| Literature DB >> 35204085 |
Abigail García-Villegas1, Alejandro Rojas-García1, María Del Carmen Villegas-Aguilar1, Patricia Fernández-Moreno1, Álvaro Fernández-Ochoa2,3, María de la Luz Cádiz-Gurrea1, David Arráez-Román1, Antonio Segura-Carretero1.
Abstract
The increasing production of tropical fruits followed by their processing results in tons of waste, such as skins or seeds. However, these by-products have been reported to be rich in bioactive compounds (BACs) with excellent properties of interest in the cosmeceutical industry: antioxidant, anti-aging, anti-inflammatory, antimicrobial and photoprotective properties. This review summarizes the tropical fruits most produced worldwide, their bioactive composition and the most important and studied therapeutic properties that their by-products can contribute to skin health, as well as the different approaches for obtaining these compounds using techniques by conventional (Soxhlet, liquid-liquid extraction or maceration) and non-conventional extractions (supercritical fluid extraction (SFE), ultrasound-assisted extraction (UAE), microwave-assisted extraction (MAE), pressurized liquid extraction (PLE) and two-phase aqueous system), followed by their identification by HPLC-MS or GC-MS analysis. Moreover, this work encompasses several studies that may prove the effects of seeds and skins from tropical fruits against oxidative stress, hyperpigmentation, acne, aging or UV radiation. Therefore, the investigation of functional components present in tropical fruit by-products under a circular bioeconomy model could be of great interest for the cosmeceutical industry and a very promising option for obtaining new cosmeceutical formulations.Entities:
Keywords: by-products; cosmeceuticals; green extraction; phenolic compounds; skin health; tropical fruits
Year: 2022 PMID: 35204085 PMCID: PMC8868306 DOI: 10.3390/antiox11020203
Source DB: PubMed Journal: Antioxidants (Basel) ISSN: 2076-3921
Figure 1Worldwide production of the major tropical and subtropical fruits.
Different green extraction used to obtain bioactives from tropical fruit by-products.
| Fruit | By-Product | Composition Solvent | Extraction Method | Characterization Method | Major Compounds Extracted/Identified | Ref. |
|---|---|---|---|---|---|---|
| Mango | Seed Kernel | EtOH (50%) | Agitation for 1 h at room temperature and 2000 rpm | HPLC-UV/Vis | Gallic acid, caffeic acid, rutin, Penta-O-galloyl-b-D-glucose, galloylglucose species with galloyl moieties (greater than five) | [ |
| Peel | EtOH | UAE at 25 kHz; MAE at 2450 mHz | HPLC/ESI/MS | Phenolic compounds and flavonoids | [ | |
| Lactic acid, | MAE at 436.45 W, 19.66 min | HPLC | Mangiferin | [ | ||
| EtOH | MAE + UAE (2450 MHz and 25 KHz, respectively) | HPLC/ESI/MS | Polyphenols | [ | ||
| Pineapple | Core | Phosphate buffer | Agitation | MALDI-TOF-TOF | Glycylendopeptidases | [ |
| H2O | Autohydrolysis | HPLC | Gallic, hydroxybenzoic, chlorogenic, coumaric and caffeic acids and epicatechin | [ | ||
| Rind | N-Hexane | Cold extraction | GC-MS | Limonene, alpha-farnesene, trans caryophyllene and myrcene | [ | |
| Avocado | Seed | EtOH | MAE at 71.64 °C for 14.69 min | HPLC-ESI-MS | Perseitol, procyanidins, hydroxytyrosol glycoside, caffeoylquinic acid, coumaroylquinic acid, catechin and epicatechin | [ |
| EtOH/H2O (80:20, | UAE for 15 min at 25 °C | HPLC-MS/MS | Procyanidin B1, catechin, epicatechin and trans-5- O-cafeoyl-D-quinic acid | [ | ||
| Peel | EtOH (36%) | MAE for 39 min at 130 °C | HPLC-ESI-TOF/ | Quinic acid, citric acid, syringic acid, procyanidins, catechin, epicatechin, rutin, quercetin derivates, naringenin and kaempferol | [ | |
| MeOH (80%) | Maceration at 15 °C for 24 h | UPLC-ESI-MS/MS | Procyanidins, quinic acid, citric acid, catechin, epicatechin, rutin, quercetin, caffeic acid, ferulic acid and kaempferol | [ | ||
| EtOH/H2O (50:50, | PLE at 200 °C for 20 min at 11 MPa | HPLC-DAD-ESI-TOF-MS | Pyrocatechol, vanillic acid, catechin, epicatechin, procyanidins, rutin, quercetin, kaempferol, sakuranetina and naringenin | [ | ||
| Custard Apple | Seed | EtOH (80%) | Agitation at 200 rpm for 1 week | GC-MS | β -stigmasterol, β -sitosterol and dihydrobrassicasterol | [ |
| MeOH/H2O (80:20, | UAE for 15 min at room temperature | HPLC-DAD-ESI-QTOF-MS | Catechin, epicatechin, procyanidins, vanillic acid, quinic acid, hydroxybenzoic acid and syringic acid | [ | ||
| Peel | MeOH (15%) | SFE with CO2 for 3 h at 75 °C and 100 bars | UPLC-ESI-MS | Aporphine, boldine, flaucine, anonaine, xilopine and pehnolamide | [ | |
| EtOH (70%) | Agitation in the dark for 12 h at 4 °C and 120 rpm | LC-ESI-QTOF-MS/MS and HPLC-PDA | Kaphtaric acid, chlorogenic acid, p-hydroxybenzoic acid, coumaric acid, ferulic acid, sinapinic acid and resveratrol | [ | ||
| Leaves | EtOH/H2O (75:25, | Maceration for 3 days in the dark at room temperature | HPLC-ESI-DAD-MS/MS | Catequin, epicatechin, kaempferol-3- O- glucoside, anonaine, quercetin-3- O -glucoside and pronuciferin | [ | |
| EtOH/H2O (80:20) and Acetone/H2O (70:30) | UAE for 20 min | HPLC-ESI-TOF-MS | Neochlorogenic acid, rutin, epicatechin, catechin, procyanidins, trigonelline, quinic acid, citric acid, kaempferol and quercetin | [ | ||
| Papaya | Seed | CO2-EtOH(5, 8%) | SFE with CO2-EtOH for 180 min at 50 °C and 20 MPa | HPLC-ESI-MS/MS | Chlorogenic acid, caffeic acid, ferulic acid, p-hydroxybenzoic acid and p-coumaric acid | [ |
| Distilled Water | SWE for 5 min at 150 °C | LC-ESI-MS/MS | Ferulic acid, mandelic acid, vanillic acid, caffeic acid, chlorogenic acid and myricetin | [ | ||
| Peel | EtOH (70%) | Agitation for 12 h at 4 °C and 120 rpm | LC-ESI-QTOF-MS/MS y HPLC-PDA | Gallic acid, kaphtharic acid, | [ | |
| EtOH (23.32%) | MAE for 3 min at 340 W | GC-MS | Phenolic compounds and flavonoids | [ | ||
| Leaves | MeOH | Maceration for 72 h at room temperature | - | Phytol, β-sitosterol, γ-tocopherol, δ-tocopherol and hexadecanoic acid | [ | |
| H2O | UAE for 10–20 min | HPLC-DAD-QTOF-MS/MS | Caffeoylquinic acid, coumaric acid derivatives, ferulic acid derivatives, rutin, kaempferol glucoside and rhamnoside | [ | ||
| Guava | Seed | MeOH | Guava seed oil: Agitation for 1 min at 20 °C | RP-UHPLC-DAD-HESI-MS/MS; GC-MS | Vanillic acid, vanillin, syringaldehyde, abscisic acid and cinnamic acid, β-sitosterol, α-tocopherol, γ-tocopherol and campesterol | [ |
| EtOH/H2O | UAE for 2 min | LC-ESI-MS/MS | Salicylic acid, cinnamic acid, p-coumaric acid, vanillic acid, ferulic acid, ellagic acid, gallic acid, galangin, naringenin, catechin and quercetin | [ | ||
| Peel | MeOH/H2O (9:1, | UAE | UHPLC-DAD-MS/MS | Gallic acid and derivatives, derivatives of cinnamic acid, caffeoylquinic acids, flavanols, proanthocyanidins, ellagitannins and anthocyanidins | [ | |
| Leaves | Distilled H2O | Boiling at 90 °C for 30 min | LC/MS | Quercetin, 3-synapoylquinic acid, esculin, gallocatequin, ellagic acid, gallic acid and citric acid | [ | |
| EtOH (70%) | UAE for 30 min at 340 W | HPLC-ESI-TOF-MS | Rutin, quercetin, quercitrin, kaempferol and avicularin | [ | ||
| Litchi | Seed | EtOH (95%) | Direct reflux extraction for 2 h at 90 °C | HPLC | Catechin, epicatechin, litchiol A and litchiol B | [ |
| Peel | Phosphate buffer | Enzyme extractionPressurized hot-water extraction | HPLC | Polyphenolic content | [ | |
| Pass. Fruit | Seed | EtOH (70%) | Agitation for 30 min at 80 °C | HPLC-DAD | Flavonoids | [ |
| Peel | EtOH (70%) | HAE for 2 min | UHPLC-PDA | Isoorientin, orientin and sovitexin | [ | |
| Leaves | Aqueous solutions of ionic liquids (ILs) | IL-MA-SLE | HPLC-PDA | Rutin, quercetin and apigenin | [ |
Abbreviations: EtOH (Ethanol), HPLC (High Performance Liquid Chromatography), Vis (Visible), UAE (Ultrasound-Assisted Extraction), MAE (Microwave-Assisted Extraction), ESI (Electrospray Ionization), MS (Mass Spectrum), NaOAc (Sodium Acetate), MALDI (Matrix-Assisted Laser Desorption/Ionization), TOF (Time Of Flight), GC (Gas Chromatography), QTOF (Quadrupole Time Of Flight), MeOH (Methanol), UPLC (Ultra Performance Liquid Chromatography), PLE (Pressurized Liquid Extraction), DAD (Diode-Array Detection), SFE (Supercritical Fluid Extraction), LC (Liquid Chromatography), PDA (Photodiode-Array Detection), SWE (Subcritical Water Extraction), RP (Reversed Phase), UHPLC (Ultra High Performance Liquid Chromatography), HESI (Heated Electrospray Ionization), HAE (Homogenizer-Assisted), IL-MA-SLE (Ionic Liquid Microwave-Assisted Solid-Liquid Extraction).
Properties of cosmeceuticals made with tropical fruit by-products.
| Fruit | Wastes | Extract Type | Assay | Activity | Effect | Results | Ref. |
|---|---|---|---|---|---|---|---|
| Mango | Seed | 95% ethanolic shook, refluxed or using acid hydrolysis extracts | In vitro | Anti-tyrosinase (skin lighter) | In vitro antioxidant activity (DPPH, chelating activity, etc.) and inhibition of tyrosinase; in vivo acute skin irritation tests | TPC: 286–90 mg GAE/g | [ |
| Two different 95% ethanolic extracts from | In vitro | Anti-wrinkle and anti-hyperpigmentation | Antioxidant activity, inhibition of tyrosinase and hyaluronidase and skin irritation on in vivo clinical tests | TPC: 138.71/170.63 mg GAE/g | [ | ||
| Ethanolic extract | In vitro | Anti-acne | Antimicrobial activity against | [ | |||
| Mango oil | In vivo | Anti-wrinkle, wound healing, emollient effect | Antiseptic, healing, soothing and cooling activities, wound repair and closure, minimum scar formation | Foot-care cream provided emolliency, which rebuilt the skin’s protective lipid barrier and actively replenished moisture. | [ | ||
| Hydroethanolic extract | In vitro | Anti-aging and anti-hyperpigmentation | Antioxidant and anti-enzymatic activity; anti-inflammatory and cytotoxic activities, ability to prevent DNA damage and to inhibit NO | TPC: 800 mg GAE/g; DPPH: 7.35 mg Tr./g | [ | ||
| Leaves | Hydroethanolic extract | In vitro | Anti-tyrosinase (skin lighter) | In vitro antioxidant activity (DPPH) and inhibition of tyrosinase | TPC: (40.00 ± 0.84) mg GAE/g | [ | |
| Pulp | Aqueous extract | In vivo | Photoprotection | UVB protection and anti-photoaging activity | 100 mg of mango extract/kg body weight per day inhibited UVB-induced increases in skin thickness, wrinkle formation and collagen fiber loss. | [ | |
| Ethanolic and aqueous extracts | In vitro | Photoprotection | UVB protection | TPC Ethanol: (3.04 ± 2.52) mg GAE/g | [ | ||
| Leaves, peel and bark | Mangiferin | In vitro and ex vivo | Anti-elastase and anti-collagenase | Anti-aging activity | Mangiferin’s ability to permeate through the stratum corneum barrier and to the living skin layers verified. | [ | |
| Avocado | Seed | Ethanolic extract (polyhydric fatty alcohols) | In vitro | Anti-inflammatory and photoprotection | Increased cell viability, decreased sunburn cells, improves DNA repair in and reduces UVB-induced IL-6 and PGE 2 production in keratinocytes | CPD (photoproducts) removal in cells treated with PFA at concentrations 1 and 5 μg/mL was 92.3% and 74.5%. | [ |
| Ethyl acetate extract (catechin) | In vitro | Anti-hyperpigmentation | Tyrosinase inhibition | Skin lightening agents through inhibiting the tyrosinase action. | [ | ||
| Leaves | Hydroethanolic extract in gel form at 10% (catechin, chlorogenic acid and rutin) | In vivo | Photoprotection | Reduced UVB radiation-induced mechanical allodynia in rats and presented an antinociceptive effect in a UVB radiation-induced burn model | Compounds in highest concentration: (+) Catechin (302.2 ± 4.9 μg/g), chlorogenic acid (130 ± 5.1 μg/g) and rutin (102.4 ± 0.9 μg/g). | [ | |
| Pulp | Avocado oil (phytochemicals) | In vivo | Wound healing and anti-inflammatory | Significant increase of epithelial tissue from wounds and in tensile strength proportional to collagen deposition, and reduction of inflammatory cells in scar tissue | Promote collagen synthesis and decrease the number of inflammatory cells during the skin wound healing process. | [ | |
| Ethanolic extract of avocado (100 mg/kg) | In vivo | Wound healing | Suppression of symptoms of induced atopic dermatitis, of serum levels of IgE, of histamine and of inflammatory cytokines (TNF-α and IL-6), NF-ΚB and caspase-1 in skins lesions similar to atopic dermatitis | Significant reduction in the symptoms of atopic dermatitis such as itching, erythema, edema and dryness in mice | [ | ||
| Seed and Peel | Ethanolic extract of avocado peels and seeds (epicatechin and procyanidin B2) | In vitro | Anti-oxidant and anti-inflammatory | HOCl, ROO· and O2· removal capacity, and suppression of TNF-α and NO release on RAW macrophages at a concentration of 10 ug/mL of extract | TPC APE: 120.3 mg/g and ASE: 59.2 mg/g. | [ | |
| Pineapple | Stem | Tacorin | In vitro and in vivo (rats) | Wound healing | Decrease of wound area by reducing the expression of TNF-α, promoting the expression of TGF-β and maintaining the expression of MMP-2 on treated rats | Tacorin treatment (80 mg/kg body weight per day) increased cell viability promoting regeneration, proliferation, cell growth and maturation. | [ |
| Crown | Dialyzed extract | In vitro | Anti-collagenase activity | Tissue remodeling and wound healing process | Topical application of the leaf extract in soft tissue injuries and hematomas where the extract can prevent the microbes to invade the host through the wound. | [ | |
| Pulp, stem, peel, core and crown | Dialyzed extract (Bromelain) | In vitro | Anti-acne | Antimicrobial activity against | PPPE exhibited highest inhibitory effects. | [ | |
| Papaya | Seed | Ethanolic extracts | In vivo | Wound healing and antimicrobial | Significant collagen deposition and fibroblast activity, antimicrobial activity against | Powerful healing, antimicrobial and anti-inflammatory activity. | [ |
| Pulp | Hydroethanolic extract | In vitro | Anti-oxidant and anti-aging | H2O2 scavenging activity and free radical scavenging (DPPH) | Anti-aging and skin renewing activity. | [ | |
| PBS extracts | In vivo | Anti-inflammatory and anti-oxidant | Significantly increased activity of SOD, catalase and glutathione peroxidase, and suppression of COX-2 activity | Important antioxidant, anti-inflammatory and healing effect on skin wounds. | [ | ||
| Leaves | Ethanolic extracts (caffeic acid and rutin) | In vitro | Photoprotection | Free radical scavenging (DPPH), decreased UVB-induced expression of MMP-1, MMP-3 and IL-6 and increased TGF-β1 and expression of procollagen mRNA | Possible agent for treating skin conditions and photoaging. | [ | |
| Methanolic extracts | In vitro | Wound healing | Free radical removal (DPPH), migration and proliferation of new cells in the wound area and increased collagen synthesis | In vitro wound healing ability using human skin fibroblasts. | [ | ||
| Fermented preparation | Fermented papaya preparation | In vivo | Anti-aging, anti-oxidant and skin improvement | Improved hydration, elasticity and skin color, and increased expression of aquaporin-3, decreased levels of MDA and significantly increased levels of SOD and NO production | Significant improvement in skin hydration and elasticity. | [ | |
| Custard Apple | Pericarp | Proanthocyanidin extract (catechin and epicatechin) | In vitro | Anti-hyperpigmentation | Tyrosinase inhibition | Prevent melanin build-up and serious skin conditions, such as melasma, freckles, age spots and actinic damage. | [ |
| Pulp, peel and seed | Ethanolic extracts | In vitro | Anti-oxidant | Antioxidant capacity by scavenging free radicals (ORAC, ABTS and FOLIN) | Eliminate free radicals, reduce oxidative stress and prevent cell damage. | [ | |
| Leaves | Methanolic extracts | In vitro | Anti-hyperpigmentation | Inhibit α-MSH-induced melanogenesis in B16F10 cells and melanogenic-related enzymes, such as tyrosinase, TRP1 and TRP2 | Dermatological anti-hyperpigmenting agent for the treatment of skin diseases. | [ | |
| Litchi | Leaves | Ethanolic 70% | In vitro | Photoprotection | Antioxidant and photochemoprotective activity against H2O2, UVA and UVB; photoprotector agent against UV-induced DNA damage | No irritating agent/do not promote cytotoxicity in fibroblasts (0.1–100 μg/mL). | [ |
| Seed | Ethanolic 75% | In vivo | Anti-oxidant and anti-inflammatory | Reduce cytokines and proinflammatory factors, and induce endogenous antioxidant protein expression | Decreased levels of NF-κB, TNF-α, IL-6 and IL-1β. | [ | |
| Peel | Standardized extract | In vitro and in vivo | Antioxidant, anti-hyperpigmentation and anti-tyrosinase (skin lighter) | Anti-melanogenesis and anti-tyrosinase effects | TPC: (35.91 ± 2.14) g GAE/g. | [ | |
| Pericarp | Standardized extract (quercetin, rosmarinic acid and gallic acid) | In vivo | Anti-aging and anti-hyperpigmentation | Suppression of cellular melanin production via tyrosinase and tyrosinase-related protein inhibitory mechanisms; inhibition against MMP-2 | Formulated into a stable non-irritating topical serum at 0.05% and 0.1%. | [ | |
| Vinegar and juice | In vitro | Photoprotection | Reduce oxidative stress and proinflammatory factors and prevent photo-damage in HaCaT keratinocytes, resulting in an anti-photoaging effect | Cell viability improved after UVB exposure (vinegar 0.06% and juice 0.63%). | [ | ||
| Passion Fruit | Seed | Ethanolic 96% | In vitro | Anti-acne | Antimicrobial activity against | The minimum concentration of the extract to have an antibacterial effect was 5% (MIZ: 8.5 mm). | [ |
| 40% methanolic water extract | In vitro | Photoprotection | Enhancement of the UVB protective efficacy with PFE for skin cancer and photo-damage protection | Different compositions of cosmetics with 0, 0.1 and 0.3% of PFE. | [ | ||
| 40% methanolic water extract divided in hexane, EtOAc and aqueous fractions | In vitro | Antioxidant and anti-tyrosinase (skin lighter) | Anti-aging and anti-wrinkle effects based on its potent antioxidant activity; UV protection efficacy and photoaging protection | TPC (EtOAc): (58.3 ± 1.1) g GAE/100 g. | [ | ||
| Piceatannol | In vitro | Photoprotection | Suppression of MMP-1 induction in the fibroblasts by piceatannol pre-treatment | Increased GSH level by 17% (6.25 μg/mL), 33% (12.5 μg/mL) and 77% (25 μg/mL). | [ | ||
| Guava | Leaves | Methanolic extract | In vitro | Anti-hyperpigmentation | Anti-melanogenesis and anti-tyrosinase effects, inhibition of ORAI1 channel | Tyrosinase: 59.8% ± 1.3% (330 μg/mL). | [ |
| Commercial extract | In vivo | Anti-sebum | Reduction of greasiness of T-zone skin | Tannin content: (85.90 ± 1.90) mg/l. | [ | ||
| Methanolic extract (triterpenes) | In vivo | Antitumor | Inhibitory effect on inflammation in ear edema and on tumor promotion | Inh. Rat. edema: 75 (1 mg/ear). | [ | ||
| Pulp, peels and seeds | Water/ethyl alcohol standardized in ellagic acid | In vitro | Photoprotection | Relevant antioxidant activity | DPPH (IC50): 19.80 μg/mL. | [ |
Abbreviations: TPC (Total Phenolic Content), GAE (Gallic Acid Equivalent), MSE (Mango Seed Extract), ID50 (50% Infectious Dose), DPPH (Diphenyl-picrylhydrazyl), IC50 (Half maximal inhibitory concentration), MMPases (Matrix Metalloproteinases), HAase (Hyaluronidase), PFA (Polyhydric Fatty Acids), CPD (Cyclobutane Pyrimidine Dimers), TNF (Tumor Necrosis Factor), IL (Interleukin), APE (Avocado Peel Extract), ASE (Avocado Seed Extract), PPPE (Pineapple Peel Purified Extract), MIC (Minimum Inhibitory Concentration), SOD (Superoxide Dismutase), MSH (Melanocyte Stimulating Hormones), TRP (Tyrosinase Related Proteins), NRf2 (Nuclear Factor Erythroid 2 Related Factor 2), PFE (Passion Fruit Extract), SPF (Sun Protection Factor).
Figure 2Some highlighted phenolic compounds: mangiferin (a), resveratrol (b), quercetin (c), piceatannol (d), kaempferol (e), myricetin (f), p-coumaric acid (g), catequin (h), caffeic acid (i) and ellagic acid (j).