Boateng Eric, Olsén Erik, Kamanzi Albert, Zhang Yao, Zhao Bin, Cullis Pieter R, Leslie Sabrina
Michael Smith Laboratories, University of British Columbia, 2185 East Mall, Vancouver V6T 1Z4, British Columbia, Canada.
Department of Physics, University of Gothenburg, Origovägen 6B, Gothenburg 41296, Sweden.
Nano Lett. 2025 Aug 13;25(32):12158-12165. doi: 10.1021/acs.nanolett.5c02232. Epub 2025 Aug 3.
Detailed characterization of the size, mass, payload, and structure of suspended mRNA-lipid nanoparticles (LNPs) is necessary to improve our understanding of how these heterogeneous properties influence therapeutic efficacy and potency. Methods currently in use face limitations in reporting ensemble-average particle properties or requiring dedicated home-built microscopes that are beyond the reach of nanoparticle developers. In this work, we overcome these limitations by combining a commercially available confocal microscope and a convex lens-induced confinement (CLiC) instrument to achieve simultaneous characterization and correlation of the size, mass, refractive index, and nucleic acid payload of individual LNPs. We established the accuracy and precision of our method using nanosized beads and used it to investigate the size, payload, and water content of LNPs in different solvent pH. By employing readily available microscopy tools, we open the door to widespread adoption of our quantitative, in-solution nanoparticle characterization method.
详细表征悬浮的信使核糖核酸-脂质纳米颗粒(LNP)的大小、质量、载药量和结构,对于增进我们对这些异质性特性如何影响治疗效果和效力的理解至关重要。目前使用的方法在报告总体平均颗粒特性方面存在局限性,或者需要专用的自制显微镜,而纳米颗粒开发者难以企及。在这项工作中,我们通过结合商用共聚焦显微镜和凸透镜诱导限制(CLiC)仪器,克服了这些局限性,以实现对单个LNP的大小、质量、折射率和核酸载药量的同步表征和关联。我们使用纳米珠确定了我们方法的准确性和精密度,并将其用于研究不同溶剂pH下LNP的大小、载药量和含水量。通过采用现成的显微镜工具,我们为广泛采用我们的定量溶液内纳米颗粒表征方法打开了大门。