Bioactive Flavonoids from Citrus Fruits: Comparison
View Latest Version
Please note this is a comparison between Version 2 by Vivi Li and Version 1 by Mohamed ADDI.

Citrus species are one of the world’s popular fruit crops, cultivated all over the world for their economic and nutritional values. Citrus, like other fruits and vegetables, are an important source of several antioxidant molecules (polyphenols, ascorbic acid, and carotenoids) that can inhibit the harmful effects of free radicals on the human body; due to their functional values and health-promoting properties, Citrus species are considered valuable fruits not only in agri-food industry, but also in pharmaceutical industry. Flavonoids are among the major constituents of polyphenols found in different parts of Citrus fruits (skin, peels, seed, pulp membrane, and juice). Flavonoids have different biological properties (antiviral, antifungal, and antibacterial activities). Several studies have also shown the health-related properties of Citrus flavonoids, especially antioxidant, anticancer, anti-inflammation, anti-aging, and cardiovascular protection activities.

  • Citrus genus
  • bioactive molecules
  • flavonoids
  • therapeutic effects
  • extraction methods

1. Introduction

Citrus genus is one of the world’s leading fruit crops cultivated for food processing as well as fresh juice production. The genus Citrus belongs to the family Rutaceae, containing several species such as orange types, sweet and sour oranges, lemon, tangerines (mandarins), and tangors. Each species or hybrid cross has one or more varieties. Besides being a rich source of vitamins A, C, and E, mineral elements, and dietary fibers, Citrus fruits are a great source of secondary metabolites, such as polyphenols and terpenoids [1]. Flavonoids and phenolic acids are the main classes of phenolic compounds found in Citrus fruits [2]. In general, the fruit skin contains a higher concentration of antioxidant substances than the other parts of the fruit [3]. Citrus flavonoid contents and profiles vary significantly from one species to another [4]. Citrus peel, which represents between 50% and 65% of the total weight of the fruits, is a rich source of bioactive compounds, including natural antioxidants such as flavonoids [5]. Several studies showed that Citrus flavonoids are found to have anti-inflammatory, anti-cancer, anti-bacterial, anti-aging, and cardiovascular protection activities [6,7][6][7].

2. Citrus Flavonoids: Structure, Classification and Biosynthesis

2.1. Structure and Classification of Flavonoids from Citrus

Flavonoids are an important class of natural products; particularly, they belong to polyphenol compounds and are synthesized by plants via primary or secondary metabolisms that protect against short-term or long-term threats and play a major function in plant development and reproduction [12][8]. Flavonoids are found widespread throughout the plant kingdom and are associated with many health benefits [13][9]. They are a major class of phytochemicals discovered in citrus fruits, especially in peels, pulp, and seeds. Flavonoids are small molecular weight polyphenolic substances that have the same basic skeleton of fifteen carbons (C6-C3-C6), consisting of two phenyl rings (A and B) connected by a heterocyclic pyran or pyron ring (C) in the center, depending on their substituents. Flavonoids are subdivided into flavanols, anthocyanidins, flavanones, flavones, and chalcones [14][10]. The generic flavonoid structure and the numbering system used to distinguish the carbon positions around the molecule are shown in Table 21. The three phenolic rings that make up the flavonoid molecule are called pyran rings. Citrus flavonoids are divided into three principal types, namely, flavanones, flavones, and flavonols [15][11]. In Table 21, the classification of Citrus flavonoids and the chemical structures of major flavonoids are presented. The main flavonoids found in Citrus species are hesperidin, narirutin, naringin and eriocitrin.
Table 21. Basic structures of Citrus flavonoid subclasses [16][12].
Citrus Flavonoids Structure Backbone Examples
31],34], and naringin (0.54 to 0.65 mg/g peel dry basis) [32,33][29][30]. Naringin is the most abundant flavonoid in grapefruit and bitter orange peel, conferring a characteristic bitter taste (10.26 to 14.40 mg/g peel dry basis) [29,35][26][32]. Citrus peels contain also polymethoxyl flavones, such as sinensetin (0.08 to 0.29 mg/g dry bassis), nobiletin (0.2 to 14.05 mg/g dry basis), tangeretin (0.16 to 7.99 mg/g dry basis) and heptamethoxyflavone [26,36,37,38][23][33][34][35]. The glycosylated flavones are present in small quantities in Citrus peel, such as diosmin, rhoifoline, isorhoifoline, luteolin. Other flavonoids are present in very small quantities in citrus peel, such as flavonols (quercetin, rutin, myricetin, and kaempferol) [39][36]. Several studies have shown that the extracts of seeds and leaves of Citrus contain high quantities of phenolic compounds, such as flavonoids [40,41][37][38]. Naringin is the most abundant flavonoid in grapefruit seeds (0.2 mg/g seeds) [41][38]. The flavonoid content in Citrus peel is much higher than in the seeds. They appear in plants and foods mostly as glycosides [42][39].
Table 32. Flavonoid composition of some Citrus juices [4,43,44][4][40][41].
  Flavanones Flavones Total Flavonoids Content
  Hesperidin Narirutin Naringin Didymin Eriocitrin Diosmin 6,8-di-C-Glu-Diosmetin 6,8-di-C-Glu-Apigenin Sinensitin
Flavanones Applsci 12 00029 i001 Hesperetin R1=O-CH3
Orange 28.6 5.2 - 1.89 0.31 0.09 0.35 5.72 0.37 18.34
R2=OH
Sour orange - - 1.97 - - 0.15 - - - - Naringenin R1=OH
Mandarin orange 24.3 3.92 - 1.44 0.31 - - - 1.05 - R2=H
Clementine 39.9 4.64 0.08 - - 1.25 0.2 0.5 - 19.23 Flavanones glycosides Applsci 12 00029 i002 Narirutin R1=O-CH3
Lemon R2=H
R3=7-O-rutinoside
20.5 Naringin R1=OH
- R2=H
R3=O-7-Rhamnoglucoside
Flavones Applsci 12 00029 i003 Apigenin R1=OH
R2=R3=H
- Luteolin R1=R2=OH
R3=H
Polymethoxylated Flavones Applsci 12 00029 i004 Nobiletin R1=H
R2=R3=OCH3
Tangeretin R1=R3=H
R2=OCH3
Flavonols Applsci 12 00029 i005 Quercetin R1=R2=R3=OH
Kaempferol R1=R3=OH
R2=H

2.2. Biosynthesis of Flavonoids

The flavonoid pathway is preceded by the general phenylpropanoid pathway, in which three enzymes are involved in the conversion of the amino acid phenylalanine to 4-coumaroyl-CoA. the first enzyme, phenylalanine ammonia lyase (PAL:EC 4.3.1.24) catalyzes the conversion of the amino acid phenylalanine to trans-cinnamic acid, with the release of ammonia (NH3), then the two other enzymes (the enzyme cinnamate 4-hydroxylase (C4H:EC 1.14.14.91), followed by 4-coumarate-CoA ligase (4CL:EC 6.2.1.12)), catalyze the reaction that leads to obtain 4-coumaroyl-CoA, which is an important precursor in the flavonoid pathway [12,13][8][9]. The biosynthesis of flavonoids is originated from the phenylpropanoids pathway and initiated by two precursors named malonyl-CoA and p-coumaroyl-CoA (Figure 1). After the condensation of three acetate units from malonyl-CoA with one molecule of p-coumaroyl-CoA, naringenin chalcones are formed. Naringenin chalcone, a major pigment of many flowers, leaves and fruits, is converted to naringenin by chalcone isomerase (CHI) or non-enzymatically in vitro [14,15][10][11]. This reaction catalyzed by chalcone synthase (CHS:EC 2.3.1.74) is thought to be the key regulatory step in the synthesis of flavonoids. It catalyzes the stereospecific isomerization of chalcones to their corresponding (2S)-flavanones via an acid base catalysis mechanism; the unstable chalcone form is normally isomerized by the enzyme chalcone isomerase (CHI:EC 5.5.1.6) to form the structural precursors for a broad range of flavonoids, such as flavonols, flavanones, anthocyanin glycosides and other derived compounds (Figure 1).
Applsci 12 00029 g001 550
Figure 1. Plant flavonoids biosynthetic pathway [15][11]. Enzymes for each step are indicated as follows: PAL, phenylalanine ammonia-lyase; C4H, cinnamate 4-hydroxylase; 4CL, 4-coumarate-CoA ligase; CHS, chalcone synthase; CHI, chalcone isomerase; F3H, flavanone 3-hydroxylase; F3′H, flavonoid 3′-hydroxylase; DFR, dihydro-flavonol 4-reductase; FNS, flavonol synthase; FLS, flavonol synthase; LAR, leucoanthocyanidin reductase; ANS, anthocyanidin synthase; UFGT, UDP-glucose: flavonoid-3-O-glycosyltransferase.
(2S)-Flavanones are converted stereospecifically to the respective (2R,3R)-dihydroflavonols (DHFs) by flavanone 3-hydroxylase (F3H:EC 1.14.11.9) in this case to dihydrokaempferol, then converted by the enzyme flavonoid 3′-hydroxylase (F3′H:EC 1.14.14.82) to dihydroquercetin. In Citrus species, the two dihydroflavanols are then converted into flavonols under the action of flavonols synthetase (FLS:EC 1.14.20.6). UDP-glucose flavanone-7-O-glucosyltransferase (UFGT:EC 2.4.1.115) and UDP-rhamnose flavanone glucoside rhamnosyltransferase (UFGRT) catalyze the conversion of the flavanone aglycones into their glucosides and rhamnoglucosides [16][12]. Dihydroflavonol-4-reductase (DFR:EC 1.1.1.219) is a key enzyme required for both anthocyanin biosynthesis and proanthocyanidin accumulation and is involved in the conversion of dihydroflavonols to leucoanthocyanidins [17][13].
Flavan-3-ols, such as catechin and epicatechin, are synthetized from leucoanthocyanidin and anthocyanidin. Leucoanthocyanidin can be converted to flavan-3-ol (for example, catechin) by leucoanthocyanidin reductase (LAR:EC 1.17.1.3) or to anthocyanidin by anthocyanidin synthase (ANS:EC 1.14.20.4). Anthocyanidin as well can be converted to flavan-3-ol (for example, epicatechin) by anthocyanidin reductase (ANR:EC 1.3.1.77), or glycosylated to form anthocyanin [18][14].

3. Flavonoid Composition in Different Parts of Citrus Fruits

It has been found that Citrus flavonoids are present in almost all the parts of Citrus fruits in different species. Several studies showed that peels are the main sources of polyphenols in Citrus fruits [19][15]. Seed and peel extracts from numerous Citrus species have proved to be an important source of flavonoids, such as polymethoxyflavones (PMFs), flavanones, and glycosylated flavanones [20][16]. More than 5000 flavonoid molecules have been identified [21][17]. Citrus juice is also a major source of flavanone glycosides. Moreover, the contents and types of flavonoids vary among different Citrus species and fruit parts [21][17]. Flavanones are the most important flavonoids in Citrus species. Hesperedin and naringenin are the predominant flavanones in Citrus fruits [16][12]. They can be found in all plant parts: stem, branches, bark, flowers, leaves, roots, rhizomes, seeds, fruits, peels, etc. Flavones are the second major group of flavonoids in Citrus, with flavonols in third place because their content is much lower than the other flavonoids [17,18][13][14]. The content of these components depends upon the age of the plant; most Citrus species accumulate substantial quantities of flavonoids during organ development. Another study showed that flavonoids content might be affected by the maturity of the fruit, the post-harvesting treatments and the extracting processes [22][18]. Juice preparation and the processing of fresh Citrus fruits may decrease flavonoids content by 50% due to their water washing methods [23[19][20],24], or by elimination of the richest parts of the fruit [25][21]. In this review, we gather some relevant data for the most abundant flavonoid component in sweet orange (C. sinensis), sour orange (C. aurantium), mandarin orange (C. reticulata), clementine (C. Clementina), lemon (C. limon), and grapefruit (C. Pardisi) juices and peel. It should be noted that Citrus peel exhibit higher contents of flavanones than other parts of the fruit [11][22]. Depending on their varieties, grapefruit and sour orange are very rich in naringin. Other Citrus species such as sweet orange, and lemon have low quantities of naringin (Table 32). Pupin et al. [26][23] studied the composition of flavanone glycosides in various orange juice varieties and concluded that narirutin and hesperidin are the most abundant compounds. Hesperidin is present in high levels in clementine, sweet orange, mandarin orange and lemon (39.9–20.5 mg/100 mL juice), while naringin (23 mg/100 mL juice) and narirutin (7.6 mg/100 mL juice), glycosides of naringenin, are especially more abundant in grapefruit (Table 32) [27][24]. In lemon, eriocitrin is present in high level (16.17 mg/100 mL juice) [26][23]. Didymin is a typical flavonoid glycoside also known as neoponcirin used in Asian countries as a dietary antioxidant [28][25]. This flavonoid is mainly present in orange, mandarin and grapefruit (1.89–0.30 mg/100 mL juice) (Table 32). The most abundant flavanones in Citrus peel are naringin andhesperidin. These flavanones are all glycosylated either by rutinose (6-O-α-l-rhamnosyl-d-glucose) or by neohesperidose (2-O-α-l-rhamnosyl-d-glucose) linked in position 7 [28][25]. Hesperidin (0.002 to 9.42 mg/g peel dry basis) [29,30][26][27] is the main flavanone in all lemon cultivars while levels of diosmin and eriocitrin are the lowest [31][28]. Mandarin peel is rich in hesperidin (3.95 to 80.90 mg/g peel dry basis) [32[29][30],33], narirutin (7.66 to 15.3 mg/g peel dry basis) [22[18][
-
16.17
3.12
4.95 1.17 - -
Grapefruit 0.93 7.60 23.0 0.3 0.41 - - - - -
Mean values are expressed in mg/100 mL of juice.

4. Citrus Flavonoid Extraction Techniques

Citrus flavonoids were discovered to be omnipresent in practically all portions of Citrus fruits from various species [45][42]. Extraction is a crucial stage in the analytical process, and its success has a significant impact on the quality of the final results [46][43]. Flavonoids can only be isolated, detected, and characterized after using the appropriate extraction procedure. Generally, to extract bioactive compounds, several processes can be used, many of which have largely remained constant for hundreds of years. All of these strategies share the same goals: (a) extracting selected bioactive chemicals from complicated plant samples; (b) improving analytical method selectivity and avoiding the presence of interferents that could alter the analysis; and (c) improving bioassay sensitivity by increasing the concentration of targeted compounds before analysis [46,47,48][43][44][45].

4.1. Conventional Extraction Techniques

Various traditional extraction procedures can be used to extract bioactive chemicals from plant sources. The recovery of bioactive chemicals from plant matrices, using common solvents, is referred to as conventional extraction (with or without heat treatment) [49][46]. The majority of these approaches rely on the extraction power of the various solvents in use, as well as the use of heat and/or mixing. The known conventional procedures for extracting bioactive chemicals from plants are (1) maceration, (2) infusion, (3) decoction, (4) hot continuous extraction (Soxhlet extraction), (5) hydrodistillation, and (6) percolation.

4.2. Non-Conventional Extraction Techniques

Degradation of targeted compounds due to high temperatures and long extraction times in solvents is a major problem encountered in classic extraction techniques. On this basis, finding various extraction strategies to overcome this difficulty becomes a critical step to improve extraction efficiency and/or selectivity. Or, using dedicated aids/energy-intensive intrants, such as microwave-assisted extraction [50][47], pressurized liquid extraction [51][48], supercritical fluid extraction [52][49], ultrasound-assisted extraction, cold plasma-assisted extraction [53][50], high pressure assisted extraction [54][51], pulsed electric field assisted extraction [55][52], and enzyme-assisted extraction [56][53], is well documented in the scientific literature as an efficient alternative. In general, while studying plant-derived chemicals, the method and solvents utilized for extraction must be carefully adopted [57][54]. In this context, some of the non-conventional extraction methods are discussed.

4.2.1. Ultrasound Assisted Extraction (UAE)

Ultrasound-assisted extraction is a new technology that is being used to extract natural products that previously took many hours to extract using traditional methods. Initially, it was employed to preserve food, but in the last decade, it has also been utilized to extract beneficial substances (mainly polyphenols). Because of the simplicity of the method, benefits such as reduced extraction time, increased extract yield, and the use of water as a solvent, which reduces the usage of organic solvents, are documented. Therefore, to avoid unwanted reactions generated by the UAE and maximize the extraction yield, the extraction parameters (e.g., extraction duration, solvent system, and, if possible, U.S. frequency) should be tuned prior to developing the extraction process [58][55]. Londoño-Londoño et al. 2010, conducted the extraction of Citrus peel flavonoids from C. sinensis, C. latifolia, and C. reticulata under optimal ultrasonic conditions of 60 kHz, 40 °C, for 1 h, using methanol as a solvent [59][56].

4.2.2. Supercritical Fluid Extraction (SFE)

Supercritical extraction is a modern technique that uses gases that have exceeded their critical pressure and temperature, resulting in a fluid with qualities in between a gas and a liquid [60][57]. Supercritical CO2 extraction (using CO2 as a solvent, mainly due to its adaptability, availability, and low cost), is a preferred approach for extracting numerous active compounds. Despite the fact that any gas can be employed as a supercritical fluid [61][58] because flavonoids are polar molecules, SFE requires the presence of a cosolvent, such as ethanol or methanol [62][59]. A study was carried out to extract nobiletin and tangeritin from C. depressa var Hayata. The authors tested both methanol and ethanol as solvents. Under the conditions reported in their paper, Lee et al. [36][33] found that SFE provides a higher amount of flavonoids (+7%) than UAE.

References

  1. Zhou, Z.Q. Citrus Fruits Nutrition; Science Press: Beijing, China, 2012.
  2. González-Molina, E.; Domínguez-Perles, R.; Moreno, D.A.; García-Viguera, C. Natural bioactive compounds of Citrus limon for food and health. J. Pharm. Biomed. Anal. 2010, 51, 327–345.
  3. Awad, M.A.; de Jager, A.; van der Plas, L.H.W.; van der Krol, A.R. Flavonoid and chlorogenic acid changes in skin of ‘Elstar’ and ‘Jonagold’apples during development and ripening. Sci. Hortic. 2001, 90, 69–83.
  4. Peterson, J.J.; Dwyer, J.T.; Beecher, G.R.; Bhagwat, S.A.; Gebhardt, S.E.; Haytowitz, D.B.; Holden, J.M. Flavanones in oranges, tangerines (mandarins), tangors, and tangelos: A compilation and review of the data from the analytical literature. J. Food Compos. Anal. 2006, 19, S66–S73.
  5. Li, B.B.; Smith, B.; Hossain, M.M. Extraction of phenolics from citrus peels: I. Solvent extraction method. Sep. Purif. Technol. 2006, 48, 182–188.
  6. Benavente-Garcia, O.; Castillo, J. Update on uses and properties of citrus flavonoids: New findings in anticancer, cardiovascular, and anti-inflammatory activity. J. Agric. Food Chem. 2008, 56, 6185–6205.
  7. Zou, Z.; Xi, W.; Hu, Y.; Nie, C.; Zhou, Z. Antioxidant activity of Citrus fruits. Food Chem. 2016, 196, 885–896.
  8. Ververidis, F.; Trantas, E.; Douglas, C.; Vollmer, G.; Kretzschmar, G.; Panopoulos, N. Biotechnology of flavonoids and other phenylpropanoid-derived natural products. Part I: Chemical diversity, impacts on plant biology and human health. Biotechnol. J. 2007, 2, 1214–1234.
  9. Vogt, T. Phenylpropanoid Biosynthesis. Mol. Plant. 2010, 3, 2–20.
  10. Austin, M.B.; Noel, J.P. The chalcone synthase superfamily of type III polyketide synthases. Nat. Prod. Rep. 2003, 20, 79–110.
  11. Tai, D.; Tian, J.; Zhang, J.; Song, T.; Yao, Y. A Malus crabapple chalcone synthase gene, McCHS, regulates red petal color and flavonoid biosynthesis. PLoS ONE. 2014, 9, e110570.
  12. Lewinsohn, E.; Britsch, L.; Mazur, Y.; Gressel, J. Flavanone glycoside biosynthesis in citrus: Chalcone synthase, UDP-glucose: Flavanone-7-O-glucosyl-transferase and-rhamnosyl-transferase activities in cell-free extracts. Plant Physiol. 1989, 91, 1323–1328.
  13. Li, Y.; Liu, X.; Cai, X.; Shan, X.; Gao, R.; Yang, S.; Han, T.; Wang, S.; Wang, L.; Gao, X. Dihydroflavonol 4-Reductase Genes from Freesia hybrida Play Important and Partially Overlapping Roles in the Biosynthesis of Flavonoids. Front. Plant Sci. 2017, 8, 428.
  14. Liu, C.; Wang, X.; Shulaev, V.; Dixon, R.A. A role for leucoanthocyanidin reductase in the extension of proanthocyanidins. Nat. Plants. 2016, 2, 1–7.
  15. Wang, L.; Wang, J.; Fang, L.; Zheng, Z.; Zhi, D.; Wang, S.; Li, S.; Ho, C.-T.; Zhao, H. Anticancer activities of citrus peel polymethoxyflavones related to angiogenesis and others. BioMed Res. Int. 2014, 2014, 453972.
  16. Xi, W.; Zhang, Y.; Sun, Y.; Shen, Y.; Ye, X.; Zhou, Z. Phenolic composition of Chinese wild mandarin (Citrus reticulata Balnco.) pulps and their antioxidant properties. Ind. Crops Prod. 2014, 52, 466–474.
  17. Harborne, J.B. The Flavonoids: Advances in Research Since 1980; Springer: Berlin/Heidelberg, Germany, 2013.
  18. Xu, G.; Ye, X.; Liu, D.; Ma, Y.; Chen, J. Composition and distribution of phenolic acids in Ponkan (Citrus poonensis Hort. ex Tanaka) and Huyou (Citrus paradisi Macf. Changshanhuyou) during maturity. J. Food Compos. Anal. 2008, 21, 382–389.
  19. Sánchez-Moreno, C.; Plaza, L.; Elez-Martínez, P.; De Ancos, B.; Martín-Belloso, O.; Cano, M.P. Impact of high pressure and pulsed electric fields on bioactive compounds and antioxidant activity of orange juice in comparison with traditional thermal processing. J. Agric. Food Chem. 2005, 53, 4403–4409.
  20. Polydera, A.C.; Stoforos, N.G.; Taoukis, P.S. Effect of high hydrostatic pressure treatment on post processing antioxidant activity of fresh Navel orange juice. Food Chem. 2005, 91, 495–503.
  21. Del Caro, A.; Piga, A.; Vacca, V.; Agabbio, M. Changes of flavonoids, vitamin C and antioxidant capacity in minimally processed citrus segments and juices during storage. Food Chem. 2004, 84, 99–105.
  22. Krueger, R.R.; Navarro, L. Citrus Germplasm Resources. In Citrus Genetics, Breeding and Biotechnology; CAB International: Wallingford, UK, 2007.
  23. Pupin, A.M.; Dennis, M.J.; Toledo, M.C.F. Flavanone glycosides in Brazilian orange juice. Food Chem. 1998, 61, 275–280.
  24. Tomás-Barberán, F.A.; Clifford, M.N. Dietary hydroxybenzoic acid derivatives–nature, occurrence and dietary burden. J. Sci. Food Agric. 2000, 80, 1024–1032.
  25. Yao, Q.; Lin, M.-T.; Zhu, Y.-D.; Xu, H.-L.; Zhao, Y.-Z. Recent trends in potential therapeutic applications of the dietary flavonoid didymin. Molecules 2018, 23, 2547.
  26. Wang, Y.-C.; Chuang, Y.-C.; Hsu, H.-W. The flavonoid, carotenoid and pectin content in peels of citrus cultivated in Taiwan. Food Chem. 2008, 106, 277–284.
  27. Russo, M.; Bonaccorsi, I.; Torre, G.; Sarò, M.; Dugo, P.; Mondello, L. Underestimated sources of flavonoids, limonoids and dietary fibre: Availability in lemon’s by-products. J. Funct. Foods. 2014, 9, 18–26.
  28. Del Río, J.A.; Fuster, M.D.; Gómez, P.; Porras, I.; Garcıa-Lidón, A.; Ortuño, A. Citrus limon: A source of flavonoids of pharmaceutical interest. Food Chem. 2004, 84, 457–461.
  29. Hayat, K.; Hussain, S.; Abbas, S.; Farooq, U.; Ding, B.; Xia, S.; Jia, C.; Zhang, X.; Xia, W. Optimized microwave-assisted extraction of phenolic acids from citrus mandarin peels and evaluation of antioxidant activity in vitro. Sep. Purif. Technol. 2009, 70, 63–70.
  30. Tumbas, V.T.; Ćetković, G.S.; Đilas, S.M.; Čanadanović-Brunet, J.M.; Vulić, J.J.; Knez, Ž.; Škerget, M. Antioxidant activity of mandarin (Citrus reticulata) peel. Acta Period. Technol. 2010, 195–203.
  31. Cheigh, C.-I.; Chung, E.-Y.; Chung, M.-S. Enhanced extraction of flavanones hesperidin and narirutin from Citrus unshiu peel using subcritical water. J. Food Eng. 2012, 110, 472–477.
  32. Giannuzzo, A.N.; Boggetti, H.J.; Nazareno, M.A.; Mishima, H.T. Supercritical fluid extraction of naringin from the peel of Citrus paradisi. Phytochem. Anal. 2003, 14, 221–223.
  33. Lee, Y.-H.; Charles, A.L.; Kung, H.-F.; Ho, C.-T.; Huang, T.-C. Extraction of nobiletin and tangeretin from Citrus depressa Hayata by supercritical carbon dioxide with ethanol as modifier. Ind. Crops Prod. 2010, 31, 59–64.
  34. Li, W.; Wang, Z.; Wang, Y.; Jiang, C.; Liu, Q.; Sun, Y.; Zheng, Y. Pressurised liquid extraction combining LC–DAD–ESI/MS analysis as an alternative method to extract three major flavones in Citrus reticulata ‘Chachi’ (Guangchenpi). Food Chem. 2012, 130, 1044–1049.
  35. Toledo-Guillén, A.R.; Higuera-Ciapara, I.; García-Navarrete, G.; De la Fuente, J.C. Extraction of Bioactive Flavonoid Compounds from Orange (Cit-rus sinensis) Peel Using Supercritical CO2. Atherosclerosis 2010, 178, 25–32.
  36. Zhang, J. Flavonoids in Grapefruit and commercial grapefruit juices: Concentration, distribution, and potential health benefi ts. Proc. Proc. Fla. State Hortic. Soc. 2007, 120, 288–294.
  37. Al-Anbari, A.K.H.; Hasan, M.A. Antioxidant activity in some citrus leaves and seeds ethanolic extracts. In Proceedings of the International Conference on Advances in Agricultural, Biological and Environmental Sciences (AABES), London, UK, 22–23 July 2015; pp. 22–23.
  38. Yu, J.; Dandekar, D.V.; Toledo, R.T.; Singh, R.K.; Patil, B.S. Supercritical fluid extraction of limonoids and naringin from grapefruit (Citrus paradisi Macf.) seeds. Food Chem. 2007, 105, 1026–1031.
  39. Tripoli, E.; La Guardia, M.; Giammanco, S.; Di Majo, D.; Giammanco, M. Citrus flavonoids: Molecular structure, biological activity and nutritional properties: A review. Food Chem. 2007, 104, 466–479.
  40. Peterson, J.J.; Beecher, G.R.; Bhagwat, S.A.; Dwyer, J.T.; Gebhardt, S.E.; Haytowitz, D.B.; Holden, J.M. Flavanones in grapefruit, lemons, and limes: A compilation and review of the data from the analytical literature. J. Food Compos. Anal. 2006, 19, S74–S80.
  41. Rao, M.J.; Wu, S.; Duan, M.; Wang, L. Antioxidant Metabolites in Primitive, Wild, and Cultivated Citrus and Their Role in Stress Tolerance. Molecules 2021, 26, 5801.
  42. Wang, S.; Yang, C.; Tu, H.; Zhou, J.; Liu, X.; Cheng, Y.; Luo, J.; Deng, X.; Zhang, H.; Xu, J. Characterization and Metabolic Diversity of Flavonoids in Citrus Species. Sci. Rep. 2017, 7, 10549.
  43. Ledesma-Escobar, C.A.; de Castro, M.D.L. Towards a comprehensive exploitation of citrus. Trends Food Sci. Technol. 2014, 39, 63–75.
  44. Smith, R.M. Before the injection—modern methods of sample preparation for separation techniques. J. Chromatogr. A 2003, 1000, 3–27.
  45. Azmir, J.; Zaidul, I.S.M.; Rahman, M.M.; Sharif, K.M.; Mohamed, A.; Sahena, F.; Jahurul, M.H.A.; Ghafoor, K.; Norulaini, N.A.N.; Omar, A.K.M. Techniques for extraction of bioactive compounds from plant materials: A review. J. Food Eng. 2013, 117, 426–436.
  46. Barba, F.J.; Putnik, P.; Bursać Kovačević, D.; Poojary, M.M.; Roohinejad, S.; Lorenzo, J.M.; Koubaa, M. Impact of conventional and non-conventional processing on prickly pear (Opuntia spp.) and their derived products: From preservation of beverages to valorization of by-products. Trends Food Sci. Technol. 2017, 67, 260–270.
  47. Pina-Pérez, M.C.; Rivas, A.; Martínez, A.; Rodrigo, D. Effect of thermal treatment, microwave, and pulsed electric field processing on the antimicrobial potential of açaí (Euterpe oleracea), stevia (Stevia rebaudiana Bertoni), and ginseng (Panax quinquefolius L.) extracts. Food Control. 2018, 90, 98–104.
  48. Ciulu, M.; Quirantes-Piné, R.; Spano, N.; Sanna, G.; Borrás-Linares, I.; Segura-Carretero, A. Evaluation of new extraction approaches to obtain phenolic compound-rich extracts from Stevia rebaudiana Bertoni leaves. Ind. Crops Prod. 2017, 108, 106–112.
  49. Uwineza, P.A.; Gramza-Michałowska, A.; Bryła, M.; Waśkiewicz, A. Antioxidant Activity and Bioactive Compounds of Lamium album Flower Extracts Obtained by Supercritical Fluid Extraction. Appl. Sci. 2021, 11, 7419.
  50. Kujundžić, D.; Jambrak, A.R.; Vukušić, T.; Stulić, V.; Kljusurić, J.G.; Banović, M.; Herceg, Z. Near-infrared spectroscopic characterization of steviol glycosides extracted from Stevia rebaudiana Bertoni using high-power ultrasound and gas-phase plasma. J. Food Nutr. Res. 2017, 56, 109–120.
  51. Barba, F.J.; Terefe, N.S.; Buckow, R.; Knorr, D.; Orlien, V. New opportunities and perspectives of high pressure treatment to improve health and safety attributes of foods. A review. Food Res. Int. 2015, 77, 725–742.
  52. Tamborrino, A.; Urbani, S.; Servili, M.; Romaniello, R.; Perone, C.; Leone, A. Pulsed electric fields for the treatment of olive pastes in the oil extraction process. Appl. Sci. 2020, 10, 114.
  53. Zuorro, A.; Lavecchia, R.; González-Delgado, Á.D.; García-Martinez, J.B.; L’Abbate, P. Optimization of enzyme-assisted extraction of flavonoids from corn husks. Processes 2019, 7, 804.
  54. Vongsak, B.; Sithisarn, P.; Mangmool, S.; Thongpraditchote, S.; Wongkrajang, Y.; Gritsanapan, W. Maximizing total phenolics, total flavonoids contents and antioxidant activity of Moringa oleifera leaf extract by the appropriate extraction method. Ind. Crops Prod. 2013, 44, 566–571.
  55. Ledesma-Escobar, C.A.; Priego-Capote, F.; Luque de Castro, M.D. Chapter 9—Relevance and Analysis of Citrus Flavonoids. In Polyphenols in Plants, 2nd ed.; Academic Press: Cambridge, MA, USA, 2019; pp. 133–150. ISBN 978-0-12-813768-0.
  56. Londoño-Londoño, J.; de Lima, V.R.; Lara, O.; Gil, A.; Pasa, T.B.C.; Arango, G.J.; Pineda, J.R.R. Clean recovery of antioxidant flavonoids from citrus peel: Optimizing an aqueous ultrasound-assisted extraction method. Food Chem. 2010, 119, 81–87.
  57. McHugh, M.; Krukonis, V. Supercritical Fluid Extraction: Principles and Practice; Elsevier: Amsterdam, The Netherlands, 2013; ISBN 0080518176.
  58. Machado, B.A.S.; Pereira, C.G.; Nunes, S.B.; Padilha, F.F.; Umsza-Guez, M.A. Supercritical fluid extraction using CO2: Main applications and future perspectives. Sep. Sci. Technol. 2013, 48, 2741–2760.
  59. Díaz-Reinoso, B.; Moure, A.; Domínguez, H.; Parajó, J.C. Supercritical CO2 Extraction and Purification of Compounds with Antioxidant Activity. J. Agric. Food Chem. 2006, 54, 2441–2469.
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/)
ScholarVision Creations
Feedback