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Find the perfect Ecolab
resin for your monoclonal
antibody purification needs.
Jako światowy lider w technologii żywic opracowujemy i produkujemy małe kulki, które są wykorzystywane w najbardziej regulowanych gałęziach przemysłu na świecie do oddzielania, usuwania lub odzyskiwania bardzo specyficznych pierwiastków i związków.
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(Obecnie tylko w języku angielskim)
With 40 years of manufacturing expertise and 30 years of regulatory experience, we supply leading separation, purification and extraction technologies to support chromatography and biocatalysis applications in healthcare and life sciences.
Jesteśmy światowym liderem w technologii separacji, oczyszczania i ekstrakcji na bazie żywic, która zapewnia zrównoważone rozwiązania dla naszego środowiska, firm i opieki zdrowotnej.
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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.
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.
“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.”
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