首页|HPLC-MS/MS法分析18%吡虫啉·氟酰脲悬浮剂含量

HPLC-MS/MS法分析18%吡虫啉·氟酰脲悬浮剂含量

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[目的]采用HPLC-MS/MS建立18%吡虫啉·氟酰脲悬浮剂含量检测方法.[方法]采用高效液相色谱-串联质谱法,以25%水(2mmol/L乙酸铵)溶液+75%乙腈(0.1%甲酸)为流动相,使用以Agilent Zorbax SB C185 μm填料的不锈钢柱和MSD检测器,对试样中的吡虫啉和氟酰脲进行测定,外标法定量.[结果]该分析方法的吡虫啉和氟酰脲线性相关系数分别为0.9996和0.9999,变异系数分别为1.14%和5.50%,平均回收率分别为88.21%和79.78%.[结论]该方法操作简单,准确度、精密度及灵敏度均满足要求,可用于18%吡虫啉·氟酰脲悬浮剂含量检测.
Analysis of Imidacloprid · Novaluron 18% SC by HPLC-MS/MS
[Aims] The aims were to establish a HPLC-MS/MS method to detect the imidacloprid · novaluron 18% suspension agent.[Methods] The separation and quantitative analysis of imidacloprid and novaluronin the samples were conducted by HPLC-MS/MS and MSD detector with the mixture of 2 mmol/L ammonium acetate solution and acetonitfile (within 0.1% formic) (25:75,by vol) as mobile phase and with ZORBAX SB-C18 column as fix phase.[Results] The results showed that the linear correlation coefficients for imidacloprid and novaluron were 0.9996 and 0.9999,the variation coefficients were l.14 and 5.50%,the average recovery rates were 88.21 and 79.78%,respectively.[Conclusions] The method is simple,the accuracy,precision and sensitivity can meet the requirement,which is suitable for analysis of imidacloprid · novaluron 18% suspension agent.

imidaclopridnovaluronsuspension agentHPLC-MS/MS

陈迎丽、林绍霞、何钰、王睿、杨鸿波、宋光林

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贵州大学,贵阳550002

贵州省分析测试研究院,贵阳550002

吡虫啉 氟酰脲 悬浮剂 高效液相色谱-串联质谱法

贵州茶叶品质高质化技术与信息化合作研究黔科合院地合[2012]7003号

2015DFA41280

2016

农药
沈阳化工研究院有限公司

农药

CSTPCDCSCD北大核心
影响因子:0.665
ISSN:1006-0413
年,卷(期):2016.55(12)
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