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PEG-PEI共聚物/DNA复合物的物理化学性能研究

Study on Physicochemical Property of PEG-PEI Copolymer/DNA Complexes

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【作者】 张璇潘仕荣胡海梅

【Author】 ZHANG Xuan1,2,PAN Shi-rong2,HU Hai-mei3(1.Shenzhen Institute of Mental Health,Shenzhen 518020,China;2.First Affiliated Hospital,Sun Yat-sen University,Guangzhou 510080,China;3.Guangdong Pharmaceutical University,Guangzhou 510224,China)

【机构】 深圳市精神卫生研究所中山大学附属第一医院广东药学院

【摘要】 目的研究合成的非病毒基因载体材料PEG-PEI共聚物与DNA形成复合物的各项物理化学性能指标,为PEG-PEI共聚物作为非病毒基因载体介导体内外基因传递的研究奠定基础。方法将含PEG不同相对分子质量和接枝量的PEG-PEI共聚物,与DNA形成复合物。测定了PEG-PEI/DNA复合物的粒径、Zeta电位,结构形态、在水溶液中的溶解性及共聚物的缓冲容量,分析了接枝PEG对各项物理化学性能的影响。结果接枝了PEG后,PEG-PEI/DNA复合物的粒径都明显减小,Zeta电位有一定程度的下降,接枝相对分子质量较大的PEG可使Zeta电位下降较多,亲水链段PEG对降低粒子间的聚集和增加溶解性起到了关键性的作用。接枝PEG的量对引起的内含体破裂并释放DNA的质子海绵效应不会产生明显影响。结论形成PEG-PEI共聚物后,对PEI/DNA复合物的物理化学性能有一定的改善作用,使复合物更适宜用于体内基因转导。

【Abstract】 OBJECTIVE To study physicochemical property of PEG-PEI/DNA complexes so as to provide foundation to the research of PEG-PEI copolymers as carriers for gene delivery in vivo and in vitro.METHODS The PEG PEI /DNA complexes were formed with different molecular weight of PEG and degree of PEG-PEI copolymer.The complex size,Zeta potential,morphology,solubility of copolymer/DNA complexes and buffering capacity of PEG-PEI copolymer were measured,and the effection of PEG-PEI copolymer on the physicochemical property of DNA complexes was investigated.RESULTS After PEG-PEI coplymer,particle sizes of PEG-PEI/DNA complexes evidently decreased,and Zeta potential decreased to a certain extent.The longer the PEG chain,the lower zeta potential of the complexes.Hydrophilic PEG in copolymer was very important for reducing aggregation between particles and increasing solubility.The degree of PEG-PEI copolymer had no obvious influence on the disruption of endosomal compartments and DNA releasing from endosomes via the proton sponge mechanism.CONCLUSION After PEG-PEI copolymer,the physicochemical property of PEI/DNA complexes could be improved,and could be used in gene delivery in vivo.

  • 【文献出处】 中国药学杂志 ,Chinese Pharmaceutical Journal , 编辑部邮箱 ,2010年01期
  • 【分类号】R318.0
  • 【被引频次】7
  • 【下载频次】839
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