生物制造
生物制药
下游(制造业)
生化工程
过程开发
细胞培养
下游加工
生物过程
生物技术
过程(计算)
质量(理念)
上游和下游(DNA)
合成生物学
计算机科学
风险分析(工程)
计算生物学
制造工程
上游(联网)
业务
生物
工程类
运营管理
生物化学
哲学
古生物学
操作系统
认识论
遗传学
计算机网络
作者
Róisín O’Flaherty,Adam Bergin,Evangelia Flampouri,Letícia Martins Mota,Ismael Obaidi,Andrew Quigley,Yongjing Xie,Michael Butler
标识
DOI:10.1016/j.biotechadv.2020.107552
摘要
The manufacturing of recombinant protein is traditionally undertaken in mammalian cell culture. Today, speed, cost and safety are the primary considerations for process improvements in both upstream and downstream manufacturing. Leaders in the biopharmaceutical industry are striving for continuous improvements to increase throughput, lower costs and produce safer more efficacious drugs. This can be achieved through advances in cell line engineering, process development of cell culture, development of chemically defined media and increased emphasis on product characterization. In the first part, this review provides a historical perspective on approved biotherapeutics by regulatory bodies which pave the way for next-generation products (including gene therapy). In the second part, it focuses on the application of in vitro and in vivo cell line engineering approaches, modern process development improvements including continuous manufacturing, recent developments in media formulation, and improvements in critical quality attribute determinations for products produced predominantly in mammalian cells.
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