| Literature DB >> 32438474 |
Yamin Li1, Rachel Jarvis2, Kuixin Zhu1, Zachary Glass1, Roza Ogurlu1, Peiyang Gao1, Peixuan Li1, Jinjin Chen1, Yingjie Yu1, Yongjie Yang2, Qiaobing Xu1.
Abstract
Developing safe and efficient delivery systems for therapeutic biomacromolecules is a long-standing challenge. Herein, we report a newly developed combinatorial library of cholesteryl-based disulfide bond-containing biodegradable cationic lipidoid nanoparticles. We have identified a subset of this library which is effective for protein and mRNA delivery in vitro and in vivo. These lipidoids showed comparable transfection efficacies but much lower cytotoxicities compared to the Lpf2k in vitro. In vivo studies in adult mice demonstrated the successful delivery of genome engineering protein and mRNA molecules in the skeletal muscle (via intramuscular injection), lung and spleen (via intravenous injection), and brain (via lateral ventricle infusion).Entities:
Keywords: genome engineering; lipidoid nanoparticle; mRNA delivery; protein delivery; stimuli responsive
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Year: 2020 PMID: 32438474 PMCID: PMC7679290 DOI: 10.1002/anie.202004994
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336