Dispersive liquid-liquid microextraction followed by magnetic nanoparticles retrieval of extract for separation and preconcentration of tetracycline from real samples before its selective spectrophotometric determination based on azo dye formation

被引:1
|
作者
Bafghi, Mohammad Reza Fattahi [1 ]
Shabani, Ali Mohammad Haji [1 ]
Dadfarnia, Shayessteh [1 ]
Yazdi, Mahnaz Nozohour [1 ]
机构
[1] Yazd Univ, Fac Sci, Dept Chem, Safaieh 89195741, Yazd, Iran
来源
SEPARATION SCIENCE PLUS | 2022年 / 5卷 / 08期
关键词
dispersive liquid-liquid microextraction; Fe3O4; nanoparticle; magnetic solid-phase extraction; spectrophotometric method; tetracycline; SOLID-PHASE EXTRACTION; WATER SAMPLES; MILK SAMPLES; ANTIBIOTICS; RESIDUES; CHROMATOGRAPHY; DOXYCYCLINE; DRUGS; ASSAY; EGG;
D O I
10.1002/sscp.202200018
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A sensitive and selective method is reported for the determination of the low amount of tetracycline in real samples. The tetracycline is extracted and preconcentrated by dispersive liquid-liquid microextraction followed by retrieval of the extract with magnetic solid-phase extraction. The extracted analyte is determined by a selective spectrophotometric method based on the formation of a water-soluble violet mono azo dye between the tetracycline and diazotized p-nitroaniline in the basic medium. The dispersive liquid-liquid microextraction was performed using acetonitrile as the disperser solvent and 1-octanol as the extracting solvent. The extracted tetracycline in the dispersive liquid-liquid microextraction step was retrieved by dispersed hydrophobic oleic-acid-modified Fe3O4 magnetic nanoparticles. Thus, the method enjoyed the high surface area and strong magnetism properties of these nanoparticles avoiding the time-consuming centrifugation or column-passing processes. Finally, the tetracycline was eluted from the magnetic solid phase into 0.5 ml of ethanol, and coupled with diazotized p-nitroaniline in the basic medium for spectrophotometric quantification. Under the optimum conditions, good linearity (in the range of 7.6-650.0 mu g/L with R-2 = 0.9987), low detection limit (2.3 mu g/L), and preconcentration factor of 30.0 were obtained. The proposed method was successively applied to the determination of tetracycline in different samples.
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页码:407 / 415
页数:9
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