Maximizing Processing Efficiency in Bioprocessing: Strategies for Cost-Effective Scale-Up


In the fast-evolving world of bioprocessing, optimizing each step of the downstream process is crucial for achieving maximum productivity and cost-effectiveness. As laboratories strive to enhance yield while minimizing expenses, the importance of processing eluates as they emerge has become paramount. This blog explores the nuances of processing efficiency, shedding light on potential bottlenecks—such as quality control steps and prolonged downstream processes—that can hinder overall progress. 

In this discussion, Field Application Specialists Jon Baker and William Bowen navigate these critical topics, offering expert analysis on how bioprocessing professionals can leverage these strategies for enhanced productivity and substantial savings across multiple batches. 

We will also examine how bed height impacts various types of chromatography resins, revealing insights on how adopting shorter bed heights can lead to significant cost savings and improved throughput. While this approach can transform workflows, it's essential to balance factors like flow rates and binding dynamics, especially for exceptions such as size exclusion resins. 

Processing Cycles with Shorter, Smaller Columns 

After performing multiple cycles with a shorter, smaller column, one may wonder whether to pull alerts before moving to the next step or to start processing each column as it becomes available. In an ideal world, processing each eluate as it comes out would yield the highest productivity, allowing for seamless transitions through each stage of the downstream process. However, real-world scenarios often present bottlenecks or pauses. For example, quality control steps might need to be completed before progressing, or a subsequent stage—such as dial filtration or ultrafiltration—may take longer than the chromatography step. In such cases, it would be prudent to process one or more eluents and closely monitor the time required for each potential step. 

 

The Applicability of Shorter Bed Heights 

When it comes to the idea of using shorter bed heights, it applies to any resin type utilizing a bind-elute process. In our recent webinar, we explored the relationship between capacity and residence time. While working in flow-through mode, it's crucial to consider purity versus residence time; longer residence times may result in binding more impurities, ultimately yielding a cleaner sample. However, size exclusion resins—such as gel filtration—require extended processing runs at lower flow rates, where this strategy might not be effective. 

“Shorter bed heights can lead to significant cost savings and improved throughput, but it's essential to balance flow rates and binding dynamics for optimal results.” 

When Not to Target Reduced Bed Height 

While, in theory, extremely low bed heights are possible, chromatography performance can become hardware-limited. A certain level of back pressure is essential for effective column operation. If the liquid entering the column doesn't have adequate pressure, it may flow preferentially through the center of the packed bed, resulting in lower resolution. Typically, a bed height of less than five centimeters would be pushing the limits. Some chromatography systems require specific back pressure to function efficiently, which is more commonly seen at lab scale than at process scale. 


Estimating Potential Savings 

The potential savings from adjusting bed height vary significantly based on what you're benchmarking. For instance, if you're using a 20-centimeter bed height and drop to a 10-centimeter bed height, you could achieve up to 50% cost reduction. If you're working with a larger bead resin that has a lower binding capacity (e.g., 50 grams per liter instead of 70), the results may differ. Depending on the size of the columns and whether you're dealing with toxicity or preclinical batches, you could save several hundred thousand dollars. When applied across multiple molecules, these savings can compound considerably. 


Scaling Up Bed Height for Commercial Use 

Scaling up while increasing bed height is straightforward. Generally, the goal is to maintain both the bed height and linear flow rate during scaling. Instead, focus on column volumes per hour, applicable regardless of bed height. This strategy ensures consistent capacity and binding dynamics. Just be cautious; if you’re operating close to pressure limits at a low bed height, monitor closely to avoid exceeding specifications when transitioning to a higher bed height. Using column volumes per hour is a practical way to measure flow rate when changing bed height. 

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