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首页> 外文期刊>Biotechnology Progress >A mechanistic model to account for the Donnan and volume exclusion effects in ultrafiltration/diafiltration process of protein formulations
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A mechanistic model to account for the Donnan and volume exclusion effects in ultrafiltration/diafiltration process of protein formulations

机译:一种机制模型,以考虑寡南和蛋白质配方渗滤过程中的唐南和体积排斥效应

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摘要

Ultrafiltration/diafiltration (UF/DF) is a typical step in protein drug manufacturing process to concentrate and exchange the protein solution into a desired formulation. However, significant offset of pH and composition from the target formulation have been frequently observed after UF/DF, posing challenges to the stability, performance, and consistency of the final drug product. Such shift can often be attributed to the Donnan and volume exclusion effects. In order to predict and compensate for those effects, a mechanistic model is developed based on the protein charge, mass and charge balances, as well as the equilibrium condition across the membrane. The integrated UF/DF model can be used to predict both the dynamic behavior and the final outcome of the process. Examples of the modeling results for the pH and composition variation during the UF/DF operations are presented for two monoclonal antibody proteins. The model predictions are in good agreement with a comprehensive experimental data set that covers different process steps, protein concentrations, solution matrices, and process scales. The results show that significant pH and excipient concentration shifts are more likely to occur for high protein concentration and low ionic strength matrices. As a special example, a self-buffering protein formulation shows unique pH behavior during DF, which could also be captured with the dynamic model. The capability of the model in predicting the performance of UF/DF process as a function of protein characteristics and formulation conditions makes it a useful tool to improve process understanding and facilitate process development.
机译:超滤/渗滤(UF / DF)是蛋白质药物制造方法的典型步骤,以浓缩并将蛋白质溶液交换为所需的制剂。然而,在UF / DF之后经常观察到来自目标制剂的pH和组合物的显着偏移,对最终药品的稳定性,性能和一致性构成挑战。这种偏移通常可以归因于DONNAN和体积排除效果。为了预测和补偿这些效果,基于蛋白质电荷,质量和电荷余额以及膜穿过的平衡条件开发机械模型。集成的UF / DF模型可用于预测该过程的动态行为和最终结果。对于两种单克隆抗体蛋白质,给出了UF / DF操作期间pH和组成变化的建模结果的实例。模型预测与涵盖不同工艺步骤,蛋白质浓度,溶液矩阵和工艺尺度的综合实验数据集具有良好的一致性。结果表明,对于高蛋白质浓度和低离子强度基质,更可能发生显着的pH和赋形剂浓度偏移。作为一个特殊实例,自缓冲蛋白质制剂在DF期间显示出独特的pH行为,这也可以用动态模型捕获。模型在预测UF / DF过程的性能作为蛋白质特征和配方条件的函数中的能力使其成为改善过程理解和促进过程开发的有用工具。

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