Development and validation of ELISA method for quantification of Q-1802 in serum and its application to pharmacokinetic study in ICR Mouse

被引:2
作者
Meng, Qinghe [1 ]
Hao, Yimeng [2 ]
Yang, Mo [3 ]
Du, Yejie [4 ]
Wang, Shuling [1 ]
机构
[1] Shenyang Pharmaceut Univ, Shenyang, Peoples R China
[2] Fudan Univ, Sch Pharm, Dept Pharmacol, Shanghai, Peoples R China
[3] Medicilon Preclin Res Shanghai LLC, Shanghai, Peoples R China
[4] Qure Biotechnol Shanghai Co Ltd, Shanghai, Peoples R China
关键词
Bispecific antibody; CLDN18.2; Pharmacokinetics; ELISA; Assay validation; CANCER;
D O I
10.1016/j.jpba.2024.116138
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Q-1802 is a humanized bispecific antibody targeting programmed death-ligand 1 (PD-L1) and Claudin 18.2 (CLDN18.2). It can bind to CLDN18.2 and mediate antibody-dependent cell-mediated cytotoxicity against tumor cells. The Fc segment of the antibody recognizing PD-L1 blocks PD-1 signaling and activates innate immunity and adaptive immunity. In this study, we report the development, validation, and application of sensitive and highthroughput enzyme-linked immunosorbent assays (ELISA) to measure the concentrations of Q-1802 in ICR mouse serum. The assay is sensitive, with a lower limit of quantification of 50 ng/mL, has a broad dynamic range of 50-3200 ng/mL, and exhibits excellent precision and accuracy. These assays were successfully applied to in vitro serum stability and pharmacokinetic (PK) studies. In conclusion, we have developed and validated a highly sensitive and selective method for measuring Q-1802 in ICR mouse serum. The development and validation steps of assays met the required criteria for validation, which suggested that these can be applied to quantify Q-1802, as well as in PK studies.
引用
收藏
页数:6
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