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Current Pharmaceutical Design

Editor-in-Chief

ISSN (Print): 1381-6128
ISSN (Online): 1873-4286

Review Article

Evaluation and Exploitation of Bioactive Compounds of Walnut, Juglans regia

Author(s): Alexa Croitoru, Denisa Ficai, Luminiţa Craciun, Anton Ficai* and Ecaterina Andronescu

Volume 25, Issue 2, 2019

Page: [119 - 131] Pages: 13

DOI: 10.2174/1381612825666190329150825

Price: $65

Abstract

In the last few years, great importance has been given to natural materials (such as walnuts, peanuts, chestnuts) due to their medicinal and pharmaceutical uses induced by the presence of natural agents, including polyphenols. Juglans regia is a traditional plant that has been used since ancient times in traditional medicine for the treatment of various diseases like microbial infections, stomach ache, thyroid dysfunctions, cancer, heart diseases and sinusitis. Recently, scientific attention for the phytochemical profile of walnut by-products is increasing due to their valuable active constituents. Natural polyphenols are important compounds present in walnut with valuable properties that have been studied for the treatment of inflammation, cancer or anti-ageing effect. The use of nanocarriers as a drug delivery system is now a promising strategy to get more stable products and is easier to apply in a medical, therapeutic and pharmaceutical environment. The aim of this work was to review the latest information provided by scientific investigators regarding the nutritional value, bioactive compounds, antioxidant and antitumor activity of walnut by-product extracts. Moreover, this review provides comprehensive information on the nanoencapsulation of bioactive constituents for application in clinical medicine, particularly in cancer research.

Keywords: Phenolic compounds, Juglans regia, antioxidant activity, anti-cancer, drug delivery, supports.

[1]
Abu Taha N, Al-wadaan MA. Utility and importance of walnut, Juglans regia Linn: A review. Afr J Microbiol Res 2011; 5: 5796-805.
[2]
Altuntas E, Erkol M. Physical Properties of Shelled and Kernel Walnuts as Affected by the Moisture Content. Czech J Food Sci 2010; 28: 547-56.
[3]
Amaral JS, Valentão P, Andrade PB, Martins RC, Seabra RM. Do cultivar, geographical location and crop season influence phenolic profile of walnut leaves? Molecules 2008; 13(6): 1321-32.
[4]
Rabrenovic B, Dimic E, Maksimovic M, Sobajic S, Gajic-Krstajic L. Determination of Fatty Acid and Tocopherol Compositions and the Oxidative Stability of Walnut (Juglans regia L.) Cultivars Grown in Serbia. Czech J Food Sci 2011; 29: 74-8.
[5]
Şen SM, Karadeniz T. The Nutritional Value of Walnut. J Hygienic Eng Des 2015; 11: 68-71.
[6]
Franci Štampar. Extraction of phenolic compounds from green walnut fruits in different solvents. Acta Agric Slov 2009; 93: 11-5.
[7]
Popovici C. Soxhlet extraction and characterisation of natural compounds from walnut (Juglans regia L.) by-products. Ukr Food J 2013; 2: 328-36.
[8]
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: 255-63.
[9]
Gharibzahedi SM, Mousavi SM, Hamedi M, Khodaiyan F. Determination and characterization of kernel biochemical composition and functional compounds of Persian walnut oil. J Food Sci Technol 2014; 51(1): 34-42.
[10]
Sharafati-Chaleshtori R, Sharafati-Chaleshtori F, Rafieian M. Biological characterization of Iranian walnut (Juglans regia) leaves. Turk J Biol 2011; 35: 635-9.
[11]
Santos A, Barros L, Calhelha RC, et al. Leaves and decoction of Juglans regia L.: Different performances regarding bioactive compounds and in vitro antioxidant and antitumor effects. Ind Crops Prod 2013; 51: 430-6.
[12]
Vieira V, Prieto MA, Barros L, Coutinho JAP, Ferreira ICFR, Ferreira O. Enhanced extraction of phenolic compounds using choline chloride based deep eutectic solvents from Juglans regia L. Ind Crops Prod 2018; 115: 261-71.
[13]
Moori Bakhtiari KE. Antibacterial Activity of the Hydro-Alcoholic Extract of Juglans regia L. Stem Bark on Human Bacterial Infection. Int Arch Health Sci 2015; 2: 139-43.
[14]
Oliveira I, Sousa A, Ferreira IC, Bento A, Estevinho L, Pereira JA. Total phenols, antioxidant potential and antimicrobial activity of walnut (Juglans regia L.) green husks. Food Chem Toxicol 2008; 46: 2326-31.
[15]
Noumi E, Snoussi M, Trabelsi N, et al. Antibacterial, anticandidal and antioxidant activities of Salvadora persica and Juglans regia L. extracts. J Med Plants Res 2011; 5: 4138-46.
[16]
Fernandez-Agullo A, Pereira E, Freire MS, et al. Influence of solvent on the antioxidant and antimicrobial properties of walnut (Juglans regia L.) green husk extracts. Ind Crops Prod 2013; 42: 126-32.
[17]
Cosmulescu S, Trandafir I, Nour V. Seasonal variation of the main individual phenolics and juglone in walnut (Juglans regia) leaves. Pharm Biol 2014; 52(5): 575-80.
[18]
Alexe A-M, Vizireanu C. Optimization of the extraction process in order to isolate antioxidant compounds from walnut leaves. Food Sci 2014; 8: 56-9.
[19]
Cosmulescu S, Botu M, Achim G, Baciu A, Gruia M, Trandafir I. Polyphenol Content in Walnut (Juglans regia L.) Mature Leaves. Acta Hortic 2014; (1050): 205-12.
[20]
Cosmulescu S, Trandafir I, Achim G, Botu M, Baciu A, Gruia M. Phenolics of Green Husk in Mature Walnut Fruits. Not Bot Horti Agrobot Cluj-Napoca 2010; 38: 53-6.
[21]
Panth N, Paudel KR, Karki R. Phytochemical profile and biological activity of Juglans regia. J Integr Med 2016; 14(5): 359-73.
[22]
Pantsi WG, Bester DJ, Esterhuyse AJ, Aboua G. Dietary Antioxidant Properties of Vegetable Oils and Nuts – The Race Against Cardiovascular Disease Progression. Antioxid Antidiab Agents Hum Health 2014; pp. 209-38.
[23]
Vieira V, Prieto MA, Barros L, Coutinho JAP, Ferreira O, Ferreira ICFR. 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: 341-52.
[24]
Mehmet Musa Özcan Cİ. Derya Arslan. Physico-chemical properties, fatty acid and mineral content of some walnuts (Juglans regia L.) types. Agric Sci 2010; 1: 62-7.
[25]
Nergiz-Ünal R, Kuijpers MJE, de Witt SM, et al. Atheroprotective effect of dietary walnut intake in ApoE-deficient mice: involvement of lipids and coagulation factors. Thromb Res 2013; 131(5): 411-7.
[26]
Stampar F, Solar A, Hudina M, Veberic R, Colaric M. Traditional walnut liqueur - cocktail of phenolics. Food Chem 2006; 95: 627-31.
[27]
Najah Ali Mohammed YKH. Comparison of antimicrobial activities of methanol extracts Juglans regio against Staphylococcus aureus, and Streptoccus mutans with ciprofloxacin: in vitro. Al-Mustansiriyah J Sci 2012; 23: 1-6.
[28]
Alicja Michalczyk, Anna Kiełcz. The use of components of the extract from the leaves of walnut Juglans regia L. against the fungus Ascosphaera apis. Chemik 2014; 68: 117-22.
[29]
Shin P-K, Zoh Y, Choi J, Kim M-S, Kim Y, Choi S-W. Walnut phenolic extracts reduce telomere length and telomerase activity in a colon cancer stem cell model. Nutr Res Pract 2019; 13(1): 58-63.
[30]
Lee J, Kim YS, Lee J, et al. Walnut Phenolic Extract and Its Bioactive Compounds Suppress Colon Cancer Cell Growth by Regulating Colon Cancer Stemness. Nutrients 2016; 8(7): 8.
[31]
Nagel JM, Brinkoetter M, Magkos F, et al. Dietary walnuts inhibit colorectal cancer growth in mice by suppressing angiogenesis. Nutrition 2012; 28(1): 67-75.
[32]
Hardman WE. Walnuts have potential for cancer prevention and treatment in mice. J Nutr 2014; 144(4)(Suppl.): 555S-60S.
[33]
Rai S, Kureel AK, Dutta PK, Mehrotra GK. Phenolic compounds based conjugates from dextran aldehyde and BSA: Preparation, characterization and evaluation of their anti-cancer efficacy for therapeutic applications. Int J Biol Macromol 2018; 110: 425-36.
[34]
Saenglee S, Jogloy S, Patanothai A, Senawong T. Cytotoxic effects of peanut phenolic compounds possessing histone deacetylase inhibitory activity on human colon cancer cell lines. Turk J Biol 2016; 40: 1258-71.
[35]
Maisuthisakul P. Microencapsulation of extract from mango seed kernel waste. UTCC 2011; pp. 1-240.
[36]
Petti S, Scully C. Polyphenols, oral health and disease: A review. J Dent 2009; 37(6): 413-23.
[37]
D’Archivio M, Filesi C, Varì R, Scazzocchio B, Masella R. Bioavailability of the polyphenols: status and controversies. Int J Mol Sci 2010; 11(4): 1321-42.
[38]
Sen Li GC, Zhang C. Man Wu, Shuyan Wu, Qing Liu. Research progress of natural antioxidants in foods for the treatment of diseases. Food Science and Human Wellness 2014; 3: 110-6.
[39]
Melo MNO, Oliveira AP, Wiecikowski AF, et al. Phenolic compounds from Viscum album tinctures enhanced antitumor activity in melanoma murine cancer cells. Saudi Pharm J 2018; 26(3): 311-22.
[40]
Reboredo-Rodríguez P, Varela-López A, Forbes-Hernández TY, et al. Phenolic Compounds Isolated from Olive Oil as Nutraceutical Tools for the Prevention and Management of Cancer and Cardiovascular Diseases. Int J Mol Sci 2018; 19(8): 1-21.
[41]
Kuete V, Mbaveng AT, Nono ECN, et al. Cytotoxicity of seven naturally occurring phenolic compounds towards multi-factorial drug-resistant cancer cells. Phytomedicine 2016; 23(8): 856-63.
[42]
Bujdoso G, Vegvari G, Hajnal V, Ficzek G, Toth M. Phenolic Profile of the Kernel of Selected Persian Walnut (Juglans regia L.) Cultivars. Not Bot Horti Agrobot Cluj-Napoca 2014; 42: 24-9.
[43]
Popovici C, Gitin L, Alexe P. Characterization of walnut (Juglans regia L) green husk extract obtained by supercritical carbon dioxide fluid extraction. J Food Pack 2013; pp. 1-5.
[44]
Ioannou I, Ghoul M. Biological Activities and Effects of Food Processing on Flavonoids as Phenolic Antioxidants 2012; 101-24.
[45]
Pereira JA, Oliveira I, Sousa A, Ferreira IC, Bento A, Estevinho L. Bioactive properties and chemical composition of six walnut (Juglans regia L.) cultivars. Food Chem Toxicol 2008; 46: 2103-11.
[46]
Kshitij Agarwal GSC. In Vitro Antioxidant Activity of Different Extract of Bark of Juglans Regia. IJIPR 2012; 3: 199-202.
[47]
Anjum S, Gani A, Ahmad M, et al. Antioxidant and Antiproliferative Activity of Walnut Extract (Juglans regia L.) Processed by Different Methods and Identification of Compounds Using GC/MS and LC/MS Technique. J Food Process Preserv 2017; 41: 1-9.
[48]
Pereira JA, Oliveira I, Sousa A, et al. Walnut (Juglans regia L.) leaves: phenolic compounds, antibacterial activity and antioxidant potential of different cultivars. Food Chem Toxicol 2007; 45: 2287-95.
[49]
Zhang XB, Zou CL, Duan YX, Wu F, Li G. Activity guided isolation and modification of juglone from Juglans regia as potent cytotoxic agent against lung cancer cell lines. BMC Complement Altern Med 2015; 15: 396.
[50]
Catanzaro E, Greco G, Potenza L, Calcabrini C, Fimognari C. Natural Products to Fight Cancer: A Focus on Juglans regia. Toxins 2018; 10: 1-38.
[51]
Alshatwi AA, Hasan TN, Shafi G, et al. Validation of the Antiproliferative Effects of Organic Extracts from the Green Husk of Juglans regia L. on PC-3 Human Prostate Cancer Cells by Assessment of Apoptosis-Related Genes. Evid Based Complement Alternat Med 2012; 2012103026
[52]
Hasan TN. B LG, Shafi G, Al-Hazzani AA, Alshatwi AA. Anti-proliferative effects of organic extracts from root bark of Juglans Regia L. (RBJR) on MDA-MB-231 human breast cancer cells: role of Bcl-2/Bax, caspases and Tp53. Asian Pac J Cancer Prev 2011; 12(2): 525-30.
[53]
Negi AS, Luqman S, Srivastava S, Krishna V, Gupta N, Darokar MP. Antiproliferative and antioxidant activities of Juglans regia fruit extracts. Pharm Biol 2011; 49(6): 669-73.
[54]
He Z, Chen AY, Rojanasakul Y, Rankin GO, Chen YC. Gallic acid, a phenolic compound, exerts anti-angiogenic effects via the PTEN/AKT/HIF-1α/VEGF signaling pathway in ovarian cancer cells. Oncol Rep 2016; 35(1): 291-7.
[55]
Fernandez-Ochoa A, Borras-Linares I, Perez-Sanchez A, et al. Phenolic compounds in rosemary as potential source of bioactive compounds against colorectal cancer: In situ absorption and metabolism study. J Funct Foods 2017; 33: 202-10.
[56]
Vieira DB, Gamarra LF. Advances in the use of nanocarriers for cancer diagnosis and treatment. Einstein (Sao Paulo) 2016; 14(1): 99-103.
[57]
Swami A, Shi JJ, Gadde S, Votruba AR, Kolishetti N, Farokhzad OC. Nanoparticles for Targeted and Temporally Controlled Drug Delivery 2012; 9-29.
[58]
Munin A, Edwards-Lévy F. Encapsulation of natural polyphenolic compounds; a review. Pharmaceutics 2011; 3(4): 793-829.
[59]
Conte RCA, Napoletano A, Valentino A, et al. Polyphenols Nanoencapsulation for Therapeutic Applications. Biomol Res Ther 2016; 5: 1-13.
[60]
Ballesteros LF, Ramirez MJ, Orrego CE, Teixeira JA, Mussatto SI. Encapsulation of antioxidant phenolic compounds extracted from spent coffee grounds by freeze-drying and spray-drying using different coating materials. Food Chem 2017; 237: 623-31.
[61]
Sánchez-Carranza JN, Alvarez L, Marquina-Bahena S, et al. Phenolic Compounds Isolated from Caesalpinia coriaria Induce S and G2/M Phase Cell Cycle Arrest Differentially and Trigger Cell Death by Interfering with Microtubule Dynamics in Cancer Cell Lines. Molecules 2017; 22(4): 1-14.
[62]
Jia ZH, Dumont MJ, Orsat V. Encapsulation of phenolic compounds present in plants using protein matrices. Food Biosci 2016; 15: 87-104.
[63]
Fang ZX, Bhandari B. Encapsulation of polyphenols - a review. Trends Food Sci Technol 2010; 21: 510-23.
[64]
Ge K, Ren HH, Sun WT, et al. Walnut kernel-like mesoporous silica nanoparticles as effective drug carrier for cancer therapy in vitro. J Nanopart Res 2016; 18: 1-11.
[65]
Alshatwi AA, Athinarayanan J, Vaiyapuri Subbarayan P. Green synthesis of platinum nanoparticles that induce cell death and G2/M-phase cell cycle arrest in human cervical cancer cells. J Mater Sci Mater Med 2015; 26(1): 5330.
[66]
Rodriguez R, Kondo H, Nyan M, et al. Implantation of green tea catechin α-tricalcium phosphate combination enhances bone repair in rat skull defects. J Biomed Mater Res B Appl Biomater 2011; 98(2): 263-71.
[67]
Samutprasert P, Chiablaem K, Teeraseranee C, et al. Epigallocatechin gallate-zinc oxide co-crystalline nanoparticles as an anticancer drug that is non-toxic to normal cells. Rsc Adv 2018; 8: 7369-76.
[68]
Tamanai-Shacoori Z, Chandad F, Rébillard A, Cillard J, Bonnaure-Mallet M. Silver-zeolite combined to polyphenol-rich extracts of Ascophyllum nodosum: potential active role in prevention of periodontal diseases. PLoS One 2014; 9(10)e105475
[69]
Xiao L, Mertens M, Wortmann L, et al. Enhanced in vitro and in vivo cellular imaging with green tea coated water-soluble iron oxide nanocrystals. ACS Appl Mater Interfaces 2015; 7(12): 6530-40.
[70]
Cirillo G, Hampel S, Klingeler R, et al. Antioxidant multi-walled carbon nanotubes by free radical grafting of gallic acid: new materials for biomedical applications. J Pharm Pharmacol 2011; 63(2): 179-88.
[71]
Cirillo G, Vittorio O, Hampel S, et al. Quercetin nanocomposite as novel anticancer therapeutic: improved efficiency and reduced toxicity. Eur J Pharm Sci 2013; 49(3): 359-65.
[72]
Abdolahad M, Janmaleki M, Mohajerzadeh S, Akhavan O, Abbasi S. Polyphenols attached graphene nanosheets for high efficiency NIR mediated photodestruction of cancer cells. Mater Sci Eng C 2013; 33(3): 1498-505.
[73]
Vico TA, Arce VB, Fangio MF, et al. Two choices for the functionalization of silica nanoparticles with gallic acid: characterization of the nanomaterials and their antimicrobial activity against Paenibacillus larvae. J Nanopart Res 2016; 18: 1-13.
[74]
Cadena MB, Preston GM, Van der Hoorn RAL, Townley HE, Thompson IP. Species-specific antimicrobial activity of essential oils and enhancement by encapsulation in mesoporous silica nanoparticles. Ind Crops Prod 2018; 122: 582-90.
[75]
Chen Y, Wang J, Liu JH, Lu LH. Metal-Phenolic Encapsulated Mesoporous Silica Nanoparticles for pH-Responsive Drug Delivery and Magnetic Resonance Imaging. Z Phys Chem 2018; 232: 1733-40.
[76]
di Leo N, Battaglini M, Berger L, et al. A catechin nanoformulation inhibits WM266 melanoma cell proliferation, migration and associated neo-angiogenesis. Eur J Pharm Biopharm 2017; 114: 1-10.
[77]
Khan N, Bharali DJ, Adhami VM, et al. Oral administration of naturally occurring chitosan-based nanoformulated green tea polyphenol EGCG effectively inhibits prostate cancer cell growth in a xenograft model. Carcinogenesis 2014; 35(2): 415-23.
[78]
de Pace RCC, Liu X, Sun M, et al. Anticancer activities of (-)-epigallocatechin-3-gallate encapsulated nanoliposomes in MCF7 breast cancer cells. J Liposome Res 2013; 23(3): 187-96.
[79]
Arulmozhi V, Pandian K, Mirunalini S. Ellagic acid encapsulated chitosan nanoparticles for drug delivery system in human oral cancer cell line (KB). Colloids Surf B Biointerfaces 2013; 110: 313-20.
[80]
Hu B, Wang Y, Xie MH, Hu GL, Ma FG, Zeng XX. Polymer nanoparticles composed with gallic acid grafted chitosan and bioactive peptides combined antioxidant, anticancer activities and improved delivery property for labile polyphenols. J Funct Foods 2015; 15: 593-603.
[81]
Sadri M, Arab-Sorkhi S, Vatani H, Bagheri-Pebdeni A. New wound dressing polymeric nanofiber containing green tea extract prepared by electrospinning method. Fibers Polym 2015; 16: 1742-50.
[82]
Shiu JC, Ho MH, Yu SH, Chao AC, Su YR, Chen WJ, et al. Preparation and characterization of caffeic acid grafted chitosan/CPTMS hybrid scaffolds. Carbohydr Polym 2010; 79: 724-30.
[83]
Ngobili TA, Shah H, Park JP, et al. Remodeling of tannic acid crosslinked collagen type I induces apoptosis in ER+ breast cancer cells. Anticancer Res 2015; 35(3): 1285-90.
[84]
Albu MG, Ghica MV, Giurginca M, Trandafir V, Popa L, Cotrut C. Spectral Characteristics and Antioxidant Properties of Tannic Acid Immobilized on Collagen Drug-Delivery Systems. Rev Chim-Bucharest 2009; 60: 666-72.
[85]
Wu H, He L, Gao MM, Gao SY, Liao XP, Shi B. One-step in situ assembly of size-controlled silver nanoparticles on polyphenol-grafted collagen fiber with enhanced antibacterial properties. New J Chem 2011; 35: 2902-9.
[86]
Dai Y, Guo J, Wang TY, et al. Self-Assembled Nanoparticles from Phenolic Derivatives for Cancer Therapy. Adv Healthc Mater 2017; 6(16): 1-7.
[87]
Dai Y, Guo J, Wang TY, et al. Self-Assembled Nanoparticles from Phenolic Derivatives for Cancer Therapy. Adv Healthc Mater 2017; 6(16): 6.
[88]
Aytac Z, Kusku SI, Durgun E, Uyar T. Encapsulation of gallic acid/cyclodextrin inclusion complex in electrospun polylactic acid nanofibers: Release behavior and antioxidant activity of gallic acid. Mater Sci Eng C 2016; 63: 231-9.
[89]
Shirode AB, Bharali DJ, Nallanthighal S, Coon JK, Mousa SA, Reliene R. Nanoencapsulation of pomegranate bioactive compounds for breast cancer chemoprevention. Int J Nanomedicine 2015; 10: 475-84.
[90]
Li J, Fu R, Li L, et al. Co-delivery of dexamethasone and green tea polyphenols using electrospun ultrafine fibers for effective treatment of keloid. Pharm Res 2014; 31(7): 1632-43.
[91]
Xing ZC, Meng W, Yuan J, Moon S, Jeong Y, Kang IK. In vitro assessment of antibacterial activity and cytocompatibility of quercetin-containing PLGA nanofibrous scaffolds for tissue engineering. J Nanomater 2012; 2012: 1-7.
[92]
Oliver S, Thomas DS, Kavallaris M, Vittorio O, Boyer C. Efficient functionalisation of dextran-aldehyde with catechin: potential applications in the treatment of cancer. Polym Chem-UK 2016; 7: 2542-52.
[93]
Oliver S, Yee E, Kavallaris M, Vittorio O, Boyer C. Water Soluble Antioxidant Dextran-Quercetin Conjugate with Potential Anticancer Properties. Macromol Biosci 2018; 18(4)e1700239
[94]
Shutava TG, Balkundi SS, Vangala P, et al. Layer-by-Layer-Coated Gelatin Nanoparticles as a Vehicle for Delivery of Natural Polyphenols. ACS Nano 2009; 3(7): 1877-85.
[95]
da Rosa CG, Borges CD, Zambiazi RC, et al. Encapsulation of the phenolic compounds of the blackberry (Rubus fruticosus). Lebensm Wiss Technol 2014; 58: 527-33.
[96]
Thitilertdecha P, Rowan MG, Guy RH. Topical formulation and dermal delivery of active phenolic compounds in the Thai medicinal plant--Clerodendrum petasites S. Moore. Int J Pharm 2015; 478(1): 39-45.

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