湖北农业科学 ›› 2022, Vol. 61 ›› Issue (6): 131-133.doi: 10.14088/j.cnki.issn0439-8114.2022.06.025

• 检测分析 • 上一篇    下一篇

金线草药材薄层鉴别及含量测定

李杉1, 覃子龙2, 陆梅元1, 马秀梅3, 曾海生3   

  1. 1.广西壮族自治区食品药品审评查验中心,南宁 530029;
    2.柳州市质量检验检测研究中心,广西 柳州 545001;
    3.右江民族医学院附属医院,广西 百色 533000
  • 收稿日期:2021-09-26 出版日期:2022-03-25 发布日期:2022-04-18
  • 通讯作者: 陆梅元(1981-),工程师,主要从事药品流通、医疗器械审评查验及中药相关研究工作,(电子信箱)182830367@qq.com。
  • 作者简介:李杉(1985-),女,广西南宁人,主管药师,主要从事药物分析研究,(电话)17891193205(电子信箱)188097724@qq.com。
  • 基金资助:
    2020年度广西高校中青年教师科研基础能力提升项目(2020KY13034); 广西壮族自治区中医药管理局科研课题(GZZC2019147); 右江民族医学院附属医院2019年度第一批高层次人才科研项目(Y20196311)

Thin layer identification and content determination of Antenoron filiforme (Thunb.) Roberty et Vantier

LI Shan1, QIN Zi-long2, LU Mei-yuan1, MA Xiu-mei3, ZENG Hai-sheng3   

  1. 1. Guangxi District Food and Drug Review and Inspection Center,Nanning 530029,China;
    2. Liuzhou Quality Inspection and Testing Research Center,Liuzhou 545001,Guangxi,China;
    3. The Affiliated Hospital of Youjiang Medical University for Nationalities,Baise 533000,Guangxi,China
  • Received:2021-09-26 Online:2022-03-25 Published:2022-04-18

摘要: 采用薄层色谱法(TLC),以甲苯∶乙酸乙酯∶甲酸(10∶3∶1.5)为展开剂,展开,晾干,喷3%三氯化铝-乙醇溶液,晾干,置紫外灯(360 nm)下检视。采用高效液相色谱法,以色谱柱Eclipse XDB-C18柱 (250 mm×4.6 mm,5 μm),10 μL进样,乙腈-0.1%的磷酸水溶液为流动相,梯度洗脱,流速1.0 mL/min,柱温30 ℃,检测波长360 nm,建立金线草(Antenoron filiforme)药材薄层鉴别方法以及含量测定。结果表明,对金线草药材进行薄层鉴别,斑点清洗,分离度好,能有效鉴别出金线草。同时,在30 min内完成对3种黄酮成分的分析,各成分间均达到基线分离,芦丁、槲皮素、山奈酚的线性范围分别为2.12~100.80 μg/mL(r=0.999 4)、25.50~758.86 μg/mL(r=0.999 8)、2.62~250.48 μg/mL(r=0.999 5),平均加样回收率(n=6)分别为98.42%、101.21%、97.92%。

关键词: 金线草(Antenoron filiforme), 芦丁, 槲皮素, 山奈酚, 薄层鉴别, 高效液相色谱

Abstract: Using thin layer chromatography (TLC), using toluene: ethyl acetate: formic acid (10∶3∶1.5) as the developing agent, unfold, dry, spray 3% aluminum trichloride-ethanol solution, dry, and set the UV lamp (360 nm) view. Using high performance liquid chromatography, the column Eclipse XDB-C18 (250 mm×4.6 mm, 5 μm), 10 μL injection, acetonitrile-0.1% phosphoric acid aqueous solution as the mobile phase, gradient elution, flow rate was 1.0 mL/min, the temperature was 30 ℃, and the detection wavelength was 360 nm, establishing the thin-layer identification method and content determination method of Antenoron filiforme. Results showed that thin layer identification of Antenoron filiforme, spot cleaning, good separation, can effectively identify Antenoron filiforme. This method completed the analysis of the three flavonoid components within 30 minutes, and each component reached a baseline separation. The linear ranges of rutin, quercetin and kaempferol were 2.12~100.80 μg/mL(r=0.999 4), 25.50~758.86 μg/mL(r=0.999 8), 2.62~250.48 μg/mL (r=0.999 5), respectively. The average recovery rates (n=6) were 98.42%, 101.21%, and 97.92%, respectively.

Key words: Antenoron filiforme, rutin, quercetin, kaempferol, thin layer identification, high performance liquid chromatography

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