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采用混合模式整体柱搅拌棒吸附萃取结合液相色谱法对蜂蜜中硝基咪唑残留进行简单灵敏的测定。

Simple and sensitive determination of nitroimidazole residues in honey using stir bar sorptive extraction with mixed mode monolith followed by liquid chromatography.

作者信息

Huang Xiaojia, Lin Jianbin, Yuan Dongxing

机构信息

State Key Laboratory of Marine Environmental Science, Environmental Science Research Center, Xiamen University, Xiamen, P. R. China.

出版信息

J Sep Sci. 2011 Aug;34(16-17):2138-44. doi: 10.1002/jssc.201000880. Epub 2011 Mar 10.

Abstract

In the present study, we developed a simple and sensitive method for the simultaneous determination of metronidazole (MTZ), ronidazole (RNZ), dimetridazole (DMZ), and tinidazole (TNZ) in honey. Honey samples were diluted with water, then directly treated by stir bar sorptive extraction (SBSE) based on poly(methacrylic acid-3-sulfopropyl ester potassium salt-co-divinylbenzene) monolithic material. The analytes were analyzed by HPLC equipped with diode array detector. In the optimized process, several parameters, including the composition of desorption solvent, pH value and ionic strength in sample matrix, extraction, and desorption time, were investigated in detail. Under the optimized conditions, the detection limits (S/N=3) and quantification limits (S/N=10) of the proposed method for the target compounds were achieved within the range of 0.47-1.52 and 1.54-5.0 μg/kg from spiked honey sample, respectively. The calibration curves showed the linearity ranging from 2 to 200 μg/kg for dimetridazole and tinidazole, 5-200 μg/kg for metronidazole and ronidazole. Method repeatability presented as intra- and interday precisions were found with the RSDs <4.43 and 4.41%, respectively. Finally, the developed method was successfully applied to the determination of nitroimidazoles in different honey samples and satisfactory recoveries of spiked target compounds were in the range of 71.1-114%.

摘要

在本研究中,我们开发了一种简单且灵敏的方法,用于同时测定蜂蜜中的甲硝唑(MTZ)、罗硝唑(RNZ)、二甲硝唑(DMZ)和替硝唑(TNZ)。蜂蜜样品用水稀释,然后基于聚(甲基丙烯酸 - 3 - 磺丙酯钾盐 - 共 - 二乙烯基苯)整体材料通过搅拌棒吸附萃取(SBSE)直接处理。分析物通过配备二极管阵列检测器的高效液相色谱法进行分析。在优化过程中,详细研究了几个参数,包括解吸溶剂的组成、样品基质中的pH值和离子强度、萃取和解吸时间。在优化条件下,加标蜂蜜样品中目标化合物的该方法检测限(S/N = 3)和定量限(S/N = 10)分别在0.47 - 1.52和1.54 - 5.0 μg/kg范围内。校准曲线显示二甲硝唑和替硝唑的线性范围为2至200 μg/kg,甲硝唑和罗硝唑为5 - 200 μg/kg。方法重复性以日内和日间精密度表示,相对标准偏差(RSD)分别<4.43%和4.41%。最后,所开发的方法成功应用于不同蜂蜜样品中硝基咪唑的测定,加标目标化合物的回收率令人满意,在71.1 - 114%范围内。

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