272
Table 7.3 (continued)
Sources
Target compounds
Deep eutectic solvent
Extraction
process
Quantification
method
Compounds’
recovery
from deep
eutectic
solvent
References
Lycium
barbarum
fruits
Myricetin; morin; rutin; luteolin;
hyperoside; quercitrin; apigenin
Choline chloride/ptoluene sulfonic acid 1:2
Heating +
stirring
HPLC-UV
(C18-WR)
Antisolvent Ali et al.
(2019)
UAE
Wine lees
Total anthocyanins; anthocyanin-3-Omonoglucosides;
delphinidin-3-O-glucoside
Choline chloride/malic
acid 1:1
UAE
HPLC-DAD (C18)
Bosiljkov
et al. (2017)
Petunidin-3-O-glucoside; malvidin-3-Oglucoside; anthocyanin-3-(6-O-pcoumaroyl)monoglucosides;
peonidin-3-(6-O-p-coumaroyl)
monoglucoside; malvidin-3-(6-O-pcoumaroyl)monoglucoside
Bisulfite bleaching
procedure
Nobis tangerine
peel
Narirutin; hesperidin; sinensetin;
nobiletin
Choline chloride/
levulinic acid/N-methyl
urea 1:1.2:0.8
UAE
UHPLC-UV (C18) Antisolvent Xu et al.
(2019)
Tangeretin; kaempferol-3-O-rutinoside;
isosinensetin;
3,5,6,7,8,3′,4′-pentamethoxyflavone;
5-hydroxy-6,7,8,3′,4′pentamethoxyflavone
UHPLC-QOrbitrap-MS/MS
Mulberry
Cyanidin-3-O-glucoside
Choline chloride/citric
acid/glucose 1:1:1
High-speed
homogenization
and cavitationburst extraction
(HSH-CBE)
CBE
UV-VIS
spectrophotometry
RP-HPLC-UV
(C18W)
Guo et al.
(2019)
L. Percevault et al.