶质粒的电荷比为0.8至1.0时,复合物实现了完全中和,多聚体的平均粒径范围为129.8±0.9至151.8±3.4nm。合成共聚物的体外转染效率比起始低分子量PEI提高了三倍,同时细胞活力保持在80%以上。