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Polymeric vesicles from amino acid homopolymers

机译:氨基酸均聚物的聚合囊泡

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Non viral gene delivery systems are being developed from poly-L-lysine incorporating targeting ligands which form a transfection competent ionic complex with the gene of interest. These systems are found to transfect cells well in culture but in vivo gene expression is very low and of a transient nature. A system capable of sustained transfection is obviously required. Previously we have developed polymeric vesicles by the simple attachment of hydrophobic groups to a carbohydrate polymer - glycol chitosan and in this communication report the development of polymeric vesicles from amino acid homopolymers poly-L-lysine and poly-L-ornithine. Previously poly-L-lysine gene delivery systems have been prepared by the attachment of hydrophobic groups (phospholipids) and hydrophilic groups (polyethylene glycol). However the current approach describes the conjugation of both hydrophobic groups (palmitoyl) and hydrophilic groups (polyethylene glycol) to poly-L-lysine or poly-L-ornithine.
机译:非病毒基因递送系统是由掺入靶向配体的聚-L-赖氨酸开发的,所述靶向配体与目标基因形成可转染的离子复合物。发现这些系统可以很好地转染培养物中的细胞,但是体内基因表达非常低并且具有瞬时性质。显然需要一种能够持续转染的系统。以前,我们已经通过将疏水基团简单地连接到碳水化合物聚合物-乙二醇壳聚糖上来开发了聚合物囊泡,在本通讯中,我们报道了由氨基酸均聚物聚-L-赖氨酸和聚-L-鸟氨酸开发的聚合物囊泡。以前,已经通过疏水基团(磷脂)和亲水基团(聚乙二醇)的连接制备了聚-L-赖氨酸基因递送系统。然而,目前的方法描述了疏水基团(棕榈酰)和亲水基团(聚乙二醇)与聚-L-赖氨酸或聚-L-鸟氨酸的缀合。

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