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用于脂质纳米颗粒生产的三维对称组装微流控装置。

Three-dimensional, symmetrically assembled microfluidic device for lipid nanoparticle production.

作者信息

Kimura Niko, Maeki Masatoshi, Sasaki Kosuke, Sato Yusuke, Ishida Akihiko, Tani Hirofumi, Harashima Hideyoshi, Tokeshi Manabu

机构信息

Graduate School of Chemical Sciences and Engineering, Hokkaido University Kita 13 Nishi 8, Kita-ku Sapporo 060-8628 Japan +81-11-706-6745 +81-11-706-6744.

Division of Applied Chemistry, Faculty of Engineering, Hokkaido University Kita 13 Nishi 8, Kita-ku Sapporo 060-8628 Japan

出版信息

RSC Adv. 2021 Jan 5;11(3):1430-1439. doi: 10.1039/d0ra08826a. eCollection 2021 Jan 4.

Abstract

Sub 100 nm-sized lipid nanoparticles (LNPs) have been widely used in drug delivery systems (DDSs). The size of the LNPs is an important parameter for the DDS performance, such as biodistribution and gene silencing using siRNAs. However, the LNPs prepared by the conventional preparation method show a wide size distribution. To improve the LNP size distribution, we developed a microfluidic device, named the iLiNP™ device, in a previous study. This device could produce LNPs in the size range of 20 to 150 nm, but the size distribution of the large-sized LNPs needs to be further improved. From the viewpoint of the LNP formation process, a homogeneous and slow rate dilution of ethanol plays an important role in improving the large-size LNP size distribution. In this study, we developed a three-dimensional, symmetrically assembled microfluidic device named the 3D-iLiNP device with the aim of precise size control of large-sized LNPs. We designed the 3D-iLiNP device using a computational fluid dynamics simulation and demonstrated that the 3D-iLiNP device can improve the LNP size distribution. The gene silencing activity of four kinds of siRNA-loaded LNPs was investigated and experiments to elucidate the effect of the LNP size distribution. The results revealed that the LNPs with a size between 90 and 120 nm showed higher gene silencing activity than those with other sizes. The 3D-iLiNP device is expected to improve DDS performance by precisely controlling the size of LNPs.

摘要

小于100纳米的脂质纳米颗粒(LNPs)已广泛应用于药物递送系统(DDSs)。LNPs的尺寸是影响DDS性能的一个重要参数,如生物分布和使用小干扰RNA(siRNAs)的基因沉默。然而,通过传统制备方法制备的LNPs尺寸分布较宽。为了改善LNPs的尺寸分布,我们在之前的一项研究中开发了一种微流控装置,名为iLiNP™ 装置。该装置能够制备尺寸在20至150纳米范围内的LNPs,但大尺寸LNPs的尺寸分布仍需进一步改善。从LNP形成过程的角度来看,乙醇的均匀缓慢稀释在改善大尺寸LNP尺寸分布方面起着重要作用。在本研究中,我们开发了一种三维对称组装的微流控装置,名为3D-iLiNP装置,旨在精确控制大尺寸LNPs的尺寸。我们使用计算流体动力学模拟设计了3D-iLiNP装置,并证明该装置可以改善LNPs的尺寸分布。研究了四种负载siRNA的LNPs的基因沉默活性,并进行了实验以阐明LNP尺寸分布的影响。结果显示,尺寸在90至120纳米之间的LNPs比其他尺寸的LNPs具有更高的基因沉默活性。3D-iLiNP装置有望通过精确控制LNPs的尺寸来提高DDS性能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b8d/8693528/664d746b7141/d0ra08826a-f1.jpg

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