摘要
采用高效液相色谱法同时测定了口服液中的咖啡酸和阿魏酸含量,用Shim-pack VP—ODS柱(150mm×4.6mm,0.3μm),流动相:乙腈-3%的冰醋酸水溶液(体积比为11:89),流速:1.0mL/min,检测波长:321nm.咖啡酸和阿魏酸的浓度与峰面积呈良好的线性关系,其线性范围分别为0.126~63.0/μg/mL(r=0.9997)和0.120-24.0μg/mL(r=0.9999),平均回收率(n=3)分别为100.7%和99.9%,相对标准偏差(RSD)分别为2.11%和2.12%,检出限分别为42ng/mL和43ng/mL,样品中咖啡酸和阿魏酸的平均含量分别为3.26μg/mL和2.36μg/mL.
An HPLC method was established for the simultaneous determination of ferulic acid and caffeic acid in oral liquid. The Shim-pack VP-ODS column (150 min×4. 6 mm, 0. 3 μm) was used with a mobile phase of acetonitrile -3% acetic acid (11 : 89 by volume). The contents of ferulic acid and caffeic acid were detected at a wavelength of 321 nm. The flow rate was 1.0 mL/min and the injection volume was 20 μL. The calibration curve was linear in the range of 0. 126--63.0 μg/mL (r=0. 999 7) for caffeic acid and 0. 120--24.0 μg/mL (r=0. 999 9) for ferulic acid. The average recovery (n=3) was 100. 7% with RSD 2.11%/00 for caffeic acid and was 99.9% with RSD 2.12% for ferulic acid. The detection limit was 42 ng/mL for caffeic acid and 43 ng/mL for ferulic acid. The average content of the samples was 3.26μg/mL for caffeic acid and 2.36 μg/mL for ferulic acid.
出处
《西南大学学报(自然科学版)》
CAS
CSCD
北大核心
2009年第5期47-50,共4页
Journal of Southwest University(Natural Science Edition)
基金
重庆市科委自然科学基金资助项目(CSTC-2007BB0367)