Biopolymers based-dispersive solid phase extraction combined with deep eutectic solvent-based dispersive liquid-liquid microextraction for the extraction of several pesticides from fruit juices prior to GC-FID analysis

被引:0
|
作者
Alineia, Mina [1 ]
Khosrowshahi, Elnaz Marzi [2 ]
Farajzadeh, Mir Ali [3 ,4 ]
Mogaddam, Mohammad Reza Afshar [2 ,5 ]
Ayazi, Zahra [1 ]
机构
[1] Azarbaijan Shahid Madani Univ, Fac Sci, Dept Chem, POB 53714-161, Tabriz, Iran
[2] Tabriz Univ Med Sci, Food & Drug Safety Res Ctr, Tabriz, Iran
[3] Univ Tabriz, Fac Chem, Dept Analyt Chem, Tabriz, Iran
[4] Near East Univ, Engn Fac, Mersin 10, TR-99138 Nicosia, North Cyprus, Turkiye
[5] Tabriz Univ Med Sci, Pharmaceut Anal Res Ctr, Tabriz, Iran
关键词
Dispersive solid phase extraction; Dispersive liquid-liquid microextraction; Deep eutectic solvent; Biopolymer; Gas chromatography; Fruit juice; CHROMATOGRAPHY; EXPOSURE; WATER;
D O I
10.1007/s11696-023-03050-5
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new analytical method based on a combination of dispersive solid phase extraction with dispersive liquid-liquid microextraction was developed for the extraction of several pesticides (diazinon, prometryn, haloxyfop methyl, hexaconazole, and fenpropathrin) in fruit juice samples. For this purpose, firstly, the pesticides were extracted by a mixture of bio-sorbents (chitosan: agarose: cellulose with a weight ratio of 4:1:1) from fruit juices and in the following they were more concentrated by a deep eutectic solvent-based dispersive liquid-liquid microextraction procedure. The effective parameters influencing both steps were investigated and optimized through a "one-factor-at-a-time" approach. Based on the figures of merit evaluated for the developed method, calibration curves were linear in the range of 0.70-4000 ng mL-1. Limits of detection and quantification were in the ranges of 0.09-0.21 and 0.30-0.70 ng mL-1, respectively. The precision of the developed method was evaluated by performing the method on six aqueous standard solutions (10 ng mL-1 of each pesticide) in a same day and various days. The obtained relative standard deviations for intra- and inter-day precisions were in the ranges of 2.9-5.9% and 5.2-6.3%, respectively. The developed method was successfully employed for multi-residue determination of pesticides in some fruit samples. The relative recoveries were from 88 to 101%.
引用
收藏
页码:7669 / 7679
页数:11
相关论文
共 50 条