A novel, green and safe ultrasound-assisted emulsification liquid phase microextraction based on alcohol-based deep eutectic solvent for determination of patulin in fruit juices by spectrophotometry

[Display omitted] •DES based UA-ELPME was applied to extract patulin from fruit juices for the first time.•The variables affecting extraction efficiency was evaluated and optimized.•Alcohol-based DES was quickly prepared.•The method allows the determination of patulin in trace level.•The method was...

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Veröffentlicht in:Journal of food composition and analysis 2019-09, Vol.82, p.103256, Article 103256
Hauptverfasser: Altunay, Nail, Elik, Adil, Gürkan, Ramazan
Format: Artikel
Sprache:eng
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Zusammenfassung:[Display omitted] •DES based UA-ELPME was applied to extract patulin from fruit juices for the first time.•The variables affecting extraction efficiency was evaluated and optimized.•Alcohol-based DES was quickly prepared.•The method allows the determination of patulin in trace level.•The method was validated with spiked samples. In the study, a novel, green and safe microextraction procedure was developed for the determination and extraction of patulin, α, β-unsaturated lactone (4-hydroxy-4H-furo[3,2-c] pyran-2-(6H)-one), in fruit juice samples by using ultrasound-assisted emulsification liquid phase microextraction based on alcohol-based deep eutectic solvent coupled to micro-volume ultraviolet-visible spectrophotometry. The method is based on formation of chelate complex or nucleophilic adduct formation between patulin and Mg(II) in presence of nucleophilic metal chelating tris-buffer at pH 8.0, and then extraction of the formed complex into the micro-drops of deep eutectic solvent by donor-acceptor mechanism. The optimum conditions for the effective extraction of patulin from fruit juices were 500 μL of deep eutectic solvent, 75 μmol L−1 of Mg(II) solution, pH 8.0, ultrasound time of 12 min, respectively. The patulin in enriched phase was detected by micro-volume ultraviolet-visible spectrophotometry at 304 nm. Under optimal conditions, the linear response range of the method was from 7.5 to 420 μg L−1 with a detection limit of 2.2 μg L−1. After the validation study, the applicability of the method were tested by analysis of the fruit juice samples. The average recovery for spiked fruit juices was ranged from 90.2% to 106.9%, with relative standard deviations lower than 4.2%.
ISSN:0889-1575
1096-0481
DOI:10.1016/j.jfca.2019.103256