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作 者:刘英 李韵之 陈列忠[2] 王彦华[2] 许振岚[2] 蒋金花[2] 汤涛[2] 陈文学[1] 王强[1,2] 张昌朋[2]
机构地区:[1]海南大学食品学院,海南海口570228 [2]浙江省农业科学院农产品质量标准研究所,省部共建国家重点实验室培育基地-浙江省植物有害生物防控重点实验室,农业部农药残留检测重点实验室,浙江杭州310021
出 处:《浙江农业学报》2018年第2期261-267,共7页Acta Agriculturae Zhejiangensis
基 金:国家重点研发项目子课题(2016YFD0200204-);公益性行业(农业)科研专项经费项目(201503107-12)
摘 要:为建立芹菜根、茎、叶中吡虫啉、唑螨酯残留的Qu ECh ERS-LC-MS/MS分析方法,采用Qu ECh ERS方法对样品进行提取和净化,通过液相色谱-串联三重四极杆质谱联用仪(LC-MS/MS)测定样品中吡虫啉、唑螨酯残留。结果表明:添加质量分数为0.05~1.00 mg·kg^(-1)时,吡虫啉在芹菜根、茎、叶中的平均添加回收率为77.15%~103.48%,RSDs为1.40%~9.97%;唑螨酯在芹菜根、茎、叶中的平均添加回收率为77.35%~100.42%,RSDs为2.01%~6.95%。吡虫啉、唑螨酯的检出限(LODs)分别是0.120、0.015μg·kg^(-1);吡虫啉在芹菜根、茎、叶的定量限(LOQs)分别为1.65、0.87、1.08μg·kg^(-1);唑螨酯在芹菜根、茎、叶的LOQs分别是1.24、0.75、0.78μg·kg^(-1)。该方法操作简单,回收率、精密度均符合农药残留分析的要求,适合实验室大量样品的检测。In this study,a simple and practical Qu ECh ERS-liquid chromatography-tandem mass spectrometry( LCMS/MS) method was established to detect the residues of imidacloprid and fenpyroximate in the roots,stems,leaves of celery. The samples were extracted and purified by Qu ECh ERS method,and analyzed by LC-MS/MS. Results showed that the average recoveries of imidacloprid in roots,stems,leaves of celery were 77. 15%-103. 48% at three spiking levels from 0. 05 mg·kg^(-1) to 1. 00 mg·kg^(-1) with relative standard deviations( RSDs) of 1. 40%-9. 97%. The average recoveries of fenpyroximate in roots,stems,leaves of celery were 77. 35%-100. 42% at three spiking levels from 0. 05 mg·kg^(-1) to 1. 00 mg·kg^(-1) with relative standard deviations( RSDs) of 2. 01%-6. 95%.Limit of detections( LODs) were estimated to be 0. 120 μg·kg^(-1) for imidacloprid,and 0. 015 μg·kg^(-1) for fenpyroxi-mate,respectively. Limit of quantitations( LOQs) for imidacloprid in the roots,stems,leaves of celery were 1. 65,0. 87 and 1. 08 μg·kg^(-1),respectively. LOQs for fenpyroximate were 1. 24 μg·kg^(-1)( roots),0. 75 μg·kg^(-1)( stems)and 0. 78 μg·kg^(-1)( leaves). The celery samples were detected using this established method,the recovery and the precision were in accordance with the requirements of pesticide residue analysis. The method was suitable for the detection of a large number of samples in the laboratory.
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