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

BIOANALYSIS(2020)

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Abstract
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).
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Key words
first-in-human,FP208,human plasma,mTOR inhibitor,mTORC1,mTORC2,pharmacokinetics,protein precipitation method,UHPLC-MS,MS,validation
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