4.5 Article

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

期刊

JOURNAL OF SEPARATION SCIENCE
卷 44, 期 21, 页码 4025-4036

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/jssc.202100269

关键词

deep eutectic solvents; dispersive liquid-liquid microextraction; dispersive solid phase extraction; gas chromatography-mass spectrometry; polycyclic aromatic hydrocarbons

资金

  1. Research Council ofTabrizUniversity of Medical Sciences [65523, 65321]

向作者/读者索取更多资源

A new and efficient extraction procedure was proposed for the simultaneous extraction of four hydroxylated metabolites polycyclic aromatic hydrocarbons from urine samples. The method showed wide linear ranges, low limits of detection and quantification, satisfactory enrichment factors and extraction recoveries, and acceptable relative standard deviations after optimization and validation according to International Council Harmonization guidelines. The introduced method was successfully applied for determination of the analytes in urine samples obtained from tobacco smokers.
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.

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