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液相色谱-串联质谱法检测地表水中的人用和兽用药物及农药

Liquid Chromatography-Tandem Mass Spectrometry Detection of Human and Veterinary Drugs and Pesticides in Surface Water.

作者信息

Zhang Xiang-Pu, Zhang Shu, Xu Chun-Yan, Li Wei-Wei, Ling Hai-Bo, Luo Yang, Jian Kang, Li Tao, Yi Chuan

机构信息

National Key Laboratory of Environmental Health Risk Assessment for Environmental Protection, Hubei Provincial Academy of Eco-Environmental Sciences, Wuhan 430070, China.

Wuhan Ecological Environmental Monitoring Center, Department of Ecology and Environment of Hubei Province, Wuhan 430070, China.

出版信息

Int J Anal Chem. 2023 Oct 16;2023:6350669. doi: 10.1155/2023/6350669. eCollection 2023.

Abstract

Antibiotics and pesticides are widespread in most rivers and lakes due to the overuse of antibiotics and pesticides, but there are few methods for simultaneous analysis of antibiotics and pesticides in aquatic environments. To address this knowledge gap, a concise and sensitive analytical method is proposed in which three classes of human and veterinary drugs (sulfonamides, macrolides, and hormones) and two classes of pesticides (organophosphorus and neonicotinoids) are simultaneously extracted and determined in surface water. The solid-phase extraction column with Cleanert PEP-2 was preconditioned sequentially with 6 mL of methanol, ultrapure water, and citric acid buffer (pH 3.0) each for simultaneous extraction and further purification. The forty-seven target analytes were analysed by LC-MS/MS in positive and negative ion modes. The LC separation was performed using a Sigma-Aldrich C column with 0.1% formic acid in water and acetonitrile as a gradient eluting mobile phase in positive ion mode. The internal standard method was used to overcome the inevitable matrix effects in LC-MS/MS analysis. The matrix effects of most target analytes were in the range of 27-151%. The recoveries of forty analytes in the three concentrations (10, 50, and 100 ng L) of surface water spiked samples ranged from 41 to 127%. The method quantitative limits of the analytes were in the range of 0.40-5.49 ng L. Application of the method to analyze samples in the eight runoff outlets of the Pearl River Delta showed that some antibiotics and pesticides were detected, and the concentration of parathion was as high as 154 ng L. A powerful tool for quickly and efficiently screening for contaminants in surface water has been presented.

摘要

由于抗生素和农药的过度使用,它们在大多数河流和湖泊中广泛存在,但在水生环境中同时分析抗生素和农药的方法却很少。为了填补这一知识空白,本文提出了一种简洁灵敏的分析方法,可同时提取并测定地表水中的三类人用和兽用药物(磺胺类、大环内酯类和激素类)以及两类农药(有机磷类和新烟碱类)。采用Cleanert PEP - 2固相萃取柱,依次用6 mL甲醇、超纯水和柠檬酸缓冲液(pH 3.0)进行预处理,以实现同时萃取和进一步净化。通过LC - MS/MS在正离子和负离子模式下对47种目标分析物进行分析。在正离子模式下,使用Sigma - Aldrich C柱,以含0.1%甲酸的水和乙腈作为梯度洗脱流动相进行LC分离。采用内标法克服LC - MS/MS分析中不可避免的基质效应。大多数目标分析物的基质效应在27% - 151%范围内。在加标浓度为10、50和100 ng/L的地表水样品中,40种分析物的回收率在41% - 127%之间。分析物的方法定量限在0.40 - 5.49 ng/L范围内。将该方法应用于珠江三角洲八个径流口的样品分析,结果表明检测到了一些抗生素和农药,其中对硫磷的浓度高达154 ng/L。本文提供了一种快速高效筛查地表水中污染物的有力工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df02/10593548/6e1791ffb82b/IJAC2023-6350669.001.jpg

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