人参皂苷Rb1和Rg1体外消化产物的UHPLC-TSQ MS分析

Analysis of Ginsenosides Rb1 and Rg1 Digestion Products in vitro Based on UHPLC-TSQ MS

  • 摘要: 本研究采用超高效液相色谱-三重四极杆质谱(ultra-high-performance liquid chromatography-triple quadrupole mass spectrometry,UHPLC-TSQ MS)法分析人参皂苷Rb1和Rg1在模拟唾液、胃液和肠液中的降解产物。在人参皂苷Rb1的消化产物中发现了Rd、Rg3、Rg5、Rk1,其中在肠液中还发现了F2,表明F2是肠液中特有的降解产物,降解途径为Rb1→Rd→Rg3→Rg5/Rk1,Rb1→Rd→F2。在人参皂苷Rg1的消化产物中发现了F1和Rh1,降解途径为Rg1→F1和Rg1→Rh1。定量结果表明:降解产物含量在消化液中随时间而变化;在胃液中,Rg3、Rd、Rg5、F1、Rh1和Rk1的达峰时间分别为1、2、4、2、2、4 h;在肠液中,7种降解产物的达峰时间均为4~6 h。另外,皂苷在唾液中的降解较胃液和肠液温和,而在胃肠道中的降解更广泛;在消化过程中,Rg1比Rb1更易降解。人参皂苷在消化道内会发生水解反应生成多种小分子皂苷,为Rb1和Rg1开发和利用提供了重要的化学与生物学基础。

     

    Abstract: A method of ultra-high-performance liquid chromatography-triple quadrupole mass spectrometry (UHPLC-TSQ MS) was used to study the products of protopanaxadiol ginsenoside Rb1 and protopanaxatriol ginsenoside Rg1 in simulated digestion solution in vitro for researching the digestion characteristics of ginsenoside. The resullt showed that ginsenoside Rd, Rg3, Rg5, and Rk1 are found in the digestion products of ginsenoside Rb1. In addition, ginsenoside F2 is found in the simulated intestinal juice, suggesting that it is the peculiar degradation product. Therefore, the degradation pathways of ginsenoside Rb1 are as follows: ginsenoside Rb1→ginsenoside Rd→insenoside Rg3→ginsenoside Rg5/Rk1, ginsenoside Rb1→ginsenoside Rd→ginsenoside F2. In the digestive fluids of Rg1, both F1 and Rh1 are identified. The degradation pathways of ginsenoside Rg1 are determined to be: ginsenoside Rg1→ginsenoside F1 and ginsenoside Rg1→ginsenoside Rh1. The results showed that the contents of degradation products in simulated saliva, simulated gastric juice and simulated intestinal juice change with the digestion time. The digestion products ginsenoside Rd, Rg3, Rg5 and Rk1 of ginsenoside Rb1 are the highest after 2-6 h of simulated gastric juice digestion. Ginsenoside F2 is only produced in simulated intestinal juice to digest, in simulated intestinal juice to digest after 4 h content to the maximum. In simulated intestinal fluid, the degradation products of ginsenosides Rb1 and Rg1 are the highest at 4-6 h of digestion. Ginsenoside Rg1 is degraded in the mock digest to generate F1 and Rh1. Degradation products in simulated saliva, gastric juice and intestinal juice content gradually increased, in simulated gastric juice to digest its content reached the highest after 2 h. The degradation of ginsenosides in simulated saliva is milder compared to simulated gastric juice and simulated intestinal juice. However, the degradation products in simulated gastric juice are more abundant than in simulated intestinal juice. In the process of digestion, ginsenoside Rg1 degrades more easily than Rb1. Ginsenosides Rg1 and Rb1 are hydrolyzed in the digestive tract to produce a variety of small molecular saponins, which provide an important chemical and biological basis for the development and utilization of ginsenosides.

     

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