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织物相吸附萃取结合超高效液相色谱串联质谱法测定环境水体中细胞毒性药物残留的方法优化与应用

Optimization and application of fabric phase sorptive extraction coupled to ultra-high performance liquid chromatography tandem mass spectrometry for the determination of cytostatic drug residues in environmental waters.

作者信息

Santana-Viera Sergio, Guedes-Alonso Rayco, Sosa-Ferrera Zoraida, Santana-Rodríguez José Juan, Kabir Abuzar, Furton Kenneth G

机构信息

Instituto Universitario de Estudios Ambientales y Recursos Naturales (i-UNAT), Universidad de Las Palmas de Gran Canaria, 35017, Las Palmas de Gran Canaria, Spain.

Instituto Universitario de Estudios Ambientales y Recursos Naturales (i-UNAT), Universidad de Las Palmas de Gran Canaria, 35017, Las Palmas de Gran Canaria, Spain.

出版信息

J Chromatogr A. 2017 Dec 22;1529:39-49. doi: 10.1016/j.chroma.2017.10.070. Epub 2017 Nov 4.

DOI:10.1016/j.chroma.2017.10.070
PMID:29132820
Abstract

Every year, hundreds of tons of organic pollutants reach the environment through effluents released from wastewater treatment plants worldwide, and many of these compounds have harmful effects on the aquatic ecosystem. A new class of emerging pollutants of high concern is cytostatic drugs, which are designed to treat different types of cancers by attacking cells. Environmental concentrations of cytostatic drugs are known to be in the range of ngL, and for this reason, it is imperative to develop analytical methods of extraction and preconcentration to allow for subsequent instrumental analysis of these drugs. In this work, a rapid, simple and green method for the analysis of seven cytostatic drug compounds that are commonly used in anti-cancer therapies was developed using a novel extraction process based on a powerful miniaturized technique, fabric phase sorptive extraction (FPSE) coupled to ultra-high performance liquid chromatography tandem mass spectrometry (UHPLC-MS/MS). The major parameters that affect the extraction process were optimized. The new method shows good linearity, with a relative standard deviation (RSD) of less than 12%. Relative recoveries higher than 40% were obtained for the studied compounds, and the detection limit of the method was within the values at which these compounds are usually found in environmental water (0.20ngL to 80ngL). The Limit of Quantification ranged from 0.68 to 267ngL. Significant suppression of the signal due to the matrix effect, a common shortcoming attributed to interference from the extraction process as well as the use of ionization mode, was not observed. Subsequently, the method was applied to real wastewater samples from an effluent obtained from a hospital area and three wastewater treatment plants located in Gran Canaria Island, Spain.

摘要

每年,数百吨有机污染物通过全球污水处理厂排放的废水进入环境,其中许多化合物对水生生态系统具有有害影响。一类备受关注的新型新兴污染物是细胞抑制药物,其旨在通过攻击细胞来治疗不同类型的癌症。已知细胞抑制药物在环境中的浓度范围为纳克/升,因此,开发萃取和预浓缩分析方法以便随后对这些药物进行仪器分析势在必行。在这项工作中,基于强大的小型化技术——织物相吸附萃取(FPSE),结合超高效液相色谱串联质谱(UHPLC-MS/MS),开发了一种快速、简单且绿色的分析方法,用于分析七种常用于抗癌治疗的细胞抑制药物化合物。对影响萃取过程的主要参数进行了优化。新方法显示出良好的线性,相对标准偏差(RSD)小于12%。所研究的化合物相对回收率高于40%,该方法的检测限在环境水中这些化合物通常的含量范围内(0.20纳克/升至80纳克/升)。定量限范围为0.68至267纳克/升。未观察到由于基质效应导致的信号显著抑制,基质效应是萃取过程以及电离模式干扰导致的常见缺点。随后,该方法应用于来自西班牙大加那利岛某医院区域的废水以及三个污水处理厂的实际废水样品。

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