Table 6.
Principle | Sources | Compounds extracted | Process conditions | Reference |
---|---|---|---|---|
Extract targeted analytes from a sample matrix into a small amount of S using high Ts and pressures | Rosmarinus officinalis L. (rosemary) leaves | Rosmarinic acid, Carnosic acid, Carnosol |
183 °C, 130 bar, and 3 min |
Hirondart et al. 2020 |
Silybum marianum L. Gaertner fruits | Silymarin | Acetone, 125 °C, 10 min, and 60 bar | Wianowska and Wiśniewski 2015 | |
Feijoa leaf | Gallic acid, Catechin and Isoquercetin | Ethanol–water, 80 °C | Santos et al. 2021 | |
Orange peel | Hesperidin, Naringin, Narirutin, tangeretin, naringenin, hesperidin | 75% ethanol, 65 °C, 40 min, and 10 MPa | Anticona et al. 2020 | |
underutilized chia seeds | Omega 3-rich oils (ALA and Linoleic acid) | Ethanol, 60 °C, and 10 min | Villanueva-Bermejo, 2019 | |
Moringa oleifera leaves | Phenolic compounds |
35% ethanol, 128 °C, 20 min |
Rodríguez-Pérez et al. 2016 | |
Neochloris oleoabundans | Carotenoids | Ethanol, 100 °C, 20 min, 1500 psi, 0.6 g algae + 2 g sea-sand | Castro-Puyana et al. 2017 | |
Fucus vesiculosus | Gallic, Protocatechuic, and Gentisic acids |
58.65% ethanol, 137.18 °C, and 4.68 min, |
Sumampouw et al. 2021 | |
Chlorella sp. microalgae | Phenolic compounds |
Water, 100 °C and 250 °C, and 5 to 20 min |
Zakaria et al. 2020 |