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In vitro metabolites characterization of ponatinib in human liver microsomes using ultra‐high performance liquid chromatography combined with Q‐Exactive‐Orbitrap tandem mass spectrometry
Author(s) -
Gao Lei,
Xu Qiqi,
Liu Qingqing,
Lang Xiuzhuang
Publication year - 2020
Publication title -
biomedical chromatography
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.4
H-Index - 65
eISSN - 1099-0801
pISSN - 0269-3879
DOI - 10.1002/bmc.4819
Subject(s) - chemistry , ponatinib , orbitrap , microsome , potassium cyanide , chromatography , biochemistry , demethylation , pharmacology , in vitro , mass spectrometry , cyanide , biology , inorganic chemistry , signal transduction , dna methylation , dasatinib , gene expression , tyrosine kinase , gene
Ponatinib is an oral drug for the treatment of chronic myeloid leukemia and acute lymphoblastic leukemia, which has been reported to increase the risk of hepatotoxicity. The aim of this study was to characterize the metabolites of ponatinib in human liver microsomes as well as its reactive metabolites. Ponatinib was incubated with human liver microsomes in the presence of NADPH and trapping agents (glutathione or potassium cyanide). The metabolites were characterized by liquid chromatography in combination with Q‐Exactive‐Orbitrap‐MS. Under the current conditions, six metabolites were detected and structurally identified on the basis of their accurate masses, fragmentation patterns, and retention times. M3 ( N ‐demethylation) was unambiguously identified by matching its retention time and fragment ions with those of its reference standard. N ‐demethylation and oxygenation were proved to be the predominant metabolic pathways of ponatinib. In addition, two reactive metabolites (cyano adducts) were detected in human liver microsomes in the presence of potassium cyanide and NADPH, suggesting that ponatinib underwent CYP450‐mediated metabolic activation, which could be one of the causative mechanisms for its hepatotoxicity. The current study provides new information regarding the metabolic profiles of ponatinib and would be helpful in understanding the effectiveness and toxicity of ponatinib, especially the mechanism of hepatotoxicity.