首页> 外文期刊>Journal of Agricultural and Food Chemistry >In-Capillary Derivatization and Stacking Electrophoretic Analysis of γ-Aminobutyric Acid and Alanine in Tea Samples To Redeem the Detection after Dilution To Decrease Matrix Interference
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In-Capillary Derivatization and Stacking Electrophoretic Analysis of γ-Aminobutyric Acid and Alanine in Tea Samples To Redeem the Detection after Dilution To Decrease Matrix Interference

机译:茶样品中γ-氨基丁酸和丙氨酸的毛细管内衍生和堆叠电泳分析,以稀释后用于赎回检测以减少基质干扰

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An in-capillary derivatization and stacking capillary electrophoresis (CE) technique has been applied to redeem the detection of dilute analytes in the analysis of γ-aminobutyric acid (GABA) and alanine (Ala) in tea samples. Extracts from samples were diluted to eliminate matrix interference before introduction into the CE system. GABA and Ala in the diluted sample zone were derivatized with o-phthaldialdehyde/2-mercaptoethanol (OPA/2-ME) to form fluorescence-labeled products in the stacking process, and the labeled derivatives were then enriched by online stacking. Optimal conditions for the stacking, such as the concentration of the background buffer solution, the matrix of the sample zone (sample solution), and the volume of the sample injection, were investigated and then applied to real sample analysis. Under optimum conditions, the detections were linear in the range of 5.0 nM-2.5 μM with the square of correlation coefficients (R~2) of 0.9995 and 0.9992 for GABA and Ala, respectively. Detection limits were found to be 0.7 and 0.8 nM for GABA and Ala, respectively. Tea samples were analyzed with recoveries between 92.33 and 97.87% and between 94.36 and 96.46% for GABA and Ala, respectively. This method is a rapid, convenient, and sensitive process for determining GABA and Ala in complicated matrix samples such as tea samples.
机译:毛细管内衍生和堆叠毛细管电泳(CE)技术已用于赎回茶样品中γ-氨基丁酸(GABA)和丙氨酸(Ala)分析中的稀释分析物。在引入CE系统之前,将样品的提取物稀释以消除基质干扰。将稀释样品区中的GABA和Ala用邻苯二甲醛/ 2-巯基乙醇(OPA / 2-ME)衍生化以在堆叠过程中形成荧光标记的产物,然后通过在线堆叠富集标记的衍生物。研究了用于堆叠的最佳条件,例如背景缓冲溶液的浓度,样品区域的基质(样品溶液)和样品进样的体积,然后将其应用于真实样品分析。在最佳条件下,检测值在5.0 nM-2.5μM范围内呈线性,GABA和Ala的相关系数(R〜2)的平方分别为0.9995和0.9992。发现GABA和Ala的检出限分别为0.7和0.8 nM。分析茶叶样品时,GABA和Ala的回收率分别为92.33至97.87%和94.36至96.46%。该方法是一种快速,方便且灵敏的方法,用于测定复杂基质样品(例如茶样品)中的GABA和Ala。

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