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Abstract

Flavonoids are a diverse group of plant derived polyphenolic compound that exhibit a wide range of biological activities, making them a focus of extensive research in recent years. This review explores the multifunctional properties of flavonoids, including their antioxidant, anti-inflammatory, anticancer, antimicrobial and cardioprotective effects. Furthermore, it empathizes how flavonoids can help prevent chronic illnesses like diabetes, cardiovascular disease and neurological diseases. These through analysis emphasizes how flavonoids are used in both nutrition and medicine.

Keywords

Flavonoids, Antioxidants, Cardioprotective, Anti-cancer, antiviral, anti-bacterial, antiaging.

Introduction

A particular class of plant organs, including leaves, fruits, roots, and stems can accumulate polyphenols, which are chemical products of secondary plant metabolism. They are broad class of bioactive compounds with the variety of biological roles. All vascular plants contain flavonoids, which are phenolic compounds  (Karak, 2019). They have several beneficial biochemical and antioxidant properties linked to a number of illnesses, including atherosclerosis, cancer, and Alzheimer’s diseases. Flavonoids are a vital part of many pharmacological, cosmetic, nutraceutical and medicinal applications and are associated with a variety of health advantages. This is due to their ability to modify important cellular enzyme functions as well as their antioxidative, anti-inflammatory, anti-mutagenic, and anti-carcinogenic qualities. They are also known to be potent inhibitors of certain enzymes, such as xanthine oxidase (XO), lipoxygenase, cyclo-oxygenase and phosphoionositide 3-kinase (A.N.Panche, 2016). In 1930, a Hungarian scientist named Albert Szent-Gyorgyino conducted an experiment that resulted in the discovery of flavonoids using a novel chemical that was extracted from orange. It was initially categorized as vitamin P, but later on, researchers determined that it was actually a flavonoid. Other types have also been found. Amidst scientific and human evidence demonstrating its range of biological and therapeutic effects. The flavonoids category has emphasized its significance since this historical event. Over 8,000 distinct flavonoids have been identified to date. They belong to a class of polyphenolic chemicals with low molecular weights. Their primary classes fall under a variety of names, including anthocyanins, isoflavones, flavonols, flavones and flavanones (Juca, 2018). Plants naturally produce flavonoid compounds, which are found in different parts of the plant. Vegetables use flavonoids to promote growth and defend against plaques. These low molecular weight phenolic chemicals are abundantly distributed across the plant world. They are a key class of chemicals found in higher plants. Many flavonoids are easily identified as floral colours in most angiosperm families. However, they can be found in all parts not just flowers. The term ‘dietary flavonoids’ refer to the abundance of flavonoids found in plant-based foods and drinks, including fruits, vegetables, tea, chocolate and wine. Flavonoids functions as UV filters, signal molecules, allopathic compounds and protective agent against biotic and abiotic stress in plants, phytoalexins, detoxifying agents, and antimicrobial defence compounds. Flavonoids can improve cold hardiness, drought resistance, plant heat acclimatization and freezing tolerance (A.N.Panche, 2016). Because of their strong antioxidant potential in both in vitro and in vivo systems, flavonoids are believed to have health promoting qualities. Flavonoids can activate the enzyme systems that protect humans (kumar, 2013). The extraction, isolation, and characterization of these compounds from various plant families has been the focus of recent research. This has led to the focus of recent research. This has led to the development of modern, environmental friendly extraction techniques, such as microwave-assisted extraction, ultrasound-assisted extraction, supercritical fluid extraction, pressurized liquid extraction, matrix solid phase dispersion, pulsed electric field extraction and enzyme-assisted extraction which may also have industrial applicability in a number of sectors, including the food, pharmaceutical, and cosmetic industries. Traditional extraction methods, such as maceration, decoction, percolation, and Soxhlet extraction have been replaced by these techniques (liga, 2023)

Biological Activities of Flavonoids:

In addition to their primary antioxidant function, flavonoids have a wide range of biological actions that contribute to human heath. These include anti-inflammatory, anti-ulcer, antiviral, anti-cancer, anti-diabetic, and cytotoxic properties, among others (Karak, 2019).

Antioxidant Activity:

Numerous investigations have demonstrated the wide ranging nutritional benefits of flavonoids to antioxidant activity. The majority of chemical tests for antioxidants demonstrate pathways for scavenging free radicals. Reactive chemical substances called antioxidant shield cells in plants, animals, and humans from the harm that reactive oxygen species (ROS) can cause. One of the finest phytochemicals for preventing disease is flavonoids, which function as antioxidants. The configuration of functional groups in the flavan nucleus determines antioxidant activity (Karak, 2019). Direct scavenging of ROS, (b) inhibition of ROS formation through the chelation of trace elements (quercetin for example, has iron-chelating and iron stabilizing properties) or inhibition of the enzyme involved in the production of free radicals (such as glutathione S-transferase, microsomal monooxygenase, mitochondrial succinoxidase, NADH oxidase, xanthine oxidase) are some of the antioxidant action mechanisms of flavonoids and (c) activation of antioxidant. A combination of some of these processes, such as radical scavenging action and enzyme activity suppression, may also occur. The majority of flavonoids appear as glycosides, and the number and position of sugar linkages influence the flavonoids antioxidant effects. Aglycone forms, on the other hand, are less readily available despite having a greater antioxidant capability (dias, 2021).

Anti-inflammatory Activity:

The intricate biological reactions of bodily tissues to damaging stimuli, including pathogens infection, damaged cells, tissue injury, and chemical irritation, is known as inflammation. It is a defence mechanism that includes blood vessels, immune cells and molecular mediators. The release of chemical mediators at the site of tissue damage and the migration of immune cells from blood vessels start this. Leukaemia sepsis, asthma, sclerosis, atherosclerosis, porosis, allergic rhinitis illnesses, colitis, rheumatoid arthritis and other conditions have been linked to flavonoids crucial involvement in inflammation. In order to eradicate invading pathogens and heal damaged tissues, this  process is followed by the recruitment of inflammatory cells and the release of ROS, RNS and proinflammatory cytokines (Karak, 2019).

Anti-bacterial Activity:

Flavonoids have the ability to combat germs through a variety of techniques. By causing bacterial membrane disruption, they can break lipid bilayers and prevent a number of functions, including the generation of ATP cells envelopes, biofilms, nucleic acids, and electron transfer chains. Catechin epicatechin and epigallocatechin galatte, as well as the flavonol  quercetin, appears to cause an oxidative burst, which raises the generation of ROS and damages the permeates membranes. Apigenin can break down the structure of membranes and result in membrane leakage by disorganizing and confounding the membrane lipids. While quercetin, luteolin, myricetin, and baicalein prevents bacterial DNA replication,  flavonoids such as apigenin, chrysin, naringenin, kaempferol, quercetin, daidzein, and geninstein disrupt the formation of biofilms (dias, 2021).

Antiaging Activity:

The effect of oxidative damage, which is caused by macromolecules like carbohydrates, DNA, proteins, and lipids that gradually build up in the cells, is one of the cause of aging. This buildup result from the body’s normal metabolic processes, which generate waste products that the body can’t always properly get rid of as we age. According to a study the high polyphenolic content of acai pulp has a high capacity to eliminate superoxide and peroxyl radicals, indicating antiaging properties. flavonoids with their antioxidant capacity, may represent a viable source of elimination of this metabolic waste. Drinking red wine has also been linked to a lower risk of developing age related illnesses (Juca, 2018).

Anticancer Activity:

The potential anti cancer property of flavonoids, which are found in fruit, fruit juices, and vegetables have been well investigated. For example cranberry juice is widely drunk in North America because of its ability to prevent urinary tract infections, which is mostly attributed to cranberry protocyanidins. Phenolic substances found in cranberry fruit include triterpenoids, a range of phenolic acids, the most important of which is p-hydroxycinamic acid, catechins flavan-3-ols, and flavonoids (flavonols and protoanthrocyanidins). Cranberry extracts have been found to prevent oxidative damage to neurons, vascular endothelium, and LDL oxidation based on preliminary research. Cranberry extracts are therefore seen to be a promising candidate for anti-tumor activity due to their antioxidant properties (Atmani, 2009).

Antiviral Activity:

Since the 1914s and many reports show that naturally occurring flavonoids exhibit a remarkable antiviral activity. They aid in the Suppression of several enzymes involved in the viral life cycle. It has been noted how flavonoids structural and functional relationships relate to their ability to inhibit enzymes.  Flavon-3-ol was found to be more effective than flavones and flavonones in selective inhibition of  HIV-1 & HIV-2 and similar immunodeficiency virus causing infections. The different study show that quercetin, hesperetin, and naringin also possess anti dengue activity (Karak, 2019).

CONCLUSION

It is well recognised that phytochemical substances, particularly flavonoids can be used to prevent and cure diseases. Fruits and vegetables naturally contain flavonoids. These phytochemicals, known as flavonoids, have a variety of biological characteristics that are advantageous to human health. In human diets, they are abundant in naturally occurring antioxidants. flavonoids help prevent numerous diseases by effectively counteracting the negative effect of free radicals. Antioxidant, free radicals scavenger, anti inflammatory, anti bacterial, antiviral, antiaging and particularly anti-cancer capabilities are only a few of the many cellular targets they interact with. The dietary sources and several significant biological activity of flavonoids that contribute to their positive effects on human health are highlighted in this review. Their industrial uses extend beyond the realm of therapeutic candidate compounds and nutraceuticals.

REFERENCES

  1. Fernandez SP, Wasowski C, Loscalzo LM, Granger RE, Johnston GAR, Paladini AC and Marder M: Central nervous system depressant action of flavonoid glycosides. European Journal of Pharmacology 2006; 539: 168-176.
  2. Burak M & Imen Y (1999) Flavonoids and their antioxidant properties. Turkiye Klin Tip Bil Derg 19, 296-304.
  3. Ovando C, Hernandez D, Hernandez E, et al. (2009) Chemical studies of anthocyanins: a review. Food Chem 113, 859–871.
  4. Lee Y, Yuk D, Lee J, et al. (2009) Epigallocatechin-3-gallate prevents lipopolysaccharide-induced elevation of β-amyloid generation and memory deficiency. Brain Res 1250, 164–174.
  5.  Metodiewa D, Kochman A & Karolczak S (1997) Evidence for antiradical and antioxidant properties of four biologically active N, N, diethylaminoethyl ethers of flavanone oximes: a comparison with natural polyphenolic flavonoid (rutin) action. Biochem Mol Biol Int 41, 1067-1075.
  6. Hayashi T, Sawa K, Kawasaki M, et al. (1988) Inhibition of cow’s milk xanthine oxidase by flavonoids. J Nat Prod 51, 345–348.
  7. Walker E, Pacold M, Perisic O, et al. (2000) Structural determinations of phosphoinositide 3-kinase inhibition by wortmannin, LY294002, quercetin, myricetin, and staurosporine. Mol Cell 6, 909–919.
  8. Kumar S, Pandey A. 2013. Chemistry and biological activities of C. longa. Trends Food Sci Technol. 2013:533–548.
  9. Nijveldt RJ, van Nood E, van Hoorn DE, Boelens PG, van Norren K, van Leeuwen PA. 2001. Flavonoids: a review of probable mechanisms of action and potential applications. Am J Clin Nutr. 74:418–425.
  10. van Acker SABE, Van Den Berg D, Tromp MNJL, Griffioen DH, Van Bennekom WP, Van Der Vijgh WJF, Bast A. 1996. Structural aspects of antioxidant activity of flavonoids. Free Radic Biol Med. 20:331–342.
  11. Havsteen B (2002) The biochemistry and medical significance of the flavonoids. Pharmacol Ther 96, 67–202.
  12. Dewick PM (2001) The shikimate pathway: aromatic amino acids and phenylpropanoids. In Medicinal Natural Products: a Biosynthetic Approach, 2nd ed., pp. 137–186 [PM Dewick, editor]. Chichester: John Wiley.
  13. Griesbach R (2005) Biochemistry and genetics of flower color. Plant Breed Rev 25, 89–114.
  14. Takahashi A & Ohnishi T (2004) The significance of the study about the biological effects of solar ultraviolet radiation using the exposed facility on the international space station. Biol Sci Space 18, 255–260.
  15. Samanta A, Das G & Das S (2011) Roles of flavonoids in plants. Int J Pharm Sci Tech 6,12–35.
  16. N. C. Cook and S. Samman, “Review: flavonoids-chemistry, metabolism, cardioprotective effects and dietary sources,” Journal of Nutritional Biochemistry, vol. 7, no. 2, pp. 66–76, 1996.
  17. C. A. Rice-Evans, N. J. Miller, P. G. Bolwell, P. M. Broamley, and J. B. Pridham, “The relative antioxidant activities of plant derived polyphenolic flavonoids,” Free Radical Research, vol. 22, no. 4, pp. 375–383, 1995.
  18. Dias, M.C.; Pinto, D.C.G.A.; Silva, A.M.S. Plant Flavonoids: Chemical Characteristics and Biological Activity. Molecules 2021, 26, 5377. [CrossRef] [PubMed]
  19. Tzanova, M.; Atanasov, V.; Yaneva, Z.; Ivanova, D.; Dinev, T. Selectivity of Current Extraction Techniques for Flavonoids from Plant Materials. Processes 2020, 8, 1222. [CrossRef]
  20. Chávez-González, M.L.; Sepúlveda, L.; Verma, D.K.; Luna-García, H.A.; Rodríguez-Durán, L.V.; Ilina, A.; Aguilar, C.N. Conventional and Emerging Extraction Processes of Flavonoids. Processes 2020, 8, 434. [CrossRef]
  21. Vessal M, Hemmati M and Vasei M: Antidiabetic effects of quercetin in streptozocin-induced diabetic rats. Comp Biochem Physiol 2003; 135: 357-364.
  22. Ghasemzadeh A and Jaafar HZE: Anticancer and antioxidant activities of young Malaysian ginger (Zingiber officinale Roscoe) varieties grown under different CO2 concentration. Jour. Med. Plant Res 1986; 5:3247-3255.
  23. Zhang J, Wu Y and Zhao X: Chemopreventive effect of flavonoids from Ougan (Citrus reticulata cv. Suavissima) fruit against cancer cell proliferation and migration. J Funct Foods 2014; 10: 511-519.
  24. Kelly EH, Anthony RT and Dennis JB: Flavonoid antioxidants: Chemistry, metabolism and structure-activity relationships. Nutri.Biochem 2002; 13(10): 572-584.
  25. Kukic J, Petrovic C and Niketic: Antioxidant activity of four endemic Stachys taxa. Biol Pharmaceut Bull 2006; 29: 725-729.
  26. Kumar, S.; Pandey, A.K. Chemistry and biological activities of flavonoids: An Overview. Sci. World J. 2013, 2013, 162750.[CrossRef] [PubMed]
  27. Agrawal, A.D. Pharmacological activity of flavonoids: A Review. Int. J. Pahrmaceut. Sci. Nano 2011, 4, 1394–1398 [CrossRef]
  28. Sandoval, V.; Sanz-Lamora, H.; Arias, G.; Marrero, P.F.; Haro, D.; Relat, J. Metabolic impact of flavonoids consumption in obesity: From central to peripheral. Nutrients 2020, 12, 2393. [CrossRef] [PubMed]
  29. Kaleem, M.; Ahmad, A. Flavonoids as nutraceuticals. In Therapeutic, Probiotic, and Unconventional Foods; Grumezescu, M.A., Holban, A.M., Eds.; Academic Press: Cambridge, MA, USA, 2018; pp.137–155. [CrossRef]
  30. Pan MH, Lai CS and Ho CT: Anti-inflammatory activity of natural dietary flavonoids. Food and Function 2010; 1(1): 15-31.
  31. Jucá, M.M.; Filho, F.M.S.C.; de Almeida, J.C.; Mesquita, D.S.; Barriga, J.R.M.; Dias, K.C.F.; Barbosa, T.M.; Vasconcelos, L.C.; Leal, L.K.A.M.; Ribeiro, J.R.; et al. Flavonoids: Biological activities and therapeutic potential. Nat. Prod. Res. 2020, 5, 692–705.[CrossRef]
  32. Górniak, I.; Bartoszewski, R.; Króliczewski, J. Comprehensive review of antimicrobial activities of plant flavonoids. Phytochem. Rev. 2019, 18, 241–272. [CrossRef]
  33. Fathima, A.; Rao, J.R. Selective toxicity of Catechin—a natural flavonoid towards bacteria. Appl. Microbiol. Biotechnol. 2016, 100, 6395–6402. [CrossRef]
  34. Xu, X.; Zhou, X.D.; Wu, C.D. Tea catechin epigallocatechin gallate inhibits Streptococcus mutans biofilm formation by suppressing gtf genes. Arch. Oral Biol. 2012, 57, 678–683. [CrossRef]
  35. Vasconcelos SML, Goulart MOF, Moura JBDF, Manfredini V, Benfato MDS, Kubota LT. 2007. Especies reativas de oxigenio e de nitrogenio, antioxidantes e marcadores de dano oxidativo em sangue humano: Principais metodos anal?ticos para sua determinacao. Quim Nova. 30:1323–1338.
  36. Mamede MEDO, Pastore GM. 2004. Compostos fenolicos do vinho: estrutura e acao antioxidante. B Ceppa. 22:233–252.
  37. Portinho JA, Zimmermann LM, Bruck MR. 2012. Efeitos Beneficos do Aca? Beneficial effects of aca?. Int J Nutrology. 5:15–20.
  38. Cerqueira F, Cordeiro-Da-Silva A, Araujo N, Cidade H, Kijjoa A, Nascimento MSJ. 2003. Inhibition of lymphocyte proliferation by prenylated flavones: artelastin as a potent inhibitor. Life Sci. 73:2321–2334.
  39. Neto CC. Cranberry and blueberry: Evidence for protective effects against cancer and vascular disease. Mol Nutr Food Res 2007; 51: 653-64.
  40. Porter ML, Krueger CG, Wiebe DA, Cunningham DG, Reed JD. Cranberry proanthocyanidins associate with low-density lipoprotein and inhibit in vitro Cu2+-induced oxidation. J Sci Food Agric 2001; 81: 1306-13.
  41. Neto CC, Sweeney-Nixon ML, Lamoureaux TL, Solomon F. Cranberry phenolics: Effects on oxidase processes, neuron cell death and tumor cell growth. Phenolic compounds in foods and natural health products. Washington, DC: ACS Books 2005; pp. 271-82.
  42. Youdim KA, McDonald J, Kalt W, Joseph JA. Potential role of dietary flavonoids in reducing microvascular endothelium vulnerability to oxidative and inflammatory insults. J Nutr Biochem 2002; 13: 282-88.
  43. Gerdin B and Srensso E: Inhibitory effect of the flavonoid on increased microvascular permeability induced by various agents in rat skin. International Journal of Microcirculation, Clinical and Experimental 1983; 2(1): 39-46.
  44.  Zandi K, Teoh BT, Sam SS, Wong PF, Mustafa MR and Abubakar S: Antiviral activity of four types of bioflavonoid against dengue virus type-2. Vir Jour 2011; 8: 560.

Reference

  1. Fernandez SP, Wasowski C, Loscalzo LM, Granger RE, Johnston GAR, Paladini AC and Marder M: Central nervous system depressant action of flavonoid glycosides. European Journal of Pharmacology 2006; 539: 168-176.
  2. Burak M & Imen Y (1999) Flavonoids and their antioxidant properties. Turkiye Klin Tip Bil Derg 19, 296-304.
  3. Ovando C, Hernandez D, Hernandez E, et al. (2009) Chemical studies of anthocyanins: a review. Food Chem 113, 859–871.
  4. Lee Y, Yuk D, Lee J, et al. (2009) Epigallocatechin-3-gallate prevents lipopolysaccharide-induced elevation of β-amyloid generation and memory deficiency. Brain Res 1250, 164–174.
  5.  Metodiewa D, Kochman A & Karolczak S (1997) Evidence for antiradical and antioxidant properties of four biologically active N, N, diethylaminoethyl ethers of flavanone oximes: a comparison with natural polyphenolic flavonoid (rutin) action. Biochem Mol Biol Int 41, 1067-1075.
  6. Hayashi T, Sawa K, Kawasaki M, et al. (1988) Inhibition of cow’s milk xanthine oxidase by flavonoids. J Nat Prod 51, 345–348.
  7. Walker E, Pacold M, Perisic O, et al. (2000) Structural determinations of phosphoinositide 3-kinase inhibition by wortmannin, LY294002, quercetin, myricetin, and staurosporine. Mol Cell 6, 909–919.
  8. Kumar S, Pandey A. 2013. Chemistry and biological activities of C. longa. Trends Food Sci Technol. 2013:533–548.
  9. Nijveldt RJ, van Nood E, van Hoorn DE, Boelens PG, van Norren K, van Leeuwen PA. 2001. Flavonoids: a review of probable mechanisms of action and potential applications. Am J Clin Nutr. 74:418–425.
  10. van Acker SABE, Van Den Berg D, Tromp MNJL, Griffioen DH, Van Bennekom WP, Van Der Vijgh WJF, Bast A. 1996. Structural aspects of antioxidant activity of flavonoids. Free Radic Biol Med. 20:331–342.
  11. Havsteen B (2002) The biochemistry and medical significance of the flavonoids. Pharmacol Ther 96, 67–202.
  12. Dewick PM (2001) The shikimate pathway: aromatic amino acids and phenylpropanoids. In Medicinal Natural Products: a Biosynthetic Approach, 2nd ed., pp. 137–186 [PM Dewick, editor]. Chichester: John Wiley.
  13. Griesbach R (2005) Biochemistry and genetics of flower color. Plant Breed Rev 25, 89–114.
  14. Takahashi A & Ohnishi T (2004) The significance of the study about the biological effects of solar ultraviolet radiation using the exposed facility on the international space station. Biol Sci Space 18, 255–260.
  15. Samanta A, Das G & Das S (2011) Roles of flavonoids in plants. Int J Pharm Sci Tech 6,12–35.
  16. N. C. Cook and S. Samman, “Review: flavonoids-chemistry, metabolism, cardioprotective effects and dietary sources,” Journal of Nutritional Biochemistry, vol. 7, no. 2, pp. 66–76, 1996.
  17. C. A. Rice-Evans, N. J. Miller, P. G. Bolwell, P. M. Broamley, and J. B. Pridham, “The relative antioxidant activities of plant derived polyphenolic flavonoids,” Free Radical Research, vol. 22, no. 4, pp. 375–383, 1995.
  18. Dias, M.C.; Pinto, D.C.G.A.; Silva, A.M.S. Plant Flavonoids: Chemical Characteristics and Biological Activity. Molecules 2021, 26, 5377. [CrossRef] [PubMed]
  19. Tzanova, M.; Atanasov, V.; Yaneva, Z.; Ivanova, D.; Dinev, T. Selectivity of Current Extraction Techniques for Flavonoids from Plant Materials. Processes 2020, 8, 1222. [CrossRef]
  20. Chávez-González, M.L.; Sepúlveda, L.; Verma, D.K.; Luna-García, H.A.; Rodríguez-Durán, L.V.; Ilina, A.; Aguilar, C.N. Conventional and Emerging Extraction Processes of Flavonoids. Processes 2020, 8, 434. [CrossRef]
  21. Vessal M, Hemmati M and Vasei M: Antidiabetic effects of quercetin in streptozocin-induced diabetic rats. Comp Biochem Physiol 2003; 135: 357-364.
  22. Ghasemzadeh A and Jaafar HZE: Anticancer and antioxidant activities of young Malaysian ginger (Zingiber officinale Roscoe) varieties grown under different CO2 concentration. Jour. Med. Plant Res 1986; 5:3247-3255.
  23. Zhang J, Wu Y and Zhao X: Chemopreventive effect of flavonoids from Ougan (Citrus reticulata cv. Suavissima) fruit against cancer cell proliferation and migration. J Funct Foods 2014; 10: 511-519.
  24. Kelly EH, Anthony RT and Dennis JB: Flavonoid antioxidants: Chemistry, metabolism and structure-activity relationships. Nutri.Biochem 2002; 13(10): 572-584.
  25. Kukic J, Petrovic C and Niketic: Antioxidant activity of four endemic Stachys taxa. Biol Pharmaceut Bull 2006; 29: 725-729.
  26. Kumar, S.; Pandey, A.K. Chemistry and biological activities of flavonoids: An Overview. Sci. World J. 2013, 2013, 162750.[CrossRef] [PubMed]
  27. Agrawal, A.D. Pharmacological activity of flavonoids: A Review. Int. J. Pahrmaceut. Sci. Nano 2011, 4, 1394–1398 [CrossRef]
  28. Sandoval, V.; Sanz-Lamora, H.; Arias, G.; Marrero, P.F.; Haro, D.; Relat, J. Metabolic impact of flavonoids consumption in obesity: From central to peripheral. Nutrients 2020, 12, 2393. [CrossRef] [PubMed]
  29. Kaleem, M.; Ahmad, A. Flavonoids as nutraceuticals. In Therapeutic, Probiotic, and Unconventional Foods; Grumezescu, M.A., Holban, A.M., Eds.; Academic Press: Cambridge, MA, USA, 2018; pp.137–155. [CrossRef]
  30. Pan MH, Lai CS and Ho CT: Anti-inflammatory activity of natural dietary flavonoids. Food and Function 2010; 1(1): 15-31.
  31. Jucá, M.M.; Filho, F.M.S.C.; de Almeida, J.C.; Mesquita, D.S.; Barriga, J.R.M.; Dias, K.C.F.; Barbosa, T.M.; Vasconcelos, L.C.; Leal, L.K.A.M.; Ribeiro, J.R.; et al. Flavonoids: Biological activities and therapeutic potential. Nat. Prod. Res. 2020, 5, 692–705.[CrossRef]
  32. Górniak, I.; Bartoszewski, R.; Króliczewski, J. Comprehensive review of antimicrobial activities of plant flavonoids. Phytochem. Rev. 2019, 18, 241–272. [CrossRef]
  33. Fathima, A.; Rao, J.R. Selective toxicity of Catechin—a natural flavonoid towards bacteria. Appl. Microbiol. Biotechnol. 2016, 100, 6395–6402. [CrossRef]
  34. Xu, X.; Zhou, X.D.; Wu, C.D. Tea catechin epigallocatechin gallate inhibits Streptococcus mutans biofilm formation by suppressing gtf genes. Arch. Oral Biol. 2012, 57, 678–683. [CrossRef]
  35. Vasconcelos SML, Goulart MOF, Moura JBDF, Manfredini V, Benfato MDS, Kubota LT. 2007. Especies reativas de oxigenio e de nitrogenio, antioxidantes e marcadores de dano oxidativo em sangue humano: Principais metodos anal?ticos para sua determinacao. Quim Nova. 30:1323–1338.
  36. Mamede MEDO, Pastore GM. 2004. Compostos fenolicos do vinho: estrutura e acao antioxidante. B Ceppa. 22:233–252.
  37. Portinho JA, Zimmermann LM, Bruck MR. 2012. Efeitos Beneficos do Aca? Beneficial effects of aca?. Int J Nutrology. 5:15–20.
  38. Cerqueira F, Cordeiro-Da-Silva A, Araujo N, Cidade H, Kijjoa A, Nascimento MSJ. 2003. Inhibition of lymphocyte proliferation by prenylated flavones: artelastin as a potent inhibitor. Life Sci. 73:2321–2334.
  39. Neto CC. Cranberry and blueberry: Evidence for protective effects against cancer and vascular disease. Mol Nutr Food Res 2007; 51: 653-64.
  40. Porter ML, Krueger CG, Wiebe DA, Cunningham DG, Reed JD. Cranberry proanthocyanidins associate with low-density lipoprotein and inhibit in vitro Cu2+-induced oxidation. J Sci Food Agric 2001; 81: 1306-13.
  41. Neto CC, Sweeney-Nixon ML, Lamoureaux TL, Solomon F. Cranberry phenolics: Effects on oxidase processes, neuron cell death and tumor cell growth. Phenolic compounds in foods and natural health products. Washington, DC: ACS Books 2005; pp. 271-82.
  42. Youdim KA, McDonald J, Kalt W, Joseph JA. Potential role of dietary flavonoids in reducing microvascular endothelium vulnerability to oxidative and inflammatory insults. J Nutr Biochem 2002; 13: 282-88.
  43. Gerdin B and Srensso E: Inhibitory effect of the flavonoid on increased microvascular permeability induced by various agents in rat skin. International Journal of Microcirculation, Clinical and Experimental 1983; 2(1): 39-46.
  44.  Zandi K, Teoh BT, Sam SS, Wong PF, Mustafa MR and Abubakar S: Antiviral activity of four types of bioflavonoid against dengue virus type-2. Vir Jour 2011; 8: 560.

Photo
Vaibhavi Vishe
Corresponding author

Research Scholar of Siddhi’s Institute of Pharmacy, Nandgaon

Photo
Nikita Kor
Co-author

Research Scholar of Siddhi’s Institute of Pharmacy, Nandgaon

Photo
Pradnya Tarmale
Co-author

Research Scholar of Siddhi’s Institute of Pharmacy, Nandgaon

Photo
Pratiksha Sonawane
Co-author

Assistant Professor of Siddhi’s Institute of Pharmacy, Nandgaon

Vaibhavi Vishe*, Nikita Kor, Pradnya Tarmale, Pratiksha Sonawane, Biological Activity of Flavonoids, Int. J. of Pharm. Sci., 2025, Vol 3, Issue 6, 1672-1678. https://doi.org/10.5281/zenodo.15619295

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