Factorial design optimization of experimental variables in preconcentration of carbamates pesticides in water samples using solid phase extraction and liquid chromatography-electrospray-mass spectrometry determination

被引:48
作者
El Atrache, Latifa Latrous [1 ,2 ]
Ben Sghaier, Rafika [1 ]
Kefi, Bochra Bejaoui [3 ]
Haldys, Violette [4 ,5 ]
Dachraoui, Mohamed [1 ]
Tortajada, Jeanine [4 ,5 ]
机构
[1] Univ Tunis Manar, Fac Sci Tunis, Lab Chim Analyt & Electrochim, Tunis 2092, Tunisia
[2] Univ Tunis Manar, Inst Preparat Etud Ingenieurs Manar, Tunis 2092, Tunisia
[3] Inst Natl Rech & Anal Physicochim, Tunis 2020, Tunisia
[4] Univ Evry Val Essonne, Lab Anal & Modelisat Biol & Environm, F-91025 Evry, France
[5] CNRS, UMR 8587, Paris, France
关键词
Carbamates pesticides; Experimental design; Solid phase extraction; Water; Method validation; COPPER DETERMINATION; ASSISTED EXTRACTION; DOEHLERT MATRIX; MICROEXTRACTION; SYSTEM; QUANTIFICATION; INSECTICIDES; PRODUCTS; RESIDUES; SOIL;
D O I
10.1016/j.talanta.2013.09.032
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
An experimental design was applied for the optimization of extraction process of carbamates pesticides from surface water samples. Solid phase extraction (SPE) of carbamates compounds and their determination by liquid chromatography coupled to electrospray mass spectrometry detector were considered. A two level full factorial design 2(k) was used for selecting the variables which affected the extraction procedure. Eluent and sample volumes were statistically the most significant parameters. These significant variables were optimized using Doehlert matrix. The developed SPE method included 200 mg of C-18 sorbent, 143.5 mL of water sample and 5.5 mL of acetonitrile in the elution step. For validation of the technique, accuracy, precision, detection and quantification limits, linearity, sensibility and selectivity were evaluated. Extraction recovery percentages of all the carbamates were above 90% with relative standard deviations (R.S.D.) in the range of 3-11%. The extraction method was selective and the detection and quantification limits were between 0.1 and 0.5 mu g L-1, and 1 and 3 mu g L-1, respectively. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:392 / 398
页数:7
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