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期刊名称:药物分析杂志 主管单位:中国科学技术协会 主办单位:中国药学会承办:中国食品药品检定研究院 主编:金少鸿 地址:北京天坛西里2号 邮政编码:100050 电话:010-67012819,67058427 电子邮箱:ywfx@nifdc.org.cn 国际标准刊号:ISSN 0254-1793 国内统一刊号:CN 11-2224/R 邮发代号:2-237
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UPLC同时测定野菊花药材中10个黄酮和有机酸的含量
Simultaneous determination of flavonoids and organic acids in Chrysanthemum indicum by UPLC
分类号:R917
出版年·卷·期(页码):2019,39 (3):451-457
DOI:
10.16155/j.0254-1793.2017.01.01
-----摘要:-------------------------------------------------------------------------------------------
目的:建立UPLC同时测定野菊花药材中绿原酸、咖啡酸、1,3-二咖啡酰奎宁酸、木犀草素-7-O-β-D-葡萄糖苷、3,4-二咖啡酰奎宁酸、3,5-二咖啡酰奎宁酸、4,5-二咖啡酰奎宁酸、木犀草素、蒙花苷及芹菜素10个成分含量的方法。方法:采用Agilent Eclipse Plus C18色谱柱(2.1 mm×100 mm,1.8μm);以甲醇(A)-0.3%磷酸水溶液(B)为流动相,梯度洗脱,流速0.4 mL·min-1;检测波长326 nm;柱温25℃。结果:10个成分在38 min内均达到基线分离,线性关系良好(r>0.999 2,n=6);平均回收率均在96.4%~103.2%(RSD<2.0%,n=6);测定的6批样品中上述10个成分含量范围分别为1.018~3.430、0.079~0.365、0~0.269、1.198~2.754、0.185~0.765、1.135~6.659、0.587~2.808、0.103~1.663、0.495~13.050、0.214~0.933 mg·g-1。结论:本方法操作简单,准确性和重复性良好。可用于野菊花药材的多成分同步测定,为野菊花的全面质量评价和质量控制提供科学依据。
-----英文摘要:---------------------------------------------------------------------------------------
Objective: To establish a ultra-performance liquid chromatography (UPLC) method for the simultaneous determination of chlorogenic acid, caffeic acid, 1, 3-dicaffeoylquinic acid, luteolin-7-O-β-D-glucoside, 3, 4-dicaffeoylquinic acid, 3, 5-dicaffeoylquinic acid, 4, 5-dicaffeoylquinic acid, luteolin, linarin and apigenin in Chrysanthemum indicum. Methods: The separation was carried out on an Agilent Eclipse Plus C18 (2.1 mm×100 mm, 1.8 μm) column eluted with methanol (A) and 0.3% phosphoric acid (B) with gradient mode at a flow rate of 0.4 mL·min-1. The column temperature was 25℃ and the detection wavelength was set at 326 nm. Results: Good separation of chlorogenic acid, caffeic acid, 1, 3-dicaffeoylquinic acid, luteolin-7-O-β-D-glucoside, 3, 4-dicaffeoylquinic acid, 3, 5-dicaffeoylquinic acid, 4, 5-dicaffeoylquinic acid, luteolin, linarin and apigenin was achieved within 38 min. Calibration curves of the ten components showed good linear relationship (r>0.999 2, n=6). The average recoveries were within 96.4%-103.2% (RSD<2.0%, n=6). The content ranges of the above mentioned 10 components in 6 batches of samples were 1.018-3.430, 0.079-0.365, 0-0.269, 1.198-2.754, 0.185-0.765, 1.135-6.659, 0.587-2.808, 0.103-1.663, 0.495-13.050 and 0.214-0.933 mg·g-1, respectively. Conclusion: The method is simple, accurate and repeatable and can be used for simultaneous determination of multi-components in Chrysanthemum indicum, which provides scientific base for comprehensive evaluation and quality control of the herb.
-----参考文献:---------------------------------------------------------------------------------------
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