液相色谱-柱后衍生法测定水产品中磺胺类药物检测条件优化

    Optimization of testing conditions for determination of sulfonamides residues in aquatic products by post-column derivation high performance liquid chromatography

    • 摘要: 在水产品中八种磺胺类药物测定的高效液相色谱-柱后衍生法方法标准的基础上,对检测条件进行优化和改进,实现了水产品中八种磺胺类(磺胺嘧啶、磺胺噻唑、磺胺甲基嘧啶、磺胺二甲基嘧啶、磺胺甲噁唑、磺胺多辛、磺胺异噁唑、磺胺喹噁啉)药物残留的高灵敏检测。磺胺嘧啶、磺胺噻唑、磺胺甲基嘧啶和磺胺二甲基嘧啶线性范围:0.025~0.5 μg/mL;磺胺甲噁唑、磺胺多辛、磺胺异噁唑线性范围:0.05~1.0 μg/mL;磺胺喹噁啉线性范围:0.1~2.0 μg/mL。线性相关系数均大于0.9990。对鲈鱼空白样品进行八种磺胺类药物的加标实验,加标量为5 μg/kg~100 μg/kg时,回收率在84.2%~109%之间,相对标准偏差为1.64%~10.6%。

       

      Abstract: The testing conditions were optimized base on the standard of determinating eight sulfonamides in aquatic products by post-column derivation high performance liquid chromatography (HPLC) method. In the optimized conditions, eight sulfonamides (sulfadiazine, sulfathiazole, sulfamerazine, sulfamethazine, sulfamethoxazole, sulfamethoxypyridazine, sulfisoxazole, sulfaquinoxaline) residues in aquatic products were separated and detected. The calibration curves were linear in a concentrations range of 0.025~0.5 μg/mL for sulfadiazine, sulfathiazole, sulfamerazine, sulfamethazine; 0.05~1.0 μg/mL for sulfamethoxazole, sulfamethoxypyridazine, sulfisoxazole and 0.1~2.0 μg/mL for sulfaquinoxaline, with r>0.9990.The average recovery was 84.2%~109% and the relative standard deviation was in the range of 1.64%~10.6% for spiked weever sample with 5 μg/kg~100 μg/kg of sulfonamides.

       

    /

    返回文章
    返回