首页> 外文期刊>Biomedical Chromatography: An International Journal Devoted to Research in Chromatographic Methodologies and Their Applications in the Biosciences >Simultaneous separation and analysis of camptothecin alkaloids in real samples by large-volume sample stacking in capillary electrophoresis
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Simultaneous separation and analysis of camptothecin alkaloids in real samples by large-volume sample stacking in capillary electrophoresis

机译:大体积样品堆叠在毛细管电泳中的实际样品中摄像石生物碱的同时分离与分析

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摘要

Large-volume sample stacking (LVSS) is commonly used as an effective online preconcentration method in capillary zone electrophoresis (CZE). In this paper, the method LVSS combined with CZE has been proposed to analyze camptothecin alkaloids. Optimum separation can be achieved in the following conditions: pH9.0; 25mm borate buffer containing 20mm sulfobutylether--cyclodextrin and 20mm ionic liquid 1-ethyl-3-methyllimidazole l-lactate; applied voltage 20kV; and capillary temperature 25 degrees C. The LVSS was optimized as hydrodynamic injection 4s at 5.0psi and the polarity switching time was 0.17min. Under the above conditions, the analytes could be separated completely in 20min and the detector response was increased compared with conventional hydrodynamic injection. The limits of detection were between 0.20 and 0.78g/L. A good linearity was obtained with correlation coefficients from 0.9991 to 0.9997. The recoveries ranged from 97.72 to 103.2% and the results demonstrated excellent accuracy. In terms of the migration time and peak area, the experiment was reproducible. The experimental results indicated that baseline separation can be obtained and this method is suitable for the quantitative determination of camptothecin alkaloids in real samples.
机译:大体积样品堆叠(LVSS)通常用作毛细管区电泳(CZE)中的有效的在线预浓度方法。本文已经提出了与CZE结合的方法,以分析喜树碱生物碱。在以下条件下可以实现最佳分离:ph9.0;含有20mM磺基醚的25mm硼酸盐缓冲液 - 环糊精和20mM离子液体1-乙基-3-甲基咪唑L-乳酸;施加电压20kV;和毛细管温度25摄氏度。LVSS被优化为5.0psi下的流体动力学注射4s,极性切换时间为0.17分钟。在上述条件下,分析物可以完全分离在20分钟中,与常规的流体动力学注射相比,探测器反应增加。检测限为0.20和0.78g /升。通过0.9991至0.9997的相关系数获得良好的线性度。回收率范围为97.72至103.2%,结果表明了优异的准确性。就迁移时间和峰面积而言,实验是可再现的。实验结果表明,可以获得基线分离,并且该方法适用于真实样品中摄像石生物碱的定量测定。

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