The Advanced Centre for Biochemical Engineering, Dept of Biochemical Engineering, University College London, London WC1E 7JE, UK.
Biotechnol Prog. 2012 Sep-Oct;28(5):1292-302. doi: 10.1002/btpr.1591. Epub 2012 Jul 31.
High throughput approaches to facilitate the development of chromatographic separations have now been adopted widely in the biopharmaceutical industry, but issues of how to reduce the associated analytical burden remain. For example, acquiring experimental data by high level factorial designs in 96 well plates can place a considerable strain upon assay capabilities, generating a bottleneck that limits significantly the speed of process characterization. This article proposes an approach designed to counter this challenge; Strategic Assay Deployment (SAD). In SAD, a set of available analytical methods is investigated to determine which set of techniques is the most appropriate to use and how best to deploy these to reduce the consumption of analytical resources while still enabling accurate and complete process characterization. The approach is demonstrated by investigating how salt concentration and pH affect the binding of green fluorescent protein from Escherichia coli homogenate to an anion exchange resin presented in a 96-well filter plate format. Compared with the deployment of routinely used analytical methods alone, the application of SAD reduced both the total assay time and total assay material consumption by at least 40% and 5%, respectively. SAD has significant utility in accelerating bioprocess development activities.
高通量方法已广泛应用于生物制药行业,以促进色谱分离的开发,但如何降低相关分析负担的问题仍然存在。例如,通过 96 孔板中的高级析因设计获取实验数据可能会对检测能力造成相当大的压力,从而形成一个瓶颈,极大地限制了过程特性的速度。本文提出了一种旨在应对这一挑战的方法; 策略检测部署(SAD)。在 SAD 中,研究了一组可用的分析方法,以确定最适合使用的技术集,并确定如何最好地部署这些技术以减少分析资源的消耗,同时仍然能够准确和完整地进行过程特性描述。该方法通过研究盐浓度和 pH 值如何影响大肠杆菌匀浆中绿色荧光蛋白与阴离子交换树脂在 96 孔过滤板形式中的结合来证明。与单独使用常规分析方法相比,SAD 的应用将总检测时间和总检测材料消耗分别至少减少了 40%和 5%。SAD 在加速生物工艺开发活动方面具有重要的实用价值。