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Proceeding Paper

By-Products of Walnut (Juglans regia) as a Source of Bioactive Compounds for the Formulation of Nutraceuticals and Functional Foods †

1
Nutrition and Bromatology Group, Department of Analytical and Food Chemistry, Faculty of Food Science and Technology, University of Vigo, Ourense Campus, E32004 Ourense, Spain
2
Mountain Research Center (CIMO), Polytechnic Institute of Braganza, Campus Santa Apolónia, 5300-253 Braganza, Portugal
*
Authors to whom correspondence should be addressed.
Presented at the 2nd International Electronic Conference on Nutrients, 15–31 March 2022; Available online: https://iecn2022.sciforum.net/.
Biol. Life Sci. Forum 2022, 12(1), 35; https://doi.org/10.3390/IECN2022-12396
Published: 14 March 2022
(This article belongs to the Proceedings of The 2nd International Electronic Conference on Nutrients)

Abstract

:
The scarcity of natural resources and higher incidence of diseases related to inappropriate eating habits have prompted the search of food and nutraceutical products with functional properties that are also respectful of the environment. Agro-industrial by-products are a profitable source for obtaining bioactive compounds, with various biological properties, including antioxidant, anti-inflammatory, and anticancer properties, which contribute to immunity and reduce the negative effects of infections, inflammation, and oxidative stress. In the case of the walnut (Juglans regia) oil industry, various by-products are generated, among which we can mention pomace, green shell, shell, skin and leaves. Therefore, there is an opportunity for the recovery of waste, the recovery of target molecules and the formulation of new products, whether they are nutraceuticals, pharmaceuticals, or food additives, contributing to the circular economy and consumer health. Walnut is commonly characterized by its high content of lipids (58–65%), mainly polyunsaturated fatty acids, tocopherols and phytosterols. In addition, the current literature states that its by-products are rich in phenolic compounds, mainly phenolic acids and flavonoids. In accordance, the antioxidant potential of different extracts of nuts, shells and leaves has bee studied using different methods such as the reduction potency assay, scavenging effect of DPPH (2,2-diphenyl-1-picrylhydrazyl) and inhibition of lipid oxidation by β-carotene linoleate system, with EC50 values less than 1 mg/mL. The results obtained showed that all walnut extracts have a strong antioxidant capacity against ROS species. For this reason, this work focuses on the bibliographic review of the bioactive compounds present in the by-products of the walnut industry, as well as mentioning their biological properties and possible applications in the food sector.

1. Introduction

The walnut is the fruit of the walnut tree (Juglans regia; Juglandaceae family). There are two species, the Persian or English walnut and the black walnut. It is harvested all over the world, but China, the United States and Europe stand out as major producers. It is well-known for its broad nutritional attributes, sensory properties, and health benefits. Whole walnuts are usually consumed, but they are also employed in various food preparations such as cakes, cookies, energy bars, salads or ice cream. In some countries such as Slovenia, green walnuts are used in the preparation of a liqueur. Regarding the contribution of nutrients, they contain lipids, mainly unsaturated fatty acids, phytosterols and tocopherols, as well as proteins, vitamins, minerals and a significant amount of antioxidant compounds such as phenolic compounds [1]. These nutrients are bioactive components since they provide beneficial properties for the health of the consumer. Current research has shown that walnut consumption can provide natural antioxidants and it has a protective role against diseases influenced by oxidative stress such as cancer and cardiovascular diseases [2,3]. On the other hand, it is known that non-edible parts such as leaves, shell, skin, green shell, and bark have been used in traditional medicine for the treatment of different ailments. For example, in some countries, an infusion of walnut leaves is used for its antioxidant and antimicrobial properties. In addition, an extract of the green peel has been used to treat skin diseases and inflammation [4]. The industrialization of the fruit causes a large amount of plant residues. In this sense, it is estimated that 70% of the fruit is transformed into residue, mainly peel, bagasse, green peel, skin, and leaves (Figure 1), which contain a significant number of bioactive compounds valuable for their use and exploitation. These residues are commonly disposed of in landfills, burned, or used for composting. However, a most efficient use of this waste would be a circular economy strategy, that would reduce environmental impact and at the same time boost economic sector. In this sense, the agricultural residues of the walnut have been widely investigated in the search for natural products. There is evidence that all parts of the walnut tree can be used as a source of compounds that express an important antioxidant, antimicrobial, antidiabetic, immunomodulatory, hepatoprotective, and anti-inflammatory potential [3,5,6]. Therefore, this review aims to discuss the recent scientific literature on the importance of the walnut, including the different parts of its fruit, as well as to mention its biological properties and possible applications in the food industry.

2. By-Products Derived from Walnut

The walnut is made up of four different parts (Figure 1). The green outer layer is known as the hull or shell; when the fruit ripens, it cracks. It must be separated manually from the middle shell, which we know as the walnut. This is a hard layer that surrounds the seed, and, in the same way, it must be broken mechanically to release the seed or nucleus, which is the edible part. In addition, the seed is covered by a thin brown layer called the skin. In the following section, we have compiled several bioactive compounds identified in these by-products (Table 1).

2.1. Walnut Husk

Walnut husk is a characteristic by-product of walnut cultivation; it is generated in the harvest, when the ripe fruit breaks to give rise to the fruit. In rural areas, it is used as a source of energy for heating. In traditional medicine, it is used for the treatment of skin diseases and pain relief. It has been reported that this by-product has significant amounts of phenolic compounds and flavonoids [4], so its recovery would be useful. For the preparation of the extract, it is necessary to choose the most appropriate solvent and extraction technique. In this sense, it is reported that better TPC and TFC results are achieved, as well as better antioxidant activities in extracts treated with mixtures of water/ethanol or water/methanol [13]. TPC recovery for extracts derived from walnut shells has been reported to oscillate between 32.61 to 166.7 mg GAE/100 g DW [12,13,14], and total flavonoids from 22.91 to 423.97 mg CE/100 g DW [19]. Generally, Soxhlet extraction is the conventional technique that allows greater recovery of TPC and TFC. However, ultrasound-assisted extraction has also shown promising results [20]. Among the main phenolic compounds present in the walnut shell, hydrolysable tannins have been identified, mainly ellagic acid, with 98.3 ± 5.56 mg GAEs/L extract reported, and tannic acid, with 120.4 ± 4.19 mg GAEs/L extract [7,21]. In addition, the presence of 27 naphthoquinones and their derivatives has been reported, with juglone being the most important with 1404 ± 96.8 mg GAEs/L extract [21]. In addition, the presence of gallic acid and protocatechuic acid has been reported, with 122 ± 10.0 and 23.0 ± 4.78 mg/100 g DW, respectively [22]. Regarding the compounds belonging to the group of flavonoids, (+)-catechin 530.80 ± 15.39 mg GAEs/L extract and La (-)-epicatechin 350.33 ± 11.91 mg GAEs/L extract stand out [19]. Additionally, the DPPH radical scavenging activity of walnut shells has been evaluated in different studies, reporting values for the half effective concentration (IC50) in the range of 0.30–0.80 mg/mL [12,13,14]. Other authors determined antioxidant activity by FRAP, showing a result of 0.45 ± 0.04 mmol Fe2+/g DS [20].
Currently, the green walnut shell has different applications in the industry. For example, it is used for the elimination of dangerous materials and heavy metal ions in industrial effluents, as well as for the elimination of synthetic dyes or other dangerous compounds. In addition, considering the presence of juglone, a natural dye, this by-product can be used as a hair dye. It is also a profitable, valuable, environmentally friendly compound [23]. For the food industry, it is described as a natural antioxidant that could replace the use of synthetic additives [24] and can be also used as a functional additive in the meat industry as a low-cost source of valuable source of phytochemicals [24].

2.2. Skin

The walnut skin is the thin brown layer that protects the seed from oxidation and microbial contamination. It represents 5 to 8% of the fruit and it is eliminated in the processing of the walnut, because it can cause a slight astringency and bitterness. Regarding phytochemical composition, it has been described to be the main source of polyphenols from the nut [5,8]. In this sense, several studies reported concentrations of the three most abundant phenolic compounds (juglone, syringic acid and ellagic acid) up to 20 times higher in the skin, compared to the seed [8]. In addition, it is reported that the concentration of phenolic compounds increases gradually from the fruiting stage to the mature stage, reporting TPC and TFC values of 52.05–279.3 mg GAE/g DW and 8.95 mg RE/g FW, respectively [5,25]. As can be seen, the presence of non-flavonoid-type phenolic compounds stands out [25]. Reports stated that most of the compounds present in the walnut skin belong to hydrolyzable tannins, such as digalloyl-glucose, ellagic acid galloyl pentose or galloyl methylgalloyl dexoyhexoside isomer. The high content of phenolic compounds gives this by-product important biological properties, such as antioxidant, antimicrobial, and anticancer capacity [3,5,7].

2.3. Shell

It is an inert, hard and biodegradable material, which constitutes about 70% of the total weight of the fruit. Thus, it is the most abundant by-product of the walnut. A study reported a chemical composition of 3.4% ash, 50.3% lignin, 22.4% hemicellulose and 23.9% cellulose [4]. Despite its high potential as a source of chemicals, it has been traditionally used as a source of energy for heating, an abrasive agent to clean and polish metals, plastics, wood, and as a filter medium to separate oil, hazardous materials, and heavy metals. Currently, due to this biofiltration potential, it is used to treat water extracted from oil fields and wastewater. In recent years, research has focused on the production of antioxidants and antimicrobials from walnut shells [4], which have been linked to the presence of phenolic compounds. In this sense, the recovery of these compounds through three extraction methods (ultrasonic bath, ultrasonic probe and standard agitation method) has been study, recovering TPC of 51.2 mg of gallic acid equivalents/g of dry weight (GAE /g DW), respectively [9]. In agreement, another study reported TPC values of 49.10–63.60 mg gallic acid equivalents/g dry weight (GAE/g DW) [26]. Further analysis identified lignans (0.30 mg/g), stilbenes (0.02 mg/g) and flavonoids (0.69 mg/g). Antioxidant properties of walnut shell have been corroborated by DPPH assay, reporting values of 3.14–7.17 µg/mL [9].

2.4. Leaves

Leaves are generated in large quantities during harvest. They have been used in traditional medicine for the treatment of hemorrhoids, venous insufficiency and for their anthelmintic, depurative, antidiarrheal properties [15]. In this by-product, juglone is reported as the main phenolic compound, among other flavonoids [5]. The appropriate mass solvents for the recovery of phenolic compounds, water, ethanol and methanol have been reported as the most efficient [5]. In this sense, a study achieved the highest recovery of TPC and TFC in a methanolic extract, reporting values of 120.28 ± 2.32, 59.44 ± 0.87 mg/g DE, respectively. They also report on a higher presence of TPC in young leaves compared to mature leaves [27]. Another study identified ten phenolic compounds, namely 3- and 5-caffeoylquinic acids, 3- and 4-p-coumaroylquinic acids, p-coumaric acid, quercetin 3- galactoside, quercetin 3-pentoside derivative, quercetin 3-arabinoside, quercetin 3-xyloside and quercetin 3-rhamnoside in walnut leaves [15].

Author Contributions

Conceptualization, F.C. and M.C.; methodology, C.L.-L.; software, O.T.; validation, P.O., H.C. and F.C.; formal analysis, F.C.; investigation, C.L.-L.; resources, M.A.P. and J.X.; data curation, F.C.; writing—original draft preparation, F.C.; writing—review and editing, M.A.P.; visualization, M.A.P.; supervision, M.A.P. and J.S.-G. All authors have read and agreed to the published version of the manuscript.

Funding

Authors are grateful to the Bio Based Industries Joint Undertaking (JU) under grant agreement No. 888003 UP4HEALTH Project (H2020-BBI-JTI-2019). The JU receives support from the European Union’s Horizon 2020 research and innovation program and the Bio-based Industries Consortium. The project SYSTEMIC Knowledge Hub on Nutrition and Food Security has received funding from national research funding parties in Belgium (FWO), France (INRA), Germany (BLE), Italy (MIPAAF), Latvia (IZM), Norway (RCN), Portugal (FCT) and Spain (AEI) in a joint action with JPI HDHL, JPI-OCEANS and FACCE-JPI launched in 2019 under the ERA-NET ERA-HDHL.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Acknowledgments

The research that led to these results was supported by MICINN, supporting the Ramón y Cajal scholarship for M.A. Prieto (RYC-2017-22891) and the Juan de la Cierva Formación grant for T. Oludemi (FJC2019-042549-I); by Xunta de Galicia, supporting the EXCELENCIA-ED431F 2020/12 program and the predoctoral fellowships of M. Carpena (ED481A 2021/313) and A.G. Pereira (ED481A-2019/0228). The research leading to these results was supported by the European Union through the “NextGenerationEU” program supporting the “Margarita Salas” grant awarded to P. Garcia-Perez, and the EcoChestnut Project (Erasmus+ KA202), which supports the work of J. Echave, and the program BENEFICIOS DO CONSUMO DAS ESPECIES TINTORE-RA-(CO-0019-2021), which supports the work of F. Chamorro. Authors are grateful to the Bio Based Industries Joint Undertaking (JU) under grant agreement No. 888003 UP4HEALTH Project (H2020-BBI-JTI-2019) that supports the work of P. Otero and C. Lourenço-Lopes.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Gunduc, N.; El, S.N. Assessing Antioxidant Activities of Phenolic Compounds of Common Turkish Food and Drinks on In Vitro Low-Density Lipoprotein Oxidation. J. Food Sci. 2003, 68, 2591–2595. [Google Scholar] [CrossRef]
  2. Yang, J.; Liu, R.H.; Halim, L. Antioxidant and antiproliferative activities of common edible nut seeds. LWT Food Sci. Technol. 2009, 42, 1–8. [Google Scholar] [CrossRef]
  3. Catanzaro, E.; Greco, G.; Potenza, L.; Calcabrini, C.; Fimognari, C. Natural products to fight cancer: A focus on Juglans regia. Toxins 2018, 10, 469. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  4. Jahanban-Esfahlan, A.; Ostadrahimi, A.; Tabibiazar, M.; Amarowicz, R. A comprehensive review on the chemical constituents and functional uses of walnut (Juglans spp.) husk. Int. J. Mol. Sci. 2019, 20, 3920. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  5. Jahanban-Esfahlan, A.; Ostadrahimi, A.; Tabibiazar, M.; Amarowicz, R. A comparative review on the extraction, antioxidant content and antioxidant potential of different parts of walnut (Juglans regia L.) fruit and tree. Molecules 2019, 24, 2133. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  6. Medic, A.; Jakopic, J.; Solar, A.; Hudina, M.; Veberic, R. Walnut (J. regia) agro-residues as a rich source of phenolic compounds. Biology 2021, 10, 535. [Google Scholar] [CrossRef]
  7. Akbari, V.; Jamei, R.; Heidari, R.; Esfahlan, A.J. Antiradical activity of different parts of Walnut (Juglans regia L.) fruit as a function of genotype. Food Chem. 2012, 135, 2404–2410. [Google Scholar] [CrossRef]
  8. Colaric, M.; Veberic, R.; Solar, A.; Hudina, M.; Stampar, F. Phenolic acids, syringaldehyde, and juglone in fruits of different cultivars of Juglans regia L. J. Agric. Food Chem. 2005, 53, 6390–6396. [Google Scholar] [CrossRef]
  9. Han, H.; Wang, S.; Rakita, M.; Wang, Y.; Han, Q.; Xu, Q. Effect of Ultrasound-Assisted Extraction of Phenolic Compounds on the Characteristics of Walnut Shells. Food Nutr. Sci. 2018, 09, 1034–1045. [Google Scholar] [CrossRef] [Green Version]
  10. Wang, X.; Zhao, M.; Su, G.; Cai, M.; Zhou, C.; Huang, J.; Lin, L. The antioxidant activities and the xanthine oxidase inhibition effects of walnut (Juglans regia L.) fruit, stem and leaf. Int. J. Food Sci. Technol. 2015, 50, 233–239. [Google Scholar] [CrossRef]
  11. Slatnar, A.; Mikulic-Petkovsek, M.; Stampar, F.; Veberic, R.; Solar, A. Identification and quantification of phenolic compounds in kernels, oil and bagasse pellets of common walnut (Juglans regia L.). Food Res. Int. 2015, 67, 255–263. [Google Scholar] [CrossRef]
  12. Oliveira, I.; Sousa, A.; Ferreira, I.C.F.R.; Bento, A.; Estevinho, L.; Pereira, J.A. Total phenols, antioxidant potential and antimicrobial activity of walnut (Juglans regia L.) green husks. Food Chem. Toxicol. 2008, 46, 2326–2331. [Google Scholar] [CrossRef] [PubMed]
  13. Fernández-Agulló, A.; Pereira, E.; Freire, M.S.; Valentão, P.; Andrade, P.B.; González-álvarez, J.; Pereira, J.A. Influence of solvent on the antioxidant and antimicrobial properties of walnut (Juglans regia L.) green husk extracts. Ind. Crops Prod. 2013, 42, 126–132. [Google Scholar] [CrossRef]
  14. Sfahlan, A.J.; Mahmoodzadeh, A.; Hasanzadeh, A.; Heidari, R.; Jamei, R. Antioxidants and antiradicals in almond hull and shell (Amygdalus communis L.) as a function of genotype. Food Chem. 2009, 115, 529–533. [Google Scholar] [CrossRef]
  15. Rather, M.A.; Dar, B.A.; Dar, M.Y.; Wani, B.A.; Shah, W.A.; Bhat, B.A.; Ganai, B.A.; Bhat, K.A.; Anand, R.; Qurishi, M.A. Chemical composition, antioxidant and antibacterial activities of the leaf essential oil of Juglans regia L. and its constituents. Phytomedicine 2012, 19, 1185–1190. [Google Scholar] [CrossRef]
  16. Vieira, V.; Prieto, M.A.; Barros, L.; Coutinho, J.A.P.; Ferreira, O.; Ferreira, I.C.F.R. Optimization and comparison of maceration and microwave extraction systems for the production of phenolic compounds from Juglans regia L. for the valorization of walnut leaves. Ind. Crops Prod. 2017, 107, 341–352. [Google Scholar] [CrossRef] [Green Version]
  17. Santos, A.; Barros, L.; Calhelha, R.C.; Dueñas, M.; Carvalho, A.M.; Santos-Buelga, C.; Ferreira, I.C.F.R. Leaves and decoction of Juglans regia L.: Different performances regarding bioactive compounds and in vitro antioxidant and antitumor effects. Ind. Crops Prod. 2013, 51, 430–436. [Google Scholar] [CrossRef]
  18. Almeida, I.F.; Fernandes, E.; Lima, J.L.F.C.; Costa, P.C.; Fernanda Bahia, M. Walnut (Juglans regia) leaf extracts are strong scavengers of pro-oxidant reactive species. Food Chem. 2008, 106, 1014–1020. [Google Scholar] [CrossRef]
  19. Cosmulescu, S.; Trandafir, I.; Nour, V.; Ionica, M.; Tutulescu, F. Phenolics content, antioxidant activity and color of green walnut extracts for preparing walnut liquor. Not. Bot. Horti Agrobot. Cluj-Napoca 2014, 42, 551–555. [Google Scholar] [CrossRef] [Green Version]
  20. Tabaraki, R.; Rastgoo, S. Comparison between conventional and ultrasound-assisted extractions of natural antioxidants from walnut green husk. Korean J. Chem. Eng. 2014, 31, 676–683. [Google Scholar] [CrossRef]
  21. Stampar, F.; Solar, A.; Hudina, M.; Veberic, R.; Colaric, M. Traditional walnut liqueur—Cocktail of phenolics. Food Chem. 2006, 95, 627–631. [Google Scholar] [CrossRef]
  22. Jakopic, J.; Solar, A.; Colaric, M.; Hudina, M.; Veberic, R.; Stampar, F. The influence of ethanol concentration on content of total and individual phenolics in walnut alcoholic drink. Acta Aliment. 2008, 37, 233–239. [Google Scholar] [CrossRef]
  23. Beiki, T.; Najafpour, G.D.; Hosseini, M. Evaluation of antimicrobial and dyeing properties of walnut (Juglans regia L.) green husk extract for cosmetics. Color. Technol. 2018, 134, 71–81. [Google Scholar] [CrossRef]
  24. Salejda, A.M.; Janiewicz, U.; Korzeniowska, M.; Kolniak-Ostek, J.; Krasnowska, G. Effect of walnut green husk addition on some quality properties of cooked sausages. LWT Food Sci. Technol. 2016, 65, 751–757. [Google Scholar] [CrossRef]
  25. Sheng, F.; Hu, B.; Jin, Q.; Wang, J.; Wu, C.; Luo, Z. The analysis of phenolic compounds in walnut husk and pellicle by uplc-q-orbitrap hrms and hplc. Molecules 2021, 26, 13. [Google Scholar] [CrossRef]
  26. Herrera, R.; Hemming, J.; Smeds, A.; Gordobil, O.; Willför, S.; Labidi, J. Recovery of bioactive compounds from hazelnuts and walnuts shells: Quantitative–qualitative analysis and chromatographic purification. Biomolecules 2020, 10, 1363. [Google Scholar] [CrossRef]
  27. Salimi, M.; Majd, A.; Sepahdar, Z.; Azadmanesh, K.; Irian, S.; Ardestaniyan, M.H.; Hedayati, M.H.; Rastkari, N. Cytotoxicity effects of various Juglans regia (walnut) leaf extracts in human cancer cell lines. Pharm. Biol. 2012, 50, 1416–1422. [Google Scholar] [CrossRef]
Figure 1. Valorization of walnut by-products following circular economy approaches, extracting compounds with biological properties for bio-based products in different industrial sectors.
Figure 1. Valorization of walnut by-products following circular economy approaches, extracting compounds with biological properties for bio-based products in different industrial sectors.
Blsf 12 00035 g001
Table 1. Compounds and functional ingredients recovered from walnut residues with various extraction methods and their applications.
Table 1. Compounds and functional ingredients recovered from walnut residues with various extraction methods and their applications.
Biomass SourceBy-ProductCompound(s)Extraction MethodBiological PropertyApplicationRefs.
NutSkinTPC
4615–6059 mg GAE/100 g 1 DW
TFC
810–1495 mg CE/100 g 1 DW
Soxhlet
MeOH, 60 °C, 30 min
DPPH
0.09–0.20 mg/mL
Natural antioxidants[7]
TPC/HPLC
syringic acid, juglone, and ellagic acid (1003.24, 317.90, and 128.98 mg/100 g)
Ultrasonic bath
MeOH/BHT
60 °C, 30 min
-Food additives[8]
ShellTPC
939–1968 mg GAE/100 g 1 DW
TFC
301–811 mg CE/100 g 1 DW
Soxhlet
MeOH, 60 °C 30 min
DPPH
0.27–0.48 mg/mL
Natural antioxidants[7]
TPC
HAE: 20.6 mg GAE/g DW
Ultrasonic bath: 25.8 mg GAE/g DW,
UAE: 51.2 mg GAE/g DW
HAE
EtOH/H2O, 25 °C, 15 min
Ultrasonic bath
EtOH/H2O, 25 °C, 15 min, 500 W
UAE
EtOH/H2O, 25 °C, 15 min, 1500 W
-Food additives[9]
TPC
14.81 mg GAE g/DW
HAE
n-hexane, 25 °C, 90 min
ORAC
3423.44 μmol Trolox g−1
Food additives[10]
BagasseTPC
7.7 mg GAE g−1 DW
Sonication
CH3OH/H2O, 60 min
DPPH
83.46–93.08%
Food additives[11]
Green huskTPC
32.61–74.08
mg (GAE)/g DW
HAE
H2O, 100 °C 45 min
DPPH
0.35–0.59 mg/mL
Food additives[12]
Antimicrobial activity:
Gram positive and Gram-negative bacteria, and fungi
<1 mg/mL
TPC
84.46 mg GAE/g DW
HAE
EtOH/H2O
MeOH/H2O
DPPH
0.33–0.70 mg/mL
Natural antioxidants[13]
TPC
43.9–166.7 mg GAE/g DW
Soxhlet
MeOH, 80 °C, 30 min
DPPH
0.30–
0.80 mg/mL
Natural antioxidants[14]
LeavesEssential oil
α and β pinene
hydrodis-tillationDPPH
34.5–56.4 μg/mL
Food additives
Antimicrobial activity:
Gram positive and Gram-negative bacteria
[15]
TPC
HAE: 3.9 a 13.7 mg GAE/g DW
MAE: 6.4 a 14.7 mg GAE/g DW
HAE
EtOH, 60 °C, 112 min.
MAE:
EtOH, 107.5 °C, 30 min
-Food additives[16]
Tocopherols: 282.20 mg/100 g DW
TPC/HPLC:
3-O-caffeoylquinic acid, Pro-cyanidins and taxifolin derivatives
HAE
H2O, 100 °C, 5 min
DPPH
0.151–0.202 mg/mL
TBARS
189.92–269.27 g/mL
Food additives[17]
HeLa
294.87 g/mL
MCF-7
209.28–242.14 g/mL
TPC
270 mg GAE/g DW
HAE
H2O/EtOH, 40 °C, 10 min
ORAC
2.17 ± 0.22 μmol Trolox/mg
Food additives[18]
Notes & abbreviations: TPC, total phenolic compounds; DPPH, 2,2-difenil-1-picrilhidrazilo; HPLC, high performance liquid chromatography; TFC, total flavonoid compounds; HAE, heat assisted extraction; MAE, microwave assisted extraction; TBARS, Thiobarbituric acid reactive substances; ORAC, Oxygen Radical Antioxidant Capacity; GAE, gallic acid equivalents; DW, dry weight; EtOH, ethanol; MeOH, methanol; H2O, water; EtOAc, ethyl acetate; Pet, petroleum; Ace, acetone; Hex, hexane; N. A., nitric acid; S. Ac., sulfuric acid; Chl, chloroform; Eg, ethylene glycol.
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Chamorro, F.; Carpena, M.; Lourenço-Lopes, C.; Taofiq, O.; Otero, P.; Cao, H.; Xiao, J.; Simal-Gandara, J.; Prieto, M.A. By-Products of Walnut (Juglans regia) as a Source of Bioactive Compounds for the Formulation of Nutraceuticals and Functional Foods. Biol. Life Sci. Forum 2022, 12, 35. https://doi.org/10.3390/IECN2022-12396

AMA Style

Chamorro F, Carpena M, Lourenço-Lopes C, Taofiq O, Otero P, Cao H, Xiao J, Simal-Gandara J, Prieto MA. By-Products of Walnut (Juglans regia) as a Source of Bioactive Compounds for the Formulation of Nutraceuticals and Functional Foods. Biology and Life Sciences Forum. 2022; 12(1):35. https://doi.org/10.3390/IECN2022-12396

Chicago/Turabian Style

Chamorro, Franklin, Maria Carpena, Catarina Lourenço-Lopes, Oludemi Taofiq, Paz Otero, Hui Cao, Jianbo Xiao, Jesus Simal-Gandara, and Miguel A. Prieto. 2022. "By-Products of Walnut (Juglans regia) as a Source of Bioactive Compounds for the Formulation of Nutraceuticals and Functional Foods" Biology and Life Sciences Forum 12, no. 1: 35. https://doi.org/10.3390/IECN2022-12396

APA Style

Chamorro, F., Carpena, M., Lourenço-Lopes, C., Taofiq, O., Otero, P., Cao, H., Xiao, J., Simal-Gandara, J., & Prieto, M. A. (2022). By-Products of Walnut (Juglans regia) as a Source of Bioactive Compounds for the Formulation of Nutraceuticals and Functional Foods. Biology and Life Sciences Forum, 12(1), 35. https://doi.org/10.3390/IECN2022-12396

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