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冷冻诱导甜菜碱掺入脂质纳米颗粒可增强mRNA递送。

Freezing induced incorporation of betaine in lipid nanoparticles enhances mRNA delivery.

作者信息

Cheng Xingdi, Zheng Xia, Tao Kun, Huo Haonan, Liu Zhang, Lu Xueguang, Wang Jianjun

机构信息

Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Colloid, Interface and Chemical Thermodynamics, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China.

Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, China.

出版信息

Nat Commun. 2025 May 20;16(1):4700. doi: 10.1038/s41467-025-60040-9.

Abstract

Lipid nanoparticles (LNPs) are key non-viral carriers for mRNA vaccines and therapeutics, but the inherent instability of mRNA necessitates sub-zero storage with cryoprotectants (CPAs) to prevent freeze-induced LNP aggregation and compromised mRNA delivery. Here we show that ice formation during freezing concentrates CPAs with LNPs in the remaining liquid-a phenomenon known as freeze concentration. This creates a steep concentration gradient of CPAs across the lipid membrane that drives passive CPAs diffusion into LNPs. By leveraging this process, we developed betaine-based CPAs that both preserve the stability of LNP and enter LNP during freeze-thaw. The incorporated betaine enhances endosomal escape and boosts mRNA delivery of LNP. In female mice, betaine-loaded LNPs elicit stronger humoral and cellular immune responses, providing dose-sparing advantages. These findings highlight freeze concentration as a promising LNP formulation strategy and underscore the role of CPA as active modulators of LNP structure and function.

摘要

脂质纳米颗粒(LNPs)是用于mRNA疫苗和治疗药物的关键非病毒载体,但mRNA固有的不稳定性需要在低温下与冷冻保护剂(CPAs)一起储存,以防止冷冻诱导的LNP聚集和mRNA递送受损。在这里,我们表明冷冻过程中的冰形成会使CPAs与LNPs在剩余液体中浓缩——这一现象称为冷冻浓缩。这会在脂质膜上形成一个陡峭的CPAs浓度梯度,驱动被动的CPAs扩散到LNPs中。通过利用这一过程,我们开发了基于甜菜碱的CPAs,它们既能保持LNP的稳定性,又能在冻融过程中进入LNP。掺入的甜菜碱增强了内体逃逸并提高了LNP的mRNA递送效率。在雌性小鼠中,负载甜菜碱的LNPs引发更强的体液免疫和细胞免疫反应,具有节省剂量的优势。这些发现突出了冷冻浓缩作为一种有前景的LNP制剂策略,并强调了CPAs作为LNP结构和功能的活性调节剂的作用。

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