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作 者:赵惠茹[1] 周晓棉[2] 冯素香[3] 靖会[1]
机构地区:[1]西安医学院药学系,陕西西安710021 [2]沈阳药科大学药学院,辽宁沈阳110016 [3]河南中医学院药学院,河南郑州450008
出 处:《华西药学杂志》2009年第4期414-416,共3页West China Journal of Pharmaceutical Sciences
摘 要:目的采用HPLC测定兔血浆中藁本内酯的浓度。方法样品经正己烷萃取后进样分析。色谱柱为Kromasil C18(150mm×4.6 mm,5μm),流动相为甲醇-水(75:25),流速1.0 ml.min-1,检测波长328 nm,测定兔灌胃100 mg.kg-1当归挥发油有效部位后的血药浓度变化。结果藁本内酯在血浆中的线性范围为0.2~6.4μg.ml^-1,最低检测浓度为0.1μg.ml^-1,日内和日间RSD均小于8%,平均回收率分别为97.18%、93.91%。兔灌胃后,Tpeak=1.28±0.12 h,Cmax=3.86±0.24μg.ml^-1,t1/2α=2.04±0.20 h。结论所建方法符合生物样品的测定要求,可用于兔血浆中藁本内酯的测定和药物动力学研究。OBJECTIVE To develope an HPLC method to assess the concentration of ligustilide in rabbit plasma.METHODS After oral administration of volatile oil at a dose of 100 mg·kg-1 to rabbit,blood samples were collected and extracted with n-hexane.The HPLC system consisted of C18(150 mm×4.6 mm,5 μm)column using MeOH-H2O(75:25) as mobile phase at a flow rate of 1.0 and detection at 328 nm.RESULTS Linear calibration was obtained over a concentration range of 0.2-6.4 μg·ml^-1 for ligustilide.The minimum limit of detection was 0.1 μg·ml^-1.The inter-day and intra-day precision were less than 8% and the recovery of ligusitilide in plasma were 97.18% and 93.91%.Pharmacokinetic parameters were estimated as follows:Tpeak 1.28±0.12 h,Cmax 3.86±0.24 μg·ml^-1,t1/2α 2.04±0.20 h,respectively.CONCLUSION This method is suitable for the pharmacokinetic study of ligustilide in rabbit.
关 键 词:高效液相色谱法 藁本内酯 药物动力学 当归挥发油
分 类 号:R917[医药卫生—药物分析学]
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