Literature DB >> 27977912

Characterization of TAP Ambr 250 disposable bioreactors, as a reliable scale-down model for biologics process development.

Ping Xu1, Colleen Clark1, Todd Ryder1, Colleen Sparks1, Jiping Zhou1, Michelle Wang1, Reb Russell1, Charo Scott1.   

Abstract

Demands for development of biological therapies is rapidly increasing, as is the drive to reduce time to patient. In order to speed up development, the disposable Automated Microscale Bioreactor (Ambr 250) system is increasingly gaining interest due to its advantages, including highly automated control, high throughput capacity, and short turnaround time. Traditional early stage upstream process development conducted in 2 - 5 L bench-top bioreactors requires high foot-print, and running cost. The establishment of the Ambr 250 as a scale-down model leads to many benefits in process development. In this study, a comprehensive characterization of mass transfer coefficient (kL a) in the Ambr 250 was conducted to define optimal operational conditions. Scale-down approaches, including dimensionless volumetric flow rate (vvm), power per unit volume (P/V) and kL a have been evaluated using different cell lines. This study demonstrates that the Ambr 250 generated comparable profiles of cell growth and protein production, as seen at 5-L and 1000-L bioreactor scales, when using kL a as a scale-down parameter. In addition to mimicking processes at large scales, the suitability of the Ambr 250 as a tool for clone selection, which is traditionally conducted in bench-top bioreactors, was investigated. Data show that cell growth, productivity, metabolite profiles, and product qualities of material generated using the Ambr 250 were comparable to those from 5-L bioreactors. Therefore, Ambr 250 can be used for clone selection and process development as a replacement for traditional bench-top bioreactors minimizing resource utilization during the early stages of development in the biopharmaceutical industry.
© 2017 American Institute of Chemical Engineers Biotechnol. Prog., 33:478-489, 2017. © 2017 American Institute of Chemical Engineers.

Entities:  

Keywords:  TAP Ambr; automated microscale bioreactor; clone selection; oxygen transfer coefficient; scale-down model; upstream process development

Mesh:

Year:  2017        PMID: 27977912     DOI: 10.1002/btpr.2417

Source DB:  PubMed          Journal:  Biotechnol Prog        ISSN: 1520-6033


  11 in total

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Review 7.  Automation in cell and gene therapy manufacturing: from past to future.

Authors:  P Moutsatsou; J Ochs; R H Schmitt; C J Hewitt; M P Hanga
Journal:  Biotechnol Lett       Date:  2019-09-20       Impact factor: 2.461

Review 8.  Developing a new class of engineered live bacterial therapeutics to treat human diseases.

Authors:  Mark R Charbonneau; Vincent M Isabella; Ning Li; Caroline B Kurtz
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Review 9.  Critical Analysis of cGMP Large-Scale Expansion Process in Bioreactors of Human Induced Pluripotent Stem Cells in the Framework of Quality by Design.

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Journal:  BioDrugs       Date:  2021-11-02       Impact factor: 5.807

Review 10.  White paper on high-throughput process development for integrated continuous biomanufacturing.

Authors:  Mariana N São Pedro; Tiago C Silva; Rohan Patil; Marcel Ottens
Journal:  Biotechnol Bioeng       Date:  2021-04-02       Impact factor: 4.530

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