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作 者:陈红 游元元[1,3] 潘晓鹃 CHEN Hong;YOU Yuanyuan;PAN Xiaojuan(School of Medicine of Chengdu Medical College Chengdu Sichuan 610500, China;The Specific Structure of Sichuan Province, the Small Molecular Drugs Research Laboratory Chengdu Sichuan 610500, China;Sichuan Provincial Academy of Traditional Chinese Medicine Chengdu Sichuan 610041, China)
机构地区:[1]成都医学院药学院,四川成都610500 [2]四川省中医药科学院,四川成都610041 [3]四川省高校结构特异性小分子药物研究重点实验室,四川成都610500
出 处:《四川中医》2018年第3期68-71,共4页Journal of Sichuan of Traditional Chinese Medicine
基 金:四川省教育厅重点项目(No.13ZC074)
摘 要:目的:建立通贤柚外果皮的HPLC指纹图谱,并测定柚皮苷、野漆树苷、异欧前胡素3种活性物质的含量。方法:色谱柱为Sepax Amethyst C18-H(250×4.60mm,5μm),流动相为乙腈~0.1%甲酸梯度洗脱,流速1.0ml/min,检测波长为283nm(柚皮苷、异欧前胡素),337nm(野漆树苷),柱温25℃,进样量20μl。结果:建立了通贤柚外果皮的HPLC指纹图谱,确定了16个共有色谱峰。3种活性物质在实验条件下得到有效分离,分别在0.041~0.409mg/m L、0.006~0.063mg/m L与0.008~0.081mg/m L范围内与峰面积呈良好的线性关系,平均加样回收率分别为98.09%、100.24%与102.53%。结论:所建立的指纹图谱与含量测定方法可用于通贤柚外果皮的质量控制。Objective: To establish the HPLC fingerprints of outer pericarp of Tongxian Pomelo and determine the content of naringin,rhoifolin and isoimperatorin. Methods: HPLC was performed on a Sepax Amethyst C18-H analytical column( 250 ×4. 60 mm,5μm) with gradient elution using acetonitrile and 0. 1% aqueous formic acid as the mobile phase at a flow rate of1. 0 ml/min^(-1). The detection wavelength was 283 nm( naringin,isoimperatorin),337 nm( rhoifolin). The column temperature was set at 25℃ and the injection valume was 20μl. Results: The HPLC fingerprint of outer pericarp of Tongxian Pomelo was established. 16 peaks were selected as the characteristic common peaks. The chromatographic peaks of 3 compounds could be separated well in the above cases. The linear ranges were 0. 041 ~ 0. 409 mg/ml,0. 006 ~ 0. 063 mg/ml and 0. 008 ~ 0. 081 mg/ml,respectively. The average recoveries were 98. 09%,100. 24% and 102. 53%,respectively. Conclusion: The established method can be used for the quality control of outer pericarp of Tongxian Pomelo.
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