Hrouzková Svetlana, Brišová Mária, Szarka Agneša
Slovak University of Technology in Bratislava, Faculty of Chemical and Food Technology, Institute of Analytical Chemistry, Radlinského 9, 812 37 Bratislava, Slovak Republic.
Slovak University of Technology in Bratislava, Faculty of Chemical and Food Technology, Institute of Analytical Chemistry, Radlinského 9, 812 37 Bratislava, Slovak Republic.
J Chromatogr A. 2017 Jul 14;1506:18-26. doi: 10.1016/j.chroma.2017.05.038. Epub 2017 May 17.
A fast, ecological, and efficient method employing vortex-assisted dispersive liquid-liquid microextraction (DLLME) method for isolation and preconcentration of selected endocrine disrupting pesticides from beverages containing some degree of alcohol was developed. The effect of several extraction parameters, such as selection of extractive solvent, its volume and extraction time, the salt addition was investigated. Four different extractive solvents (chloroform, tetrachloroethane, tetrachloromethane and toluene) and their combinations were evaluated for DLLME. Under the following conditions: 1mL of fortified sample, 80μL of tetrachloroethane, 1.5mL of water, vortex assistance for 3min at the speed of 1800rpm, and no salt addition, the method was validated. Linearity was studied in the concentration range of 0.01-250μg/L with coefficient of correlation ranging between 0.9940 and 1.0000, limits of detection and quantification ranging between 0.02-1.4μg/L and 0.07-4.7μg/L, respectively. Recoveries were satisfactory in the range of 70-120%, with the exception of diphenyl, alachlor and fenarimol at the lowest concentration level and p,p-DDE at concentration level of 100 and 250μg/L. The applicability of the developed and validated method was proved by the analysis of real samples.
开发了一种快速、生态且高效的方法,该方法采用涡旋辅助分散液液微萃取(DLLME)从含有一定程度酒精的饮料中分离和预富集选定的内分泌干扰农药。研究了几种萃取参数的影响,如萃取溶剂的选择、其体积和萃取时间、盐的添加。对四种不同的萃取溶剂(氯仿、四氯乙烷、四氯化碳和甲苯)及其组合进行了DLLME评估。在以下条件下:1mL强化样品、80μL四氯乙烷、1.5mL水、以1800rpm的速度涡旋辅助3分钟且不添加盐,对该方法进行了验证。在0.01 - 250μg/L的浓度范围内研究了线性,相关系数在0.9940至1.0000之间,检测限和定量限分别在0.02 - 1.4μg/L和0.07 - 4.7μg/L之间。回收率在70 - 120%范围内令人满意,但最低浓度水平下的联苯、甲草胺和氯苯嘧啶醇以及浓度水平为100和250μg/L时的p,p - DDE除外。通过对实际样品的分析证明了所开发和验证方法的适用性。