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深入了解脂质纳米粒的配方,优化 mRNA 疗法。

Insights into the formulation of lipid nanoparticles for the optimization of mRNA therapeutics.

机构信息

Department of Critical Care Medicine, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Chengdu, China.

出版信息

Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2024 Sep-Oct;16(5):e1992. doi: 10.1002/wnan.1992.

Abstract

mRNA-based therapeutics increasingly demonstrate significant potential in treating various diseases, including infectious diseases, cancers, and genetic disorders. Effective delivery systems are crucial for advancing mRNA therapeutics. Lipid nanoparticles (LNPs) serve as an excellent carrier, widely validated for their safety and tolerability in commercially available mRNA vaccines. Standard LNPs typically consist of four components: ionizable lipids (ILs), helper lipids, cholesterol, and polyethylene glycol-lipids (PEG-lipids), with the structural design of ILs gradually becoming a focal point of research interest. The chemical structures and formulations of the other components also significantly affect the delivery efficiency, targeting specificity, and stability of LNPs. The complex formulations of LNPs may hinder the clinical transformation of mRNA therapeutics and have raised widespread concerns about their safety. This review aims to summarize the progress of LNPs-based mRNA therapeutics in clinical trials, focusing on adverse effects that occurred during these trials. It also discusses representative innovations in LNP components, highlighting challenges and potential ways in this research field. We firmly believe this review will promote further improvements and designs of LNP compositions to optimize mRNA therapeutics. This article is categorized under: Nanotechnology Approaches to Biology > Nanoscale Systems in Biology Biology-Inspired Nanomaterials > Lipid-Based Structures.

摘要

mRNA 疗法在治疗各种疾病方面(包括传染病、癌症和遗传疾病)的潜力日益显著。有效的传递系统对于推进 mRNA 疗法至关重要。脂质纳米颗粒(LNPs)作为一种极好的载体,其在商业 mRNA 疫苗中的安全性和耐受性已得到广泛验证。标准 LNPs 通常由四种成分组成:可离子化脂质(ILs)、辅助脂质、胆固醇和聚乙二醇脂质(PEG 脂质),ILs 的结构设计逐渐成为研究关注的焦点。其他成分的化学结构和配方也显著影响 LNPs 的传递效率、靶向特异性和稳定性。LNPs 的复杂配方可能会阻碍 mRNA 疗法的临床转化,并引起人们对其安全性的广泛关注。本综述旨在总结 LNPs 基 mRNA 疗法在临床试验中的进展,重点关注这些试验中发生的不良反应。同时还讨论了 LNP 成分的代表性创新,突出了该研究领域的挑战和潜在途径。我们坚信,这篇综述将促进 LNPs 组成的进一步改进和设计,以优化 mRNA 疗法。本文属于以下分类: 生物技术中的纳米技术方法 > 生物学中的纳米级系统 仿生纳米材料 > 基于脂质的结构

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