Identification of in vivo metabolites of Citri Sarcodactylis Fructus by UHPLC–Q/Orbitrap HRMS

化学 色谱法 甲酸 代谢途径 体内 去甲基化 代谢物 轨道轨道 羟基化 葡萄糖醛酸化 电喷雾电离 新陈代谢 质谱法 生物化学 微粒体 体外 基因表达 生物技术 基因 DNA甲基化 生物
作者
Fang Deng,Xue‐Min Li,Qian‐Qian Gong,Zhen‐Xing Zheng,Li Zeng,Mengjiao Zhang,Ting‐Yin Duan,Xin Liu,Ming‐Zhi Zhang,Da‐Le Guo
出处
期刊:Phytochemical Analysis [Wiley]
卷期号:34 (8): 938-949 被引量:11
标识
DOI:10.1002/pca.3262
摘要

INTRODUCTION: Citri Sarcodactylis Fructus has the effects of relieving cough, removing phlegm, and reducing asthma, but little is known about the metabolic and distribution of its chemical constituents in vivo. Therefore, it is necessary to study the metabolism of Citri Sarcodactylis Fructus in vivo. OBJECTIVE: We aimed to (1) analyze the distribution of prototype compounds and metabolites of the chemical constituents of Citri Sarcodactylis Fructus in rat and (2) infer the metabolites and metabolic pathways of the chemical constituents. MATERIALS AND METHODS: column (3 × 100 mm, 2.6 μm) was used. The mobile phase was water containing 0.1% formic acid (eluent A) and acetonitrile containing 0.1% formic acid (eluent B) at a discharge rate of 0.3 mL/min. Mass spectra of biological samples were collected in electrospray ionization (ESI) positive ion mode in the m/z 100-1500 scan range. The obtained biological samples were then subjected to chemical analysis, including plasma, urine, feces, and heart, liver, spleen, lungs, kidneys, stomach, and small intestine tissues. Prototype compounds and metabolites were identified. RESULTS: In all, 40 prototype compounds and 78 metabolites, including 26 phase I metabolites and 52 phase II metabolites, were identified using UHPLC-Q/Orbitrap HRMS. Eight possible metabolic pathways (reduction, hydrolysis, dehydration, methylation, hydroxylation, sulfation, glucuronidation, and demethylation) were proposed. The prototype compounds were predominantly distributed in lung tissues. The metabolites were mainly distributed in plasma and kidney tissues. CONCLUSION: We systematically investigated the metabolites of Citri Sarcodactylis Fructus in vivo. We suggest metabolic pathways that might be relevant for further metabolic studies and screening of active ingredients of Citrus Sarcodactylis Fructus in vivo.
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