Fed‐batch bioreactor process scale‐up from 3‐L to 2,500‐L scale for monoclonal antibody production from cell culture

生物反应器 放大 曝气 工艺工程 比例(比率) 环境科学 过程开发 过程(计算) 生化工程 制浆造纸工业 计算机科学 化学 生物 工程类 生态学 操作系统 物理 经典力学 有机化学 量子力学
作者
Jeng‐Dar Yang,Canghai Lu,Brad Stasny,Joseph Henley,Woodrow Guinto,Carlos Gonzalez,Joseph Gleason,Monica Fung,Brett Collopy,Michael Benjamino,Jennifer Gangi,Melissa C. Hanson,Elisabeth Ille
出处
期刊:Biotechnology and Bioengineering [Wiley]
卷期号:98 (1): 141-154 被引量:98
标识
DOI:10.1002/bit.21413
摘要

This case study focuses on the scale-up of a Sp2/0 mouse myeloma cell line based fed-batch bioreactor process, from the initial 3-L bench scale to the 2,500-L scale. A stepwise scale-up strategy that involved several intermediate steps in increasing the bioreactor volume was adopted to minimize the risks associated with scale-up processes. Careful selection of several available mixing models from literature, and appropriately applying the calculated results to our settings, resulted in successful scale-up of agitation speed for the large bioreactors. Consideration was also given to scale-up of the nutrient feeding, inoculation, and the set-points of operational parameters such as temperature, pH, dissolved oxygen, dissolved carbon dioxide, and aeration in an integrated manner. It has been demonstrated through the qualitative and the quantitative side-by-side comparison of bioreactor performance as well as through a panel of biochemical characterization tests that the comparability of the process and the product was well controlled and maintained during the process scale-up. The 2,500-L process is currently in use for the routine clinical production of Epratuzumab in support of two global Phase III clinical trials in patients with lupus. Today, the 2,500 L, fed-batch production process for Epratuzumab has met all scheduled batch releases, and the quality of the antibody is consistent and reproducible, meeting all specifications, thus confirming the robustness of the process.
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