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Linear flow-velocity gradient chromatography-An efficient method for increasing the process efficiency of batch and continuous capture chromatography of proteins

机译:线性流速梯度色谱 - 提高批次和连续捕获色谱法的高效方法和蛋白质的连续捕获色谱

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摘要

A new method was proposed for increasing the capture chromatography process efficiency, linear flow-velocity gradient (LFG). The method uses a linear decreasing flow-velocity gradient with time during the sample loading. The initial flow velocity, the final flow velocity and the gradient time are the parameters to be tuned. We have developed a method for determining these parameters by using the total column capacity and the total loaded amount as a function of time. The capacity can be calculated by using the relationships between dynamic binding capacity (DBC) and residence time. By leveraging the capacity, loading amount, and the required conditions, the optimum LFG can be designed. The method was verified by ion-exchange and protein A chromatography of monoclonal antibodies (mAbs). A two-fold increase in the productivity during the sample loading was possible by LFG compared with the constant flow-velocity (CF) operation. LFG was also applied to a 4-column continuous process. The simulation showed that the cost of resin per unit amount of processed mAbs can be reduced by 13% while 1.4 times enhancement in productivity was preserved after optimization by LFG compared to CF. The process efficiency improvement is more pronounced when the isotherm is highly favorable and the loading volume is large.
机译:提出了一种用于增加捕获色谱工艺效率,线性流速 - 速度梯度(LFG)的新方法。该方法在样品负载期间使用线性减小流量梯度。初始流速,最终流速和梯度时间是要调整的参数。我们开发了一种通过使用总列容量和总加载量作为时间的总加载量来确定这些参数的方法。可以通过使用动态绑定容量(DBC)和停留时间之间的关系来计算容量。通过利用容量,装载量和所需条件,可以设计最佳的LFG。通过离子交换和蛋白质是单克隆抗体(MAb)的色谱法验证该方法。通过LFG与恒定流速(CF)操作相比,通过LFG在样品负载期间的生产率增加两倍。 LFG还应用于4柱连续过程。模拟显示,每单位加工MAB的树脂成本可以减少13%,而LFG与CF相比,通过LFG优化后,保留了生产率的增强1.4倍。当等温仪高度有利并且负载量大时,过程效率改善更加明显。

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