核糖核酸
外体
纳米载体
DNA
小干扰RNA
化学
基因沉默
RNA干扰
基因传递
微泡
纳米技术
体外
细胞生物学
生物物理学
分子生物学
纳米颗粒
材料科学
基因
生物
遗传增强
生物化学
小RNA
作者
Niko Kimura,Masatoshi Maeki,Akihiko Ishida,Hirofumi Tani,Manabu Tokeshi
出处
期刊:ACS applied bio materials
[American Chemical Society]
日期:2021-01-12
卷期号:4 (2): 1783-1793
被引量:9
标识
DOI:10.1021/acsabm.0c01519
摘要
Size-controlled lipid nanoparticle (LNP)-based DNA/RNA delivery is a leading technology for gene therapies. For DNA/RNA delivery, typically, a cationic lipid is used to encapsulate DNA/RNA into LNPs. However, the use of the cationic lipid leads to cytotoxicity. In contrast, noncationic NPs, such as exosomes, are ideal nanocarriers for DNA/RNA delivery. However, the development of a simple one-step method for the production of size-controlled noncationic NPs encapsulating DNA/RNA is still challenging because of the lack of electrostatic interactions between the cationic lipid and negatively charged DNA/RNA. Herein, we report a microfluidic-based one-step method for the production of size-controlled noncationic NPs encapsulating small interfering RNA (siRNA). Our microfluidic device, named iLiNP, enables the efficient encapsulation of siRNA, as well as control over the NP size, by varying the flow conditions. We applied this method to produce size-controlled exosome-like NPs. The siRNA-loaded exosome-like NPs did not show in vitro cytotoxicity at a high siRNA dosage. In addition, we investigated the effect of the size of the exosome-like NPs on the target gene silencing and found that the 40-50 nm-sized NPs suppressed target protein expression at a dose of 20 nM siRNA. The iLiNP-based one-step production method for size-controlled noncationic-NP-encapsulated RNA is a promising method for the production of artificial exosomes and functionally modified exosomes for gene and cell therapies.
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