Effective September 2012
Bioseparations and Downstream Processing
Strategic assay deployment as a method for countering analytical bottlenecks in high throughput process development: Case studies in ion exchange chromatography
Article first published online: 31 JUL 2012
DOI: 10.1002/btpr.1591
Copyright © 2012 American Institute of Chemical Engineers (AIChE)
Additional Information
How to Cite
Konstantinidis, S., Heldin, E., Chhatre, S., Velayudhan, A. and Titchener-Hooker, N. (2012), Strategic assay deployment as a method for countering analytical bottlenecks in high throughput process development: Case studies in ion exchange chromatography. Biotechnol Progress, 28: 1292–1302. doi: 10.1002/btpr.1591
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Effective September 2012
Publication History
- Issue published online: 10 OCT 2012
- Article first published online: 31 JUL 2012
- Accepted manuscript online: 28 JUN 2012 01:59AM EST
- Manuscript Revised: 21 JUN 2012
- Manuscript Received: 11 MAR 2012
Keywords:
- analytical bottleneck;
- anion exchange chromatography;
- high throughput process development;
- method comparison;
- multicriteria decision-making
Abstract
High throughput approaches to facilitate the development of chromatographic separations have now been adopted widely in the biopharmaceutical industry, but issues of how to reduce the associated analytical burden remain. For example, acquiring experimental data by high level factorial designs in 96 well plates can place a considerable strain upon assay capabilities, generating a bottleneck that limits significantly the speed of process characterization. This article proposes an approach designed to counter this challenge; Strategic Assay Deployment (SAD). In SAD, a set of available analytical methods is investigated to determine which set of techniques is the most appropriate to use and how best to deploy these to reduce the consumption of analytical resources while still enabling accurate and complete process characterization. The approach is demonstrated by investigating how salt concentration and pH affect the binding of green fluorescent protein from Escherichia coli homogenate to an anion exchange resin presented in a 96-well filter plate format. Compared with the deployment of routinely used analytical methods alone, the application of SAD reduced both the total assay time and total assay material consumption by at least 40% and 5%, respectively. SAD has significant utility in accelerating bioprocess development activities. © 2012 American Institute of Chemical Engineers Biotechnol. Prog., 2012

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