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用1,2 - 环氧己烷或1,2 - 环氧十二烷改性的聚(酰胺 - 胺)树枝状大分子用于增强基因递送应用。

Poly(amidoamine) Dendrimers Modified with 1,2-Epoxyhexane or 1,2-Epoxydodecane for Enhanced Gene Delivery Applications.

作者信息

Xiao Tongyu, Cao Xueyan, Hou Wenxiu, Peng Chen, Qiu Jieru, Shi Xiangyang

出版信息

J Nanosci Nanotechnol. 2015 Dec;15(12):10134-40. doi: 10.1166/jnn.2015.11693.

Abstract

We report a new non-viral gene delivery system based on hydrophobically modified poly(amidoamine) (PAMAM) dendrimers. In this study, the periphery of amine-terminated generation 5 (G5) PAMAM dendrimers was partially reacted with 1,2-epoxyhexane and 1,2-epoxydodecane, respectively. The formed hydrophobically modified G5 dendrimers (denoted as G5.NH2-C6 or G5.NH2-C12) were used to complex two different plasmid DNAs (pDNAs) encoding luciferase (Luc) and enhanced green fluorescent protein (EGFP), respectively for gene transfection studies. The polyplexes formed between vectors and pDNA were characterized by gel retardation assay, dynamic light scattering, and zeta potential measurements. We show that the G5.NH2-C6 and G5.NH2-C12 vectors are able to effectively compact the pDNA, allowing for highly efficient gene transfection into a model cell line (HeLa cells) as demonstrated by both Luc assay and confocal microscopic imaging of the EGFP expression. Under the studied N/P ratios (the molar ratio of primary amines of the dendrimers to phosphates in the pDNA backbone) at 2.5 or 5, the transfection efficiency of the dendrimer-based vectors followed the order of G5.NH2-C12 > G5.NH2-C6 > G5.NH2. This enhanced gene transfection capacity is believed to be associated with the enhanced hydrophobic interaction between the vector/pDNA complexes and the relatively hydrophobic cell membranes. The developed hydrophobically modified dendrimers may be used as a promising non-viral vector for enhanced gene delivery applications.

摘要

我们报道了一种基于疏水改性聚(酰胺胺)(PAMAM)树枝状大分子的新型非病毒基因递送系统。在本研究中,胺端基第5代(G5)PAMAM树枝状大分子的外围分别与1,2 - 环氧己烷和1,2 - 环氧十二烷进行了部分反应。形成的疏水改性G5树枝状大分子(表示为G5.NH2 - C6或G5.NH2 - C12)用于分别与两种不同的编码荧光素酶(Luc)和增强型绿色荧光蛋白(EGFP)的质粒DNA(pDNA)复合,用于基因转染研究。通过凝胶阻滞试验、动态光散射和zeta电位测量对载体与pDNA之间形成的多聚体进行了表征。我们表明,G5.NH2 - C6和G5.NH2 - C12载体能够有效地压缩pDNA,如Luc测定和EGFP表达的共聚焦显微镜成像所示,允许高效地将基因转染到模型细胞系(HeLa细胞)中。在所研究的N/P比(树枝状大分子的伯胺与pDNA主链中磷酸根的摩尔比)为2.5或5时,基于树枝状大分子的载体的转染效率遵循G5.NH2 - C12 > G5.NH2 - C6 > G5.NH2的顺序。这种增强的基因转染能力被认为与载体/pDNA复合物与相对疏水的细胞膜之间增强的疏水相互作用有关。所开发的疏水改性树枝状大分子可作为一种有前途的非病毒载体用于增强基因递送应用。

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