单克隆抗体快速纯化策略:一个案例研究。

IF 2.8 3区 工程技术 Q2 CHEMISTRY, ANALYTICAL
Qian Li, Xiaoying Liang, Hongyang Zhao, Qingquan He, Guozhu Li, Zicheng Wang, Guohong Qin, Dan Xu
{"title":"单克隆抗体快速纯化策略:一个案例研究。","authors":"Qian Li,&nbsp;Xiaoying Liang,&nbsp;Hongyang Zhao,&nbsp;Qingquan He,&nbsp;Guozhu Li,&nbsp;Zicheng Wang,&nbsp;Guohong Qin,&nbsp;Dan Xu","doi":"10.1002/jssc.70232","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Monoclonal antibodies (mAbs) are widely used in drug development for their precise targeting and lower adverse effects. Market competition drives demand for more efficient mAb production processes. We developed a mAbs purification platform integrating protein A membrane chromatography with sequential anion/cation exchange. Compared with conventional protein A column chromatography (HiTrap MabSelect PrismA), protein A membrane chromatography (HiTrap Fibro PrismA) achieved a 96% reduction in process time (7.5 vs. 190 min) with similar product quality. A tandem system (Eshmuno CP-FT + Natrix Q Micro) showed robust performance at high loads (up to 1000 g/L). Specifically, this system reduced high molecular weight impurities from 1.9% to 0.2% and host cell protein levels from 630.4 to 19.77 ppm, while maintaining a recovery yield exceeding 90%. Combined rapid affinity membrane and high-capacity tandem exchange steps reduced medium costs by 11.8%. This platform demonstrates high efficiency for mAbs purification workflows.</p>\n </div>","PeriodicalId":17098,"journal":{"name":"Journal of separation science","volume":"48 8","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rapid Purification Strategies for Monoclonal Antibodies: A Case Study\",\"authors\":\"Qian Li,&nbsp;Xiaoying Liang,&nbsp;Hongyang Zhao,&nbsp;Qingquan He,&nbsp;Guozhu Li,&nbsp;Zicheng Wang,&nbsp;Guohong Qin,&nbsp;Dan Xu\",\"doi\":\"10.1002/jssc.70232\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n <p>Monoclonal antibodies (mAbs) are widely used in drug development for their precise targeting and lower adverse effects. Market competition drives demand for more efficient mAb production processes. We developed a mAbs purification platform integrating protein A membrane chromatography with sequential anion/cation exchange. Compared with conventional protein A column chromatography (HiTrap MabSelect PrismA), protein A membrane chromatography (HiTrap Fibro PrismA) achieved a 96% reduction in process time (7.5 vs. 190 min) with similar product quality. A tandem system (Eshmuno CP-FT + Natrix Q Micro) showed robust performance at high loads (up to 1000 g/L). Specifically, this system reduced high molecular weight impurities from 1.9% to 0.2% and host cell protein levels from 630.4 to 19.77 ppm, while maintaining a recovery yield exceeding 90%. Combined rapid affinity membrane and high-capacity tandem exchange steps reduced medium costs by 11.8%. This platform demonstrates high efficiency for mAbs purification workflows.</p>\\n </div>\",\"PeriodicalId\":17098,\"journal\":{\"name\":\"Journal of separation science\",\"volume\":\"48 8\",\"pages\":\"\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-08-06\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of separation science\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://analyticalsciencejournals.onlinelibrary.wiley.com/doi/10.1002/jssc.70232\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of separation science","FirstCategoryId":"5","ListUrlMain":"https://analyticalsciencejournals.onlinelibrary.wiley.com/doi/10.1002/jssc.70232","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0

摘要

单克隆抗体(mab)因其靶向准确、不良反应小而广泛应用于药物开发。市场竞争推动了对更高效的单克隆抗体生产工艺的需求。我们开发了一种结合蛋白a膜层析和顺序阴离子/阳离子交换的单克隆抗体纯化平台。与传统的蛋白A柱色谱法(HiTrap MabSelect PrismA)相比,蛋白A膜色谱法(HiTrap Fibro PrismA)在产品质量相似的情况下,加工时间缩短了96%(7.5分钟比190分钟)。串联系统(Eshmuno CP-FT + Natrix Q Micro)在高负载(高达1000 g/L)下表现出强劲的性能。具体来说,该系统将高分子量杂质从1.9%降低到0.2%,将宿主细胞蛋白水平从630.4 ppm降低到19.77 ppm,同时保持了超过90%的回收率。结合快速亲和膜和大容量串联交换步骤降低了11.8%的介质成本。该平台证明了单克隆抗体纯化流程的高效率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Rapid Purification Strategies for Monoclonal Antibodies: A Case Study

Rapid Purification Strategies for Monoclonal Antibodies: A Case Study

Rapid Purification Strategies for Monoclonal Antibodies: A Case Study

Rapid Purification Strategies for Monoclonal Antibodies: A Case Study

Monoclonal antibodies (mAbs) are widely used in drug development for their precise targeting and lower adverse effects. Market competition drives demand for more efficient mAb production processes. We developed a mAbs purification platform integrating protein A membrane chromatography with sequential anion/cation exchange. Compared with conventional protein A column chromatography (HiTrap MabSelect PrismA), protein A membrane chromatography (HiTrap Fibro PrismA) achieved a 96% reduction in process time (7.5 vs. 190 min) with similar product quality. A tandem system (Eshmuno CP-FT + Natrix Q Micro) showed robust performance at high loads (up to 1000 g/L). Specifically, this system reduced high molecular weight impurities from 1.9% to 0.2% and host cell protein levels from 630.4 to 19.77 ppm, while maintaining a recovery yield exceeding 90%. Combined rapid affinity membrane and high-capacity tandem exchange steps reduced medium costs by 11.8%. This platform demonstrates high efficiency for mAbs purification workflows.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of separation science
Journal of separation science 化学-分析化学
CiteScore
6.30
自引率
16.10%
发文量
408
审稿时长
1.8 months
期刊介绍: The Journal of Separation Science (JSS) is the most comprehensive source in separation science, since it covers all areas of chromatographic and electrophoretic separation methods in theory and practice, both in the analytical and in the preparative mode, solid phase extraction, sample preparation, and related techniques. Manuscripts on methodological or instrumental developments, including detection aspects, in particular mass spectrometry, as well as on innovative applications will also be published. Manuscripts on hyphenation, automation, and miniaturization are particularly welcome. Pre- and post-separation facets of a total analysis may be covered as well as the underlying logic of the development or application of a method.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信