Börjesdotter Anna-Maria, Bolinsson Hans, Dagø Thomas, Herranz-Trillo Fátima, Palmiero Umberto Capasso, Schagerlöf Herje, Nilsson Lars
Lund University, Naturvetarvägen 14, 221 00 Lund, Sweden.
Lund University, Naturvetarvägen 14, 221 00 Lund, Sweden.
Int J Pharm. 2025 Jan 5;668:124940. doi: 10.1016/j.ijpharm.2024.124940. Epub 2024 Nov 10.
This study employs asymmetric flow field-flow fractionation online coupled with small angle X-ray scattering at a synchrotron beamline, along with multiple downstream detectors, including multi-angle light scattering, dual wavelength UV and dRI. This setup enables size-resolved characterization of lipid nanoparticles, allowing for a detailed comparison between empty and cargo-loaded lipid nanoparticles intended for nucleic acid delivery. Batch-mode characterization techniques, including cryogenic transmission electron microscopy and dynamic light scattering, alongside collection of fractions for offline characterization with liquid chromatography-charged aerosol detection, allowed for determination of the particle morphology, hydrodynamic radius, and the lipid composition over the size distribution. Cargo-containing and empty lipid nanoparticles show differences in density, and loaded particles exhibit a broader size distribution and a higher frequency of blebs at the surface. Both samples consist of spherical core-shell structured particles, with no distinguishable internal structure. A pivotal finding, often assumed until now, is that the mole fraction of each individual lipid component closely matches the original formulation. This work contributes to a more detailed understanding of lipid nanoparticles, supporting their continued development and rational design in medical applications.
本研究采用不对称流场-流分级法与同步加速器光束线上的小角X射线散射在线联用,并配备多个下游探测器,包括多角度光散射、双波长紫外和示差折光检测器。这种设置能够对脂质纳米颗粒进行尺寸分辨表征,从而对用于核酸递送的空脂质纳米颗粒和载有货物的脂质纳米颗粒进行详细比较。批处理模式表征技术,包括低温透射电子显微镜和动态光散射,以及收集馏分用于离线液相色谱-带电气溶胶检测表征,可确定颗粒形态、流体动力学半径以及尺寸分布上的脂质组成。含货物的脂质纳米颗粒和空脂质纳米颗粒在密度上存在差异,载有货物的颗粒表现出更宽的尺寸分布以及表面更高频率的泡状突起。两个样品均由球形核壳结构颗粒组成,没有可区分的内部结构。一个至今常被假定的关键发现是,每种脂质成分的摩尔分数与原始配方紧密匹配。这项工作有助于更详细地了解脂质纳米颗粒,支持它们在医学应用中的持续开发和合理设计。