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Development and Validation of Capillary Electrophoresis Method for Simultaneous Determination of Six Pharmaceuticals in Different Food Samples Combining On-line and Off-line Sample Enrichment Techniques

机译:毛细管电泳法同时测定不同食物样品中六种药物的毛细管电泳方法的开发与验证结合在线和离线样品富集技术

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A rapid and highly sensitive capillary electrophoresis method was developed combining on-line and off-line sample enrichment techniques that are capable to determine six widely used pharmaceuticals, viz. amoxicillin, carbamazepine, diclofenac, indomethacin, ibuprofen, and paracetamol from various food samples. A new sample preconcentration technique, i.e., in situ aggregated microextraction, was utilized to extract the analytes from various food samples. The process was carried out by the formation of aggregate phase in situ in the aqueous sample by ion association between oppositely charged surfactants, viz. TironA (R) and cetyltrimethylammonium bromide. The separation and quantification of analytes were carried out in micellar electrokinetic chromatography mode at -20 kV. In short, the uncoated fused silica capillaries were filled with 80 mM phosphate buffer solution (pH 6.0) to act as leading electrolyte, and the samples were dissolved in 100 mM borate buffer and injected by electrokinetic mode applying -10 kV for 600 s. The method showed good linearity in between 0.06 and 50 mu g/L for all six pharmaceuticals. Good repeatability and recoveries were obtained for all analytes in the range of 94.45-106.32% using optimized experimental conditions. The limit of detection ranged from 0.02 to 0.08 mu g/L, and the limit of quantification ranged from 0.06 to 0.25 mu g/L for six pharmaceuticals. The sensitivity of the developed micellar electrokinetic chromatography method was increased about 2500-folds compared to conventional capillary zone electrophoresis method. Finally, the developed analytical procedure was applied successfully for the detection of selected pharmaceuticals in fruits, urine, and river water samples.
机译:快速且高灵敏度的毛细管电泳方法是组合在线和离线样品富集技术,该技术能够确定六种广泛使用的药品,ZIZ。 Amoxicillin,Carbamazepine,Diclofenac,Indomethacin,布洛芬和来自各种食物样品的扑热息痛。利用新的样品预浓缩技术,即原位聚集的微萃取物,从各种食物样品中提取分析物。通过在相对的带电表面活性剂,VIZ之间形成通过离子结合在水性样品中形成聚集相的方法进行。赤龙(r)和西甲基三甲基溴化物。分析物的分离和定量在-20kV下以胶束电动色谱模式进行。简而言之,将未涂覆的熔融石英毛细管填充有80mM磷酸盐缓冲溶液(pH6.0)以充当电解质,并将样品溶于100mM硼酸盐缓冲液中并通过电动模式喷射,施加-10kV 600秒。该方法显示出所有六种药物的0.06至50μg/ l的良好线性。使用优化的实验条件,在94.45-106.32%的所有分析物中获得良好的重复性和回收率。检测极限范围为0.02至0.08μmg/ l,定量限为六种药物的0.06至0.25μg/ l。与常规毛细管区电泳法相比,开发的胶束电动色谱法的敏感性增加约2500倍。最后,成功地应用了发育的分析程序,用于检测水果,尿和河水样品中所选药物。

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