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不同产地白花败酱草中异荭草苷和异牡荆苷的含量测定 被引量:5

Determination of Isovitexin and Isoorientin from Patrinia Villosa Juss by HPLC
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摘要 目的建立白花败酱草中异荭草苷和异牡荆苷含量的高效液相色谱(HPLC)法。方法药材经甲醇超声提取后进行色谱分析,色谱柱为YWGC18柱(150mm×4.6mm,5μm),流动相为乙腈-水-乙酸(22∶78∶1),流速1.0mL/min,检测波长270nm。结果异荭草苷和异牡荆苷分离良好,含量分别在0.012~0.037mg/mL和0.026~0.082mg/mL范围内与峰面积线性关系良好,平均加样回收率分别为96.1%(RSD=0.89%)和98.1%(RSD=1.43%)。结论HPLC法简便、快速,可用于白花败酱草的质量控制。 Objective To establish a method for the determination of isovitexin and isoorientin from Patrinia villosa Juss. Methods The medi- cinat materiats after ultrasound-assisted extraction was analyzed by HPLC with a YWG C18(150 mm ×4.6 mm, 5 μm) column, and the solvent system composed of CH3CN-H20-HAc(22:78:1) was used as the mobile phase at the flow rate of 1.0 mL/min, and the detection wavelength was set at 270 nm. Results An excellent separation was achieved under the optimized conditions, and the linear ranges were 0.012-0.037 mg/mL and 0.026-0. 082 mg/mL for isovitexin and isoorientin, respectively, and the average recovery rates were 96. 1% (RSD =2.06% ) and 96. 7% (RSD =2.24% ). Conclusion The HPLC method is rapid, fast and suitable for the quality control of Patrinia villosa Juss.
作者 陈雁
出处 《中国药业》 CAS 2008年第16期24-25,共2页 China Pharmaceuticals
关键词 白花败酱草 异荭草苷 异牡荆苷 含量分析 Patrinia villosa Juss, isovitexin isoorientin content determination
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  • 1何福江,杨建萍.败酱属植物化学成分与药理研究概况[J].甘肃医药,1993,12(3):161-163. 被引量:12
  • 2Jinyong Peng. Preparative separation of isovitexin and isoorientin from Patrinia villosa Juss by high- speed counter-current chromatography[J]. Journal of Chromatography A, 2005, 1 074 ( 1 - 2) : 111 - 115.
  • 3Toshihiro Kumazawa. An effective synthesis of isoorientin: the regioselective synthesis of a 6-C- glucosylflavone[J] . Carbohydrate Research, 2000, 329(3): 507.
  • 4Gong Cheng, Flavonoids from Ziziphus jujube Mill var. spinosa[J ], Tetrahedron, 2000, 56(45): 8915 - 8920.

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