超高效液相色谱-串联质谱法测定黄芪中黄芪甲苷的含量
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(天津市疾病预防控制中心,天津 300011)

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夏义平 男 主管技师 研究方向为理化检验 E-mail:xyp_76@163.com

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天津市卫生计生委科技基金(2014KY21)


Determination of astragaloside IV in Radix astragali by ultra high performance luquid chromatography-tandem mass spectrometry
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(Tianjin Center for Disease Control and Prevention,Tianjin 300011,China)

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    摘要:

    建立超高效液相色谱-串联质谱法测定黄芪中黄芪甲苷的含量。方法 黄芪经甲醇-氨水(3∶1,V/V)超声提取30 min,采用多反应监测(MRM)模式,以m/z 785.4/143.108和m/z 785.4/473.391为定性离子对,m/z 785.4/143.108为定量离子对,外标法测定黄芪甲苷。结果 黄芪甲苷在60.0~12 000 ng/ml浓度范围内有良好线性关系(r=0.999 3),平均回收率为91.7%,最低检测限为68.2 μg/kg。结论 该方法具有简便、快速和灵敏度高的特点,可用于黄芪中黄芪甲苷的测定。

    Abstract:

    To establish a method for determination of astragaloside IV in Radix astragali by UPLC-MS/MS.Methods Radix astragali was extracted with methanol-ammonia (3∶1, V/V) for 30 min by ultrasonic, the astragaloside IV was monitored via the ESI+ionization model and quantified by multiple reaction monitoring(MRM), using m/z 785.4/143.108 and m/z 785.4/473.391 as qualitative ion pair and m/z 785.4/143.108 as quantitative ion pair. Results The calibration curve of astragaloside IV was in good linearity over the ranges of 60.0-12 000 ng/ml (r=0.999 3), the average recovery was 91.7%, and the detection limit was 68.2 μg/kg. Conclusion This method was accurate, rapid, easy to operate, and the methodology validation showed that it was suitable for the determination of astragaloside IV in Radix astragali.

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夏义平,李建平,党亚敏,渠志华,王辰.超高效液相色谱-串联质谱法测定黄芪中黄芪甲苷的含量[J].中国食品卫生杂志,2016,28(5):624-627.

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  • 收稿日期:2016-01-27
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  • 在线发布日期: 2016-10-18
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