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通过多柱逆流溶剂梯度纯化法从批处理到连续色谱纯化治疗性肽。

From batch to continuous chromatographic purification of a therapeutic peptide through multicolumn countercurrent solvent gradient purification.

机构信息

Dept. of Chemistry and Pharmaceutical Sciences, University of Ferrara, via L. Borsari 46, 44121 Ferrara, Italy.

Institute for Chemical and Bioengineering, ETH Zurich, Vladimir-Prelog-Weg 1, 8093 Zurich, Switzerland.

出版信息

J Chromatogr A. 2020 Aug 16;1625:461304. doi: 10.1016/j.chroma.2020.461304. Epub 2020 Jun 3.

Abstract

A twin-column Multicolumn Countercurrent Solvent Gradient Purification (MCSGP) process has been developed for the purification of a therapeutic peptide, glucagon, from a crude synthetic mixture. This semi-continuous process uses two identical columns operating either in interconnected or in batch mode, thus enabling the internal recycle of the portions of the eluting stream which do not comply with purity specifications. Because of this feature, which actually results in the simulated countercurrent movement of the stationary phase with respect to the mobile one, the yield-purity trade-off typical of traditional batch preparative chromatography can be alleviated. Moreover, the purification process can be completely automatized. Aim of this work is to present a simple procedure for the development of the MCSGP process based on a single batch experiment, in the case of a therapeutic peptide of industrial relevance. This allowed to recover roughly 90% of the injected glucagon in a purified pool with a purity of about 90%. A comparison between the performance of the MCSGP process and the classical single column batch process indicates that percentage increase in the recovery of target product is +23% when transferring the method from batch conditions to MCSGP, with an unchanged purity of around 89%. This improvement comes at the expenses of a reduction of about 38% in productivity.

摘要

双柱多柱逆流溶剂梯度净化(MCSGP)工艺已被开发用于从粗合成混合物中纯化治疗肽胰高血糖素。该半连续工艺使用两个相同的柱,以相互连接或分批模式运行,从而能够对不符合纯度规格的洗脱流部分进行内部再循环。由于这个特点,实际上实现了固定相对于流动相的模拟逆流运动,因此可以减轻传统批处理制备色谱中典型的产率-纯度权衡。此外,该纯化过程可以完全自动化。本工作的目的是介绍一种简单的方法,用于在工业相关治疗肽的情况下,基于单次批量实验开发 MCSGP 工艺。该方法可在纯度约为 90%的纯化池中回收约 90%的注入胰高血糖素。MCSGP 工艺与经典单柱批处理工艺的性能比较表明,将方法从批处理条件转移到 MCSGP 时,目标产物的回收率增加了 23%,而纯度保持在 89%左右不变。这种改进是以生产率降低约 38%为代价的。

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