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A multiclass method for the determination of pharmaceuticals in drinking water by solid phase extraction and ultra-high performance liquid chromatography-tandem mass spectrometry

机译:通过固相萃取和超高效液相色谱 - 串联质谱法测定饮用水中药物的多烷基方法

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摘要

In this work, a simple method for the determination of 20 pharmaceuticals of different classes in drinking water using solid phase extraction (SPE) and ultra-high performance liquid chromatography with tandem mass spectrometry (UHPLC-MS/MS) was developed and validated. Different sorbents, solvents and elution volumes were evaluated. The optimized conditions of the extraction step were the Strata (TM)-X cartridge, samples without pH adjustment but with addition of 0.1% (w/v) of EDTA, eluting solvent 1% (v/v) acetic acid in acetonitrile/methanol 1 : 1 (v/v) and an elution volume of 1 mL. Recovery results were adequate ranging from 70 to 119%, with relative standard deviation (RSD) # 19%. The limits of quantification and detection of the method were from 0.01 to 0.1 mg L-1 and from 0.003 to 0.03 mg L-1, respectively, considered suitable for monitoring of these compounds in drinking water. The proposed method was successfully applied in real samples. Atenolol, carbamazepine and paracetamol were found in some samples at concentrations <= 0.027 mu g L-1.
机译:在这项工作中,开发了一种使用固相萃取(SPE)和超高效液相色谱法测定饮用水中不同类别的20药物的简单方法和串联质谱(UHPLC-MS / MS)。评估不同的吸附剂,溶剂和洗脱体积。提取步骤的优化条件是Strata(TM)-X盒,没有pH调节的样品,但是加入0.1%(w / v)的EDTA,洗脱乙腈/甲醇中的溶剂1%(v / v)乙酸1:1(v / v)和1ml的洗脱体积。恢复结果足以从70〜119%的范围,相对标准偏差(RSD)#19%。定量和检测该方法的限制分别为0.01至0.1mg L-1和0.003至0.03mg L-1,认为适于监测这些化合物在饮用水中。该方法以实际样品成功应用。在浓度<=0.027μg1-1的一些样品中发现了阿扎罗尔,尿嘧啶素和扑热息痛。

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