2019年冠状病毒病(COVID-19)
信使核糖核酸
医学
体内分布
核酸
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
病毒学
冠状病毒
药理学
生物
疾病
基因
传染病(医学专业)
体外
遗传学
病理
作者
Yuta Suzuki,Hiroshi Ishihara
标识
DOI:10.1016/j.dmpk.2021.100424
摘要
Nucleic acid therapeutics are developing into precise medicines that can manipulate specific genes. However, the development of safe and effective delivery system for the target cells has remained a challenge. Lipid nanoparticles (LNPs) have provided a revolutionary delivery system that can ensure multiple clinical translation of RNA-based candidates. In 2018, Patisiran (Onpattro) was first approved as an LNP-based siRNA drug. In 2020, during the coronavirus disease 2019 (COVID-19) outbreak, LNPs have enabled the development of two SARS-CoV-2 mRNA vaccines, Tozinameran (Comirnaty or Pfizer-BioNTech COVID-19 vaccine) and Elasomeran (Spikevax or COVID-19 vaccine Moderna) for conditional approval. Here, we reviewed the state-of-the-art LNP technology employed in three approved drugs (one siRNA-based and two mRNA-based drugs) and discussed the differences in their mode of action, formulation design, and biodistribution.
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