有效的宿主细胞蛋白清除:生物制药过程中膜吸附剂和树脂的研究。

IF 2.8 3区 医学 Q2 BIOCHEMICAL RESEARCH METHODS
Ernest Šprager , Veronika Reisinger , Jonas Sommer , Tinkara Lekić , Nina Pucelj , Tina Kljun , Mojca Lunder , Jožica Vašl , Tomaž Bratkovič
{"title":"有效的宿主细胞蛋白清除:生物制药过程中膜吸附剂和树脂的研究。","authors":"Ernest Šprager ,&nbsp;Veronika Reisinger ,&nbsp;Jonas Sommer ,&nbsp;Tinkara Lekić ,&nbsp;Nina Pucelj ,&nbsp;Tina Kljun ,&nbsp;Mojca Lunder ,&nbsp;Jožica Vašl ,&nbsp;Tomaž Bratkovič","doi":"10.1016/j.jchromb.2025.124796","DOIUrl":null,"url":null,"abstract":"<div><div>In recent years, biopharmaceutical purification processes have shifted towards more productive and cost-effective methods. Membrane technology has emerged as viable alternative to conventional resins, capable of delivering similar product quality while facilitating a simpler and more flexible downstream purification process. This study compares the impurity removal efficiency of three anion-exchange media types (quaternary amine-functionalized agarose resin (Q Sepharose™ Fast Flow), cellulose membrane adsorber (Sartobind® Q), and a hybrid purifier, composed of two complementary anion-exchange media, a quaternary ammonium functional non-woven and a guanidinium functional polyamide membrane (3M™ Polisher ST)) in a flow-through mode during a monoclonal antibody product purification. The content of residual major impurities—host cell proteins (HCPs) and aggregates—were investigated using a design of experiments (DoE) approach, varying pH, ionic strength, and loading densities. Membrane-based devices exhibited high impurity removal capacity, with 3M™ Polisher ST capable of reducing HCP levels from 8000 ppm down to as low as 10 ppm at competitive loading densities in this case study. The presence of critical HCPs, such as esterases capable of hydrolysing ester bonds in polysorbates, was monitored using high-throughput enzyme assays and liquid chromatography-tandem mass spectrometry. Orthogonal HCP analytical methods were required for more informed process development, as esterase presence did not follow the same trend as the general HCP population. All chromatographic media were further tested for their robustness by conducting breakthrough experiments at an optimal pH of 6.5 and conductivity of 4 mS/cm. An additional orthogonal polishing step was required as anion-exchange chromatography alone was insufficient at clearing aggregates. Among options evaluated, 3M™ Polisher ST demonstrated the greatest potential for simplifying the purification process and enhancing productivity.</div></div>","PeriodicalId":348,"journal":{"name":"Journal of Chromatography B","volume":"1267 ","pages":"Article 124796"},"PeriodicalIF":2.8000,"publicationDate":"2025-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Efficient host cell protein clearance: A study of membrane adsorbers and resins in biopharmaceutical processes\",\"authors\":\"Ernest Šprager ,&nbsp;Veronika Reisinger ,&nbsp;Jonas Sommer ,&nbsp;Tinkara Lekić ,&nbsp;Nina Pucelj ,&nbsp;Tina Kljun ,&nbsp;Mojca Lunder ,&nbsp;Jožica Vašl ,&nbsp;Tomaž Bratkovič\",\"doi\":\"10.1016/j.jchromb.2025.124796\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>In recent years, biopharmaceutical purification processes have shifted towards more productive and cost-effective methods. Membrane technology has emerged as viable alternative to conventional resins, capable of delivering similar product quality while facilitating a simpler and more flexible downstream purification process. This study compares the impurity removal efficiency of three anion-exchange media types (quaternary amine-functionalized agarose resin (Q Sepharose™ Fast Flow), cellulose membrane adsorber (Sartobind® Q), and a hybrid purifier, composed of two complementary anion-exchange media, a quaternary ammonium functional non-woven and a guanidinium functional polyamide membrane (3M™ Polisher ST)) in a flow-through mode during a monoclonal antibody product purification. The content of residual major impurities—host cell proteins (HCPs) and aggregates—were investigated using a design of experiments (DoE) approach, varying pH, ionic strength, and loading densities. Membrane-based devices exhibited high impurity removal capacity, with 3M™ Polisher ST capable of reducing HCP levels from 8000 ppm down to as low as 10 ppm at competitive loading densities in this case study. The presence of critical HCPs, such as esterases capable of hydrolysing ester bonds in polysorbates, was monitored using high-throughput enzyme assays and liquid chromatography-tandem mass spectrometry. Orthogonal HCP analytical methods were required for more informed process development, as esterase presence did not follow the same trend as the general HCP population. All chromatographic media were further tested for their robustness by conducting breakthrough experiments at an optimal pH of 6.5 and conductivity of 4 mS/cm. An additional orthogonal polishing step was required as anion-exchange chromatography alone was insufficient at clearing aggregates. Among options evaluated, 3M™ Polisher ST demonstrated the greatest potential for simplifying the purification process and enhancing productivity.</div></div>\",\"PeriodicalId\":348,\"journal\":{\"name\":\"Journal of Chromatography B\",\"volume\":\"1267 \",\"pages\":\"Article 124796\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-09-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Chromatography B\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1570023225003502\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Chromatography B","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1570023225003502","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

摘要

近年来,生物制药纯化过程已转向更高效和成本效益的方法。膜技术已经成为传统树脂的可行替代品,能够提供类似的产品质量,同时促进更简单、更灵活的下游净化过程。本研究比较了三种阴离子交换介质类型(季胺功能化琼脂糖树脂(Q Sepharose™Fast Flow)、纤维素膜吸附剂(Sartobind®Q)和混合净化器(由两种互补阴离子交换介质、季铵功能无纺布和胍功能聚酰胺膜(3M™Polisher ST)组成)在流动模式下对单克隆抗体产物纯化的杂质去除效率。使用实验设计(DoE)方法,在不同的pH值、离子强度和负载密度下,研究了残留的主要杂质——宿主细胞蛋白(HCPs)和聚集物的含量。在本案例研究中,基于膜的设备表现出很高的杂质去除能力,在竞争负载密度下,3M™Polisher ST能够将HCP水平从8000ppm降低到10ppm。使用高通量酶分析和液相色谱-串联质谱法监测关键HCPs的存在,例如能够水解聚山梨酸酯中的酯键的酯酶。由于酯酶的存在与一般HCP人群的趋势不同,因此需要采用正交HCP分析方法以获得更多信息。在最佳pH为6.5,电导率为4 mS/cm的条件下,通过突破性实验进一步测试了所有色谱介质的稳健性。由于单独的阴离子交换色谱法不足以清除聚集体,因此需要一个额外的正交抛光步骤。在评估的选项中,3M™Polisher ST在简化净化过程和提高生产率方面表现出最大的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficient host cell protein clearance: A study of membrane adsorbers and resins in biopharmaceutical processes
In recent years, biopharmaceutical purification processes have shifted towards more productive and cost-effective methods. Membrane technology has emerged as viable alternative to conventional resins, capable of delivering similar product quality while facilitating a simpler and more flexible downstream purification process. This study compares the impurity removal efficiency of three anion-exchange media types (quaternary amine-functionalized agarose resin (Q Sepharose™ Fast Flow), cellulose membrane adsorber (Sartobind® Q), and a hybrid purifier, composed of two complementary anion-exchange media, a quaternary ammonium functional non-woven and a guanidinium functional polyamide membrane (3M™ Polisher ST)) in a flow-through mode during a monoclonal antibody product purification. The content of residual major impurities—host cell proteins (HCPs) and aggregates—were investigated using a design of experiments (DoE) approach, varying pH, ionic strength, and loading densities. Membrane-based devices exhibited high impurity removal capacity, with 3M™ Polisher ST capable of reducing HCP levels from 8000 ppm down to as low as 10 ppm at competitive loading densities in this case study. The presence of critical HCPs, such as esterases capable of hydrolysing ester bonds in polysorbates, was monitored using high-throughput enzyme assays and liquid chromatography-tandem mass spectrometry. Orthogonal HCP analytical methods were required for more informed process development, as esterase presence did not follow the same trend as the general HCP population. All chromatographic media were further tested for their robustness by conducting breakthrough experiments at an optimal pH of 6.5 and conductivity of 4 mS/cm. An additional orthogonal polishing step was required as anion-exchange chromatography alone was insufficient at clearing aggregates. Among options evaluated, 3M™ Polisher ST demonstrated the greatest potential for simplifying the purification process and enhancing productivity.
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 Chromatography B
Journal of Chromatography B 医学-分析化学
CiteScore
5.60
自引率
3.30%
发文量
306
审稿时长
44 days
期刊介绍: The Journal of Chromatography B publishes papers on developments in separation science relevant to biology and biomedical research including both fundamental advances and applications. Analytical techniques which may be considered include the various facets of chromatography, electrophoresis and related methods, affinity and immunoaffinity-based methodologies, hyphenated and other multi-dimensional techniques, and microanalytical approaches. The journal also considers articles reporting developments in sample preparation, detection techniques including mass spectrometry, and data handling and analysis. Developments related to preparative separations for the isolation and purification of components of biological systems may be published, including chromatographic and electrophoretic methods, affinity separations, field flow fractionation and other preparative approaches. Applications to the analysis of biological systems and samples will be considered when the analytical science contains a significant element of novelty, e.g. a new approach to the separation of a compound, novel combination of analytical techniques, or significantly improved analytical performance.
×
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