Polyphenols from Byproducts: Their Applications and Health Effects
Abstract
1. Introduction
2. Plant Derived Phenolic Compounds and Their Bioactivities
2.1. Antioxidant Activities of Phenolic Compounds
2.2. Antiviral Activities of Phenolic Compounds
2.3. Antimicrobial Activities of Phenolic Compounds
2.4. Therapuetic Potential of Phenolic Compounds
3. Application Areas of Phenolic Compounds from Plant Byproducts
3.1. Extraction Methods
3.1.1. Conventional Extraction Technologies
3.1.2. Green Extraction Technologies
3.2. Food Industry
3.3. Cosmetic Applications
3.4. Pharmaceutical and Health Applications
3.5. Sustainable Materials and Packaging
4. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Conflicts of Interest
References
- Bertelli, A.; Biagi, M.; Corsini, M.; Baini, G.; Cappellucci, G.; Miraldi, E. Polyphenols: From Theory to Practice. Foods 2021, 10, 2595. [Google Scholar] [CrossRef]
- Mukherjee, C.; Chakraborty, S. Study of Dietary Polyphenols from Natural Herbal Sources for Providing Protection against Human Degenerative Disorders. Biocatal. Agric. Biotechnol. 2021, 33, 101956. [Google Scholar] [CrossRef]
- Cutrim, C.S.; Cortez, M.A.S. A Review on Polyphenols: Classification, Beneficial Effects and Their Application in Dairy Products. Int. J. Dairy Technol. 2018, 71, 564–578. [Google Scholar] [CrossRef]
- Quideau, S.; Deffieux, D.; Douat-Casassus, C.; Pouységu, L. Plant Polyphenols: Chemical Properties, Biological Activities, and Synthesis. Angew. Chem. Int. Ed. 2011, 50, 586–621. [Google Scholar] [CrossRef]
- Lang, Y.; Gao, N.; Zang, Z.; Meng, X.; Lin, Y.; Yang, S.; Yang, Y.; Jin, Z.; Li, B. Classification and Antioxidant Assays of Polyphenols: A Review. J. Future Foods 2024, 4, 193–204. [Google Scholar] [CrossRef]
- Grosso, G. Effects of Polyphenol-Rich Foods on Human Health. Nutrients 2018, 10, 1089. [Google Scholar] [CrossRef]
- Cao, H.; Saroglu, O.; Karadag, A.; Diaconeasa, Z.; Zoccatelli, G.; Conte-Junior, C.A.; Gonzalez-Aguilar, G.A.; Ou, J.; Bai, W.; Zamarioli, C.M.; et al. Available Technologies on Improving the Stability of Polyphenols in Food Processing. Food Front. 2021, 2, 109–139. [Google Scholar] [CrossRef]
- Coşkun, N.; Sarıtaş, S.; Jaouhari, Y.; Bordiga, M.; Karav, S. The Impact of Freeze Drying on Bioactivity and Physical Properties of Food Products. Appl. Sci. 2024, 14, 9183. [Google Scholar] [CrossRef]
- Picot-Allain, C.; Mahomoodally, M.F.; Ak, G.; Zengin, G. Conventional versus Green Extraction Techniques—A Comparative Perspective. Curr. Opin. Food Sci. 2021, 40, 144–156. [Google Scholar] [CrossRef]
- Feng, W.; Hao, Z.; Li, M. Isolation and Structure Identification of Flavonoids. In Flavonoids—From Biosynthesis to Human Health; Justino, G.C., Ed.; InTech: London, UK, 2017; ISBN 978-953-51-3423-7. [Google Scholar]
- Perron, N.R.; Brumaghim, J.L. A Review of the Antioxidant Mechanisms of Polyphenol Compounds Related to Iron Binding. Cell Biochem. Biophys. 2009, 53, 75–100. [Google Scholar] [CrossRef]
- Urquiaga, I.; Leighton, F. Plant Polyphenol Antioxidants and Oxidative Stress. Biol. Res. 2000, 33, 55–64. [Google Scholar] [CrossRef]
- Leri, M.; Scuto, M.; Ontario, M.L.; Calabrese, V.; Calabrese, E.J.; Bucciantini, M.; Stefani, M. Healthy Effects of Plant Polyphenols: Molecular Mechanisms. Int. J. Mol. Sci. 2020, 21, 1250. [Google Scholar] [CrossRef] [PubMed]
- Rasouli, H.; Farzaei, M.H.; Khodarahmi, R. Polyphenols and Their Benefits: A Review. Int. J. Food Prop. 2017, 20, 1700–1741. [Google Scholar] [CrossRef]
- Dubrovina, A.S.; Kiselev, K.V. Regulation of Stilbene Biosynthesis in Plants. Planta 2017, 246, 597–623. [Google Scholar] [CrossRef] [PubMed]
- Cucciolla, V.; Borriello, A.; Oliva, A.; Galletti, P.; Zappia, V.; Ragione, F.D. Resveratrol: From Basic Science to the Clinic. Cell Cycle 2007, 6, 2495–2510. [Google Scholar] [CrossRef]
- Ko, J.-H.; Sethi, G.; Um, J.-Y.; Shanmugam, M.K.; Arfuso, F.; Kumar, A.P.; Bishayee, A.; Ahn, K.S. The Role of Resveratrol in Cancer Therapy. Int. J. Mol. Sci. 2017, 18, 2589. [Google Scholar] [CrossRef]
- Mondal, A.; Bennett, L.L. Resveratrol Enhances the Efficacy of Sorafenib Mediated Apoptosis in Human Breast Cancer MCF7 Cells through ROS, Cell Cycle Inhibition, Caspase 3 and PARP Cleavage. Biomed. Pharmacother. 2016, 84, 1906–1914. [Google Scholar] [CrossRef]
- Giampieri, F.; Cianciosi, D.; Alvarez-Suarez, J.M.; Quiles, J.L.; Forbes-Hernández, T.Y.; Navarro-Hortal, M.D.; Machì, M.; Casanova, R.D.J.P.; Espinosa, J.C.M.; Chen, X.; et al. Anthocyanins: What Do We Know until Now? J. Berry Res. 2023, 13, 1–6. [Google Scholar] [CrossRef]
- Badshah, S.L.; Faisal, S.; Muhammad, A.; Poulson, B.G.; Emwas, A.H.; Jaremko, M. Antiviral Activities of Flavonoids. Biomed. Pharmacother. 2021, 140, 111596. [Google Scholar] [CrossRef]
- Cushnie, T.P.T.; Lamb, A.J. Antimicrobial Activity of Flavonoids. Int. J. Antimicrob. Agents 2005, 26, 343–356, Correction in Int. J. Antimicrob. Agents 2006, 27, 181. [Google Scholar] [CrossRef]
- Friedman, M. Overview of Antibacterial, Antitoxin, Antiviral, and Antifungal Activities of Tea Flavonoids and Teas. Mol. Nutr. Food Res. 2007, 51, 116–134. [Google Scholar] [CrossRef] [PubMed]
- Ahmad, A.; Kaleem, M.; Ahmed, Z.; Shafiq, H. Therapeutic Potential of Flavonoids and Their Mechanism of Action against Microbial and Viral Infections—A Review. Food Res. Int. 2015, 77, 221–235. [Google Scholar] [CrossRef]
- Imanishi, N.; Tuji, Y.; Katada, Y.; Maruhashi, M.; Konosu, S.; Mantani, N.; Terasawa, K.; Ochiai, H. Additional Inhibitory Effect of Tea Extract on the Growth of Influenza A and B Viruses in MDCK Cells. Microbiol. Immunol. 2002, 46, 491–494. [Google Scholar] [CrossRef]
- Lani, R.; Hassandarvish, P.; Shu, M.-H.; Phoon, W.H.; Chu, J.J.H.; Higgs, S.; Vanlandingham, D.; Abu Bakar, S.; Zandi, K. Antiviral Activity of Selected Flavonoids against Chikungunya Virus. Antivir. Res. 2016, 133, 50–61. [Google Scholar] [CrossRef]
- Papakyriakopoulou, P.; Velidakis, N.; Khattab, E.; Valsami, G.; Korakianitis, I.; Kadoglou, N.P. Potential Pharmaceutical Applications of Quercetin in Cardiovascular Diseases. Pharmaceuticals 2022, 15, 1019. [Google Scholar] [CrossRef]
- He, W. Epigallocatechin Gallate Inhibits HBV DNA Synthesis in a Viral Replication—Inducible Cell Line. World J. Gastroenterol. 2011, 17, 1507. [Google Scholar] [CrossRef] [PubMed]
- Ancuceanu, R.; Lascu, B.E.; Drăgănescu, D.; Dinu, M. In Silico ADME Methods Used in the Evaluation of Natural Products. Pharmaceutics 2025, 17, 1002. [Google Scholar] [CrossRef]
- Wu, W.; Yang, L.; Zhang, S.; Hao, D.; Yang, Y.; Li, X.; Wu, G.; Zhang, L.; Luo, Z. Development of a New Characteristic Parameter—Waveform Index of Finger Blood Volume Pulse. Comput. Assist. Surg. 2016, 21, 6–10. [Google Scholar] [CrossRef][Green Version]
- Johari, J.; Kianmehr, A.; Mustafa, M.; Abubakar, S.; Zandi, K. Antiviral Activity of Baicalein and Quercetin against the Japanese Encephalitis Virus. Int. J. Mol. Sci. 2012, 13, 16785–16795. [Google Scholar] [CrossRef]
- Phadungsombat, J.; Lin, M.Y.-C.; Srimark, N.; Yamanaka, A.; Nakayama, E.E.; Moolasart, V.; Suttha, P.; Shioda, T.; Uttayamakul, S. Emergence of Genotype Cosmopolitan of Dengue Virus Type 2 and Genotype III of Dengue Virus Type 3 in Thailand. PLoS ONE 2018, 13, e0207220. [Google Scholar] [CrossRef] [PubMed]
- Nahmias, Y.; Goldwasser, J.; Casali, M.; Van Poll, D.; Wakita, T.; Chung, R.T.; Yarmush, M.L. Apolipoprotein B–Dependent Hepatitis C Virus Secretion Is Inhibited by the Grapefruit Flavonoid Naringenin. Hepatology 2008, 47, 1437–1445. [Google Scholar] [CrossRef]
- Li, B.Q.; Fu, T.; Dongyan, Y.; Mikovits, J.A.; Ruscetti, F.W.; Wang, J.M. Flavonoid Baicalin Inhibits HIV-1 Infection at the Level of Viral Entry. Biochem. Biophys. Res. Commun. 2000, 276, 534–538. [Google Scholar] [CrossRef]
- Fabbrini, M.; D’Amico, F.; Barone, M.; Conti, G.; Mengoli, M.; Brigidi, P.; Turroni, S. Polyphenol and Tannin Nutraceuticals and Their Metabolites: How the Human Gut Microbiota Influences Their Properties. Biomolecules 2022, 12, 875. [Google Scholar] [CrossRef]
- Ordoñez, R.; Atarés, L.; Chiralt, A. Biodegradable Active Materials Containing Phenolic Acids for Food Packaging Applications. Compr. Rev. Food Sci. Food Saf. 2022, 21, 3910–3930. [Google Scholar] [CrossRef]
- Czerkas, K.; Olchowik-Grabarek, E.; Łomanowska, M.; Abdulladjanova, N.; Sękowski, S. Antibacterial Activity of Plant Polyphenols Belonging to the Tannins against Streptococcus Mutans—Potential against Dental Caries. Molecules 2024, 29, 879. [Google Scholar] [CrossRef] [PubMed]
- Kaczmarek, B. Tannic Acid with Antiviral and Antibacterial Activity as A Promising Component of Biomaterials—A Minireview. Materials 2020, 13, 3224. [Google Scholar] [CrossRef]
- Cardoso-Gutierrez, E.; Aranda-Aguirre, E.; Robles-Jimenez, L.E.; Castelán-Ortega, O.A.; Chay-Canul, A.J.; Foggi, G.; Angeles-Hernandez, J.C.; Vargas-Bello-Pérez, E.; González-Ronquillo, M. Effect of Tannins from Tropical Plants on Methane Production from Ruminants: A Systematic Review. Vet. Anim. Sci. 2021, 14, 100214. [Google Scholar] [CrossRef] [PubMed]
- Roldan, M.B.; Cousins, G.; Muetzel, S.; Zeller, W.E.; Fraser, K.; Salminen, J.-P.; Blanc, A.; Kaur, R.; Richardson, K.; Maher, D.; et al. Condensed Tannins in White Clover (Trifolium repens) Foliar Tissues Expressing the Transcription Factor TaMYB14-1 Bind to Forage Protein and Reduce Ammonia and Methane Emissions in Vitro. Front. Plant Sci. 2022, 12, 777354. [Google Scholar] [CrossRef] [PubMed]
- Tuyen, P.; Xuan, T.; Khang, D.; Ahmad, A.; Quan, N.; Tu Anh, T.; Anh, L.; Minh, T. Phenolic Compositions and Antioxidant Properties in Bark, Flower, Inner Skin, Kernel and Leaf Extracts of Castanea crenata Sieb. et Zucc. Antioxidants 2017, 6, 31. [Google Scholar] [CrossRef]
- Molino, S.; Pilar Francino, M.; Ángel Rufián Henares, J. Why Is It Important to Understand the Nature and Chemistry of Tannins to Exploit Their Potential as Nutraceuticals? Food Res. Int. 2023, 173, 113329. [Google Scholar] [CrossRef]
- Lafay, S.; Gil-Izquierdo, A. Bioavailability of Phenolic Acids. Phytochem. Rev. 2008, 7, 301–311. [Google Scholar] [CrossRef]
- Clifford, M.N. Chlorogenic Acids and Other Cinnamates—Nature, Occurrence, Dietary Burden, Absorption and Metabolism. J. Sci. Food Agric. 2000, 80, 1033–1043. [Google Scholar] [CrossRef]
- Caruso, G.; Godos, J.; Privitera, A.; Lanza, G.; Castellano, S.; Chillemi, A.; Bruni, O.; Ferri, R.; Caraci, F.; Grosso, G. Phenolic Acids and Prevention of Cognitive Decline: Polyphenols with a Neuroprotective Role in Cognitive Disorders and Alzheimer’s Disease. Nutrients 2022, 14, 819. [Google Scholar] [CrossRef]
- Kumar, N.; Goel, N. Phenolic Acids: Natural Versatile Molecules with Promising Therapeutic Applications. Biotechnol. Rep. 2019, 24, e00370. [Google Scholar] [CrossRef]
- Rashedinia, M.; Rasti Arbabi, Z.; Sabet, R.; Emami, L.; Poustforoosh, A.; Sabahi, Z. Comparison of Protective Effects of Phenolic Acids on Protein Glycation of BSA Supported by In Vitro and Docking Studies. Biochem. Res. Int. 2023, 2023, 9984618. [Google Scholar] [CrossRef]
- Rashmi, H.B.; Negi, P.S. Phenolic Acids from Vegetables: A Review on Processing Stability and Health Benefits. Food Res. Int. 2020, 136, 109298. [Google Scholar] [CrossRef]
- Cui, Q.; Du, R.; Liu, M.; Rong, L. Lignans and Their Derivatives from Plants as Antivirals. Molecules 2020, 25, 183. [Google Scholar] [CrossRef]
- Jang, W.Y.; Kim, M.-Y.; Cho, J.Y. Antioxidant, Anti-Inflammatory, Anti-Menopausal, and Anti-Cancer Effects of Lignans and Their Metabolites. Int. J. Mol. Sci. 2022, 23, 15482. [Google Scholar] [CrossRef] [PubMed]
- Baldi, S.; Tristán Asensi, M.; Pallecchi, M.; Sofi, F.; Bartolucci, G.; Amedei, A. Interplay between Lignans and Gut Microbiota: Nutritional, Functional and Methodological Aspects. Molecules 2023, 28, 343. [Google Scholar] [CrossRef] [PubMed]
- Barker, D. Lignans. Molecules 2019, 24, 1424. [Google Scholar] [CrossRef]
- Guo, Y.; Sun, Q.; Wu, F.; Dai, Y.; Chen, X. Polyphenol-Containing Nanoparticles: Synthesis, Properties, and Therapeutic Delivery. Adv. Mater. 2021, 33, 2007356. [Google Scholar] [CrossRef]
- Williamson, G. The Role of Polyphenols in Modern Nutrition. Nutr. Bull. 2017, 42, 226–235. [Google Scholar] [CrossRef]
- Hügel, H.M.; Jackson, N.; May, B.; Zhang, A.L.; Xue, C.C. Polyphenol Protection and Treatment of Hypertension. Phytomedicine 2016, 23, 220–231. [Google Scholar] [CrossRef]
- Ochmian, I.; Figiel-Kroczyńska, M.; Lachowicz, S. The Quality of Freeze-Dried and Rehydrated Blueberries Depending on Their Size and Preparation for Freeze-Drying. Acta Univ. Cibiniensis Ser. E Food Technol. 2020, 24, 61–78. [Google Scholar] [CrossRef]
- Sandoval-Acuña, C.; Ferreira, J.; Speisky, H. Polyphenols and Mitochondria: An Update on Their Increasingly Emerging ROS-Scavenging Independent Actions. Arch. Biochem. Biophys. 2014, 559, 75–90. [Google Scholar] [CrossRef] [PubMed]
- Megías, C.; Pastor-Cavada, E.; Torres-Fuentes, C.; Girón-Calle, J.; Alaiz, M.; Juan, R.; Pastor, J.; Vioque, J. Chelating, Antioxidant and Antiproliferative Activity of Vicia Sativa Polyphenol Extracts. Eur. Food Res. Technol. 2009, 230, 353–359. [Google Scholar] [CrossRef]
- Na, H.-K.; Surh, Y.-J. Modulation of Nrf2-Mediated Antioxidant and Detoxifying Enzyme Induction by the Green Tea Polyphenol EGCG. Food Chem. Toxicol. 2008, 46, 1271–1278. [Google Scholar] [CrossRef] [PubMed]
- Fraga, C.G.; Oteiza, P.I.; Hid, E.J.; Galleano, M. (Poly)Phenols and the Regulation of NADPH Oxidases. Redox Biol. 2023, 67, 102927. [Google Scholar] [CrossRef]
- Valgimigli, L. Lipid Peroxidation and Antioxidant Protection. Biomolecules 2023, 13, 1291. [Google Scholar] [CrossRef]
- Scalbert, A.; Johnson, I.T.; Saltmarsh, M. Polyphenols: Antioxidants and Beyond. Am. J. Clin. Nutr. 2005, 81, 215S–217S. [Google Scholar] [CrossRef]
- Rudrapal, M.; Khairnar, S.J.; Khan, J.; Dukhyil, A.B.; Ansari, M.A.; Alomary, M.N.; Alshabrmi, F.M.; Palai, S.; Deb, P.K.; Devi, R. Dietary Polyphenols and Their Role in Oxidative Stress-Induced Human Diseases: Insights into Protective Effects, Antioxidant Potentials and Mechanism(s) of Action. Front. Pharmacol. 2022, 13, 806470. [Google Scholar] [CrossRef]
- Apel, K.; Hirt, H. REACTIVE OXYGEN SPECIES: Metabolism, Oxidative Stress, and Signal Transduction. Annu. Rev. Plant Biol. 2004, 55, 373–399. [Google Scholar] [CrossRef]
- Gebicki, J.M.; Nauser, T. Fast Antioxidant Reaction of Polyphenols and Their Metabolites. Antioxidants 2021, 10, 1297. [Google Scholar] [CrossRef]
- Obrenovich, M.E.; Nair, N.G.; Beyaz, A.; Aliev, G.; Reddy, V.P. The Role of Polyphenolic Antioxidants in Health, Disease, and Aging. Rejuvenation Res. 2010, 13, 631–643. [Google Scholar] [CrossRef] [PubMed]
- Chiva-Blanch, G.; Visioli, F. Polyphenols and Health: Moving beyond Antioxidants. J. Berry Res. 2012, 2, 63–71. [Google Scholar] [CrossRef]
- Bucciantini, M.; Leri, M.; Nardiello, P.; Casamenti, F.; Stefani, M. Olive Polyphenols: Antioxidant and Anti-Inflammatory Properties. Antioxidants 2021, 10, 1044. [Google Scholar] [CrossRef]
- Mazzocchi, A.; Leone, L.; Agostoni, C.; Pali-Schöll, I. The Secrets of the Mediterranean Diet. Does [Only] Olive Oil Matter? Nutrients 2019, 11, 2941. [Google Scholar] [CrossRef] [PubMed]
- Fabiani, R.; Rosignoli, P.; De Bartolomeo, A.; Fuccelli, R.; Servili, M.; Montedoro, G.F.; Morozzi, G. Oxidative DNA Damage Is Prevented by Extracts of Olive Oil, Hydroxytyrosol, and Other Olive Phenolic Compounds in Human Blood Mononuclear Cells and HL60 Cells. J. Nutr. 2008, 138, 1411–1416. [Google Scholar] [CrossRef]
- Cicerale, S.; Lucas, L.; Keast, R. Biological Activities of Phenolic Compounds Present in Virgin Olive Oil. Int. J. Mol. Sci. 2010, 11, 458–479. [Google Scholar] [CrossRef] [PubMed]
- Cicerale, S.; Lucas, L.; Keast, R. Antimicrobial, Antioxidant and Anti-Inflammatory Phenolic Activities in Extra Virgin Olive Oil. Curr. Opin. Biotechnol. 2012, 23, 129–135. [Google Scholar] [CrossRef]
- Liu, W.; Wang, Z.; Xia, Y.; Kuang, H.; Liu, S.; Li, L.; Tang, C.; Yin, D. The Balance of Apoptosis and Autophagy via Regulation of the AMPK Signal Pathway in Aging Rat Striatum during Regular Aerobic Exercise. Exp. Gerontol. 2019, 124, 110647. [Google Scholar] [CrossRef]
- Erdman, V.V.; Nasibullin, T.R.; Tuktarova, I.A.; Somova, R.S.; Mustafina, O.E. Association Analysis of Polymorphic Gene Variants in the JAK/STAT Signaling Pathway with Aging and Longevity. Russ. J. Genet. 2019, 55, 728–737. [Google Scholar] [CrossRef]
- Harris, J.; Lang, T.; Thomas, J.P.W.; Sukkar, M.B.; Nabar, N.R.; Kehrl, J.H. Autophagy and Inflammasomes. Mol. Immunol. 2017, 86, 10–15. [Google Scholar] [CrossRef]
- Bostancıklıoğlu, M. An Update on the Interactions between Alzheimer’s Disease, Autophagy and Inflammation. Gene 2019, 705, 157–166. [Google Scholar] [CrossRef] [PubMed]
- Hassanpour, S.H.; Doroudi, A. Review of the Antioxidant Potential of Flavonoids as a Subgroup of Polyphenols and Partial Substitute for Synthetic Antioxidants. Avicenna J. Phytomed. 2023, 13, 354–376. [Google Scholar] [CrossRef] [PubMed]
- Gutiérrez-del-Río, I.; López-Ibáñez, S.; Magadán-Corpas, P.; Fernández-Calleja, L.; Pérez-Valero, Á.; Tuñón-Granda, M.; Miguélez, E.M.; Villar, C.J.; Lombó, F. Terpenoids and Polyphenols as Natural Antioxidant Agents in Food Preservation. Antioxidants 2021, 10, 1264. [Google Scholar] [CrossRef] [PubMed]
- Bešlo, D.; Golubić, N.; Rastija, V.; Agić, D.; Karnaš, M.; Šubarić, D.; Lučić, B. Antioxidant Activity, Metabolism, and Bioavailability of Polyphenols in the Diet of Animals. Antioxidants 2023, 12, 1141. [Google Scholar] [CrossRef]
- Cesa, S.; Carradori, S.; Bellagamba, G.; Locatelli, M.; Casadei, M.A.; Masci, A.; Paolicelli, P. Evaluation of Processing Effects on Anthocyanin Content and Colour Modifications of Blueberry (Vaccinium spp.) Extracts: Comparison Between HPLC-DAD and CIELAB Analyses. Food Chem. 2017, 232, 114–123. [Google Scholar] [CrossRef]
- Da Silva, F.L.; Escribano-Bailón, M.T.; Pérez Alonso, J.J.; Rivas-Gonzalo, J.C.; Santos-Buelga, C. Anthocyanin Pigments in Strawberry. LWT Food Sci. Technol. 2007, 40, 374–382. [Google Scholar] [CrossRef]
- Mustafa, A.M.; Angeloni, S.; Abouelenein, D.; Acquaticci, L.; Xiao, J.; Sagratini, G.; Maggi, F.; Vittori, S.; Caprioli, G. A New HPLC-MS/MS Method for the Simultaneous Determination of 36 Polyphenols in Blueberry, Strawberry and Their Commercial Products and Determination of Antioxidant Activity. Food Chem. 2022, 367, 130743. [Google Scholar] [CrossRef]
- Zhang, W.; Shen, Y.; Li, Z.; Xie, X.; Gong, E.S.; Tian, J.; Si, X.; Wang, Y.; Gao, N.; Shu, C.; et al. Effects of High Hydrostatic Pressure and Thermal Processing on Anthocyanin Content, Polyphenol Oxidase and β-Glucosidase Activities, Color, and Antioxidant Activities of Blueberry (Vaccinium spp.) Puree. Food Chem. 2021, 342, 128564. [Google Scholar] [CrossRef]
- Lachowicz-Wiśniewska, S.; Pratap-Singh, A.; Ochmian, I.; Kapusta, I.; Kotowska, A.; Pluta, S. Biodiversity in Nutrients and Biological Activities of 14 Highbush Blueberry (Vaccinium corymbosum L.) Cultivars. Sci. Rep. 2024, 14, 22063. [Google Scholar] [CrossRef]
- Saracila, M.; Untea, A.E.; Oancea, A.G.; Varzaru, I.; Vlaicu, P.A. Comparative Analysis of Black Chokeberry (Aronia melanocarpa L.) Fruit, Leaves, and Pomace for Their Phytochemical Composition, Antioxidant Potential, and Polyphenol Bioaccessibility. Foods 2024, 13, 1856. [Google Scholar] [CrossRef]
- Dobros, N.; Zielińska, A.; Siudem, P.; Zawada, K.D.; Paradowska, K. Profile of Bioactive Components and Antioxidant Activity of Aronia melanocarpa Fruits at Various Stages of Their Growth, Using Chemometric Methods. Antioxidants 2024, 13, 462. [Google Scholar] [CrossRef]
- Halim, M.A.; Kanan, K.A.; Nahar, T.; Rahman, M.J.; Ahmed, K.S.; Hossain, H.; Mozumder, N.H.M.R.; Ahmed, M. Metabolic Profiling of Phenolics of the Extracts from the Various Parts of Blackberry Plant (Syzygium cumini L.) and Their Antioxidant Activities. LWT 2022, 167, 113813. [Google Scholar] [CrossRef]
- Varzaru, I.; Oancea, A.G.; Vlaicu, P.A.; Saracila, M.; Untea, A.E. Exploring the Antioxidant Potential of Blackberry and Raspberry Leaves: Phytochemical Analysis, Scavenging Activity, and In Vitro Polyphenol Bioaccessibility. Antioxidants 2023, 12, 2125. [Google Scholar] [CrossRef] [PubMed]
- Sánchez-Velázquez, O.A.; Mulero, M.; Cuevas-Rodríguez, E.O.; Mondor, M.; Arcand, Y.; Hernández-Álvarez, A.J. In Vitro Gastrointestinal Digestion Impact on Stability, Bioaccessibility and Antioxidant Activity of Polyphenols from Wild and Commercial Blackberries (Rubus spp.). Food Funct. 2021, 12, 7358–7378. [Google Scholar] [CrossRef] [PubMed]
- Muzolf-Panek, M.; Waśkiewicz, A. Relationship between Phenolic Compounds, Antioxidant Activity and Color Parameters of Red Table Grape Skins Using Linear Ordering Analysis. Appl. Sci. 2022, 12, 6146. [Google Scholar] [CrossRef]
- Kupe, M.; Karatas, N.; Unal, M.S.; Ercisli, S.; Baron, M.; Sochor, J. Phenolic Composition and Antioxidant Activity of Peel, Pulp and Seed Extracts of Different Clones of the Turkish Grape Cultivar ‘Karaerik’. Plants 2021, 10, 2154. [Google Scholar] [CrossRef]
- Bocsan, I.C.; Măgureanu, D.C.; Pop, R.M.; Levai, A.M.; Macovei, Ș.O.; Pătrașca, I.M.; Chedea, V.S.; Buzoianu, A.D. Antioxidant and Anti-Inflammatory Actions of Polyphenols from Red and White Grape Pomace in Ischemic Heart Diseases. Biomedicines 2022, 10, 2337. [Google Scholar] [CrossRef]
- Yu, J.; Li, W.; You, B.; Yang, S.; Xian, W.; Deng, Y.; Huang, W.; Yang, R. Phenolic Profiles, Bioaccessibility and Antioxidant Activity of Plum (Prunus salicina Lindl). Food Res. Int. 2021, 143, 110300. [Google Scholar] [CrossRef]
- Johnson, J.B.; Hoyos, B.E.; Mani, J.S.; Reynolds, M.; Altvater, J.; Naiker, M. Identification of Phenolics Responsible for the High Antioxidant Activity in Burdekin Plum (Pleiogynium timoriense) Fruit. Food Chem. Adv. 2022, 1, 100081. [Google Scholar] [CrossRef]
- Trang, A.; Khandhar, P.B. Physiology, Acetylcholinesterase. In StatPearls; StatPearls Publishing: Treasure Island, FL, USA, 2025. [Google Scholar]
- Abd El-Aziz, N.M.; Eldin Awad, O.M.; Shehata, M.G.; El-Sohaimy, S.A. Antioxidant and Anti-Acetylcholinesterase Potential of Artichoke Phenolic Compounds. Food Biosci. 2021, 41, 101006. [Google Scholar] [CrossRef]
- Iglesias-Carres, L.; Bruno, A.; D’Antuono, I.; Linsalata, V.; Cardinali, A.; Neilson, A.P. In Vitro Evidences of the Globe Artichoke Antioxidant, Cardioprotective and Neuroprotective Effects. J. Funct. Foods 2023, 107, 105674. [Google Scholar] [CrossRef]
- Phan, T.-H.-A.; Nguyen, T.-P.; Tran, T.-T.-A. Extracting, Evaluating Biological Activities of Phenolic Compounds from Yellow Onion Peels (Allium cepa L.) and Their Applicability for Fish Preservation. IOP Conf. Ser. Earth Environ. Sci. 2021, 947, 012042. [Google Scholar] [CrossRef]
- Oyawoye, O.M.; Olotu, T.M.; Nzekwe, S.C.; Idowu, J.A.; Abdullahi, T.A.; Babatunde, S.O.; Ridwan, I.A.; Batiha, G.E.; Idowu, N.; Alorabi, M.; et al. Antioxidant Potential and Antibacterial Activities of Allium cepa (Onion) and Allium sativum (Garlic) against the Multidrug Resistance Bacteria. Bull. Natl. Res. Cent. 2022, 46, 214. [Google Scholar] [CrossRef]
- Demir, R.; Sarıtaş, S.; Bechelany, M.; Karav, S. Lactoferrin: Properties and Potential Uses in the Food Industry. Int. J. Mol. Sci. 2025, 26, 1404. [Google Scholar] [CrossRef] [PubMed]
- Ma, H.; Zhang, H.; Abubaker, M.A.; Al-Wraikat, M.; Li, L.; Liu, Y. Goat Lactoferrin–Pterostilbene Complexes as Novel Edible Functional Proteins with Enhanced Ultraviolet Stabilization and Antioxidant Properties. Food Hydrocoll. 2025, 158, 110538. [Google Scholar] [CrossRef]
- Davidova, S.; Galabov, A.S.; Satchanska, G. Antibacterial, Antifungal, Antiviral Activity, and Mechanisms of Action of Plant Polyphenols. Microorganisms 2024, 12, 2502. [Google Scholar] [CrossRef]
- Song, J.-M.; Lee, K.-H.; Seong, B.-L. Antiviral Effect of Catechins in Green Tea on Influenza Virus. Antivir. Res. 2005, 68, 66–74. [Google Scholar] [CrossRef]
- Manjunathan, R.; Periyaswami, V.; Mitra, K.; Rosita, A.S.; Pandya, M.; Selvaraj, J.; Ravi, L.; Devarajan, N.; Doble, M. Molecular Docking Analysis Reveals the Functional Inhibitory Effect of Genistein and Quercetin on TMPRSS2: SARS-COV-2 Cell Entry Facilitator Spike Protein. BMC Bioinform. 2022, 23, 180. [Google Scholar] [CrossRef] [PubMed]
- Li, T.; Zhu, J.; Yu, Q.; Zhu, Y.; Wu, C.; Zheng, X.; Chen, N.; Pei, P.; Yang, K.; Wang, K.; et al. Dietary Flavonoid Quercetin Supplement Promotes Antiviral Innate Responses Against Vesicular Stomatitis Virus Infection by Reshaping the Bacteriome and Host Metabolome in Mice. Mol. Nutr. Food Res. 2024, 68, 2300898. [Google Scholar] [CrossRef] [PubMed]
- Zainal, N.; Chang, C.-P.; Cheng, Y.-L.; Wu, Y.-W.; Anderson, R.; Wan, S.-W.; Chen, C.-L.; Ho, T.-S.; AbuBakar, S.; Lin, Y.-S. Resveratrol Treatment Reveals a Novel Role for HMGB1 in Regulation of the Type 1 Interferon Response in Dengue Virus Infection. Sci. Rep. 2017, 7, 42998. [Google Scholar] [CrossRef]
- Luo, R.; Li, S.; Yang, C.; Tang, B.; Li, L.; Luo, C. Curcumin Inhibits the Development of Pancreatic Cancer by Targeting the Circ_0079440/miR-522-3p/EIF4A1 Pathway. Cell Biochem. Biophys. 2024, 83, 377–390. [Google Scholar] [CrossRef]
- Peng, Y.; Zheng, J.; Zhou, Y.; Li, J. Characterization of a Novel Curcumin Analog P1 as Potent Inhibitor of the NF-κB Signaling Pathway with Distinct Mechanisms. Acta Pharmacol. Sin. 2013, 34, 939–950. [Google Scholar] [CrossRef] [PubMed][Green Version]
- Iqbal, N.; Poór, P. Plant Protection by Tannins Depends on Defence-Related Phytohormones. J. Plant Growth Regul. 2025, 44, 22–39. [Google Scholar] [CrossRef]
- Gescher, K.; Kühn, J.; Lorentzen, E.; Hafezi, W.; Derksen, A.; Deters, A.; Hensel, A. Proanthocyanidin-Enriched Extract from Myrothamnus flabellifolia Welw. Exerts Antiviral Activity against Herpes Simplex Virus Type 1 by Inhibition of Viral Adsorption and Penetration. J. Ethnopharmacol. 2011, 134, 468–474. [Google Scholar] [CrossRef]
- Hu, Y.; Li, Y.; Zhu, H.; Wang, D.; Zhou, J.; Li, B. Screening and Comparative Study of Four Anti-PEDV Candidate Drugs in Vitro. Anal. Biochem. 2025, 701, 115804. [Google Scholar] [CrossRef]
- De Angelis, M.; Della-Morte, D.; Buttinelli, G.; Di Martino, A.; Pacifici, F.; Checconi, P.; Ambrosio, L.; Stefanelli, P.; Palamara, A.T.; Garaci, E.; et al. Protective Role of Combined Polyphenols and Micronutrients against Influenza A Virus and SARS-CoV-2 Infection In Vitro. Biomedicines 2021, 9, 1721. [Google Scholar] [CrossRef]
- Mandal, M.K.; Domb, A.J. Antimicrobial Activities of Natural Bioactive Polyphenols. Pharmaceutics 2024, 16, 718. [Google Scholar] [CrossRef]
- Rasaily, S.; Haldipur, A.C.; Srividya, N. LC-Q-TOF-MS Phenolic Profiling, Data Mining for Antiviral Compounds, and in Silico Analysis against SARS-CoV-2 in Heritage-Pigmented Rice Metabolome. Food Biosci. 2025, 63, 105613. [Google Scholar] [CrossRef]
- Capasso, L.; De Masi, L.; Sirignano, C.; Maresca, V.; Basile, A.; Nebbioso, A.; Rigano, D.; Bontempo, P. Epigallocatechin Gallate (EGCG): Pharmacological Properties, Biological Activities and Therapeutic Potential. Molecules 2025, 30, 654. [Google Scholar] [CrossRef] [PubMed]
- Eggers, M.; Jungke, P.; Wolkinger, V.; Bauer, R.; Kessler, U.; Frank, B. Antiviral Activity of Plant Juices and Green Tea against SARS-CoV-2 and Influenza Virus. Phytother. Res. 2022, 36, 2109–2115. [Google Scholar] [CrossRef]
- Kumar, D.; Sharma, N.; Aarthy, M.; Singh, S.K.; Giri, R. Mechanistic Insights into Zika Virus NS3 Helicase Inhibition by Epigallocatechin-3-Gallate. ACS Omega 2020, 5, 11217–11226. [Google Scholar] [CrossRef]
- Da Conceição, P.J.P.; Ayusso, G.M.; Carvalho, T.; Duarte Lima, M.L.; Marinho, M.D.S.; Moraes, F.R.; Galán-Jurado, P.E.; González-Santamaría, J.; Bittar, C.; Zhang, B.; et al. In Vitro Evaluation of the Antiviral Activity of Polyphenol (−)-Epigallocatechin-3-Gallate (EGCG) Against Mayaro Virus. Viruses 2025, 17, 258. [Google Scholar] [CrossRef] [PubMed]
- Bibi, S.; Nisar, M.; Rafique, S.; Waqas, M.; Zahoor, M.; Idrees, M.; Nazir, N.; Ihsan, M.; Salmen, S.H.; Alharbi, S.A.; et al. Harnessing Nature’s Gifts: Salix Nigra and Its Potential for Combating Hepatitis C Virus (HCV). ACS Omega 2023, 8, 42987–42999. [Google Scholar] [CrossRef]
- Hassan, S.T.S.; Šudomová, M.; Mazurakova, A.; Kubatka, P. Insights into Antiviral Properties and Molecular Mechanisms of Non-Flavonoid Polyphenols against Human Herpesviruses. Int. J. Mol. Sci. 2022, 23, 13891. [Google Scholar] [CrossRef] [PubMed]
- Prabhu, S.; Kalaimathi, K.; Thiruvengadam, M.; Ayyanar, M.; Shine, K.; Amalraj, S.; Ceasar, S.A.; Priya, S.P.; Prakash, N. Antiviral Mechanisms of Dietary Polyphenols: Recent Developments as Antiviral Agents and Future Prospects in Combating Nipah Virus. Phytochem. Rev. 2024. [Google Scholar] [CrossRef]
- Chojnacka, K.; Skrzypczak, D.; Izydorczyk, G.; Mikula, K.; Szopa, D.; Witek-Krowiak, A. Antiviral Properties of Polyphenols from Plants. Foods 2021, 10, 2277. [Google Scholar] [CrossRef]
- Srivastava, R.; Dubey, N.K.; Sharma, M.; Kharkwal, H.; Bajpai, R.; Srivastava, R. Boosting the Human Antiviral Response in Conjunction with Natural Plant Products. Front. Nat. Prod. 2025, 3, 1470639. [Google Scholar] [CrossRef]
- Agrawal, P.K.; Agrawal, C.; Blunden, G. Quercetin: Antiviral Significance and Possible COVID-19 Integrative Considerations. Nat. Prod. Commun. 2020, 15, 1934578X20976293. [Google Scholar] [CrossRef]
- Sharapov, A.D.; Fatykhov, R.F.; Khalymbadzha, I.A.; Zyryanov, G.V.; Chupakhin, O.N.; Tsurkan, M.V. Plant Coumarins with Anti-HIV Activity: Isolation and Mechanisms of Action. Int. J. Mol. Sci. 2023, 24, 2839. [Google Scholar] [CrossRef] [PubMed]
- Garozzo, A.; Timpanaro, R.; Stivala, A.; Bisignano, G.; Castro, A. Activity of Melaleuca alternifolia (Tea Tree) Oil on Influenza Virus A/PR/8: Study on the Mechanism of Action. Antivir. Res. 2011, 89, 83–88. [Google Scholar] [CrossRef]
- Mieres-Castro, D.; Ahmar, S.; Shabbir, R.; Mora-Poblete, F. Antiviral Activities of Eucalyptus Essential Oils: Their Effectiveness as Therapeutic Targets against Human Viruses. Pharmaceuticals 2021, 14, 1210. [Google Scholar] [CrossRef] [PubMed]
- Garozzo, A.; Timpanaro, R.; Bisignano, B.; Furneri, P.M.; Bisignano, G.; Castro, A. In Vitro Antiviral Activity of Melaleuca Alternifolia Essential Oil. Lett. Appl. Microbiol. 2009, 49, 806–808. [Google Scholar] [CrossRef]
- Feng, A.; Si, T.; Du, B.; Sun, Q.; Yang, Y.; Rong, R. Antiviral Potential of Essential Oils and Their Plant Sources, Delivery Methods, and Drug Development Strategies with Special Focus on Their Mechanisms: A Comprehensive Review. Phytochem. Rev. 2025, 24, 1667–1689. [Google Scholar] [CrossRef]
- Elshafie, H.S.; Camele, I.; Mohamed, A.A. A Comprehensive Review on the Biological, Agricultural and Pharmaceutical Properties of Secondary Metabolites Based-Plant Origin. Int. J. Mol. Sci. 2023, 24, 3266. [Google Scholar] [CrossRef]
- Kreiser, T.; Zaguri, D.; Sachdeva, S.; Zamostiano, R.; Mograbi, J.; Segal, D.; Bacharach, E.; Gazit, E. Inhibition of Respiratory RNA Viruses by a Composition of Ionophoric Polyphenols with Metal Ions. Pharmaceuticals 2022, 15, 377. [Google Scholar] [CrossRef] [PubMed]
- Zhang, X.; Yang, J.; Liu, F.; Mo, M.; Farooq, M.; Li, J.; Yao, C.; Wei, W. Antiviral Activity of Morus alba L. Extract against Pseudorabies Virus. J. Ethnopharmacol. 2025, 336, 118719. [Google Scholar] [CrossRef]
- Quirós-Fallas, M.I.; Vargas-Huertas, F.; Quesada-Mora, S.; Azofeifa-Cordero, G.; Wilhelm-Romero, K.; Vásquez-Castro, F.; Alvarado-Corella, D.; Sánchez-Kopper, A.; Navarro-Hoyos, M. Polyphenolic HRMS Characterization, Contents and Antioxidant Activity of Curcuma longa Rhizomes from Costa Rica. Antioxidants 2022, 11, 620. [Google Scholar] [CrossRef]
- Lei, J.; Kusov, Y.; Hilgenfeld, R. Nsp3 of Coronaviruses: Structures and Functions of a Large Multi-Domain Protein. Antivir. Res. 2018, 149, 58–74. [Google Scholar] [CrossRef]
- Li, C.-W.; Chao, T.-L.; Lai, C.-L.; Lin, C.-C.; Pan, M.Y.-C.; Cheng, C.-L.; Kuo, C.-J.; Wang, L.H.-C.; Chang, S.-Y.; Liang, P.-H. Systematic Studies on the Anti-SARS-CoV-2 Mechanisms of Tea Polyphenol-Related Natural Products. ACS Omega 2024, 9, 23984–23997. [Google Scholar] [CrossRef]
- Tang, C.; Carrera Montoya, J.; Fritzlar, S.; Flavel, M.; Londrigan, S.L.; Mackenzie, J.M. Polyphenol Rich Sugarcane Extract (PRSE) Has Potential Antiviral Activity against Influenza A Virus in Vitro. Virology 2024, 590, 109969. [Google Scholar] [CrossRef] [PubMed]
- Tang, C.; Flavel, M.; Londrigan, S.L.; Mackenzie, J.M. Polyphenol Rich Sugarcane Extract Restricts Select Respiratory Viruses Depending on Their Mode of Entry. Virology 2025, 606, 110500. [Google Scholar] [CrossRef] [PubMed]
- Mileto, D.; Riva, A.; Cutrera, M.; Moschese, D.; Mancon, A.; Meroni, L.; Giacomelli, A.; Bestetti, G.; Rizzardini, G.; Gismondo, M.R.; et al. New Challenges in Human Monkeypox Outside Africa: A Review and Case Report from Italy. Travel Med. Infect. Dis. 2022, 49, 102386. [Google Scholar] [CrossRef]
- Rout, M.; Mishra, S.; Dey, S.; Singh, M.K.; Dehury, B.; Pati, S. Exploiting the Potential of Natural Polyphenols as Antivirals against Monkeypox Envelope Protein F13 Using Machine Learning and All-Atoms MD Simulations. Comput. Biol. Med. 2023, 162, 107116. [Google Scholar] [CrossRef] [PubMed]
- Manzoor, Z.; Sajad, A.; Qadiri, S.S.N.; Shah, F.A.; Dar, S.A.; Mandu, S.M. Polyphenols as Antiviral Agents: Assessing Their Potential Usage and Benefits in Aquaculture. Aquac. Int. 2025, 33, 106. [Google Scholar] [CrossRef]
- Sharma, S.; Ghosh, P.; Kar, C.; Ghosh, R. Anticipating Viral Challenges: A Perspective on Phytochemicals against Existing and Emerging Viruses. Anti-Infect. Agents 2025, 23, e22113525312781. [Google Scholar] [CrossRef]
- Ghosh, S.; Basu, S.; Anbarasu, A.; Ramaiah, S. A Comprehensive Review of Antimicrobial Agents Against Clinically Important Bacterial Pathogens: Prospects for Phytochemicals. Phytother. Res. 2025, 39, 138–161. [Google Scholar] [CrossRef]
- Zhong, W.; Tang, M.; Xie, Y.; Huang, X.; Liu, Y. Tea Polyphenols Inhibit the Activity and Toxicity of Staphylococcus aureus by Destroying Cell Membranes and Accumulating Reactive Oxygen Species. Foodborne Pathog. Dis. 2023, 20, 294–302. [Google Scholar] [CrossRef]
- Wang, L.; Li, T.; Wu, C.; Fan, G.; Zhou, D.; Li, X. Unlocking the Potential of Plant Polyphenols: Advances in Extraction, Antibacterial Mechanisms, and Future Applications. Food Sci. Biotechnol. 2025, 34, 1235–1259. [Google Scholar] [CrossRef]
- Bae, J.-Y.; Seo, Y.-H.; Oh, S.-W. Antibacterial Activities of Polyphenols against Foodborne Pathogens and Their Application as Antibacterial Agents. Food Sci. Biotechnol. 2022, 31, 985–997. [Google Scholar] [CrossRef]
- Nassarawa, S.S.; Nayik, G.A.; Gupta, S.D.; Areche, F.O.; Jagdale, Y.D.; Ansari, M.J.; Hemeg, H.A.; AL-Farga, A.; Alotaibi, S.S. Chemical Aspects of Polyphenol-Protein Interactions and Their Antibacterial Activity. Crit. Rev. Food Sci. Nutr. 2023, 63, 9482–9505. [Google Scholar] [CrossRef]
- Makarewicz, M.; Drożdż, I.; Tarko, T.; Duda-Chodak, A. The Interactions between Polyphenols and Microorganisms, Especially Gut Microbiota. Antioxidants 2021, 10, 188. [Google Scholar] [CrossRef]
- Slobodníková, L.; Fialová, S.; Rendeková, K.; Kováč, J.; Mučaji, P. Antibiofilm Activity of Plant Polyphenols. Molecules 2016, 21, 1717. [Google Scholar] [CrossRef]
- Bernal-Gallardo, J.O.; Molina-Torres, J.; Angoa-Pérez, M.V.; Cárdenas-Valdovinos, J.G.; García-Ruíz, I.; Ceja-Díaz, J.A.; Mena-Violante, H.G. Phenolic Compound Content and the Antioxidant and Antimicrobial Activity of Wild Blueberries (Vaccinium stenophyllum Steud.) Fruits Extracts during Ripening. Horticulturae 2021, 8, 15. [Google Scholar] [CrossRef]
- Li, W.; Yang, R.; Ying, D.; Yu, J.; Sanguansri, L.; Augustin, M.A. Analysis of Polyphenols in Apple Pomace: A Comparative Study of Different Extraction and Hydrolysis Procedures. Ind. Crops Prod. 2020, 147, 112250. [Google Scholar] [CrossRef]
- Geana, E.-I.; Ciucure, C.T.; Niculescu, V.-C.; Marinas, I.C.; Pircalabioru, G.G.; Dutu, D.; Trusca, R.; Oprea, O.-C.; Ficai, A.; Andronescu, E. Valorization of Apple Pomace by Obtaining Some Bioactive Ingredients with Antioxidant, Antimicrobial and Prebiotic Activities. Food Bioprod. Process. 2025, 150, 182–197. [Google Scholar] [CrossRef]
- Tienaho, J.; Liimatainen, J.; Myllymäki, L.; Kaipanen, K.; Tagliavento, L.; Ruuttunen, K.; Rudolfsson, M.; Karonen, M.; Marjomäki, V.; Hagerman, A.E.; et al. Pilot Scale Hydrodynamic Cavitation and Hot-Water Extraction of Norway Spruce Bark Yield Antimicrobial and Polyphenol-Rich Fractions. Sep. Purif. Technol. 2025, 360, 130925. [Google Scholar] [CrossRef]
- Sun, S.; Huang, S.; Shi, Y.; Shao, Y.; Qiu, J.; Sedjoah, R.-C.A.-A.; Yan, Z.; Ding, L.; Zou, D.; Xin, Z. Extraction, Isolation, Characterization and Antimicrobial Activities of Non-Extractable Polyphenols from Pomegranate Peel. Food Chem. 2021, 351, 129232. [Google Scholar] [CrossRef] [PubMed]
- Feng, Y.; Lin, J.; He, G.; Liang, L.; Liu, Q.; Yan, J.; Yao, Q. Compositions and Biological Activities of Pomegranate Peel Polyphenols Extracted by Different Solvents. Molecules 2022, 27, 4796. [Google Scholar] [CrossRef]
- Ruan, J.-H.; Li, J.; Adili, G.; Sun, G.-Y.; Abuduaini, M.; Abdulla, R.; Maiwulanjiang, M.; Aisa, H.A. Phenolic Compounds and Bioactivities from Pomegranate (Punica granatum L.) Peels. J. Agric. Food Chem. 2022, 70, 3678–3686. [Google Scholar] [CrossRef]
- Morgene, M.F.; Botelho-Nevers, E.; Grattard, F.; Pillet, S.; Berthelot, P.; Pozzetto, B.; Verhoeven, P.O. Staphylococcus aureus Colonization and Non-Influenza Respiratory Viruses: Interactions and Synergism Mechanisms. Virulence 2018, 9, 1354–1363. [Google Scholar] [CrossRef]
- Zhang, H.; Wang, M.; Yu, G.; Pu, J.; Tian, K.; Tang, X.; Du, Y.; Wu, H.; Hu, J.; Luo, X.; et al. Comparative Analysis of the Phenolic Contents and Antioxidant Activities of Different Parts of Two Pomegranate (Punica granatum L.) Cultivars: ‘Tunisia’ and ‘Qingpi’. Front. Plant Sci. 2023, 14, 1265018. [Google Scholar] [CrossRef]
- Turlewicz-Podbielska, H.; Augustyniak, A.; Pomorska-Mól, M. Viral Co-Infections of the Porcine Respiratory Tract: Insight into the Local Cytokine Response. Med. Weter. 2022, 78, 212–221. [Google Scholar] [CrossRef]
- Kumar, N.; Pratibha; Neeraj; Sami, R.; Khojah, E.; Aljahani, A.H.; Al-Mushhin, A.A.M. Effects of Drying Methods and Solvent Extraction on Quantification of Major Bioactive Compounds in Pomegranate Peel Waste Using HPLC. Sci. Rep. 2022, 12, 8000. [Google Scholar] [CrossRef] [PubMed]
- Wu, W.; Jiang, S.; Liu, M.; Tian, S. Simultaneous Process Optimization of Ultrasound-Assisted Extraction of Polyphenols and Ellagic Acid from Pomegranate (Punica granatum L.) Flowers and Its Biological Activities. Ultrason. Sonochem. 2021, 80, 105833. [Google Scholar] [CrossRef] [PubMed]
- Sahlabgi, A.; Lupuliasa, D.; Stanciu, G.; Lupșor, S.; Vlaia, L.L.; Rotariu, R.; Predescu, N.C.; Rădulescu, C.; Olteanu, R.-L.; Stănescu, S.-G.; et al. The Development and Comparative Evaluation of Rosemary Hydroalcoholic Macerate-Based Dermatocosmetic Preparations: A Study on Antioxidant, Antimicrobial, and Anti-Inflammatory Properties. Gels 2025, 11, 149. [Google Scholar] [CrossRef] [PubMed]
- Munggari, I.P.; Kurnia, D.; Deawati, Y.; Julaeha, E. Current Research of Phytochemical, Medicinal and Non-Medicinal Uses of Uncaria gambir Roxb.: A Review. Molecules 2022, 27, 6551. [Google Scholar] [CrossRef]
- Alkufeidy, R.M.; Ameer Altuwijri, L.; Aldosari, N.S.; Alsakabi, N.; Dawoud, T.M. Antimicrobial and Synergistic Properties of Green Tea Catechins against Microbial Pathogens. J. King Saud Univ. Sci. 2024, 36, 103277. [Google Scholar] [CrossRef]
- Rodríguez-Melcón, C.; Alonso-Calleja, C.; García-Fernández, C.; Carballo, J.; Capita, R. Minimum Inhibitory Concentration (MIC) and Minimum Bactericidal Concentration (MBC) for Twelve Antimicrobials (Biocides and Antibiotics) in Eight Strains of Listeria monocytogenes. Biology 2021, 11, 46. [Google Scholar] [CrossRef]
- Jubair, N.; R., M.; Fatima, A.; Mahdi, Y.K.; Abdullah, N.H. Evaluation of Catechin Synergistic and Antibacterial Efficacy on Biofilm Formation and acrA Gene Expression of Uropathogenic E. coli Clinical Isolates. Antibiotics 2022, 11, 1223. [Google Scholar] [CrossRef] [PubMed]
- Erttmann, S.F.; Gekara, N.O. Hydrogen Peroxide Release by Bacteria Suppresses Inflammasome-Dependent Innate Immunity. Nat. Commun. 2019, 10, 3493. [Google Scholar] [CrossRef]
- Ayub, A.; Cheong, Y.K.; Castro, J.C.; Cumberlege, O.; Chrysanthou, A. Use of Hydrogen Peroxide Vapour for Microbiological Disinfection in Hospital Environments: A Review. Bioengineering 2024, 11, 205. [Google Scholar] [CrossRef]
- Xu, W.; Lin, Z.; Cortez-Jugo, C.; Qiao, G.G.; Caruso, F. Antimicrobial Phenolic Materials: From Assembly to Function. Angew. Chem. Int. Ed. 2025, 64, e202423654. [Google Scholar] [CrossRef]
- Wang, L.; Li, T.; Wu, C.; Shi, J.; Fan, G.; Zhou, D.; Li, X. Inhibitory Effect of Polyphenol Extract of Osmanthus fragrans on Alternaria alternata and Development of a Novel Antimicrobial Film. Food Biosci. 2025, 64, 105882. [Google Scholar] [CrossRef]
- Prabhu, S.; Molath, A.; Choksi, H.; Kumar, S.; Mehra, R. Classifications of Polyphenols and Their Potential Application in Human Health and Diseases. Int. J. Physiol. Nutr. Phys. Educ. 2021, 6, 293–301. [Google Scholar] [CrossRef]
- Manso, T.; Lores, M.; De Miguel, T. Antimicrobial Activity of Polyphenols and Natural Polyphenolic Extracts on Clinical Isolates. Antibiotics 2021, 11, 46. [Google Scholar] [CrossRef] [PubMed]
- Lund, M.N. Reactions of Plant Polyphenols in Foods: Impact of Molecular Structure. Trends Food Sci. Technol. 2021, 112, 241–251. [Google Scholar] [CrossRef]
- De Oliveira Souza, G.G.; Gonçalves Castro, J.W.; Nascimento, L.L.L.; Inácio Da Silva, M.; Duarte Leite, D.O.; Garcia Santos, G.J.; Janaine Camilo, C.; Alencar De Menezes, I.R.; Martins Da Costa, J.G. Chemical Profile, Antioxidant and Antimicrobial Activity of Marine Sponge Species Combined with Multivariate Statistical Analyses: Desmapsamma anchorata, Dysidea etheria and Echinodictyum dendroides. Chem. Biodivers. 2025, 22, e202402156. [Google Scholar] [CrossRef]
- Zaki-Germi, S.; Afshar, D.; Akbari, A.; Nikfarjam, N. Multifunctional Bionanocomposite Hydrogels Based on Gelatin Methacrylate and Polyphenolic 2D Nanoparticles Decorated with Antimicrobial Bis(Imidazolium)-Based Ionic Liquids. Compos. Sci. Technol. 2025, 262, 111059. [Google Scholar] [CrossRef]
- Kawee-ai, A. Advancing Gel Systems with Natural Extracts: Antioxidant, Antimicrobial Applications, and Sustainable Innovations. Gels 2025, 11, 125. [Google Scholar] [CrossRef]
- Jalouli, M.; Rahman, M.A.; Biswas, P.; Rahman, H.; Harrath, A.H.; Lee, I.-S.; Kang, S.; Choi, J.; Park, M.N.; Kim, B. Targeting Natural Antioxidant Polyphenols to Protect Neuroinflammation and Neurodegenerative Diseases: A Comprehensive Review. Front. Pharmacol. 2025, 16, 1492517. [Google Scholar] [CrossRef]
- Di Sotto, A.; Di Giacomo, S. Plant Polyphenols and Human Health: Novel Findings for Future Therapeutic Developments. Nutrients 2023, 15, 3764. [Google Scholar] [CrossRef]
- Mehmood, A.; Usman, M.; Patil, P.; Zhao, L.; Wang, C. A Review on Management of Cardiovascular Diseases by Olive Polyphenols. Food Sci. Nutr. 2020, 8, 4639–4655. [Google Scholar] [CrossRef] [PubMed]
- García-Conesa, M.-T.; Larrosa, M. Polyphenol-Rich Foods for Human Health and Disease. Nutrients 2020, 12, 400. [Google Scholar] [CrossRef]
- Zhang, Z.; Li, X.; Sang, S.; McClements, D.J.; Chen, L.; Long, J.; Jiao, A.; Jin, Z.; Qiu, C. Polyphenols as Plant-Based Nutraceuticals: Health Effects, Encapsulation, Nano-Delivery, and Application. Foods 2022, 11, 2189. [Google Scholar] [CrossRef] [PubMed]
- Niu, C.; Zhang, J.; Okolo, P.I. Therapeutic Potential of Plant Polyphenols in Acute Pancreatitis. Inflammopharmacology 2025, 33, 785–798. [Google Scholar] [CrossRef]
- Dong, Y.; Li, J.; Dai, Y.; Zhang, X.; Jiang, X.; Wang, T.; Zhao, B.; Liu, W.; Sun, H.; Du, P.; et al. A Novel Nanocarrier Based on Natural Polyphenols Enhancing Gemcitabine Sensitization Ability for Improved Pancreatic Cancer Therapy Efficiency. Mater. Today Bio 2025, 30, 101463. [Google Scholar] [CrossRef] [PubMed]
- An, Y.; Sun, J.-X.; Ma, S.-Y.; Xu, M.-Y.; Xu, J.-Z.; Liu, C.-Q.; Wang, S.-G.; Xia, Q.-D. From Plant Based Therapy to Plant-Derived Vesicle-Like Nanoparticles for Cancer Treatment: Past, Present and Future. Int. J. Nanomed. 2025, 20, 3471–3491. [Google Scholar] [CrossRef]
- Solanki, R.; Rawat, L.; Tabasum, S.; Pal, S.; Patel, S.; Sabarwal, A. A Comprehensive Review of Anti-Cancer Mechanisms of Polyphenol Honokiol and Nano Carrier-Based Approaches to Enhance Its Therapeutic Potential. Phytochem. Rev. 2025. [Google Scholar] [CrossRef]
- Feng, T.; Wan, Y.; Dai, B.; Liu, Y. Anticancer Activity of Bitter Melon-Derived Vesicles Extract against Breast Cancer. Cells 2023, 12, 824. [Google Scholar] [CrossRef] [PubMed]
- Tajik, T.; Baghaei, K.; Moghadam, V.E.; Farrokhi, N.; Salami, S.A. Extracellular Vesicles of Cannabis with High CBD Content Induce Anticancer Signaling in Human Hepatocellular Carcinoma. Biomed. Pharmacother. 2022, 152, 113209. [Google Scholar] [CrossRef] [PubMed]
- Puspadewi, R.; Milanda, T.; Muhaimin, M.; Chaerunisaa, A.Y. Nanoparticle-Encapsulated Plant Polyphenols and Flavonoids as an Enhanced Delivery System for Anti-Acne Therapy. Pharmaceuticals 2025, 18, 209. [Google Scholar] [CrossRef]
- Kaparekar, P.S.; Anandasadagopan, S.K. The Potential Role of Bioactive Plant-Based Polyphenolic Compounds and Their Delivery Systems—As a Promising Opportunity for a New Therapeutic Solution for Acute and Chronic Wound Healing. Curr. Pharmacol. Rep. 2022, 8, 321–338. [Google Scholar] [CrossRef]
- Froldi, G.; Ragazzi, E. Selected Plant-Derived Polyphenols as Potential Therapeutic Agents for Peripheral Artery Disease: Molecular Mechanisms, Efficacy and Safety. Molecules 2022, 27, 7110. [Google Scholar] [CrossRef]
- Chen, D.; Sun, Y. Current Status of Plant-Based Bioactive Compounds as Therapeutics in Alzheimer’s Diseases. J. Integr. Neurosci. 2025, 24, 23090. [Google Scholar] [CrossRef]
- Xu, R.; Zhou, Y.; Niu, H.; Xue, S.; Fu, L.; Huang, Q.; Sun, Y. Kiwifruit Polyphenols Regulate Mitophagy to Promote Intestinal Barrier Function: Based on Proteomics, In Vitro and In Vivo Study. Food Biosci. 2025, 64, 105847. [Google Scholar] [CrossRef]
- Madrigal-Gamboa, V.; Jiménez-Arias, J.; Hidalgo, O.; Quesada, S.; Pérez, A.M.; Azofeifa, G. Membrane Processing Effect of Blackberry (Rubus adenotrichos) on Cytotoxic and Pro-apoptotic Activities against Cancer Cell Lines. J. Food Process. Preserv. 2021, 45, e15575. [Google Scholar] [CrossRef]
- Castejón-Vega, B.; Kyriakidis, N.C.; Alcócer-Gómez, E.; Giampieri, F.; González-Paramás, A.M.; Cordero, M.D.; Alvarez-Suarez, J.M. Modulatory Effect of Andean Blackberry Polyphenols on Genes Related to Antioxidant and Inflammatory Responses, the NLRP3 Inflammasome, and Autophagy. J. Berry Res. 2024, 14, 41–59. [Google Scholar] [CrossRef]
- Hu, X.; Xie, J.; Bai, Y.-Y.; Hong, Z.-S.; Zhang, L.; Gong, W.-Y.; Pan, Y.-X.; Wang, W.-J.; Su, M.; Sheng, J.; et al. Extraction, In Vitro Hypoglycaemic Activity and Active Ingredient Analysis of Polyphenols from Walnut Green Husk. J. Funct. Foods 2024, 122, 106508. [Google Scholar] [CrossRef]
- Kim, Y.; Keogh, J.; Clifton, P. Polyphenols and Glycemic Control. Nutrients 2016, 8, 17. [Google Scholar] [CrossRef]
- Farazi, M.; Houghton, M.J.; Nicolotti, L.; Murray, M.; Cardoso, B.R.; Williamson, G. Inhibition of Human Starch Digesting Enzymes and Intestinal Glucose Transport by Walnut Polyphenols. Food Res. Int. 2024, 189, 114572. [Google Scholar] [CrossRef]
- Yassin, M.T.; Mostafa, A.A.-F.; Al Askar, A.A. In Vitro Evaluation of Biological Activities and Phytochemical Analysis of Different Solvent Extracts of Punica granatum L. (Pomegranate) Peels. Plants 2021, 10, 2742. [Google Scholar] [CrossRef] [PubMed]
- Saad, P.G.; Castelino, R.D.; Ravi, V.; Al-Amri, I.S.; Khan, S.A. Green Synthesis of Silver Nanoparticles Using Omani Pomegranate Peel Extract and Two Polyphenolic Natural Products: Characterization and Comparison of Their Antioxidant, Antibacterial, and Cytotoxic Activities. Beni-Suef Univ. J. Basic Appl. Sci. 2021, 10, 29. [Google Scholar] [CrossRef]
- Olszowy-Tomczyk, M.; Garbaczewska, S.; Wianowska, D. Correlation Study of Biological Activity with Quercetin and Phenolics Content in Onion Extracts. Molecules 2022, 27, 8164. [Google Scholar] [CrossRef]
- Kim, Y.; Kim, Y.-J.; Shin, Y. Comparative Analysis of Polyphenol Content and Antioxidant Activity of Different Parts of Five Onion Cultivars Harvested in Korea. Antioxidants 2024, 13, 197. [Google Scholar] [CrossRef]
- Bozinou, E.; Pappas, I.S.; Patergiannakis, I.-S.; Chatzimitakos, T.; Palaiogiannis, D.; Athanasiadis, V.; Lalas, S.I.; Chatzilazarou, A.; Makris, D.P. Evaluation of Antioxidant, Antimicrobial, and Anticancer Properties of Onion Skin Extracts. Sustainability 2023, 15, 11599. [Google Scholar] [CrossRef]
- Mirmojarabian, S.; Karimi, A.; Lorigooini, Z.; Javadi-Farsani, F.; Soltani, A.; Moradi, M.-T. Phytochemical Properties and Antiviral Effect of Green Tea (Camellia sinensis) Extract on Adenovirus In Vitro. J. Shahrekord Univ. Med. Sci. 2022, 24, 104–110. [Google Scholar] [CrossRef]
- Teixeira Oliveira, J.; Machado Da Costa, F.; Gonçalvez Da Silva, T.; Dotto Simões, G.; Dos Santos Pereira, E.; Quevedo Da Costa, P.; Andreazza, R.; Cavalheiro Schenkel, P.; Pieniz, S. Green Tea and Kombucha Characterization: Phenolic Composition, Antioxidant Capacity and Enzymatic Inhibition Potential. Food Chem. 2023, 408, 135206. [Google Scholar] [CrossRef] [PubMed]
- Deo, A.S.; Devi, P.J.A.; Sijisha, K.S.; Anusha, R.; Mishra, T.; Mathew, S.; Abraham, K.M.; Jagadish, R.; Priya, S. Comparative Studies on the Antioxidant, Anticancer and Anti-Inflammatory Activities of Green Tea, Orthodox Black Tea and CTC Black Tea. J. Food Sci. Technol. 2024, 61, 1315–1325. [Google Scholar] [CrossRef]
- Ranasinghe, M.; Alghaithi, M.; Mugdil, P.; Sundarakani, B.; Stathopoulos, C.; Maqsood, S. Fiber and Polyphenol Enriched Biscuits Using Date Palm Byproduct: Physiochemical Characteristics, Sensory Properties, In Vitro Digestion, and Storage Stability. J. Food Sci. 2025, 90, e17667. [Google Scholar] [CrossRef]
- Ranasinghe, M.; Sivapragasam, N.; Mostafa, H.; Airouyuwa, J.O.; Manikas, I.; Sundarakani, B.; Maqsood, S.; Stathopoulos, C. Valorizing Date Seeds in Biscuits: A Novel Approach to Incorporate Bioactive Components Extracted from Date Seeds Using Microwave-Assisted Extraction. Resour. Environ. Sustain. 2024, 15, 100147. [Google Scholar] [CrossRef]
- Mustafa, I.; Chin, N.L. Antioxidant Properties of Dried Ginger (Zingiber officinale Roscoe) Var. Bentong. Foods 2023, 12, 178. [Google Scholar] [CrossRef]
- Almehizia, A.A.; Al-Omar, M.A.; Naglah, A.M.; Zen, A.A.; Rouf, M.A.; Nupur, A.H.; Rahamn, M.S.; Adam, A.M.A.; Mazumder, M.A.R. Incorporation of Ginger Peel Polyphenol into Yogurt Improves Its Stability: Physicochemical and Microbiological Characterizations. Bull. Chem. Soc. Ethiop. 2024, 39, 201–213. [Google Scholar] [CrossRef]
- Gonzales, E.; Bustamante, A.; García-Díaz, D.; Sanhueza, L.; Orellana, J.F.; Fredes, C.; Jiménez, P.; Chávez, V.; Echeverría, F. Assessing Quality and Polyphenol in Vitro Bioaccessibility in Healthy Jelly Gummies with Microencapsulated and Non-Encapsulated Pomegranate Peel Extract. Food Chem. 2025, 470, 142611. [Google Scholar] [CrossRef]
- Bansode, V.; Chandra Panda, T.; Jaddu, S.; Sahoo, S.; Subrahmanyam, K.; Vignesh, V.; Niranjan, T.; Chandra Pradhan, R.; Dwivedi, M. Enhancing Nutritional Potential: Plasma-Activated Water Treatment on Sweet Orange Peel Powder—Polyphenols, Flavonoids, Antioxidants, and Anti-Nutrients Optimization. IEEE Trans. Plasma Sci. 2025, 53, 51–62. [Google Scholar] [CrossRef]
- Medina-Herrera, N.; Martínez-Ávila, G.C.G.; Robledo-Jiménez, C.L.; Rojas, R.; Orozco-Zamora, B.S. From Citrus Waste to Valuable Resources: A Biorefinery Approach. Biomass 2024, 4, 784–808. [Google Scholar] [CrossRef]
- Ngongoni, K.N.; Pfukwa, T.M.; Mapiye, C. Keeping Quality of Raw Ground Beef Patties Fortified with Polyphenols Extracted from Acacia mearnsii Bark and Leaves. Meat Sci. 2025, 219, 109665. [Google Scholar] [CrossRef]
- Rusindo-Rodríguez, I.M.; Ramos-Sánchez, V.H.; Chávez-Flores, D.; Delgado, E.; Chávez-Martínez, A.; Luján-Torres, V.E.; Orozco-Mena, R.E.; Sepúlveda, D.R.; Gutiérrez-Méndez, N. Co-Crystals of Lactose-Polyphenols Created from Two Food-Related By-Products: Cheese Whey and Maize Inflorescences. Food Bioprocess Technol. 2025, 18, 4513–4528. [Google Scholar] [CrossRef]
- Telesca, L.; Belluscio, A.; Criscoli, A.; Ardizzone, G.; Apostolaki, E.T.; Fraschetti, S.; Gristina, M.; Knittweis, L.; Martin, C.S.; Pergent, G.; et al. Seagrass Meadows (Posidonia oceanica) Distribution and Trajectories of Change. Sci. Rep. 2015, 5, 12505. [Google Scholar] [CrossRef]
- Piechowiak, T.; Skóra, B.; Grzelak-Błaszczyk, K.; Sójka, M. Extraction of Antioxidant Compounds from Blueberry Fruit Waste and Evaluation of Their In Vitro Biological Activity in Human Keratinocytes (HaCaT). Food Anal. Methods 2021, 14, 2317–2327. [Google Scholar] [CrossRef]
- Bencresciuto, G.F.; Carnevale, M.; Paris, E.; Gallucci, F.; Santangelo, E.; Migliori, C.A. A Sustainable Alternative for Cosmetic Applications: NADES Extraction of Bioactive Compounds from Hazelnut By-Products. Sustainability 2025, 17, 1516. [Google Scholar] [CrossRef]
- Sanhueza, L.; Melo, R.; Montero, R.; Maisey, K.; Mendoza, L.; Wilkens, M. Synergistic Interactions between Phenolic Compounds Identified in Grape Pomace Extract with Antibiotics of Different Classes against Staphylococcus aureus and Escherichia coli. PLoS ONE 2017, 12, e0172273. [Google Scholar] [CrossRef] [PubMed]
- Daglia, M. Polyphenols as Antimicrobial Agents. Curr. Opin. Biotechnol. 2012, 23, 174–181. [Google Scholar] [CrossRef]
- Armari, M.; Zavattaro, E.; Trejo, C.F.; Galeazzi, A.; Grossetti, A.; Veronese, F.; Savoia, P.; Azzimonti, B. Vitis Vinifera L. Leaf Extract, a Microbiota Green Ally against Infectious and Inflammatory Skin and Scalp Diseases: An In-Depth Update. Antibiotics 2024, 13, 697. [Google Scholar] [CrossRef]
- Tsiapali, O.I.; Ayfantopoulou, E.; Tzourouni, A.; Ofrydopoulou, A.; Letsiou, S.; Tsoupras, A. Unveiling the Utilization of Grape and Winery By-Products in Cosmetics with Health Promoting Properties. Appl. Sci. 2025, 15, 1007. [Google Scholar] [CrossRef]
- Salih, N.K.-E.M.; Alam, M.Z.; Haris, S.; Kamal-Eldin, A.; Al-Marzouqi, A.H. Prospective Applications of Phenolic Compounds in Processing By-Products of Date Fruits (Phoenix dactylifera L.). Discov. Food 2025, 5, 198. [Google Scholar] [CrossRef]
- Tapia-Quirós, P.; Montenegro-Landívar, M.F.; Reig, M.; Vecino, X.; Cortina, J.L.; Saurina, J.; Granados, M. Recovery of Polyphenols from Agri-Food By-Products: The Olive Oil and Winery Industries Cases. Foods 2022, 11, 362. [Google Scholar] [CrossRef]
- Galanakis, C.M.; Tsatalas, P.; Galanakis, I.M. Implementation of Phenols Recovered from Olive Mill Wastewater as UV Booster in Cosmetics. Ind. Crops Prod. 2018, 111, 30–37. [Google Scholar] [CrossRef]
- Barba, F.J.; Zhu, Z.; Koubaa, M.; Sant’Ana, A.S.; Orlien, V. Green Alternative Methods for the Extraction of Antioxidant Bioactive Compounds from Winery Wastes and By-Products: A Review. Trends Food Sci. Technol. 2016, 49, 96–109. [Google Scholar] [CrossRef]
- Rojo-Poveda, O.; Ribeiro, S.O.; Anton-Sales, C.; Keymeulen, F.; Barbosa-Pereira, L.; Delporte, C.; Zeppa, G.; Stévigny, C. Evaluation of Cocoa Bean Shell Antimicrobial Activity: A Tentative Assay Using a Metabolomic Approach for Active Compound Identification. Planta Med. 2021, 87, 841–849. [Google Scholar] [CrossRef]
- Disca, V.; Travaglia, F.; Carini, C.; Coïsson, J.D.; Cravotto, G.; Arlorio, M.; Locatelli, M. Improving the Extraction of Polyphenols from Cocoa Bean Shells by Ultrasound and Microwaves: A Comparative Study. Antioxidants 2024, 13, 1097. [Google Scholar] [CrossRef] [PubMed]
- Moreno-Chamba, B.; Salazar-Bermeo, J.; Martínez-Madrid, M.C.; Lizama, V.; Martín-Bermudo, F.; Berná, G.; Neacsu, M.; Saura, D.; Martí, N.; Valero, M. Bound Galloylated Compounds in Persimmon Upcycled Dietary Fiber Modulate Microbial Strains Associated to Human Health after in Vitro Digestion. LWT 2022, 156, 113011. [Google Scholar] [CrossRef]
- Moreno-Chamba, B.; Salazar-Bermeo, J.; Navarro-Simarro, P.; Narváez-Asensio, M.; Martínez-Madrid, M.C.; Saura, D.; Martí, N.; Valero, M. Autoinducers Modulation as a Potential Anti-Virulence Target of Bacteria by Phenolic Compounds. Int. J. Antimicrob. Agents 2023, 62, 106937. [Google Scholar] [CrossRef]
- Lopes, J.D.C.; Madureira, J.; Margaça, F.M.A.; Cabo Verde, S. Grape Pomace: A Review of Its Bioactive Phenolic Compounds, Health Benefits, and Applications. Molecules 2025, 30, 362. [Google Scholar] [CrossRef]
- Albrahim, J.S.; El-Fakharany, E.M.; El-Gendi, H.; Saleh, A.K.; El-Maradny, Y.A. Therapeutic Perspectives of Mangifera indica L. Peel Extract: Phytochemical Profile, Antimicrobial, Anticancer, and Antiviral Efficacy. Biomass Convers. Biorefin. 2025, 15, 11371–11394. [Google Scholar] [CrossRef]
- Siol, M.; Sadowska, A. Chemical Composition, Physicochemical and Bioactive Properties of Avocado (Persea americana) Seed and Its Potential Use in Functional Food Design. Agriculture 2023, 13, 316. [Google Scholar] [CrossRef]
- Gandhi, G.R.; Jothi, G.; Antony, P.J.; Balakrishna, K.; Paulraj, M.G.; Ignacimuthu, S.; Stalin, A.; Al-Dhabi, N.A. Gallic Acid Attenuates High-Fat Diet Fed-Streptozotocin-Induced Insulin Resistance via Partial Agonism of PPARγ in Experimental Type 2 Diabetic Rats and Enhances Glucose Uptake through Translocation and Activation of GLUT4 in PI3K/p-Akt Signaling Pathway. Eur. J. Pharmacol. 2014, 745, 201–216. [Google Scholar] [CrossRef]
- Nunes, A.R.; Alves, G.; Falcão, A.; Lopes, J.A.; Silva, L.R. Phenolic Acids from Fruit By-Products as Therapeutic Agents for Metabolic Syndrome: A Review. Int. J. Mol. Sci. 2025, 26, 3834. [Google Scholar] [CrossRef] [PubMed]
- Santana-Gálvez, J.; Cisneros-Zevallos, L.; Jacobo-Velázquez, D. Chlorogenic Acid: Recent Advances on Its Dual Role as a Food Additive and a Nutraceutical against Metabolic Syndrome. Molecules 2017, 22, 358. [Google Scholar] [CrossRef] [PubMed]
- Zubairu, I.K.; Rakariyatham, K.; Bai-Ngew, S.; Leksawasdi, N.; Regenstein, J.M.; Lao, F.; Hong, H.; Shin, W.-S.; Alzahrani, K.J.; Phimolsiripol, Y. Nutritional and Therapeutic Potential of Longan Fruit By-Products for Liver Diseases: Pathway to Functional Foods. Curr. Nutr. Rep. 2025, 14, 28. [Google Scholar] [CrossRef]
- Servin-Uribe, R.I.; Castilla-Ramírez, P.; Ramírez, I.F.P.; Jiménez, J.P.; Reynoso-Camacho, R. In Vivo Differential Effects of Extractable and Non-Extractable Phenolic Compounds from Grape Pomace on the Regulation of Obesity and Associated Metabolic Alterations. Plant Foods Hum. Nutr. 2025, 80, 37. [Google Scholar] [CrossRef]
- Frusciante, L.; Geminiani, M.; Shabab, B.; Olmastroni, T.; Roncucci, N.; Mastroeni, P.; Salvini, L.; Lamponi, S.; Trezza, A.; Santucci, A. Enhancing Industrial Hemp (Cannabis sativa) Leaf By-Products: Bioactive Compounds, Anti-Inflammatory Properties, and Potential Health Applications. Int. J. Mol. Sci. 2025, 26, 548. [Google Scholar] [CrossRef]
- Laaraj, N.; Bouhrim, M.; Kharchoufa, L.; Tiji, S.; Bendaha, H.; Addi, M.; Drouet, S.; Hano, C.; Lorenzo, J.M.; Bnouham, M.; et al. Phytochemical Analysis, α-Glucosidase and α-Amylase Inhibitory Activities and Acute Toxicity Studies of Extracts from Pomegranate (Punica granatum) Bark, a Valuable Agro-Industrial By-Product. Foods 2022, 11, 1353. [Google Scholar] [CrossRef] [PubMed]
- Qiu, Z.; Zheng, Z.; Xiao, H. Sustainable Valorization of Garlic Byproducts: From Waste to Resource in the Pursuit of Carbon Neutrality. Compr. Rev. Food Sci. Food Saf. 2025, 24, e70151. [Google Scholar] [CrossRef]
- Fernandez, S.P.; González, R.E. Nutritional Quality, Bioactive Compounds, and Antioxidant Activity of Nine Clones of Fresh Garlic and Its Black Garlic Derivative: A Comparative Study. Biol. Life Sci. Forum 2024, 40, 29. [Google Scholar]
- Cava, R.; Ladero, L. Using Polyphenol-Rich Extracts from Tropical Fruit Byproducts to Control Lipid and Protein Oxidation in Cooked Chicken Models. Eur. Food Res. Technol. 2024, 250, 2809–2820. [Google Scholar] [CrossRef]
- Fernandes, R.A.; Ferreira, N.; Lopes, S.; Freitas, B.; Santos, J.; Martins, J.M.; Carvalho, L.H. Antioxidant Particleboards Produced from Forest By-Products with Application in the Food Packaging Industry. Polymers 2025, 17, 216. [Google Scholar] [CrossRef]
- Panja, P. Green Extraction Methods of Food Polyphenols from Vegetable Materials. Curr. Opin. Food Sci. 2018, 23, 173–182. [Google Scholar] [CrossRef]
- Ameer, K.; Shahbaz, H.M.; Kwon, J. Green Extraction Methods for Polyphenols from Plant Matrices and Their Byproducts: A Review. Compr. Rev. Food Sci. Food Saf. 2017, 16, 295–315. [Google Scholar] [CrossRef]
- Dzah, C.S.; Duan, Y.; Zhang, H.; Serwah Boateng, N.A.; Ma, H. Latest Developments in Polyphenol Recovery and Purification from Plant By-Products: A Review. Trends Food Sci. Technol. 2020, 99, 375–388. [Google Scholar] [CrossRef]
- Alexandre, E.M.C.; Araújo, P.; Duarte, M.F.; De Freitas, V.; Pintado, M.; Saraiva, J.A. High-Pressure Assisted Extraction of Bioactive Compounds from Industrial Fermented Fig by-Product. J. Food Sci. Technol. 2017, 54, 2519–2531. [Google Scholar] [CrossRef]
- Okur, I.; Oztop, M.H.; Alpas, H. Optimization and Comparison of High-Pressure-Assisted Extraction of Phenolic Compounds from Olive Pomace. ACS Food Sci. Technol. 2022, 2, 1862–1869. [Google Scholar] [CrossRef]
- Panda, D.; Saharan, V.K.; Manickam, S. Controlled Hydrodynamic Cavitation: A Review of Recent Advances and Perspectives for Greener Processing. Processes 2020, 8, 220. [Google Scholar] [CrossRef]
- Wu, Z.; Ferreira, D.F.; Crudo, D.; Bosco, V.; Stevanato, L.; Costale, A.; Cravotto, G. Plant and Biomass Extraction and Valorisation under Hydrodynamic Cavitation. Processes 2019, 7, 965. [Google Scholar] [CrossRef]
- Farías-Campomanes, A.M.; Rostagno, M.A.; Coaquira-Quispe, J.J.; Meireles, M.A.A. Supercritical Fluid Extraction of Polyphenols from Lees: Overall Extraction Curve, Kinetic Data and Composition of the Extracts. Bioresour. Bioprocess. 2015, 2, 45. [Google Scholar] [CrossRef]
- Bessa, C.; Francisco, T.; Dias, R.; Mateus, N.; Freitas, V.D.; Pérez-Gregorio, R. Use of Polyphenols as Modulators of Food Allergies. From Chemistry to Biological Implications. Front. Sustain. Food Syst. 2021, 5, 623611. [Google Scholar] [CrossRef]
- Słota, P.; Harasym, J.; Jacukowicz-Sobala, I. Supercritical Fluid Extraction—A Sustainable and Selective Alternative for Tannin Recovery from Biomass Resources. Appl. Sci. 2025, 15, 5914. [Google Scholar] [CrossRef]
- Dobroslavić, E.; Elez Garofulić, I.; Šeparović, J.; Zorić, Z.; Pedisić, S.; Dragović-Uzelac, V. Pressurized Liquid Extraction as a Novel Technique for the Isolation of Laurus nobilis L. Leaf Polyphenols. Molecules 2022, 27, 5099. [Google Scholar] [CrossRef]
- Nieto, J.A.; Santoyo, S.; De Sá, M.; Baoshan, S.; Reglero, G.; Jaime, L. Comprehensive Study of Sustainable Pressurized Liquid Extractions to Obtain Bioavailable Antioxidant Phenolic Compounds from Grape Seed By-Products. Processes 2024, 12, 2308. [Google Scholar] [CrossRef]
- Savic, I.M.; Savic Gajic, I.M. Optimization of Ultrasound-Assisted Extraction of Polyphenols from Wheatgrass (Triticum aestivum L.). J. Food Sci. Technol. 2020, 57, 2809–2818. [Google Scholar] [CrossRef]
- Kumari, B.; Tiwari, B.K.; Hossain, M.B.; Rai, D.K.; Brunton, N.P. Ultrasound-assisted Extraction of Polyphenols from Potato Peels: Profiling and Kinetic Modelling. Int. J. Food Sci. Technol. 2017, 52, 1432–1439. [Google Scholar] [CrossRef]
- Pogorzelska-Nowicka, E.; Hanula, M.; Pogorzelski, G. Extraction of Polyphenols and Essential Oils from Herbs with Green Extraction Methods—An Insightful Review. Food Chem. 2024, 460, 140456. [Google Scholar] [CrossRef] [PubMed]
- López-Salazar, H.; Camacho-Díaz, B.H.; Ocampo, M.L.A.; Jiménez-Aparicio, A.R. Microwave-Assisted Extraction of Functional Compounds from Plants: A Review. BioResources 2023, 18, 6614–6638. [Google Scholar] [CrossRef]
- Tanruean, K.; Luangkamin, S.; Srisurat, T.; Bunmusik, W.; Suttiarporn, P. Optimization of Microwave-Assisted Extraction Process for Production of Polyphenol-Rich Crude Extract from Cinnamomum iners Leaves. Appl. Sci. 2025, 15, 1265. [Google Scholar] [CrossRef]
- Das, S.; Nadar, S.S.; Rathod, V.K. Integrated Strategies for Enzyme Assisted Extraction of Bioactive Molecules: A Review. Int. J. Biol. Macromol. 2021, 191, 899–917. [Google Scholar] [CrossRef]
- De Camargo, A.C.; Regitano-d’Arce, M.A.B.; Biasoto, A.C.T.; Shahidi, F. Enzyme-Assisted Extraction of Phenolics from Winemaking by-Products: Antioxidant Potential and Inhibition of Alpha-Glucosidase and Lipase Activities. Food Chem. 2016, 212, 395–402. [Google Scholar] [CrossRef] [PubMed]
- Lakka, A.; Bozinou, E.; Stavropoulos, G.; Samanidis, I.; Athanasiadis, V.; Dourtoglou, V.G.; Makris, D.P.; Lalas, S.I. Enhancement of Polyphenols Recovery from Rosa canina, Calendula officinalis and Castanea sativa Using Pulsed Electric Field. Beverages 2021, 7, 63. [Google Scholar] [CrossRef]
- Carpentieri, S.; Ferrari, G.; Pataro, G. Optimization of Pulsed Electric Fields-Assisted Extraction of Phenolic Compounds From White Grape Pomace Using Response Surface Methodology. Front. Sustain. Food Syst. 2022, 6, 854968. [Google Scholar] [CrossRef]
- Dai, Y.; Van Spronsen, J.; Witkamp, G.-J.; Verpoorte, R.; Choi, Y.H. Natural Deep Eutectic Solvents as New Potential Media for Green Technology. Anal. Chim. Acta 2013, 766, 61–68. [Google Scholar] [CrossRef]
- Mustafa, A.; Turner, C. Pressurized Liquid Extraction as a Green Approach in Food and Herbal Plants Extraction: A Review. Anal. Chim. Acta 2011, 703, 8–18. [Google Scholar] [CrossRef]
- Rosales, T.K.O.; Fabi, J.P. Valorization of Polyphenolic Compounds from Food Industry By-Products for Application in Polysaccharide-Based Nanoparticles. Front. Nutr. 2023, 10, 1144677. [Google Scholar] [CrossRef] [PubMed]
- Drosou, C.; Kyriakopoulou, K.; Laina, K.T.; Bimpilas, A.; Tsimogiannis, D.; Krokida, M. Revolutionizing Wine Waste: Advanced Techniques for Polyphenol Recovery from White Wine Byproducts. Agriculture 2025, 15, 648. [Google Scholar] [CrossRef]
- Paiva, A.; Craveiro, R.; Aroso, I.; Martins, M.; Reis, R.L.; Duarte, A.R.C. Natural Deep Eutectic Solvents—Solvents for the 21st Century. ACS Sustain. Chem. Eng. 2014, 2, 1063–1071. [Google Scholar] [CrossRef]
- Liu, Y.; Li, R.; Wang, Q.; Liu, X.; Gong, Z. Polyphenols and Flavonoids in Water Caltrop Shells from Different Producing Areas of China: Identification, Green Extraction and Quantitative Analysis. Ind. Crops Prod. 2025, 225, 120606. [Google Scholar] [CrossRef]
- Dushkova, M.; Mitova, M.; Bakardzhiyski, I.; Miteva-Petrova, M.; Menkov, N. Application of Ultrafiltration for Recovery of Bioactive Phenolic Compounds from Rose Wastewater. Appl. Sci. 2025, 15, 2040. [Google Scholar] [CrossRef]
- Huang, J.; Liu, Y.; Han, F.; Fang, Z.; Yang, L.; Zhuang, M.; Zhang, Y.; Lv, H.; Wang, Y.; Ji, J.; et al. Genetic Diversity and Population Structure Analysis of 161 Broccoli Cultivars Based on SNP Markers. Hortic. Plant J. 2021, 7, 423–433. [Google Scholar] [CrossRef]
- Ghimire, U.; Pliakoni, E.; Yu, F.; Brecht, J.K.; Liu, T. Identifying Genes Regulated during Natural, on-Plant Senescence in Broccoli (Brassica oleracea) in Contrast to Postharvest Senescence. Postharvest Biol. Technol. 2023, 206, 112535. [Google Scholar] [CrossRef]
- Rivas, M.Á.; Benito, M.J.; Martín, A.; De Guía Córdoba, M.; Gizaw, Y.; Casquete, R. Development of Supercritical Technology to Obtain Improved Functional Dietary Fiber for the Valorization of Broccoli By-product. J. Sci. Food Agric. 2025, 105, 2203–2214. [Google Scholar] [CrossRef]
- Shah, M.A.; Tariq, S.; Abuzar, S.M.; Ilyas, K.; Qadees, I.; Alsharif, I.; Anam, K.; Almutairi, R.T.; Al-Regaiey, K.A.; Babalghith, A.O.; et al. Peel Waste of Citrus Fruits: A Valuable and Renewable Source of Polyphenols for the Treatment of Diabesity. Curr. Res. Biotechnol. 2024, 7, 100204. [Google Scholar] [CrossRef]
- Wang, S.; Feng, Y.; Yu, X.; Yang, Z.; Jiao, P.; Niu, Q. Integrated Deep Eutectic Solvent Extraction and Resin Adsorption for Recovering Polyphenols from Citrus reticulata Blanco Peels: Process Optimization, Compositional Analysis, and Activity Determination. Sep. Purif. Technol. 2025, 355, 129560. [Google Scholar] [CrossRef]
- Marchetti, F.; Gugel, I.; Costa, S.; Baldisserotto, A.; Foletto, A.; Gugel, I.; Baldini, E.; Manfredini, S.; Vertuani, S. A Sustainable Approach to Valuable Polyphenol and Iridoid Antioxidants from Medicinal Plant By-Products. Antioxidants 2024, 13, 1014. [Google Scholar] [CrossRef] [PubMed]
- Rocchetti, G.; Blasi, F.; Montesano, D.; Ghisoni, S.; Marcotullio, M.C.; Sabatini, S.; Cossignani, L.; Lucini, L. Impact of Conventional/Non-Conventional Extraction Methods on the Untargeted Phenolic Profile of Moringa oleifera Leaves. Food Res. Int. 2019, 115, 319–327. [Google Scholar] [CrossRef] [PubMed]
- Armenta, S.; Garrigues, S.; Esteve-Turrillas, F.A.; De La Guardia, M. Green Extraction Techniques in Green Analytical Chemistry. TrAC Trends Anal. Chem. 2019, 116, 248–253. [Google Scholar] [CrossRef]
- Coşkun, N.; Sarıtaş, S.; Bechelany, M.; Karav, S. Polyphenols in Foods and Their Use in the Food Industry: Enhancing the Quality and Nutritional Value of Functional Foods. Int. J. Mol. Sci. 2025, 26, 5803. [Google Scholar] [CrossRef]
- Kammerer, D.R.; Kammerer, J.; Valet, R.; Carle, R. Recovery of Polyphenols from the By-Products of Plant Food Processing and Application as Valuable Food Ingredients. Food Res. Int. 2014, 65, 2–12. [Google Scholar] [CrossRef]
- Bai, T.; Wang, X.; Du, W.; Cheng, J.; Zhang, J.; Zhang, Y.; Klinjapo, R.; Asavasanti, S.; Yasurin, P. Recent Advances, Challenges, and Functional Applications of Natural Phenolic Compounds in the Meat Products Industry. Antioxidants 2025, 14, 138. [Google Scholar] [CrossRef]
- Benito-González, I.; López-Rubio, A.; Martínez-Abad, A.; Ballester, A.-R.; Falcó, I.; González-Candelas, L.; Sánchez, G.; Lozano-Sánchez, J.; Borrás-Linares, I.; Segura-Carretero, A.; et al. In-Depth Characterization of Bioactive Extracts from Posidonia Oceanica Waste Biomass. Mar. Drugs 2019, 17, 409. [Google Scholar] [CrossRef]
- Galante, M.; Brassesco, M.E.; Maragoni Santos, C.; Beres, C.; Fai, A.E.C.; Cabezudo, I. Grape Pomace as a Natural Source of Antimicrobial Agents for Food Preservation. Front. Nutr. 2025, 12, 1650450. [Google Scholar] [CrossRef]
- Yilmaz, Y.; Toledo, R.T. Major Flavonoids in Grape Seeds and Skins: Antioxidant Capacity of Catechin, Epicatechin, and Gallic Acid. J. Agric. Food Chem. 2004, 52, 255–260. [Google Scholar] [CrossRef] [PubMed]
- Di Stefano, V.; Buzzanca, C.; Melilli, M.G.; Indelicato, S.; Mauro, M.; Vazzana, M.; Arizza, V.; Lucarini, M.; Durazzo, A.; Bongiorno, D. Polyphenol Characterization and Antioxidant Activity of Grape Seeds and Skins from Sicily: A Preliminary Study. Sustainability 2022, 14, 6702. [Google Scholar] [CrossRef]
- Rajasekharan, R.; Paul, S.A.; Madhavan, A.; Sindhu, R.; Binod, P.; Awasthi, M.K.; Pandey, A. Green Strategies for Extraction of Nanocellulose from Agricultural Wastes—Current Trends and Future Perspectives. In Green Sustainable Process for Chemical and Environmental Engineering and Science; Elsevier: Amsterdam, The Netherlands, 2023; pp. 269–288. ISBN 978-0-323-95156-2. [Google Scholar]
- Duarte, P.F.; Chaves, M.A.; Borges, C.D.; Mendonça, C.R.B. Avocado: Characteristics, Health Benefits and Uses. Ciênc. Rural 2016, 46, 747–754. [Google Scholar] [CrossRef]
- Zuo, X.; Gu, Y.; Wang, C.; Zhang, J.; Zhang, J.; Wang, G.; Wang, F. A Systematic Review of the Anti-Inflammatory and Immunomodulatory Properties of 16 Essential Oils of Herbs. Evid. Based Complement. Alternat. Med. 2020, 2020, 8878927. [Google Scholar] [CrossRef]
- Chagas, M.D.S.S.; Behrens, M.D.; Moragas-Tellis, C.J.; Penedo, G.X.M.; Silva, A.R.; Gonçalves-de-Albuquerque, C.F. Flavonols and Flavones as Potential anti-Inflammatory, Antioxidant, and Antibacterial Compounds. Oxid. Med. Cell. Longev. 2022, 2022, 9966750. [Google Scholar] [CrossRef]
- Belgacem, I.; Li Destri Nicosia, M.G.; Pangallo, S.; Abdelfattah, A.; Benuzzi, M.; Agosteo, G.E.; Schena, L. Pomegranate Peel Extracts as Safe Natural Treatments to Control Plant Diseases and Increase the Shelf-Life and Safety of Fresh Fruits and Vegetables. Plants 2021, 10, 453. [Google Scholar] [CrossRef]
- Jang, H.-J.; Lee, H.-J.; Yoon, D.-K.; Ji, D.-S.; Kim, J.-H.; Lee, C.-H. Antioxidant and Antimicrobial Activities of Fresh Garlic and Aged Garlic By-Products Extracted with Different Solvents. Food Sci. Biotechnol. 2018, 27, 219–225. [Google Scholar] [CrossRef]
- Tresserra-Rimbau, A.; Lamuela-Raventos, R.M.; Moreno, J.J. Polyphenols, Food and Pharma. Current Knowledge and Directions for Future Research. Biochem. Pharmacol. 2018, 156, 186–195. [Google Scholar] [CrossRef] [PubMed]
- Mourtzinos, I.; Goula, A. Polyphenols in Agricultural Byproducts and Food Waste. In Polyphenols in Plants; Elsevier: Amsterdam, The Netherlands, 2019; pp. 23–44. ISBN 978-0-12-813768-0. [Google Scholar]
- Saini, R.K.; Khan, M.I.; Kumar, V.; Shang, X.; Lee, J.-H.; Ko, E.-Y. Bioactive Compounds of Agro-Industrial By-Products: Current Trends, Recovery, and Possible Utilization. Antioxidants 2025, 14, 650. [Google Scholar] [CrossRef]

| Industrial Application Area | Experiment Area | Phenolic Compound Byproduct Source | Type of Phenolic Compound | Type of Extraction Method | Bioactivity and Results of Applications | Reference |
|---|---|---|---|---|---|---|
| Food Industry | Syrup production Food additives in biscuits | Date palm and seed extract Date seed powder | Flavonoids Anthocyanins | Microwave-assisted extraction method | Increase in antioxidant activity The dose of sample affected the texture as hardness Balance in taste and texture Enhancement in nutritional value | [204,205] |
| Fortification in yogurt (0.5%, 1.0%, and 1.5%) | Ginger peel extracts | Gingerol Anthocyanins Flavonoids | Ultrasound-assisted extraction Conventional solvent extraction using hot water, 80% ethanol, and 100% ethanol | Yogurt samples that are fortified with 1.5% ginger peel extracts enhanced the antioxidant activity Increase in water-holding capacity Increase in stability of pH Fortified yogurts exhibited darker colors due to higher phenolic content Microbiological tests that were carried out with S. thermophilus and L. bulgaricus resulted in longer shelf life potential with suppressed yeast and mold formation | [206,207] | |
| Jelly gummy | Pomegranate peel extracts | Punicalagin (both α and β form) Ellagic acid Gallic acid Coumaric acid Catechin Protocatechuic acid Chlorogenic acid Epicatechin Caffeic acid 4-Hydroxybenzaldehyde Benzoic acid Ferulic acid Quercetin | Conventional solid–liquid extraction | Bioavailability enhancement Increased firmness in texture Similar hardness between samples | [208] | |
| Investigation of bioavailability enhancement using plasma-activated water method | Sweet orange peels | Benzoic acid Ferulic acid Caffeic acid Myricetin 3,5,6,7,4′-pentamethoxyflavone 3,5,6,7,3′,4′-hexamethoxyflavone Naringin Protocatechuic acid Apigenin Naringenin Hesperidin Hesperetin Flavonoids Narirutin Tannins Sinapinic acid Isovanillic acid 4-coumaric acid Tangeretin Neohesperidin | Plasma-activated water method | Decrease in unwanted compounds, which increased the bioavailability | [209,210] | |
| Raw ground beef patties | Acacia bark and leaves | Flavonols, Proanthocyanidins Bioflavonoids/polyflavonoids Hydrolyzable tannins Hydroxybenzoic acids Hydroxycinnamic acids Dihydrochalcones Abundantly: Epicatechin p-coumaroyltrifolin B Procyanidin B5 (−)-epigallocatechin Procyanidin C1 | Conventional solid–liquid extraction | Both samples exhibited an increase in shelf life and stability Higher antioxidant capacity Reduction in color deterioration Reduction in lipid peroxidation | [211] | |
| Investigation of encapsulation efficiency with lactose crystals | Cheese whey and maize inflorescences | Chlorogenic acid Maysin | Hot-aqueous extraction and encapsulation | Increasement in antioxidant capacity, stability, and bioavailability Protection from degradation | [212] | |
| Investigation of effect in bioavailability | Posidonia oceanica (seagrass) | Flavonoids Stilbenes Coumarins Tannins Lignans | Solid–liquid extraction | Antifungal activity against Penicillium italicum, Botrytis cinerea, Penicillium digitatum, Penicillium expansum, Aspergillus niger, and Geotrichum candidum Antiviral activity against murine norovirus and feline calicivirus Potential in food preservation | [213] | |
| Human keratinocytes HaCaT cells | Blueberry pomace | Cyanidin-3-glucoside Quercetin-3-glucoside | Ultrasound-assisted extraction | High antioxidant activity Preservation of HaCaT cells from oxidative stress Developmental potential as food additives | [214] | |
| Cosmetic Applications | Investigation with NADES extraction process to enhance bioavailability | Hazelnut skin and shell | (−)-epicatechin (+)-catechin Phloridzin Quercetin-3-O-rhamnoside Myricetin-3-O-rhamnoside | NADES extraction | Protection against UV-induced damage Enhancement in photostability Antioxidant and skin-healing properties Promoter in process of inhibition of lipid peroxidation and the aging process | [215] |
| Investigation with antibiotics (β-lactams, amphenicols, tetracyclines, and quinolones) | Grape pomace | Catechins Resveratrol Gallic acid | Solid–liquid extraction Supercritical Fluid extraction Ultrasound-assisted extraction Microwave-assisted extraction Enzyme-assisted High-Voltage Electric Discharge Ohmic Heating High-Pressure Processing Deep Eutectic Solvents (DESs) | Inhibition of antibacterial enzymes, including peroxidase, lactase, pectinases, xylanases, and cellulases Antimicrobial properties against E. coli, S. Typhimurium, S. aureus, P. aeruginosa, and L. monocytogenes Synergistic effect on the inhibition of S. aureus and E. coli Potential as cosmeceuticals and nutraceuticals by inhibiting Cutibacterium acnes, as well as reducing inflammation and redness | [216,217,218,219] | |
| Investigation of their effect on food quality and methodology efficiency | Date seed powder | Protocatechuic acid p-hydroxybenzoic acid Vanillic acid Syringic acid Caffeic acid Coumaric acid Ferulic acid p-hydroxycinnamic acid Chlorogenic acid Quercetin-3-O-glucoside Catechin Procyanidin Anthocyanins Proanthocyanidins | Conventional solvent extraction | Strong antioxidant activity Potential to enhance food quality as food additives and functional oils | [220] | |
| Investigation into bioavailability and potential applications | Olive byproducts | Hydroxytyrosol Tyrosol Oleuropein Caffeic acid Rutin Resveratrol Catechins | Ultrasound-assisted extraction Microwave-assisted extraction Enzyme-assisted extraction Supercritical Fluid extraction Pressurized Liquid extraction Ohmic Heating Pulsed Electrical Field | Potential as natural antioxidants in food, oil, and beverages Sustainable biomass waste sources | [221,222] | |
| Investigation into bioavailability and potential applications | Wine byproducts | Hydroxytyrosol Tyrosol Oleuropein Caffeic acid Rutin Resveratrol Catechins | Ultrasound-assisted extraction Microwave-assisted extraction Enzyme-assisted extraction Supercritical Fluid extraction Pressurized Liquid extraction Ohmic Heating Pulsed Electrical Field | UV-protectant and anti-aging properties Sustainable biomass waste sources Natural antioxidants | [221,223] | |
| Pharmaceutical and Health Applications | Investigation on bioactivity | Cacao bean shells | Quercetin Kaempferol Proanthocyanidins | Microwave-assisted extraction Ultrasound-assisted extraction | Rich phenolic content Antimicrobial activity against S. mutans 7-methylxanthine metabolite did not exhibit inhibitory effect against S. mutans alone | [224,225] |
| Investigation into bioactivity and potential health applications | Persimmon byproducts | Gallic acid Quercetin | Solid-assisted extraction | Antimicrobial activities: Inhibition of E. coli and biofilm activity Synergistic effect with gentamicin against S. aureus Potential candidate by inhibiting bacterial adhesion to HaCaT and Caco-2 cells Antiviral activity by inhibiting biofilm formation, blocking β-lactamase | [226,227] | |
| Investigation of bioactivity and effect of using a DES extraction–resin adsorption system | Grape pomace | Quercetin-3-O-rutinoside Quercetin-O-pentoside Myricetin-O-rutinoside Gallic acid Caffeic acid Syringic acid Vanillic acid Chlorogenic acid p-coumaric acid Petunidin-rutinoside Malvidin-rutinoside β-Type (epi)catechin tetramer Quercetin-glucuronide p-coumaric acid Malvidin-3-O-glucoside Malvidin-3-O-(p-coumaroyl)glucoside (+)-catechin (−)-epicatechin Syringic acid (−)-gallocatechin | Solid–liquid extraction Supercritical Fluid extraction Ultrasound-assisted extraction Microwave-assisted extraction Enzyme-assisted High-Voltage Electric Discharge Ohmic Heating High-Pressure Processing Deep Eutectic Solvents (DESs) | Improving lipid profiles that are effective for cardiovascular diseases Being able to preserve their antioxidant and α-glucosidase with DES extraction–resin adsorption system | [228] | |
| In vitro study with Vero cells and HepG-2 liver cells | Mango peel extract | Gallic acid Chlorogenic acid | * | Antimicrobial activity against S. aureus and S. mutans Antiviral activity adenovirus-7 and HSV-1 Cytotoxicity effect against HepG-2 liver cancer cells | [229] | |
| Investigation into bioactivity | Avocado seed powder | Quercetin Gallic acid | Conventional solid–liquid extraction | Antimicrobial activity against E. coli, S. aureus, Salmonella spp., P. aeruginosa, and C. albicans Anti-inflammatory activity against TNF-α, IL-6, and IL-1β pathways and COX-2 and iNOS enzymes | [230] | |
| Investigation into bioactivity | Cherry seed | Caffeic acid Ferulic acid Gallic acid Protocatechuic acid | Conventional solid–liquid extraction Ultrasound-assisted extraction Enzyme-assisted extraction Supercritical Fluid extraction | Modulation of lipid metabolism and insulin sensitivity Promote glucose utilization Contribution to glucose intake | [231,232,233] | |
| Investigation into bioactivity | Longan fruit | Proanthocyanidins Phenolic acids | Ultrasound-assisted extraction Enzyme-assisted extraction Microwave-assisted extraction | High antioxidant and anti-inflammatory activities Potential candidates against NAFD and obesity | [234] | |
| In vivo experiment with d-galactose-induced aging mice | Walnut oil process byproducts | Procyanidin dimer B2 isomer I Procyanidin dimer B1 isomer II Malvidin hexoside Malvidin Coumaroyl-hexoside Petunidin hexoside (−)-epicatechin Quercetin Glucuronide Myricetin Rhamnoside (+)-catechin (iso)-rhamnetin Myricetin | Conventional solid–liquid extraction | Restore in antioxidant and SOD activity with WKP hydrolysates Improvement in liver and kidney tissue morphology Reduction in MDA concentration Reduction in expression of SREBP-1c by pretreatment of malvidin hexosides | [235] | |
| In vitro study to investigate the potential in joint disorders using macrophage- and chondrocyte-like cell lines | Hemp leaf | Cannabinoids Flavonoids | Heat-reflux extraction | Reduction in symptoms of osteoarthritis Improvement in joint function | [236] | |
| In vivo study for investigation of their antidiabetic activity | Pomegranate tree (Punica granatum) bark | Flavonoids Phenolic acids Tannins | Soxhlet extraction | Inhibition of α-glucosidase and α-amylase | [237] | |
| Investigation into sustainable methods to evaluate bioactivity | Garlic byproducts | Flavonoids | Supercritical Fluid extraction | No significant improvement observed Lack of standardization and material assessment | [238,239] | |
| Sustainable Materials and Packaging | Investigation into their bioactivities in cooked chicken noodle | Mango, papaya and loquat byproducts | - In mango: Mangiferin Catechin Quercetin Kaempferol Rhamnetin Anthocyanins Gallic acid Ellagic acid Propyl gallate Methyl gallate Benzoic acid Protocatechuic acid - In loquat: 3-p-coumaroylquinic acid Caffeoylquinic acid 5-feruloylquinic acid Quercetin Kaempferol derivatives, including galactoside, glucoside, and rhamnoside - In papaya: Ferulic acid Mandelic acid Syringic acid Vanillic acid Myricetin Conifer aldehyde | Conventional solid–liquid extraction | Strongest antioxidant activity in mango seed extracts Higher phenolic content in seed extracts than peel extracts Better color maintenance in mango seed extracts Reduction in lipid and protein oxidation in mango peel extracts Partial effect of papaya and loquat extracts in reduction in lipid and protein oxidation | [240] |
| Investigation into their potential in food-packaging industry using polyphenols and citric acid | Poplar bark and veneer | * | Chemical-assisted solid–liquid extraction | Resulted in high antioxidant activity, mechanical resistance, and bonding properties | [241] |
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2026 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.
Share and Cite
Demir, R.; Sarıtaş, S.; Bechelany, M.; Karav, S. Polyphenols from Byproducts: Their Applications and Health Effects. Antioxidants 2026, 15, 87. https://doi.org/10.3390/antiox15010087
Demir R, Sarıtaş S, Bechelany M, Karav S. Polyphenols from Byproducts: Their Applications and Health Effects. Antioxidants. 2026; 15(1):87. https://doi.org/10.3390/antiox15010087
Chicago/Turabian StyleDemir, Ranya, Sümeyye Sarıtaş, Mikhael Bechelany, and Sercan Karav. 2026. "Polyphenols from Byproducts: Their Applications and Health Effects" Antioxidants 15, no. 1: 87. https://doi.org/10.3390/antiox15010087
APA StyleDemir, R., Sarıtaş, S., Bechelany, M., & Karav, S. (2026). Polyphenols from Byproducts: Their Applications and Health Effects. Antioxidants, 15(1), 87. https://doi.org/10.3390/antiox15010087

