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PEI-海藻酸钠纳米复合材料:核酸的高效非病毒载体。

PEI-alginate nanocomposites: efficient non-viral vectors for nucleic acids.

机构信息

Institute of Genomics and Integrative Biology (CSIR), Delhi University Campus, Mall Road, Delhi 110007, India.

出版信息

Int J Pharm. 2010 Jan 29;385(1-2):194-202. doi: 10.1016/j.ijpharm.2009.10.041. Epub 2009 Oct 27.

Abstract

Branched polyethylenimine (PEI, 25 kDa) was ionically interacted with varying amount of alginic acid to block different proportion (2.6-5.7%) of amines in PEI to form a series of nanocomposites, PEI-Al. These nanocomposites, upon interaction with DNA, protected it against DNase I. Among various complexes evaluated, PEI-Al(4.8%)/DNA displayed the highest transfection efficiency in HEK293, COS-1 and HeLa cells that was approximately 2-8-folds higher than Superfect, Fugene, PEI (750 kDa)-Al(6.26%) and PEI alone. The projected nanocomposites were nearly non-toxic to cells in vitro. Furthermore, the concentration of PEI-Al(4.8%) needed to deliver GFP-specific siRNA in COS-1 cells was 20 times lower than PEI (750 kDa)-Al(6.26%). Intracellular trafficking of PEI-Al(4.8%) with or without complexed DNA in HeLa cells shows that both appear in the nucleus after 1 h.

摘要

支化聚亚乙基亚胺(PEI,25 kDa)与不同量的海藻酸离子相互作用,以阻止 PEI 中的不同比例(2.6-5.7%)的胺基形成一系列纳米复合物,PEI-Al。这些纳米复合物与 DNA 相互作用后,可防止 DNA 酶 I 对其的降解。在评估的各种复合物中,PEI-Al(4.8%)/DNA 在 HEK293、COS-1 和 HeLa 细胞中的转染效率最高,约为 Superfect、Fugene、PEI(750 kDa)-Al(6.26%) 和 PEI 单独使用的 2-8 倍。预测的纳米复合物在体外对细胞几乎没有毒性。此外,在 COS-1 细胞中递送 GFP 特异性 siRNA 所需的 PEI-Al(4.8%)的浓度比 PEI(750 kDa)-Al(6.26%)低 20 倍。PEI-Al(4.8%)与或不与复合 DNA 在 HeLa 细胞中的细胞内运输显示,两者在 1 小时后均出现在细胞核中。

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