Magnetic restricted-access carbon nanotubes for dispersive solid phase extraction of organophosphates pesticides from bovine milk samples

被引:43
作者
do Lago, Ayla Campos [1 ]
da Silva Cavalcanti, Marcello Henrique [1 ]
Rosa, Mariana Azevedo [1 ]
Silveira, Alberto Thalison [1 ]
Teixeira Tarley, Cesar Ricardo [2 ]
Figueiredo, Eduardo Costa [1 ]
机构
[1] Fed Univ Alfenas Unifal MG, Lab Toxicant & Drug Anal, Gabriel Monteiro da Silva St 700, BR-37130000 Alfenas, MG, Brazil
[2] Univ Estadual Londrina, Dept Chem, Rodovia Celso Garcia Cid 445,Km 380, BR-86057970 Londrina, Parana, Brazil
关键词
Restricted-access carbon nanotubes; Dispersive-solid phase extraction; Magnetic restricted-access carbon nanotubes; Organophosphates; Pesticides; Milk; LIQUID-CHROMATOGRAPHY; ENVIRONMENTAL WATER; ONLINE EXTRACTION; ADSORPTION; NANOCOMPOSITE; DRUGS; MICROEXTRACTION; COMPOSITE; EXPOSURE; SORBENT;
D O I
10.1016/j.aca.2019.12.039
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Magnetic restricted-access carbon nanotubes (M-RACNTs) were synthesised and used for dispersive solid phase extraction of organophosphates (chlorpyriphos, malathion, disulfoton, pirimiphos) from commercial bovine raw milk samples. Due to their magnetic susceptibility, M-RACNTs were easily separated from the samples/solvents using a neodymium magnet, and the extracted organophosphates were analysed by gas chromatography-mass spectrometry. The protein exclusion capacity was about 100%. Kinetic and isotherm data (for M-RACNTs - malathion interaction) were adequately adjusted to the pseudo-second order and Sips models, respectively, and the maximum adsorption capacity was about 0.55 mg g(-1). The method presented linear ranges from 5.0 to 40.0 mu g L-1 for all analytes, with determination coefficients from 0.9902 to 0.9963. The intra-assay precisions (as relative standard deviation) and accuracies (as relative error) ranged from 10.47 to 19.85% and from -0.18 to -18.80%, respectively, whereas the inter-assay precisions ranged from 6.48 to 18.76% and from -0.22 to 19.49%, respectively for 5.0, 20.0 and 40.0 mu g L-1 organophosphates levels. The organophosphates were not stable at 4 and 24 h (relative errors ranged from -39.30 to 72.07% and -69.64 to 75.95%, respectively). Limits of detection ranged from 0.36 to 0.95 mu g L-1, and 5 mu g L-1 was defined as the limit of quantification for all the analytes. The proposed method was applied in the determination of organophosphates in five commercial milk samples, and no pesticides were detected. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:11 / 23
页数:13
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