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作 者:张敏[1] 闫超杰 付海滨[3] 李修平[4] 徐宜宏[3]
机构地区:[1]沈阳农业大学工程学院,辽宁沈阳110866 [2]锦州出入境检验检疫局,辽宁锦州121013 [3]沈阳出入境检验检疫局,辽宁沈阳110016 [4]济宁出入境检验检疫局,山东济宁272100
出 处:《食品与发酵工业》2014年第2期192-195,共4页Food and Fermentation Industries
基 金:沈阳市2012年科学技术计划农业攻关项目(No.F10-235-4-00)
摘 要:建立了一种简单、快速,同时检测水果中赤霉素、多效唑和烯效唑残留量的固相萃取-高效液相色谱(SPE—HPLC)方法。该方法经80%甲醇水提取样品,C18固相萃取小柱净化,采用DAD检测器220nm紫外扫描检测。结果表明:3种植物生长调节剂在0.5~10μg/mL内线性关系良好(r≥0.999);检出限分别为赤霉素0.002mg/kg、多效唑0.04mg/kg、烯效唑0.02mg/kg;在0.2~0.8mg/kg加标水平下,3种植物生长调节剂平均回收率为78%~91%;相对标准偏差为2.4%~5.4%。A simple and rapid SPE-HPLC method for the determination of Gibberellin, Paclobutrazol and Unicon- azole residues in fruits was developed. The sample was extracted with 80% methanol -water solution, then was puri- fied by Cls column and detected in 220 nm with a DAD detector. Linear ranges of three plant growth regulators were in the range of 0.5 - 10 μg/mL with correlation coefficients more than 0. 999. The minimum detection limit of Gib- berellin, Paclobutrazol and Uniconazole were 0. 002 mg/kg, 0.04 mg/kg and 0.02 mg/kg respectively. The average recoveries at s tions (RSDs) piked concentration levels of 0.2 -0.8 mg/kg ranged from 78% to 91% , with relative standard devia- of 2.4% -5.4%.
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