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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%.
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页码:7669 / 7679
页数:11
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