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作 者:覃洁萍[1] 姚蓉[1] 李芸[2] 王丽丽[1] 许晨霞[1] 李伟[1]
机构地区:[1]广西中医学院,南宁市明秀东路179号530001 [2]广西中医学院制药厂,530023
出 处:《广西中医药》2008年第4期58-60,共3页Guangxi Journal of Traditional Chinese Medicine
基 金:广西自然科学基金资助项目(桂科自0447076)
摘 要:目的:建立扶芳藤药材中卫矛醇的含量测定方法。方法:采用HPLC法,色谱柱为Lichrospher5-NH2柱(250mm×4.6mm,5μm);流动相为乙腈-水(90:10);流速为1.0ml/min;柱温为28℃;检测器为PL-ELS2100型蒸发光散射检测器(漂移管温度65℃,雾化室温度50℃,气体流量为:0.9L/min)。结果:卫矛醇在2.91~29.1μg范围内,其峰面积的自然对数(Y)与进样量的自然对数(X)呈良好的线性关系,r=0.9998;平均加样回收率100.78%,RSD为2.36%(n=6)。结论:该方法简便,重复性好,结果准确,可作为扶芳藤药材中卫矛醇的含量测定方法。Objective:To establish a method for the determination of dulcitol in Fortune euonymus stem. Method: The way of HPLC-ELSD was used. Chromatographic column was Lichrospher5-NH2 column (250 mm× 4.6 mm, 5μm) and the mobile phase was a mixture of acetonitrile-water (90:10) with 1.0ml.min^-1 as the flow rate. Column temperature was at 28℃ and the detector was PL-ELS2100 ELSD (diift tube Temp:65℃,atomizer chamber Temp:50℃ ,gas flow:0.9 mL/min). Results: When dulcitol was in the rang of 2.91-29.1μg, the natural logarithm(Y) of peak area and the natural logarithm(X) of sample size showed a satisfactory linear relationship R = 0.9998;the average recovery of application of sample was 100.75% and RSD was 2.3%(n= 6). Conclusion: The method is easy which has a good repeatability and an accurate result. It can be the method for the determination of dulcitol in Fortune euonymus stem.
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