UHPLC-Q-TOF-MS/MS method based on four-step strategy for metabolites of hinokiflavone in vivo and in vitro

被引:43
作者
Chen, Yuting [1 ]
Feng, Xue [1 ]
Li, Luya [1 ]
Zhang, Xiaowei [2 ]
Song, Kewei [3 ]
Diao, Xinpeng [1 ]
Sun, Yupeng [1 ]
Zhang, Lantong [1 ]
机构
[1] Hebei Med Univ, Sch Pharm, Dept Pharmaceut Anal, Shijiazhuang 050017, Hebei, Peoples R China
[2] Hebei Med Univ, Hosp 2, Shijiazhuang 050000, Hebei, Peoples R China
[3] Fourth Hosp Shijiazhuang, Shijiazhuang 050017, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
Hinokiflavone; UHPLC-Q-TOF-MS/MS; Metabolism; In vivo; Rat liver microsomes; Rat intestinal flora; SELAGINELLA-TAMARISCINA; IDENTIFICATION; AMENTOFLAVONE; PATHWAY; ACID; RATS;
D O I
10.1016/j.jpba.2019.02.034
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Hinokiflavone (HF), belonging to biflavonoids, possesses excellent pharmacological activities, including anti-inflammatory, antioxidant and antitumor activity. Nevertheless, its metabolism in vivo (rats) and in vitro (rat liver microsomes and intestinal flora) is presently not characterized. In this study, ultra-high-performance liquid chromatography coupled with hybrid triple quadrupole time-of-flight mass spectrometry (UHPLC-Q-TOF-MS) based on four-step strategy was a rapid method for the detection of HF metabolites. A total of 41 metabolites in vivo, 49 metabolites in vitro were characterized. It also verified that intestinal tract exceeds the liver in the biotransformation of HF. More significant, the main metabolic pathways for HF were mainly bio-transformed to various mono-flavone resulting from the rupture of connective C-O bonds, which exhibited a large distinction with other biflavones. Noteworthily, glutamine conjugation and glycine conjugation were considered as unique metabolic pathways of HF. The information obtained from this study contributes to better understanding of pharmacological mechanism of HF. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:19 / 29
页数:11
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