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  2. A Comprehensive Screening and Identification of Genistin Metabolites in Rats Based on Multiple Metabolite Templates Combined with UHPLC-HRMS Analysis

A Comprehensive Screening and Identification of Genistin Metabolites in Rats Based on Multiple Metabolite Templates Combined with UHPLC-HRMS Analysis

  • Molecules. 2018 Jul 26;23(8):1862. doi: 10.3390/molecules23081862.
Yaoyue Liang 1 Wenjing Zhao 2 Chenxiao Wang 3 Zijian Wang 4 Zhibin Wang 5 Jiayu Zhang 6
Affiliations

Affiliations

  • 1 School of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing 100029, China. [email protected].
  • 2 School of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing 100029, China. [email protected].
  • 3 School of Chinese Pharmacy, Beijing University of Chinese Medicine, Beijing 100029, China. [email protected].
  • 4 Beijing Research Institution of Chinese Medicine, Beijing University of Chinese Medicine, Beijing 100029, China. [email protected].
  • 5 Beijing Research Institution of Chinese Medicine, Beijing University of Chinese Medicine, Beijing 100029, China. [email protected].
  • 6 Beijing Research Institution of Chinese Medicine, Beijing University of Chinese Medicine, Beijing 100029, China. [email protected].
Abstract

Genistin, an isoflavone belonging to the phytoestrogen family, has been reported to possess various therapeutic effects. In the present study, the genistin metabolites in rats were investigated by UHPLC-LTQ-Orbitrap mass spectrometer in both positive and negative ion modes. Firstly, the data sets were obtained based on data-dependent acquisition method and then 10 metabolite templates were established based on the previous reports. Then diagnostic product ions (DPIs) and neutral loss fragments (NLFs) were proposed to efficiently screen and ascertain the major-to-trace genistin metabolites. Meanwhile, the calculated Clog P values were used to identify the positional isomers with different retention times. Consequently, a total of 64 metabolites, including prototype drug, were positively or putatively characterized. Among them, 40 metabolites were found according to the templates of genistin and genistein, which was the same as the previous research method. After using other metabolite templates, 24 metabolites were added. The results demonstrated that genistin mainly underwent methylation, hydrogenation, hydroxylation, glucosylation, glucuronidation, sulfonation, acetylation, ring-cleavage and their composite reactions in vivo biotransformation. In conclusion, the research not only revealed the genistein metabolites and metabolic pathways in vivo comprehensively, but also proposed a method based on multiple metabolite templates to screen and identify metabolites of other natural compounds.

Keywords

UHPLC-LTQ-Orbitrap mass spectrometer; genistin; metabolic profiling; multiple metabolite templates.

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