Vaudreuil Marc-Antoine, Vo Duy Sung, Munoz Gabriel, Furtos Alexandra, Sauvé Sébastien
Department of Chemistry, Université de Montréal, Montréal, QC, Canada.
Department of Chemistry, Université de Montréal, Montréal, QC, Canada.
Talanta. 2020 Dec 1;220:121407. doi: 10.1016/j.talanta.2020.121407. Epub 2020 Jul 22.
With the consumption of chemotherapy agents, residues of anticancer drugs may be increasingly found in hospital and municipal wastewaters. Quantification of these highly polar micropollutants remains challenging due to poor chromatographic retention on typical reversed phases. This study investigated different solid-phase extraction (SPE) materials for automated on-line preconcentration of complex matrices (hospital and municipal wastewaters) and various chromatographic column options. A hyper crosslinked hydroxylated polystyrene-divinylbenzene copolymer SPE sorbent coupled on-line with hydrophilic interaction liquid chromatography tandem mass spectrometry (HILIC-MS/MS) yielded suitable limits of detection (LOD: 1-2 ng L) for 5-fluorouracil (5-FU) and 2',2'-difluorodeoxyuridine (dFdU). Optimization of chromatographic conditions led to a single LC-MS/MS method for the analysis of other cytostatic drugs including cytarabine (CYT), gemcitabine (GEM), methotrexate (MTX), ifosfamide (IFO), cyclophosphamide (CYC) and capecitabine (CAP). The filter membrane for sample pre-treatment, HPLC mobile phase additives, and on-line SPE loading parameters were also investigated. The methods were validated in wastewater matrix with suitable determination coefficients (R range: 0.9982-0.9999), LODs (0.5-5 ng L), accuracy (78-111%), intraday precision (2.6-12%), and interday precision (2.1-13%). The occurrence of cytostatic drugs was examined in field-collected water samples from hospital effluents and municipal wastewater treatment plants (WWTP) in Canada. CAP (3.7-64 ng L), dFdU (6.1-300 ng L), and MTX (1.8-68 ng L) were frequently detected across both matrix types, while IFO was detected in hospital wastewater (23-140 ng L) but not in municipal WWTPs.
随着化疗药物的使用,医院和城市废水中可能会越来越多地发现抗癌药物残留。由于这些高极性微污染物在典型反相色谱上的保留性较差,对其进行定量分析仍然具有挑战性。本研究调查了不同的固相萃取(SPE)材料,用于复杂基质(医院和城市废水)的自动在线预浓缩以及各种色谱柱选项。一种超交联羟基化聚苯乙烯 - 二乙烯基苯共聚物SPE吸附剂与亲水作用液相色谱串联质谱(HILIC - MS/MS)在线联用,对5 - 氟尿嘧啶(5 - FU)和2',2'-二氟脱氧尿苷(dFdU)产生了合适的检测限(LOD:1 - 2 ng/L)。色谱条件的优化产生了一种单一的LC - MS/MS方法,用于分析其他细胞毒性药物,包括阿糖胞苷(CYT)、吉西他滨(GEM)、甲氨蝶呤(MTX)、异环磷酰胺(IFO)、环磷酰胺(CYC)和卡培他滨(CAP)。还研究了用于样品预处理的滤膜、HPLC流动相添加剂和在线SPE进样参数。这些方法在废水基质中得到验证,具有合适的测定系数(R范围:0.9982 - 0.9999)、检测限(0.5 - 5 ng/L)、准确度(78 - 111%)、日内精密度(2.6 - 12%)和日间精密度(2.1 - 13%)。对加拿大医院废水和城市污水处理厂(WWTP)现场采集的水样中细胞毒性药物的存在情况进行了检测。在两种基质类型中均频繁检测到CAP(3.7 - 64 ng/L)、dFdU(6.1 - 300 ng/L)和MTX(1.8 - 68 ng/L),而IFO在医院废水中被检测到(23 - 140 ng/L),但在城市污水处理厂中未检测到。