Nanoelectroporation and controllable intracellular delivery into localized single cell with high transfection and cell viability

T. Santra, J. Borana, Pen-Cheng Wang, F. Tseng
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引用次数: 3

Abstract

Physical introduction of foreign biomolecules such as genes, proteins, DNA and RNA into living cells with high efficiency is a challenging task for biological and therapeutic research. Bulk electroporation technique, where high electric field pulses were applied to millions of cells together in-between two large electrodes, though widely employed, however is nonspecific resulting in variable efficiency with low cell viability. Here we demonstrate controllable nano-electroporation platform for HeLa cell and human Caucasian Gastric Adenocarcinoma (AGS) cell to achieve high efficient bimolecular delivery with high cell viability. Our system consists of 40nm triangular Indium Tin Oxide (ITO) metal tip with 60nm electrode gap to provide high intense electric filed into the local region of the single cell membrane. Therefore biomolecules can be delivered by much enhance electrophoresis and diffusion effects during pulsing process through a small specific nano-region of the single cell, where remaining other area of the cell membrane unaffected. This microfluidic device has great ability to offer spatial, temporal and qualitative dosage control as well as very high transfection efficiency and high cell viability.
纳米电穿孔和可控的细胞内递送到局部单细胞,具有高转染和细胞活力
将外源生物分子如基因、蛋白质、DNA和RNA高效地物理导入活细胞是生物学和治疗研究的一项具有挑战性的任务。大块电穿孔技术,将高电场脉冲应用于两个大电极之间的数百万个细胞,虽然被广泛应用,但其非特异性导致效率可变,细胞存活率低。在此,我们为HeLa细胞和人高加索胃腺癌(AGS)细胞构建了可控的纳米电穿孔平台,以实现高效的双分子递送和高细胞活力。我们的系统由40nm的三角形氧化铟锡(ITO)金属尖端和60nm的电极间隙组成,可以在单细胞膜的局部区域提供高强度的电场。因此,在脉冲过程中,生物分子可以通过单细胞的一个小的特定纳米区域通过更强的电泳和扩散效应来传递,而细胞膜的其他区域不受影响。该微流控装置具有空间、时间和定性剂量控制能力强,转染效率高,细胞存活率高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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