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用于从食品样品中提取苯并咪唑并通过高效液相色谱分析的磁性石墨烯平台的原位合成。

In Situ Synthesis of a Magnetic Graphene Platform for the Extraction of Benzimidazoles from Food Samples and Analysis by High-Performance Liquid Chromatography.

作者信息

Zhang Qianchun, Liu Yulan, Wang Xingyi, Li Huimin, Chen Junyu

机构信息

School of Biology and Chemistry, Xingyi Normal University for Nationalities, Xingyi 562400, China.

出版信息

J Anal Methods Chem. 2017;2017:3018198. doi: 10.1155/2017/3018198. Epub 2017 May 4.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6bd5/5435904/9e1286522f39/JAMC2017-3018198.001.jpg

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