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作 者:郝荣荣[1] 杨倩[1] 曹蔚[1] 肖会敏[1] 王四旺[1]
机构地区:[1]第四军医大学药学院天然药物学教研室,陕西西安710032
出 处:《现代生物医学进展》2014年第20期3840-3843,3856,共5页Progress in Modern Biomedicine
基 金:陕西省"13115"科技创新工程技术研究中心基金(S2010ZDGC105)
摘 要:目的:建立同时测定椒目及椒目仁油中α-亚麻酸含量的HPLC方法。方法:用固定相为Kromasil C18柱(250mm×4.6mm,5μm),流动相为乙腈-1%醋酸溶液(90:10),检测波长为205nm,流速为1.0mL·min-1,柱温:25℃,进样量:10此,测定椒目及椒目仁油中α-亚麻酸的含量;结果:α-亚麻酸在(22-500)μg·mL-1浓度范围内线性关系良好,5批椒目和椒目仁油中α-亚麻酸的平均含量分别为4.56%,32.72%,平均回收率分别为99.87%,98.97%。结论:所建方法操作简便,准确可靠,重现性良好,可有效的控制椒目及椒目仁油的质量。Objective: To establish the HPLC method to determine the content of α-linolenic acid in the Zanthoxylum bungeanum Maxim and the seeds oil from Zanthoxylum bungeanum Maxim. Methods: With the stationary phase for Kromasil C18 column (250 mm ×4.6mm,5μm), mobile phase of acetonitrile and 1% acetic acid solution (90:10), detection wavelength of 205 nm, flow rate of 1.0 mL min -i, column temperature: 25 ℃, sample quantity: 10 uL.to determine the content of α-linolenic acid in the Zanthoxylum bungeanum Maxim and the seeds oil from Zanthoxylum bungeanum Maxim. Results: Linear range of a-linolenic acid was (22-500) μg-mL-1 , and the average contents of a-linolenic acid were 4.56% and 32.72%, the average recoveries of a-linolenic acid were 99.87% and 98.97% for Zanthoxylum bungeanum Maxim and the seeds oil from Zanthoxylum bungeanum Maxim respectively. Conclusion: The method is simple, accurate, reliable and with good reproducibility, which can effectively control the quality of Zanthoxylurn bungeanum Maxim and the seeds oil from Zanthoxylum hungeanum Maxim.
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