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作 者:李艳[1] 高英[1] 辛永涛[1] 张静[1] 李卫民[1]
出 处:《中国实验方剂学杂志》2015年第4期68-70,共3页Chinese Journal of Experimental Traditional Medical Formulae
摘 要:目的:石榴酸(C18:3)在结构上为顺9,反11,顺13-十八碳三烯酸,为长链烃类,在200-400nm没有吸收,无法直接用紫外检测器进行检测,本实验采用柱前衍生化方法,使石榴酸带上一个强发色团,使其在200-400nm有最大吸收,建立石榴籽油中指标性成分石榴酸的柱前衍生化HPLC分析方法。方法:以ω-溴代苯乙酮作为衍生化试剂,以三乙醇眩为相转移催化剂,对石榴籽油进行柱前衍生化,色谱条件采用Diamonsi C18色谱柱(4.6mm×250mm,5μm),检测波长272nm,以甲醇-乙腈-水(68.5:20:11.5)为流动相,柱温30℃,流速1.0mL·min^-1。结果:石榴酸在0.0266-0.1330g·L^-1(r=0.999)线件关系良好,平均加样回收率为98.7%,RSD1.8%。结论:该法稳定性、重复性好,定量准确,可作为石榴籽油中“榴酸的定量方法,用于评价和控制石榴籽油的质量。Objective: As the long chain hydrocarbons, punicic acid (C18:3) on the structure of 9 (Z) , 11 (E), 13 (Z) -octadecatrienoic acid, which was in 200-400 nm absorption-free and can't be measured directly by UV detector. This experiment adopted column derivatization methods, made the punicic acid with a strong ehromophore in maximum absorption in 200-400nm. The determination method of punicicacid in pomegranate seed oil by HPLC was established in this thesis. Method: The punicic acid were derivatized with ω-bromoacetophenone as derivative reagent, triethanolamine as catalyst, the Diamonsi Clseolumn (4.6 mm×250 mm, 5μm) was used. The detection wavelength was set at 272 nm, column temperature 30℃, with methanol- acetonitrile-water (68.5: 20:11.5) aseluent, the flow rate was 1.0 mL·min^-1 Result : The standard curves of punicic acid is linear within in the range of 0.0266-0.1330g·L^-1 and the coefficient is 0.999. The average recovery of punieie acid is 98.7% , RSD is 1.8%. Conclusion: The method is reproducible and accurate, which can be used as the determination method of punicic acid inpomegranate seed oil, and used for the quality control of pomegranate seed oil.
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