产量(工程)
工艺工程
肽合成
比例(比率)
过程(计算)
制造工艺
材料科学
计算机科学
化学
肽
工程类
冶金
物理
操作系统
复合材料
量子力学
生物化学
作者
Michael O. Frederick,Raymond A. Boyse,Timothy M. Braden,Joel R. Calvin,Bradley M. Campbell,Shujauddin M. Changi,Stephanie R. Coffin,Carmel Condon,Olivia Gowran,Jennifer McClary Groh,Stephen R. Groskreutz,Zachary D. Harms,Ashley A. Humenik,Neil J. Kallman,Nicholas D. Klitzing,Michael E. Kopach,Juliana K. Kretsinger,Gordon R. Lambertus,J. T. Lampert,Laura M. Maguire
标识
DOI:10.1021/acs.oprd.1c00108
摘要
The large-scale manufacture of complex synthetic peptides is challenging due to many factors such as manufacturing risk (including failed product specifications) as well as processes that are often low in both yield and overall purity. To overcome these liabilities, a hybrid solid-phase peptide synthesis/liquid-phase peptide synthesis (SPPS/LPPS) approach was developed for the synthesis of tirzepatide. Continuous manufacturing and real-time analytical monitoring ensured the production of high-quality material, while nanofiltration provided intermediate purification without difficult precipitations. Implementation of the strategy worked very well, resulting in a robust process with high yields and purity.
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