Table 4.
Survey on the applications of PLE to obtain flavonoids from natural sources using environmentally-friendly organic solvents.
Sample | Solvent (%) | PLE conditions (mode, reactor volume, extraction time, solvent flow rate) | Temperature (°C) | Pressure (bar) | Target compounds | Yield or recovery | Reference |
---|---|---|---|---|---|---|---|
Goldenberry | Ethanol (70%) | Dynamic, 7.5 mL, 10–60 min, 1–3 mL/min | N/I | 100–200 | Quercetin Rutin_hydrate Mangiferin |
0.57 mg/L 1.20 mg/L 3.57 mg/L |
Corazza et al., 2018 |
Grape marc | Ethanol (50–100%) Water-ethanol acidified |
N/I, 50 mL, 220 min, 5 g/min | 40–100 | 100 | Anthocyanins | 10.21 mg malvidin-3-O-glucoside/g dr | Pereira et al., 2019 |
Citrus by-products | Ethanol (50–99.5%) | Dynamic, 10 mL, 5–40 min, 2.37 g/min | 45–65 | 100 | Hesperidin | 19.3 mg/g dry peel | Barrales et al., 2018 |
Passion fruit rinds | Ethanol (70–100%) | Dynamic, 10 mL, 60 min, 2.7–3 mL/min | 30–60 | 100 | Isoorientin Vicenin Orientin Isovitexin Vitexin |
118 μg/g dried rind 85 μg/g dried rind 25 μg/g dried rind 34 μg/g dried rind 17 μg/g dried rind |
Viganó et al., 2016 |
Waxy barley | Ethanol (5–20%) | Static, 100 mL, 15–55 min, 2–6 mL/min | 135–175 | 150 | Catechin, Naringinin, Morin, Rutin, and Quercetin | N/I | Benito-Román et al., 2015 |
Dracocephalun kotschyi | Methanol | Static and dynamic, 100 mL, N/I, 0.4–0.8 | 50–80 | 20–40 | Quercetin Luteolin |
6.13 mg/g 13.25 μg/g |
Kamali et al., 2016 |
Lippia citriodora leaves | Ethanol (15–85%) | Static, 33 mL, 5–20 min, N/I | 40–180 | 110 | Luteolin-7-diglucuronide, apigenin-7-diglucuronide, chrysoeriol-7-diglucuronide, acacetin-7-diglucuronide, methyl quercetin, dimethyl kaempferol, and dimethyl quercetin | N/I | Leyva-Jiménez et al., 2018 |
Moringa oleifera leaves | Ethanol (55–100%) | Static, N/I, 60–210 min, N/I | 110–140 | N/I | Quercetin and kaempferol | N/I | Wang et al., 2017 |