Zhang Heyang, Barz Matthias
Division of BioTherapeutics, Leiden Academic Centre for Drug Research (LACDR), Leiden University, 2333CC Leiden, Netherlands.
Division of BioTherapeutics, Leiden Academic Centre for Drug Research (LACDR), Leiden University, 2333CC Leiden, Netherlands; Department of Dermatology, University Medical Center of the Johannes Gutenberg-University, 55128 Mainz, Germany.
J Control Release. 2025 May 10;381:113559. doi: 10.1016/j.jconrel.2025.02.055. Epub 2025 Feb 27.
Lipid nanoparticles (LNPs) are the most established and clinically advanced platform for RNA delivery. While significant efforts have been made to improve RNA delivery efficiency for improved protein production, the interplay between physiological stability, target specificity, and therapeutic efficacy of RNA-LNPs remains largely unexplored. This review highlights the crucial, yet often overlooked, impact of in vivo stability or instability of RNA-LNPs in contact with biological fluids on delivery performance. We discuss the various factors, including lipid composition, particle surface properties and interactions with proteins in physiological conditions, and provide an overview of the current methods for assessing RNA-LNP stability in biological fluids, such as dynamic laser light scattering, liquid chromatography, and fluorescent and radiolabeled techniques. In the final part, we propose strategies for enhancing stability, with a focus on shielding lipids. Therefore, this work highlights the importance of investigating and understanding the balance between stability and instability of LNPs in the biological context to achieve a more meaningful correlation between formulation properties and in vivo performance.
脂质纳米颗粒(LNPs)是目前最成熟且临床应用最先进的RNA递送平台。尽管人们为提高RNA递送效率以改善蛋白质生产付出了巨大努力,但RNA-LNPs的生理稳定性、靶向特异性和治疗效果之间的相互作用在很大程度上仍未得到探索。本综述强调了RNA-LNPs在与生物流体接触时体内稳定性或不稳定性对递送性能的关键但常被忽视的影响。我们讨论了各种因素,包括脂质组成、颗粒表面性质以及在生理条件下与蛋白质的相互作用,并概述了当前评估生物流体中RNA-LNP稳定性的方法,如动态激光散射、液相色谱以及荧光和放射性标记技术。在最后一部分,我们提出了增强稳定性的策略,重点是屏蔽脂质。因此,这项工作强调了在生物学背景下研究和理解LNPs稳定性与不稳定性之间平衡的重要性,以便在制剂性质和体内性能之间建立更有意义的关联。