Kichler Antoine, Chillon Miguel, Leborgne Christian, Danos Olivier, Frisch Benoît
Généthon III-CNRS URA 1923, 1 Rue de l'Internationale, Evry, France.
J Control Release. 2002 Jun 17;81(3):379-88. doi: 10.1016/s0168-3659(02)00080-9.
Polyethylenimines (PEIs) are among the most efficient synthetic DNA carriers. High levels of reporter gene expression can be obtained with these agents on a variety of cells. Nevertheless, the gap between their efficiency and that required for therapeutic approaches is still important. With the aim to improve the in vivo transfection properties of PEIs, we have synthesized a conjugate consisting of the linear polymer of 22 kDa covalently modified with polyethyleneglycol (PEG) residues. The resulting conjugate was able to complex DNA and allowed the preparation of highly concentrated polyplexes, in contrast to non-modified PEIs. Administration by nasal instillation of PEI-PEG/DNA complexes in mice resulted in significant levels of transgene expression. Luciferase activity was greatest 24 h after delivery and decreased thereafter. Our results show that the grafting of PEGs can improve some of the properties of PEIs.
聚乙烯亚胺(PEIs)是最有效的合成DNA载体之一。使用这些试剂可在多种细胞上获得高水平的报告基因表达。然而,它们的效率与治疗方法所需的效率之间的差距仍然很大。为了提高PEIs的体内转染特性,我们合成了一种共轭物,它由22 kDa的线性聚合物与聚乙二醇(PEG)残基共价修饰而成。与未修饰的PEIs相比,所得共轭物能够与DNA形成复合物,并可制备高浓度的多聚体。通过滴鼻法将PEI-PEG/DNA复合物给予小鼠后,可导致显著水平的转基因表达。荧光素酶活性在给药后24小时最高,此后下降。我们的结果表明,PEG的接枝可以改善PEIs的一些特性。