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固相萃取-高效液相色谱法同时测定果蔬中吡虫啉和多菌灵残留量

Simultaneous determination of imidacloprid and carbendazim residues by SPE-HPLC

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【作者】 杨宇霞韩建欣李慧赵欣

【Author】 YANG Yuxia;HAN Jianxin;LI Hui;ZHAO Xin;Shanxi biological research institute Co.,Ltd;

【机构】 山西省生物研究院有限公司

【摘要】 建立了固相萃取-高效液相色谱同时测定果蔬中吡虫啉和多菌灵含量的方法。试样用乙腈提取,经Cleanert-NH2固相萃取小柱净化,流动相定容后,采用高效液相色谱法测定。以甲醇-水(32∶68)为流动相,流速1.0 m L/min,于270 nm波长下检测。结果表明,吡虫啉和多菌灵分别在0.02μg/m L~1.0μg/m L和0.05μg/m L~5.0μg/m L范围内线性良好,相关系数均0.999 9以上;回收率在85.1%~100.5%之间,相对标准偏差为1.6%~6.6%(n=6)。该方法简便、高效,适用于果蔬中吡虫啉和多菌灵含量的同时测定。

【Abstract】 A method for the simultaneous determination of imidacloprid and carbendazim in fruits and vegetables was developed by solid-phase extraction and high performance liquid chromatography(SPE-HPLC). The samples was extracted with acetonitrile and purified by a Cleanert-NH2 solid-phase extraction(SPE) cartridge. The extract was analyzed by HPLC with methanol-water(32∶68) as the mobile phase. The flow rate of the mobile phase was 1.0 m L/min and the detection wavelength was 270 nm. The results showed that imidacloprid and carbendazim had good linearity in the concentration ranges of 0.02 μg/m L ~1.0 μg/m L and 0.05 μg/m L ~5.0 μg/m L respectively, the correlation coefficient was above 0.9999, the recovery was 85.1% ~100.5%, and the relative standard deviation was1.6%~6.6%(n=6). The method is simple, efficient and suitable for the simultaneous determination of imidacloprid and carbendazim in fruits and vegetables.

  • 【分类号】O657.72;TS255.7
  • 【被引频次】9
  • 【下载频次】434
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