NIBRT - The National Institute for Bioprocessing Research and Training, Foster Avenue, Mount Merrion, Blackrock, Co. Dublin, A94 X099, Ireland.
Spirogen, a Member of the AstraZeneca Group, QMB Innovation Centre, 42 New Road, London, E1 2AX, United Kingdom.
J Pharm Biomed Anal. 2021 Oct 25;205:114287. doi: 10.1016/j.jpba.2021.114287. Epub 2021 Jul 28.
Antibody-drug conjugates (ADCs) are an emerging class of oncology treatments combining the unique specificity of monoclonal antibodies with the highly cytotoxic properties of small molecule compounds. Pyrrolobenzodiazepines (PBDs) are highly potent agents capable of inhibiting cellular DNA replication which leads to apoptosis. To ensure efficacy and patient safety upon administration of such toxic and heterogeneous molecules, their structure and quality attributes must be closely monitored. Size exclusion chromatography (SEC) is a powerful, fast and robust tool for the separation of compounds varying in molecular weight. When using volatile components in the chromatographic mobile phase, SEC has also been shown to be amenable for interfacing to mass spectrometry, providing potential for reliable identification of protein isoforms across the size variants present. Here, we present a SEC-MS method developed for the characterisation of PBD-based ADCs on the intact molecular level. We demonstrate that information on ADC monomers such as the glycoform distribution and the average drug-antibody ratio (DAR) can be obtained in 15 minutes of analysis time. Qualitative and quantitative information on low and high molecular weight impurities such as aggregates and fragments, fundamental for critical quality attribute analysis of biopharmaceuticals, can be generated simultaneously. SEC-MS enables the characterisation of multiple product quality attributes of complex biotherapeutics at the same time.
抗体药物偶联物 (ADC) 是一类新兴的肿瘤治疗药物,它将单克隆抗体的独特特异性与小分子化合物的高细胞毒性结合在一起。吡咯并苯并二氮杂卓 (PBD) 是一种高效能的药物,能够抑制细胞 DNA 复制,从而导致细胞凋亡。为了确保在给予此类有毒和异质分子时的疗效和患者安全性,必须密切监测其结构和质量属性。尺寸排阻色谱 (SEC) 是一种强大、快速且稳健的工具,可用于分离分子量不同的化合物。当在色谱流动相中使用挥发性成分时,SEC 也已被证明适用于与质谱联用,从而有可能在存在各种大小变异体的情况下可靠地鉴定蛋白质异构体。在这里,我们提出了一种 SEC-MS 方法,用于在完整分子水平上对基于 PBD 的 ADC 进行特性分析。我们证明,在 15 分钟的分析时间内,可以获得有关 ADC 单体的信息,例如糖型分布和平均药物抗体比 (DAR)。同时可以生成有关低分子量和高分子量杂质(如聚集体和片段)的定性和定量信息,这对于生物制药的关键质量属性分析至关重要。SEC-MS 能够同时对复杂生物治疗药物的多个产品质量属性进行特性分析。