李嘉, 张颖, 姜平川, 张赟赟. 广西不同产地壮药玉叶金花中Mussaendoside G的含量测定[J]. 中国现代应用药学, 2014, 31(12): 1478-1480.
    引用本文: 李嘉, 张颖, 姜平川, 张赟赟. 广西不同产地壮药玉叶金花中Mussaendoside G的含量测定[J]. 中国现代应用药学, 2014, 31(12): 1478-1480.
    LI JIA, ZHANG Ying, JIANG Pingchuan, ZHANG Yunyun. Determination of Mussaendoside G in Mussaenda Pubescens in Different Areas of Guangxi Province by HPLC[J]. The Chinese Journal of Modern Applied Pharmacy, 2014, 31(12): 1478-1480.
    Citation: LI JIA, ZHANG Ying, JIANG Pingchuan, ZHANG Yunyun. Determination of Mussaendoside G in Mussaenda Pubescens in Different Areas of Guangxi Province by HPLC[J]. The Chinese Journal of Modern Applied Pharmacy, 2014, 31(12): 1478-1480.

    广西不同产地壮药玉叶金花中Mussaendoside G的含量测定

    Determination of Mussaendoside G in Mussaenda Pubescens in Different Areas of Guangxi Province by HPLC

    • 摘要: 目的 建立高效液相色谱法测定玉叶金花中mussaendoside G的含量。方法 色谱柱为Techmate C18(4.6 mm× 250 mm,5 μm),流动相:乙腈-水(38∶62),检测波长:265 nm,流速:1.0 mL·min-1。结果 mussaendoside G在0.06~ 0.60 mg·mL-1(r=0.999 9)内线性关系良好,平均回收率为99.34%,RSD为2.32%。不同产地玉叶金花中mussaendoside G的含量相差较大。结论 此方法简便、快捷、准确,可用于玉叶金花药材的质量控制。

       

      Abstract: OBJECTIVE To establish an HPLC method for the simultaneous determination of mussaendoside G in Mussaenda pubescens in different areas of Guangxi province. METHODS Mussaendoside G was separated on Techmate C18 (4.6 mm×250 mm, 5 μm) column and detected at 265 nm. The mobile phase was acetonitrile-water(38∶62). The flow rate was 1.0 mL·min-1. RESULTS Mussaendoside G was 1inear within the range of 0.06-0.60 mg·mL-1(r=0.999 9). The average recovery was 99.34%(RSD=2.32%). The contents of mussaendoside G in different areas were different. CONCLUSION The method is simple, rapid, and it can be used for the quality control of Mussaenda pubescens.

       

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