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作 者:于桂芳[1,2] 秦建平[1,2] 李家春[1,2] 王婧[1,2] 毕宇安[1,2] 王振中[1,2] 萧伟[1,2]
机构地区:[1]江苏康缘药业股份有限公司,江苏连云港222001 [2]中药制药过程新技术国家重点实验室,江苏连云港222001
出 处:《中国实验方剂学杂志》2013年第15期82-85,共4页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家科技部973计划项目(2010CB735604)
摘 要:目的:建立同时测定林蛙油中α-亚麻酸、亚油酸和油酸含量的HPLC方法。方法:Alltima C18色谱柱(4.6 mm×250 mm,5μm),以乙腈-0.1%磷酸(80∶20)为流动相,流速1 mL.min-1,柱温30℃,检测波长203 nm。结果:α-亚麻酸在4.76~152.16 mg.L-1(r=1),亚油酸在15.36~491.59 mg.L-1(r=0.999 8),油酸在47.28~1512.80 mg.L-1(r=0.999 9)呈良好的线性关系;平均回收率α-亚麻酸为95.8%,RSD 1.79%(n=6);亚油酸为98.6%,RSD 1.32%(n=6);油酸为99.3%,RSD 1.59%(n=6)。结论:该法操作简便,结果准确,专属性强,重复性好,可作为林蛙油质量控制的参考。Objective: To establish a HPLC method for the determination of α-linolenic acid,linoleic acid and oleic acid in Oviductus Ranae.Method: Alltima C18(4.6 mm × 250 mm,5 μm) column was used with mobile phase of acetonitrile-0.1% phosphoric acid(80 ∶ 20);the flow rate was 1 mL.min-1;the column temperature was kept at 30 ℃;the detection wavelength was set at 203 nm.Result: The linear ranges of αlinolenic acid,linoleic acid and oleic acid were 4.755-152.16 mg.L-1(r =1),15.362-491.59 mg.L-1(r = 0.999 8) and 47.275-1512.8 mg.L-1(r = 0.999 9) respectively.The average recoveries were 95.8% with RSD 1.79% for α-linolenic acid,98.6% with RSD 1.32% for linoleic acid,99.3% with RSD 1.59% for oleic acid.Conclusion: The method is simple,accurate,convenient,specific and repeatable,which can be used to control the quality of α-linolenic acid,linoleic acid and oleic acid in Oviductus Ranae.
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