基于超高效液相色谱-四极杆飞行时间质谱鉴定清心滋肾方入血化学成分

Identification of Plasma Absorbed Components of Qingxin Zishen Prescription by UPLC-Q-TOF MS

  • 摘要: 本研究基于超高效液相色谱-四极杆飞行时间质谱(UPLC-Q-TOF MS)法鉴定了清心滋肾方(QZP)的入血成分。将雌性SD大鼠连续灌胃48.5 g/kg QZP 3天后,收集血浆样品,利用固相萃取法去除蛋白,采用Agilent ZORBAX SB C18色谱柱(4.6 mm×100 mm,1.8 µm)分离,以0.1%甲酸水溶液和甲醇-乙腈溶液(1:1,V/V)为流动相进行梯度洗脱,在电喷雾离子源正、负离子模式下采集数据。根据精确质荷比、二级质谱信息、对照品信息及相关文献鉴定QZP入血成分,并对化合物来源进行归属,总结了环烯醚萜苷和双苄基异喹啉类生物碱化合物的特征碎片和裂解规律。结果表明,大鼠血浆中共有40种来自QZP的入血原型成分,包括27种生物碱、9种环烯醚萜苷、2种黄酮碳苷、1种酚酸和1种脂肪酸。本方法可对QZP入血成分进行快速全面的分析鉴定,为阐明其药效物质基础提供依据。

     

    Abstract: It has been confirmed in clinic that Qingxin Zishen Prescription (QZP) is effective and safe in relieving vasomotor symptoms. However, its active components have not been elucidated. In this study, a method based on ultra-performance liquid chromatography quadrupole-time of flight mass spectrometry (UPLC-Q-TOF MS) was developed to identify the plasma absorbed components of QZP. After continuous intragastric administration of 48.5 g/kg QZP for 3 days to female SD rats, plasma samples were collected and then pre-treated by solid phase extraction (SPE) to remove proteins in plasma. Then, chromatographic separation of the plasma samples was performed on an Agilent ZORBAX SB C18 column (4.6 mm×100 mm, 1.8 µm) using a gradient elution with a mobile phase composed of 0.1% formic acid aqueous solution (A) and methanol-acetonitrile (1:1, V/V, B) prior to MS analysis. The column temperature was kept at 40 ℃. The MS and MS2 analysis were performed with the electrospray ionization (ESI) source under both positive and negative ion modes from m/z 100 to 1300. Intelligent dynamic background deduction, information dependent acquisition and highly sensitive mode were used to collect the data. According to the accurate m/z values of MS and MS2 information, data from reference substance and related literature, the absorbed components in plasma were identified. In total, forty prototypes from QZP are identified and inferred in the plasma samples, including 27 alkaloids, 9 iridoid glycosides, 2 flavonoid carbon glycosides, 1 phenolic acid and 1 fatty acid. Among them, alkaloids are mainly from Nelumbo nucifera Gaertn, Coptis chinensis Franch, Ziziphus jujuba Mill. var. spinosa (Bunge) Hu ex H. F. Chou, and Uncaria rhynchophylla (Miq.) Miq. ex Havil. Iridoid glycosides are mainly from Rehmannia glutinosa Libosch. and Cornus officinalis Sieb. et Zucc. Furthermore, the fragmentation pathways and characteristic fragment ions of iridoid glycosides and dibenzylisoquinoline alkaloids were summarized. This study provides not only a rapid and comprehensive analysis method for the plasma absorbed components of QZP, but also a scientific fundamental for elucidating the material basis of action of QZP.

     

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