...
首页> 外文期刊>Biotechnology and Bioengineering >Advances in inline quantification of co-eluting proteins in chromatography: Process-data-based model calibration and application towards real-life separation issues
【24h】

Advances in inline quantification of co-eluting proteins in chromatography: Process-data-based model calibration and application towards real-life separation issues

机译:色谱中共洗脱蛋白的在线定量研究的进展:基于过程数据的模型校准及其在现实生活中分离问题的应用

获取原文
获取原文并翻译 | 示例

摘要

Pooling decisions in preparative liquid chromatography for protein purification are usually based on univariate UV absorption measurements that are not able to differentiate between product and co-eluting contaminants. This can result in inconsistent pool purities or yields, if there is a batch-to-batch variability of the feedstock. To overcome this analytical bottleneck, a tool for selective inline quantification of co-eluting model proteins using mid-UV absorption spectra and Partial Least Squares Regression (PLS) was presented in a previous study and applied for real-time pooling decisions. In this paper, a process-data-based method for the PLS model calibration will be introduced that allows the application of the tool towards chromatography steps of real-life processes. The process-data-based calibration method uses recorded inline mid-UV absorption spectra that are correlated with offline fraction analytics to calibrate PLS models. In order to generate average spectra from the inline data, a Visual Basic for Application macro was successfully developed. The process-data-based model calibration was established using a ternary model protein system. Afterwards, it was successfully demonstrated in two case studies that the calibration method is applicable towards real-life separation issues. The calibrated PLS models allowed a successful quantification of the co-eluting species in a cation-exchange-based aggregate and fraction removal during the purification of monoclonal antibodies and of co-eluting serum proteins in an anion-exchange-based purification of Cohn supernatant I. Consequently, the presented process-data-based PLS model calibration in combination with the tool for selective inline quantification has a great potential for the monitoring of future chromatography steps and may contribute to manage batch-to-batch variability by real-time pooling decisions. Biotechnol. Bioeng. 2015;112: 1406-1416. (c) 2015 Wiley Periodicals, Inc.
机译:用于蛋白质纯化的制备型液相色谱中的合并决策通常基于无法区分产物和共洗脱污染物的单变量UV吸收测量值。如果原料之间存在批次差异,这可能导致池纯度或产量不一致。为克服这一分析瓶颈,在先前的研究中提供了一种使用中紫外吸收光谱和偏最小二乘回归(PLS)进行共洗脱模型蛋白的选择性在线定量分析的工具,该工具可用于实时合并决策。在本文中,将介绍一种用于PLS模型校准的基于过程数据的方法,该方法允许将该工具应用于实际过程的色谱步骤。基于过程数据的校准方法使用已记录的在线中紫外吸收光谱(与离线馏分分析相关)来校准PLS模型。为了从内联数据生成平均光谱,成功开发了Visual Basic for Application宏。使用三元模型蛋白质系统建立了基于过程数据的模型校准。之后,在两个案例研究中成功证明了校准方法适用于现实生活中的分离问题。校准的PLS模型可以成功定量定量基于阳离子交换的聚集体中的共洗脱物种,并在纯化单克隆抗体和基于阴离子交换的Cohn上清液I纯化过程中共同洗脱的血清蛋白时去除馏分因此,所提出的基于过程数据的PLS模型校准与用于选择性在线定量分析的工具相结合,具有监测未来色谱步骤的巨大潜力,并可能有助于通过实时合并决策来管理批次间的差异。生物技术。生恩2015; 112:1406-1416。 (c)2015年威利期刊有限公司

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号