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作 者:孙艳涛[1,2] 赵兰英[1] 李婷婷[1] 赵磊[3] 姜大雨[1,2]
机构地区:[1]吉林师范大学化学学院,四平136000 [2]吉林师范大学环境友好材料制备与应用省部共建教育部重点实验室,四平136000 [3]吉林省四平市食品药品检验所,四平136000
出 处:《医药导报》2014年第1期100-102,共3页Herald of Medicine
基 金:吉林省教育厅十二五基金项目(2012177)
摘 要:目的建立高效液相色谱(HPLC)切换波长法同时测定牛蒡子中3种活性成分含量。方法应用TC.C18色谱柱(4.6mm×250mm,5μm);流动相为甲醇-0.4%冰醋酸,梯度洗脱;流速1.0mL·min-1;检测波长为280与326nm切换;进样量10μL;温度25℃。结果绿原酸、牛蒡子苷和牛蒡子苷元分别在0.0273—5.4600,0.1500~18.0000和0.0303—6.0600肛g范周内呈良好线性,线性方程分别为Y=1]06.476X-11.452,Y=1026.014X+20.391和y=287.661X+4.045;平均加样回收率分别为99.55%,99.42%和99.40%。结论该方法快速、准确、重复性好,可用于牛蒡子中多组分含量的同时测定及质量控制。Objective To establish an HPLC method for simuhaneous determination of three active components in Fructus arctii. Methods The HPLC analysis was carried out on TC-CIs(4.6 mm×250 mm,5μm) column at the temperature of 25 ℃. The mobile phase composed of methanol and 0. 4% glacial acetic acid with gradient elution at a flow rate of 1.0 mL · rain-~. The detection wavelength was 280 nm shifted to 326 nm. The sample loading volume was 10μL. Results The linear range for chlorogenie acid, arctiin, and arctigenin was 0. 027 3-5. 460 0, 0. 150 0- 18. 000 0, and 0. 030 3- 6. 060 μg, respectively. The linear equation was Y= 1 106. 476X- 11. 452, Y= 1 026. 014X+20. 391, and Y= 287. 661X+ 4.045, respectively. The average recovery of cblorogenic acid, arctiin, and arctigenin was 99.55%, 99.42% and 99.40%, respectively. Conclusion The method is quick, accurate, and reproducible. It can be used for content determination and quality control for Fructus arctii.
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