A polymer-based dispersive solid phase extraction combined with deep eutectic solvent based-dispersive liquid-liquid microextraction for the determination of four hydroxylated polycyclic aromatic hydrocarbons from urine samples

被引:12
作者
Jouyban, Abolghasem [1 ,2 ,3 ]
Nemati, Mahboob [1 ,4 ]
Farazajdeh, Mir Ali [5 ,6 ]
Nabil, Ali Akbar Alizadeh [1 ]
Mogaddam, Mohammad Reza Afshar [1 ,2 ,3 ]
机构
[1] Tabriz Univ Med Sci, Food & Drug Safety Res Ctr, Tabriz, Iran
[2] Tabriz Univ Med Sci, Pharmaceut Anal Res Ctr, Tabriz, Iran
[3] Tabriz Univ Med Sci, Fac Pharm, Tabriz, Iran
[4] Minist Hlth & Med Educ, Halal Res Ctr, Tehran, Iran
[5] Univ Tabriz, Dept Analyt Chem, Fac Chem, Tabriz, Iran
[6] Near East Univ, Engn Fac, Mersin, Turkey
关键词
deep eutectic solvents; dispersive liquid-liquid microextraction; dispersive solid phase extraction; gas chromatography-mass spectrometry; polycyclic aromatic hydrocarbons;
D O I
10.1002/jssc.202100269
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A new and efficient extraction procedure was proposed and used for the simultaneous extraction of four hydroxylated metabolites polycyclic aromatic hydrocarbons from urine samples. The extraction procedure was started by dissolving an organic polymer into a water-miscible organic solvent (iso-propanol) and its injection into the sample solution. The sorbent was re-precipitated in all parts of the solution as tiny particles and the analytes were adsorbed onto the sorbent. After that, the sorbent was separated and the adsorbed analytes were eluted by choline chloride: dichloroacetic acid deep eutectic solvent. The elution solvent was mixed with choline chloride-3,3-dimethyl butyric acid deep eutectic solvent and the mixture was applied in dispersive liquid-liquid microextraction procedure for more concentration of the analytes. After optimization, the method validation was followed according to International Council Harmonization guidelines and the results showed that wide linear ranges (26-500 000 ng/L) and low limits of detection (3.6-7.2 ng/L) and quantification (11-26 ng/L) were obtained. Satisfactory enrichment factors (435-475) and extraction recoveries (87-95%), and acceptable relative standard deviations (equal or less than 8.6%) were obtained. Finally, the introduced method was successfully applied for determination of the analytes in urine samples obtained from tobacco smokers.
引用
收藏
页码:4025 / 4036
页数:13
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