Analytical Development, Cambridge, Massachusetts, USA.
Gene Therapy-Process Development, Cambridge, Massachusetts, USA.
Hum Gene Ther. 2022 Jan;33(1-2):103-108. doi: 10.1089/hum.2021.136. Epub 2021 Sep 20.
Adeno-associated viruses (AAVs) are nonenveloped viruses that have become popular gene transfer vectors to deliver DNA to target cells in clinical gene therapy. Iodixanol-based density gradient is one of the widely used purification methods for serotype-independent AAVs. However, residual iodixanol in AAV could be a safety concern, and further purification to remove this process-related impurity is typically needed. An analytical assay with high sensitivity is essential for the detection of residual iodixanol to ensure the safety of AAV products. We developed a liquid chromatography-mass spectrometry method with the limit of quantification of 0.01 μg/mL for residual iodixanol measurement in AAVs. The method also demonstrated linearity over four orders of magnitude that allows quantifying a high iodixanol concentration in in-process samples with excellent recovery and accuracy. In addition, we further explored a highly efficient purification method for removal of the residual iodixanol, to minimize the safety concern from iodixanol as a process impurity.
腺相关病毒(AAV)是非包膜病毒,已成为将 DNA 递送至临床基因治疗中靶细胞的热门基因转移载体。基于碘海醇的密度梯度离心法是用于非依赖血清型 AAV 的广泛使用的纯化方法之一。然而,AAV 中的残留碘海醇可能存在安全隐患,通常需要进一步纯化以去除该过程相关杂质。具有高灵敏度的分析检测方法对于检测残留碘海醇以确保 AAV 产品的安全性至关重要。我们开发了一种液相色谱-质谱法,用于检测 AAV 中残留碘海醇的定量下限为 0.01μg/mL。该方法还在四个数量级范围内表现出线性,允许对高浓度的碘海醇进行过程样品的定量分析,具有良好的回收率和准确性。此外,我们进一步探索了一种高效的纯化方法来去除残留的碘海醇,以最大限度地减少碘海醇作为工艺杂质的安全隐患。