可操作性
生物制造
生产力
背景(考古学)
工艺工程
产品(数学)
产能利用率
比例(比率)
可靠性工程
工程类
生物技术
经济
数学
物理
生物
宏观经济学
古生物学
微观经济学
量子力学
几何学
作者
William C. Yang,Daniel F. Minkler,Rashmi Kshirsagar,Thomas Ryll,Yao‐ming Huang
标识
DOI:10.1016/j.jbiotec.2015.10.009
摘要
Biomanufacturing factories of the future are transitioning from large, single-product facilities toward smaller, multi-product, flexible facilities. Flexible capacity allows companies to adapt to ever-changing pipeline and market demands. Concentrated fed-batch (CFB) cell culture enables flexible manufacturing capacity with limited volumetric capacity; it intensifies cell culture titers such that the output of a smaller facility can rival that of a larger facility. We tested this hypothesis at bench scale by developing a feeding strategy for CFB and applying it to two cell lines. CFB improved cell line A output by 105% and cell line B output by 70% compared to traditional fed-batch (TFB) processes. CFB did not greatly change cell line A product quality, but it improved cell line B charge heterogeneity, suggesting that CFB has both process and product quality benefits. We projected CFB output gains in the context of a 2000-L small-scale facility, but the output was lower than that of a 15,000-L large-scale TFB facility. CFB's high cell mass also complicated operations, eroded volumetric productivity, and showed our current processes require significant improvements in specific productivity in order to realize their full potential and savings in manufacturing. Thus, improving specific productivity can resolve CFB's cost, scale-up, and operability challenges.
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