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超声或加速溶剂萃取,然后进行 U-HPLC-高质量精度 MS 分析,用于筛选土壤和植物样品中的药物和杀菌剂。

Ultrasonic or accelerated solvent extraction followed by U-HPLC-high mass accuracy MS for screening of pharmaceuticals and fungicides in soil and plant samples.

机构信息

University Dunarea de Jos Galaţi-Faculty of Food Science and Engineering, Str. Domnească 47, 800008 Galaţi, Romania.

出版信息

Talanta. 2012 Jan 15;88:653-62. doi: 10.1016/j.talanta.2011.11.054. Epub 2011 Nov 26.

Abstract

Different veterinary pharmaceuticals are used in agricultural livestock becoming a source of environment contamination. Furthermore, no regulation exists for the concentration limits of pharmaceuticals in soil or water. Monitoring programs for environment contamination with pharmaceuticals are needed, requiring new sensitive and selective screening methods. The present study focuses on developing a method for the simultaneous scanning of forty-two compounds (pharmaceuticals, azole biocides and fungicides) in soil and plant material samples. For extraction purposes the use of ultrasonic assisted and accelerated solvent extraction (ASE) were compared. The extract was purified and concentrated by applying a solid phase extraction step followed by ultra-high-performance-chromatographic separation and accurate-mass spectrometric detection using Exacte Orbitrap technology (FWHM 50,000). The effects of the different extraction solvents and conditions on the extraction efficiency were tested. Although both extraction approaches are applicable the optimal extraction efficiency was obtained by applying accelerated solvent extraction using solvent mixtures containing acetone for soil and methanol for plant samples. An ASE process has been validated for the determination of selected pharmaceuticals and fungicides in soil and in plant material. The recoveries from soil samples were >70% for more than 68% of the compounds. The levels of detection were ≤10 μg kg(-1) for 93% of the compounds tested. The recoveries from plant material were >70% for 64% of the compounds tested. The levels of detection were ≤10 μg kg(-1) for 66% of the compounds. The developed method was used to screen soil and plant material collected throughout the Netherlands and oxytetracycline residues were detected.

摘要

不同的兽医药品在农业牲畜中使用,成为环境污染的源头。此外,土壤或水中药品的浓度限制没有规定。需要对环境中药物污染进行监测计划,这需要新的敏感和选择性筛选方法。本研究专注于开发一种同时扫描土壤和植物材料样品中四十二种化合物(药品、唑类杀菌剂和杀真菌剂)的方法。为了萃取目的,比较了超声波辅助和加速溶剂萃取(ASE)的使用。通过应用固相萃取步骤,然后通过超高效色谱分离和使用 Exacte Orbitrap 技术(FWHM 50,000)进行精确质量质谱检测,对提取物进行了纯化和浓缩。测试了不同萃取溶剂和条件对萃取效率的影响。尽管这两种萃取方法都适用,但通过应用含有丙酮的加速溶剂萃取和甲醇萃取植物样品的溶剂混合物,可以获得最佳的萃取效率。已经验证了 ASE 过程用于土壤和植物材料中选定药品和杀真菌剂的测定。土壤样品的回收率>70%,超过 68%的化合物。检测限为≤10μgkg(-1),测试的 93%的化合物符合要求。植物材料的回收率>70%,64%的化合物符合要求。检测限为≤10μgkg(-1),66%的化合物符合要求。开发的方法用于筛选在荷兰各地收集的土壤和植物材料,并检测到土霉素残留。

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