Cysteine-Based Coupling: Challenges and Solutions

被引:31
|
作者
You, Jianwei [1 ,2 ]
Zhang, Juan [1 ]
Wang, Jun [2 ]
Jin, Mingzhi [2 ]
机构
[1] China Pharmaceut Univ, Sch Life Sci & Technol, Nanjing 210009, Peoples R China
[2] WuXi Biol Co Ltd, Shanghai 200131, Peoples R China
关键词
NEXT-GENERATION; PHARMACOLOGICAL-PROPERTIES; DRUG; CONJUGATE; STABILITY; LINKER; STRATEGIES; IMPROVE; TARGET; POTENT;
D O I
10.1021/acs.bioconjchem.1c00213
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Antibody-drug conjugates (ADCs) have attracted great attention in recent years in the wake of an accelerated FDA approval rate and several large-scale acquisitions. To date, there are ten ADC drugs on the market and more than 70 in various stages of clinical trials. Yet, due to the complicated nature of ADC molecules, considerations need to cover many aspects for the success of ADCs, including target specificity, linker-payload stability, tumor permeability, and clearance rate. This topical review summarizes and discusses current methods used to increase stability and homogeneity of ADCs of cysteine conjugation. We believe that they will lead to improvement of efficacy and pharmacokinetics (PK) of ADC drugs.
引用
收藏
页码:1525 / 1534
页数:10
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