Huang Yong, Sun Hui-Yuan, Qin Xiao-Li, Li Yong-Jun, Liao Shang-Gao, Gong Zi-Peng, Lu Yuan, Wang Yong-Lin, Wang Ai-Min, Lan Yan-Yu, Zheng Lin
Provincial Key Laboratory of Pharmaceutics in Guizhou Province, Guizhou Medical University, 4 Beijing Road, Guiyang 550004, China.
School of Pharmacy, Guizhou Medical University, 4 Beijing Road, Guiyang 550004, China.
Molecules. 2017 Feb 25;22(3):353. doi: 10.3390/molecules22030353.
The principal active constituents of are phenolic acids and flavonoids, such as gallic acid, quercitrin, and quercetin. The aim of this study was to develop and validate a method to determine the three constituents and the corresponding conjugated metabolites of in vivo and to conduct pharmacokinetic studies on the herb, a well-known Miao medicinal plant in China. Gallic acid, quercitrin, and quercetin were analysed by ultra-performance liquid chromatography-electrospray ionization-tandem mass spectrometry (UPLC-ESI-MS/MS). Protein precipitation in plasma samples was performed using methanol. For the determination of total forms of analytes, an additional process of hydrolysis was conducted using β-glucuronidase and sulphatase. The analytes were separated on a BEH C column (50 mm × 2.1 mm; i.d., 1.7 μm) and quantified by multiple reaction monitoring (MRM) mode. The linear regression showed high linearity over a 729-fold dynamic range for the three analytes. The relative standard deviations of intra- and inter-day measurements were less than 9.5%, and the method was accurate to within -11.1% to 12.5%. The extraction recoveries for gallic acid, quercitrin, and quercetin were 94.3%-98.8%, 88.9%-98.8%, and 95.7%-98.5%, respectively. All samples were stable under short- and long-term storage conditions. The validated method was successfully applied to a comparative pharmacokinetic study of gallic acid, quercitrin, and quercetin in their free and total forms in rat plasma. The study revealed significantly higher exposure of the constituents in total forms for gallic acid and quercetin, while quercitrin was detected mainly in its corresponding free form in vivo. The established method was rapid and sensitive for the simultaneous quantification of free and total forms of multiple constituents of extract in plasma.
其主要活性成分是酚酸和黄酮类化合物,如没食子酸、槲皮苷和槲皮素。本研究的目的是开发并验证一种方法,用于测定该植物体内这三种成分及其相应的共轭代谢物,并对这种中国著名的苗族药用植物进行药代动力学研究。没食子酸、槲皮苷和槲皮素采用超高效液相色谱-电喷雾电离-串联质谱法(UPLC-ESI-MS/MS)进行分析。血浆样品中的蛋白质沉淀采用甲醇进行。为了测定分析物的总形式,使用β-葡萄糖醛酸酶和硫酸酯酶进行额外的水解过程。分析物在BEH C柱(50 mm×2.1 mm;内径,1.7μm)上分离,并通过多反应监测(MRM)模式进行定量。线性回归显示,这三种分析物在729倍的动态范围内具有高线性。日内和日间测量的相对标准偏差均小于9.5%,该方法的准确度在-11.1%至12.5%以内。没食子酸、槲皮苷和槲皮素的提取回收率分别为94.3%-98.8%、88.9%-98.8%和95.7%-98.5%。所有样品在短期和长期储存条件下均稳定。该验证方法成功应用于大鼠血浆中没食子酸、槲皮苷和槲皮素游离形式和总形式的比较药代动力学研究。研究表明,没食子酸和槲皮素总形式的成分暴露量显著更高,而槲皮苷在体内主要以其相应的游离形式被检测到。所建立的方法对于同时定量血浆中该植物提取物多种成分的游离形式和总形式快速且灵敏。