Computer assisted liquid chromatographic method development for the separation of therapeutic proteins

被引:28
作者
Tyteca, Eva [1 ]
Veuthey, Jean-Luc [2 ]
Desmet, Gert [1 ]
Guillarme, Davy [2 ]
Fekete, Szabolcs [2 ]
机构
[1] Vrije Univ Brussel, Dept Chem Engn, Pl Laan 2, B-1050 Brussels, Belgium
[2] Univ Geneva, Univ Lausanne, Sch Pharmaceut Sci, Blvd dYvoy 20, CH-1211 Geneva 4, Switzerland
基金
瑞士国家科学基金会;
关键词
HYDROPHOBIC INTERACTION CHROMATOGRAPHY; ION-EXCHANGE CHROMATOGRAPHY; ELECTROSTATIC-INTERACTION CHROMATOGRAPHY; HYDROPHILIC INTERACTION CHROMATOGRAPHY; ANTIBODY CHARGE VARIANTS; GRADIENT-ELUTION; MONOCLONAL-ANTIBODIES; POLYELECTROLYTE SOLUTIONS; COUNTERION CONDENSATION; IMMUNOGLOBULIN G1;
D O I
10.1039/c6an01520d
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
This review summarizes the use of computer assisted liquid chromatographic method development for the analytical characterization of protein biopharmaceuticals. Several modes of chromatography including reversed-phase liquid chromatography (RPLC), ion exchange chromatography (IEX), hydrophobic interaction chromatography (HIC) and some perspectives are discussed. For all these chromatographic modes, the most important variables for tuning retention and selectivity are exposed. Then, the retention models that were applied in the literature in RPLC, IEX and HIC are described and critically discussed. Finally, some representative examples of separation of therapeutic proteins and mAbs are shown, to illustrate the possibilities offered by the retention modeling approach. At the end, the reliability of the models was excellent, whatever the chromatographic mode, and the retention time prediction errors were systematically below 2%. In addition, a significant amount of time can be saved during method development and robustness testing.
引用
收藏
页码:5488 / 5501
页数:14
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