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Direct Interrogation of DNA Content Distribution inNanoparticles by a Novel Microfluidics-Based Single-Particle Analysis

机译:直接询问DNA含量分布新型基于微流体的单颗粒分析方法制备纳米颗粒

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摘要

Nonviral gene delivery holds great promise not just as a safer alternative to viral vectors in traditional gene therapy applications, but also for regenerative medicine, induction of pluripotency in somatic cells, and RNA interference for gene silencing. Although it continues to be an active area of research, there remain many challenges to the rational design of vectors. Among these, the inability to characterize the composition of nanoparticles and its distribution has made it difficult to probe the mechanism of gene transfection process, since differences in the nanoparticle-mediated transfection exist even when the same vector is used. There is a lack of sensitive methods that allow for full characterization of DNA content in single nanoparticles and its distribution among particles in the same preparation. Here we report a novel spectroscopic approach that is capable of interrogating nanoparticles on a particle-by-particle basis. Using PEI/DNA and PEI-g-PEG/DNA nanoparticles as examples, we have shown that the distribution of DNA content among these nanoparticles was relatively narrow, with the average numbers of DNA of 4.8 and 6.7 per particle,respectively, in PEI/DNA and PEI-g-PEG/DNA nanoparticles.This analysis enables a more accurate description of DNA content inpolycation/DNA nanoparticles. It paves the way toward comparativeassessments of various types of gene carriers and provides insightsinto bridging the efficiency gap between viral and nonviral vehicles.
机译:非病毒基因的传递不仅在传统的基因治疗应用中作为病毒载体的安全替代品,而且在再生医学,体细胞多能性诱导以及基因沉默的RNA干扰方面都具有广阔的前景。尽管它仍然是一个活跃的研究领域,但对向量的合理设计仍然存在许多挑战。其中,由于即使使用相同的载体,纳米粒子介导的转染也存在差异,因此无法表征纳米粒子的组成及其分布使得难以探究基因转染过程的机制。缺乏灵敏的方法来完全表征单个纳米颗粒中DNA的含量及其在同一制剂中在颗粒之间的分布。在这里,我们报告了一种新颖的光谱方法,该方法能够逐个颗粒地询问纳米颗粒。以PEI / DNA和PEI-g-PEG / DNA纳米粒子为例,我们显示了这些纳米粒子中DNA含量的分布相对较窄,每个粒子的平均DNA数为4.8和6.7,分别在PEI / DNA和PEI-g-PEG / DNA纳米颗粒中。该分析可以更准确地描述DNA含量聚阳离子/ DNA纳米粒子。它为比较法铺平了道路评估各种类型的基因载体并提供见解弥合病毒和非病毒车辆之间的效率差距。

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