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Structural investigations of novel triblock cationic copolymer/DNA complexes

机译:新型三嵌段阳离子共聚物/ DNA复合物的结构研究

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A series of biodegradable triblock copolymers poly (ethylene glycol)-g-polyethylenimine-b-poly (dimethylaminoethyl l-glutamine) (PEG-g-PEI-b-PDMAEG) as novel vectors for gene therapy were synthesized and evaluated.Poly (ethylene glycol)-g-polyethylenimiene (PEG-g-PEI) was firstly obtained by linking of PEG and PEI using isophorone diisocyanate (IPDI) as coupling reagent.The anionic copolymerization of γ-benzyl l-glutamtae N-carboxyanhydride (BLG-NCA) using PEG-g-PEI as a macroinitiator was carried out,followed by aminolysis with 2-dimethylaminoethylamine to obtain the target water soluble triblock copolymer.The structures from PEG-g-PEI precursor to the triblock copolymers were confirmed by FT-IR.The particle sizes,zeta potentials of polyplexes were evaluated.All polyethylenimine derivates were revealed to compact plasmid DNA effectively to give polyplexes with suitable size (~100 nm) and moderate ζ-potentials (10-15 mV) at N/P ratios of 30.The relationship between the composition of PEG-g-PEI-b-PDMAEG and the size,the ζ-potentials of corresponding copolymer/DNA complexes were also investigated.
机译:合成并评估了一系列可生物降解的三嵌段共聚物聚(乙二醇)-g-聚乙烯亚胺-b-聚(二甲基氨基乙基1-谷氨酰胺)(PEG-g-PEI-b-PDMAEGEG)作为基因治疗的新型载体。首先以异佛尔酮二异氰酸酯(IPDI)为偶联剂,通过PEG与PEI的键合,得到PEG-g-PEI(PEG-g-PEI).γ-苄基L-谷氨酰胺N-羧基酐(BLG-NCA)的阴离子共聚。以PEG-g-PEI为大分子引发剂,然后用2-二甲基氨基乙胺进行氨解,得到目标水溶性三嵌段共聚物.FT-IR证实了PEG-g-PEI前体与三嵌段共聚物的结构。揭示了所有聚乙烯亚胺衍生物均能有效地压紧质粒DNA,从而以N / P值为30的大小提供合适大小(〜100 nm)和适度ζ电位(10-15 mV)的复合物。 P的组成关系还研究了EG-g-PEI-b-PDMAEG的大小,相应的共聚物/ DNA复合物的大小,ζ电势。

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