Nan Zhang, Xinyuan Pei, Huiyang Fu, Shiyu Miao, Qingqing Zhu, Zhengbo Dai, Yi Chi, Guohua Zhu, Ligang Hu, Rong Jin and Chunyang Liao
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A sensitive method combining ultra-high performance liquid chromatography-triple quadrupole tandem mass spectrometry (UHPLC-MS/MS) and gas chromatography-mass spectrometry (GC-MS) was developed for the simultaneous determination of three typical classes of phenolic EDCs in aquatic environments, including parabens, bisphenols, and SPAs. Solid-phase extraction (SPE) parameters and instrumental conditions were optimized, achieving recoveries of 64.7%–123% and 64.0%–111% for blank spikes and matrix spikes, respectively, with relative standard deviation below 18%. Detection and quantification limits were determined to be 0.228–0.940 ng L<small><sup>−1</sup></small> and 0.758–3.13 ng L<small><sup>−1</sup></small>, respectively. The method was successfully applied to 23 surface water samples, and 10 EDCs were detected. Notably, bisphenols and SPAs in the Qiantang River displayed a clear increasing trend toward the downstream. SPAs exhibited the highest concentrations, with oxidation by the π-system being the predominant pathway responsible for the transformation to degradants like BHT-Q and BHT-quinol. 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引用次数: 0
摘要
全球对新出现的污染物,特别是内分泌干扰化学物质(EDCs)的关注,推动了对先进检测方法的需求。酚类EDCs,如对羟基苯甲酸酯、双酚类和合成酚类抗氧化剂(SPAs),广泛存在于环境中,对生殖系统和代谢构成威胁。随着研究的不断进步,同时检测这些酚类EDCs的高通量技术的发展已成为当务之急。建立了超高效液相色谱-三重四极杆串联质谱联用(UHPLC-MS/MS)和气相色谱-质谱联用(GC-MS)同时测定水生环境中3类典型酚类EDCs(对羟基苯甲酸酯类、双酚类和spa类)的灵敏方法。对固相萃取(SPE)参数和仪器条件进行了优化,空白峰和基质峰的回收率分别为64.7% ~ 123%和64.0% ~ 111%,相对标准偏差小于18%。检测限和定量限分别为0.228 ~ 0.940 ng L−1和0.758 ~ 3.13 ng L−1。该方法成功应用于23份地表水样品,检测到10种EDCs。其中,钱塘江双酚类和spa向下游呈明显的增加趋势。SPAs的浓度最高,π体系的氧化是转化为BHT-Q和bht -醌等降解物的主要途径。该方法可对水中多种酚类EDCs进行可靠的检测和定量,为EDCs污染的环境监测、风险评估和监管管理提供了有价值的工具。
Development and validation of an integrated UHPLC-MS/MS and GC-MS method for the simultaneous analysis of three categories of phenolic endocrine disrupting chemicals in surface water†
The global concern over emerging contaminants, particularly endocrine-disrupting chemicals (EDCs), has driven the need for advanced detection methods. Phenolic EDCs, such as parabens, bisphenols, and synthetic phenolic antioxidants (SPAs), are widely distributed in the environment and pose risks to reproductive systems and metabolism. With ongoing advancements in research, the development of high-throughput technologies for the simultaneous detection of these phenolic EDCs has become a pressing priority. A sensitive method combining ultra-high performance liquid chromatography-triple quadrupole tandem mass spectrometry (UHPLC-MS/MS) and gas chromatography-mass spectrometry (GC-MS) was developed for the simultaneous determination of three typical classes of phenolic EDCs in aquatic environments, including parabens, bisphenols, and SPAs. Solid-phase extraction (SPE) parameters and instrumental conditions were optimized, achieving recoveries of 64.7%–123% and 64.0%–111% for blank spikes and matrix spikes, respectively, with relative standard deviation below 18%. Detection and quantification limits were determined to be 0.228–0.940 ng L−1 and 0.758–3.13 ng L−1, respectively. The method was successfully applied to 23 surface water samples, and 10 EDCs were detected. Notably, bisphenols and SPAs in the Qiantang River displayed a clear increasing trend toward the downstream. SPAs exhibited the highest concentrations, with oxidation by the π-system being the predominant pathway responsible for the transformation to degradants like BHT-Q and BHT-quinol. This method offers reliable detection and quantification of multiple phenolic EDCs in water, providing a valuable tool for environmental monitoring, risk assessment, and regulatory management of EDCs contamination.