Fruit Seeds as Sources of Bioactive Compounds: Sustainable Production of High Value-Added Ingredients from By-Products within Circular Economy

The circular economy is an umbrella concept that applies different mechanisms aiming to minimize waste generation, thus decoupling economic growth from natural resources. Each year, an estimated one-third of all food produced is wasted; this is equivalent to 1.3 billion tons of food, which is worth around US$1 trillion or even $2.6 trillion when social and economic costs are included. In the fruit and vegetable sector, 45% of the total produced amount is lost in the production (post-harvest, processing, and distribution) and consumption chains. Therefore, it is necessary to find new technological and environmentally friendly solutions to utilize fruit wastes as new raw materials to develop and scale up the production of high value-added products and ingredients. Considering that the production and consumption of fruits has increased in the last years and following the need to find the sustainable use of different fruit side streams, this work aimed to describe the chemical composition and bioactivity of different fruit seeds consumed worldwide. A comprehensive focus is given on the extraction techniques of water-soluble and lipophilic compounds and in vitro/in vivo functionalities, and the link between chemical composition and observed activity is holistically explained.


Introduction
According to Homrich et al. [1], the circular economy (CE) is an umbrella concept that applies different mechanisms aiming to minimize waste generation, thus decoupling economic growth from natural resources. European Union (EU) countries are leading this concept by promoting the responsive and cyclical use of resources and contributing to sustainability [2]. From the economic standpoint, CE Not only technological applications containing fruit side streams have been studied, but also the optimization of extraction parameters aiming to increase the level of bioactive compounds, namely phenolic compounds and carotenoids, to produce bioactive-rich extracts and then further add into different foods [37]. For instance, Takii et al. [38] studied the effects of ethanol (EtOH), extraction time, and temperature on the extraction rate of phenolic compounds and antioxidants from banana peel, whereas Wong et al. [39] optimized the extraction conditions of total phenolic content and antioxidant activity of passion fruit peel using the same factors (e.g., EtOH concentration in the extracting solution, time, and temperature). In the same line of research, Dorta et al. [40] assessed the effects of EtOH, water, and acetone as solvents and different temperatures on the extraction of antioxidants from mango peel and seeds. Table 1 contains some studies [15,28, regarding the extraction of bioactive compounds from fruit seeds and the bioactivity already studied. It is clear that new studies regarding fruit seeds should be focused on the optimization of extraction conditions and on the extraction techniques so that new value-added extracts can be potentially used as ingredients by pharmaceutical and food sectors. The extraction methods are highlighted to provide useful information about new techniques that can be explored industrially for scale-up process, and therefore enlarge the use of natural side streams as raw materials to obtain bioactive-rich extracts. Aside from that, conventional extracting techniques, such as maceration, are time consuming, which can limit its applicability in the industrial sector.
Considering that the production and consumption of fruits has increased over the last years and following the need to find sustainable uses of underutilized fruit byproducts, this work aimed to describe the chemical composition and bioactivity of different fruit seeds consumed worldwide. A comprehensive focus is given on the extraction techniques of water-soluble and lipophilic compounds and in vitro/in vivo functionalities, and the link between chemical composition and observed activity is holistically explained. Anti-inflammatory activity [65] 50 mM acetate buffer at 1:10 w/v 0.81 g GAE/100g Gallic acid p-Coumaric acid Syringic acid (+)-Catechin Resveratrol Malvidin-3-O-glucoside TEAC [68]  Apples are mainly consumed fresh; however, 25-33% of fruits are processed into juice, cider, jams, and other products. Globally, the most used processed apple product is the juice. The recovery of juice in the industrial processing is around 70-75%, whereas 25-30% w/w of apple pomace is generated. Seeds account for 2-4% w/w of the pomace [11,74]. Considering the massive production of apples, seeds represent a significant side stream.
The oil content of apple seeds varies from 17% to 29% v/w, and the main fatty acids are oleic (27.0-46.5% w/w) and alpha linoleic acid (43.8-60.0% w/w). Other prominent fatty acids are palmitic, stearic, and arachidic acids [75][76][77][78][79]. A high percentage of unsaturated fatty acids makes apple seed oil nutritionally favorable, having positive effects on lowering low-density lipoproteins (LDL) cholesterol and preventing risks of cardiovascular diseases [79]. Apple seed oil is also a rich source of tocopherols, sterols, and phospholipids [76,77,80]. According to Tian et al. [78], apple seed oil is active against bacteria, mildews were less sensitive to apple seed oil than yeasts, and the minimum inhibitory concentration (MIC) of apple seed oil ranged from 0.3 to 0.6 mg/mL. The observed biological activities showed that the oil had a good potential for uses in the food industry and pharmacy.
The nutritional value of protein from defatted apple seed meal was relatively low in the murine study performed by Opyd et al. [81]. However, the protein content of apple seeds is quite high, varying from 34 to 50% w/w, and it is rich in sulfur-containing amino acids. The fiber content of seeds is 3.9-4.3% w/w. Seeds also contain significant amounts of minerals such as phosphorus, potassium, magnesium, calcium, and iron, in the order of 720, 650, 510, 210 and 110 mg/100 g, respectively [78,79].
Apple phytochemicals and especially phloridzin may have many beneficial health effects. It has anti-inflammatory and antioxidant activities, and it reduces hyperglycemia by blocking renal glucose resorption and intestinal glucose absorption through inhibition of the sodium-glucose symporters [38,[82][83][84][85]. According to the more recent murine study by Shin et al. [86], phloridzin may prevent diet-induced obesity, hepatic steatosis, inflammation, fibrosis, and insulin resistance. Phloridzin can be potentially used as treatment for type 2 diabetes, as a weight loss agent for obesity, and in the acute management of hyperglycemia [83].
Although apple seeds seem to be an interesting nutritional source, the presence of toxic cyanogenic glycosides critically limit their utilization as a food ingredient. The amygdalin content of seeds from 15 apple cultivars varied from 1 to 4 mg/g. These amygdalin contents could generate 0.06-0.2 mg cyanide equivalents per gram of apple seeds [87]. These values are relatively high, because acute cyanide toxicity can occur in humans at doses between 0.5 and 3.5 mg/kg body weight [88]. However, many processing techniques can reduce the cyanide content. Processing allows contact between cyanogenic glycosides and endogenous enzymes, which results in the hydrolytic breakdown of cyanogenic glycosides to hydrogen cyanide [87]. According to a murine study from Opyd et al. [81] a daily dose of 160 mg/kg body weight of apple seed meal for two weeks did not exert any observable adverse effects. The results showed increased protein digestibility as well as exerted beneficial effects on the intestinal tract, blood lipid profile, and antioxidant status of rats.
In conclusion, apple seeds are rich in nutrients, high-quality oil, and polyphenols, and can be a rich source of functional ingredients for health-promoting foods, feeds, nutraceuticals, and cosmetics.
However, the contents of bioactivities vary significantly between various cultivars. In addition, for utilizing apple seeds, there is a risk concerning cyanogenic glucosides that must be considered, and the seeds must be processed in such a way that amygdalin is not physiologically toxic.

Grape (Vitis Labrusca and Vitis Vinifera)
Grapes are an important cash crop throughout the world. The berries stand out for their bright color, juicy flavor, and high nutrient content, and they are rich in vitamins, anthocyanins, carotenoids, and several antioxidant compounds, which are substances that can effectively remove free radicals and delay senility in the body [89,90].
As reported by The Plant List [91], the grape genus Vitis includes 68 species. Responsible for studying multiple genera, the Department of Agriculture (USDA) and the Natural Resources The basis of the phenolic composition of grapes and derived products is flavonoids, such as anthocyanins, flavones, and flavonols; stilbenes, such as trans-resveratrol; and phenolic acids, as gallic, vanillic, syringic, and caffeic [53]. Fiume et al. [92] suggested that amongst all the phenolic extractables in grapes, about 10% are present in the pulp, 28-35% are present in the peel, and 60-70% are present in the seeds. Several studies claim that there are several biological activities in grape phenolic compounds, both in vitro and in vivo, viz. anti-angiogenic, anti-proliferative, pro-apoptotic, antioxidant, and other functions [93][94][95][96][97]. Specific phenolic compounds extracted from grapevines studied by According to Yang et al. [101], the mechanism of action that could prevent tumor initiation may be related to the antioxidant, anti-inflammatory, and anti-proliferative activity of grape phenolic compounds.
As stated in a review by Salehi et al. [104], V. vinifera wines contain a variety of phenolic compounds, such as hydroxybenzoic acids (e.g., gallate dimers), hydroxycinnamic acids (e.g., trans-caffeic acid), pyranoanthocyanins, flavonols (e.g., quercetin and myricetin), flavones (e.g., luteolin), and flavanols in their polymeric forms (e.g., procyanidins dimers). Tkacz et al. [105] document that the average amount of total polyphenolic compounds in white grape seeds (Vitis vinifera cv. Pinot Gris) exceeds by at least nine times the value found in the pulp and by more than five times what is found in the peel. The antioxidant activity was highest in seeds and lowest in pulp, as in a study by Yilmaz et al. [106].
Composed of skin, stems, and seeds, grape pomace represents the largest waste in the wine and juice industry [107,108]. The seeds represent about 5% of the fruit weight, generating approximately 40-50% of solid residues in the production process [109]. Grape seed oil has several applications, mainly in cosmetic formulations. It can contribute to nutraceutical effects due to its composition and antioxidant capacity [28]. Widely available in vegetables and fruits, flavan-3-ols represent the most common group of typical flavonoids of the human diet, and are present in higher concentrations in fruit seeds [110].
Consisting of high oil and polyphenols, grape seeds also contain oligosaccharides that display prebiotic activity [111,112]. According to Bordiga et al. [113], the oligosaccharides identified in grape seeds using chromatography can be considered, in some combinations, as a "functional ingredient" with potential prebiotic activity for L. acidophilus P18806, allowing improved growth during in vitro fermentation. Since grape seeds and skins are more valuable sources in compounds with high biological activity than fruit pulp, further studies to determine the biological properties with in vivo and in vitro testing of the morphological parts of the grape are very important for designing food products with high-sensory health-related quality. Moreover, seeds are an integral part of bagasse; thus, increasing their use in the food, pharmaceutical, and cosmetic industries would be economically justified.
Deolindo et al. [64] state that the hydroethanolic extracts of grape seed (Vitis labrusca cv. Bordeaux) have not only chemical antioxidant activity (based on DPPH analysis, where 3637 ± 4 mg AAE/100 g was obtained for the seeds and 1033 ± 10 mg AAE/100 g for the skin, extracted with a 60% v/v ethanolic solution), but also the potential to inhibit ACE-I (angiotensin-I-converting enzyme) activity in vitro. Salehi et al. [114] justify the inhibition of ACE-I activity to phenolic compounds in grape juice, peel, and seeds mainly due to the presence of (+)-catechin, (-)-epicatechin, (+)-gallocatechin and (+)-epigallocatechin, these substances being alternatives to the use of synthetic drugs to control or prevent hypertension.
Harbeoui et al. [65] confirmed the anti-inflammatory ability of the ethanol/water extract (80:20, v/v) of Vitis vinifera L. grape seeds by inhibiting the expression and production of different inflammatory markers. The authors also suggested that the different mechanisms involved in this anti-inflammatory activity could be due to the synergism between several phenolic compounds, as well as the specific structural elements of flavonoids (dominant fraction), constituting the primary determinants of anti-inflammatory activity.
Studies of the extract (ethanol/acidic water) of seed oils from cold-pressed fresh grapes, performed by Cecchi et al. [28], demonstrate in vitro inhibitory activity against PTP-1B (protein tyrosine phosphatase 1B enzyme), which is an overexpressed enzyme in type 2 diabetes, showing maximum inhibition values (98%) for Vitis vinifera cv. Sauvignon Blanc and minimal inhibition (40%) for Vitis vinifera cv. Cabernet Sauvignon. The authors assert an inhibitory activity exerted by the isolated phenolic fraction of these oils, and argue that these results urge for further studies, so that it is possible to confirm the action of grape seed oils and understand the mechanism behind them.

Pomegranate (Punica granatum)
The pomegranate (Punica granatum) is a fruit belonging to the Punicaceae family, which is native to Iran and is currently cultivated worldwide due to its great ability to adapt to various climatic conditions [43]. Pomegranates are mainly composed of bark, arils, and seeds, where residues can represent up to 50% of the total weight of the fruit [115]. Recent studies have sought to find methods to avoid wasting these residues by assessing the following: phenolic composition and antioxidant activity [42]; concentration of linoleic acid isomers [43]; in vitro and in vivo anthelmintic activity in relation to Ascaridia galli [116]; enrichment of fatty acid profile and reduced activity of desaturases in rat livers [117]; and decreased risk of non-communicable chronic diseases such as cancer, cardiovascular disease, diabetes, and obesity [44].
The antioxidant activity of pomegranate has been analysed in several studies. These included antioxidant activity by the DPPH method; antioxidant activity by the ABTS method; β-carotene by the bleaching method; antioxidant activity by electron paramagnetic resonance (EPR) spectrometry; metal-chelating ability; and oxygen radical absorbance capacity (ORAC) [41,[43][44][45]. In these studies, pomegranate seeds showed antioxidant activity in all the methods that were used. Derakhshan et al. [42] evaluated the positive correlation between phenolic compound content and antioxidant activity using the β-carotene bleaching method. It was concluded that different methods should be employed to assess the types of antioxidant mechanism of action, such as single electron transfer, transition metal chelator capacity, and hydrogen atom transfer [118].
Biological assays with different protocols and experimental conditions are often used to evaluate natural products. In addition to identifying phenolic compounds, Ambigaipalan et al. [44] also studied the inhibitory effects of α-glucosidase and pancreatic lipase, the inhibition of peroxyl and hydroxyl radical-induced super stranded scission, and the inhibition of LDL cholesterol oxidation, confirming the effectiveness of the pomegranate seeds in the assays. Ferreira et al. [119] performed in vivo studies using mice and nanoemulsions of pomegranate seed oil for improving the photostability and antinociceptive effects of non-steroidal anti-inflammatory drugs. Zarepourfard et al. [120] performed in vivo assays on cloned goats to confirm that dietary supplementation with pomegranate seeds can improve sperm motility and viability after freeze-thawing, as well as maintaining developmental competence. Additionally, Białek et al. [117] performed dietary supplementation with pomegranate seed oil in Sprague-Dawley rats. The fatty acid content, lipid oxidation biomarker levels, and the activity of the main enzymes that catalyse lipid metabolism, confirmed that pomegranate seed oil is an alternative source of conjugated linoleic acids.
The use of pomegranate seeds for industrial purposes is already underway. A study by Van Nieuwenhove et al. [43] included pomegranate extracts as a component for the enrichment of conjugated linolenic acids in yoghurt. By using the DPPH method, there was a confirmed enrichment of the fatty acid profile, as well as an increase in antioxidant activity in the fermented products, while maintaining their nutritional, microbiological, and sensory characteristics. However, in vitro and in vivo evaluations of antimicrobial, cytotoxic, and antioxidant activity may be improved methods to study pomegranate seed extracts in greater detail.

Camu-Camu (Myrciaria Dubia H.B.K. McVaugh)
Camu-camu is a fruit species from the Myrtaceae family that naturally grows near rivers and lakes in the Amazon basin [121]. Pulp and peel extraction industries often use its fruits and seeds, which accounts for 50% of the total fruit weight and great loos if discarded [15].
The camu-camu seeds are a potentially rich source of phenolic compounds, while their functional and biological effects were previously reported. Studies such as those by Fidelis [15,[46][47][48][49] have verified the high concentrations of phenolic compounds in the seeds, which are even higher than the concentrations from camu-camu pulp. Fidelis et al. [15] identified the presence of bioactive compounds by HPLC coupled to diode array detection. Fifteen phenolic compounds (phenolic acids, flavonoids, and trans-resveratrol) were identified in aqueous, ethanolic, and propanone extracts. There was a significant difference (p < 0.05) in the content of all the bioactive compounds among the three obtained extracts, except for 2-hydroxycinnamic acid. Differences in the solubility and polarity of the compounds may explain these differences, as varying polarity of solvents can result in a different compound being extracted.
Do Carmo et al. [49] performed five extractions with different proportions of water and EtOH for the in vitro evaluation of phenolic composition, antioxidant activity, cytotoxicity, and the inhibition of cisplatin-induced chromosomal aberrations. The extract with 50% of each solvent presented the highest concentrations of total phenolic compounds. The highest antioxidant capacity evaluated by three different methods (DPPH radical scavenging; ferric reducing-antioxidant power, FRAP; and Folin-Ciocalteu reducing capacity) also inhibited the growth of four cancer cell lines without cytotoxic effects on normal cells. In addition, the extract also presented a protective effect by decreasing the cisplatin-induced chromosomal break index by 37%.
Myoda et al. [46] analysed the antioxidant activity of camu-camu seeds through DPPH radical elimination and reduction power tests. They used five fractions of crude extract obtained with different proportions of water and methanol and verified the effectiveness of the extract on in vitro antioxidant activity. The aforementioned study evaluated the antimicrobial activity of the five fractions of the extract against Staphylococcus aureus, Escherichia coli, and Saccharomyces cerevisiae bacteria. Here, antibacterial action was only observed in relation to Staphylococcus aureus bacteria. A further study by Kaneshima et al. [122] isolated C-glycosidic ellagitannins in camu-camu seed extracts, which showed antioxidant action against DPPH and ABTS radicals.
The evaluation of antibacterial and cytotoxic effects was performed by Camere-Colarossi et al. [123], who compared methanolic extracts of camu-camu pulp and seeds. Both extracts showed antibacterial activities against Streptococcus mutans (ATCC 25175) and Streptococcus sanguinis (ATCC 10556) bacteria. However, the seed extract presented the largest inhibitory halos, while the extracts showed no cytotoxic effects at the concentrations used.
Regarding in vivo studies, Yazawa et al. [124] studied the methanolic extracts of camu-camu seeds, and found anti-inflammatory action in carrageenan-induced paw oedema in murine models. Studies of camu-camu pulp are more frequently found in the literature [125][126][127][128][129]. However, it was stressed to use the waste that is generated while obtaining the pulp. In vitro and in vivo research with camu-camu seeds should be further developed, because this residue is recognized as a source of high concentrations of bioactive compounds and antioxidants.

Plums (Prunus sp.)
Plums (Prunus sp.) are among the most popular processed fruits. The global production of plums has been increasing and reached 11.8 million tons in 2017 [12]. Most often, plums are processed into dry fruits, jams, and juices, which generate tons of seeds as by-products. Thus, utilization of the seeds is of growing interest due to environmental and economic aspects.
The oil content of plum seeds varies from 23% (w/w) to 53% (w/w) per dry weight basis, depending mainly on the variety [73]. The dominant fatty acids in plum seed oil are oleic and linolenic acids; oleic acid constitutes 46-71% of the oil, and linoleic acid constitutes 23-45% of the oil, depending on the variety [73]. Based on the high content of unsaturated fatty acids, plum seeds have potential to lower LDL cholesterol and prevent cardiovascular diseases [79]. The oil is also rich in bioactive compounds, such as carotenoids, tocopherols, tocotrienols, phytosterols, and squalene [73]. The content of tocochromanols in 100 g of the oil is reported to be up to 209 mg, the content of total carotenoids is reported to be up to 3 mg, the content of phytosterols is reported to be up to 1579 mg, and the content of squalene is reported to be up to 80 mg [73]. Although the content of the bioactives varies greatly between the varieties, β-sitosterol and γ-tocopherol remain the main lipophilic compounds in plum seed oils. The contents of β-sitosterol constitutes are 209-1259 mg/100 g of oil and γ-tocopherol constitutes are 61 and 182 mg/100 g of oil [73].
Phytosterols, such as plant stanols and sterols, are steroid compounds that have a significant impact on human health. For example, phytosterols can reduce the levels of cholesterol in blood serum [130]. For example, tocochromanols include tocopherol and tocotrienol, which are active forms of vitamin E. They have important functions in human nutrition, and they possess various physiological and biological activities, such as the prevention of cardiovascular diseases and diabetes (e.g., [131]). Carotenoids are natural isoprenoid pigments with various biological and physiological functions, such as antioxidant and antitumor activities (e.g., [132]). One of the most common carotenoids in the plants is β-carotene, which exhibits pro-vitamin A activity. Squalene (2,6,10,15,19,23-hexamethyl-2,6,10,14,18,20-tetracosahexane) is a biochemical precursor of vitamin D, cholesterol, and steroid hormones, and thus is of high importance for human health [133].
In addition to the healthy fatty acids, lipophilic bioactives, and polyphenols, plum seeds have been characterized as a source of functional proteins and bioactive peptides. The protein content of plum seeds is up to 40% on a dry matter basis [134]. High-intensity ultrasound treatment has been applied for extracting the proteins [134,135]. The produced protein concentrates have been shown to possess good solubility, emulsifying, and foaming properties, as well as gel and film formation capacity. These functional properties indicate that the plum seed protein concentrates could meet the complex requirements of manufactured food products. For example, excellent emulsifying and gel-forming properties are needed in sausage products and emulsifying and film-forming capacities enable the production of emulsion-based edible films. In addition, proteins can be used for the production of biologically active peptides. This far, plum seed protein-derived peptides have shown antioxidant and antihypertensive (angiotensin I converting enzyme inhibitory) properties in vitro [134,136]. Bioactive peptides have been produced by hydrolyzing the plum seed proteins with proteolytic enzymes. Among the tested enzymes, alcalase most efficiently released the antioxidant and potentially antihypertensive peptides. The peptide sequences IYSPH, IYTPH, IFSPR, and VAIP have been reported to relate to the potential antihypertensive activity [136].
In summary, plum seeds are rich sources of nutrients, especially oils and proteins, and a wide variety of natural bioactive compounds. Based on these compounds, plum seeds have potential for exploitation in health-enhancing functional foods, nutraceuticals, extending the shelf life and active ingredients in food and cosmetic products. However, it needs to be taken into account that the concentration of the bioactive compounds varies significantly between the different varieties, and also, the seeds contain toxic cyanogenic glycosides, which need to be diminished during processing.
2.6. Jabuticaba (Plinia jaboticaba and Plinia cauliflora Mart. Kausel) Jabuticabeira belongs to the Myrtaceae family, and it is a native species of Brazil with great economic importance. It is produced mainly in the states of Minas Gerais, Espirito Santo, Rio de Janeiro, São Paulo, and Paraná [137]. Due to its high water and sugar content, jabuticaba is highly perishable, and is not widely consumed in its fresh form. On the other hand, its pulp is usually extracted to make jams, wines, liqueurs, and vinegars [54]. According to Jorge et al. [138], the residues generated in the extraction of this fruit are seeds and peel, which represent approximately 50% of the fruit. The purposeful processing of these residues would reduce the production of organic wastes and add value to the food products, because they are a rich source of bioactive compounds, e.g., dietary fiber, minerals, and phenolic compounds [139].
Extraction is fundamental to obtain accurate results in relation to the studied matrix. To evaluate the phenolic compound content in jabuticaba seeds, Paludo et al. [53] performed optimized extraction using three solvents (water, EtOH, and methanol) and compared combinations of these solvents.
The EtOH:water composition (60:40 v/v) had the highest extraction efficiency and proved the presence of high levels of phenolic compounds in the jabuticaba seeds. Inada et al. [54] evaluated the technological potential of the fractions (peel, seeds, and pulp) of jabuticaba and determined the antioxidant capacity and chemical composition. In the identification of phenolic compounds, soluble and insoluble fractions were extracted, and gallic acid was found to be the main compound present in jabuticaba seeds. The fractions showed in vitro antioxidant capacity in the methods used (Folin-Ciocalteu; ferric-reducing ability, Trolox equivalent antioxidant capacity, and oxygen radical antioxidant capacity). A positive correlation was observed between total phenolic compounds and antioxidant capacity, regardless of the assay, indicating that these bioactive compounds are effective in antioxidant action.
Similarly, Hacke et al. [55] performed the extraction and chemical characterization of antioxidant and antimicrobial compounds from jabuticaba seeds. The effects of three solvents (water, ethyl alcohol, and propanone) were analysed, and the binary combination of water and propanone (60:40 v/v) obtained the best results regarding phenolic content and antioxidant activity using the DPPH method After optimization, the crude extract was purified, and ellagic acid and ellagitannin compounds were identified using electrospray ionization coupled with tandem mass spectrometry (ESI-MS/MS). Alezandro et al. [56] evaluated jabuticaba fractions and also reported the presence of ellagic acid derivatives in jabuticaba seeds. In this same study, the methanolic extract of jabuticaba seeds presented higher antioxidant capacity when compared to the skin and pulp extracts, regardless of the method used (Folin-Ciocalteu reducing capacity, DPPH scavenging ability, or ferric-reducing ability). This study demonstrates how important it is to consume the whole fruit, because each fraction has its own particular importance and helps to maintain health.
Jorge et al. and Lima et al. [138,140] evaluated the profile of fatty acids and organic acids in jabuticaba seeds, respectively. Regarding fatty acids, polyunsaturated fatty acid concentrations were obtained, with a predominance of linoleic acid and α-linolenic acid. The organic acids that were detected included citric acid, succinic acid, malic acid, oxalic acid, and acetic acid. Such compounds are essential in maintaining health, because they contain beneficial properties for the body such as antioxidant, antimicrobial, and anti-inflammatory capacity.
In a practical use of jabuticaba seeds, Baldin et al. [139] evaluated the antioxidant and antimicrobial activity of the microencapsulated aqueous extract of jabuticaba residues (bark and seeds) used as dyes in the manufacture of mortadella. The addition of the extract provided better sensory acceptance, and did not interfere with the chemical composition, lipid oxidation, and bacterial development. According to the authors, the addition of natural extracts is promising and represents great potential for application during the manufacture of products enriched with natural antioxidants.
Jabuticaba peel has been identified as a potential source of bioactive compounds with biological activities. In vivo studies were performed by Batista et al. [141], who obtained an improvement in the triglyceride excretion and hepatic lipid peroxidation in rats fed a high-fat diet enriched with lyophilized jabuticaba peel. Palozi et al. [142] showed that the oral use of ethanolic extracts of jabuticaba peel in rabbits did not cause significant changes in respiratory, cardiovascular, and central nervous system functions, ensuring pharmacological safety for the use of this residue. However, biological studies of jabuticaba seeds are scarce, and further research is required to assure the complete safety of these potential sources of bioactive compounds. Hacke et al. [55] evaluated the protective effects of jabuticaba seed extract using in vivo micromolecular assays on murine bone marrow cells combined with cyclophosphamide. Ellagitannins (castalagin, vescalagin, and pedunculagin) were the main compounds isolated from jabuticaba seed extracts, which protected DNA from damage and accelerated DNA reparation.
Future research regarding jabuticaba seeds, particularly in relation to in vitro antioxidant, antimicrobial, and antiproliferative activities, as well as in vivo analysis, may provide more specific information on how to best utilize these residues.

Avocado (Persea americana Mill.)
Persea americana (Lauraceae), commonly known as avocado, is native to Mexico and Central America, and can be widely found throughout tropical countries. Most of avocado's chemicals and bioactivity studies are focused on pulp, but little is known about the seed. Extensive research on this part of the fruit may be of great interest due to its anti-inflammatory properties (decreasing the generation of interleukin-6 pro-inflammatory mediators, IL-6; and prostaglandin-E2, PGE2; anti-cancer, antioxidant, and antihypertensive factors). Numerous chemical characterizations have shown a large number of polyphenols, such as catechins, procyanidins and other tannins, flavonoids, triterpenes, and unsaturated fatty acids in avocado seeds [143,144].
In vivo studies performed by Athaydes et al. [61] demonstrated that avocado seed extracts with ethyl acetate have gastroprotective activity and can be used as an adjunctive treatment for indomethacin-induced gastric mucosal injury. Uchenna et al. [145] have shown promising component values in avocado seeds as a source of energy, protein, and bioactive phytochemicals to stimulate growth and metabolism. Additionally, the authors reported that the inclusion of avocado seeds in diets has also lowered cholesterol levels and suppressed hyperglycemia in rats.
Studies on avocado seed pigmentation conducted by Hatzakis et al. [146] demonstrated that the seed has perseorangan as the most abundant component, which may contribute to its final coloration. The authors stated that further research is needed to characterize the usefulness of this compound as a food coloring additive and to identify its biosynthetic precursors and potential natural derivatives. Likewise, toxicological studies should be performed on cells and mice to ascertain its safety. In vitro and in vivo studies of the extract from avocado seeds could be an alternative to better understand its biological activities and encourage its use as an ingredient in the cosmetic, pharmaceutical, and food industries.

Passion Fruit (Passiflora edulis Sims)
Passiflora, originally from the tropical and warm climates of South America, is the largest genus in the Passifloraceae family, containing about 500 different species. Due to their pleasant natural and intense bittersweet flavor, Passiflora fruits, popularly known as passion fruit, are much appreciated in the world. In the food industry, its juice is the main source of nutritional properties, mainly due to the presence of many phytochemical constituents such as phenolic compounds. Although hundreds of Passiflora species can be found worldwide, only a few are identified as edible. In addition, these fruits contribute to some beneficial health properties, such as antioxidant, anti-inflammatory, antipyretic, analgesic, sedative, and hypotensive activities [67,[147][148][149]. Passiflora fruits are also rich in minerals (calcium and phosphorus), retinol, ascorbic acid, thiamine, riboflavin, and niacin [150].
Studying tropical fruit by-products water extracts (mix of shell and seed in powder form), Albuquerque et al. [66] assert their potential to act or be a source of antioxidant dietary fiber. The passion fruit extract evaluated in the study is capable of acting as a prebiotic with antioxidant activity when analyzed through ORAC (oxygen radical antioxidant capacity) and DPPH. Using various types of extractions including maceration, (MAC), ultrasound-assisted leaching (UE), supercritical fluid extraction (SFE), and solvents (hexane, ethanol, ethanol/water and ethyl acetate), Oliveira et al. [69] demonstrated the antimicrobial activity of passion fruit (P. edulis sp.) seed in E. coli and L. innocua, presenting minimum inhibitory concentration (MIC) values of 8.0 mg/mL in the combination of maceration extraction (ethanol/water) and UE (ethanol/water); and 8.0 mg/mL in the combination of supercritical fluid extraction-150/300 bar 40 • C and 4.0 mg/mL 150 bar 50 • C, respectively. Lam and Ng [155], studying a new dimeric protein from passion fruit seeds, P. edulis (passiflin), determined specific antifungal activity against Rhizoctonia solani with an IC 50 of 16 µM and a potent inhibitory action on breast cancer cells (MCF-7) with an IC 50 of 15 µM.
Lourith and Kanlayavattanakul [156], studying the ethanolic extract of P. edulis seeds, state that the processing residue of passion fruit juice (seed) is a source of functional compounds, and the antioxidant fraction, determined by DPPH, FRAP, and ABTS analyses, works as a sunscreen with an effective protection against UV rays, as well as a skin-whitening agent. The sun protection capability of the extracts was confirmed by the fact that it contains quercetin and rosmarinic acid in its composition, which have potential action against photooxidative damage. Thus, this eco-friendly antioxidant is considered safe and effective for health-beneficial uses, and therefore, passion fruit seed can be used as an ingredient in the development of cosmetics, especially anti-aging and anti-wrinkle products, which are effective in protecting against UV, combating photoaging.
Malacrida and Jorge [157] confirmed through the study of passion fruit seed methanolic extract that the antioxidant amount present in the seed can serve as a dietary source of natural antioxidants, helping to prevent diseases by combating free radicals in vivo or as a food additive, increasing the stability and quality of food products. This antioxidant activity is attributed to phenolic compounds (linoleic, oleic, palmitic, and stearic) and to the presence of δ-tocopherol and γ-tocopherol (natural antioxidants). The authors further state that oil extraction from passion fruit seeds could add value to products, which is generally discarded as waste. The seed can also be used as a raw material in different industries, including food, detergents, cosmetics, supplements, vitamins, and biodiesel.
The results obtained by Macagnan et al. [158] suggest that apple, orange, and passion fruit by-products positively influence lipids and glucose metabolism, without negative effects in vivo, not affecting the growth of mice studied during the experiment period. By-products promoted a significant reduction in triglyceride and hepatic cholesterol levels and exerted important effects on postprandial glucose control. Furthermore, the authors found that these fiber sources are important for intestinal health without affecting the regularity of intestinal transit, demonstrating that apple pomace, orange pomace, and passion fruit peel can be considered as fonts of dietary fiber with relevant functional properties to health promotion and protection.
The bioactive compounds found in berry seeds mainly are phenolic compounds, fatty acids, and tocopherols. Previous studies shown in Table 2 showed a large deviation in the total content of phenolic compounds in each berry species. It is difficult to compare the abundance of phenolics among different berry seeds, since the values are influenced by many factors, such as cultivars of berries, cultivation condition, extraction solvents, and analytical methods. The primary phenolic compounds in seeds are dependent on the berry species. Ayoub et al. [19] compared the phenolic profiles of seed meals of blackberry, raspberry (black), and blueberry.
The antioxidant activity of berry seeds has been studied extensively [19,[159][160][161][162][163][164][165][167][168][169][170]. Most of the studied seed oils or seed extracts have shown strong capacities of directly scavenging free radicals, chelating metal cations, or inhibiting the oxidation (or DNA damage) caused by free radicals. Yet, the compounds responsible for anti-oxidative effects have not been determined, which is likely due to the large chemical diversity that was found in the extracts. The related conclusions have been drawn only based on the correlation between antioxidant results and the concentration of chemical components. Furthermore, it is difficult to rank berry seed extracts based on their antioxidant effects due to different extraction solvents applied. For example, Helbig and co-workers evaluated both the hexane and water extracts of several seed press residues using the trolox equivalent antioxidant capacity -TEAC method [159]. The results showed that the antioxidant capacity of both hexane and water extracts decreased in the order of elderberry > blackcurrant > cranberry > bilberry. Similarity might be caused by the presence of different bioactive compounds in extracts. Additionally, considering the nature of free radicals, the inhibitory effects of certain berry seeds might differ in various antioxidant assays. Yang et al. reported the peroxyl radical scavenging capacities of supercritical CO 2 extracted berry seed oils [163]. The activity was positively correlated with the content of tocopherols and tocotrienols in the seed oils. Among the seed oils studied, raspberry seed oils exhibited the best activity against peroxyl radicals, but the lowest efficacy of inhibiting lipid oxidation compared to seed oils from the other species of the Rubus and Vaccinium families. In contrast, bilberry seed oil was a potent inhibitor against lipid oxidation, yet weakened with scavenging peroxyl radicals [163]. In the same research, the authors reported the protective effects of sea buckthorn seed oil against oxidative damages of DNA.
Regarding other bioactivities of berry seed extracts, Basu et al. [176] confirmed that that supercritical CO 2 -extracted sea buckthorn seed oil had a significant anti-atherogenic activity when administrated to normal or hypercholesterolemic rabbits. The ethanolic extracts of sea buckthorn seeds strongly inhibited the growth of Enterecoccus durans (68%), Candida albicans (68%), and Bacillus cereus (64%). This was attributed to the high levels of total phenolic compounds, which were represented primarily with condensed tannins [161]. Puupponen-Pimiä et al. [169] evaluated two fractions of acetone extracts of cloudberry seeds in liquid cultures of selected microbial strains. Both fine and seed coarse seed fractions showed strong antibacterial efficacy on the growth of Staphylococcus aureus and Escherichia coli, whereas inhibition was observed on C. albicans and Saccharomyces cerevisiae. It was speculated that high contents of casuarictin/potentillin and sanguiin H2 isomers in the fractions might be responsible for the strong antimicrobial activity [171]. In the same study, the anti-inflammatory abilities of cloudberry seeds were estimated in a dose-dependent manner and caused a significant decrease on pro-inflammatory factors (bacterial lipopolysaccharide induced nitric oxide, NO, IL-6, and inducible nitric oxide synthase, iNOS). As compared to the seed fine faction, the coarse counterpart had the stronger anti-inflammatory effects at the concentration of 1-3 µg/mL, which was associated with the presence of quercetin derivatives [171]. The methanolic extracts of seeds of blackberry and elderberry were tested against bacterial lipopolysaccharide-induced NO and CCL20 in macrophages. The results revealed that blackberry seed extracts had a strong anti-inflammatory property, inhibiting 60% of NO and over 90% of CCL20 production at the dose level of 50 µg/mL. Nevertheless, no inhibitory effect was detected in elderberry seed extracts [165].
The clinical evidence on the health-promoting effects of berry seeds has been summarized by Yang and Kortesniemi [177]. Dietary supplementations with berry seed oils have shown positive impacts on atopic dermatitis [178], plasma lipid profiles [178,179], and platelet aggregation [180,181]. The beneficial effects were due to the high content of polyunsaturated fatty acids with favorable ratios of ω6/ω3 that were close to the recommendation given by the global experts. However, other lipophilic components such as phytosterols, tocopherols, and tocotrienols may also play an important role. [101,163,181] reported that the supplementation with 2 g of sea buckthorn oil (extracted from both seed and pulp) for three months has been shown to have a positive effect on human subjects between 20 and 70 years old suffering from dry eye symptoms [179]. Moreover, Linnamaa et al. [182] suggested that the prevalence of atopic dermatitis in infants could be reduced by dietary intervention using blackcurrant seed oil, when administered to both women during pregnancy and lactation, and to the babies after weaning.

Extraction Technologies of Water-Soluble and Lipophilic Bioactive Compounds
The extraction of bioactive compounds has a long tradition using conventional solvent extraction techniques based on different organic solvents. However, the demand for improving the extraction yield of the target bioactive compounds from plant matrices and the pressure on the environmental friendliness of the production process indicated the need for the development of novel extraction techniques that are based on benign pre-extraction technology by the implementation of enzymes [183]. Marathe et al. [184] described the effectiveness of the enzymatic hydrolysis in the reduction of cellular wall thickness to ensure the better passage of the solvent toward compounds that may be bound in the wall. This way, the extraction will eventually lead to higher yields, more efficiency, a reduction in the processing time and the solvent used, and at the end, a prospective technological solution that is sustainability and commercially viable.
Different enzymes can be used to facilitate the extraction of bioactive compounds, e.g., phenolics from grape seed as an example. Fernández et al. [185] compared the effectiveness of pectinases, cellulases, and tannases, and the blend of these enzymes. All the studied enzymes increased the total phenolic content in the extracts (versus controls) with a 1.18-1.34-fold increased yield. Comprehensive collection on the findings for enzymatic aids in processing for the extraction of polyphenols was recently published by Gligor et al. [186]. This review gives information on the use of hemicellulases and lignanases for the hydrolysis and oxidizing of cellular walls. However, González-García et al. [136] describe that the use of lignanases is not viable for food industrial applications, due to the formation of low-molecular reactive compounds in the oxidation process. The authors reported that although there are positive outcomes regarding the efficiency and environmental friendliness of enzyme-assisted extractions, the high costs and low popularity slows down their prevalence for food industrial applications.
Recently, the combination of these enzymes with microwave, ultrasound, supercritical fluid extraction, or high-pressure extraction was described in order to overcome the drawbacks mentioned above. The target compounds that strongly bind to the cell walls usually will not be fully released with enzymatic digestion by polysaccharide-degrading enzymes or hemicellulases [187]. It was reported that approximately 24% of the total phenolics are bound in the food matrices with polysaccharides (e.g., hemicellulose, cellulose, and pectin), and with certain biomolecules, as proteins. From this point of view, enzymatic utilization of a different nature can significantly enhance the recovery of the phenolics. Pap et al. [188] showed that the enzymatic depectinization of the blackcurrant juice by pectinase significantly increased the amount of available flavonols, but a similar observation for anthocyanins were not observed. Fernandes and Carvalho [189] furthermore explained that the treatment with cellulases, hemicellulases, and pectines resulted in the formation of smaller oligosaccharide chains and the liberation of compounds, such as oils and proteins.
Ultrasound techniques are based on the acoustic cavitation in which small vapor-filled bubbles are generated. These bubbles will eventually explode and result in high pressure and temperature in the cell walls [190]. Ultrasound waves that are exploited for the treatments of different food materials are generally over 20 kHz [191]. The application of ultrasound extraction (US) for polyphenols from different fruit seeds has already been covered in the literature. Segovia et al. [62] studied the batch and continuous US for recovering polyphenols from avocado seeds. These authors also modeled the extraction process and described that the film theory and Fick's law models could sufficiently describe the US process, for both batch and continuous phase. Such a mathematical modeling provides understanding on the proceeding of the extraction.
Da Porto et al. [192] investigated the extraction of oils and polyphenols in US from grape seeds and compared the results with conventional extraction. The results indicated that the removal of oil was almost as efficient with US as with Soxhlet when a power of 150 W for 30 min was used. Comparing the polyphenolic extraction from grape seed by maceration versus US, these authors reported that the preliminary treatment with US increased the yield of polyphenols in maceration. However, a significant decrease of polyphenolic content was observed with double US treatments, when both the oil removal and the polyphenolic extraction were done by the US. Since polyphenolic compounds are naturally heat sensitive, this observation can be attributed to the significantly higher temperatures and pressures in the US hot spots [193] and consequential breakdown of the polyphenols.
Opposite to ultrasounds, microwaves are non-ionizing radiations at frequencies between 300 MHz to 300 GHz [194]. Considering the mechanism of microwave action, they are different in nature in a way that heating, and the extent of the absorbed heat will depend on the ability of polar solvents to absorb the microwave energy. Ionic conduction and dipole rotation of the solvent will result with heating, which is selective in nature, and opposite to conventional extractions where generally, the vessel is heated, and the solvent absorbs the heat through it. Li et al. [195] reported the effectiveness of the microwave-assisted extraction (MAE) of polyphenols from grape seeds. The authors optimized the MAE of the grape seeds in a five-level, three independent variable central composite rotatable design, and concluded that the yield of polyphenols in MAE extracts were comparable to that of US extraction and conventional extraction. However, a significant benefit was the much shorter time that was required for the extraction. The length of the process is always a crucial factor, since some of the compounds, especially heat-sensitive ones, may start to degrade during the course of the processing. On the other hand, Bucić-Kojić et al. [196] developed a statistical model for the description of the kinetics of grape seed phenolics depending on the temperature. The understanding and the implementation of such modeling is an extremely useful tool in process scale-up and industrial application as well.
Pressurized hot water extraction also plays an important role in novel extraction techniques. This extraction technology is gaining more interest for the production of bioactive compounds. Here, the pressure is adjusted to keep the water in its liquid state, and the temperature is between the boiling and critical point [197]. This technology benefits from the changes of the dielectric constant of water, as increasing the temperature up to 200-350 • C will decrease the dielectric constant of the water and provide similar polarities to those that methanol, EtOH, or acetone have at room temperature [198]. The hot water is usually recirculated, or the process can be also multi-staged. The complexity of the technology increases when matrices with multiple compounds are used in real applications, since the operation parameters must be well manipulated in order to extract the desired compound without the other contaminants. However, it is important to avoid undesirable changes of the target compounds that could deteriorate during the extraction. Plaza and Marina [199] published a comprehensive review on the potential application of the pressurized hot water extraction. The application for the extraction of phenolic compounds, diterpenes, triperpenes, polysaccharides, and proteins from different plant materials, peels, leaves, seeds, barks, and wastes were covered, and a positive trend for their future importance was indicated by this technology. Beside, several authors reported the results of the study on the extraction of polyphenolic compounds [198,200] from grape peels and pomegranate seed residues [201] for anthocyanins from grape pomace [202].
In supercritical fluid extraction, the most commonly used solvent is carbon dioxide, which due to its low critical temperature allows the extraction of thermally sensitive compounds [184,203]. Still, the challenge is related to the high cost of processing as compared to a low yield of extracted compounds. Nonetheless, the nature of the CO 2 as a solvent enables the extraction of compounds with non-polar character. However, when used alone in the extraction, it is inadequate for the extraction of highly polar compounds, e.g., polyphenols being one of them [204]. Due to this, for the most polyphenolic recovery from plant seeds, the CO 2 is combined with other solvents, (e.g., ethanol) for potential applications in food production. Castro-Vargas et al. [129] extracted bioactives from guava seeds with supercritical CO 2 extraction combined with EtOH, and found a correlation between the applied pressure and temperature on the antioxidant activity of the extracts.
Yilmaz et al. [203] pointed out that the challenge with the valorization of the grape seeds is the residual oil obtained along with the phenolic compounds. Hexane is commonly used for the conventional extraction of oil, but it needs additional evaporation step(s) to remove the residual solvent after the defatting. The authors reported that with the co-addition of ethanol in the supercritical extraction, with a suitable adjustment of pressure and temperature, proanthocyanidins were successfully recovered from the grape seeds. Da Porto and Natolino [205] used response surface optimization to estimate the optimum process parameters for the extraction of polyphenols from white grape seeds in a two-stage supercritical CO 2 extraction. The optimization was carried out by studying the effects of pressure, the amount of ethanol as co-solvent, and the CO 2 flow rate for the number of total polyphenols and proanthocyanidins in the extracts. The results indicated that the optimization was crucial in order to make a good compromise between the concentration of the valuable compounds of the extracts, and also the length of the extraction process to ensure the economic feasibility for industrial application.
The above summary describes the most common novel extraction techniques that are combined with the enzymatic treatments of the plant materials. However, Ran et al. [206] recently reported the application of the conventional extraction of proanthocyanidins from grape seeds with boosting the extraction with the addition of ionic liquids as adjuvants. The authors reported on the increase of the extraction efficiency when adding ionic liquids. However, they also concluded that further studies are required to benefit fully from the utilization of ionic liquids, including the recovery and reuse of the solvents. On the other hand, the widespread application of ionic liquids in food industrial processes are hindered due to the lack of proper information on their toxicity, and stability and bioactivity limits [207].
When the most promising technological concept is selected for the extraction of bioactive compounds from plant seeds, the extract of the target compounds can undergo downstream processing, such as (pre)concentration by the membrane technology and drying. Shi et al. [208] showed that the concentration of polyphenols with membranes was useful after the extraction with 50% ethanol and 50% water mixtures when a 0.22-µm membrane was applied. Pap et al. [209] also reported on the concentration of anthocyanins and flavonols of blackcurrants in juice by using a reverse osmosis process. An approximate 1.5-fold increase of anthocyanins and flavonols was observed when the process was combined with pectinase enzyme treatment. Conidi et al. [210] successfully implemented a multistep ultrafiltration (150 kDa and 2 kDa membranes) of pomegranate juice to separate anthocyanins from glucose and fructose, and to produce end-products as nutraceuticals and food additives. These findings emphasized the importance of the proper selection of membranes to separate and pre-concentrate the bioactive compounds before the final drying. Due to the heat sensitivity of the bioactives, drying is a challenging step in the downstream processing. For instance, although freeze-drying well preserves the compounds, its widespread industrial application for extract processing will be likely impeded because of the price.
As final remarks, enzyme-assisted extraction, and its combination with novel extraction techniques are gaining importance. There is an increased need to improve the performance of these processes so that they become more resource efficient. In the case of the enzymatic treatment, these should focus on selecting the proper enzyme(s) or blend, and process optimization for operating under the optimal pH, temperature, and enzyme-to-substrate ratio that are defined by their kinetics. The length of the enzymatic treatment is also an important factor to be optimized to reach economic yields. It is also important to consider that chosen enzymes have high stability against the effects that these novel techniques exhibit during the processing. In the case of the novel co-extraction techniques, the operational parameters usually involved are the microwave and ultrasound power, temperatures, pressures, solvent-to-solid ratio, pH, and the extraction time. A target compound is usually determined by the nature of the solvent or solvent mixtures.
As a summary of the extraction technologies, Table 3 [211][212][213][214][215][216][217][218] gathers some studies linking the chemical compounds of fruit seeds and their respective bioactivity with the extracting technology used. The antioxidant activity results showed that the methanol and ethanol fractions were more effective radical scavengers than chloroform, ethyl acetate and n-hexane.
Both alcoholic fractions showed potential toward tyrosinase, xanthine oxidase and urease inhibition.
Among the TAAs, ursolic acid, betulinic acid and maslinic acid showed effective radical scavenging activity.
All TAAs showed lower inhibitory activity towards free radicals in vitro than the apple pomace extracts. Apple pomace methanol extract and ursolic acid revealed prominent anticancer activity on Hela, Skov-3, Caski, and NCL cancer cell lines, respectively.  Phloridzin represented 52-67% and 75-83% of the total phenolics measured by the Folin-Ciocalteu assay and HPLC method, respectively.
Chewing gum could be a suitable delivering material for phloridzin uptake originated from apple seeds.
Apple pomace obtained after processing of a When apple pomace HWE were added to yogurt formulations, a final product with improved fiber content and antioxidant properties was achieved in comparison to control sample (plain yogurt). Higher total phenols and DPPH radical scavenging activity was found in Red Delicious apple pomace extracts.
Extraction solvent was not found as significant extraction parameter. The DPPH scavenging ability of the extracts ranged from 27.1 to 54.6 ± 6.9 mg trolox/L, depending on the extraction parameters.
In most cases, extraction time and the particle size of the sample had significant effect on the extraction yield and longer extraction times lead to increased TPC in the extract.
UAEE found to be superior techniques to extract TPC from apple pomace due to the synergistic effects of US and enzymes.
The antioxidant activity decreased with the extraction time and enzyme dosage. Total phenols and AA were significantly (p < 0.05) influenced by the FWR and its interaction with the electric filed intensity and time.
With the increase in electric filed intensity from 1 kV/cm to 3 kV/cm, a significant (p < 0.05) increase of 4.8% TPC and 4.4% AA was observed.
A significant (p < 0.05) decrease of 3.8% and 2.6% was observed in total phenols and AA, respectively with the increase in treatment time from 500 µs to 875 µs followed by no significant (p > 0.05) change in both total phenols and AA. The optimum condition of PEF treatment was found as 12.5% (w/v) FWR, 2 kV/cm electric field intensity and 500 µs treatment time with a specific energy input of 3.0 kJ/kg.
Obtained results indicated that the PEF treatment could be useful tool for the processing of food with enhanced levels of phenolic antioxidants.

Final Comments and Upcoming Research Prospects
The potential use of fruit seeds for the recovery of phytochemicals is of pivotal importance within circular economy premises of production and utilization of natural resources. Bioactive-rich extracts may be used for either pharmaceutical or food sectors, and in some cases for both. Future research should focus on the optimization of innovative extraction techniques and on the biological effects of the bioactive-rich extracts using different in vitro and in vivo protocols. In addition, after checking to ensure that the extracts are safe from the chemical and toxicological standpoints, applications in cosmetics and food models should be conducted to assess the effectiveness of such extracts regarding their antioxidant, antimicrobial, anti-proliferative, antilipidemic, hypoglycemic, and anti-inflammatory effects.
Author Contributions: The review was conceived and designed by D.G. We declare that the data were collected, interpreted and analyzed by all authors named in this article. All authors read, made significant changes and approved the manuscript for publication.