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采用分散液液微萃取技术提取和浓缩牛奶中的三唑类农药,然后用 GC-FID 和 GC-MS 进行测定。

Extraction and preconcentration technique for triazole pesticides from cow milk using dispersive liquid-liquid microextraction followed by GC-FID and GC-MS determinations.

机构信息

Department of Analytical Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz, Iran.

出版信息

J Sep Sci. 2011 Jun;34(11):1309-16. doi: 10.1002/jssc.201000928. Epub 2011 Apr 13.

Abstract

A simple and rapid dispersive liquid-liquid microextraction (DLLME) technique coupled with gas chromatography-flame ionization detection (GC-FID) and gas chromatography-mass spectrometry (GC-MS) was developed for the extraction, preconcentration, and analysis of triazole pesticides (penconazole, hexaconazole, tebuconazole, triticonazole, and difenoconazole) in cow milk samples. Initially to 5 mL milk sample, NaCl and acetonitrile were added as salting-out agent and extraction solvent, respectively. After manual shaking, the mixture was centrifuged. In the presence of sodium chloride, a two-phase system was formed: upper phase, acetonitrile containing triazole pesticides and lower phase, aqueous phase containing soluble compounds and the precipitated proteins. After the extraction of pesticides from milk, a portion of supernatant phase (acetonitrile) was removed, mixed with chloroform at microliter level and rapidly injected by syringe into 5 mL distilled water. In this process, triazole pesticides were extracted into fine droplets of chloroform (as extraction solvent). After centrifugation, the fine droplets of chloroform were sedimented in bottom of the conical test tube. Finally, GC-FID and GC-MS were used for the separation and determination of analytes in the sedimented phase. Some important parameters like type of solvent for extraction of pesticides from milk, salt amount, the volume of extraction solvent, etc., which affect the extraction efficiency, were completely studied. Under the optimum conditions, enrichment factors were in the range of 156-380. The linear ranges of calibration curves were wide and limits of detection (LODs) and limits of quantification (LOQs) were between 4-58 and 13-180 μg/L, respectively. This method is very simple and rapid, requiring <15 min for sample preparation.

摘要

建立了一种简单快速的分散液液微萃取(DLLME)技术,结合气相色谱-火焰离子化检测(GC-FID)和气相色谱-质谱(GC-MS),用于从牛奶样品中提取、预浓缩和分析三唑类农药(戊唑醇、己唑醇、丙环唑、三唑酮和烯唑醇)。最初,向 5 mL 牛奶样品中加入 NaCl 和乙腈作为盐析剂和萃取溶剂。手动摇匀后,将混合物离心。在氯化钠存在下,形成了一个两相体系:上层为含有三唑类农药的乙腈相,下层为含有可溶性化合物和沉淀蛋白质的水相。在从牛奶中萃取农药后,取出一部分上清液(乙腈),与氯仿混合,用微量注射器迅速注入 5 mL 去离子水。在这个过程中,三唑类农药被萃取到氯仿(萃取溶剂)的微小液滴中。离心后,氯仿的微小液滴沉降在锥形试管的底部。最后,GC-FID 和 GC-MS 用于分离和测定沉淀相中分析物。研究了一些重要的参数,如从牛奶中萃取农药的溶剂类型、盐量、萃取溶剂的体积等,这些参数会影响萃取效率。在最佳条件下,富集因子在 156-380 范围内。校准曲线的线性范围很宽,检测限(LOD)和定量限(LOQ)分别为 4-58 和 13-180 μg/L。该方法非常简单快速,样品制备时间<15 min。

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