Sonochemical synthesis of deep eutectic solvent-coated magnetic nanoparticles and their application in magnetic dispersive micro solid phase extraction-dispersive liquid-liquid microextraction of polycyclic aromatic hydrocarbons from mascara

被引:18
作者
Dilmaghani, Araz Bazzaz [1 ,2 ]
Monajjemzadeh, Farnaz [2 ,3 ]
Mogaddam, Mohammad Reza Afshar [3 ,4 ]
Farajzadeh, Mir Ali [5 ,6 ]
机构
[1] Tabriz Univ Med Sci, Student Res Comm, Tabriz, Iran
[2] Tabriz Univ Med Sci, Fac Pharm, Pharmaceut & Food Control Dept, Tabriz, Iran
[3] Tabriz Univ Med Sci, Food & Drug Safety Res Ctr, Tabriz, Iran
[4] Tabriz Univ Med Sci, Pharmaceut Anal Res Ctr, Tabriz, Iran
[5] Univ Tabriz, Fac Chem, Dept Analyt Chem, Tabriz, Iran
[6] Near East Univ, Engn Fac, Mersin 10, TR-99138 Nicosia, North Cyprus, Turkey
关键词
Polycyclic aromatic hydrocarbon; Mascara; Magnetic dispersive micro solid phase extraction; Deep eutectic solvent coated magnetic nanoparticles; CHROMATOGRAPHY;
D O I
10.1016/j.microc.2022.107665
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In this study, application of magnetic dispersive micro solid phase extraction of polycyclic aromatic hydrocarbons from mascara was reported. The extracted analytes were concentrated by a dispersive liquid-liquid microextraction procedure to reach high enrichment factors and low detection limits. In this work, deep eutectic solvent-coated iron nanoparticles were synthesized sonochemically and characterized by energy-dispersive X-ray spectroscopy, scanning electron microscopy, Furrier transform infrared spectrometry, and vibrating sample magnetometry. The extraction procedure was done by extracting the analytes from mascara into an aqueous solution composed of methanol and deionized water. Then the sorbent was added into the solution and the mixture was vortexed. After that the sorbent was separated from the aqueous solution and the analytes were desorbed by methanol with the aid of vortexing. Whole of the elution solvent was collected and mixed with carbon tetrachloride and dispersed into sodium chloride solution. Validation data showed that limits of detection and quantification were within the ranges of 0.33-0.57 and 1.1-1.9 ng/g, respectively. Relative standard deviation values were <= 8.6%. The extraction recovery values were in the range of 80-95%. The new method was successfully used for the analysis of the studied compounds in five mascara samples and three analytes were detected in all samples at ng/g level.
引用
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页数:9
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