Determination of Rotenone Residues in Foodstuffs by Solid-Phase Extraction (SPE) and Liquid Chromatography/Tandem Mass Spectrometry (LC-MS/MS)  被引量:5

Determination of Rotenone Residues in Foodstuffs by Solid-Phase Extraction (SPE) and Liquid Chromatography/Tandem Mass Spectrometry (LC-MS/MS)

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作  者:XU Dun-ming ZHOU Yu LIN Li-yi ZHANG Zhi-gang ZHANG Jin LU Sheng-yu YANG Fang HUANG Peng-ying 

机构地区:[1]Xiamen Entry-Exit Inspection and Quarantine Bureau, Xiamen 361026, P.R. China [2]Fujian Entry-Exit Inspection and Quarantine Bureau, Fuzhou 350001, P.R.China

出  处:《Agricultural Sciences in China》2010年第9期1299-1308,共10页中国农业科学(英文版)

基  金:supported by the Fujian Provincial Department of Science and Technology, China(2006F3002);Xiamen Science and Technology Bureau,China (3502Z20072003, 3502Z20092008 and3502Z20092009);Ministry of Agriculture,China (200903034)

摘  要:We developed a novel approach to determine rotenone residues in foodstuffs, by integrating solid-phase extraction (SPE) and liquid chromatography/tandem mass spectrometry (LC-MS/MS) technologies, to achieve high sensitivity and selectivity. In our method, the solvent extraction with n-hexane-dichloromethane (50:50, v/v) and cleanup with florisil SPE cartridges using ethyl acetate-ethyl ether (25:75, v/v) as eluents provided adequate recovery of rotenone. The detection of rotenone was then carried out by LC-MS/MS using acetonitrile-water with the 0.1% formic acid (w/v) as the mobile phase. The multiple reaction monitoring (MRM) scheme employed in the approach involved the transitions of the precursor ion to three selected product ions, in which one pair for quantification was m/z 395.3 〉 213.2 and the other two pairs for identification were m/z 395.3 〉 192.2 and 395.3 〉 367.0. The limits of quantification (LOQs) of the method ranged from 0.001 to 0.005 mg kg-1 depending on the matrix. Intra- and inter-day precisions (relative standard deviations, RSDs) for rotenone were less than 7.1 and 14.8%, respectively. Results from repetitive analysis suggested good reproducibility of the method for rotenone residue detection. The recoveries at three concentrations (LOQ, 10LOQ and 100LOQ) ranged from 79.3-118.3% in cabbage, potato, onion, carrot, apple, orange, banana, lichee, tea, and Shiitake mushroom. The proposed procedure was then applied to the analysis of 129 real samples collected from Xiamen, Fujian Province, China. The existence of rotenone was found in two tea products with concentrations of 0.012 and 0.016 mg kg-1, respectively. The method has great potential for routine analysis of monitoring rotenone residue in foodstuffs.We developed a novel approach to determine rotenone residues in foodstuffs, by integrating solid-phase extraction (SPE) and liquid chromatography/tandem mass spectrometry (LC-MS/MS) technologies, to achieve high sensitivity and selectivity. In our method, the solvent extraction with n-hexane-dichloromethane (50:50, v/v) and cleanup with florisil SPE cartridges using ethyl acetate-ethyl ether (25:75, v/v) as eluents provided adequate recovery of rotenone. The detection of rotenone was then carried out by LC-MS/MS using acetonitrile-water with the 0.1% formic acid (w/v) as the mobile phase. The multiple reaction monitoring (MRM) scheme employed in the approach involved the transitions of the precursor ion to three selected product ions, in which one pair for quantification was m/z 395.3 〉 213.2 and the other two pairs for identification were m/z 395.3 〉 192.2 and 395.3 〉 367.0. The limits of quantification (LOQs) of the method ranged from 0.001 to 0.005 mg kg-1 depending on the matrix. Intra- and inter-day precisions (relative standard deviations, RSDs) for rotenone were less than 7.1 and 14.8%, respectively. Results from repetitive analysis suggested good reproducibility of the method for rotenone residue detection. The recoveries at three concentrations (LOQ, 10LOQ and 100LOQ) ranged from 79.3-118.3% in cabbage, potato, onion, carrot, apple, orange, banana, lichee, tea, and Shiitake mushroom. The proposed procedure was then applied to the analysis of 129 real samples collected from Xiamen, Fujian Province, China. The existence of rotenone was found in two tea products with concentrations of 0.012 and 0.016 mg kg-1, respectively. The method has great potential for routine analysis of monitoring rotenone residue in foodstuffs.

关 键 词:ROTENONE LC-MS/MS FOODSTUFF residue SPE 

分 类 号:O657.63[理学—分析化学] S859.84[理学—化学]

 

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