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首页> 外文期刊>Analytical Sciences >Capillary Electrophoresis-Amperometric Determination of Antioxidant Propyl Gallate and Butylated Hydroxyanisole in Foods
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Capillary Electrophoresis-Amperometric Determination of Antioxidant Propyl Gallate and Butylated Hydroxyanisole in Foods

机译:毛细管电泳-安培法测定食品中的抗氧化剂没食子酸丙酯和丁基化羟基苯甲醚

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Capillary electrophoretic separation coupled with end-column amperometric detection for the simultaneous quantification of butylated hydroxyanisole (BHA) and propyl gallate (PG) in food was developed. Important factors affecting separation and detection, such as the running buffer, separation voltage, and detection potential, were investigated in detail. An improved working electrode preparation method was used, where a carbon disk of 33 µm in diameter was sealed in a tip and positioned opposite the outlet of a capillary. The experiments indicated that the preparation method was simple, and the obtained electrode exhibited good flexibility and stability for the determination of phenolic antioxidants. The separation was carried out within 5 min using a 50 cm length capillary, with a solution containing 5 mM phosphate and 5 mM borax of pH 8.84 as a separation buffer, and a separation potential of 20 kV. Amperometric detection was achieved with an applied potential of 0.70 V versus Ag|AgCl| saturated KCl. There was excellent linearity between the peak current and the concentrations of the analytes in the range of 1.8 - 180.2 µg/mL for BHA and 10.6 - 212.2 µg/mL for PG, respectively. Relative standard deviations of 4.92% for BHA and 5.27% for PG were obtained, respectively. The developed method was successfully applied for the determination of antioxidants in several commercial foods.
机译:开发了毛细管电泳分离与末端色谱安培检测相结合的食品中丁基化羟基茴香醚(BHA)和没食子酸丙酯(PG)的同时定量方法。详细研究了影响分离和检测的重要因素,例如运行缓冲液,分离电压和检测电位。使用了一种改进的工作电极制备方法,其中将直径为33 µm的碳盘密封在尖端中,并与毛细管出口相对。实验表明,制备方法简单,所得电极具有良好的柔性和稳定性,可用于测定酚类抗氧化剂。使用长度为50 cm的毛细管在5分钟内进行分离,其中含有5 mM磷酸盐和5 mM pH为8.84的硼砂的溶液作为分离缓冲液,分离电位为20 kV。相对于Ag | AgCl |,施加0.70 V的电位可实现安培检测饱和氯化钾。 BHA和PG的峰值电流和分析物浓度之间的线性关系极佳,分别为1.8-180.2 µg / mL和10.6-212.2 µg / mL。 BHA和PG的相对标准偏差分别为4.92%和5.27%。所开发的方法已成功用于几种商业食品中抗氧化剂的测定。

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