连续流动
工艺工程
遏制(计算机编程)
过程(计算)
计算机科学
制造工程
环境科学
工程类
生化工程
操作系统
程序设计语言
作者
Kevin P. Cole,Jennifer McClary Groh,Martin D. Johnson,Christopher L. Burcham,Bradley M. Campbell,William D. Diseroad,Michael R. Heller,John R. Howell,Neil J. Kallman,Thomas M. Koenig,Scott A. May,Richard D. Miller,David Mitchell,David P. Myers,Steven S. Myers,Joseph L. Phillips,Christopher S. Polster,Timothy White,Jim Cashman,D. Declan Hurley
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2017-06-16
卷期号:356 (6343): 1144-1150
被引量:297
标识
DOI:10.1126/science.aan0745
摘要
Advances in drug potency and tailored therapeutics are promoting pharmaceutical manufacturing to transition from a traditional batch paradigm to more flexible continuous processing. Here we report the development of a multistep continuous-flow CGMP (current good manufacturing practices) process that produced 24 kilograms of prexasertib monolactate monohydrate suitable for use in human clinical trials. Eight continuous unit operations were conducted to produce the target at roughly 3 kilograms per day using small continuous reactors, extractors, evaporators, crystallizers, and filters in laboratory fume hoods. Success was enabled by advances in chemistry, engineering, analytical science, process modeling, and equipment design. Substantial technical and business drivers were identified, which merited the continuous process. The continuous process afforded improved performance and safety relative to batch processes and also improved containment of a highly potent compound.
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