A robust enzyme-linked immunosorbent assay to measure serum ramucirumab concentrations

被引:2
|
作者
Desvignes, Celine [1 ,2 ]
Ternant, David [1 ,2 ,3 ]
Lecomte, Thierry [4 ,5 ]
Lievre, Astrid [6 ,7 ]
Ohresser, Marc [2 ]
Chautard, Romain [4 ]
Raoul, William [8 ]
Paintaud, Gilles [1 ,2 ,3 ]
机构
[1] CHRU Tours, Ctr Pilote Suivi Biol Traitements Anticorps CePiB, Plateforme Rech, Tours, France
[2] Univ Tours, EA4245 Transplantat, Immunol, Inflammat, Tours, France
[3] CHRU Tours, Serv Pharmacol Med, Tours, France
[4] CHRU Tours, Serv Hepatogastroenterol & Oncol Digest, Tours, France
[5] Univ Tours, Grp Innovat & Ciblage Cellulaire, EA 7501, Tours, France
[6] CHU Pontchaillou, Serv Gastroenterol, Rennes, France
[7] INSERM, U1242, Oncogenesis Stress & Signaling, Rennes, France
[8] Univ Tours, INSERM, UMR 1069, Nutr Croissance & Canc N2C, Tours, France
关键词
enzyme-linked immunosorbent assay; monoclonal antibody; pharmacokinetics; ramucirumab; therapeutic drug monitoring;
D O I
10.4155/bio-2020-0199
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Aim: Ramucirumab, an anti-VEGFR2 monoclonal antibody, has been approved for the treatment of metastatic gastric and colorectal cancer. An assay measuring ramucirumab serum concentrations was needed to investigate its pharmacokinetics and concentration-response relationship. Results: An ELISA was developed and validated according to the international guidelines for ligand-binding assays. Ramucirumab calibration standards ranged from 0.125 to 40 mg/l. Low, middle and high quality controls were spiked at 0.2, 4 and 8 mg/l, respectively. The limits of quantification were established to be 0.125 and 10 mg/l for LLOQ and ULOQ, respectively. No cross-reactivity with anti-VEGF or anti-EGFR was detected. Conclusion: This in-house-developed ELISA is sensitive, accurate, reproducible and suitable for pharmacokinetic studies of ramucirumab.
引用
收藏
页码:565 / 574
页数:10
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