Tankiewicz Maciej, Biziuk Marek
Department of Environmental Toxicology, Faculty of Health Sciences with Subfaculty of Nursing and Institute of Maritime and Tropical Medicine, Medical University of Gdańsk, Dębowa Str. 23, 80-204, Gdańsk, Poland.
Department of Analytical Chemistry, Faculty of Chemistry, Gdańsk University of Technology, G. Narutowicza Str. 11/12, 80-233, Gdańsk, Poland.
Anal Bioanal Chem. 2018 Feb;410(5):1533-1550. doi: 10.1007/s00216-017-0798-4. Epub 2017 Dec 18.
A simple and efficient dispersive liquid-liquid microextraction technique (DLLME) was developed by using a mixture of two solvents: 40 μL of tetrachlorethylene (extraction solvent) and 1.0 mL of methanol (disperser solvent), which was rapidly injected with a syringe into 10 mL of water sample. Some important parameters affecting the extraction efficiency, such as type and volume of solvents, water sample volume, extraction time, temperature, pH adjustment and salt addition effect were investigated. Simultaneous determination of 34 commonly used pesticides was performed by using gas chromatography coupled with mass spectrometry (GC-MS). The procedure has been validated in order to obtain the highest efficiency at the lowest concentration levels of analytes to fulfill the requirements of regulations on maximum residue limits. Under the optimum conditions, the linearity range was within 0.0096-100 μg L. The limits of detection (LODs) of the developed DLLME-GC-MS methodology for all investigated pesticides were in the range of 0.0032 (endrin)-0.0174 (diazinon) μg L and limits of quantification (LOQs) from 0.0096 to 0.052 μg L. At lower concentration of 1 μg L for each pesticide, recoveries ranged between 84% (tebufenpyrad) and 108% (deltamethrin) with relative standard deviations (RSDs) (n = 7) from 1.1% (metconazole) to 11% (parathion-mehtyl). This methodology was successfully applied to check contamination of environmental samples. The procedure has proved to be selective, sensitive and precise for the simultaneous determination of various pesticides. The optimized analytical method is very simple and rapid (less than 5 min). Graphical abstract Analytical procedure for testing water samples consists of dispersive liquid-liquid microextraction (DLLME) and gas chromatography coupled with mass spectrometry (GC-MS).
通过使用两种溶剂的混合物开发了一种简单高效的分散液液微萃取技术(DLLME):40 μL 四氯乙烯(萃取溶剂)和 1.0 mL 甲醇(分散剂溶剂),用注射器将其快速注入 10 mL 水样中。研究了一些影响萃取效率的重要参数,如溶剂的类型和体积、水样体积、萃取时间、温度、pH 调节和加盐效果。采用气相色谱 - 质谱联用(GC-MS)同时测定 34 种常用农药。为了在分析物的最低浓度水平下获得最高效率以满足最大残留限量法规的要求,对该方法进行了验证。在最佳条件下,线性范围为 0.0096 - 100 μg/L。所开发的 DLLME - GC - MS 方法对所有研究农药的检测限(LOD)在 0.0032(异狄氏剂) - 0.0174(二嗪农)μg/L 范围内,定量限(LOQ)为 0.0096 至 0.052 μg/L。对于每种农药在 1 μg/L 的较低浓度下,回收率在 84%(戊唑醇)至 108%(溴氰菊酯)之间,相对标准偏差(RSD)(n = 7)为 1.1%(丙环唑)至 11%(甲基对硫磷)。该方法成功应用于检测环境样品的污染情况。该方法已被证明对于同时测定各种农药具有选择性、灵敏性和精确性。优化后的分析方法非常简单快速(不到 5 分钟)。图形摘要检测水样的分析程序包括分散液液微萃取(DLLME)和气相色谱 - 质谱联用(GC-MS)。