Department of Chemistry, University of Michigan, Ann Arbor, MI, USA.
Expert Rev Proteomics. 2024 May-Jun;21(5-6):259-270. doi: 10.1080/14789450.2024.2373707. Epub 2024 Jul 1.
The pharmaceutical industry continues to expand its search for innovative biotherapeutics. The comprehensive characterization of such therapeutics requires many analytical techniques to fully evaluate critical quality attributes, making analysis a bottleneck in discovery and development timelines. While thorough characterization is crucial for ensuring the safety and efficacy of biotherapeutics, there is a need to further streamline analytical characterization and expedite the overall timeline from discovery to market.
This review focuses on recent developments in liquid-phase separations coupled with ion mobility-mass spectrometry (IM-MS) for the development and characterization of biotherapeutics. We cover uses of IM-MS to improve the characterization of monoclonal antibodies, antibody-drug conjugates, host cell proteins, glycans, and nucleic acids. This discussion is based on an extensive literature search using Web of Science, Google Scholar, and SciFinder.
IM-MS has the potential to enhance the depth and efficiency of biotherapeutic characterization by providing additional insights into conformational changes, post-translational modifications, and impurity profiles. The rapid timescale of IM-MS positions it well to enhance the information content of existing assays through its facile integration with standard liquid-phase separation techniques that are commonly used for biopharmaceutical analysis.
制药行业继续扩大对创新生物疗法的探索。此类疗法的全面表征需要许多分析技术来全面评估关键质量属性,这使得分析成为发现和开发时间线上的瓶颈。虽然彻底的表征对于确保生物疗法的安全性和有效性至关重要,但需要进一步简化分析表征并加快从发现到市场的整体时间表。
本文综述了近年来液相分离与离子淌度-质谱联用(IM-MS)在生物疗法开发和表征中的应用。我们介绍了 IM-MS 用于改善单克隆抗体、抗体药物偶联物、宿主细胞蛋白、聚糖和核酸的表征的用途。这一讨论是基于对 Web of Science、Google Scholar 和 SciFinder 进行的广泛文献检索。
IM-MS 有可能通过提供对构象变化、翻译后修饰和杂质谱的更多了解,来增强生物疗法表征的深度和效率。IM-MS 的快速时间尺度使其能够通过与常用的生物制药分析标准液相分离技术的简便集成,增强现有分析的信息量,从而很好地定位。