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硫鎓脂质纳米颗粒实现肺部特异性 mRNA 递送。

Lung-Specific mRNA Delivery Enabled by Sulfonium Lipid Nanoparticles.

机构信息

Department of Pharmacology, State University of New York, Upstate Medical University, Syracuse, New York 13210, United States.

Department of Neuroscience and Physiology, State University of New York, Upstate Medical University, Syracuse, New York 13210, United States.

出版信息

Nano Lett. 2024 Jul 3;24(26):8080-8088. doi: 10.1021/acs.nanolett.4c01854. Epub 2024 Jun 18.

Abstract

Among various mRNA carrier systems, lipid nanoparticles (LNPs) stand out as the most clinically advanced. While current clinical trials of mRNA/LNP therapeutics mainly address liver diseases, the potential of mRNA therapy extends far beyond─yet to be unraveled. To fully unlock the promises of mRNA therapy, there is an urgent need to develop safe and effective LNP systems that can target extrahepatic organs. Here, we report on the development of sulfonium lipid nanoparticles (sLNPs) for systemic mRNA delivery to the lungs. sLNP effectively and specifically delivered mRNA to the lungs following intravenous administration in mice. No evidence of lung and systemic inflammation or toxicity in major organs was induced by sLNP. Our findings demonstrated that the newly developed lung-specific sLNP platform is both safe and efficacious. It holds great promise for advancing the development of new mRNA-based therapies for the treatment of lung-associated diseases and conditions.

摘要

在各种 mRNA 载体系统中,脂质纳米颗粒(LNPs)是最具临床应用前景的一种。目前,基于 mRNA/LNP 的治疗方法的临床试验主要针对肝脏疾病,但 mRNA 治疗的潜力远远超出了目前的认识,还有待进一步揭示。为了充分实现 mRNA 治疗的承诺,迫切需要开发安全有效的 LNP 系统,使其能够靶向肝外器官。在这里,我们报告了用于全身 mRNA 递送至肺部的硫鎓脂质纳米颗粒(sLNPs)的开发。sLNP 经静脉给药后可有效且特异地将 mRNA 递送至肺部。sLNP 不会引起肺部和全身炎症或主要器官的毒性。我们的研究结果表明,新开发的肺部特异性 sLNP 平台既安全又有效。它为推进新的基于 mRNA 的治疗肺部相关疾病和病症的治疗方法的发展提供了巨大的潜力。

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