Department of Analytical Chemistry, Faculty of Chemical Engineering and Technology, University of Zagreb, Marulićev trg 20, HR-10000, Zagreb, Croatia.
Environ Sci Pollut Res Int. 2017 Sep;24(25):20521-20539. doi: 10.1007/s11356-017-9660-7. Epub 2017 Jul 15.
In this work, a multi-class analytical method for determination of 22 frequently used pharmaceuticals was developed and validated. Analytes were from different classes for example macrolides, fluoroquinolones, tetracyclines, sulfonamides, anthelmintics, anesthetics, and others. Method was intended for analysis of aqueous samples so the sample preparation was done using solid-phase extraction (SPE). Different sorbents (C8, C18, polymeric, and ion exchange sorbents) combining different eluents (methanol, ethanol, acetonitrile, acetone, ethyl acetate) were investigated during development of sample preparation step. Samples were analyzed using HPLC-MS/MS, and therefore, chromatographic and mass spectrometer conditions were investigated. Optimal extraction efficiencies for most of the investigated analytes were obtained with Oasis HLB polymeric sorbents with acetonitrile as eluent. A study of matrix effect was carried out for wastewater treatment plant (WWTP) influent and effluent. The method was validated for linearity, detection limits and quantification limits, repeatability, and reproducibility. Method detection limits were in the range of 2.0-204.0 ng L for WWTP influent except for sulfaguanidine and dexamethasone. Also, method detection limits for WWTP effluent were from 1.0 to 115.4 ng L. Method was successfully applied for analysis of real wastewater samples from municipal wastewater treatment plant. In the influent, pharmaceuticals from all investigated groups were present and the concentrations were from 50.0 to 4914.3 ng L for influent and 26.9 to 1699.2 ng L for effluent. It was also reported that some pharmaceuticals showed higher concentrations in the wastewater effluent than in the influent.
本工作开发并验证了一种用于测定 22 种常用药物的多类别分析方法。分析物来自不同类别,例如大环内酯类、氟喹诺酮类、四环素类、磺胺类、驱虫药、麻醉剂等。该方法旨在分析水样,因此采用固相萃取(SPE)进行样品制备。在开发样品制备步骤期间,研究了不同的吸附剂(C8、C18、聚合物和离子交换吸附剂)与不同洗脱液(甲醇、乙醇、乙腈、丙酮、乙酸乙酯)的组合。采用 HPLC-MS/MS 对样品进行分析,因此对色谱和质谱条件进行了研究。对于大多数研究的分析物,Oasis HLB 聚合物吸附剂与乙腈作为洗脱液可获得最佳的萃取效率。对污水处理厂(WWTP)进水和出水进行了基质效应研究。该方法对线性、检测限和定量限、重复性和再现性进行了验证。除磺胺胍和地塞米松外,WWTP 进水的方法检测限范围为 2.0-204.0 ng L。此外,WWTP 出水的方法检测限范围为 1.0-115.4 ng L。该方法成功应用于市政污水处理厂实际废水样品的分析。在进水样品中,所有研究组别的药物均存在,浓度范围为 50.0-4914.3 ng L,出水浓度范围为 26.9-1699.2 ng L。研究还报告称,一些药物在废水出水中的浓度高于进水。