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疏水相互作用色谱-毛细管区带电泳离线联用用于监测重组单克隆抗体基于电荷的异质性

Offline Coupling of Hydrophobic Interaction Chromatography-Capillary Zone Electrophoresis for Monitoring Charge-Based Heterogeneity of Recombinant Monoclonal Antibodies.

作者信息

Sarin Deepika, Kumar Sunil, Rathore Anurag S

机构信息

Department of Chemical Engineering, Indian Institute of Technology Delhi, New Delhi, India.

出版信息

Electrophoresis. 2024 Nov;45(21-22):1927-1938. doi: 10.1002/elps.202400158. Epub 2024 Oct 14.

DOI:10.1002/elps.202400158
PMID:39402848
Abstract

A holistic understanding of the charge heterogeneity in monoclonal antibodies (mAbs) is paramount for ensuring acceptable product quality. Hence, biotherapeutic manufacturers are expected to thoroughly characterize their products via advanced analytical techniques. Recently, two-dimensional liquid chromatography (2DLC) methods have gained popularity for resolving complex charged species. Capillary electrophoresis (CE) is regarded as a sensitive and faster tool for charged species estimation in biotherapeutics. In this study, we aim to combine the separation power of chromatographic and electrophoretic tools (liquid chromatography [LC]-CE) so as to achieve maximum resolution of mAb charge variants. Hydrophobic interaction chromatography (HIC) has been used as the preferred LC mode with CE for achieving successful separation of both charge and hydrophobic variants for two of the mAbs (trastuzumab and rituximab). The standalone HIC and capillary zone electrophoresis (CZE) methods separated 4 hydrophobic variants and 7 charge variants for each mAb, whereas the 2DLC method separated 10 and 11 variants for mAbs A and B. On the other hand, the HIC-CZE-UV method resolved 29 variants in mAb A and 23 variants in mAb B. The reproducibility of the HIC-CZE-UV method was demonstrated by % change in values of retention time (RT) and peak area as <5% (mAb A), <3% (mAb B), and <12% (for both mAbs), respectively. Thus, the utility of the proposed LC-CE method for characterization of mAb charge variants has been displayed.

摘要

全面了解单克隆抗体(mAb)中的电荷异质性对于确保可接受的产品质量至关重要。因此,生物治疗药物制造商需要通过先进的分析技术对其产品进行全面表征。最近,二维液相色谱(2DLC)方法在分离复杂带电物质方面颇受青睐。毛细管电泳(CE)被认为是一种用于生物治疗药物中带电物质评估的灵敏且快速的工具。在本研究中,我们旨在结合色谱和电泳工具(液相色谱[LC]-CE)的分离能力,以实现mAb电荷变体的最大分辨率。疏水相互作用色谱(HIC)已被用作与CE联用的首选LC模式,以成功分离两种mAb(曲妥珠单抗和利妥昔单抗)的电荷和疏水变体。单独的HIC和毛细管区带电泳(CZE)方法分别为每种mAb分离出4种疏水变体和7种电荷变体,而2DLC方法为mAb A和mAb B分别分离出10种和11种变体。另一方面,HIC-CZE-UV方法在mAb A中分离出29种变体,在mAb B中分离出23种变体。HIC-CZE-UV方法的重现性通过保留时间(RT)和峰面积值的变化百分比来证明,分别为<5%(mAb A)、<3%(mAb B)和<12%(两种mAb)。因此,已展示了所提出的LC-CE方法用于表征mAb电荷变体的实用性。

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