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作 者:唐君苹[1] 曾宝[1,2] 黄孟秋[1] 肖祖平[1] 袁捷[1,2] 赖小平[1,2]
机构地区:[1]广州中医药大学,广州510006 [2]东莞广州中医药大学中医药数理工程研究院,广东东莞523808
出 处:《中南药学》2012年第11期811-814,共4页Central South Pharmacy
基 金:国家科技部重大新药创制专项(编号:2009ZX09103-388);广东省科技计划项目(编号:2009A030100014)
摘 要:目的建立巴豆油中游离型和结合型亚油酸的含量测定方法,为巴豆油的质量评价提供理论依据。方法采用RP-HPLC法,色谱条件:Kromasil 100-5C18(250 mm×4.6 mm,5μm)色谱柱;流动相:乙腈-0.1%甲酸(80:20),等度洗脱;流速:1.0 mL min-1;柱温:25℃;检测波长:210 nm。结果巴豆油中亚油酸在0.04~0.68 mg mL-1与峰面积呈良好的线性关系(Y=6.000×106X+6.916×104,r=0.999 7,n=7),平均回收率为98.0%(游离型)和98.5%(结合型)(n=6)。结论该方法简单、准确、重复性好,可为巴豆药材的质量控制提供参考。Objective To establish an RP-HPLC method for the determination of linoleic acid in crotonis oil,and to offer evidence for quality evaluation of fructus crotonis.Methods RP-HPLC method was used.The separation condition was as follows: Kromasil 100-5C18 chromatographic column(250 mm×4.6 mm,5 μm),elution was used with the mobile phase of acetonetrile-0.1% formic acid(80 : 20),the flow rate was 1.0 mL ? min-1,the column temperature was 25 ℃,and detection wavelength was 210 nm.Results The linear range of linoleic acid in crotonis oil was 0.04-0.68 mg ? mL-1.The correlation coefficient of calibration curves was 0.999 7.The average recovery was 98.0%(free type) and 98.5%(bound)(n=6).Conclusion The established method is simple,accurate,and repeatable,which will supply evidence for the quality evaluation of fructus crotonis.
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