| Literature DB >> 31757027 |
Radu Claudiu Fierascu1,2, Irina Fierascu1,2, Sorin Marius Avramescu1,3, Elwira Sieniawska4.
Abstract
Large amounts of agro-industrial waste are being generated each year, leading to pollution and economic loss. At the same time, these side streams are rich source of active compounds including antioxidants. Recovered compounds can be re-utilized as food additives, functional foods, nutra-/pharmaceuticals, cosmeceuticals, beauty products, and bio-packaging. Advanced extraction techniques are promising tools to recover target compounds such as antioxidants from agro-industrial side streams. Due to the disadvantages of classical extraction techniques (such as large amounts of solvents, increased time of extraction, large amounts of remaining waste after the extraction procedure, etc.), and advanced techniques emerged, in order to obtain more efficient and sustainable processes. In this review paper aspects regarding different modern extraction techniques related to recovery of antioxidant compounds from wastes generated in different industries and their applications are briefly discussed.Entities:
Keywords: active compounds; extraction; food waste; fruits; re-utilization; vegetables
Mesh:
Substances:
Year: 2019 PMID: 31757027 PMCID: PMC6930540 DOI: 10.3390/molecules24234212
Source DB: PubMed Journal: Molecules ISSN: 1420-3049 Impact factor: 4.411
Examples of different antioxidants from agro-industrial side-streams.
| Compound Group | Source | Extracted Compounds | Ref. |
|---|---|---|---|
| Phenolic compounds | Apple seeds | Phloridzin, ellagic acid, caffeic acid, ferrulic acid, protocatechuic acid, gallic acid | [ |
| Phenolic compounds | Avocado seeds | Procyanidin B2, epicatechin, rans-5- | [ |
| Phenolic compounds | Rapeseed cake | Sinapine, sinapic acid and canolol | [ |
| Phenolic compounds | Citrus peel | Total phenolic content | [ |
| Phenolic compounds | Coconut shell | Total phenolic content | [ |
| Phenolic compounds | Grape marc, | Total phenolic content | [ |
| Phenolic compounds | Black currant | Delphinidin 3- | [ |
| Phenolic acids, flavonoids | Grape skin | Gallic acid, caffeic acid, epicatechin, | [ |
| Flavonols | Pistachio hulls | Gallic acid, penta- | [ |
| Flavonoids, carotenoids | Passion fruit peel | β-carotene, provitamin A, quercetin, lycopene | [ |
| Carotene | Carrot pomace | α- and β-carotene | [ |
| Lycopene | Tomato peel | Lycopene | [ |
| Non phenolic compounds | Lettuce | Ascorbic acid | [ |
| Non phenolic compounds | Sugarcane molasses | Pullulan | [ |
| Non phenolic compounds | Rice bran oil | Tocopherol | [ |
Figure 1Flow chart of extraction process.
Some examples of recovery of antioxidant compounds from edible oil industry wastes 1.
| Waste | Extraction Method | Optimized Extraction Conditions | Obtained Compounds | Antioxidant Assay | Ref. |
|---|---|---|---|---|---|
| Flaxseed hulls | PEF | Electrode area (cm2)—95 | Tocopherols, polyphenols, phytosterols | - | [ |
| Palm pressed fibers | PLE, Sx, Pc | Temperature (°C)—35, 35, 78.4 | Carotenoids | - | [ |
| Palm pressed fiber | PLE | Solvents: CO2 and compressed liquefied petroleum gas | β-sitosterol, | HPX/XOD | [ |
| Palm pressed fiber | UAE | Ultrasound intensity (W.cm−2)—120 | β-sitosterol, | DPPH | [ |
| Olive leaves | ASE | Temperature (°C)—190 | Oleuropein, Luteolin-7- | DPPH | [ |
| Olive tree pruning biomass | UAE | Power (W)—400 | Phenolic compounds Flavonoids | DPPH, ABTS, FRAP | [ |
| Olive pomace | UAE, MAE, Se | Ethanol concentration (%)—90, | Hydroxytyrosol, maslinic acid, oleanolic acid | - | [ |
| Olive leaves and tree bark | SCe | Temperature (°C)—60, | α-tocopherol, squalene | - | [ |
| Olive waste | UAEH | Cellulase, pectinase | Phenolic compounds | DPPH, ABTS, FRAP | [ |
| Sunflower leaves | PLE, ESE | CO2 and mixture of solvents (ethanol in water from 0 to 100%) | Diterpenoids, flavonoids | - | [ |
| Rapeseed press-cake | HVED | High voltage pulsed power (kV)—40 | Protein, polyphenols and isothiocyanates | TEAC | [ |
| Pumpkin seeds | UAE | Frequency (GHz)—2.45 | Phenolic compounds | DPPH | [ |
1 Where: ABTS—2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid; ASE—accelerated solvent extraction; DPPH (assay)—2,2-diphenyl-1-picrylhydrazyl; ESE—enhanced solvent extraction; EtOH—ethanol; FRAP (assay)—ferric reducing ability of plasma; hex—hexane; HVED—high voltage electric discharge; MAE—microwave-assisted extraction; Pc—percolation; PEF—pulsed electric fields; PLE—pressurized liquid extraction; SCe—supercritical extraction; Se—solvent extraction; Sx—Soxhlet extraction; TEAC (assay)—Trolox equivalent antioxidant capacity; UAE—ultrasound-assisted extraction; UAEH—ultrasound-assisted enzyme hydrolysis; HPX/XOD—Hypoxanthine/xanthine oxidase system (superoxide radical scavenging activity).
Some examples of recovery of antioxidant compounds from fruits and vegetable wastes 1.
| Waste | Extraction Method | Optimized Extraction Conditions | Obtained Compounds | Antioxidant Assay | Ref. |
|---|---|---|---|---|---|
| Apple pomace | Cec | Methanol, ethanol and ethyl acetate | Phenolic compounds and triterpenic acids | DPPH, FRAP, ABTS | [ |
| Apple pomace | MAE | Solvent—70% acetone and 60% ethanol, | Phenolic compounds | DPPH | [ |
| Mango peels | ScE | Pressure (MPa)—25.0 | Carotene | - | [ |
| Orange peel | LSE | Solvent: cyclopentyl methyl ether, ethyl lactate, isopropyl alcohol, polyethylene glycol 300, isopropyl acetate, dimethyl carbonate, methyl ethyl ketone, 2-methyl-tetrahydrofuran and ethyl acetate | Limonene | - | [ |
| Cocoa shells | UAE, HC | Hexane, hydro-alcoholic solution (70:30 EtOH/H2O) | Catechins epicatechins | DPPH | [ |
| Tomato seeds | UAE | Power (W)—90 | Lycopene | - | [ |
| Tomato seeds | MAE, OT | Temperature (°C)—70 | Rutin | - | [ |
| Onion waste | SbWE(PT) | Temperature (°C)—145 | Quercitin | - | [ |
| Pomegra-nate waste | UAE | Temperature (°C)—51.5; | Carotenoids | - | [ |
1 Where: ABTS—2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid; Cec—classical extraction with centrifugation; DPPH (assay)—2,2-diphenyl-1-picrylhydrazyl; FRAP (assay)—ferric reducing ability of plasma; HC—hydrodynamic cavitation; LSE—liquid solid extraction; MAE—microwave -ssisted extraction; OT—ohmic technologies; SbWE(PT)—Subcritical water extraction with physical pretreatment; ScE—Supercritical extraction; UAE—ultrasound-assisted extraction.
Some examples of recovery of antioxidant compounds from other different industries wastes 1.
| Waste | Extraction Method | Optimized Extraction Conditions | Obtained Compounds | Antioxidant Assay | Ref. |
|---|---|---|---|---|---|
| Squid muscle | SbWE | Temperature (°C)—250 for aminoacids; 160 for peptides | Amino acids Peptides | ABTS | [ |
| Poultry wastes | SbWE | Temperature (K) 533 | Amino acids | - | [ |
| Waste chicken breast muscle | OT | Sets of high voltage short pulses and by low voltage long pulses | Proteins | DPPH | [ |
|
| MAE | Pressure (psi)—120 | Fucoidan | - | [ |
| MAE | Solvent: 55% ethanol | Phlorotannins | - | [ | |
| MAE coupled with HSCCC | Solvent: ethanolic KOH solution (1.5 mol/L) | Fucosterol, 24-methylenecholesterol, phytol | - | [ | |
|
| UAE | Solvent: 2mL of ethanol, 10mg ascorbic acid, 3mL of n-hexane, | Tocopherol | - | [ |
| PEF | The electric field (kV/cm)—20 | Carotenoids | - | [ |
1 Where: ABTS—2,2′-azino-bis(3-ethylbenzothiazoline-6-sulphonic acid; DPPH (assay)—2,2-diphenyl-1-picrylhydrazyl; HSCCC—high-speed counter current chromatography; PEF—pulsed electric fields; OT—ohmic technologies; MAE—microwave-assisted extraction; SbWE—subcritical water extraction; UAE—ultrasound-assisted extraction.
Recovery of antioxidant compounds from agro food side streams and potential applications.
| Waste | Active Compounds | Application | Ref. |
|---|---|---|---|
|
| |||
| Palm pressed fiber | β-Sitosterol, | Cosmetic formulation with high sun protection factor | [ |
| Sunflower leaves | Diterpenoids, flavonoids | Natural herbicide | [ |
| Sunflower seed | Phenolic compounds | Antioxidant additive for sunflower oil | [ |
| Soy bean waste | Proteins | Biopackaging | [ |
| Olive waste extract | Phenolic compounds | Food industry (increasing shelf life of meat) | [ |
| Olive mill wastes | Phenolic compounds | Food antioxidants | [ |
|
| |||
| Apple seeds | Phenolic compounds | Food industry | [ |
| Berries | Phenolic compounds | Pharmaceutical formulations | [ |
| Mango peels | Carotene | Antioxidant additive for edible oil | [ |
| Banana peels | Caffeic acid | Cosmetic formulations | [ |
| Citrus peels | Phenolic compounds, | Pharmaceutical formulations | [ |
| Citrus wastes | Phenolics and flavonoids | Cosmetic formulations | [ |
| Citrus peels | Terpinene, cymene | Pharmaceutical formulations | [ |
| Cocoa | Total extract | Larvicidal nanoparticles | [ |
| Grape pomace | Phenolic compounds | Food industry | [ |
|
| |||
| Tomato wastes | Lycopene | Health related applications | [ |
| Beetroot pomace | Betalains | Medicinal and food applications | [ |
| Carrot pomace | Carotenoids | Pharmaceutical formulations | [ |
| Garlic waste | Ethanolic extract | Food additive to increase products shelf life | [ |
| Onion waste | Phenolic compounds | Food industry | [ |
| Cauliflower by-products | Isothiocyanates | Food industry | [ |
|
| |||
| Meat industry wastes | Gelatin | Pharmaceutical formulations (antioxidant and antihypertensive) | [ |
| Algal biomass | Sulfated polysaccharides | Pharmaceutical formulations | [ |
| Algal biomass | α-Carnitine | Nutraceutical products | [ |
| Squid waste | Astaxanthin | Pharmaceutical industry | [ |
| Shrimps shells | Astaxanthin | Food packaging material | [ |
| Shrimps shells | Carotenoprotein | Supplementary nutritive feed | [ |