College of Pharmacy and Institute of Drug Research and Development, Chungnam National University, Daejeon 34134, Korea.
Molecules. 2019 Jul 29;24(15):2754. doi: 10.3390/molecules24152754.
A simple liquid chromatography-quadrupole-time-of-flight-mass spectrometric assay (LC-TOF-MS/MS) has been developed for the evaluation of metabolism and pharmacokinetic (PK) characteristics of monomethyl auristatin F (MMAF) in rat, which is being used as a payload for antibody-drug conjugates. LC-TOF-MS/MS method was qualified for the quantification of MMAF in rat plasma. The calibration curves were acceptable over the concentration range from 3.02 to 2200 ng/mL using quadratic regression. MMAF was stable in various conditions. There were no significant matrix effects between rat and other preclinical species. The PK studies showed that the bioavailability of MMAF was 0% with high clearance. Additionally, the metabolite profiling studies, in vitro/in vivo, were performed. Seven metabolites for MMAF were tentatively identified in liver microsome. The major metabolic pathway was demethylation, which was one of the metabolic pathways predicted by MedChem Designer. Therefore, these results will be helpful to understand the PK, catabolism, and metabolism behavior of MMAF comprehensively when developing antibody-drug conjugates (ADCs) in the future.
已开发出一种简单的液相色谱-四极杆飞行时间质谱联用(LC-TOF-MS/MS)分析方法,用于评估单甲基奥瑞他汀 F(MMAF)在大鼠中的代谢和药代动力学(PK)特征,MMAF 正在被用作抗体药物偶联物的有效载荷。LC-TOF-MS/MS 方法可用于定量测定大鼠血浆中的 MMAF。使用二次回归,校准曲线在 3.02 至 2200 ng/mL 的浓度范围内可接受。MMAF 在各种条件下均稳定。大鼠与其他临床前物种之间不存在显著的基质效应。PK 研究表明,MMAF 的生物利用度为 0%,清除率较高。此外,还进行了体外/体内代谢产物谱研究。在肝微粒体中鉴定出 7 种 MMAF 的代谢产物。主要代谢途径为去甲基化,这是 MedChem Designer 预测的代谢途径之一。因此,这些结果将有助于在未来开发抗体药物偶联物(ADC)时全面了解 MMAF 的 PK、分解代谢和代谢行为。