Sequential Assembly of Lipid Molecules Broadens Designability of Lipid-Based Nanoparticles

Niko Kimura, Shinya Sakuma
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Abstract

We present an unprecedent concept of "sequential assembly of lipid-based nanoparticles (LNPs)" by designing order of liquid-liquid interfaces based on microfluidic flow control. Unlike existing methods, our method enables to broaden the controllability of the LNP size without any changes of initial abundance ratio of lipids. We utilized a microfluidic chip having multi-inlets, and the configuration allows to change the order of the self-assembly relating to the size controllability. We demonstrated visualization of cellular uptake of LNPs with different size. From the results, we confirmed that the size was a critical factor for controlled transportation of LNPs into spheroids. The presented sequential assembly opens new paradigms of detailed analyses of live-cells.
脂质分子的顺序组装拓宽了脂质纳米颗粒的可设计性
我们提出了一种前所未有的 "脂基纳米粒子(LNPs)顺序组装 "概念,即在微流体流动控制的基础上设计液-液界面的顺序。与现有方法不同的是,我们的方法能够在不改变脂质初始丰度比的情况下扩大 LNP 大小的可控性。我们使用的微流体芯片有多个入口,这种配置可以改变与尺寸可控性有关的自组装顺序。我们展示了不同大小的 LNPs 被细胞吸收的可视化过程。从结果来看,我们证实大小是 LNPs 受控进入球体的关键因素。所展示的顺序组装为详细分析活细胞开辟了新的范例。
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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