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首页> 外文期刊>Molecules >Simultaneous Determination of Multiple Components in Guanjiekang in Rat Plasma via the UPLC-MS/MS Method and Its Application in Pharmacokinetic Study
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Simultaneous Determination of Multiple Components in Guanjiekang in Rat Plasma via the UPLC-MS/MS Method and Its Application in Pharmacokinetic Study

机译:UPLC-MS / MS法同时测定大鼠血浆冠捷康中的多种成分及其在药代动力学研究中的应用

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摘要

Guanjiekang (GJK) that is formed by five medicinal herbs including Astragali Radix, Aconiti Lateralis Radix Praeparaia, Glycyrrhizae Radix et Rhizoma, Corydalis Rhizoma and Paeoniae Radix Alba was used for the treatment of rheumatoid arthritis (RA). However, the pharmacokinetic (PK) profile of active components in GJK remains unclear. This study aims to evaluate the pharmacokinetic behavior of seven representative active constituents in GJK (i.e., benzoylhypaconine, benzoylmesaconine, paeoniflorin, tetrahydropalmatine, calycosin-7-glucoside, formononetin and isoliquiritigenin) after oral administration of GJK in rats. A rapid, sensitive and reliable ultra-performance liquid chromatography-tandem mass spectrometer (UPLC-MS/MS) method has been successfully developed for the simultaneous determination of these seven constituents in rat plasma. Chromatographic separation was achieved on a C-18 column with a gradient elution program that consists of acetonitrile and water (containing 0.1% formic acid) at a flow rate of 0.35 mL/min. Detection was performed under the multiple reaction monitoring (MRM) in the positive electrospray ionization (ESI) mode. The calibration curves exhibited good linearity (R-2 > 0.99) over a wide concentration range for all constituents. The accuracies ranged from 92.9% to 107.8%, and the intra-day and inter-day precisions at three different levels were below 15%. Our PK results showed that these seven compounds were quickly absorbed after the administration of the GJK product, and T-max ranged from 30 min to 189 min. The in vivo concentrations of paeoniflorin and isoliquiritigenin were significantly higher than the reported in vitro effective doses, indicating that they could partly contribute to the therapeutic effect of GJK. Therefore, we conclude that pharmacokinetic studies of representative bioactive chemicals after administration of complex herbal products are not only necessary but also feasible. Moreover, these seven compounds that were absorbed in vivo can be used as indicator standards for quality control and for determining pharmacokinetic behavior of herbal medicines in clinical studies.
机译:由五种药组成的冠结康(GJK),用于治疗类风湿关节炎(RA),其中包括黄芪,白附子,甘草,大黄,延胡索和白e。但是,尚不清楚GJK中活性成分的药代动力学(PK)情况。这项研究旨在评估大鼠口服GJK后GJK的七个代表性活性成分(即苯甲酰基羟紫苏碱,苯甲酰基美沙可宁,pa药苷,四氢巴马汀,calycosin-7-葡萄糖苷,前生花青素和异寡糖原蛋白)的药代动力学行为。快速,灵敏和可靠的超高性能液相色谱-串联质谱仪(UPLC-MS / MS)方法已成功开发,用于同时测定大鼠血浆中的这七个成分。使用梯度洗脱程序在C-18色谱柱上进行色谱分离,该梯度洗脱程序由乙腈和水(含0.1%甲酸)组成,流速为0.35 mL / min。在正电喷雾电离(ESI)模式下的多重反应监测(MRM)下进行检测。对于所有成分,校准曲线在宽浓度范围内均显示出良好的线性(R-2> 0.99)。精度范围从92.9%到107.8%,三个不同级别的日内和日间精度低于15%。我们的PK结果表明,施用GJK产品后这7种化合物被快速吸收,T-max介于30分钟至189分钟之间。 eon药苷和异黄体生成素的体内浓度显着高于所报道的体外有效剂量,这表明它们可能部分有助于GJK的治疗作用。因此,我们得出结论,在服用复杂草药产品后,具有代表性的生物活性化学品的药代动力学研究不仅是必要的,而且也是可行的。此外,在体内吸收的这七种化合物可用作质量控制和确定临床研究中草药药代动力学行为的指示剂标准。

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