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A novel method for continuous chromatographic separation of monoclonal antibody charge variants by combining displacement mode chromatography and step elution
Authors:Anupa Anupa  Vikrant Bansode  Nikhil Kateja  Anurag S. Rathore
Affiliation:1. School of Interdisciplinary Research, Indian Institute of Technology Delhi, New Delhi, India

Contribution: Conceptualization, Formal analysis, ​Investigation, Methodology, Writing - original draft;2. Department of Chemical Engineering, Indian Institute of Technology Delhi, New Delhi, India

Contribution: ​Investigation, Methodology, Writing - original draft;3. Department of Chemical Engineering, Indian Institute of Technology Delhi, New Delhi, India

Contribution: Formal analysis, Writing - original draft;4. Department of Chemical Engineering, Indian Institute of Technology Delhi, New Delhi, India

Abstract:Charge heterogeneity of monoclonal antibodies is considered a critical quality attribute and hence needs to be monitored and controlled by the manufacturer. Typically, this is accomplished via separation of charge variants on cation exchange chromatography (CEX) using a pH or conductivity based linear gradient elution. Although an effective approach, this is challenging particularly during continuous processing as creation of linear gradient during continuous processing adds to process complexity and can lead to deviations in product quality upon slightest changes in gradient formation. Moreover, the long length of elution gradient along with the required peak fractionation makes process integration difficult. In this study, we propose a novel approach for separation of charge variants during continuous CEX chromatography by utilizing a combination of displacement mode chromatography and salt-based step elution. It has been demonstrated that while the displacement mode of chromatography enables control of acidic variants ≤26% in the CEX eluate, salt-based step gradient elution manages basic charge variant ≤25% in the CEX eluate. The proposed approach has been successfully demonstrated using feed materials with varying compositions. On comparing the designed strategy with 2-column concurrent (CC) chromatography, the resin specific productivity increased by 95% and resin utilization increased by 183% with recovery of main species >99%. Further, in order to showcase the amenability of the designed CEX method in continuous operation, the method was examined in our in-house continuous mAb platform.
Keywords:biosimilars  cation exchange chromatography  charge variants  continuous processing  monoclonal antibodies  sample-displacement
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