Table 2. Extraction and Analysis of Phenolic Compounds Obtained from Plant Peels and Husksa.
| reference | source | best extraction conditions | extraction solvent | chromatographic analysis | TPC/TFC | phenolic compounds |
|---|---|---|---|---|---|---|
| Nayak et al. (2015)66 | Citrus sinensis peel | MAE | water–acetone (51:49, v/v) | HPLC-DAD, C18 column (4.6 mm × 250 mm, 5 μm), 30 °C, 254, 289, 520, 300, and 700 nm, 6:94 (v/v) acetic acid in water, 100% ACN, 40 min | 12.20 mg GAE/g | chlorogenic acid, catechin, rutin, gallic acid, p- coumaric acid, caffeic acid, and ferulic acid |
| T: 80 °C | ||||||
| t: 122 s | ||||||
| Po: 500W | ||||||
| F: 2.45 kHz | ||||||
| 25 mL/g | ||||||
| Wang et al. (2018)67 | red orange peel | UAE | water–ethanol (85:15, v/v) | HPLC-DAD-ESI-M2, reverse- phase amide column (15 cm × 4.6 mm), 25 °C, 320 nm, water in ACN, 40 min | n-d | tangeretin and nobiletin |
| T: 50 °C | ||||||
| t: 40 min | ||||||
| Po: 150 W | ||||||
| F: 20 kHz | ||||||
| 20 mL/g | ||||||
| Kaderides et al. (2019)68 | pomegranate peel | MAE | water–ethanol (50:50, v/v) | HPLC UV–vis, reverse-phase column (250 mm × 4.6 mm, 5 μm), 30 °C, 254 and 280 nm, 5% acetic acid in water, and CAN, 12 min | 199.4 mg GAE/g | phenolics acids, flavonoids, catechins, and procyanidins |
| T: 30 °C | ||||||
| t: 4 min | ||||||
| Po: 600W | ||||||
| F: 2.45 kHz | ||||||
| 60 mL/g | ||||||
| Mei et al. (2020)69 | Xanthoceras sorbifolia husks | UAE | water–ethanol (60:30, v/v) | HPLC UV–vis, ODS-C18 column (250 mm × 4.6 mm, 5 μm), 25 °C, 0.1% formic acid and ACN, 20 min | 23.16 mg GAE/g | gallic acid, protocatechuic acid, epicatechin, rutin, rutinoside, and quercetin |
| T: 40 °C | ||||||
| t: 40 min | ||||||
| F: 100 kHz | ||||||
| 100 mL/g | ||||||
| Figueroa et al. (2021)39 | avocado peel | MAE | water–ethanol (36:64, v/v) | HPLC-ESI-TOF/GTOF-MS, C18 column (150 nm × 4.6 nm, 1.8 μm), 25 °C, formic acid in water and ACN, 55 min | 72.04 mg GAE/g | flavonoids, catechins, procyanidins, and phenolic acids |
| T: 130 °C | ||||||
| t: 39 min | ||||||
| Po: 850 W | ||||||
| 30 mL/g | ||||||
| Dewi et al. (2022)70 | cacao pod husk | MAE | water–ethanol (50:50, v/v) | HPLC-VWD, reverse-phase column (250 mm × 4.6 mm, 5 μm), 30 °C, 30 °C, 280 nm, 0.1% of orthophosphoric acid in water, and ACN, 50 min | 100.4 mg GAE/g | catechin, quercetin, epicatechin, gallic acid, coumaric acid, and protocatechuic acid |
| T: 50 °C | ||||||
| t: 5 min | ||||||
| Po: 120 W | ||||||
| F: 2.45 kHz | ||||||
| 80 mL | ||||||
| Estrada-Gil et al. (2022)24 | rambutan peel | UAE + MAE | water (1:16, m/v) | HPLC-MS, reverse-phase (150 mm × 2.1 mm, 3 μm), 30 °C, 245, 280, 320, 550 nm, formic acid and ACN, 60 min | 176.38 mg GAE/g | geraniin, corilagin, and ellagic acid |
| UAE | ||||||
| t: 20 min | ||||||
| F: 25 kHz | ||||||
| MAE | ||||||
| T: 70 °C | ||||||
| t: 5 min | ||||||
| F: 2450 kHz | ||||||
| Anticona et al. (2022)71 | citrus peel | UAE | water–ethanol (50:50, v/v) | HPLC-UV, C18 column (250 mm × 4.6 mm, 5 μm), 280 nm, formic acid in water and ACN, 80 min | n-d | catechin, caffeic acid, vanillic acid, quercetin, naringenin, apigenin, and hesperidin |
| T: 35–40 °C | ||||||
| t: 30 min | ||||||
| Po: 400 W | ||||||
| F: 20 kHz | ||||||
| 45 mL | ||||||
| Wang et al. (2023)38 | brocade orange peels | UAE | water– methanol– DMSO (1:4:5) | UHPLC-Q-TOF-MS, C18 column (4.6 mm × 100 mm, 3.5 μm), 35 °C, formic acid and methanol, and HPLC-DAD, Aq-C18 column, same gradient, 35 °C | 24.97 mg GAE/g | caffeic acid, sinapic acid, ferulic acid, narigin, hesperidin, luteolin, rutin, sinensetin, nobiletin, and tangeretin |
| T: 26 °C | ||||||
| t: 30 min | ||||||
| Po: 60 W | ||||||
| F: 40 kHz | ||||||
| 17.6 mL/g | ||||||
| Gómez-Urios et al. (2022)72 | orange peel | magnetic stirring | choline chloride and glycerol ratio of 1:2 with 25% water | HPLC UV–vis, C18 column (250 nm × 4.6 nm, 5 μm), 280 nm, 5% acid formic in water and 40% in ACN, 80 min | 903 mg GAE/g | ascorbic acid, flavonoids, and polyphenols |
| T: 45 °C | ||||||
| t: 20 min | ||||||
| 10g/mL | ||||||
| Maimulyanti et al. (2023)34 | coffee husk from west Java, Indonesia | magnetic stirring | choline chloride and proline ratio of 1:1with 50% water | HPLC-PDA, reverse phase column (250 mm × 4.6 mm, 5 μm), 30 °C, 327 nm, 50 mM acid in distillate water and 50 mM acid in ACN, 10 min | 10.07 mg GAE/g | chlorogenic acid |
| T: 80 °C | ||||||
| t: 30 min | ||||||
| Po: 200 W | ||||||
| F: 34 kHz | ||||||
| 10 mL/g | ||||||
| Strieder et al. (2024)44 | Arabic coffee husk: green coffee beans 60:40 (w/w) | PLE | water | HPLC-PDA, Kinetex C18 column (100 mm × 4.6 mm, 2.6 μm), 50 °C, 270 and 325 nm, 0.1% acetic acid in water and in ACN, 9 min | n-d | chlorogenic acid and caffeine |
| T: 125 °C | ||||||
| P: 150 MPa | ||||||
| flow: 2 mL/min | ||||||
| 50 mL/g | ||||||
UAE: ultrasound-assisted extraction; MAE: microwave-assisted extraction; PLE: pressurized liquid extraction; HAE: homogenate-assisted extraction; TPC: total phenolic content; TFC: total flavonoid content; (UH)PLC: (ultrahigh) performance liquid chromatography; DAD/PDA: photodiode-array detector; ESI-M2: electrospray ionization coupled mass spectrometry; (Q)TOF: quadrupole time-of-flight; MS: mass spectrometry, VWD; variable wavelength detector; T: temperature; RT: room temperature; t: extraction time; SM: sample mass; P: pressure; Po: Power; A: amplitude; F: frequency; TPC: total phenolic content; TFC: total flavonoid content; GAE: gallic acid equivalent; n-d: nondetermined; ACN: acetonitrile.