化学
单克隆抗体
辣根过氧化物酶
多克隆抗体
抗体
分子生物学
生物分析
抗体-药物偶联物
免疫分析
结合
生物化学
酶
色谱法
免疫学
生物
数学分析
数学
作者
Feng Yin,Christopher L. DeCiantis,Jan Pinkas,Biplab Das,Frank Wang,Nancy Zheng,David W. Hahn,Aniruddha Amrite,Jianwen Feng,Diana Adhikari,Cheikh Kane,Jack Sikora,Justin Pittman,Rebecca J. Wates,Elizabeth Shaheen,Shawn Harriman
标识
DOI:10.1016/j.jpba.2023.115452
摘要
PYX-201 is an investigative ADC oncology drug composed of a monoclonal human immunoglobulin G (IgG) antibody targeting the extra domain B splice variant of fibronectin (EDB + FN) conjugated to an auristatin payload through a cleavable linker. Effective measurement of PYX-201 tAb is the key to ADC drug PYX-201 preclinical pharmacokinetics (PK) assessment. PYX-201 monoclonal antibody (mAb) was used as the reference standard, goat anti-human IgG polyclonal antibody (pAb) or rabbit anti-human Kappa light chain mAb was employed as the capture antibody, and mouse mAb or goat pAb anti-human IgG the crystallizable fragment (Fc) (horseradish peroxidase (HRP)) was utilized as the detection antibody in this ELISA. This assay was validated with a dynamic range 250 – 10,000 ng/mL and 250 – 6000 ng/mL in rat and monkey K2EDTA plasma, respectively. PYX-201 tAb bioanalytical ELISA assay was reported for the first time in any biological matrix. This is the first time for a bioanalytical method to be validated for a tAb from an ADC drug targeting EDB + FN in any biological matrix.
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