2016
DOI: 10.5935/0103-5053.20160042
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Determination of Pesticides in Grape Juices by QuEChERS and Liquid Chromatography-Tandem Mass Spectrometry

Abstract: In this study, we describe a liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for quantifying 25 pesticides in grape juice. This method was optimized and validated according with INMETRO (Instituto Nacional de Metrologia Qualidade e Tecnologia) for the simultaneous determination of pesticide, which are widely used in grape culture in Brazil. The method was based on the QuEChERS (quick, easy, cheap, effective, rugged and safe) methodology. We used AOAC Official Method 2007.01 and Standard Method… Show more

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Cited by 5 publications
(6 citation statements)
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“…Annastassiades et al chose citrate as the buffer and this version was named by the European Committee for Standardization (CEN) as Standard Method EN 15662 [59]. Other frequent modifications include: changes in the composition and/or proportion of the salts used in extraction [60], changes in the composition and/or proportion of the sorbents used [10,12,61], using various proportions of buffers: citrate [12,32,62,63] or acetate [12,32,63] and (in order to maintain the optimum pH of the sample within the 5-5.5 range) using appropriate acids [29,60] or bases [29]. One should also note other variants of the method that are based on omitting the cleanup step completely [40], using the sorbent deposit in the form of a column [64], replacing acetonitrile with ethyl acetate as the organic solvent [65], or introducing an additional step where the analytes are concentrated in the cleaned up extract by evaporating and/or replacing the solvent [61,66,67].…”
Section: Sample Preparationmentioning
confidence: 99%
“…Annastassiades et al chose citrate as the buffer and this version was named by the European Committee for Standardization (CEN) as Standard Method EN 15662 [59]. Other frequent modifications include: changes in the composition and/or proportion of the salts used in extraction [60], changes in the composition and/or proportion of the sorbents used [10,12,61], using various proportions of buffers: citrate [12,32,62,63] or acetate [12,32,63] and (in order to maintain the optimum pH of the sample within the 5-5.5 range) using appropriate acids [29,60] or bases [29]. One should also note other variants of the method that are based on omitting the cleanup step completely [40], using the sorbent deposit in the form of a column [64], replacing acetonitrile with ethyl acetate as the organic solvent [65], or introducing an additional step where the analytes are concentrated in the cleaned up extract by evaporating and/or replacing the solvent [61,66,67].…”
Section: Sample Preparationmentioning
confidence: 99%
“…O método analítico utilizado pela ANVISA para extração de carbaril em abacaxi, é o QuEChERS (Quick, Easy, Cheap, Effective, Rugged, Safe) [7][8][9]. Este já foi aplicado em diversas amostras de alimentos e bebidas, como: Cebola [10], soja [11], banana, mamão e pimentão [12], maçã, morango e tomate [13], laranja, [14], pera, pepino e repolho [15], mel [16], leite bovino [17], sucos de uva [18] e caldo de cana [19].…”
Section: ____________________________________________________________unclassified
“…In order to avoid the health hazards caused by pesticide residues, governments and international organizations regulate the maximum residues level (MRL) in fruit and vegetables, aiming to limit population exposure and to confirm the proper use and exact concentrations of pesticides in agricultural products [ 2 ]. The MRL values established by regulatory bodies range between 0.01–10 mg/kg, in relation to matrices and acceptable daily intake [ 3 , 4 ]. Also, 10 μg L −1 for paraquat and 90 μg L −1 for carbaryl have been reported as guideline limits for water [ 5 ].…”
Section: Introductionmentioning
confidence: 99%
“…Consequently, trace level detection and fast identification represent important aspects in analytical method selection. In general, pesticides are detected in food and water using chromatographic analytical methods such as gas and liquid chromatography in tandem with mass spectrometry [ 1 , 3 , 4 , 6 ], immunoassays and immunosensors [ 7 ], flow injection chemiluminescence [ 8 ], or fluorescence [ 9 ]. The main disadvantages of these methods are the time consumption, including prerequisite sample pre-treatment/pre-concentration, the expensive instrumentation and the toxic organic reagents required.…”
Section: Introductionmentioning
confidence: 99%