Simulation of a human serum albumin downstream process incorporating ion-exchange membrane adsorbers

In this paper a generic process model for the simulation of various downstream processes for protein purification is presented. It consists of detailed, dynamic models for ion-exchange membrane adsorbers, ion-exchange and size-exclusion chromatography and ultra-/diafiltration. For the implemented ion-exchange membrane adsorber model, the steric mass action model has been applied. The isotherm parameters have been determined experimentally for bovine serum albumin (BSA) and immunoglobulin G (IgG). The comparison between simulation results of the ion-exchange membrane and experiments for two protein mixtures containing BSA and IgG shows satisfactory agreement. Two case studies based on the purification process of human serum albumin are performed to illustrate the influence of structural changes in the process flowsheet on the process performance. The simulation results show that the replacement of an anion-exchange chromatography column by an anion-exchange membrane adsorber leads to a significant reduction in overall process time at constant yield and purity. The case studies demonstrate the applicability of the generic process model for detailed process analysis.

[1]  Steven M. Cramer,et al.  Solute affinity in ion-exchange displacement chromatography , 1996 .

[2]  W Demmer,et al.  Large-scale membrane adsorbers. , 1999, Journal of chromatography. A.

[3]  A. Polson,et al.  The Some Aspects of Diffusion in Solution and a Definition of a Colloidal Particle. , 1950 .

[4]  Lawrence B. Evans,et al.  Bioprocess Simulation: A New Tool for Process Development , 1988, Bio/Technology.

[5]  C. Wen,et al.  Longitudinal dispersion of liquid flowing through fixed and fluidized beds , 1968 .

[6]  Anita M. Katti,et al.  Fundamentals of Preparative and Nonlinear Chromatography , 1994 .

[7]  J. M. Pinto,et al.  Optimal Design of Protein Production Plants with Time and Size Factor Process Models , 2000, Biotechnology progress.

[8]  A. R. Cooper Ultrafiltration membranes and applications , 1981 .

[9]  E. Lightfoot,et al.  Predictability of chromatographic protein separations , 1992 .

[10]  Anders Axelsson,et al.  Methodologies for model calibration to assist the design of a preparative ion-exchange step for antibody purification. , 2004, Journal of chromatography. A.

[11]  P. V. Danckwerts Continuous flow systems , 1953 .

[12]  W. Deen Hindered transport of large molecules in liquid‐filled pores , 1987 .

[13]  A. Lenhoff Significance and estimation of chromatographic parameters , 1987 .

[14]  J. Fried,et al.  Breakthrough of lysozyme through an affinity membrane of cellulose‐cibacron blue , 1994 .

[15]  S. Suen,et al.  A mathematical analysis of affinity membrane bioseparations , 1992 .

[16]  S M Cramer,et al.  Comparison of linear gradient and displacement separations in ion-exchange systems. , 2002, Biotechnology and bioengineering.

[17]  H. Yeh Modified Gel-Polarization Model for Ultrafiltration in Hollow-Fiber Membrane Modules , 1996 .

[18]  A. Shiosaki,et al.  Frontal analysis of protein adsorption on a membrane adsorber. , 1994, Journal of chromatography. A.

[19]  M. A. Winkler,et al.  Chemical engineering problems in biotechnology , 1990 .

[20]  E. J. Wilson,et al.  Liquid Mass Transfer at Very Low Reynolds Numbers in Packed Beds , 1966 .

[21]  P. V. Danckwerts Continuous flow systems. Distribution of residence times , 1995 .

[22]  R. Evangelista,et al.  Process and Economic Evaluation of the Extraction and Purification of Recombinant β‐Glucuronidase from Transgenic Corn , 1998, Biotechnology progress.

[23]  Henner Schmidt-Traub,et al.  Preparative Chromatography: of Fine Chemicals and Pharmaceutical Agents , 2005 .

[24]  J. Curling Methods of plasma protein fractionation , 1980 .

[25]  Jochen Strube,et al.  Challenges in biotechnology production—generic processes and process optimization for monoclonal antibodies , 2005 .

[26]  C L Cooney,et al.  Process simulation for recombinant protein production: cost estimation and sensitivity analysis for heparinase I expressed in Escherichia coli. , 1997, Biotechnology and bioengineering.

[27]  Tingyue Gu,et al.  New approach to a general nonlinear multicomponent chromatography model , 1990 .