We use cookies to distinguish you from other users and to provide you with a better experience on our websites. Close this message to accept cookies or find out how to manage your cookie settings.
To save content items to your account,
please confirm that you agree to abide by our usage policies.
If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account.
Find out more about saving content to .
To save content items to your Kindle, first ensure no-reply@cambridge.org
is added to your Approved Personal Document E-mail List under your Personal Document Settings
on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part
of your Kindle email address below.
Find out more about saving to your Kindle.
Note you can select to save to either the @free.kindle.com or @kindle.com variations.
‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi.
‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.
This chapter focusses on chromatographic processes for protein capture. The first part provides a detailed description of the mechanistic phenomena involved in protein capture, which can be regarded as a non-competitive binary system protein/impurity, where the protein of interest strongly interacts with the chromatographic medium. Several multi-column counter-current processes allowing the implementation of the sequence of operations necessary in protein capture (load, wash, recovery, regeneration) in a continuous manner are presented in the second part of the chapter. Two process design approaches for multi-column capture processes are provided: an empirical one, which allows to obtain a first guess of the operating conditions from breakthrough curves experiments, and a model-based one, which allows a more rigorous determination of the process variables. The model-based approach is used to compare the performance of multi-column and single-column processes.
This chapter focusses on the polishing steps encountered during protein purification by chromatography. The first part provides a detailed description of the mechanistic phenomena at stake, whose complexity may greatly vary from one case to the other depending on the number and type of impurities, the selectivity for the target protein as well as non-linear and competitive effects. Several multi-column counter-current processes allowing the implementation of the polishing steps in a continuous manner are presented in the second part of the chapter. Modifications of the classical SMB process introduced to better cope with the specific needs of the biopharmaceutical industry are discussed. These modifications primarily aim at recovering more than two fractions and at implementing modifier concentration gradients. Two process design approaches for multi-column processes are presented: an empirical one, which provides a first guess of the operating conditions from single-column experiments, and a model-based one, which allows a more rigorous determination of the process variables. The model-based approach is used to compare the performance of multi-column and single-column processes.
Recommend this
Email your librarian or administrator to recommend adding this to your organisation's collection.