首页> 美国卫生研究院文献>Molecules >Simultaneous Determination and Pharmacokinetic Characterization of Glycyrrhizin Isoliquiritigenin Liquiritigenin and Liquiritin in Rat Plasma Following Oral Administration of Glycyrrhizae Radix Extract
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Simultaneous Determination and Pharmacokinetic Characterization of Glycyrrhizin Isoliquiritigenin Liquiritigenin and Liquiritin in Rat Plasma Following Oral Administration of Glycyrrhizae Radix Extract

机译:口服甘草根提取物后同时测定大鼠血浆中甘草甜素异黄体素异黄体素和黄体素的含量及药代动力学

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摘要

Glycyrrhizae Radix is widely used as herbal medicine and is effective against inflammation, various cancers, and digestive disorders. We aimed to develop a sensitive and simultaneous analytical method for detecting glycyrrhizin, isoliquiritigenin, liquiritigenin, and liquiritin, the four marker components of Glycyrrhizae Radix extract (GRE), in rat plasma using liquid chromatography-tandem mass spectrometry and to apply this analytical method to pharmacokinetic studies. Retention times for glycyrrhizin, isoliquiritigenin, liquiritigenin, and liquiritin were 7.8 min, 4.1 min, 3.1 min, and 2.0 min, respectively, suggesting that the four analytes were well separated without any interfering peaks around the peak elution time. The lower limit of quantitation was 2 ng/mL for glycyrrhizin and 0.2 ng/mL for isoliquiritigenin, liquiritigenin, and liquiritin; the inter- and intra-day accuracy, precision, and stability were less than 15%. Plasma concentrations of glycyrrhizin, isoliquiritigenin, liquiritigenin, and liquiritin were quantified for 24 h after a single oral administration of 1 g/kg GRE to four rats. Among the four components, plasma concentration of glycyrrhizin was the highest and exhibited a long half-life (23.1 ± 15.5 h). Interestingly, plasma concentrations of isoliquiritigenin and liquiritigenin were restored to the initial concentration at 4–10 h after the GRE administration, as evidenced by liquiritin biotransformation into isoliquiritigenin and liquiritigenin, catalyzed by fecal lysate and gut wall enzymes. In conclusion, our analytical method developed for detecting glycyrrhizin, isoliquiritigenin, liquiritigenin, and liquiritin could be successfully applied to investigate their pharmacokinetic properties in rats and would be useful for conducting further studies on the efficacy, toxicity, and biopharmaceutics of GREs and their marker components.
机译:甘草基被广泛用作草药,对炎症,各种癌症和消化系统疾病有效。我们旨在开发一种灵敏且同时的分析方法,以液相色谱-串联质谱法在大鼠血浆中检测甘草甜菜根提取物(GRE)的四个标志物成分-甘草甜素,异黄体生成素,黄体生成素和黄体生成素,并将该分析方法应用于药代动力学研究。甘草甜素,异黄体素,异黄体素和黄体素的保留时间分别为7.8分钟,4.1分钟,3.1分钟和2.0分钟,这表明四种分析物的分离度很好,在峰洗脱时间附近没有任何干扰峰。甘草甜素的定量下限为2 ng / mL,异异黄体生成素,liquiritigenin和liquiritin的定量下限为0.2 ng / mL;日间和日间的准确性,准确性和稳定性均低于15%。在对四只大鼠单次口服1 g / kg GRE后,在24小时内对甘草甜素,异黄体生成素,异黄体生成素和黄体生成素的血浆浓度进行定量。在这四个成分中,甘草甜素的血浆浓度最高,并且显示出长的半衰期(23.1±15.5 h)。有趣的是,在GRE给药后4-10小时,异黄体生成素和异黄体生成素的血浆浓度恢复到初始浓度,这是由粪便裂解物和肠壁酶催化的黄生成素生物转化为异黄生成素和异黄生成素的证明。综上所述,我们开发的用于检测甘草甜素,异黄体生成素,异黄体生成素和黄体生成素的分析方法可以成功地用于研究它们在大鼠中的药代动力学特性,并将有助于进一步研究GREs及其标志物成分的功效,毒性和生物药物学。

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