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采用三相溶剂系统的高效液相色谱-串联质谱法测定废水中药物的验证。

Validation of a liquid chromatography coupled with tandem mass spectrometry method for the determination of drugs in wastewater using a three-phase solvent system.

机构信息

Scuola di Ingegneria, Università degli Studi della Basilicata, Potenza, Italy.

Dipartimento di Scienze, Università degli Studi della Basilicata, Potenza, Italy.

出版信息

J Sep Sci. 2020 Mar;43(5):886-895. doi: 10.1002/jssc.201900509. Epub 2020 Jan 15.

DOI:10.1002/jssc.201900509
PMID:31849166
Abstract

Pharmaceuticals constitute one of the most important emerging classes of environmental pollutants. A three-phase solvent system of water, water containing 0.1% of formic acid and acetonitrile was successfully used to separate, by liquid chromatography with mass spectrometry (LC-MS), polarity-matched pharmaceuticals, that is, carbamazepine, clarithromycin, and erythromycin, as well as amoxicillin and metformin. Despite of polarity similarities, these pharmaceuticals were completely resolved in the analytical run time of 15 min. The optimized three-phase solvent system based-method was validated for the simultaneous analysis of six matched-polarity pharmaceuticals in wastewater samples. Good linearity (coefficient of determination more than 0.993) and precision (relative standard deviation less than 15.66%) were achieved. Recovery of analytes from the wastewater was between 0.70 and 1.18. Limits of detections ranged from 0.0001 to 0.5114 µg/L. No significant matrix effect, evaluated by post extraction addition, was observed in the electrospray ionization (ESI) source. Then, this methodology has been successfully applied to environmental study of pharmaceutical residues occurring in influent and effluent wastewater samples, from the main wastewater treatment plant in Potenza (Basilicata, Southern Italy).

摘要

药品是最重要的新兴环境污染物类别之一。我们成功地使用了水、含 0.1%甲酸的水和乙腈的三相溶剂系统,通过液相色谱-质谱联用(LC-MS)分离出极性匹配的药品,即卡马西平、克拉霉素和红霉素,以及阿莫西林和二甲双胍。尽管极性相似,但这些药品在 15 分钟的分析运行时间内完全得到了分离。基于优化的三相溶剂系统的方法已针对废水样品中六种匹配极性药品的同时分析进行了验证。该方法具有良好的线性(决定系数大于 0.993)和精密度(相对标准偏差小于 15.66%)。从废水中回收分析物的回收率在 0.70 到 1.18 之间。检测限范围为 0.0001 至 0.5114 µg/L。在电喷雾电离(ESI)源中,通过萃取后添加评估,未观察到明显的基质效应。然后,该方法已成功应用于意大利南部巴西利卡塔大区波坦扎市(Potenza)主要污水处理厂的进水和出水废水中药物残留的环境研究。

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