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作 者:干国平[1] 朱红[1] 师磊[1] 史克莉[1] 刘焱文[1]
机构地区:[1]湖北中医学院"中药资源与中药复方"省部共建教育部重点实验室,武汉430061
出 处:《中国药师》2009年第1期12-14,共3页China Pharmacist
基 金:2004年湖北省教育厅自然科学类重点科研项目(2004D009)
摘 要:目的:建立山合欢皮正丁醇部位的指纹图谱。方法:采用HPLC法,色谱柱:Kromasil C_(18)(250mm×4.6mm,5μm);流动相:甲醇-乙腈0.4%磷酸溶液,梯度洗脱;流速:1.0ml·min^(-1);柱温:23℃;检测波长:210nm;参照物:icarside E5。结果:确定了25个共有峰,得到了以淫羊藿次苷E5为参照物的保留时间和相对峰面积,并利用《中药色谱指纹图谱相似度评价系统》计算相似度。结论:采用HPLC指纹图谱技术,可作为山合欢皮药材的质量控制。To establish the HPLC fingerprints of Albizia kalkora prain from different area. Method: the HPLC separation was performed on a Kromasil C18 column (250mm × 4.6mm,5 μm), gradient elution with mobile phase was methanol-acetonitrile -0.4% phosphoric acid solution at the flow rate of 1.0 ml·min^-1,the detection wavelength was 210 nm, the icariside E5 was reference standard. Result: Twenty-five co-possessing peaks were indicated, the retention time and relative peak area were obtained, the similar degrees was obtained from the similarity evaluation system for chromatographic fingerprint of TCM (version 2004 A). Conclusion: The HPLC fingerprint method can be used in the quality control of Albizia kalkora prain.
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