转染
体内
血脑屏障
信使核糖核酸
化学
高通量筛选
全身给药
细胞生物学
医学
生物
生物化学
神经科学
基因
中枢神经系统
生物技术
作者
Emily Han,Marshall S. Padilla,Rohan Palanki,Dongyoon Kim,Kaitlin Mrksich,Jacqueline J. Li,Sophia Tang,Il‐Chul Yoon,Michael J. Mitchell
出处
期刊:Nano Letters
[American Chemical Society]
日期:2024-01-23
卷期号:24 (5): 1477-1486
被引量:14
标识
DOI:10.1021/acs.nanolett.3c03509
摘要
Lipid nanoparticle (LNP)-mediated nucleic acid therapies, including mRNA protein replacement and gene editing therapies, hold great potential in treating neurological disorders including neurodegeneration, brain cancer, and stroke. However, delivering LNPs across the blood–brain barrier (BBB) after systemic administration remains underexplored. In this work, we engineered a high-throughput screening transwell platform for the BBB (HTS-BBB), specifically optimized for screening mRNA LNPs. Unlike most transwell assays, which only assess transport across an endothelial monolayer, HTS-BBB simultaneously measures LNP transport and mRNA transfection of the endothelial cells themselves. We then use HTS-BBB to screen a library of 14 LNPs made with structurally diverse ionizable lipids and demonstrate it is predictive of in vivo performance by validating lead candidates for mRNA delivery to the mouse brain after intravenous injection. Going forward, this platform could be used to screen large libraries of brain-targeted LNPs for a range of protein replacement and gene editing applications.
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