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作 者:程猷[1,2] 薛健[1] 黄晓会[1] 彭峥国[1] 王建明[2] 庞作正[2]
机构地区:[1]中国医学科学院药用植物研究所,北京100193 [2]黑龙江中医药大学药学院,哈尔滨150040
出 处:《中国药房》2012年第15期1421-1423,共3页China Pharmacy
基 金:国家科技重大新药创制专项课题(2009ZX09502-027;2009ZX09308-006)
摘 要:目的:建立同时测定黄芪中41种有机磷农药残留的方法。方法:采用毛细管气相色谱法。样品用40mL乙腈冰浴超声提取30min,用气相色谱配备火焰光度检测器进行测定:色谱柱为ZB-1701毛细管柱(30m×0.25mm×0.25μm),进样口温度为250℃,检测器温度为250℃,不分流进样。结果:41种有机磷农药最小检出限在0.9~22.5μg.kg-1之间,平均回收率在70.6%~113.9%之间,RSD在0.2%~14.1%之间。结论:本方法操作简便,回收率、准确度、精密度均符合农药残留分析的要求,可用于黄芪中41种有机磷农药残留的快速检测。OBJECTIVE:To establish the method for the simultaneous determination of 41 residual organophosphorus pesticides in Astragali Radix.METHODS:Capillary gas chromatography was adopted.Samples were extracted on ice for 30 min ultrasound with 40 mL acetonitrile.The sample was determined by GC equipped with flame photometric detector(FPD).The ZB-1701 capillary column(30 m×0.25 mm×0.25 μm) was adopted.The injecton port temperature was 250 ℃ and detector temperature was 250 ℃ with unsplitting injection.RESULTS:The minimum detectable limit of 41 oganophpsphorus pesticides was from 0.9 to 22.5 μg·kg-1.The average recovery was 70.6%~113.9% with RSD of 0.2%~14.1%.CONCLUSION:The method is simple in operation.Recovery,accuracy and precision are all meet requirements of residual pesticides analysis.It can be used for rapid determination of 41 residual oganophpsphorus pesticides.
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