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Three-Dimensional Hydrodynamic Focusing Method for Polyplex Synthesis

机译:复合体合成的三维水力聚焦方法

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摘要

Successful intracellular delivery of nucleic acid therapeutics relies on multiaspect optimization, one of which is formulation. While there has been ample innovation on chemical design of polymeric gene carriers, the same cannot be said for physical processing of polymer--DNA nanocomplexes (polyplexes). Conventional synthesis of polyplexes by bulk mixing depends on the operators' experience. The poorly controlled bulk mixing process may also lead to batch-to-batch variation and consequent irreproducibility. Here, we synthesize polyplexes by using a three-dimensional hydrodynamic focusing (3D-HF) technique in a single-layered, planar microfluidic device. Without any additional chemical treatment or postprocessing, the polyplexes prepared by the 3D-HF method show smaller size, slower aggregation rate, and higher transfection efficiency, while exhibiting reduced cytotoxicity compared to the ones synthesized by conventional bulk mixing. In addition, by introducing external acoustic perturbation, mixing can be further enhanced, leading to even smaller nanocomplexes. The 3D-HF method provides a simple and reproducible process for synthesizing high-quality polyplexes, addressing a critical barrier in the eventual translation of nucleic acid therapeutics.
机译:核酸治疗剂的成功细胞内递送依赖于多方面的优化,其中之一是制剂。尽管在聚合基因载体的化学设计方面已经进行了充分的创新,但对于聚合物的物理加工-DNA纳米复合物(polyplex)却不能说相同。传统的通过本体混合合成多链体取决于操作者的经验。控制不佳的本体混合过程也可能导致批次之间的差异以及随之而来的不可再现性。在这里,我们通过在单层平面微流体装置中使用三维流体动力学聚焦(3D-HF)技术合成多链体。与常规本体混合法相比,通过3D-HF方法制备的多链体无需任何额外的化学处理或后处理,即可显示出较小的尺寸,较慢的聚集速率和更高的转染效率,同时显示出降低的细胞毒性。另外,通过引入外部声扰动,可以进一步增强混合,从而产生更小的纳米复合物。 3D-HF方法为合成高质量的多链体提供了一个简单且可重复的过程,解决了核酸治疗剂最终翻译中的关键障碍。

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