中医临床研究2024,Vol.16Issue(6) :16-20.DOI:10.3969/j.issn.1674-7860.2024.06.003

高效液相色谱法测定蒲公英中5种成分的含量

Determination of five components in Pugongying by HPLC

李文静 王艳萍 刘荣宏 侯玉娇 洪博
中医临床研究2024,Vol.16Issue(6) :16-20.DOI:10.3969/j.issn.1674-7860.2024.06.003

高效液相色谱法测定蒲公英中5种成分的含量

Determination of five components in Pugongying by HPLC

李文静 1王艳萍 1刘荣宏 1侯玉娇 1洪博1
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作者信息

  • 1. 齐齐哈尔医学院药学院,黑龙江 齐齐哈尔,161006
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摘要

目的:本研究采用高效液相色谱法(High Performance Liquid Chromatography,HPLC)建立了蒲公英药材中绿原酸、咖啡酸、木犀草苷、菊苣酸、木犀草素5种成分的含量测定方法,完善和提高蒲公英的质量控制方法.方法:蒲公英药材样品经过超声法提取,分离与检测采用Waters ACQUITY BEH C18色谱柱(2.1 mm× 100mm,1.8 μm),以乙腈(B)-0.4%磷酸水溶液(A)为流动相,梯度洗脱;检测波长为320nm;流速:1.0mL/min;进样量:20μL;柱温:35 ℃.通过专属性考察、线性关系考察、精密度考察、重复性考察、稳定性考察和加样回收率试验来验证方法学.结果:绿原酸、咖啡酸、木犀草苷、菊苣酸和木犀草素的质量浓度范围分别为 60~1 920 μg/mL、3.22~103 μg/mL、3.22~103 μg/mL、68.125~2 180 μg/mL 和 3.31~106 μg/mL,以各成分的质量浓度(X)为横坐标、峰面积(Y)为纵坐标进行线性回归分析,呈良好的线性关系(r>0.998 7),平均加样回收率为98.62%~101.43%,RSD为0.68%~1.86%,仪器精密度、方法重复性和方法的稳定性良好(RSD均<2%).结论:该方法分离度好,精密度、稳定性、重复性均良好,加样回收率高,可作为蒲公英的质量控制方法,为蒲公英其他方面的研究奠定基础.

Abstract

Objective:In this study,the determination method of chlorogenic acid,caffeic acid,galuteolin,cichoric acid and luteolin in Pugongying(Taraxacum mongolicum)was established by HPLC,and the quality control method of Pugongying was improved and promoted.Methods:The samples of Pugongying herb were extracted by ultrasonic method,and then separated and detected by Waters ACQUITY BEH C18 chromatographic column(2.1 mm× 100 mm,1.8 μm).Acetonitrile(B)and 0.4%phosphoric acid aqueous solution(A)were used as mobile phase with gradient elution.The detection wavelength was 320 nm.Flow rate:1.0 mL/min;Injection volume:20 μL.Column temperature:35 ℃.The methodology was validated by exclusive inspection,linear relationship test,precision test,repeatability test,stability test and recovery test.Results:The concentrations of chlorogenic acid,caffeic acid,galuteolin,cichoric acid and luteolin ranged from 60 to 1 920 μg/mL,3.22 to 103 μg/mL,3.22 to 103 μg/mL,68.125 to 2 180 μg/mL and 3.31 to 106 μg/mL,respectively.Linear regression equation was carried out with the concentration(X)of each component as the abscissa and the peak area(y)as the ordinate,showing a good linear relationship(r>0.998 7),and the av-erage recovery was 98.62%-101.43%.The RSD range was 0.68%-1.86%.The instrument precision,method repeatability and method stability were good(RSD<2%).Conclusion:The method has good separation,precision,stability,repeatability and high recovery rate.It can be used as a quality control method of Pugongying and lays a foundation for other research of Pugongying.

关键词

蒲公英/高效液相色谱/成分/含量测定

Key words

Pugongying/HPLC/Component/Content determination

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基金项目

齐齐哈尔市社会发展科技攻关计划(LSFGG-2022048)

出版年

2024
中医临床研究
中华中医药学会

中医临床研究

影响因子:0.839
ISSN:1674-7860
参考文献量17
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