首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >On-line derivatization with on-line coupled normal phase liquid chromatography-gas chromatography using the through oven transfer adsorption desorption interface: Application to the analysis of total sterols in edible oils
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On-line derivatization with on-line coupled normal phase liquid chromatography-gas chromatography using the through oven transfer adsorption desorption interface: Application to the analysis of total sterols in edible oils

机译:在线耦合正相液相色谱-气相色谱在线转化,通过直通炉转移吸附解吸接口:在食用油中总固醇分析中的应用

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In the present work on-line derivatization is combined with on-line normal phase liquid chromatography-gas chromatography (NPLC-GC) to analyze total sterols in edible oils. The method uses the TOTAD interface with an additional LC injection valve to automatically introduce the derivatization reagent. The derivatization reaction takes place in the adsorbent material located inside the liner of the TOTAD interface. The samples were saponified with potassium hydroxide in an ethanolic solution and the unsaponifiable fraction was extracted with diethyl ether. The extract was then analyzed by on-line derivatization with on-line NPLC-GC, avoiding the laborious thin layer chromatography and off-line derivatization steps used in the Official European Union (EU) method. The relative standard deviations (RSDs) from the absolute peak area were lower than 14% except for campestanol. No variability in retention time was observed. Limits of detection (LODs) were less than 8.82. mg/kg. Different edible oils were analyzed using the proposed method and the results obtained were compared with those obtained using the Official EU method. There was good agreement between both methods for all the sterols analyzed.
机译:在当前的工作中,将在线衍生化与在线正相液相色谱-气相色谱(NPLC-GC)结合使用,以分析食用油中的总固醇。该方法将TOTAD接口与附加的LC进样阀配合使用,以自动引入衍生化试剂。衍生化反应发生在位于TOTAD界面衬里内部的吸附材料中。将样品在乙醇溶液中用氢氧化钾皂化,并将不皂化的级分用乙醚萃取。然后,通过使用在线NPLC-GC在线衍生化分析提取物,避免了费力的薄层色谱分析和官方欧联(EU)方法中使用的离线衍生化步骤。除樟脑甾醇外,与绝对峰面积的相对标准偏差(RSD)低于14%。没有观察到保留时间的变化。检出限(LOD)小于8.82。毫克/千克使用提出的方法分析了不同的食用油,并将获得的结果与使用Official EU方法获得的结果进行了比较。两种方法对所有分析的固醇都有很好的一致性。

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