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使用液相色谱-串联质谱法分析沉积物中的多卤化咔唑。

Analysis of polyhalogenated carbazoles in sediment using liquid chromatography-tandem mass spectrometry.

机构信息

Fujian Provincial Key Laboratory for Coastal Ecology and Environmental Studies, Center for Marine Environmental Chemistry and Toxicology, College of the Environment and Ecology, Xiamen University, Xiamen 361102, China.

College of Environment, Zhejiang University of Technology, Hangzhou 310032, China.

出版信息

Ecotoxicol Environ Saf. 2019 Apr 15;170:148-155. doi: 10.1016/j.ecoenv.2018.11.131. Epub 2018 Dec 5.

Abstract

The purpose of this study was to develop a novel and sensitive method for the analysis of carbazole and polyhalogenated carbazoles (PHCs) in sediment using ultra performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS). Briefly, 5.0 g of freeze-dried sediment samples were extracted with dichloromethane using pressurized liquid extraction (PLE). The extract was purified with Florisil solid phase extraction cartridge, filtered through 0.22 µm polytetrafluoroethylene filter using a glass syringe, followed by LC-MS/MS analysis. Besides parameters for LC-MS/MS analysis, sample preparation procedures (including solvents for PLE, sorbents for cleanup, and filters for sample filtration) were optimized. The limits of detection and limits of quantification of target compounds were in the ranges of 3.0 × 10 to 0.22 ng g dry weight (d.w.) and 1.0 × 10 to 0.75 ng g d.w., respectively. The recoveries of target compounds in the spiked sediments at 2.0 ng g d.w. and 10 ng g d.w. were 64.8-91.8% and 70.9-124.7%, respectively, with relative standard deviations being less than 13.2%. Except that 36-BCZ had positive matrix effects of 63.3%, the sediment matrices generally displayed low or medium negative matrix effects on the other target compounds during LC-MS/MS analysis. The developed method was applied in the analysis of carbazoles and PHCs in sediment samples from Jiulong River, Fujian, China and all the target compounds were detected in the samples.

摘要

本研究旨在开发一种新颖且灵敏的超高效液相色谱-串联质谱法(UPLC-MS/MS),用于分析沉积物中的咔唑和多卤代咔唑(PHCs)。简要地说,将 5.0 g 冷冻干燥的沉积物样品用加压液体萃取(PLE)用二氯甲烷提取。用 Florisil 固相萃取小柱对提取物进行纯化,用玻璃注射器通过 0.22 µm 聚四氟乙烯滤器过滤,然后进行 LC-MS/MS 分析。除了 LC-MS/MS 分析的参数外,还优化了样品制备程序(包括 PLE 的溶剂、净化的吸附剂和样品过滤的滤器)。目标化合物的检出限和定量限范围分别为 3.0×10 至 0.22 ng g 干重(d.w.)和 1.0×10 至 0.75 ng g d.w.。在 2.0 ng g d.w.和 10 ng g d.w.的加标沉积物中,目标化合物的回收率分别为 64.8-91.8%和 70.9-124.7%,相对标准偏差均小于 13.2%。除了 36-BCZ 具有 63.3%的正基质效应外,在 LC-MS/MS 分析过程中,沉积物基质对其他目标化合物通常表现出低或中等的负基质效应。所建立的方法应用于分析来自中国福建九龙江的沉积物中的咔唑和 PHCs,所有目标化合物均在样品中被检测到。

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