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高效液相色谱法测定调胃丹中厚朴酚、和厚朴酚含量
引用本文:姜雪敏,王云龙,杨立志,任丽莉.高效液相色谱法测定调胃丹中厚朴酚、和厚朴酚含量[J].中国药业,2011,20(24):37-38.
作者姓名:姜雪敏  王云龙  杨立志  任丽莉
作者单位:黑龙江省鸡西市药品检验所,黑龙江,鸡西,158100
摘    要:目的建立调胃丹中厚朴酚、和厚朴酚的含量测定方法。方法采用Agilent Extend C18柱(250 mm×4.6 mm,5μm)为色谱柱,以乙腈-0.1%磷酸溶液(57∶43)为流动相,检测波长为294 nm,流速为1.0 mL/min。结果厚朴酚进样量在0.105 6~1.056 0μg范围内与峰面积具有良好线性关系,r=1.000 0;和厚朴酚进样量在0.044 9~0.448 8μg范围内与峰面积具有良好线性关系,r=1.000 0。厚朴酚的平均回收率为98.07%,RSD=1.14%(n=6);和厚朴酚的平均回收率为97.53%,RSD=0.60%(n=6)。结论所用方法结果简便、快速、准确,可用于调胃丹的质量控制。

关 键 词:含量测定  调胃丹  高效液相色谱法

Determination of Magnolol and Honokiol in Tiaowei Pills by HPLC
Jiang Xuemin,Wang Yunlong,Yang Lizhi,Ren Lili.Determination of Magnolol and Honokiol in Tiaowei Pills by HPLC[J].China Pharmaceuticals,2011,20(24):37-38.
Authors:Jiang Xuemin  Wang Yunlong  Yang Lizhi  Ren Lili
Institution:Jiang Xuemin,Wang Yunlong,Yang Lizhi,Ren Lili(Jixi Institute for Drug Control,Jixi,Heilongjiang,China 158100)
Abstract:Objective To establish a HPLC method for simultaneous determination of magnolol and honokiol in Tiaowei Pills. Methods The separation was performed on the Agilent Extend C18 column (250mm×4.6mm,5μm) with acetonitrile-0. 1% phosphoric acid (57:43) as the mobile phase. The UV detection wavelength was set at 294 nm and the flow rate was 1.0 mL/min. Results There was good linearity between the peak areas and concentrations in the range of 0. 105 6 - 1. 056 0 μg( r = 1. 000 0) for magnoM and 0. 044 9 -0. 448 8 μg( r = 1. 000 0) for honokiol respectively. The average recovery rates of magnolol and honokiol were 98.07%, RSD=1. 14% (n=6)and 97.53%, RSD =0. 60% (n =6),respectively. Conclusion The method is rapid, simple, accurate and can be applied for the quality control of Tiaowei Pills.
Keywords:content determination  Tiaowei Pills  HPLC  
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