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Development of a stacking-CZE method for the analysis of phenolic acids.

机译:开发了用于分析酚酸的Stacking-CZE方法。

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摘要

Eight phenolic acids were analyzed by capillary zone electrophoresis. On-line analyte preconcentration was carried out by hydrodynamic injection of large volume of sample followed by removal of the bulk of the low conductivity sample matrix by polarity switching. The optimal electrolyte system consisted of 50mM sodium tetraborate of pH 9.0 (adjusted with 0.1 M phosphoric acid) containing 2% of alpha-cyclodextrin. The separations were carried out with a fused silica capillary (effective length 50 cm, i.d. 50 microm) and monitored at 200 nm. Under optimized preconcentration conditions (sample injection 99 s at 100 mbar and the polarity switching time 1.0 min) linear calibration ranges (0.1-2.0 microg/ml, R=0.9979-0.9995), favourable limits of detection (0.01-0.025 microg/ml) and good repeatability of the peak areas (R.S.D.: 2.76-5.69%, n=6) were achieved.
机译:通过毛细管区带电泳分析了八种酚酸。在线分析物预浓缩是通过流体动力注入大体积的样品,然后通过极性切换除去大部分低电导率样品基质来进行的。最佳电解质系统由50mM pH 9.0的四硼酸钠(用0.1 M磷酸调节)组成,其中含有2%的α-环糊精。用熔融石英毛细管(有效长度50cm,即50微米)进行分离,并在200nm下监测。在优化的预浓缩条件下(在100 mbar下进样99 s,极性切换时间为1.0分钟)的线性校准范围(0.1-2.0 microg / ml,R = 0.9979-0.9995),有利的检出限(0.01-0.025 microg / ml)峰面积的重复性好(RSD:2.76-5.69%,n = 6)。

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