A novel efficient optimisation system for purification process synthesis

被引:9
|
作者
Polykarpou, Eleftheria M. [1 ,2 ]
Dalby, Paul A. [2 ]
Papageorgiou, Lazaros G. [1 ]
机构
[1] Univ London Univ Coll, Ctr Proc Syst Engn, Dept Chem Engn, London WC1E 7JE, England
[2] Univ London Univ Coll, Dept Biochem Engn, London WC1E 7JE, England
基金
英国工程与自然科学研究理事会;
关键词
Downstream processing; Mixed integer programming; Optimisation; PROTEIN-PURIFICATION; RECOMBINANT PROTEINS; MILP FORMULATIONS; EXPERT-SYSTEM; DESIGN; CHROMATOGRAPHY; TAGS; SELECTION;
D O I
10.1016/j.bej.2012.06.012
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Protein purification through chromatographic processes has been broadly used in the biopharmaceutical industry over the last decades, but still remains a major bottleneck. In this work, we address the challenge of selecting appropriate chromatographic steps, along with product collecting timeline for separating the target protein from the contaminants in a multicomponent mixture. A novel mixed integer linear programming (MILP) model for purification process synthesis is proposed. The model allows product losses and is tested on three example protein mixtures, containing up to 13 contaminants and selecting from a set of up to 21 candidate steps. The results are compared with previous literature models attempting to solve the same problem and show that the proposed approach offers significant gains in computational efficiency without compromising the quality of the solution. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:186 / 193
页数:8
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