Department of Environmental Chemistry, IDAEA-CSIC, 08034 Barcelona, Spain.
Talanta. 2009 Nov 15;80(1):363-71. doi: 10.1016/j.talanta.2009.06.077. Epub 2009 Jul 8.
A simple and sensitive method for simultaneous analysis of 43 pharmaceutical compounds in sewage sludge and sediment samples was developed and validated. The target compounds were extracted using pressurized liquid extraction (PLE) and then purified and pre-concentrated by solid phase extraction (SPE) using a hydrophilic-lipophilic balanced polymer. PLE extraction was performed on temperature of 100 degrees C, with methanol/water mixture (1/2, v/v) as extraction solvent. The quantitative analysis was performed by liquid chromatography tandem mass spectrometry using a hybrid triple quadrupole-linear ion trap mass spectrometer (LC-QqLIT-MS). Data acquisition was carried out in selected reaction monitoring (SRM) mode, monitoring two SRM transitions to ensure an accurate identification of target compounds in the samples. Additional identification and confirmation of target compounds were performed using the Information Dependent Acquisition (IDA) function. The method was validated through the estimation of the linearity, sensitivity, repeatability, reproducibility and matrix effects. The internal standard approach was used for quantification because it efficiently corrected matrix effects. Despite the strong matrix interferences, the recoveries were generally higher of 50% in both matrixes and the detection and quantification limits were very low. Beside the very good sensitivity provided by LC-QqLIT-MS, an important characteristic of the method is that all the target compounds can be simultaneously extracted, treated and analysed. Hence, it can be used for routine analysis of pharmaceuticals providing large amount of data. The method was applied for the analysis of pharmaceuticals in river sediment and wastewater sludge from three treatment plants with different treatment properties (i.e. capacity, secondary treatment, quality of influent waters). The analysis showed a widespread occurrence of pharmaceuticals in the sludge matrices.
建立并验证了一种可同时分析污水污泥和沉积物样品中 43 种药物化合物的简单灵敏的方法。采用加压液体萃取(PLE)提取目标化合物,然后使用亲水亲脂平衡聚合物通过固相萃取(SPE)进行纯化和预浓缩。PLE 萃取在 100°C 的温度下进行,以甲醇/水混合物(1/2,v/v)作为萃取溶剂。采用混合三重四极杆-线性离子阱质谱仪(LC-QqLIT-MS)进行液相色谱串联质谱定量分析。采用选择反应监测(SRM)模式进行数据采集,监测两个 SRM 跃迁,以确保样品中目标化合物的准确鉴定。使用信息相关采集(IDA)功能对目标化合物进行进一步鉴定和确认。通过线性、灵敏度、重复性、重现性和基质效应的估计对方法进行了验证。由于其能够有效校正基质效应,因此采用内标法进行定量。尽管基质存在强烈干扰,但两种基质的回收率通常均高于 50%,检测限和定量限均非常低。除了 LC-QqLIT-MS 提供的非常高的灵敏度外,该方法的一个重要特点是可以同时提取、处理和分析所有目标化合物。因此,它可用于提供大量数据的药物常规分析。该方法应用于三种具有不同处理特性(即处理能力、二级处理、进水水质)的处理厂的河流沉积物和废水污泥中的药物分析。分析表明,药物在污泥基质中广泛存在。