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抗体药物偶联物的生物分析:美国药学科学家协会抗体药物偶联物工作组立场文件。

Bioanalysis of antibody-drug conjugates: American Association of Pharmaceutical Scientists Antibody-Drug Conjugate Working Group position paper.

作者信息

Gorovits Boris, Alley Stephen C, Bilic Sanela, Booth Brian, Kaur Surinder, Oldfield Phillip, Purushothama Shobha, Rao Chetana, Shord Stacy, Siguenza Patricia

机构信息

Pfizer, 1 Burtt Road, Andover, MA 01810, USA.

出版信息

Bioanalysis. 2013 May;5(9):997-1006. doi: 10.4155/bio.13.38.

Abstract

Antibody-drug conjugates (ADCs) typically consist of a cytotoxic drug covalently bound to an antibody by a linker. These conjugates have the potential to substantially improve efficacy and reduce toxicity compared with cytotoxic small-molecule drugs. Since ADCs are generally complex heterogeneous mixtures of multiple species, these novel therapeutic products present unique bioanalytical challenges. The growing number of ADCs being developed across the industry suggests the need for alignment of the bioanalytical methods or approaches used to assess the multiple species and facilitate consistent interpretation of the bioanalytical data. With limited clinical data, the current strategies that can be used to provide insight into the relationship between the multiple species and the observed clinical safety and efficacy are still evolving. Considerations of the bioanalytical strategies for ADCs based on the current industry practices that take into account the complexity and heterogeneity of ADCs are discussed.

摘要

抗体药物偶联物(ADC)通常由一种细胞毒性药物通过连接子与抗体共价结合而成。与细胞毒性小分子药物相比,这些偶联物有潜力显著提高疗效并降低毒性。由于ADC通常是多种物质的复杂异质混合物,这些新型治疗产品带来了独特的生物分析挑战。整个行业正在研发的ADC数量不断增加,这表明需要统一用于评估多种物质的生物分析方法或途径,以便对生物分析数据进行一致的解读。鉴于临床数据有限,目前可用于深入了解多种物质与观察到的临床安全性和疗效之间关系的策略仍在不断发展。本文讨论了基于当前行业实践对ADC生物分析策略的考量,这些实践考虑到了ADC的复杂性和异质性。

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