Process Sensing and Control
Model-based analysis on the extractability of information from data in dynamic fed-batch experiments
Article first published online: 23 JAN 2013
DOI: 10.1002/btpr.1649
Copyright © 2013 American Institute of Chemical Engineers (AIChE)
Additional Information
How to Cite
Wechselberger, P., Sagmeister, P. and Herwig, C. (2013), Model-based analysis on the extractability of information from data in dynamic fed-batch experiments. Biotechnol Progress, 29: 285–296. doi: 10.1002/btpr.1649
Publication History
- Issue published online: 4 FEB 2013
- Article first published online: 23 JAN 2013
- Accepted manuscript online: 1 NOV 2012 08:23AM EST
- Manuscript Revised: 2 OCT 2012
- Manuscript Received: 23 MAY 2012
Funded by
- Austrian Science Fund. Grant Number: FWF Project P24154-N17
- Abstract
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Keywords:
- data exploitation;
- bioprocess model;
- bioprocess optimization;
- dynamic experiments;
- quality by design
Abstract
Dynamic changes of physiological bioprocess parameters, e.g. a change in the specific growth rate μ, are frequently observed during industrial manufacturing as well as bioprocess development. A quantitative description of these variations is of great interest, since it can bring elucidation to the physiological state of the culture. The goal of this contribution was to show limitations and issues for the calculation of rates with regard to temporal resolution for dynamic fed-batch experiments. The impact of measurement errors, temporal resolution and the physiological activity on the signal to noise ratio (SNR) of the calculated rates was evaluated using an in-silico approach. To make use of that in practice, a generally applicable rule of thumb equation for the estimation of the SNR of specific rates was presented. The SNR calculated by this rule of thumb equation helps with definition of sampling intervals and making a decision whether an observed change is statistically significant or should be attributed to random error. Furthermore, a generic reconciliation approach to remove random as well as systematic error from data was presented. This reconciliation technique requires only little prior knowledge. The validity of the proposed tools was checked with real data from a fed-batch culture of E. coli with dynamic variations due to feed profile. © 2013 American Institute of Chemical Engineers Biotechnol. Prog., 2013

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