首页> 外文期刊>Electrophoresis: The Official Journal of the International Electrophoresis Society >In-line coupled single drop liquid-liquid-liquid microextraction with capillary electrophoresis for determining fluoroquinolones in water samples
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In-line coupled single drop liquid-liquid-liquid microextraction with capillary electrophoresis for determining fluoroquinolones in water samples

机译:用毛细管电泳在线耦合单滴液 - 液 - 液体微萃取,用于测定水样中的氟喹啉

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A simple in-line single drop liquid-liquid-liquid microextraction (SD-LLLME) coupled with CE for the determination of two fluoroquinolones was developed. The method is capable to quantify trace amount of analytes in water samples and to improve the sensitivity of CE detection. For the SD-LLLME, a thin layer of organic phase was used to separate a drop of 0.1M NaOH hanging at the inlet of the capillary from the aqueous donor phase. By this way, the analytes were extracted to the acceptor phase through the organic layer based on their acidic/basic dissociation equilibrium. The drop was immersed into the organic phase during 10 min for extraction and then it is directly injected into the capillary for the analysis. Parameters such as type and volume of organic solvent phase, aqueous donor, and acceptor phases and extraction time and temperature were optimized. The enrichment factor was calculated, resulting 40-fold for enrofloxacin (ENR) and sixfold for ciprofloxacin (CIP). The linear range were 20-400 g/L for ENR and 60-400 g/L for CIP. The detection limits were 10.1g/L and 55.3g/L for ENR and CIP, respectively, and a good reproducibility was obtained (4.4% for ENR and 5.6% for CIP). Two real water samples were analysed applying the new method and the obtained results presented satisfactory recovery percentages (90-100.3%).
机译:加上CE两个氟喹诺酮的判断结果是简单的在线单降液 - 液 - 液微萃取(SD-LLLME)的开发。所述方法能够定量分析物的痕量水样中,并改善CE检测的灵敏度。对于SD-LLLME,使用有机相的薄层分离0.1M的NaOH挂在从水供给相的毛细管入口的下降。通过这种方式,分析物是通过根据它们的酸性/碱性的离解平衡萃取,有机层至受体相。 10分钟提取时的下降浸入到有机相中,然后将其直接注射到毛细管中用于分析。参数,例如类型和有机溶剂相的体积,水供体,和受体相和萃取时间和温度进行了优化。富集因子计算,所得的40倍为恩诺沙星(ENR)和六倍环丙沙星(CIP)。的线性范围为20-400克/升用于ENR和60-400克/升用于CIP。检测限为10.1克/ L和55.3克/ L分别为ENR和CIP,并获得良好的再现性(4.4%对ENR和CIP 5.6%)。两个实水样品进行分析应用新的方法和所获得的结果呈现令人满意的回收百分比(90-100.3%)。

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