Saito Isao, Ueno Eiji, Oshima Harumi, Matsumoto Hiroshi, Sasaki Kumiko, Maitani Tamio
Aichi Prefectural Institute of Public Health: 7-6, Nagare, Tsuji-machi, Kita-ku, Nagoya 462-8576, Japan.
Shokuhin Eiseigaku Zasshi. 2006 Aug;47(4):173-7. doi: 10.3358/shokueishi.47.173.
We studied the determination of methoprene in foods by high-performance liquid chromatography (HPLC). The sample was extracted with acetonitrile and the extract was salted out by adding sodium chloride, allowing the acetonitrile layer to separate. The acetonitrile solution was washed with hexane saturated with acetonitrile, cleaned up on a Florisil column and determined by HPLC. The recovery of methoprene from spiked samples was 74.6-82.8%. In an evaluation of this method by 6 analytical laboratories, mean recoveries from spiked samples ranged from 79.4% to 84.6%. Repeatability relative standard deviation values were 2.3-8.8% and reproducibility relative standard deviation values were 8.8-23.6%. The detection limits were 0.001-0.02 microg/g and below the detection limit of the Notified Analytical Method.
我们研究了采用高效液相色谱法(HPLC)测定食品中的烯虫酯。样品用乙腈萃取,萃取液通过加入氯化钠进行盐析,使乙腈层分离。乙腈溶液用饱和乙腈的己烷洗涤,在弗罗里硅土柱上净化,然后用HPLC测定。加标样品中烯虫酯的回收率为74.6 - 82.8%。在6个分析实验室对该方法的评估中,加标样品的平均回收率在79.4%至84.6%之间。重复性相对标准偏差值为2.3 - 8.8%,再现性相对标准偏差值为8.8 - 23.6%。检测限为0.001 - 0.02微克/克,低于通知分析方法的检测限。