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y Effect of Chemical Profiling Change of Processed Magnolia officinalis on the Pharmacokinetic Profiling of Honokiol and Magnolol in Rats

机译:加工厚朴的化学特性变化对大鼠厚朴酚和厚朴酚药代动力学谱的影响

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摘要

The stem of Magnoliae officinalis (MO) cortex is always preliminarily processed before being applied in traditional Chinese medicine. The definite bioavailability of honokiol (HO) and magnolol (MA) in processed MO (PMO) and the effect of chemical profiling change on the pharmacokinetics of HO and MA are always a greater challenge compared with those of MO. Compared with that of MO, the pharmacokinetic profiling of HO and MA in the PMO was significantly changed and the mean T-max of HO and MA was increased by 31 and 50% (P < 0.05), respectively; the mean AUC(0-t) and C-max of HO were increased by 36 and 24% (P < 0.05), respectively. Subsequently, the chemical profiling of MO and PMO was investigated by a simple and rapid LC-Q/TOF-MS coupled with multivariate analysis method. Principal component analysis and hierarchical cluster analysis of the chromatographic data demonstrated that the chemical profiling of PMO was significantly different from that of MO. Eight marker components including six alkaloids (magnocurarine, magnoflorine, roemerine and three unidentified peaks) and two lignans (obovatol and MA) were screened out by partial least-squares discriminant analysis. The results indicated that the changes of eight marker components of PMO may have an effect on the pharmacokinetic profiles of HO and MA.
机译:厚朴(MO)皮层的茎在用于中药之前总是经过初步加工。与MO相比,厚朴酚(HO)和厚朴酚(MA)在加工MO(PMO)中的确定生物利用度以及化学谱变化对HO和MA药代动力学的影响始终是一个更大的挑战。与MO相比,PMO中HO和MA的药代动力学曲线发生了显着变化,HO和MA的平均T-max分别增加了31%和50%(P <0.05); HO的平均AUC(0-t)和C-max分别增加了36%和24%(P <0.05)。随后,通过简单快速的LC-Q / TOF-MS结合多元分析方法研究了MO和PMO的化学谱。色谱数据的主成分分析和层次聚类分析表明,PMO的化学谱与MO显着不同。通过偏最小二乘判别分析筛选出八个标记物成分,包括六个生物碱(木犀草碱,厚朴碱,玫瑰红碱和三个未鉴定的峰)和两个木脂素(奥贝托尔和MA)。结果表明,PMO的八个标志物成分的变化可能会影响HO和MA的药代动力学。

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