Beckert Nicole, Dietrich Annabelle, Hubbuch Jürgen
Institute of Process Engineering in Life Sciences-Section IV: Biomolecular Separation Engineering, Karlsruhe Institute of Technology (KIT), 76131 Karlsruhe, Germany.
Pharmaceuticals (Basel). 2024 Sep 16;17(9):1217. doi: 10.3390/ph17091217.
Lipid nanoparticles (LNPs) and their versatile nucleic acid payloads bear great potential as delivery systems. Despite their complex lipid composition, their quality is primarily judged by particle characteristics and nucleic acid encapsulation. In this study, we present a holistic reversed-phase (RP)-charged aerosol detection (CAD)-based method developed for commonly used LNP formulations, allowing for intensified LNP and process characterization. We used an experimental approach for power function value (PFV) optimization termed exploratory calibration, providing a single PFV (1.3) in an appropriate linearity range for all six lipids. Followed by the procedure of method calibration and validation, linearity (10-400 ng, > 0.996), precision, accuracy, and robustness were effectively proven. To complement the commonly determined LNP attributes and to evaluate the process performance across LNP processing, the developed RP-CAD method was applied in a process parameter study varying the total flow rate (TFR) during microfluidic mixing. The RP-CAD method revealed a constant lipid molar ratio across processing but identified deviations in the theoretical lipid content and general lipid loss, which were both, however, entirely TFR-independent. The deviations in lipid content could be successfully traced back to the lipid stock solution preparation. In contrast, the observed lipid loss was attributable to the small-scale dialysis following microfluidic mixing. Overall, this study establishes a foundation for employing RP-CAD for lipid quantification throughout LNP processing, and it highlights the potential to extend its applicability to other LNPs, process parameter studies, or processes such as cross-flow filtration.
脂质纳米颗粒(LNPs)及其多样的核酸载荷作为递送系统具有巨大潜力。尽管其脂质组成复杂,但其质量主要通过颗粒特性和核酸包封来判断。在本研究中,我们提出了一种基于整体反相(RP)-带电气溶胶检测(CAD)的方法,该方法是为常用的LNP制剂开发的,可强化LNP及其工艺表征。我们采用了一种称为探索性校准的实验方法来优化幂函数值(PFV),为所有六种脂质在合适的线性范围内提供了单一的PFV(1.3)。在进行方法校准和验证程序后,有效证明了线性(10 - 400 ng,> 0.996)、精密度、准确度和稳健性。为了补充通常确定的LNP属性并评估整个LNP加工过程的工艺性能,将所开发的RP-CAD方法应用于微流控混合过程中改变总流速(TFR)的工艺参数研究。RP-CAD方法揭示了整个加工过程中脂质摩尔比恒定,但确定了理论脂质含量和一般脂质损失的偏差,然而这两者均与TFR完全无关。脂质含量的偏差可以成功追溯到脂质储备溶液的制备。相比之下,观察到的脂质损失归因于微流控混合后的小规模透析。总体而言,本研究为在整个LNP加工过程中采用RP-CAD进行脂质定量奠定了基础,并突出了将其适用性扩展到其他LNP、工艺参数研究或诸如错流过滤等工艺的潜力。