Zhang Qianchun, Liu Yulan, Wang Xingyi, Li Huimin, Chen Junyu
School of Biology and Chemistry, Xingyi Normal University for Nationalities, Xingyi 562400, China.
J Anal Methods Chem. 2017;2017:3018198. doi: 10.1155/2017/3018198. Epub 2017 May 4.
A novel method was proposed for the determination of five benzimidazoles (oxfendazole, mebendazole, flubendazole, albendazole, and fenbendazole) using magnetic graphene (G-FeO). G-FeO was synthesized via in situ chemical coprecipitation. The properties of G-FeO were characterized by various instrumental methods. G-FeO exhibited a great adsorption ability and good stability towards analytes. Various experimental parameters that might affect the extraction efficiency such as the amount of G-FeO, extraction solvent, extraction time, and desorption conditions were evaluated. Under the optimized conditions, a method based on G-FeO magnetic solid-phase extraction coupled with high-performance liquid chromatography was developed. A good linear response was observed in the concentration range of 0.100-100 g/L for the five benzimidazoles, with correlation coefficients ranging from 0.9966 to 0.9998. The limits of detection (/ = 3) of the method were between 17.2 and 32.3 ng/L. Trace benzimidazoles in chicken, chicken blood, and chicken liver samples were determined and the concentrations of oxfendazole, mebendazole, flubendazole, and fenbendazole in these samples were 13.0-20.2, 1.62-4.64, 1.94-6.42, and 0.292-1.04 ng/g, respectively. The recovery ranged from 83.0% to 115%, and the relative standard deviations were less than 7.9%. The proposed method was sensitive, reliable, and convenient for the analysis of trace benzimidazoles in food samples.
提出了一种使用磁性石墨烯(G-FeO)测定五种苯并咪唑(奥芬达唑、甲苯达唑、氟苯达唑、阿苯达唑和芬苯达唑)的新方法。通过原位化学共沉淀法合成了G-FeO。采用多种仪器方法对G-FeO的性质进行了表征。G-FeO对分析物表现出很强的吸附能力和良好的稳定性。评估了各种可能影响萃取效率的实验参数,如G-FeO的用量、萃取溶剂、萃取时间和解吸条件。在优化条件下,建立了一种基于G-FeO磁性固相萃取结合高效液相色谱的方法。五种苯并咪唑在0.100-100 g/L浓度范围内呈现良好的线性响应,相关系数在0.9966至0.9998之间。该方法的检测限(/ = 3)在17.2至32.3 ng/L之间。测定了鸡肉、鸡血和鸡肝样品中的痕量苯并咪唑,这些样品中奥芬达唑、甲苯达唑、氟苯达唑和芬苯达唑的浓度分别为13.0-20.2、1.62-4.64、1.94-6.42和0.292-1.04 ng/g。回收率在83.0%至115%之间,相对标准偏差小于7.9%。该方法灵敏可靠,便于分析食品样品中的痕量苯并咪唑。