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扩大用于慢病毒载体纯化的空间排阻膜色谱法规模

Scaling Up of Steric Exclusion Membrane Chromatography for Lentiviral Vector Purification.

作者信息

Labisch Jennifer Julia, Paul Richard, Wiese G Philip, Pflanz Karl

机构信息

Lab Essentials Applications Development, Sartorius Stedim Biotech GmbH, August-Spindler-Straße 11, 37079 Göttingen, Germany.

Institute of Technical Chemistry, Leibniz University Hannover, Callinstraße 5, 30167 Hannover, Germany.

出版信息

Membranes (Basel). 2023 Jan 24;13(2):149. doi: 10.3390/membranes13020149.

Abstract

Lentiviral vectors (LVs) are widely used in clinical trials of gene and cell therapy. Low LV stability incentivizes constant development and the improvement of gentle process steps. Steric exclusion chromatography (SXC) has gained interest in the field of virus purification but scaling up has not yet been addressed. In this study, the scaling up of lentiviral vector purification by SXC with membrane modules was approached. Visualization of the LVs captured on the membrane during SXC showed predominant usage of the upper membrane layer. Furthermore, testing of different housing geometries showed a strong influence on the uniform usage of the membrane. The main use of the first membrane layer places a completely new requirement on the scaling of the process and the membrane modules. When transferring the SXC process to smaller or larger membrane modules, it became apparent that scaling of the flow rate is a critical factor that must be related to the membrane area of the first layer. Performing SXC at different scales demonstrated that a certain critical minimum surface area-dependent flow rate is necessary to achieve reproducible LV recoveries. With the presented scaling approach, we were able to purify 980 mL LVs with a recovery of 68%.

摘要

慢病毒载体(LVs)广泛应用于基因和细胞治疗的临床试验。慢病毒载体稳定性较低,这促使人们不断开发并改进温和的工艺步骤。空间排阻色谱法(SXC)在病毒纯化领域受到关注,但放大规模的问题尚未得到解决。在本研究中,探讨了使用膜组件通过空间排阻色谱法放大慢病毒载体纯化的方法。空间排阻色谱法过程中膜上捕获的慢病毒载体的可视化显示,主要使用的是上层膜。此外,对不同外壳几何形状的测试表明,其对膜的均匀使用有很大影响。第一层膜的主要用途对工艺和膜组件的放大提出了全新的要求。当将空间排阻色谱法工艺转移到更小或更大的膜组件时,很明显流速的放大是一个关键因素,必须与第一层的膜面积相关。在不同规模下进行空间排阻色谱法表明,为实现可重复的慢病毒载体回收率,需要一定的与最小表面积相关的临界流速。采用所提出的放大方法,我们能够纯化980 mL慢病毒载体,回收率为68%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1169/9958935/afbe864f8677/membranes-13-00149-g001.jpg

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