共 50 条
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
来源:
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.
引用
收藏
页数:8
相关论文