Xiao Xue, Wang Wentao, Zhang Yamin, Jia Li
Ministry of Education Key Laboratory of Laser Life Science & Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China.
Ministry of Education Key Laboratory of Laser Life Science & Institute of Laser Life Science, College of Biophotonics, South China Normal University, Guangzhou 510631, China.
J Pharm Biomed Anal. 2017 Jun 5;140:377-383. doi: 10.1016/j.jpba.2017.03.014. Epub 2017 Mar 16.
Monoclonal antibodies (mAbs) are one of the most promising classes of therapeutic protein biopharmaceuticals. However, the complexity of mAbs poses a daunting analytical challenge for heterogeneity characterization of mAbs. In this study, inspired by blood coagulation, we adopted a fibrin coating as a novel stationary phase in open tubular (OT) column for the separation of the mAbs variants by capillary electrochromatography. The fibrin coating was prepared by in situ polymerization of fibrin in the presence of thrombin as a catalyst inside a fused-silica capillary. Scanning electron microscopy and electroosmotic flow measurement were carried out to characterize the fibrin coated OT columns. The average thickness of the fibrin coating was about 1.13μm. And the EOF of the column was pH-dependent. The electrochromatographic performance of the prepared columns was evaluated by characterization of the variants of three mAbs (cetuximab, trastuzumab and rituximab). The columns demonstrated good repeatability with the run-to-run, day-to-day and column-to-column relative standard deviations of migration times less than 2.42%. The study highlighted the potential of adsorbed proteins as stationary phases for the separation of mAbs variants. Furthermore, the study provided a new platform for characterization of heterogeneity of mAbs in pharmaceutical industry.
单克隆抗体(mAbs)是最具前景的治疗性蛋白质生物制药类别之一。然而,单克隆抗体的复杂性对其异质性表征提出了艰巨的分析挑战。在本研究中,受血液凝固的启发,我们采用纤维蛋白涂层作为开管(OT)柱中的新型固定相,通过毛细管电色谱法分离单克隆抗体变体。纤维蛋白涂层是在熔融石英毛细管内,以凝血酶作为催化剂,通过纤维蛋白的原位聚合制备而成。进行扫描电子显微镜和电渗流测量以表征纤维蛋白涂层的OT柱。纤维蛋白涂层的平均厚度约为1.13μm。并且该柱的电渗流与pH值有关。通过对三种单克隆抗体(西妥昔单抗、曲妥珠单抗和利妥昔单抗)的变体进行表征,评估了所制备柱的电色谱性能。这些柱表现出良好的重复性,运行间、日间和柱间迁移时间的相对标准偏差小于2.42%。该研究突出了吸附蛋白作为固定相用于分离单克隆抗体变体的潜力。此外,该研究为制药行业中单克隆抗体异质性的表征提供了一个新平台。