Yandrofski Katharina, Mouchahoir Trina, De Leoz M Lorna, Duewer David, Hudgens Jeffrey W, Anderson Kyle W, Arbogast Luke, Delaglio Frank, Brinson Robert G, Marino John P, Phinney Karen, Tarlov Michael, Schiel John E
Institute for Bioscience and Biotechnology Research, National Institute of Standards and Technology, Rockville, MD, United States.
Agilent Technologies, Santa Clara, CA, United States.
Front Mol Biosci. 2022 May 5;9:876780. doi: 10.3389/fmolb.2022.876780. eCollection 2022.
Biopharmaceuticals such as monoclonal antibodies are required to be rigorously characterized using a wide range of analytical methods. Various material properties must be characterized and well controlled to assure that clinically relevant features and critical quality attributes are maintained. A thorough understanding of analytical method performance metrics, particularly emerging methods designed to address measurement gaps, is required to assure methods are appropriate for their intended use in assuring drug safety, stability, and functional activity. To this end, a series of interlaboratory studies have been conducted using NISTmAb, a biopharmaceutical-representative and publicly available monoclonal antibody test material, to report on state-of-the-art method performance, harmonize best practices, and inform on potential gaps in the analytical measurement infrastructure. Reported here is a summary of the study designs, results, and future perspectives revealed from these interlaboratory studies which focused on primary structure, post-translational modifications, and higher order structure measurements currently employed during biopharmaceutical development.
生物制药,如单克隆抗体,需要使用多种分析方法进行严格表征。必须对各种材料特性进行表征并严格控制,以确保维持临床相关特征和关键质量属性。为确保方法适用于其在保证药物安全性、稳定性和功能活性方面的预期用途,需要深入了解分析方法性能指标,特别是旨在解决测量差距的新兴方法。为此,已经使用NISTmAb(一种具有生物制药代表性且公开可用的单克隆抗体测试材料)开展了一系列实验室间研究,以报告最新方法性能、统一最佳实践,并了解分析测量基础设施中的潜在差距。本文报告了这些实验室间研究的研究设计、结果和未来展望的总结,这些研究聚焦于生物制药开发过程中目前采用的一级结构、翻译后修饰和高级结构测量。