Belay Masho Hilawie, Precht Ulrich, Mortensen Peter, Marengo Emilio, Robotti Elisa
Department of Science and Technological Innovation, University of Piemonte Orientale, Viale T. Michel 11, 15121 Alessandria, Italy.
Eurofins Environment Denmark A/S, Ladelundvej 85, 6600 Vejen, Denmark.
Toxics. 2022 Feb 23;10(3):103. doi: 10.3390/toxics10030103.
The increasing use of pharmaceuticals, their presence in the aquatic environment, and the associated toxic effects, have raised concerns in recent years. In this work, a new multi-residue analytical method was developed and validated for the determination of 10 pharmaceuticals in wastewaters using online solid-phase extraction (online SPE) and liquid chromatography-tandem mass spectrometry (LC-MS/MS). The compounds included in the method were antineoplastics (cabazitaxel, docetaxel, doxorubicin, etoposide, irinotecan, methotrexate, paclitaxel, and topotecan), renin inhibitors (aliskiren), and antidepressants (maprotiline). The method was developed through several experiments on four online SPE cartridges, three reversed phase chromatography columns, and four combinations of mobile phase components. Under optimal conditions, very low limits of detection (LODs) of 1.30 to 10.6 ng L were obtained. The method was repeatable, with relative standard deviations (RSD, %) for intraday and interday precisions ranged from 1.6 to 7.8 and from 3.3 to 13.2, respectively. Recovery values ranged from 78.4 to 111.4%, indicating the reproducibility of the method. Matrix effects were mainly presented as signal suppression, with topotecan and doxorubicin being the two most affected compounds (31.0% signal suppression). The proposed method was successfully applied to hospital effluents, detecting methotrexate (4.7-9.3 ng L) and maprotiline (11.2-23.1 ng L). Due to the shorter overall run time of 15 min, including sample preparation, and reduced sample volume (0.9 mL), this on-line SPE-LC-MS/MS method was extremely convenient and efficient in comparison to the classical off-line SPE method. The proposed method was also highly sensitive and can be used for ultratrace quantification of the studied pharmaceuticals in wastewaters, providing useful data for effective environmental monitoring.
近年来,药物使用量的增加、其在水环境中的存在以及相关的毒性效应引发了人们的关注。在这项工作中,开发并验证了一种新的多残留分析方法,用于使用在线固相萃取(online SPE)和液相色谱 - 串联质谱(LC-MS/MS)测定废水中的10种药物。该方法所包含的化合物有抗肿瘤药(卡巴他赛、多西他赛、阿霉素、依托泊苷、伊立替康、甲氨蝶呤、紫杉醇和拓扑替康)、肾素抑制剂(阿利吉仑)和抗抑郁药(马普替林)。该方法通过在四个在线SPE柱、三个反相色谱柱以及流动相成分的四种组合上进行的多项实验开发而成。在最佳条件下,获得了1.30至10.6 ng/L的极低检测限(LOD)。该方法具有可重复性,日内和日间精密度的相对标准偏差(RSD,%)分别为1.6至7.8和3.3至13.2。回收率范围为78.4%至111.4%,表明该方法具有重现性。基质效应主要表现为信号抑制,拓扑替康和阿霉素是受影响最大的两种化合物(信号抑制31.0%)。所提出的方法成功应用于医院废水,检测到甲氨蝶呤(4.7 - 9.3 ng/L)和马普替林(11.2 - 23.1 ng/L)。由于包括样品制备在内的总运行时间较短,仅为15分钟,且样品体积减少(0.9 mL),与传统的离线SPE方法相比,这种在线SPE-LC-MS/MS方法极其方便和高效。所提出的方法也具有高灵敏度,可用于废水中所研究药物的超痕量定量,为有效的环境监测提供有用数据。