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高效液相色谱法同时测定香兰素与邻位香兰素 被引量:30

Simultaneous Determination of Vanillin and o-Vanillin by High Performance Liquid Chromatography
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摘要 建立了同时测定香兰素和邻位香兰素的高效液相色谱法。考察了流动相组成、柱温等因素对分析效率的影响。在流动相为5%乙酸-乙腈(60:40,体积比),流速1.0mL/min,柱温25℃的优化条件下,香兰素和邻位香兰素可在5min内实现分离。测定结果表明,香兰素和邻位香兰素在10~240mg/L范围内线性关系良好,相关系数均为0.9997;方法的检出限(S/N=3)分别为0.06、0.02mg/L;样品的加标回收率为99%~102%,相对标准偏差为0.2%~0.6%。该方法操作简单、快速,用于实际样品的分析,结果满意。 A high performance liquid chromatographic method was developed for the simultaneous separation and determination of vanillin and o-vanillin. Influences of mobile phase composition and column temperature on the separation were investigated. Under the condition of 5% acetic acid - acetonitrile (60 : 40, by volume) as mobile phase at a flow rate of 1.0 mL/min and 25 ℃, the vanillin and o-vanillin were separated in less than 5 min. The calibration curves of vanillin and o-vanillin showed good linearities in the range of 10 - 240 mg/L with both correlation coefficients of 0. 999 7. The limits of detection( S/N = 3 ) for vanillin and o-vanillin were 0.06 mg/L and 0.02 mg/L, respectively. The average recoveries at three spiked levels were in the range of 99% -102% with relative standard deviations of 0. 2% - 0.6%. The method was successfully used for the determination of vanillin and o-vanillin in real samples with satisfactory results.
出处 《分析测试学报》 CAS CSCD 北大核心 2011年第2期222-224,228,共4页 Journal of Instrumental Analysis
基金 辽宁省自然基金资助项目(20090655) 辽宁省教育厅2008年度科研计划项目(2008S184)
关键词 高效液相色谱法 香兰素 邻位香兰素 同分异构体 high performance liquid chromatography vanillin o-vanillin isomers
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