The PK bioanalysis method study of c-Met antibody-drug conjugate (RC108) in cynomolgus monkey
10.16438/j.0513-4870.2022-1350
- VernacularTitle:靶向c-Met抗体偶联药物 (RC108) 在食蟹猴中PK生物分析方法学研究
- Author:
Hong-yu ZHOU
1
;
Shu-juan WANG
2
;
Zhi-hao LIU
2
;
Ke MA
3
;
Ling WANG
2
;
Jing JIANG
1
,
4
Author Information
1. Binzhou Medical University, Yantai 264003, China
2. RemeGen Company Ltd., Yantai 265503, China
3. Junke Zhengyuan Pharmaceutical Research Company Ltd., Beijing 102206, China
4. RemeGen Company Ltd., Yantai 265503, China
- Publication Type:Research Article
- Keywords:
antibody-drug conjugate;
ligand-binding assay;
liquid chromatography tandem mass spectrometry;
quantitative analysis
- From:
Acta Pharmaceutica Sinica
2023;58(6):1663-1668
- CountryChina
- Language:Chinese
-
Abstract:
Antibody-drug conjugate (ADC) has the characteristics of low toxicity and high efficiency, and plays an important role in cancer treatment. However, due to the complexity of its structure, it brings difficulties in pharmacokinetic (PK) bioanalysis. This study established an analytical method for the detection of ADC (RC108) in cynomolgus monkey plasma by ligand-binding assay (LBA) and liquid chromatography tandem mass spectrometry (LC-MS/MS), which was used to analyze and quantify the total antibody, bound antibody and free drug in cynomolgus monkey plasma. Based on the LBA method, rabbit anti-RC108 Fab and mouse anti-MMAE (monomethyl auristatin E) mAb were pre-coated in 96-well plates as the total antibody and antibody binding reagents, respectively. The samples to be tested were added, and then the detection reagents were added in turn. Goat anti-human IgG (H+L)-HRP, chromogenic solution tetramethylbenzidine (TMB), H2SO4 terminate the reaction, read data at 450 nm/630 nm wavelength of microplate reader; LC-MS/MS analysis method quantifies MMAE concentration, and refer to relevant regulations for methodological validation. The analytical method for quantifying total antibody, bound antibody and free drug of RC108 drug obtained good accuracy and precision, and the selectivity, dilution linearity, hook effect, parallelism and stability were verified. Meet the requirements of biological analysis. Finally, a bioanalytical method for the determination of the concentration of the test substance RC108 (total antibody, conjugated antibody, free MMAE) in cynomolgus monkey plasma with high sensitivity and high throughput was established by LBA and LC-MS/MS method. Subsequent non-clinical research on PK research in cynomolgus monkeys will provide technical support.
