Waters Corporation, 1 Rue Michel Servet, Geneva 1211, Switzerland.
Waters Corporation, 1 Rue Michel Servet, Geneva 1211, Switzerland.
J Chromatogr A. 2024 Jan 11;1714:464587. doi: 10.1016/j.chroma.2023.464587. Epub 2023 Dec 17.
More and more transformative gene therapies (GTx) are reaching commercialization stage and many of them use Adeno Associated Viruses (AAVs) as their vector. Being larger than therapeutic antibodies, their size variant analysis poses an analytical challenge that must be addressed to speed up the development processes. Size exclusion chromatography (SEC) can provide critical information on the quality and purity of the product, but its full potential is not yet utilized by currently applied columns that are (i) packed with relatively large particles, (ii) prepared exclusively in large formats and (iii) built using metal hardware that is prone to secondary interactions. In this paper, we investigate the use of state-of-the-art sub-3 µm particles to address existing limitations. A prototype 2.5 µm column was found to deliver superior kinetic efficiency, significant reduction in run times and increased resolution of separations. No evidence for shear or sample sieving effects were found during comparisons with conventional 5 µm columns. Moreover, use of low adsorption hardware enabled the application of a wide range of mobile phase conditions and a chance to apply a more robust platform method for several AAV serotypes. The resulting method was tested for its reproducibility as well as utility for critical quality attribute assays, including multiangle light scattering based (MALS) measurements of size and molar mass. Thus, a new tool for higher resolution, higher throughput size variant analysis of AAVs has been described.
越来越多的变革性基因疗法(GTx)正在进入商业化阶段,其中许多疗法都使用腺相关病毒(AAV)作为载体。由于它们比治疗性抗体大,因此其大小变异分析具有分析挑战性,必须加以解决以加快开发进程。尺寸排阻色谱(SEC)可以提供有关产品质量和纯度的关键信息,但目前应用的柱(i)填充有相对较大的颗粒,(ii)专门在大格式中制备,(iii)使用易于发生二次相互作用的金属硬件制造,因此尚未充分利用其全部潜力。在本文中,我们研究了使用最先进的亚 3μm 颗粒来解决现有局限性。发现原型 2.5μm 柱具有优越的动力学效率,大大缩短了运行时间,并提高了分离分辨率。与常规 5μm 柱进行比较时,未发现剪切或样品筛分效应的证据。此外,低吸附硬件的使用使能够应用更广泛的流动相条件,并为几种 AAV 血清型应用更稳健的平台方法。该方法的重现性以及对关键质量属性分析(包括基于多角度光散射(MALS)的大小和摩尔质量测量)的实用性都进行了测试。因此,已经描述了用于 AAV 更高分辨率,更高通量的大小变异分析的新工具。