魏雅芹, 王天云, 李雅婷, 陈雨浪, 廖文星, 杜岩, 汤道权. UPLC-Q/TOF-MS/MS法分析鉴定夏佛塔苷在小鼠体内的代谢产物J. 药学学报, 2022, 57(9): 2811-2820. DOI: 10.16438/j.0513-4870.2022-0436
引用本文: 魏雅芹, 王天云, 李雅婷, 陈雨浪, 廖文星, 杜岩, 汤道权. UPLC-Q/TOF-MS/MS法分析鉴定夏佛塔苷在小鼠体内的代谢产物J. 药学学报, 2022, 57(9): 2811-2820. DOI: 10.16438/j.0513-4870.2022-0436
WEI Ya-qin, WANG Tian-yun, LI Ya-ting, CHEN Yu-lang, LIAO Wen-xing, DU Yan, TANG Dao-quan. Metabolites of schaftoside in mouse plasma, bile, urine and feces after oral administration by UPLC-Q/TOF-MS/MSJ. Acta Pharmaceutica Sinica, 2022, 57(9): 2811-2820. DOI: 10.16438/j.0513-4870.2022-0436
Citation: WEI Ya-qin, WANG Tian-yun, LI Ya-ting, CHEN Yu-lang, LIAO Wen-xing, DU Yan, TANG Dao-quan. Metabolites of schaftoside in mouse plasma, bile, urine and feces after oral administration by UPLC-Q/TOF-MS/MSJ. Acta Pharmaceutica Sinica, 2022, 57(9): 2811-2820. DOI: 10.16438/j.0513-4870.2022-0436

UPLC-Q/TOF-MS/MS法分析鉴定夏佛塔苷在小鼠体内的代谢产物

Metabolites of schaftoside in mouse plasma, bile, urine and feces after oral administration by UPLC-Q/TOF-MS/MS

  • 摘要: 采用超高效液相色谱-四极杆-飞行时间串联质谱(ultra-high performance liquid chromatography coupled with quadrupole/ time-of-flight tandem mass spectrometry, UPLC-Q/TOF-MS/MS) 技术, 对夏佛塔苷口服给药后在小鼠体内的原形成分及其代谢产物进行定性分析。动物福利和实验过程获得徐州医科大学伦理委员会的批准(批准号: XZMULL201612024)。通过分析各成分的精确分子质量、一级、二级质谱信息, 并与相应的对照品及文献比对, 从小鼠血浆、胆汁、尿液和粪便中共鉴定出1个原形成分和29个代谢产物。这些成分在小鼠体内代谢的主要途径有去羟基化、羟基化、脱糖化、糖化、氢化、甲基化、乙酰化、硫酸化、葡糖醛酸化等。研究结果可为进一步阐明夏佛塔苷的药效物质基础提供有价值的依据。

     

    Abstract: Ultra-high performance liquid chromatography coupled with quadrupole/time-of-flight tandem mass spectrometry (UPLC-Q/TOF-MS/MS) has been used to detect the metabolites of schaftoside in plasma, bile, urine and feces of mice after oral administration. The study was approved by the Experimental Animal Ethics Committee from Xuzhou Medical University (No. XZMULL201612024). Compounds were identified by analyzing their high-resolution mass spectrometry data, mass spectra, and comparison with reference substances and the literatures. The parent compound and 29 metabolites were detected in the plasma, bile, urine and feces samples of mice. The main metabolic pathways of schaftoside in mice include deglycosylation/glycosylation, hydroxylation/dehydroxylation, hydrogenation, methylation, acetylation, sulfation, and glucuronidation. This study provides references for the material basis of schaftoside in vivo.

     

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