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Effects of antibody disulfide bond reduction on purification process performance and final drug substance stability
Authors:Wai Keen Chung  Brian Russell  Yanhong Yang  Michael Handlogten  Suzanne Hudak  Mingyan Cao  Jihong Wang  David Robbins  Sanjeev Ahuja  Min Zhu
Institution:1. +1(301)398‐2799 0000-0001-7822-7131 Purification Process Sciences, MedImmune LLC, One MedImmune Way, Gaithersburg, Maryland;2. Cell Culture and Fermentation Sciences, MedImmune LLC, One MedImmune Way, Gaithersburg, Maryland;3. Analytical Sciences, MedImmune LLC, One MedImmune Way, Gaithersburg, Maryland;4. Cell Culture Sciences, Macrogenics Inc, Rockville, Maryland;5. Formulation Sciences, MedImmune LLC, One MedImmune Way, Gaithersburg, Maryland;6. Purification Process Sciences, MedImmune LLC, One MedImmune Way, Gaithersburg, Maryland;7. Protein Science, Boehringer Ingelheim Fremont Inc, Fremont, California
Abstract:Antibody disulfide bond reduction during monoclonal antibody (mAb) production is a phenomenon that has been attributed to the reducing enzymes from CHO cells acting on the mAb during the harvest process. However, the impact of antibody reduction on the downstream purification process has not been studied. During the production of an IgG2 mAb, antibody reduction was observed in the harvested cell culture fluid (HCCF), resulting in high fragment levels. In addition, aggregate levels increased during the low pH treatment step in the purification process. A correlation between the level of free thiol in the HCCF (as a result of antibody reduction) and aggregation during the low pH step was established, wherein higher levels of free thiol in the starting sample resulted in increased levels of aggregates during low pH treatment. The elevated levels of free thiol were not reduced over the course of purification, resulting in carry‐over of high free thiol content into the formulated drug substance. When the drug substance with high free thiols was monitored for product degradation at room temperature and 2–8°C, faster rates of aggregation were observed compared to the drug substance generated from HCCF that was purified immediately after harvest. Further, when antibody reduction mitigations (e.g., chilling, aeration, and addition of cystine) were applied, HCCF could be held for an extended period of time while providing the same product quality/stability as material that had been purified immediately after harvest. Biotechnol. Bioeng. 2017;114: 1264–1274. © 2017 The Authors. Biotechnology and Bioengineering Published by Wiley Periodicals Inc.
Keywords:purification  stability  antibody disulfide bond reduction  aggregate
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