Effectiveness of pressurized liquid extraction and solvent extraction for the simultaneous quantification of 14 pesticide residues in green tea using GC

2008 ◽  
Vol 31 (10) ◽  
pp. 1750-1760 ◽  
Author(s):  
Soon-Kil Cho ◽  
A. M. Abd El-Aty ◽  
Jeong-Heui Choi ◽  
Yang-Mo Jeong ◽  
Ho-Chul Shin ◽  
...  
2015 ◽  
Vol 96 ◽  
pp. 106-112 ◽  
Author(s):  
David Villanueva Bermejo ◽  
José A. Mendiola ◽  
Elena Ibáñez ◽  
Guillermo Reglero ◽  
Tiziana Fornari

2015 ◽  
Vol 94 ◽  
pp. 90-100 ◽  
Author(s):  
Fiorella P. Cardenas-Toro ◽  
Sylvia C. Alcázar-Alay ◽  
Janclei P. Coutinho ◽  
Helena Teixeira Godoy ◽  
Tânia Forster-Carneiro ◽  
...  

2015 ◽  
Vol 7 (7) ◽  
pp. 3054-3062 ◽  
Author(s):  
Feng Qiu ◽  
Zhanqi Tong ◽  
Jianyi Gao ◽  
Manyuan Wang ◽  
Muxin Gong

The running time of analyzing one sample using the developed HPLC-ESI-MS/MS method is only 4.5 min, and more than 150 samples could be assayed daily.


2020 ◽  
pp. 1-7
Author(s):  
Sue Chen ◽  
Qi An ◽  
Hong Sun ◽  
Mengqian Mao

Abstract A simple, inexpensive and sensitive method was developed for the simultaneous determination of three pesticide residues (carbendazim, thiophanate-methyl, and imidacloprid) in fruit and vegetable samples using high performance liquid chromatography (HPLC) based on a combined pretreatment of ultrasound-assisted deep eutectic solvent extraction (UA-DES-E) and liquid-liquid extraction (LLE). In this study, various types of deep eutectic solvents (DESs) were synthesized and the extraction efficiency was compared as extraction solvents. Results showed that glycerol-proline = 9:4 (GP-5) obtained the highest extraction efficiency among different types of DESs. Experiment conditions, including DES volume, extraction time and pH, were systematically optimized using single-factor experiment. Under the optimum conditions, the limits of detection (LODs) and quantification (LOQs) were in the ranges of 0.05–0.2 μg·mL−1 and 0.1–0.5 μg·mL−1, respectively. The relative recoveries of the three pesticides in the fruit and vegetable samples ranged from 85.7 to 113.0% at two spiked levels. Meanwhile, the method achieved excellent linearity with determination coefficients (r) greater than 0.999. Furthermore, the method was successfully applied to the analysis of the pesticides in real fruit and vegetable samples (apple, tomato, and grape).


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