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HPLC同时测定龙血竭及其提取物中5个有效成分的含量
引用本文:李云,萧伟,秦建平,郭瑛,祝倩倩.HPLC同时测定龙血竭及其提取物中5个有效成分的含量[J].中国中药杂志,2012,37(7):929-933.
作者姓名:李云  萧伟  秦建平  郭瑛  祝倩倩
作者单位:1. 南京中医药大学,江苏 南京 210046;中药制药过程新技术国家重点实验室(筹),江苏 连云港 222001
2. 江苏康缘药业股份有限公司,江苏 连云港 222001;中药制药过程新技术国家重点实验室(筹),江苏 连云港 222001
基金项目:国家"重大新药创制"科技重大专项(2011ZX09401-097)
摘    要:目的:建立HPLC同时测定龙血竭及其提取物中龙血素A,龙血素B,7,4’-二羟基黄酮,紫檀茋,白藜芦醇含量的方法。方法:采用Kromasil 100-5 C18(4.6 mm×250 mm,5μm)色谱柱;流动相乙腈-1%冰醋酸,梯度洗脱;流速1 mL.min-1;柱温40℃;检测波长龙血素A和龙血素B为278 nm,7,4’-二羟基黄酮、紫檀茋和白藜芦醇为319 nm。结果:5个有效成分在40 min内均达到基线分离,线性关系良好(r≥0.999 7)。龙血竭中龙血素A,龙血素B,7,4’-二羟基黄酮,紫檀茋,白藜芦醇的平均回收率分别为102.9%,96.81%,97.29%,100.7%,103.7%,RSD分别为0.23%,1.5%,0.42%,0.58%,0.34%;龙血竭提取物中龙血素A,龙血素B,7,4’-二羟基黄酮,紫檀茋,白藜芦醇的平均回收率分别为102.2%,96.93%,97.90%,102.0%,103.3%,RSD分别为1.7%,0.91%,1.4%,1.5%,1.2%。结论:本方法操作简便、结果准确,具有较好的重复性和稳定性,为龙血竭及其提取物的质量控制提供了一个很好的参考。

关 键 词:HPLC  龙血竭  龙血素A  龙血素B  7  4’-二羟基黄酮  紫檀茋  白藜芦醇
收稿时间:2011/11/25 0:00:00

Simultaneous determination of five active components in resina draconis and its extract by HPLC
LI Yun,XIAO Wei,QIN Jianping,GUO Ying and ZHU Qianqian.Simultaneous determination of five active components in resina draconis and its extract by HPLC[J].China Journal of Chinese Materia Medica,2012,37(7):929-933.
Authors:LI Yun  XIAO Wei  QIN Jianping  GUO Ying and ZHU Qianqian
Institution:Nanjing University of Chinese Medicine, Jiangsu 210000, China; State Key Laboratory of Pharmaceutical New-tech for Chinese Medicine, Lianyungang 222001, China;Jangsu Kanion pharmaceutical Co., Ltd, Lianyungang 222001, China; State Key Laboratory of Pharmaceutical New-tech for Chinese Medicine, Lianyungang 222001, China;Jangsu Kanion pharmaceutical Co., Ltd, Lianyungang 222001, China; State Key Laboratory of Pharmaceutical New-tech for Chinese Medicine, Lianyungang 222001, China;Jangsu Kanion pharmaceutical Co., Ltd, Lianyungang 222001, China; State Key Laboratory of Pharmaceutical New-tech for Chinese Medicine, Lianyungang 222001, China;Nanjing University of Chinese Medicine, Jiangsu 210000, China; State Key Laboratory of Pharmaceutical New-tech for Chinese Medicine, Lianyungang 222001, China
Abstract:Objective: To establish an HPLC method for simultaneous determination of contents of loureirin A,loureirin B,7,4′-dihydroxy flavone,pterostilbene and resveratrol in resina draconis and its extracts.Method: Kromasil 100-5C18 column(4.6 mm×250 mm,5 μm) was used with the mobile phase of acetonitrile-1% glacial acetic acid at a flow rate of 1.0 mL·min-1 and the column temperature at 40 ℃.The detective wave length of loureirin A and B was detected at 278 nm,and 7,4′-dihydroxy flavone,pterostilbene and resveratrol was at 319 nm.Result: All the five active components reached the resolved peaks within 40 min,indicating a good linearity(r≥0.999 7).The average recoveries of loureirin A,loureirin B,7,4′-dihydroxy flavone,pterostilbene and resveratrol in resina draconis were 102.9%,96.81%,97.29%,100.7% and 103.7%,with RSDs of 0.23%,1.5%,0.42%,0.58% and 0.34%,respectively.The average recoveries of loureirin A,loureirin B,7,4′-dihydroxy flavone,pterostilbene and resveratrol in extract of resina draconis were 102.2%,96.93%,97.90%,102.0% and 103.3%,with RSDs of 1.7%,0.91%,1.4%,1.5% and 1.2%,respectively.Conclusion: The method is so easy,accurate,highly repeatable and stable that it provides good reference for the quality control of resina draconis and its extracts.
Keywords:HPLC  resina draconis  loureirin A  loureirin B  7  4'-dihydroxy flavone  pterostilbene  resveratrol
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