信使核糖核酸
体内
核糖核酸
体外
化学
生物
生物化学
基因
遗传学
作者
Hiroki Tanaka,Shinya Hagiwara,Daiki Shirane,Takuma Yamakawa,Yuka Sato,Chika Matsumoto,Kota Ishizaki,Miho Hishinuma,Katsuyuki Chida,Kasumi Sasaki,Etsuo Yonemochi,Keisuke Ueda,Kenjirou Higashi,Kunikazu Moribe,Takashi Tadokoro,Katsumi Maenaka,Sakura Taneichi,Y. Nakai,Kota Tange,Yu Sakurai,Hidetaka Akita
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-01-31
卷期号:17 (3): 2588-2601
被引量:15
标识
DOI:10.1021/acsnano.2c10501
摘要
Based on the clinical success of an in vitro transcribed mRNA (IVT-mRNA) that is encapsulated in lipid nanoparticles (mRNA-LNPs), there is a growing demand by researchers to test whether their own biological findings might be applicable for use in mRNA-based therapeutics. However, the equipment and/or know-how required for manufacturing such nanoparticles is often inaccessible. To encourage more innovation in mRNA therapeutics, a simple method for preparing mRNA-LNPs is prerequisite. In this study, we report on a method for encapsulating IVT-mRNA into LNPs by rehydrating a Ready-to-Use empty freeze-dried LNP (LNPs(RtoU)) formulation with IVT-mRNA solution followed by heating. The resulting mRNA-LNPs(RtoU) had a similar intraparticle structure compared to the mRNA-LNPs prepared by conventional microfluidic mixing. In vivo genome editing, a promising application of these types of mRNA-LNPs, was accomplished using the LNPs(RtoU) containing co-encapsulated Cas9-mRNA and a small guide RNA.
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