Application of deep eutectic solvents for the extraction of phenolic compounds from extra-virgin olive oil

被引:31
作者
Fanali, Chiara [1 ]
Della Posta, Susanna [1 ]
Dugo, Laura [1 ]
Russo, Marina [1 ]
Gentili, Alessandra [3 ]
Mondello, Luigi [1 ,2 ,4 ,5 ]
De Gara, Laura [1 ]
机构
[1] Univ Campus Bio Med Roma, Unit Food Sci & Nutr, Dept Med, Rome, Italy
[2] Univ Rome Sapienza, Dept Chem Biol Pharmaceut & Environm Sci, Rome, Italy
[3] Univ Roma La Sapienza, Dept Chem, Rome, Italy
[4] Univ Messina, Dept Chem Biol Pharmaceut & Environm Sci, Chrornaleont Srl, Messina, Italy
[5] Univ Messina, Dept Chem Biol Pharmaceut & Environm Sci, BeSep Srl, Messina, Italy
关键词
deep eutectic solvents; extra-virgin olive oil; green extraction; HPLC-DAD; MS; phenolic compounds; PERFORMANCE LIQUID-CHROMATOGRAPHY; POLYPHENOLS; HEALTH; IDENTIFICATION; SEPARATION;
D O I
10.1002/elps.201900423
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A HPLC-DAD/ESI-MS method has been developed and validated for the analysis of the most representative phenolic compounds in extra-virgin olive oil (EVOO) samples using a green extraction approach based on deep eutectic solvents (DESs) at room temperature. We examined ten DESs based on choline chloride and betaine in combination with different hydrogen bond donors comprising six alcohols, two organic acids, and one urea. Five phenolic compounds, belonging to the classes of secoiridoids and phenolic alcohols, were selected for the evaluation of extraction efficiency. A betaine-based DES with glycerol (molar ratio 1:2) was found to be the most effective for extracting phenolic compounds as compared to a conventional solvent. The optimization of the extraction method involved the study of the quantity of water to be added to the DES and evaluation of the sample-to-solvent ratio optimal condition. Thirty percent of water added to DES and sample to solvent ratio 1:1 (w/v) were selected as the best conditions. The chromatographic method was validated by studying LOD, LOQ, intraday and interday retention time precision, and linearity range. Recovery values obtained spiking seed oil sample aliquots with standard compounds at 5 and 100 mu g/g concentration were in the range between 75.2% and 98.7%.
引用
收藏
页码:1752 / 1759
页数:8
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