Progression of continuous downstream processing of monoclonal antibodies: Current trends and challenges

Rapid advances in intensifying upstream processes for biologics production have left downstream processing as a bottleneck in the manufacturing scheme. Biomanufacturers are pursuing continuous downstream process development to increase efficiency and flexibility, reduce footprint and cost of goods, and improve product consistency and quality. Even after successful laboratory trials, the implementation of a continuous process at manufacturing scale is not easy to achieve. This paper reviews specific challenges in converting each downstream unit operation to a continuous mode. Key elements of developing practical strategies for overcoming these challenges are detailed. These include equipment valve complexity, favorable column aspect ratio, protein‐A resin selection, quantitative assessment of chromatogram peak size and shape, holistic process characterization approach, and a customized process economic evaluation. Overall, this study provides a comprehensive review of current trends and the path forward for implementing continuous downstream processing at the manufacturing scale.

[1]  P. Alves,et al.  Improved virus purification processes for vaccines and gene therapy , 2015, Biotechnology and bioengineering.

[2]  L. Connell‐Crowley,et al.  Cation exchange chromatography provides effective retrovirus clearance for antibody purification processes , 2012, Biotechnology and bioengineering.

[3]  Dimitrios I. Gerogiorgis,et al.  Economic Analysis of Integrated Continuous and Batch Pharmaceutical Manufacturing: A Case Study , 2011 .

[4]  N Avdalovic,et al.  Protein variant separations by cation-exchange chromatography on tentacle-type polymeric stationary phases. , 1998, Journal of chromatography. A.

[5]  J. Pezzini,et al.  Accelerated , Seamless Antibody Purification Process Intensification with Continuous Disposable Technology , 2016 .

[6]  Hadi Parastar,et al.  Multivariate Curve Resolution Methods for Qualitative and Quantitative Analysis in Analytical Chemistry , 2015 .

[7]  Kate Zhang,et al.  Identification and quantitation of vesivirus 2117 particles in bioreactor fluids from infected Chinese hamster ovary cell cultures , 2013, Biotechnology and bioengineering.

[8]  M. Schofield,et al.  Transfer of a three step mAb chromatography process from batch to continuous: Optimizing productivity to minimize consumable requirements. , 2017, Journal of biotechnology.

[9]  Duncan Low,et al.  Future of antibody purification. , 2007, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[10]  Alois Jungbauer,et al.  Protein Chromatography: Process Development and Scale-Up , 2010 .

[11]  Marc Bisschops,et al.  Continuous Chromatography Is Now Possible for Clinical Manufacturing , 2016 .

[12]  Marc Bisschops,et al.  The impact of continuous multicolumn chromatography on biomanufacturing efficiency , 2013 .

[13]  P. He,et al.  Temperature effect on peak width and column efficiency in subcritical water chromatography. , 2002, Journal of chromatographic science.

[14]  L. Castilho,et al.  Development of a 3‐step straight‐through purification strategy combining membrane adsorbers and resins , 2017, Biotechnology progress.

[15]  William G. Whitford,et al.  Single‐Use Systems Support Continuous Bioprocessing by Perfusion Culture , 2014 .

[16]  L. Lerner,et al.  A rapid method for determining dynamic binding capacity of resins for the purification of proteins. , 2008, Protein expression and purification.

[17]  Suzanne S Farid,et al.  Integrated continuous bioprocessing: Economic, operational, and environmental feasibility for clinical and commercial antibody manufacture , 2017, Biotechnology progress.

[18]  Anurag S Rathore,et al.  Comparison of different options for harvest of a therapeutic protein product from high cell density yeast fermentation broth , 2006, Biotechnology and bioengineering.

[19]  R L Fahrner,et al.  Membrane ion-exchange chromatography for process-scale antibody purification. , 2001, Journal of chromatography. A.

[20]  J. Stickel,et al.  Pressure‐Flow Relationships for Packed Beds of Compressible Chromatography Media at Laboratory and Production Scale , 2001, Biotechnology progress.

[21]  S. Hober,et al.  Protein A chromatography for antibody purification. , 2007, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[22]  Marcelo Fernández-Lahore,et al.  Chromatographic Characterization and Process Performance of Column-Packed Anion Exchange Fibrous Adsorbents for High Throughput and High Capacity Bioseparations , 2015 .

[23]  C. I. Collins,et al.  Peak shape analysis and plate theory for plasma chromatography , 1975 .

[24]  Gerhard Schembecker,et al.  Developing the biofacility of the future based on continuous processing and single-use technology. , 2015, Journal of biotechnology.

[25]  Suzanne S. Farid,et al.  Integrated economic and experimental framework for screening of primary recovery technologies for high cell density CHO cultures , 2016, Biotechnology journal.

[26]  Massimo Morbidelli,et al.  Design and operation of a continuous integrated monoclonal antibody production process , 2017, Biotechnology progress.

[27]  J. Coffman,et al.  A tandem laboratory scale protein purification process using Protein A affinity and anion exchange chromatography operated in a weak partitioning mode , 2013, Biotechnology and bioengineering.

[28]  Uwe Gottschalk,et al.  Bioseparation in Antibody Manufacturing: The Good, The Bad and The Ugly , 2008, Biotechnology progress.

[29]  R. Million,et al.  Monoclonal antibody biosimilars , 2015, Nature Reviews Drug Discovery.

[30]  Konstantin B Konstantinov,et al.  The future of industrial bioprocessing: batch or continuous? , 2015, Biotechnology and bioengineering.

[31]  Oliver Kaltenbrunner,et al.  Continuous bind‐and‐elute protein A capture chromatography: Optimization under process scale column constraints and comparison to batch operation , 2016, Biotechnology progress.

[32]  Mark Pagkaliwangan,et al.  Modeling the Downstream Processing of Monoclonal Antibodies Reveals Cost Advantages for Continuous Methods for a Broad Range of Manufacturing Scales , 2019, Biotechnology journal.

[33]  W. Berthold,et al.  Interaction of cell culture with downstream purification: a case study , 2004, Cytotechnology.

[34]  Mark Schofield,et al.  Implementation of an end-to-end continuous bioprocessing platform using novel technologies , 2017 .

[35]  Iain Beattie,et al.  Ultra-performance liquid chromatography coupled to quadrupole-orthogonal time-of-flight mass spectrometry. , 2004, Rapid communications in mass spectrometry : RCM.

[36]  Frank Riske,et al.  Periodic counter-current chromatography -- design and operational considerations for integrated and continuous purification of proteins. , 2012, Biotechnology journal.

[37]  R. Bayer,et al.  Recovery and purification process development for monoclonal antibody production , 2010, mAbs.

[38]  Jason Walther,et al.  The business impact of an integrated continuous biomanufacturing platform for recombinant protein production. , 2015, Journal of biotechnology.

[39]  Christopher Miller,et al.  High‐throughput miniaturized bioreactors for cell culture process development: Reproducibility, scalability, and control , 2014, Biotechnology progress.

[40]  Ye Zhang,et al.  Very High Density of CHO Cells in Perfusion by ATF or TFF in WAVE Bioreactor™. Part I. Effect of the Cell Density on the Process , 2013, Biotechnology progress.

[41]  Ich Topic Q5A GUIDANCE FOR INDUSTRY Viral Safety Evaluation of Biotechnology Products Derived from Cell Lines of Human or Animal Origin , 2001 .

[42]  Bharat Reddy,et al.  Staphylococcus aureus protein A induces airway epithelial inflammatory responses by activating TNFR1 , 2004, Nature Network Boston.

[43]  Sarah A Johnson,et al.  Adapting viral safety assurance strategies to continuous processing of biological products , 2017, Biotechnology and bioengineering.

[44]  Roger Brunkow,et al.  The clarification of bioreactor cell cultures for biopharmaceuticals , 2003 .

[45]  Gerhard Schembecker,et al.  Cost evaluation of antibody production processes in different operation modes , 2016 .

[46]  L. Richard Stock,et al.  The Potential Impact of Continuous Processing on the Practice and Economics of Biopharmaceutical Manufacturing , 2014 .

[47]  Kurt Brorson,et al.  The clearance of viruses and transmissible spongiform encephalopathy agents from biologicals. , 2005, Current opinion in biotechnology.

[48]  Kurt Brorson,et al.  Impact of multiple re-use of anion-exchange chromatography media on virus removal. , 2005, Journal of chromatography. A.

[49]  E. Boschetti,et al.  Composite affinity sorbents and their cleaning in place. , 1990, Journal of chromatography.

[50]  Günter Jagschies,et al.  Continuous Capture of mAbs—Points to Consider and Case Studies , 2018 .

[51]  Daniel Cummings,et al.  Integrated continuous production of recombinant therapeutic proteins , 2012, Biotechnology and bioengineering.

[52]  Ekta Mahajan,et al.  Improving affinity chromatography resin efficiency using semi-continuous chromatography. , 2012, Journal of chromatography. A.

[53]  Tim Tressel,et al.  Current Therapeutic Antibody Production and Process Optimization , 2006 .

[54]  Qualification of a chromatographic column: Why and how to do it , 2003 .

[55]  Eric Langer,et al.  Continuous Bioprocessing and Perfusion: Wider Adoption Coming as Bioprocessing Matures , 2014 .

[56]  R. Kunert,et al.  Advances in recombinant antibody manufacturing , 2016, Applied Microbiology and Biotechnology.

[57]  Christian Hakemeyer,et al.  Complete clarification solution for processing high density cell culture harvests , 2015 .

[58]  Priyabrata Pattnaik,et al.  Packing of large-scale chromatography columns with irregularly shaped glass based resins using a stop-flow method , 2014, Biotechnology progress.

[59]  Jennifer Halley,et al.  Protein A chromatography increases monoclonal antibody aggregation rate during subsequent low pH virus inactivation hold , 2015, Journal of chromatography. A.

[60]  A. Shukla,et al.  Evolving trends in mAb production processes , 2017, Bioengineering & translational medicine.

[61]  Brian Hubbard,et al.  Downstream processing of monoclonal antibodies--application of platform approaches. , 2007, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[62]  Daniel G Bracewell,et al.  Optimising the design and operation of semi-continuous affinity chromatography for clinical and commercial manufacture. , 2013, Journal of chromatography. A.

[63]  Alois Jungbauer,et al.  Continuous cell flocculation for recombinant antibody harvesting , 2017, Journal of chemical technology and biotechnology.

[64]  Gail Sofer,et al.  Process Validation in Manufacturing of Biopharmaceuticals , 2012 .

[65]  Jing Liu,et al.  A mechanistic study of Protein A chromatography resin lifetime. , 2009, Journal of chromatography. A.

[66]  Paul J. Mcdonald,et al.  Fragments of protein A eluted during protein A affinity chromatography. , 2007, Journal of chromatography. A.

[67]  Joanna Rucker-Pezzini,et al.  Single Pass Diafiltration Integrated into a Fully Continuous mAb Purification Process. , 2018, Biotechnology and bioengineering.

[68]  C. Lindsley New 2016 Data and Statistics for Global Pharmaceutical Products and Projections through 2017. , 2017, ACS chemical neuroscience.

[69]  D. Cecchini,et al.  Inactivation of viruses using novel protein A wash buffers , 2015, Biotechnology progress.

[70]  Bernhardt L Trout,et al.  Regulatory Perspectives on Continuous Pharmaceutical Manufacturing: Moving From Theory to Practice: September 26-27, 2016, International Symposium on the Continuous Manufacturing of Pharmaceuticals. , 2017, Journal of pharmaceutical sciences.

[71]  D. Walls,et al.  Protein Chromatography , 2017, Methods in Molecular Biology.

[72]  Andrew L. Zydney,et al.  Perspectives on integrated continuous bioprocessing — opportunities and challenges , 2015 .

[73]  Nigel J. Titchener-Hooker,et al.  Evaluation of a structural mechanics model to predict the effect of inserts in the bed support of chromatographic columns , 2013 .

[74]  G. Schembecker,et al.  Continuous viral inactivation at low pH value in antibody manufacturing , 2016 .

[75]  Konstantin Konstantinov,et al.  End-to-end integrated fully continuous production of recombinant monoclonal antibodies. , 2015, Journal of biotechnology.

[76]  C. Jungreuthmayer,et al.  Trend analysis of performance parameters of pre-packed columns for protein chromatography over a time span of ten years. , 2016, Journal of chromatography. A.

[77]  M Vanderlaan,et al.  Industrial Purification of Pharmaceutical Antibodies: Development, Operation, and Validation of Chromatography Processes , 2001, Biotechnology & genetic engineering reviews.

[78]  Andrew L. Zydney,et al.  Continuous downstream processing for high value biological products: A Review , 2016, Biotechnology and bioengineering.

[79]  Karan Sukhija,et al.  A Single-use Strategy to Enable Manufacturing of Affordable Biologics , 2016, Computational and structural biotechnology journal.

[80]  Alois Jungbauer,et al.  Comparison of protein A affinity sorbents II. Mass transfer properties. , 2005, Journal of chromatography. A.

[81]  S. Lute,et al.  Analysis of viral clearance unit operations for monoclonal antibodies , 2010, Biotechnology and bioengineering.

[82]  P. Duncan,et al.  Systematic evaluation of in vitro and in vivo adventitious virus assays for the detection of viral contamination of cell banks and biological products. , 2014, Vaccine.

[83]  D. Ecker,et al.  The therapeutic monoclonal antibody market , 2015, mAbs.

[84]  Feng Li,et al.  Cell culture processes for monoclonal antibody production , 2010, mAbs.

[85]  Suzanne S Farid,et al.  Process economics of industrial monoclonal antibody manufacture. , 2007, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.

[86]  Yao-ming Huang,et al.  Perfusion seed cultures improve biopharmaceutical fed‐batch production capacity and product quality , 2014, Biotechnology progress.

[87]  Alois Jungbauer,et al.  Comparison of protein A affinity sorbents. , 2003, Journal of chromatography. B, Analytical technologies in the biomedical and life sciences.