药品
抗体-药物偶联物
结合
抗体
计算生物学
医学
药理学
计算机科学
生物
免疫学
单克隆抗体
数学
数学分析
作者
Vara Prasad Chandrabatla
出处
期刊:ADC review
[InPress Media Group, LLC]
日期:2025-07-15
标识
DOI:10.14229/jadc.2025.07.15.001
摘要
Antibody-drug conjugates (ADCs) are a cutting-edge class of biopharmaceuticals that combine the selectivity of monoclonal antibodies with the cytotoxic potency of small-molecule drugs. This targeted delivery system has redefined oncology treatment by reducing systemic toxicity and improving efficacy. ADCs are composed of a tumor-targeting antibody, a cytotoxic agent, and a chemical linker, which together create a complex structure that presents various analytical challenges. These challenges include determining the drug-to-antibody ratio (DAR), ensuring specificity at the conjugation site, and assessing the stability of the linker, all of which significantly influence pharmacokinetics, pharmacodynamics, and potential toxicity. This review highlights critical analytical techniques necessary for the characterization of ADCs, emphasizing their physicochemical properties, biological activity, stability assessments, and regulatory implications. Employing robust analytical methods is essential throughout the ADC development process to guarantee both therapeutic effectiveness and safety, ultimately positioning ADCs as a vital element in contemporary cancer treatment strategies.
科研通智能强力驱动
Strongly Powered by AbleSci AI