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反相高效液相法测定滋肾利肝颗粒中芍药苷的含量(英文) 被引量:2

Determination of the Content of Paeoniflorin in Zishenligan Granule by Reversed-Phase High Performance Liquid Chromatography
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摘要 目的建立一种测定滋肾利肝颗粒中芍药苷含量的反相高效液相法。方法采用Kromasil C18柱,以甲醇-0.05mol·L^-1磷酸二氢钾溶液(32:68)为流动相,紫外检测波长230nm,流速1ml·min^-1。结果在所使用的色谱条件下,芍药苷出峰位置未见干扰,芍药苷在24.28~121.40μg·ml^-1浓度范围内线性关系良好(r=0.9999)。滋肾利肝颗粒中芍药苷的平均加样回收率为98.32%,相对标准偏差为1.34%(n=9)。结论该法操作简便,重现性好,可作为滋肾利肝颗粒生产上质量控制的一种可信工具。 Objective To establish a RP - HPLC method for determination of the content of Paeoniflorin in Zishenligan Granule. Methods The analysis was carried out by using a Kromasil C18 analytical column with methanol and 0.05mol·L^-1 potassium dihydrogen phosphate solution (32:68, v/v) as mobile phase. The UV detection wavelength was 230nm and the flow rate was 1ml·min^-1 Results Under the chromatographic conditions used, there was no interference found in the position of Paeoniflorin peak. Paeoniflorin had fine linear responses ( r = 0. 999 9) in the concentration range of 24.28 - 121.40 μg·ml^-1, the average recovery of Paeoniflorin in Zishenligan Granule was 98.32% with the relative standard deviation of 1.34% ( n = 9). Conclusion The method employed in this analysis is convenient with good repetition and can be used as a reliable tool for quality control in the production of Zishenligan Granule.
出处 《时珍国医国药》 CAS CSCD 北大核心 2006年第11期2369-2371,共3页 Lishizhen Medicine and Materia Medica Research
关键词 滋肾利肝颗粒 芍药苷 反相高效液相法 定量分析 Zishenligan Granule Paeoniflorin Reversed - Phase High Performance Liquid Chromatography Quantitative Analysis
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  • 1Committee of National Pharmacopoeia, "Pharmacopoeia of People' s Republic of China" [ S ]. Press of Chemical Industry, Beijing, 2005,Vol. 1 :I09.
  • 2Editorial Committee of Chinese Materia Medica, " Chinese Materia Medica", Essential Edition [ M ]. Shanghai Science and Technology Press, Shanghai, 1998, Vol. 1:647, 659.
  • 3戴静,方娜娜.薄层层析-紫外分光光度法测定十全大补胶囊中芍药苷含量[J].天然产物研究与开发,2003,15(3):206-207. 被引量:11
  • 4Mi ZHOU, Hong CAI, Zhuging HUANG, Yuqing SUN. HPLC Method for the Determination of Paeoniflorin in Paeonia Lactiflare Pall and its preparations[ J ]. Biomedical Chromatography, 1998, 12( 1 ) : 43.
  • 5Gang CHEN, Luyan ZHANG, Pengyuan YANG. Rapid Determination of Paeoniflorin and Three Sugars in Radix Paeoniae Alba by Capillary Electrophoresis[ J]. Analytical Sciences, 2005, 21 (3): 247.

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