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Zonal Rate Model for Axial and Radial Flow Membrane Chromatography. Part I: Knowledge Transfer Across Operating Conditions and Scales

机译:轴向和径向流膜色谱的区域速率模型。第一部分:跨运营条件和规模的知识转移

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摘要

The zonal rate model (ZRM) has previously been applied for analyzing the performance of axial flow membrane chromatography capsules by independently determining the impacts of flow and binding related non-idealities on measured breakthrough curves. In the present study, the ZRM is extended to radial flow configurations, which are commonly used at larger scales. The axial flow XT5 capsule and the radial flow XT140 capsule from Pall are rigorously analyzed under binding and non-binding conditions with bovine serum albumin (BSA) as test molecule. The binding data of this molecule is much better reproduced by the spreading model, which hypothesizes different binding orientations, than by the well-known Langmuir model. Moreover, a revised cleaning protocol with NaCl instead of NaOH and minimizing the storage time has been identified as most critical for quantitatively reproducing the measured breakthrough curves. The internal geometry of both capsules is visualized by magnetic resonance imaging (MRI). The flow in the external hold-up volumes of the XT140 capsule was found to be more homogeneous as in the previously studied XT5 capsule. An attempt for model-based scale-up was apparently impeded by irregular pleat structures in the used XT140 capsule, which might lead to local variations in the linear velocity through the membrane stack. However, the presented approach is universal and can be applied to different capsules. The ZRM is shown to potentially help save valuable material and time, as the experiments required for model calibration are much cheaper than the predicted large-scale experiment at binding conditions. Biotechnol. Bioeng. 2013; 110: 1129–1141. © 2012 Wiley Periodicals, Inc.
机译:区域速率模型(ZRM)以前已通过独立确定流量和结合的相关非理想性对测得的穿透曲线的影响而用于分析轴流膜色谱胶囊的性能。在本研究中,ZRM扩展到径向流配置,通常在较大规模下使用。在结合和非结合条件下,以牛血清白蛋白(BSA)作为测试分子,严格分析了颇尔公司生产的轴向流动XT5胶囊和径向流动XT140胶囊。该分子的结合数据通过假设不同结合方向的扩展模型比众所周知的Langmuir模型更好地再现。此外,已经确定了用NaCl代替NaOH并减少存储时间的修订清洁方案对于定量复制所测得的穿透曲线最为关键。两个胶囊的内部几何结构均通过磁共振成像(MRI)可视化。与以前研究的XT5胶囊一样,XT140胶囊的外部滞留体积中的流动更均匀。 XM140胶囊中不规则的褶皱结构明显阻碍了基于模型的放大尝试,这可能会导致通过膜叠堆的线速度发生局部变化。然而,提出的方法是通用的,并且可以应用于不同的胶囊。 ZRM被证明可以潜在地节省宝贵的材料和时间,因为模型校正所需的实验比在结合条件下预测的大规模实验便宜得多。生物技术。生恩2013; 110:1129–1141。 ©2012 Wiley Periodicals,Inc.

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