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首页> 外文期刊>Journal of chromatography, A: Including electrophoresis and other separation methods >Directly suspended droplet microextraction with in injection-port derivatization coupled to gas chromatography-mass spectrometry for the analysis of polyphenols in herbal infusions, fruits and functional foods
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Directly suspended droplet microextraction with in injection-port derivatization coupled to gas chromatography-mass spectrometry for the analysis of polyphenols in herbal infusions, fruits and functional foods

机译:直接悬浮液滴微萃取,进样口衍生化-气相色谱-质谱联用,用于分析草药输液,水果和功能食品中的多酚

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摘要

A miniaturized liquid-phase extraction procedure based on directly suspended droplet microextraction is proposed for determining different classes of polyphenols. A derivatization reaction by means of in injection-port reaction with bis(trimethylsilyl)trifluoroacetamide is carried out to convert the polar non-volatile polyphenols into volatile derivatives. The separation and detection is carried out by coupling gas chromatography with mass spectrometry in the selected ion monitoring mode. The procedure uses undecanone, a low density organic solvent, and several factors influencing the extraction, collection efficiency and derivatization reaction are optimized. Excellent linearity was obtained for the range studied (0.05-500ngmL~(-1)). The limits of detection are between 0.011 and 0.13ngmL~(-1), depending on the compound, and the limits of quantification between 0.037 and 0.43ngmL~(-1). The sensitivity and detection limits for polyphenols using the DSDME sample pretreatment method were very low. Enrichment factors are between 413 and 578. The recoveries obtained for spiked samples are satisfactory for all the compounds. The coupled miniaturized method is applied to the sensitive determination of both cis- and trans-resveratrol isomers, piceatannol, catechin, epicatechin, quercetin and fisetin in herbal infusions, fruits, juices and functional foods.
机译:提出了一种基于直接悬浮液滴微萃取的小型液相萃取方法,用于测定不同种类的多酚。通过与双(三甲基甲硅烷基)三氟乙酰胺的注入口反应进行衍生化反应,以将极性非挥发性多酚转化为挥发性衍生物。分离和检测是通过气相色谱与质谱联用在选定的离子监测模式下进行的。该方法使用十一烷酮,低密度有机溶剂,并优化了影响萃取,收集效率和衍生化反应的几个因素。在所研究的范围内(0.05-500ngmL〜(-1))获得了极好的线性。检测限在0.011至0.13ngmL〜(-1)之间,具体取决于化合物;定量限在0.037至0.43ngmL〜(-1)之间。使用DSDME样品预处理方法对多酚的灵敏度和检测限非常低。富集因子在413至578之间。加标样品的回收率对所有化合物均令人满意。耦合的小型化方法适用于中草药输液,水果,果汁和功能性食品中顺式和反式白藜芦醇异构体,苦连酚,儿茶素,表儿茶素,槲皮素和非瑟定的灵敏测定。

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