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 Qin Yin,Christopher L. DeCiantis,Jan Pinkas,Biplab Das,Frank Wang,Nancy Zheng,David W. Hahn,Aniruddha C. Amrite,Jianwen Feng,Diana Adhikari,Cheikh Kane,Jack Sikora,Justin Pittman,Rebecca J. Wates,Elizabeth Shaheen,Shawn P. 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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