识别和消除细胞培养过程的可变性

Alan Gilbert, Yao-ming Huang, T. Ryll
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引用次数: 23

摘要

关键的生物制药工业目标是稳健的,可重复的过程,导致一致的产品质量和产量。这些参数支持产品的安全性和有效性,以及对过程和供应链的控制。为了有一个一致的细胞培养过程,过程输入必须是可靠的。从历史上看,细胞培养基通过包含复杂成分(如水解物和血清)一直是变异性的来源。工业已经转向化学定义的基础和饲料介质,减少了可变性,但化学定义的介质并没有消除过程的可变性。因此,本综述将侧重于介质变异性、乳酸和氨生产的后续产出和产品质量,以及消除工艺不一致性的可能途径。
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Identifying and eliminating cell culture process variability
Critical to the biopharmaceutical industrial objectives are robust, reproducible processes which result in consistent product quality and yields. These parameters support the product safety and efficacy as well as control over the process and supply chain. To have a consistent cell culture process, process inputs must be reliable. Historically cell culture media have been a source of variability through the inclusion of complex components such as hydrolysates and sera. Industry has shifted to chemically defined basal and feed media and seen reduced variability but chemically defined media have not eliminated process variability. This review will consequently focus on media variability, the subsequent outputs of lactate and ammonia production and product quality, and the possible routes to eliminate process inconsistency.
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Bioresources and Bioprocessing a review Short Commentary on Pharmaceutical Bioprocessing Editorial in Pharmaceutical Bioprocessing Dynamics and scale-up of thePharmaceutical molecule Research on Pharmaceutical Bioprocessing a short communication
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