UHPLC-LTQ-Orbitrap质谱法鉴定染料木素在大鼠体内的代谢产物

Structural Elucidation of Genistein Metabolites in Rats Based on UHPLC-LTQ-Orbitrap Mass Spectrometry

  • 摘要: 为深入研究染料木素在大鼠体内的效应物质基础,采用超高效液相色谱-离子阱-静电轨道场质谱(UHPLC-LTQ-Orbitrap MS)技术分析染料木素在大鼠体内可能的代谢产物。大鼠单次灌胃染料木素的CMC-Na混悬液后,收集不同时间的血浆及24 h内的尿液,样品经固相萃取法处理后,采用Waters Acquity UPLC BEH C18色谱柱(1.7 μm×2.1 mm×100 mm)分离,0.1%甲酸水溶液(A)-乙腈(B)流动相系统进行梯度洗脱;在负离子扫描模式下对含药血浆、尿液及空白组样品进行质谱分析。通过分析大鼠生物样品的质谱信息,并结合相关文献,共筛选鉴定出31种染料木素代谢产物。结果表明,染料木素在大鼠体内的主要代谢途径为葡萄糖醛酸化、葡萄糖结合、羟基化、还原反应、甲基化、硫酸酯化及其复合反应。本研究初步阐明了染料木素在大鼠体内的代谢情况,推测了体内发挥药效的物质基础,可为进一步药理作用机制研究提供依据。

     

    Abstract: For further study of bioactive components of Genistein in vivo, a method of ultra-high performance liquid chromatography coupled with linear ion trap-Orbitrap mass spectrometry (UHPLC-LTQ-Orbitrap MS) was established to comprehensively profile its metabolism in rats. Genistein was suspended in 0.5% carboxymethylcellulose sodium (CMC-Na) solution. Rats in drug group were given a dose of 200 mg/kg body weight orally. 0.5% CMC-Na aqueous solution (2 mL) was administrated to rats in control group. The obtained biological samples were pretreated using solid phase extraction method to exclude protein and solid residue precipitation. Samples were separated on a Waters Acquity BEH C18 column (2.1 mm×100 mm×1.7 μm) with 0.1% formic acid aqueous solution-acetonitrile solution as the mobile phases in gradient elution, and then analyzed by LTQ-Orbitrap mass spectrometry equipped with an ESI ion source in negative mode. According to the obtained accurate mass measurements and mass fragmentation patterns, a total of 31 metabolites (including Genistein) were tentatively or unambiguously identified. The results demonstrated that Genistein underwent multiple in vivo metabolic reactions, including dehydration, methylation, glucuronide conjugation, sulfate conjugation and their composite reactions. The results not only provided novel and useful data to comprehensively understand the metabolic mechanism and material basis of Genistein for further researches of safety, toxicity and efficacy, but also indicated that the proposed strategy was reliable for a rapid discovery and identification drug related constituents in vivo.

     

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