Abstract

A model based approach has been developed and used to identify robust operating conditions for an industrial hydrophobic interaction chromatography where resin lot variability, combined with feed stream variability, was resulting in serious performance issues during the purification of a multi component therapeutic protein from crude feed material. An equilibrium dispersive model was formulated which successfully predicted the key product critical quality attribute during validation studies. The model was then used to identify operating parameter ranges that assured product quality despite the process variability. Probabilistic design spaces were generated using stochastic simulations that showed the probability that each resin lot would meet product quality specifications, over a range of possible operating conditions, accounting for the historical variability experienced in the load material composition and concentration. No operating condition was found with normal process variability where quality assurance remained >0.95 for resins that gave the highest and lowest product recoveries during process development. The lowest risk of batch failure found was 16%, and operating conditions were not robust. We then extended the stochastic methodology used to generate probabilistic design spaces, to identify the level of control required on the load material composition and concentration to bring process robustness to an acceptable level, which is not possible using DOE experimental methods due to the impractical amount of resources that would be required. Although reducing inlet variability resulted in an increase in the assurance of product quality, the results indicated that changing operating conditions according to which resin lot is in use is the favorable option.

Highlights

  • A model based approach has been developed and used to identify robust operating conditions for an industrial hydrophobic interaction chromatography where resin lot variability, combined with feed stream variability, was resulting in serious performance issues during the purification of a multi component therapeutic protein from crude feed material

  • The results show the probability of meeting product quality specifications, over a range of possible operating conditions, whilst accounting for process uncertainty based on the historical variability experienced in the load material composition and concentration

  • We assumed that all product isoforms that remain bound to the column after the load and wash steps are subsequently collected in the elution step, only the load and wash stages of the separation are simulated, and that the product related impurities and HCP's in the feed stream had a negligible impact on the separation of the product of interest, as the impurities are observed to flow through during the load phase of the chromatographic cycle

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Summary

Introduction

A model based approach has been developed and used to identify robust operating conditions for an industrial hydrophobic interaction chromatography where resin lot variability, combined with feed stream variability, was resulting in serious performance issues during the purification of a multi component therapeutic protein from crude feed material. Model based approaches to sensitivity and robustness analysis are of particular relevance to industrial separations as they can ensure purification processes are robust, which is a key requirement for bioseparations (Jakobsson et al, 2005; Degerman et al, 2009; Westerberg et al, 2012; Borg et al, 2013) These approaches enable the impact of disturbances in process parameters on meeting CQA's to be quantified quickly and efficiently, thereby indicating the risk of batch failure, with minimal time, material and analytical constraints. The additional knowledge and process understanding gained by their use may offset the extra investment of time and material for model development and validation, and fulfils regulatory guidance regarding the implementation of Quality by Design and the proposed greater use of mechanistic models (ICH, 2008a)

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