Chen Hui, Li Zheng, Li Yin-jie, Wu Xiao-wen, Wang Shi-rui, Chen Kai, Zheng Xiao-xiao, Du Qian, Tang Dao-quan
Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, Xuzhou Medical College, Xuzhou, Jiangsu, 221004, China.
Xuzhou Institute for Drug Control, Xuzhou, Jiangsu, 221002, China.
Biomed Chromatogr. 2015 Dec;29(12):1819-25. doi: 10.1002/bmc.3501. Epub 2015 May 27.
A novel UPLC-DAD method was developed and validated for the simultaneous determination of baicalin (baicalein-7-glucuronide, BG), oroxylin A-7-O-glucuronide (OAG) and wogonoside (WG) in rat plasma using rutin as the internal standard. Plasma samples were precipitated using acetonitrile containing 0.1% formic acid. Separation was performed on an Agilent Eclipse Plus C18 column (2.1 × 50 mm, 1.8 µm) using gradient acetonitrile and 0.2% formic acid water solution as mobile phase. The flow-rate was set at 0.4 mL/min and the eluate was detected at 275 nm. The method was linear over the ranges of 0.075-17.50, 0.050-12.60 and 0.056-14.10 µg/mL for BG, OAG and WG, respectively. The intra- and inter-day precisions were respectively <4.8% and 6.4%. All of the limits of detection of three analytes in rat plasma were 0.01 µg/mL, whereas the limits of quantification were, respectively, 0.035, 0.025 and, 0.025 µg/mL. This assay has been successfully applied to pharmacokinetics of BG, OAG and WG in rats after oral administration of Yinhuang granule (YHG) and comparative pharmacokinetics of BG in rats following oral administration of the pure BG, Radix Scutellariae (RS) or YHG. We speculate that some co-existing ingredients in RS or YHG may increase the absorption and elimination of BG in rat. This work may be helpful for the quality control of Yinhuang granule.
建立了一种新型超高效液相色谱-二极管阵列检测法(UPLC-DAD),以芦丁为内标,用于同时测定大鼠血浆中的黄芩苷(黄芩素-7-葡萄糖醛酸苷,BG)、木犀草素-7-O-葡萄糖醛酸苷(OAG)和汉黄芩苷(WG)。血浆样品用含0.1%甲酸的乙腈沉淀。采用梯度乙腈和0.2%甲酸水溶液作为流动相,在安捷伦Eclipse Plus C18柱(2.1×50 mm,1.8 µm)上进行分离。流速设定为0.4 mL/min,在275 nm处检测洗脱液。该方法在BG、OAG和WG的浓度范围分别为0.075 - 17.50、0.050 - 12.60和0.056 - 14.10 µg/mL时呈线性。日内和日间精密度分别<4.8%和6.4%。三种分析物在大鼠血浆中的检测限均为0.01 µg/mL,而定量限分别为0.035、0.025和0.025 µg/mL。该测定法已成功应用于大鼠口服银黄颗粒(YHG)后BG、OAG和WG的药代动力学研究,以及大鼠口服纯BG、黄芩(RS)或YHG后BG的比较药代动力学研究。我们推测RS或YHG中一些共存成分可能会增加大鼠对BG的吸收和消除。这项工作可能有助于银黄颗粒的质量控制。