叶丽香, 苏燕评, 曹大炫, 林菁, 俞昌喜. UPLC测定钩吻素子的含量及其水溶液稳定性[J]. 中国现代应用药学, 2015, 32(4): 471-474.
    引用本文: 叶丽香, 苏燕评, 曹大炫, 林菁, 俞昌喜. UPLC测定钩吻素子的含量及其水溶液稳定性[J]. 中国现代应用药学, 2015, 32(4): 471-474.
    YE Lixiang, SU Yanpin, CAO Daxuan, LIN Jing, YU Changxi. Content Determination and Stability of Koumine by UPLC[J]. The Chinese Journal of Modern Applied Pharmacy, 2015, 32(4): 471-474.
    Citation: YE Lixiang, SU Yanpin, CAO Daxuan, LIN Jing, YU Changxi. Content Determination and Stability of Koumine by UPLC[J]. The Chinese Journal of Modern Applied Pharmacy, 2015, 32(4): 471-474.

    UPLC测定钩吻素子的含量及其水溶液稳定性

    Content Determination and Stability of Koumine by UPLC

    • 摘要: 目的 建立超高效液相色谱法测定钩吻素子的含量,并考察其水溶液在室温条件下的稳定性。方法 采用Agilent Extend-C18(2.1 mm×100 mm,1.8 μm)色谱柱,以乙腈-0.2%正丁胺水溶液(30∶70)为流动相,流速0.5 mL?min-1,检测波长256 nm,测定3个批次钩吻素子的含量,并考察钩吻素子水溶液在室温条件下稳定性。结果 钩吻素子分离度良好;在10.19~112.2 μg?mL-1内线性关系良好(r=0.999 7),定量限为0.1 μg?mL-1;平均回收率为100.4%(RSD=0.45%,

      Abstract: OBJECTIVE To establish a ultra high performance liquid chromatography(UPLC) method for determination of koumine and to study the stability of koumine solution at room temperature. METHODS The analysis was achieved by Agilent Extend-C18 chromatogram column(2.1 mm×100 mm, 1.8 μm). The mobile phase composed of acetonitrile-0.2% butylamine (30∶70) at flow rate of 0.5 mL?min-1. The detection wavelength was set at 256 nm. Three batches of koumine were determined and stability of its solution was examined under room temperature. RESULTS Under the estabilished method, the separation of koumine and its main related substances was good. The linear range of koumine was 10.19-112.2 μg?mL-1(r=0.999 7) with detection limit of 0.1 μg?mL-1. The average recovery was 100.4% (RSD=0.45%, n=9). The average concentration of koumine were 99.97%(