Methods for the Generation of Single-Payload Antibody-Drug Conjugates

被引:0
|
作者
Wharton, Thomas [1 ]
Spring, David R. [1 ]
机构
[1] Univ Cambridge, Yusuf Hamied Dept Chem, Lensfield Rd, Cambridge CB2 1EW, England
基金
英国工程与自然科学研究理事会; 英国生物技术与生命科学研究理事会;
关键词
Antibodies; Antibody-drug conjugates; Drug delivery; Drug-to-antibody ratio; Cytotoxicity; STRATEGY; DELIVERY; CLICK;
D O I
10.1002/cmdc.202500132
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Antibody-drug conjugates (ADCs) have emerged as a powerful form of targeted therapy that can deliver drugs with a high level of selectivity towards a specific cell type, reducing off-target effects and increasing the therapeutic window compared to small molecule therapeutics. However, creating ADCs that are stable, homogeneous, and with controlled drug-to-antibody ratio (DAR) remains a significant challenge. Whilst a myriad of methods have been reported to generate ADCs with a DAR of 2, 4, and 8, strategies to generate DAR 1 constructs are seldom reported despite the advantages of low drug loading to tune ADC properties or to allow access to antibody-antibody and antibody-protein constructs. This concept article highlights the diversity of methods that have been employed to access single-payload ADCs and explores the outlook for the field.
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页数:8
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