Ajinomoto Co., Inc.
Ajinomoto Bio-Pharma Services.
Chem Pharm Bull (Tokyo). 2021;69(10):976-983. doi: 10.1248/cpb.c21-00258.
Antibody-drug conjugates (ADCs) are biopharmaceuticals produced by chemically linking small molecules (payloads) to antibodies that possess specific affinity for the target cell. The ADCs currently on the commercially market are the result of a stochastic conjugation of highly-potent payloads to multiple sites on the monoclonal antibody, resulting in a heterogeneous drug-antibody ratio (DAR) and drug distribution. The heterogeneity inherent to ADCs not produced site-specifically may not only be detrimental to the quality of the drug but also is less-desirable from the perspective of regulatory science. An ideal method or unified approach used to measure the DAR for ADCs, a critical aspect of their analysis and characterization, has not yet been established in the ADC field and remains an often-challenging issue for bioanalytical chemists. In this review we describe, compare, and evaluate the characteristics of various DAR determination methods for ADCs featuring recently reported technologies. The future landscape of bioconjugate DAR analysis is also discussed.
抗体药物偶联物 (ADC) 是通过化学连接小分子(有效载荷)和具有特定靶细胞亲和力的抗体而产生的生物制药。目前市售的 ADC 是将高活性有效载荷随机连接到单克隆抗体上的多个部位的结果,导致药物抗体比(DAR)和药物分布不均一。非特异性产生的 ADC 固有的不均一性不仅可能对药物质量有害,而且从监管科学的角度来看也是不理想的。一种理想的方法或统一的方法,用于测量 ADC 的 DAR,这是其分析和表征的关键方面,在 ADC 领域尚未建立,并且仍然是生物分析化学家经常面临的挑战。在这篇综述中,我们描述、比较和评估了各种 DAR 测定方法的特点,这些方法具有最近报道的技术。还讨论了生物缀合物 DAR 分析的未来前景。