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下游加工技术/捕获与最终纯化:创新、变革与改进的机遇。蛋白质纯化下游加工发展综述。

Downstream Processing Technologies/Capturing and Final Purification : Opportunities for Innovation, Change, and Improvement. A Review of Downstream Processing Developments in Protein Purification.

作者信息

Singh Nripen, Herzer Sibylle

机构信息

Bristol-Myers Squibb, Global Manufacturing and Supply, Devens, MA, 01434, USA.

Bristol-Myers Squibb, Global Manufacturing and Supply, Hopewell, NJ, 01434, USA.

出版信息

Adv Biochem Eng Biotechnol. 2018;165:115-178. doi: 10.1007/10_2017_12.

Abstract

Increased pressure on upstream processes to maximize productivity has been crowned with great success, although at the cost of shifting the bottleneck to purification. As drivers were economical, focus is on now on debottlenecking downstream processes as the main drivers of high manufacturing cost. Devising a holistically efficient and economical process remains a key challenge. Traditional and emerging protein purification strategies with particular emphasis on methodologies implemented for the production of recombinant proteins of biopharmaceutical importance are reviewed. The breadth of innovation is addressed, as well as the challenges the industry faces today, with an eye to remaining impartial, fair, and balanced. In addition, the scope encompasses both chromatographic and non-chromatographic separations directed at the purification of proteins, with a strong emphasis on antibodies. Complete solutions such as integrated USP/DSP strategies (i.e., continuous processing) are discussed as well as gains in data quantity and quality arising from automation and high-throughput screening (HTS). Best practices and advantages through design of experiments (DOE) to access a complex design space such as multi-modal chromatography are reviewed with an outlook on potential future trends. A discussion of single-use technology, its impact and opportunities for further growth, and the exciting developments in modeling and simulation of DSP rounds out the overview. Lastly, emerging trends such as 3D printing and nanotechnology are covered. Graphical Abstract Workflow of high-throughput screening, design of experiments, and high-throughput analytics to understand design space and design space boundaries quickly. (Reproduced with permission from Gregory Barker, Process Development, Bristol-Myers Squibb).

摘要

为了实现生产力最大化,上游工艺面临着越来越大的压力,尽管这是以将瓶颈转移到纯化环节为代价的。由于驱动因素是经济性,现在的重点是消除下游工艺的瓶颈,因为下游工艺是高制造成本的主要驱动因素。设计一个整体高效且经济的工艺仍然是一个关键挑战。本文综述了传统和新兴的蛋白质纯化策略,特别强调了用于生产具有生物制药重要性的重组蛋白的方法。文中既探讨了创新的广度,也审视了该行业目前面临的挑战,力求保持公正、公平和平衡。此外,范围涵盖了针对蛋白质纯化的色谱和非色谱分离,尤其着重于抗体。还讨论了诸如集成的上游/下游工艺策略(即连续加工)等完整解决方案,以及自动化和高通量筛选(HTS)带来的数据量和质量的提升。通过实验设计(DOE)来进入诸如多模式色谱等复杂设计空间的最佳实践和优势也进行了综述,并展望了潜在的未来趋势。对一次性技术、其影响和进一步增长的机会,以及下游工艺建模与模拟方面的令人兴奋的进展进行了讨论,从而完善了这一概述。最后,还涵盖了3D打印和纳米技术等新兴趋势。图形摘要高通量筛选、实验设计和高通量分析的工作流程,以快速了解设计空间和设计空间边界。(经百时美施贵宝公司工艺开发部的Gregory Barker许可转载)

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