In human monoclonal antibody (HuMAb) processes, nonaffinity purification schemes have been developed as viable alternatives to affinity schemes, especially when cell culture expression levels have been increased significantly. Primary recovery by tangential flow filtration (TFF) for concentration and diafiltration plays a crucial role in a nonaffinity purification platform with cation exchange as a capture step. A nonaffinity purification scheme, including an optimized primary recovery TFF step, is comparable to Protein A-based purification processes in overall process efficiency, product recovery, and quality.
Tangential flow filtration is a common unit operation either for cell culture clarification and concentration or just for concentration of the cell culture supernatant in biopharmaceutical manufacturing where affinity or nonaffinity capture is used. As a platform approach, exploring nonaffinity capture as a viable alternative to Protein A has yielded efficient purification schemes. These nonaffinity schemes with three, two, or one chromatography steps have been successfully developed for HuMAbs.1,2 Cell culture harvest needs to be preconditioned by concentration and buffer exchange to the appropriate pH and conductivity to have a uniform and maximum load on CEX column. For this primary recovery step to fulfill both concentration and diafiltration, a TFF step is generally optimized for different process parameters. During the diafiltration step, significant slow precipitation from the cell culture harvest is formed as the pH and conductivity are decreased. Development and optimization of TFF is crucial for the nonaffinity purification platform not only for the optimal loading condition on CEX, but also for determining the cost efficiency of the purification schemes.The Role of Primary Recovery TFF in Non-Protein A Purification Schemes
Binding to CEX resin requires below-neutral pH and low conductivity for HuMAbs. The lower the pH, the higher the binding capacity, thereby, reducing capture chromatography cycles. However, the low pH requirement can lead to challenges because of gradual precipitation during diafiltration. Therefore, assessing the influence of several process parameters is essential to optimize the TFF step during primary recovery.
Primary recovery TFF plays a more significant role in the non-affinity scheme than in the affinity scheme not only because it is a batch-volume reduction and feed conditioning step for the capture, but it is also a partial purification step.
Batch Volume Reduction
During the primary recovery TFF, the clarified harvest bulk is concentrated several fold, which will reduce batch processing time on capture chromatography especially for high-binding CEX resins. With more high-binding CEX resins competing in the market, development scientists have the luxury of evaluating and choosing the highest binding resins with high processing flow rates.3 Even for the resins that can be operated at very high flow rate, the load time would be significant without volume reduction at primary recovery step.
Feed Conditioning to Capture Chromatography