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刊物信息

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-PDA同时测定三黄方药液10种成分含量

Simultaneous determination of ten ingredients in Sanhuangfang ethanol extract by UPLC-PDA

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出版年·卷·期(页码):2016,36 (8):0-0
DOI: 10.16155/j.0254-1793.2017.01.01
-----摘要:-------------------------------------------------------------------------------------------

目的:建立UPLC-PDA法同时测定三黄方药液中黄柏碱、黄芩苷、小檗碱、黄芩素、芦荟大黄素、汉黄芩素、大黄酸、大黄素、大黄酚、大黄素甲醚10种成分的含量。方法:采用Waters ACQUITY BEH C18(2.1 mm×100 mm,1.7 μm)色谱柱,以乙腈-0.1%磷酸水溶液为流动相,梯度洗脱,流速0.3 mL·min-1,柱温30℃,检测波长284 nm。结果:在一定浓度范围内,三黄方药液中10种成分均呈良好的线性关系(r>0.999);平均加样回收率为96.73%~101.7%(RSD<3%,n=6)。3批样品中黄柏碱、黄芩苷、小檗碱、黄芩素、芦荟大黄素、汉黄芩素、大黄酸、大黄素、大黄酚、大黄素甲醚含量分别在0.226~0.233、5.85~6.00、1.92~2.00、0.140~0.151、0.031 4~0.037 5、0.043 6~0.044 7、0.081 5~0.083 1、0.032 8~0.040 6、0.102~0.105、0.340~0.350 mg·mL-1结论:经方法学验证,本法可用于三黄方药液的质量控制。

-----英文摘要:---------------------------------------------------------------------------------------

Objective: To establish a UPLC-PDA method for simultaneous determination of ten ingredients, including phellodendrine,baicalin,berberine,baicalein,aloe-emodin,wogonin,rhein,emodin,chrysophanol and physcion,in Sanhuangfang ethanol extract.Methods: The chromatographic analysis was carried out on an ACQUITY BEH C18 column(2.1 mm×100 mm,1.7 μm).The mobile phase consisted of acetonitrile-0.1% phosphoric acid solution with gradient elution at a flow rate of 0.3 mL·min-1.The column temperature was 30℃,and the detection wavelengths were set at 284 nm.Results: Within a certain concentration range,the ten ingredients all showed good linear relationship(r>0.999) and the average recoveries were with the range of 96.73%-101.7% (RSD<3%,n=6).The contents of phellodendrine,baicalin,berberine,baicalein,aloe-emodin,wogonin,rhein, emodin,chrysophanol and physcion in 3 samples were 0.226-0.233,5.85-6.00,1.92-2.00,0.140-0.151, 0.031 4-0.037 5,0.043 6-0.044 7,0.081 5-0.083 1,0.032 8-0.040 6,0.102-0.105,and 0.340-0.350 mg·mL-1, respectively.Conclusion: The established method can be used for the quality control of Sanhuangfang ethanol extract.

-----参考文献:---------------------------------------------------------------------------------------

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