首页> 外文期刊>Journal of chromatography, B. Analytical technologies in the biomedical and life sciences >Comparative pharmacokinetics of baicalin and wogonoside by liquid chromatography-mass spectrometry after oral administration of Xiaochaihu Tang and Radix scutellariae extract to rats
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Comparative pharmacokinetics of baicalin and wogonoside by liquid chromatography-mass spectrometry after oral administration of Xiaochaihu Tang and Radix scutellariae extract to rats

机译:大鼠小柴胡汤和黄cut提取物口服液相色谱-质谱联用对黄ical苷和牛磺酸皂苷的比较药代动力学

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The aim of this study was to compare the pharmacokinetics of baicalin and wogonoside in rats following oral administration of Xiaochaihu Tang (Minor Radix Bupleuri Decoction) and Radix scutellariae extract. Thus, a specific LC-MS method was developed and validated for the determination of these flavonoids in the plasma of rats after oral administration Xiaochaihu Tang and Radix scutellariae extract. Chromatographic separation was performed on a Zorbax SB C_(18) column (150mm×4.6mm, i.d.: 5μm) with 0.1% formic acid in water and acetonitrile by linear gradient elution. Baicalin, wogonoside and carbamazepine (internal standard, I.S.) were detected in select-ion-monitoring (SIM) mode with a positive electrospray ionization (ESI) interface. The following ions: m/z 447 for baicalin, m/z 461 for wogonoside and m/z 237 for the I.S. were used for quantitative determination. The calibration curves were linear over the concentration ranges from 0.1231 to 6.156μgmL~(-1) for baicalin and 0.08832 to 4.416μgmL~(-1) for wogonoside. The lower limit of detection (LLOD) based on a signal-to-noise ratio of 2 was 0.06155μgmL~(-1) for baicalin and 0.04416μgmL~(-1) for wogonoside. Intra-day and inter-day precisions (RSD%) were within 10% and accuracy (RE%) ranged from -6.4 to 4.4%. The extraction recovery at three QC concentrations ranged from 74.7 to 86.0% for baicalin and from 71.3 to 83.7% for wogonoside. The plasma concentrations of baicalin and wogonoside in rats at designated time periods after oral administration were successfully determined using the validated method, pharmacokinetic parameters were estimated by a non-compartment model. Following oral administration of Xiaochaihu Tang and Radix scutellariae extract, the t_(1/2) of baicalin was 3.60±0.90 and 5.64±1.67, the C_(max1) was 1.64±0.99 and 5.66±2.02, the t_(max1) was 0.13±0.05 and 0.20±0.07, the C_(max2) was 2.43±0.46 and 3.18±1.66, and the t_(max2) were 6.40±1.67 and 5.66±2.02, respectively. Following oral administration of Xiaochaihu Tang and Radix scutellariae extract, the t_(1/2) of wogonoside was 4.97±1.68 and 7.71±1.55, the C_(max1) was 1.39±0.83 and 1.45±0.37, the t_(max1) was 0.21±0.20 and 0.17±0.01, the C_(max2) was 1.90±0.55 and 1.42±0.70, and the t_(max2) was 5.60±1.67 and 5.20±1.79, respectively. A significant difference (p<0.05) was observed for t_(1/2), and the elimination of baicalin and wogonoside in Xiaochaihu Tang was increased.
机译:这项研究的目的是比较小柴胡汤(小柴胡汤)和黄提取物口服后黄ical苷和Wogonoside在大鼠中的药代动力学。因此,开发了一种专用的LC-MS方法,并通过口服小柴胡汤和黄ix提取物对大鼠血浆中这些类黄酮的测定进行了验证。通过Zorbax SB C_(18)色谱柱(150mm×4.6mm,i.d .:5μm)进行色谱分离,采用0.1%甲酸的水溶液和乙腈溶液通过线性梯度洗脱进行分离。在具有正电喷雾电离(ESI)接口的选择离子监测(SIM)模式下检测到黄ical苷,wogonoside和卡马西平(内标,IS)。以下离子:黄ical苷m / z 447,皂甙类化合物m / z 461,I.S. m / z 237。用于定量测定。对于黄ical苷,浓度范围为0.1231至6.156μgmL〜(-1),对于单酚苷,浓度范围为0.08832至4.416μgmL〜(-1)是线性的。基于黄in苷的信噪比为2的检测下限(LLOD)为0.06155μgmL〜(-1),而山w苷为0.04416μgmL〜(-1)。日内和日间精度(RSD%)均在10%以内,精度(RE%)介于-6.4至4.4%之间。黄ical苷在三种QC浓度下的提取回收率范围分别为74.7%至86.0%和wogonoside的范围为71.3%至83.7%。使用验证的方法成功确定了口服给药后指定时间段大鼠黄ical苷和Wogonoside的血浆浓度,并通过非隔离室模型估算了药代动力学参数。口服小柴胡汤和黄cut提取物后,黄ical苷的t_(1/2)为3.60±0.90和5.64±1.67,C_(max1)为1.64±0.99和5.66±2.02,t_(max1)为0.13 ±0.05和0.20±0.07,C_(max2)分别为2.43±0.46和3.18±1.66,t_(max2)分别为6.40±1.67和5.66±2.02。口服小柴胡汤和黄提取物后,窝参皂苷的t_(1/2)为4.97±1.68和7.71±1.55,C_(max1)为1.39±0.83和1.45±0.37,t_(max1)为0.21 ±0.20和0.17±0.01,C_(max2)分别为1.90±0.55和1.42±0.70,t_(max2)分别为5.60±1.67和5.20±1.79。 t_(1/2)差异有统计学意义(p <0.05),并且小柴胡汤中黄ical苷和Wogononoside的清除率增加。

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