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化学学报
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化学学报 ›› 2007, Vol. 65 ›› Issue (19): 2181-2186. 上一篇    下一篇

研究论文

聚乙二醇嵌段树枝状聚赖氨酸共聚物的合成及其基因载体研究

崔亮1,2, 李洋2, 侯小东3, 宫文娟3, 徐宇虹*,1, 曹阿民*,2   

  1. (1上海交通大学药学院 上海 200237)
    (2中国科学院上海有机化学研究所 上海 200032)
    (3上海交通大学化学化工学院 上海 200237)
  • 投稿日期:2007-04-18 修回日期:2007-05-29 发布日期:2007-10-14
  • 通讯作者: 徐宇虹, 曹阿民

Studies on the Synthesis of Poly(ethylene glycol)-b-dendritic Poly(l-lysine)s and Their Application as Gene Carriers

CUI Liang1; LI Yang2; HOU Xiao-Dong3; GONGWen-Juan3; XU Yu-Hong*,1; CAO A-Min*,2   

  1. (1 School of Pharmacy, Shanghai Jiaotong University, Shanghai 200237)
    (2 Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032)
    (3 School of Chemistry and Chemical Engineering, Shanghai Jiaotong Univer-sity, Shanghai 200237)
  • Received:2007-04-18 Revised:2007-05-29 Published:2007-10-14
  • Contact: XU Yu-Hong; CAO A-Min

PDF

991

被引次数

25

采用液相多肽合成法制备得到窄分子量分布、结构可控的生物相容性聚乙二醇嵌段共聚树枝状聚赖氨酸阳离子功能大分子(PEG-b-Dendritic PLL). 运用1H NMR核磁共振、凝胶电泳以及荧光淬灭滴定手段对所得阳离子两嵌段大分子的化学结构及其与质粒DNA (pDNA)结合作用与复合行为进行了研究. 结果表明聚乙二醇嵌段树枝状聚赖氨酸与pDNA分子可以在缓冲溶液中形成稳定的胶束, pDNA与阳离子树枝赖氨酸嵌段通过静电相互作用形成胶束核, 其水溶性聚乙二醇嵌段形成水溶性胶束壳, 提高了阳离子大分子/pDNA复合胶束的稳定性. 同时发现随着阳离子嵌段树枝状赖氨酸代数的增加, 阳离子两嵌段大分子与pDNA的结合作用增强, 有利于其作为基因转染生物功能载体的应用.

关键词: 聚乙二醇嵌段树枝状赖氨酸, 阳离子大分子, pDNA载体, 凝胶电泳, 荧光淬灭滴定

New water-soluble diblock poly(ethylene glycol)-b-dendritic poly(l-lysine) with diverse den-dritic generations were molecularly designed and synthesized with well-defined structures. The chemical structures of the diblock cationic copolymers were characterized by 1H NMR. Furthermore, agarose gel electrophoresis and fluorescence titration assays were implemented to evaluate the plasmid DNA (pDNA) binding affinities of the synthesized new block copolymers, indicating higher DNA binding affinities of the diblock copolymers with 4 and 5 generation (PLL). Moreover, the dynamic light scattering was applied to characterize the polyplexes nanoparticles of the cationic carrier/pDNA, indicating the water-soluble PEG-b-dendritic PLL and pDNA could complex to form stable “core-shell” structure nanoparticles, and the biocompatible PEG shell could possibly decrease cytotoxicity of the complexed polyplexes nanoparticle during cell gene transfection. Therefore, these new structural diblock cationic macromolecules may be further developed as potential gene carriers with high efficacy.

Key words: PEG-b-dendritic PLL, cationic gene carrier, agarose gel electrophoresis, fluorescence titration, polyplex nanoparticles