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Separation and Quantification of Diazinon in Water Samples Using Liquid-Phase Microextraction-Based Effervescent Tablet-Assisted Switchable Solvent Method Coupled to Gas Chromatography-Flame Ionization Detection Publisher Pubmed



Kakaei H1, 2 ; Shahtaheri SJ3, 4 ; Abdi K5 ; Rahimi Kakavandi N1
Authors
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Authors Affiliations
  1. 1. Department of Occupational Health Engineering, School of Health, Ilam University of Medical Sciences, Ilam, Iran
  2. 2. Health and Environment Research Center, Ilam University of Medical Sciences, Ilam, Iran
  3. 3. Department of Occupational Health Engineering, School of Health, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Institute for Environmental Research Center for Water Quality Research, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Department of Nuclear Pharmaceutical Group, School of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran

Source: Biomedical Chromatography Published:2023


Abstract

This study used a liquid-phase microextraction-based effervescent tablet-assisted switchable solvent method coupled to gas chromatography-flame ionization detection as an eco-efficient, convenient-to-use, cost-effective, sensitive, rapid, and efficient method for extracting, preconcentrating, and quantifying trace amounts of diazinon in river water samples. As a switchable solvent, triethylamine (TEA) was used. In situ generation of CO2 using effervescent tablet containing Na2CO3 and citric acid changed the hydrophobic TEA to the hydrophilic protonated triethylamine carbonate (P-TEA-C). CO2 removal from the specimen solution using NaOH caused P-TEA-C to be converted into TEA and led to phase separation, during which diazinon was extracted into the TEA phase. The salting-out process was helpful in enhancing extraction efficiency. In addition, a number of significant parameters that affect extraction recovery were examined. Under optimum conditions, the limit of detection and limit of quantitation were 0.06 and 0.2 ng/ml, respectively. The extraction recovery percentage and pre-concentration factor were obtained at 95 and 190%, respectively, and the precision (inter- and intra-day, relative standard deviation %, n = 5) was <5%. © 2023 John Wiley & Sons Ltd.
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