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HPLC法同时测定大黄、厚朴药对提取物中7个成分的含量
引用本文:王婧宁,王梦瑶,张振秋,何秀菊,郝淞瑶,刘畅.HPLC法同时测定大黄、厚朴药对提取物中7个成分的含量[J].辽宁中医杂志,2014(4):763-766.
作者姓名:王婧宁  王梦瑶  张振秋  何秀菊  郝淞瑶  刘畅
作者单位:[1]辽宁中医药大学药学院,辽宁大连116600 [2]中国刑事警察学院,辽宁沈阳110035
基金项目:辽宁省科技厅课题(2013020176)
摘    要:目的:建立同时测定大黄、厚朴药对提取物中7个成分(芦荟大黄素、大黄酸、大黄素、大黄酚、大黄素甲醚、和厚朴酚、厚朴酚)含量的HPLC方法。方法:采用Agilent Eclipse XDB-C18(250 mm×4.6 mm,5μm)色谱柱,以甲醇(A)-0.1%磷酸水(B)为流动相,梯度洗脱,015 min,82%A→85%A;1515 min,82%A→85%A;1535 min,85%A→90%A;3535 min,85%A→90%A;3540 min,90%A→82%A;4040 min,90%A→82%A;4042 min,82%A→82%A,流速1.0 mL·min-1,检测波长为254 nm,柱温30℃。结果:大黄、厚朴药对提取物中7个成分芦荟大黄素、大黄酸、大黄素、大黄酚、大黄素甲醚、和厚朴酚、厚朴酚进样量分别在0.0279042 min,82%A→82%A,流速1.0 mL·min-1,检测波长为254 nm,柱温30℃。结果:大黄、厚朴药对提取物中7个成分芦荟大黄素、大黄酸、大黄素、大黄酚、大黄素甲醚、和厚朴酚、厚朴酚进样量分别在0.027900.2790μg(r=0.9992),0.061760.2790μg(r=0.9992),0.061760.6176μg(r=0.9991),0.050400.6176μg(r=0.9991),0.050400.5040μg(r=0.9997),0.19950.5040μg(r=0.9997),0.19951.995μg(r=0.9992),0.041281.995μg(r=0.9992),0.041280.4128μg(r=0.9993),0.46440.4128μg(r=0.9993),0.46444.644μg(r=0.9994),0.64324.644μg(r=0.9994),0.64326.432μg(r=0.9991)范围内与峰面积呈良好线性关系;平均回收率(n=5)分别为98.5%、99.4%、99.2%、98.5%、99.5%、99.0%、98.4%。结论:该方法准确可靠、重复性好,可用于大黄、厚朴药对提取物的质量控制。

关 键 词:大黄  厚朴  芦荟大黄素  大黄酸  大黄素  大黄酚  大黄素甲醚  和厚朴酚  厚朴酚  高效液相色谱

Simultaneous Determination of Seven Ingredients in Combination Extracts of Rhei Radix et Rhizoma and Magnoliae Officinalis by HPLC
WANG Jingning,WANG Mengyao,ZHANG Zhenqiu,HE Xiuju,HAO Songyao,LIU Chang.Simultaneous Determination of Seven Ingredients in Combination Extracts of Rhei Radix et Rhizoma and Magnoliae Officinalis by HPLC[J].Liaoning Journal of Traditional Chinese Medicine,2014(4):763-766.
Authors:WANG Jingning  WANG Mengyao  ZHANG Zhenqiu  HE Xiuju  HAO Songyao  LIU Chang
Institution:( College of Pharmacy, Liaoning University of Traditional Chinese Medicine, Dalian 116600, Liaoning, China)
Abstract:Objective .. To develop an HPLC method for determination of 7 indicative components ( aloe - emodin, rhein, emodin,chrysophanol,physcion, honokio, magnolia) in Rhei Radix et Rhizoma and Magnoliae Officinalis. Methods: Agilent Eclipse XDB - C18 ( 250 mm×4.6 mm,5 μm) was adopted ; the mobile phase was methanol (A) - 0.1% phosphoric acid solution (B) with gradient elution (0 - 15 min,82% A→85 % A ; 15 - 35 min, 85 % A→90% A ; 35 - 40 min, 90% A→82% A ;40 - 42 min, 82% A-→82% A) of methanol - water of 0.1% phosphoric acid at a flow rate of 1.0 mL ·min -1 and the detection wavelength was 254 nm; the column temperature was set at 30 ℃. Results : The content of 7 indicative components in Rhei Radix et Rhizoma and Magnoliae Officinalis was stable. The method had a good linearity in the ranges of 0.02790 - 0.2790 p.g ( r = 0.9992) for aloe - emodin ;0. 06176 - 0.6176μg ( r = 0.9991 ) for rhein ;0. 05040 - 0. 5040 ixg ( r = 0. 9997 ) for emodin ;0. 1995 - 1. 995 ug( r = 0. 9992 ) for chrysophanol ;0. 04128 - 0. 4128 ug( r = 0. 9993 ) for physcion ;0. 4644 -- 4. 644μg ( r = 0. 9994 ) for honokio ;0. 6432 6. 432 μg (r = 0. 9991 ) for magnolia. The average recoveries (n = 5 ) were 98.5% ,99.4% ,99.2% , 98.5% , 99.5% , 99. 0%, 98.4%, respectively. Conclusion:This method is dependable, simple and practical and may be used to control quality of Rhei Radix et Rhizoma and Magnoliae Officinalis.
Keywords:Rhei Radix et Rhizoma  Magnoliae Officinalis  aloe - emodin  rhein  emodin  chrysophanol  physcion  honokio  magnolia  HPLC
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