Morrica Patrizia, Fidente Paola, Seccia Serenella
Department of Pharmaceutical and Toxicological Chemistry, University of Napoli 'Federico II', Via D. Montesano 49, 80131 Napoli, Italy.
Biomed Chromatogr. 2005 Jan;19(1):107-10. doi: 10.1002/bmc.426.
A multi-residue method for the simultaneous extraction from drinking water using solid-phase extraction on LiChrolut EN [poly(styrene-divinylbenzene), PSDVB] and determination of nine N-methylcarbamate pesticides (NMCs) (aldicarb, its metabolites i.e. aldicarb sulfone and aldicarb sulfoxide and carbaryl, carbofuran, dioxacarb, ethiofencarb, methomyl and propoxur) using reversed-phase liquid chromatography was studied. A 1000-fold pre-concentration was achieved and the method was used for determination of the nine pesticides in water, with limits of detection in the range 3-15 ng L(-1). For all compounds the recoveries determined at the 0.1 and 1 microg L(-1) level generally ranged from 85 to 104% with relative standard deviations (RSD) of 1.4-8.8%.
研究了一种多残留方法,该方法采用LiChrolut EN[聚(苯乙烯-二乙烯基苯),PSDVB]固相萃取从饮用水中同时萃取,并使用反相液相色谱法测定九种N-甲基氨基甲酸酯类农药(NMCs)(涕灭威及其代谢物涕灭威砜、涕灭威亚砜、西维因、克百威、恶虫威、乙硫苯威、灭多威和残杀威)。实现了1000倍预浓缩,该方法用于测定水中的九种农药,检测限在3-15 ng L(-1)范围内。对于所有化合物,在0.1和1 μg L(-1)水平测定的回收率一般在85%至104%之间,相对标准偏差(RSD)为1.4%-8.8%。