Effective extraction of parabens from toothpaste by vortex-assisted liquid-phase microextraction based on low viscosity deep eutectic solvent

[Display omitted] •Deep eutectic solvents with low viscosity were prepared by quaternary ammonium salts and methanol/ethanol.•A DES-VALPME procedure has been developed for the extraction of parabens from toothpaste samples.•The proposed method was simpler and requires shorter extraction time. An eff...

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Bibliographic Details
Published inMicrochemical journal Vol. 179; p. 107590
Main Authors Cao, Jiangping, Shi, Lei, He, Yifei, Liu, Yuwen, Zhao, Faqiong
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.08.2022
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Summary:[Display omitted] •Deep eutectic solvents with low viscosity were prepared by quaternary ammonium salts and methanol/ethanol.•A DES-VALPME procedure has been developed for the extraction of parabens from toothpaste samples.•The proposed method was simpler and requires shorter extraction time. An efficient, green and reliable method, namely deep eutectic solvent-based vortex-assisted liquid-phase microextraction (DES-VALPME) was proposed for the rapid extraction and sensitive high performance liquid chromatography coupled with variable wavelength detector (HPLC-VWD) determination of methylparaben (MP), ethylparaben (EP), propylparaben (PP) and butylparaben (BP) in toothpaste samples as a proof-of-concept example of trace analysis of personal care and cosmetic products. Compared with traditional DES suffering from higher viscosity, a class of six low viscosity DESs were synthesized by simply dissolving quaternary ammonium salts (hydrogen bond acceptors, HBAs) in methanol or ethanol (hydrogen bond donors, HBDs) at ambient temperature. Initial studies indicated that the DES consisting of tetrabutylammonium chloride (TBAC) and ethanol at a molar ratio of 1:5 achieved the highest extraction efficiency for all target analytes. The influence of type, molar ratio and volume of DES, extraction temperature and vortex time on the extraction efficiency was investigated and optimized systematically. Under the selected conditions, the method displayed satisfactory linearity in the range of 0.05–10 μg/g (R2 ≥ 0.9995), acceptable recoveries for the real samples (varied from 79.4% to 108.6%), good precision (with relative standard deviation ≤ 5.2 %), as well as lower limits of detection (in the range of 0.01–0.02 μg/g). This study demonstrates that the separation and determination of PBs with the developed DES-VALPME-HPLC-VWD technique is simple, efficient, sensitive and inexpensive.
ISSN:0026-265X
1095-9149
DOI:10.1016/j.microc.2022.107590