Zhang Jiye, Yang Guangde, Lin Rong, Hu Zheng
School of Medicine, Xi'an Jiaotong University, Shaanxi, People's Republic of China.
Biomed Chromatogr. 2011 Apr;25(4):450-7. doi: 10.1002/bmc.1466. Epub 2010 Aug 23.
The purpose of this study was to simultaneously investigate the pharmacokinetics of five bioactive compounds in rat plasma after oral administration of Buyang Huanwu decoction (BYHWD) using high-performance liquid chromatography coupled with mass spectrometry (HPLC-MS). The separations were performed on a Thermo Hypersil Gold C(18) analytical column (50 × 2.1 mm, 3 µm) with the column temperature kept at 30°C. The quantitative analysis was performed using a quadrupole mass spectrometer detector operated under selected ion monitoring mode. A linear gradient elution of A (0.1% formic acid solution) and B (100% acetonitrile) was used at a flow rate of 0.2 mL/min. The method was validated within the concentration ranges 1.8-450, 6.0-1500, 2.0-500, 1.2-300 and 1.2-150 ng/mL for paeoniflorin, calycosin-7-O-β-d-glucoside, ononin, calycosin and formononetin, respectively. The calibration curves were linear with correlation coefficients > 0.99. The lower limits of quantitations were < 6.0 ng/mL. The method was further applied to assess the pharmacokinetics of the five bioactive constituents of BYHWD in rat plasma.
本研究旨在采用高效液相色谱-质谱联用(HPLC-MS)技术,同时考察大鼠口服补阳还五汤(BYHWD)后血浆中5种生物活性成分的药代动力学。分离在Thermo Hypersil Gold C(18)分析柱(50×2.1 mm,3 µm)上进行,柱温保持在30°C。定量分析采用在选择离子监测模式下操作的四极杆质谱仪检测器进行。以0.2 mL/min的流速使用A(0.1%甲酸溶液)和B(100%乙腈)进行线性梯度洗脱。该方法在芍药苷、毛蕊异黄酮-7-O-β-D-葡萄糖苷、芒柄花苷、毛蕊异黄酮和刺芒柄花素的浓度范围分别为1.8 - 450、6.0 - 1500、2.0 - 500、1.2 - 300和1.2 - 150 ng/mL内进行了验证。校准曲线呈线性,相关系数>0.99。定量下限<6.0 ng/mL。该方法进一步应用于评估补阳还五汤中5种生物活性成分在大鼠血浆中的药代动力学。