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织物相吸附萃取结合超高效液相色谱-串联质谱法用于分析污水样品中的苯并三唑类紫外线稳定剂。

Fabric phase sorptive extraction followed by UHPLC-MS/MS for the analysis of benzotriazole UV stabilizers in sewage samples.

作者信息

Montesdeoca-Esponda Sarah, Sosa-Ferrera Zoraida, Kabir Abuzar, Furton Kenneth G, Santana-Rodríguez José Juan

机构信息

Departamento de Química, Universidad de Las Palmas de G.C., 35017, Las Palmas de Gran Canaria, Spain.

International Forensic Research Institute, Department of Chemistry and Biochemistry, Florida International University, Miami, FL, USA.

出版信息

Anal Bioanal Chem. 2015 Oct;407(26):8137-50. doi: 10.1007/s00216-015-8990-x. Epub 2015 Sep 7.

Abstract

A fast and sensitive sample preparation strategy using fabric phase sorptive extraction followed by ultra-high-performance liquid chromatography and tandem mass spectrometry detection has been developed to analyse benzotriazole UV stabilizer compounds in aqueous samples. Benzotriazole UV stabilizer compounds are a group of compounds added to sunscreens and other personal care products which may present detrimental effects to aquatic ecosystems. Fabric phase sorptive extraction is a novel solvent minimized sample preparation approach that integrates the advantages of sol-gel derived hybrid inorganic-organic nanocomposite sorbents and the flexible, permeable and hydrophobic surface chemistry of polyester fabric. It is a highly sensitive, fast, efficient and inexpensive device that can be reused and does not suffer from coating damage, unlike SPME fibres or stir bars. In this paper, we optimized the extraction of seven benzotriazole UV filters evaluating the majority of the parameters involved in the extraction process, such as sorbent chemistry selection, extraction time, back-extraction solvent, back-extraction time and the impact of ionic strength. Under the optimized conditions, fabric phase sorptive extraction allows enrichment factors of 10 times with detection limits ranging from 6.01 to 60.7 ng L(-1) and intra- and inter-day % RSDs lower than 11 and 30 % for all compounds, respectively. The optimized sample preparation technique followed by ultra-high-performance liquid chromatography and tandem mass spectrometry detection was applied to determine the target analytes in sewage samples from wastewater treatment plants with different purification processes of Gran Canaria Island (Spain). Two UV stabilizer compounds were measured in ranges 17.0-60.5 ng mL(-1) (UV 328) and 69.3-99.2 ng mL(-1) (UV 360) in the three sewage water samples analysed.

摘要

已开发出一种快速灵敏的样品前处理策略,即采用织物相吸附萃取,随后进行超高效液相色谱和串联质谱检测,以分析水性样品中的苯并三唑类紫外线稳定剂化合物。苯并三唑类紫外线稳定剂化合物是添加到防晒霜和其他个人护理产品中的一类化合物,可能会对水生生态系统产生有害影响。织物相吸附萃取是一种新型的溶剂用量最少的样品前处理方法,它整合了溶胶-凝胶衍生的杂化无机-有机纳米复合吸附剂的优点以及聚酯织物灵活、可渗透和疏水的表面化学性质。它是一种高度灵敏、快速、高效且廉价的装置,可重复使用,且不会像固相微萃取纤维或搅拌棒那样出现涂层损坏的问题。在本文中,我们优化了七种苯并三唑类紫外线过滤剂的萃取过程,评估了萃取过程中涉及的大多数参数,如吸附剂化学性质的选择、萃取时间、反萃取溶剂、反萃取时间以及离子强度的影响。在优化条件下,织物相吸附萃取的富集倍数为10倍,检测限在6.01至60.7 ng L⁻¹之间,所有化合物的日内和日间相对标准偏差分别低于11%和30%。将优化后的样品前处理技术与超高效液相色谱和串联质谱检测相结合,用于测定西班牙大加那利岛不同净化工艺的污水处理厂污水样品中的目标分析物。在所分析的三个污水样品中,两种紫外线稳定剂化合物的含量分别在17.0 - 60.5 ng mL⁻¹(UV 328)和69.3 - 99.2 ng mL⁻¹(UV 360)范围内。

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