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Identification of gelsemine metabolites in rat liver S9 by high‐performance liquid chromatography/quadrupole‐time‐of‐flight mass spectrometry
Author(s) -
Yang Kun,
Huang YaJun,
Xiao Sa,
Liu YanChun,
Sun ZhiLiang,
Liu YiSong,
Tang Qi,
Liu ZhaoYing
Publication year - 2017
Publication title -
rapid communications in mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 136
eISSN - 1097-0231
pISSN - 0951-4198
DOI - 10.1002/rcm.8012
Subject(s) - chemistry , chromatography , high performance liquid chromatography , metabolite , mass spectrometry , metabolism , metabolic pathway , in vivo , trichloroacetic acid , liquid chromatography–mass spectrometry , demethylation , biochemistry , microbiology and biotechnology , biology , gene expression , gene , dna methylation
Rationale Gelsemine has been extensively studied because of its anti‐tumor, immunomodulatory, insecticidal itching and other significant effects. However, limited information on the pharmacokinetics and metabolism of gelsemine has been reported. Therefore, the purpose of the present study was to investigate the in vitro metabolism of gelsemine in rat liver S9 by using rapid and accurate high‐performance liquid chromatography/ quadrupole‐time‐of‐flight mass spectrometry (HPLC/QqTOF‐MS). Methods The incubation mixture was processed with 15% trichloroacetic acid. Multiple scans of gelsemine metabolites and accurate mass measurements were automatically performed simultaneously through data‐dependent acquisition in only 30 min. The structural elucidations of these metabolites were performed by comparing their changes in accurate molecular masses and product ions with those of the parent drug. Results Five metabolites of gelsemine were identified in rat liver S9. Of these, four metabolites of gelsemine were identified for the first time. The present results showed that the metabolic pathways of gelsemine are oxidation, demethylation, and dehydrogenation in rat liver S9. Conclusions In this study, metabolites of gelsemine in liver S9 were identified and elucidated firstly using the HPLC/QqTOF‐MS method. The proposed metabolic pathways of gelsemine in liver S9 will provide a basis for further studies of the in vivo metabolism of gelsemine in animals and humans.

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