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Simultaneous determination of pharmaceutical and personal care products in wastewater by capillary electrophoresis with head-column field-amplified sample stacking

机译:毛细管电泳-头柱场放大样品叠加同时测定废水中的药品和个人护理产品

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A sensitive and reliable method using capillary zone electrophoresis with UV-diode array detection (CZE-DAD) has been developed and validated for trace determination of nineteen pharmaceutical and personal care products (PPCPs) in wastewater. Due to the lack of sensitivity of UV-vis detection, a solid-phase extraction (SPE) method for off-line preconcentration and cleanup of water samples, in combination with an on-line preconcentration methodology named head-column field-amplified sample stacking (FASS), has been applied. Several parameters affecting separation and FASS efficiency were investigated in detail, including the buffer pH and concentration, organic modifier, sample matrix, water plug, and electrokinetic injection voltage and time. Under the optimal FASS-CZE conditions, high efficiency was achieved and nineteen PPCPs were baseline separated within 27 min. The accuracy of this assay was ensured by spiking of real samples with standard known concentrations and the intra-day and inter-day relative standard deviations (RSDs) were below 5.6 and 6.3%, respectively. The average recoveries for water samples with the studied PPCPs were greater than 64.7 ?± 1.1%. The limits of detection (LODs) were estimated to range from 1.4 to 46.4 ng La?’1 for the studied compounds. This method was successfully applied for the simultaneous determination of PPCPs in wastewater samples from a sewage treatment plant.
机译:已经开发了一种灵敏且可靠的方法,该方法使用毛细管区带电泳和UV二极管阵列检测(CZE-DAD),并已用于痕量测定废水中的19种药物和个人护理产品(PPCP)。由于缺乏紫外线可见检测的灵敏度,因此采用离线萃取和水样固相萃取(SPE)方法,并结合称为柱头现场放大样品堆叠的在线预浓缩方法(FASS),已应用。详细研究了影响分离和FASS效率的几个参数,包括缓冲液pH和浓度,有机改性剂,样品基质,水塞以及电动进样电压和时间。在最佳FASS-CZE条件下,可实现高效率,并且在27分钟内基线分离了19种PPCP。通过掺加标准已知浓度的真实样品来确保该测定的准确性,并且日内和日间相对标准偏差(RSD)分别低于5.6%和6.3%。使用所研究的PPCP的水样品的平均回收率大于64.7±1.1%。对于所研究的化合物,检出限(LOD)估计为1.4到46.4 ng La?1。该方法成功地用于同时测定污水处理厂废水样品中的PPCP。

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