Literature DB >> 16520938

Simultaneous determination of 405 pesticide residues in grain by accelerated solvent extraction then gas chromatography-mass spectrometry or liquid chromatography-tandem mass spectrometry.

Guo-Fang Pang1, Yong-Ming Liu, Chun-Lin Fan, Jin-Jie Zhang, Yan-Zhong Cao, Xue-Min Li, Zeng-Yin Li, Yan-Ping Wu, Tong-Tong Guo.   

Abstract

A new method has been established for simultaneous determination of 405 pesticide residues in grain, using accelerated solvent extraction (ASE), solid-phase extraction (SPE), and GC-MS and LC-MS-MS. The method was based on appraisal of the GC-MS and LC-MS-MS characteristics of 660 pesticides, their efficiency of extraction from grain, and their purification. Samples of grain (10 g) were mixed with Celite 545 (10 g) and the mixture was placed in a 34-mL cell of an accelerated solvent extractor and extracted with acetonitrile in the static state for 3 min with two cycles at 1,500 psig and at 80 degrees C. For the 362 pesticides determined by GC-MS, half of the extracts were cleaned with an Envi-18 cartridge and then further cleaned with Envi-Carb and Sep-Pak NH2 cartridges in series. The pesticides were eluted with acetonitrile-toluene, 3:1, and the eluates were concentrated and used for analysis after being exchanged with hexane twice. For the 43 pesticides determined by LC-MS-MS the other half of the extracts were cleaned with Sep-Pak Alumina N cartridge and further cleaned with Envi-Carb and Sep-Pak NH2 cartridges. Pesticides were eluted with acetonitrile-toluene, 3:1. After evaporation to dryness the eluates were diluted with acetonitrile-water, 3:2, and used for analysis. In the linear range of each pesticide the linear correlation coefficient r was equal to or greater than 0.956 and 94% of linear correlation coefficients were greater than 0.990. At low, medium, and high fortification levels, at the limit of detection (LOD), twice the LOD and ten times LOD, respectively, recoveries ranged from 42 to 132%; for 382 pesticides, or 94.32%, recovery was from 60 to 120%. The relative standard deviation (RSD) was always below 38% and was below 30% for 391 pesticides, or 96.54%. The LOD was 0.0005-0.3000 mg kg(-1). The proposed method is suitable for determination of 405 pesticide residues in grain such as maize, wheat, oat, rice, and barley, etc.

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Year:  2006        PMID: 16520938     DOI: 10.1007/s00216-005-0237-9

Source DB:  PubMed          Journal:  Anal Bioanal Chem        ISSN: 1618-2642            Impact factor:   4.142


  4 in total

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Authors:  Hong-cheng Liu; Qi-wan Li; Li-bin Tang
Journal:  J Zhejiang Univ Sci B       Date:  2007-04       Impact factor: 3.066

2.  Determination of diniconazole in agricultural samples by sol-gel immunoaffinity extraction procedure coupled with HPLC and ELISA.

Authors:  Zhenjiang Liu; Yahui Jin; Minghua Wang
Journal:  PLoS One       Date:  2012-10-08       Impact factor: 3.240

3.  Current literature in mass spectrometry.

Authors: 
Journal:  J Mass Spectrom       Date:  2007-01       Impact factor: 1.982

4.  Modification and re-validation of the ethyl acetate-based multi-residue method for pesticides in produce.

Authors:  Hans G J Mol; Astrid Rooseboom; Ruud van Dam; Marleen Roding; Karin Arondeus; Suryati Sunarto
Journal:  Anal Bioanal Chem       Date:  2007-06-12       Impact factor: 4.142

  4 in total

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