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作 者:向孙敏[1] 韩丽[1] 刘李梅[1] 张超[1] 王莹[1] 谢兴亮[2]
机构地区:[1]成都中医药大学,中药资源系统研究与开发利用省部共建国家重点实验室培育基地,成都611137 [2]成都医学院药学院,成都610083
出 处:《中国实验方剂学杂志》2013年第14期13-16,共4页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家科技重大专项“十二五”重大新药创制项目(2012ZX09102201-103)
摘 要:目的:建立愈肠宁胶囊中苦参提取物生物碱类成分的HPLC指纹图谱的检测方法。方法:采用Kromasil NH2氨基柱(4.6 mm×250 mm,5μm),流动相乙腈-乙醇(8∶1)-3%磷酸水梯度洗脱,流速0.8 min.mL-1,检测波长220 nm,对10批苦参提取物进行HPLC指纹图谱检测,采用"中药色谱指纹图谱评价系统2004年版"进行评价。结果:苦参提取物采用氨基柱各峰分离效果好,确定了15个共有峰,并对其中4个色谱峰进行了指认,10批提取物的相似度均>0.9,提取物与药材指纹图谱间存在相关性。结论:该方法精密度、重复性、稳定性较好,为苦参提取物的质量控制提供了一种检测方法。Objective: To establish HPLC fingerprint detection for alkaloids from extract of Sophora flavescens in Yuchangning capsules.Method: Amino Kromasil NH2 column(4.6 mm × 250 mm,5 μm) was adopted,gradient eluted with mobile phase of acetonitrile-ethanol(8 ∶ 1)-3% phosphoric acid water,flow rate was 0.8 min.mL-1,detection wavelength was 220 nm.10 batches of extract of S.flavescens were detected by HPLC fingerprint,then evaluated with 2004 edition of ‘chromatographic fingerprint evaluation system of Chinese medicine’.Result: By taking Kromasil NH2 column,peaks separation of extract of S.flavescens was better,identified 15 common peaks and 4 of them were assigned.Similarity of these 10 batches extract was more than 0.9,correlation between fingerprints of extract and raw materials existed.Conclusion: This method had good precision,repeatability and stability,it could provide a detection method for quality control of extract of S.flavescens.
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