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抱茎苦荬菜药材中木犀草素-7-O-β-D-吡喃葡萄糖苷的分离与含量测定 被引量:7

Separation and quantitative determination of luteolin-7-O-β-D-glucopyranoside in the Ixeris sonchifolia(Bge.)Hance
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摘要 目的建立分离、测定抱茎苦荬菜药材中木犀草素-7-O-β-D-葡萄糖苷的方法。方法采用醇提取、氯仿萃取与硅胶柱分离等手段来分离木犀草素-7-O-β-D-葡萄糖苷;采用RP-HPLC法进行含量测定,色谱条件为:Diamonsin C18(250mm×4.6mm,5μm)色谱柱,以质量分数为0.2%的磷酸溶液-甲醇(体积比为67:33)为流动相,检测波长为260nm,流速为0.8mL·min^-1。结果木犀草素-7-O-β-D-葡萄糖苷质量浓度在4.80-24.0mg·L^-1内线性关系良好(r=0.9997,n=5),平均回收率为99.4%,相对标准差(RSD)为0.97%。结论本法适合测定抱茎苦荬菜药材中木犀草素-7-O-β-D-葡萄糖苷的含量。 Objective To develop a RP-HPLC method for the determination of the content of luteolin-7-O-β-D-D-glucopyranoside in Ixeris sonchifolia (Bge.)Hance. Methods The luteolin-7-O-β-D-glucopyranoside was obtained by the extraction with 70 % EtOH and precipitated by the method of column chromatography. It was separated on a Diamonsin C18 (4.6 mm × 250 mm, 5 μm) column with CH3OH-H2O(0.2 96 H3 PO4) (33 : 67)as the mobile phase, The UV detective wavelength was set at 260 nm, the flow rate was 0.8 ml/min. Results The average recovery is 99.4 %, and RSD is 0.97 %. The linear calibration curves are obtained in the ranges of 4.8-24.0 mg·L^-1. Conclusions The method is simple and accurate. It can be applied to the determination of the concentration of the luteolin-7-O-β-D-glucopyranoside.
出处 《沈阳药科大学学报》 CAS CSCD 北大核心 2006年第8期518-520,共3页 Journal of Shenyang Pharmaceutical University
关键词 抱茎苦荬菜 木犀草素-7-O-β-D-吡喃葡萄糖苷 高效液相色谱法 含量测定 Ixeris sonchifolia ( Bge. ) Hance luteolin-7-O-β-D-glucopyranoside RP-HPLC content determination
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参考文献2

  • 1Asada H, Miyase T, Fukushima S. Sesquiterpene lactones from Ixeris tamagawaensis Kitam [J ]. Chem Pharrn Bull, 1984, 32(5) :1724 - 1728.
  • 2Asada H, Miyase T, Fukushima S. Sesquiterpene lactones from Ixeris tamagawensis Kitam II [J]. Chem Pharm Bull, 1984, 32(8) : 3036 - 3042.

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