Gene Editing Center, School of Life Science and Technology, ShanghaiTech University, Shanghai 201210, China.
Interdisciplinary Research Center on Biology and Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 201210, China.
Nano Lett. 2022 Aug 24;22(16):6580-6589. doi: 10.1021/acs.nanolett.2c01784. Epub 2022 Aug 15.
Lipid nanoparticles (LNPs) carrying therapeutic mRNAs hold great promise in treating lung-associated diseases like viral infections, tumors, and genetic disorders. However, because of their thermodynamically unstable nature, traditional LNPs carrying mRNAs need to be stored at low temperatures, which hinders their prevalence. Herein, an efficient lung-specific mRNA delivery platform named five-element nanoparticles (FNPs) is developed in which helper-polymer poly(β-amino esters) (PBAEs) and DOTAP are used in combination. The new strategy endows FNPs with high stability by increasing the charge repulsion between nanoparticles and the binding force of the aliphatic chains within the nanoparticles. The structure-activity relationship (SAR) shows that PBAEs with E1 end-caps, higher degrees of polymerization, and longer alkyl side chains exhibit higher hit rates. Lyophilized FNP formulations can be stably stored at 4 °C for at least 6 months. Overall, a novel delivery platform with high efficiency, specificity, and stability was developed for advancing mRNA-based therapies for lung-associated diseases.
携带治疗性 mRNA 的脂质纳米颗粒 (LNPs) 在治疗与肺部相关的疾病方面具有巨大的潜力,如病毒感染、肿瘤和遗传疾病。然而,由于其热力学不稳定的性质,传统的携带 mRNA 的 LNPs 需要低温储存,这阻碍了它们的普及。在此,开发了一种名为五元素纳米颗粒 (FNPs) 的高效肺特异性 mRNA 递药平台,其中使用了助聚合物聚(β-氨基酯)(PBAEs)和 DOTAP。新策略通过增加纳米颗粒之间的电荷排斥和纳米颗粒内脂族链的结合力,赋予 FNPs 高稳定性。结构-活性关系(SAR)表明,具有 E1 端帽、更高聚合度和更长烷基侧链的 PBAEs 具有更高的命中率。冻干的 FNP 制剂可以在 4°C 下稳定储存至少 6 个月。总之,为了推进与肺部相关的疾病的基于 mRNA 的治疗,开发了一种具有高效、特异性和稳定性的新型递药平台。