Model-Based Process Challenge of an Industrial Ion-Exchange Chromatography Step

被引:39
|
作者
Westerberg, Karin [1 ]
Hansen, Ernst Broberg [2 ]
Degerman, Marcus [3 ]
Hansen, Thomas Budde [3 ]
Nilsson, Bernt [1 ]
机构
[1] Lund Univ, Dept Chem Engn, SE-22100 Lund, Sweden
[2] Novo Nordisk AS, DK-2880 Bagsvaerd, Denmark
[3] Novo Nordisk AS, DK-2820 Gentofte, Denmark
基金
瑞典研究理事会;
关键词
Chromatography; Process modeling; Quality by design; Robustness; Sensitivity analysis; SENSITIVITY-ANALYSIS; PREPARATIVE CHROMATOGRAPHY; ROBUSTNESS ANALYSIS; DESIGN; QUALITY; OPTIMIZATION; PURIFICATION; UNCERTAINTY;
D O I
10.1002/ceat.201000560
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The separation of one weakly and one strongly binding impurity from a therapeutic protein by ion-exchange chromatography was studied with a mechanistic model. The effect of disturbances in eight potentially critical process parameters on two critical quality attributes was evaluated. It was found that the outgoing concentration of the weakly binding impurity was only affected by the ingoing concentration of this impurity, while the target product purity was affected by the amounts of buffer and acid used to prepare the elution buffers and the protein concentration and purity of the feed. Full factor analysis of these parameters showed that there were interaction effects between the parameters due to the pH dependence of the chromatographic separation. Sampling-based robustness analysis estimated the probability of batch failure to be above 1?%. The model improved the analysis as it was possible to study the effects of more process parameters and their interactions than would have been possible in an experimental study.
引用
收藏
页码:183 / 190
页数:8
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