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Development of Effervescence-Assisted Switchable Polarity Solvent Homogeneous Liquid-Phase Microextraction for the Determination of Permethrin and Deltamethrin in Water Samples Prior to Gas Chromatography–Flame Ionization Detection Publisher Pubmed



Asadi T1, 2 ; Rahimi Kakavandi N3, 4 ; Nili Ahmadabadi A1 ; Heshmati A5 ; Ranjbar A1, 5 ; Abdi K6 ; Ezoddin M7
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Authors Affiliations
  1. 1. Department of Pharmacology and Toxicology, School of Pharmacy, Hamadan University of Medical Sciences, Hamadan, Iran
  2. 2. Students Research Center, Hamadan University of Medical Sciences, Hamadan, Iran
  3. 3. Department of Toxicology & Pharmacology, Faculty of Pharmacy, Tehran University of Medical Sciences (TUMS), Tehran, Iran
  4. 4. Students’ Scientific Research Center, Tehran University of Medical Sciences (TUMS), Tehran, Iran
  5. 5. Nutrition Health Research Center, Hamadan University of Medical Sciences, Hamadan, Iran
  6. 6. Department of Radiopharmacy and Medicinal Chemistry, Faculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran
  7. 7. Department of Chemistry, Payame Noor University, Tehran, Iran

Source: Biomedical Chromatography Published:2022


Abstract

An effervescent tablet-assisted switchable polarity solvent–based homogeneous liquid-phase microextraction combined with gas chromatography with flame ionization detection has been conducted for the separation, preconcentration, and detection of permethrin and deltamethrin in the river water specimens. Triethylamine (TEA) was utilized as the switchable polarity solvent in this method. The switching process was carried out by the dissolution of an effervescent tablet including an effervescency agent (sodium carbonate) and a proton donor agent (citric acid). Changing the pH of the specimen solution enhanced the conversion of TEA into protonated triethylamine carbonate through the tablet that generated carbon dioxide bubbles in situ. Finally, the addition of sodium hydroxide changed the ionization state of TEA and separated the two phases. Influential factors in the extraction were investigated. According to optimal situations, the limit of detection and the limit of quantification were 0.16 and 0.5 μg L−1 for permethrin and 0.03 and 0.1 μg L−1 for deltamethrin, respectively. The preconcentration factor was 194 in river water samples and inter- and intra-day precision (relative standard deviation %; n = 5) was <5%. The extraction recovery was obtained in the range of 93.0%–97% for permethrin and deltamethrin in water samples. © 2021 John Wiley & Sons, Ltd.
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