材料科学
RNA干扰
纳米颗粒
脾脏
纳米技术
细胞生物学
生物物理学
生物
生物化学
核糖核酸
免疫学
基因
作者
Amogh Vaidya,Stephen D. Moore,Sumanta Chatterjee,Erick D. Guerrero,Minjeong Kim,Lukas Farbiak,Sean A. Dilliard,Daniel J. Siegwart
标识
DOI:10.1002/adma.202313791
摘要
Inhibition of disease-causing mutations using RNA interference (RNAi) has resulted in clinically approved medicines with additional candidates in late stage trials. However, targetable tissues currently in preclinical development are limited to liver following systemic intravenous (IV) administration because predictable delivery of siRNA to non-liver tissues remains an unsolved challenge. Here, evidence of durable extrahepatic gene silencing enabled by siRNA Selective ORgan Targeting lipid nanoparticles (siRNA SORT LNPs) to the kidneys, lungs, and spleen is provided. LNPs excel at dose-dependent silencing of tissue-enriched endogenous targets resulting in 60%-80% maximal knockdown after a single IV injection and up to 88% downregulation of protein expression in mouse lungs after two doses. To examine knockdown potency and unbiased organ targeting, B6.129
科研通智能强力驱动
Strongly Powered by AbleSci AI