Bernardi Gabrieli, Kemmerich Magali, Ribeiro Lucila C, Adaime Martha B, Zanella Renato, Prestes Osmar D
Laboratory of Pesticide Residue Analysis (LARP), Chemistry Department, Federal University of Santa Maria, Santa Maria, RS, 97105-900 Brazil.
Laboratory of Pesticide Residue Analysis (LARP), Chemistry Department, Federal University of Santa Maria, Santa Maria, RS, 97105-900 Brazil.
Talanta. 2016 Dec 1;161:40-47. doi: 10.1016/j.talanta.2016.08.015. Epub 2016 Aug 9.
An effective method has been developed and validated for the determination of residues of 55 pesticides in tobacco. The proposed sample preparation method is based on acetonitrile extraction, low-temperature precipitation (LTP) and dispersive solid phase extraction (d-SPE) clean-up. Gas chromatography and ultra-high performance liquid chromatography analysis, both coupled to tandem mass spectrometry (GC-MS/MS and UHPLC-MS/MS), were used for determination. LTP is easy to perform and was crucial to obtain a clean extract. Method quantification limit for the pesticides were between 25 and 75µgkg. Extraction recoveries obtained for blank samples spiked at 25, 75, 125 and 250µgkg levels ranged from 63 to 161% with relative standard deviations (RSD)≤20%. The method was successfully applied to the analysis of thirteen different tobacco samples, providing to be a robust procedure for routine analysis. The compounds pirimiphos methyl and isofenphos presented residues in the range of 35-51µgkg.
已开发并验证了一种测定烟草中55种农药残留的有效方法。所提出的样品制备方法基于乙腈萃取、低温沉淀(LTP)和分散固相萃取(d-SPE)净化。采用气相色谱和超高效液相色谱分析,并与串联质谱联用(GC-MS/MS和UHPLC-MS/MS)进行测定。低温沉淀操作简便,对于获得纯净提取物至关重要。农药的方法定量限在25至75μg/kg之间。在25、75、125和250μg/kg水平加标的空白样品的萃取回收率在63%至161%之间,相对标准偏差(RSD)≤20%。该方法成功应用于13种不同烟草样品的分析,是一种适用于常规分析的可靠方法。甲基嘧啶磷和异柳磷的残留量在35 - 51μg/kg范围内。