Department of Environmental Chemistry, Institute of Environmental Assessment and Water Research (IDAEA-CSIC), Jordi Girona 18-26, E-08034 Barcelona, Spain.
J Chromatogr A. 2013 Mar 8;1280:64-74. doi: 10.1016/j.chroma.2013.01.031. Epub 2013 Jan 14.
A fully automated on-line solid-phase extraction-liquid chromatography-tandem mass spectrometry (SPE-LC-MS/MS) method has been developed for the determination of 13 cytostatics and 4 metabolites in aqueous matrices, including groundwater, surface water, and raw and treated wastewater. On-line SPE is performed by loading 5 mL of water sample at pH 2 through a PLRP-s cartridge. MS/MS is performed with an electrospray (ESI) interface operating in the positive ion mode and registering two selected reaction monitoring (SRM) transitions per compound. Quantification is carried out by the isotope dilution method using 15 different isotope-labelled compounds, specific for the target analytes, as internal standards (IS). The main advantages of the method are high sensitivity, with limits of determination in groundwater, surface water, and raw and treated wastewater below 5 ng L(-1) for all compounds except for gemcitabine (6.9-9.3 ng L(-1)), temozolomide (26-50 ng L(-1)), imatinib (80-180 ng L(-1)) and etoposide (38-65 ng L(-1)), repeatability, with relative standard deviations (RSDs) in most cases below 15%, and selectivity and reliability of results. The method is also fairly simple and fast, with an analysis time per sample (excluding the manual steps, i.e., sample filtration, pH adjustment, and addition of IS) of 40 min. Application of the method to influent wastewater samples collected daily during eight consecutive days from a wastewater treatment plant (WWTP) from Catalonia showed the presence of methotrexate, ifosfamide, capecitabine, tamoxifen and 6(α)-hydroxypaclitaxel but at fairly low concentrations (up to 43 ng L(-1)).
已开发出一种全自动固相萃取-液相色谱-串联质谱法(SPE-LC-MS/MS),用于测定水基质(包括地下水、地表水以及原水和处理后的废水)中的 13 种细胞抑制剂和 4 种代谢物。在线 SPE 通过在 pH 2 下将 5 mL 水样加载到 PLRP-s 柱上来进行。MS/MS 采用电喷雾(ESI)接口,以正离子模式运行,并为每个化合物注册两个选择反应监测(SRM)转换。通过使用 15 种不同的同位素标记化合物(针对目标分析物特异性)作为内标(IS)的同位素稀释法进行定量。该方法的主要优点是灵敏度高,除吉西他滨(6.9-9.3ng/L)、替莫唑胺(26-50ng/L)、伊马替尼(80-180ng/L)和依托泊苷(38-65ng/L)外,所有化合物在地下水、地表水以及原水和处理后的废水中的测定限值均低于 5ng/L,重现性好,大多数情况下相对标准偏差(RSD)低于 15%,结果具有选择性和可靠性。该方法还相当简单和快速,每个样品的分析时间(不包括手动步骤,即样品过滤、pH 调整和添加 IS)为 40 分钟。该方法应用于来自加泰罗尼亚的一家废水处理厂(WWTP)连续 8 天每天收集的进水废水样品中,结果表明存在甲氨蝶呤、异环磷酰胺、卡培他滨、他莫昔芬和 6(α)-羟基紫杉醇,但浓度相当低(高达 43ng/L)。