双波长HPLC同时测定八角莲中4′-去甲基鬼臼毒素鬼臼毒素 槲皮素 山柰素的含量
投稿时间:2018-06-24     点此下载全文
引用本文:钟水生,顾炳仁,周坚,张华锋,王亚琼,郝刚.双波长HPLC同时测定八角莲中4′-去甲基鬼臼毒素鬼臼毒素 槲皮素 山柰素的含量[J].中国现代中药,2018,20(12):1565-1568
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作者中文名作者英文名单位中文名单位英文名E-Mail
钟水生 ZHONG Shui-sheng 苏州市药品检验检测研究中心,江苏苏州215100 Suzhou Institute for Drug Control,Suzhou Jiangsu 215100,China 钟水生,主管中药师,研究方向:仪器分析及药品质量控制;Tel:(0512)68223525,E-mail:cpu-zhongshuisheng@163.com 
顾炳仁 GU Bing-ren 苏州市药品检验检测研究中心,江苏苏州215101 Suzhou Institute for Drug Control,Suzhou Jiangsu 215101,China  
周坚 ZHOU Jian 苏州市药品检验检测研究中心,江苏苏州215102 Suzhou Institute for Drug Control,Suzhou Jiangsu 215102,China  
张华锋 ZHANG Hua-feng 苏州市药品检验检测研究中心,江苏苏州215103 Suzhou Institute for Drug Control,Suzhou Jiangsu 215103,China  
王亚琼 WANG Ya-qiong 苏州市药品检验检测研究中心,江苏苏州215104 Suzhou Institute for Drug Control,Suzhou Jiangsu 215104,China  
郝刚 HAO gang 苏州市药品检验检测研究中心,江苏苏州215105 Suzhou Institute for Drug Control,Suzhou Jiangsu 215105,China  
中文摘要:目的:建立同时测定八角莲中木脂素类成分4′-去甲基鬼臼毒素、鬼臼毒素和黄酮类成分槲皮素、山柰素含量的方法。方法:采用Dikma C18 plus(250 mm×4.6 mm ,5 μm)色谱柱;流动相为甲醇-0.1%磷酸水溶液(50∶50);流速为1 mL·min-1;检测波长分别为290、360 nm。结果:4′-去甲基鬼臼毒素、鬼臼毒素、槲皮素、山柰素分别在进样量0.294 4~3.680、0.961 6~12.020、0.086 3~1.079 3、0.102 3~1.279 μg与峰面积呈现良好的线性关系;4个成分各个水平的方法回收率(n=9)均在97.1~102.1%。结论:该方法简便、准确,重复性良好,适用于八角莲中4′-去甲基鬼臼毒素、鬼臼毒素、槲皮素、山柰素4种成分的同时测定,能为八角莲药材和饮片的质量控制和临床应用提供依据。
中文关键词:八角莲  鬼臼毒素  4′-去甲基鬼臼毒素  槲皮素  山柰素  双波长HPLC
 
Simultaneous Determination of 4′-Demethylpodophyotoxin,Podophyllotoxin
Abstract:Objective:To establish a dual-wavelength HPLC method for simultaneous determination of 4′-demethylpodophyotoxin,odophyllotoxin,quercetin and kaempferide in Dysosmae Pleianthae Radix et Rhizoma.Methods:A Dikma C18 plus column(250 mm×4.6 mm,5 μm)was adopted,the mobile phase was a mixture of methanol and 0.1% phosphate acid solution(50:50)at a flow rate of 1 mL·min-1.Result:Good linearities were observed within the scope of 0.294 4-3.68 μg for 4′-demethylpodophyotoxin,0.961 6-12.02 μg for podophyllotoxin,0.086 34-1.079 3 μg for quercetin and 0.102 3-1.279 μg for kaempferide,respectively.The recoveries for the four components at each level were all in the range between 97.1-102.1%.Conclusion:The method was validated to be simple,accurate and robust,and applicable for the simultaneous measurement of the four components,thus provide basis for the quality control of Dysosmae Pleianthae Radix et Rhizoma.
keywords:Dysosmae Pleianthae Radix et Rhizoma  podophyllotoxin  4′-demethylpodophyotoxin  quercetin  kaempferide  dual-wavelength HPLC
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