UHPLC-MS/MS method to determine FP-208 in human plasma and its application to a pharmacokinetic study.

Huanhuan Wang,Teng Wang, Zhanqing Wang, Zhenjian Du,Qian Zhao,Ji Jiang,Pei Hu

BIOANALYSIS(2020)

引用 1|浏览6
暂无评分
摘要
Aim: FP-208 is a novel and effective small-molecule inhibitor blocking the mammalian target of rapamycin complex-1/mammalian target of rapamycin complex-2/PI3Ka. To investigate the pharmacokinetic profile of FP-208, a rapid and reliable analytical method was needed to be established to determine FP-208 in the plasma of patients with solid tumors. Materials & methods: FP208 was separated on a charged surface hybrid (CSH) C18 column (2.1 mm x 50 mm, 1.7 mu m) after the plasma samples were purified using a protein precipitation method. Detection was performed on an AB Sciex 5500 mass spectrometer in the positive electrospray ionization mode. The established method was validated according to the bioanalytical guidelines. Conclusion: For the first time, the developed and validated method was successfully applied in the first-in-human study for FP-208 in patients with solid tumors after oral administration (Number: CTR20180683).
更多
查看译文
关键词
first-in-human,FP208,human plasma,mTOR inhibitor,mTORC1,mTORC2,pharmacokinetics,protein precipitation method,UHPLC-MS,MS,validation
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要