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新型光流控药物输送系统,用于高效细胞转染。

Novel opto-fluidic drug delivery system for efficient cellular transfection.

机构信息

Laboratoire Physique des Lasers, Atomes et Molécules - UMR 8523, Université de Lille, 59655, Villeneuve d'Ascq, France.

Institut d'Électronique, de Microélectronique et de Nanotechnologie - UMR CNRS 8520, Université de Lille, 59655, Villeneuve d'Ascq, France.

出版信息

J Nanobiotechnology. 2023 Feb 6;21(1):43. doi: 10.1186/s12951-023-01797-3.

DOI:10.1186/s12951-023-01797-3
PMID:36747263
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9901003/
Abstract

Intracellular drug delivery is at the heart of many diagnosis procedures and a key step in gene therapy. Research has been conducted to bypass cell barriers for controlled intracellular drug release and made consistent progress. However, state-of-the-art techniques based on non-viral carriers or physical methods suffer several drawbacks, including limited delivery yield, low throughput or low viability, which are key parameters in therapeutics, diagnostics and drug delivery. Nevertheless, gold nanoparticle (AuNP) mediated photoporation has stood out as a promising approach to permeabilize cell membranes through laser induced Vapour NanoBubble (VNB) generation, allowing the influx of external cargo molecules into cells. However, its use as a transfection technology for the genetic manipulation of therapeutic cells is hindered by the presence of non-degradable gold nanoparticles. Here, we report a new optofluidic method bringing gold nanoparticles in close proximity to cells for photoporation, while avoiding direct contact with cells by taking advantage of hydrodynamic focusing in a multi-flow device. Cells were successfully photoporated with [Formula: see text] efficiency with no significant reduction in cell viability at a throughput ranging from [Formula: see text] to [Formula: see text]. This optofluidic approach provides prospects of translating photoporation from an R &D setting to clinical use for producing genetically engineered therapeutic cells.

摘要

细胞内药物输送是许多诊断程序的核心,也是基因治疗的关键步骤。已经进行了研究来绕过细胞屏障以进行受控的细胞内药物释放,并取得了一致的进展。然而,基于非病毒载体或物理方法的最先进技术存在几个缺点,包括有限的输送产率、低通量或低存活率,这些都是治疗学、诊断学和药物输送的关键参数。尽管如此,金纳米颗粒(AuNP)介导的光穿孔已成为一种有前途的方法,可以通过激光诱导的蒸气纳米泡(VNB)产生来使细胞膜穿孔,从而允许外部货物分子进入细胞。然而,由于存在不可降解的金纳米颗粒,其作为治疗细胞遗传操作的转染技术的用途受到阻碍。在这里,我们报告了一种新的光流控方法,该方法将金纳米颗粒置于靠近细胞的位置进行光穿孔,同时通过在多流装置中利用流体动力学聚焦避免与细胞直接接触。以高达[Formula: see text]的通量成功地对细胞进行了光穿孔,而细胞活力没有明显下降,效率达到[Formula: see text]。这种光流控方法为将光穿孔从研发环境转化为临床应用以产生基因工程治疗细胞提供了前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9904/9901003/f216b703d3fe/12951_2023_1797_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9904/9901003/07f936eb7827/12951_2023_1797_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9904/9901003/d61c2b7dc3fb/12951_2023_1797_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9904/9901003/806f03e6de34/12951_2023_1797_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9904/9901003/f216b703d3fe/12951_2023_1797_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9904/9901003/07f936eb7827/12951_2023_1797_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9904/9901003/d61c2b7dc3fb/12951_2023_1797_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9904/9901003/806f03e6de34/12951_2023_1797_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9904/9901003/f216b703d3fe/12951_2023_1797_Fig4_HTML.jpg

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