Developing the biofacility of the future based on continuous processing and single-use technology
Autor: | Gerhard Schembecker, Martin Lobedann, Benjamin Maiser, Stephan Klutz, Jorgen Magnus, Maike Temming, Jens Niklas, Peter Schwan |
---|---|
Rok vydání: | 2014 |
Předmět: |
Chromatography
Drug Industry business.industry Process (engineering) Computer science Scale (chemistry) Antibodies Monoclonal Bioengineering General Medicine Hydrogen-Ion Concentration Applied Microbiology and Biotechnology Pilot plant Chemical engineering Downstream (manufacturing) Proof of concept Analytics Facility Design and Construction Production (economics) Virus Inactivation Upstream (networking) Process engineering business Staphylococcal Protein A Filtration Biotechnology |
Zdroj: | Journal of biotechnology. 213 |
ISSN: | 1873-4863 |
Popis: | To maintain or strengthen their market position, biopharmaceutical producers have to adapt their production facilities to a drastically changed market environment. Contrary to currently used large scale batch-wise operated production facilities, where stainless steel equipment is widely applied, small scale and flexible production processes are desired. Consequently, the concept of the “biofacility of the future” has been developed, which combines the attributes fast, flexible, small, inexpensive and sustainable. Four design principles build the facility’s basis and are presented within this work: continuous processing, 100% single-use equipment, closed processing and adopting the ballroom concept. However, no publication presents a completely continuously operated platform process for the production of monoclonal antibodies up to now. Therefore, this work establishes the proof of concept regarding continuous antibody manufacturing. A pilot plant for the production of monoclonal antibodies has been built 100% in single-use equipment. It was operated fully continuous and automated in the upstream and the downstream part. The concepts that allow continuously operating the pilot plant are presented within this work, i.e., continuously operated filtration, continuously operated viral inactivation, continuously operated chromatography and a continuously operated formulation. Analytics showed that the produced product was within specification limits of industrial bulk drug substances. |
Databáze: | OpenAIRE |
Externí odkaz: |