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  •   University of Thessaly Institutional Repository
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  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Insights on the impact of deep eutectic solvents on the composition of the extracts from lemon (Citrus limon L.) peels analyzed by a novel RP-LC–QTOF-MS/MS method

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Author
Kalogiouri N.P., Palaiologou E., Papadakis E.N., Makris D.P., Biliaderis C.G., Mourtzinos I.
Date
2022
Language
en
DOI
10.1007/s00217-022-04100-0
Keyword
Chlorine compounds
Citrus fruits
Flavonoids
Liquid chromatography
Mass spectrometry
Polyphenolic compounds
Solvent extraction
Solvents
Citrus limon
Deep eutectic solvents
ESI-QTOF-MS
LC-QTOF-MS/MS
LC–QTOFMS, non-target
Lemon
Lemon peel
Non-target screenings
P-coumaric acid
Peel
Eutectics
Springer Science and Business Media Deutschland GmbH
Metadata display
Abstract
Extraction of polyphenolic compounds from lemon peels using deep eutectic solvents (DES) was investigated. A choline chloride-based DES paired with glycerol was used as the extraction solvent, alternative to conventional ones. Response surface methodology (RSM) was employed to optimize the extraction parameters, namely, the water concentration (CW), the liquid to solid ratio (RL/S) and the duration of the extraction (t) in terms of total phenol content and radical scavenging activity; the conditions that can be recommended as optimum for the recovery of the phenolic compounds were 55% (w/v), 13 mL g−1 and 36 min, respectively. The composition of the obtained extracts under optimum conditions was compared with extracts prepared in ethanol and water. A novel reversed phase ultra-pressure electrospray liquid chromatographic time-of-flight mass spectrometric method (RP-UPLC–ESI–QTOF-MS) was developed and validated for the determination of individual bioactive compounds in the extracts through target, suspect, and non-target screening. The developed RP-UPLC–ESI–QTOF-MS methodology was validated and presented adequately low limits of detection (LODs) and limits of quantification (LOQs) over the ranges 8.64 (quercetin)–30.4 μg L−1 (p-coumaric acid), and 25.9 (quercetin)–91.2 μg L−1 (p-coumaric acid), respectively. The RSD% of the within-day and between-day assays were lower than 3.2, and 9.8, respectively, demonstrating good method precision. Overall, 10 compounds were determined and quantified through target screening, as well as 4 suspect, and 9 non-target compounds were tentatively identified in the extracts by means of suspect and non-target screening, respectively. © 2022, The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.
URI
http://hdl.handle.net/11615/74202
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