首页|HPLC法同时测定云南红大戟中三种蒽醌类化合物的含量

HPLC法同时测定云南红大戟中三种蒽醌类化合物的含量

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目的: 建立HPLC法同时测定红大戟药材中芦西定、5-羟基巴戟醌与红大戟素的含量.方法: 采用 Waters Xbridge C18色谱柱(250 mm×4.6 mm,5 μm),以0.05%磷酸为流动相A,以乙腈为流动相B,梯度洗脱;流速为1.0 ml·min-1,检测波长为280 nm,柱温为30℃. 结果: 芦西定、5-羟基巴戟醌、红大戟素的线性范围分别为0.147~29.400 μg·ml-1(r=0.999 6)、0.126~25.200 μg·ml-1 (r=0.999 9)、0.135~27.000μg·ml-1 (r=0.999 5),平均加样回收率分别为98.50%(RSD=1.20%)、98.72%(RSD=0.73%)、101.10%(RSD=1.12%)(n=6).结论: 本文建立的方法经方法学验证可用于评价红大戟药材质量.
Simutaneous Determination of Three Anthraquinone Components in Knoxia Valerianoides by HPLC
Objective: To develop an HPLC method for the simultaneous determination of 3 anthraquinones components in Knoxia valerianoides.Methods: The separation was performed on a Waters Xbridge C18column(250 mm×4.6 mm,5 μm), the mobile phase A was 0.05% phosphoric acid, and acetonitrile served as the mobile phase B, and the analysis was with gradient elution;the flow rate was 1.0 ml·min-1;the detection wavelength was 280 nm;the column temperature was 30℃.Results: The linearity of lucidin, 3-hydroxymorindone and knoxiadin was 0.147-29.400 μg·ml-1 (r=0.999 6), 0.126-25.200μg·ml-1 (r=0.999 9) and 0.135-27.000μg·ml-1 (r=0.999 5), and the average recovery was 98.50%(RSD=1.20%), 98.72%(RSD=0.73%) and 101.10%(RSD=1.12%)(n=6), respectively.Conclusion: The developed method for the simultaneous determination of 3 components can be used to control the quality of Yunnan Knoxia valerianoides.

Knoxia valerianoidesHPLCLucidin3-HydroxymorindoneKnoxiadin

吴陈军、王嘉林、程金鹏、赵静、李艳

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南通市食品药品监督检验中心 江苏南通 226006

河南洛阳市食品药品检验所

云南昭通市农业科学院

中国中医研究院

河南科技大学药学院

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红大戟 高效液相色谱 芦西定 3-羟基巴戟醌 红大戟素

2017

中国药师
国家药品监督管理局高级研修学院,武汉医药(集团)股份有限公司

中国药师

CSTPCD
影响因子:0.944
ISSN:1008-049X
年,卷(期):2017.20(6)
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