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机构地区:[1]吉林市食品药品检验所,吉林吉林132000 [2]空军总医院药学部,北京100142
出 处:《中国医院用药评价与分析》2013年第10期914-917,共4页Evaluation and Analysis of Drug-use in Hospitals of China
摘 要:目的:建立固相萃取-气相色谱-质谱联用法同时测定白术中8种有机氯农药残留量。方法:样品以丙酮超声提取,采用氨基固相萃取柱进行净化,气相色谱-质谱联用技术进行测定。结果:8种有机氯农药在10~1 000μg/L范围内呈良好的线性关系,8种农药的检测限在0.3~2.0μg/kg之间,定量限在1.0~6.0μg/kg之间,3个水平添加回收率在82.07%~105.13%之间,相对标准偏差(RSD)〈6%(n=9)。结论:本方法灵敏度高,重现性好,可用于白术中8种有机氯农药残留量的检测。OBJECTIVE:To establish an SPE-GC-MS (Solid Phase Extraction-Gas Chromatography-Mass Spectrometry) method for the simultaneously determination of 8 organoehlorine pesticides in Atractylodes Macrocephala. METHODS: The sample was extracted ultrasonically using acetone, purified using NH2-solid phase extraction column and determined by GC-MS. RESULTS: The linear range of the 8 organochlorine pesticides was 10-1 000 μg/L, and their limits of detection (LOD) ranged within 0. 3-2. 0μg/kg and limits of quantitation (LOQ) ranged at 1.0-6.0μg/kg. The average fortified recovery rates at three levels ranged at 82.07%-105.13% with relative standard deviations (RSD) less than 6% (n = 9 ). CONCLUSION: The method is sensitive and reproducible and it can be used for the detection of pesticide residues of 8 organochlorine in Atractylodes Macrocephala.
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