Bangladesh J Pharmacol. 2016; 11: S18-S25

Available Online: 19 February 2016 DOI: 10.3329/bjp.v11iS1.26419

Isolation of flavonoids from onion skin and their effects on K562 cell viability

Guo-Qing Shi1, Jing Yang1, Jiang Liu2, Sheng-Nan Liu1, Han-Xue Song1, Wen-En Zhao3 and Yan-Qi Liu1

1School of Food and Bioengineering, Zhengzhou University of Light Industry, Henan, Zhengzhou 450 002, P. R. China; 2National Engineering Laboratory for Further Processing of Wheat and Corn, Henan University of Technology, Henan, Zhengzhou 450 000, P. R. China; 3School of Chemical Engineering and Energy, Zhengzhou University, Henan, Zhengzhou 450 052, P. R. China.

Principal Contact

Abstract

To investigate the anti-proliferative activity of flavonoids from onion skins, extraction by 50% ethanol (v/v), soxhlet polar fractionation, pH gradient separation, thin-layer chromatography, and recrystallization methods were used to isolate and purify flavonoids from dry onion skins. Anti-proliferative activities of some flavonoids obtained on leukemia K562 cell line were deter-mined by MTT assay. Results showed that flavonoids of onion skins were mainly in form of quercetin, kaempferol, isorhamnetin, apigenin-7-O-β-D-glucopyranoside, quercetin-3-O-β-D-glucopyranoside, kaempferol-7-O-β-D-glucopyranoside and rutin. Quercetin and kaempferol decreased K562 cell viability, and quercetin had stronger effect. However, isorhamnetin and rutin exhibited certain proliferation-promoting effects. It suggests that ortho hydroxyl groups on B ring of onion flavonoids might be the key structural elements of their cytotoxic effects on K562 cells, and hydroxyl groups in position 3 or carbonyl groups in position 4 might be one of the structural effect elements.


Introduction

Onion (Allium cepa L.) is considered to be one of the world’s oldest cultivated vegetable, and contains high level of dietary flavonoids (Slimestad et al., 2007), which are present in much higher concentrations in the onion skin than they are in the fleshy bulb (Kim and Kim, 2006; Yao et al., 2004; Sellappan and Akoh, 2002). There is a growing body of evidence indicating that flavonoids may exhibit health-promoting effects (Griffiths et al., 2002).

The results of several studies have shown that the physiological functions of flavonoids are dependent on their structures, because flavonoids with different structures exhibit a variety of different biological activities (Kefalas et al., 2006).

The isolation and identification of flavonoids from onion skin would not only enhance our understanding of the material basis for their biological activities, but could also provide a theoretical basis for the utilization of these compounds in a number of other areas of research.

Significant research efforts have been directed towards the characterization of onion and onion skin flavonoids during the last decade (Soltoft et al., 2009; Pérez-Gregorio et al., 2010; Kiassos, et al., 2009; Jin, et al., 2011) which has led to a significant increase in our understanding of these compounds. Despite these studies, information pertaining to the systematic isolation and identification of flavonols from discarded onion skin remains scarce.


Materials and Methods

Dry red onion skins were collected from Zhengzhou North Central Vegetable Wholesale Market, China. Onion skin powder was obtained through the sequential cleaning, drying and grounding of the onion skins.

Extraction

Two hundred grams of onion skin powder was extracted with 6 L of 50% aqueous ethanol at 72°C for 2 hours in a water bath. The resulting extract was then cooled to ambient temperature and filtered through filter paper. This procedure was repeated two times and the combined extracts were concentrated under vacuum on a rotary evaporator near to cream, which was absorbed onto diatomaceous earth and dried in the air.

Soxhlet polar fractionation

The dried diatomaceous earth samples were sequentially extracted with petroleum ether, diethyl ether, and ethyl acetate using a soxhlet extractor. Each solvent extraction procedure was conducted for 12 hours. The petroleum ether phase was discarded, whereas the diethyl ether and ethyl acetate extracts were collected for further processing.

pH gradient separation

The diethyl ether phase was extracted three times with 2% (w/v) NaHCO3 solution, and the pH of the combined aqueous extracts was adjusted with concentrated hydrochloric acid to pH 2. The acidified aqueous was then extracted with diethyl ether before being evaporated to dryness under vacuum to give the NaHCO3 components of the diethyl ether phase. The organic phase was sequentially extracted with 5% (w/v) Na2CO3 and 1% (w/v) NaOH solutions to give the corresponding diethyl ether phase components. The ethyl acetate phase was subjected to the same separation method to give the NaHCO3, Na2CO3, and NaOH components of the ethyl acetate phase.

Isolation

The NaOH components of the diethyl ether and ethyl acetate phases were discarded because they contained very low levels of flavonoids. The flavonoids in the NaHCO3 and Na2CO3 components of the diethyl ether and ethyl acetate phases were isolated by preparative TLC (developing solvents: toluene/ethyl, formate/formic acid, and toluene/ethyl formate/ethanol/formic acid) and recrystallized from chloroform and methanol to give seven flavonoids (Table I).

Table I
Flavonoids isolated from onion skins
SourceNumberCompound name
The NaHCO3 components of diethyl ether phase Compound 1Isorhamnetin
Compound 2Quercetin
Compound 3Kaempferol
The Na2CO3 components of diethyl ether phaseCompound 5Quercetin-3-O-β-D-glucopyranoside
The NaHCO3 components of ethyl acetate phase Compound 7Rutin
Compound 2Quercetin
The Na2CO3 components of ethyl acetate phase Compound 4Apigenin-7-O-β-D-glucopyranoside
Compound 6Kaempferol-7-O-β-D-glucopyranoside

Identification reactions

HCl-Mg reaction was used for the identification of the flavonoids. Briefly, a few milligrams of Mg powder were added to 1 mL ethanol solutions of the samples (0.1 mg/mL). A few drops of concentrated hydrochloric were added to the solutions, and the resulting mixtures were heated in a water bath when necessary. The formation of a red or purple color indicated the occurrence of a positive reaction.

Molisch reaction was used for the identification of glycosidic units. Solution I was made as follows: α-naphthol (1 g) was accurately weighed into a volumetric flask and dissolved and diluted to 10 mL with 75% ethanol. Solution II was concentrated sulfuric acid. Two or three drops of solution I were added to 1 mL of ethanol or an aqueous solution of the flavonoid sample, and the resulting solution was thoroughly mixed. A small amount of solution II was then slowly added to the sample mixture along the wall of the tube. Notably, the interface between the samples solution and solution II became purple in color for a positive reaction.

Cell culture and drug treatment

K562 cells were cultured in RPMI 1640 medium supplemented with decomplemented fetal bovine serum (10%, v/v), penicillin (100 IU/mL), and streptomycin (100 μg/mL) in a humidified incubator under 5% CO2 and 95% air at 37°C.

The flavonoids were added to the cells using dimethyl sulfoxide (DMSO) as a solvent. The concentrations of the DMSO solutions were adjusted to be the same in all of experiments, and the final concentrations were never greater than 0.5% (v/v). The control group received the same amount of DMSO without any flavonoids.

Cell viability was measured using an MTT assay. Briefly, the K562 cells were seeded into 96-well culture plates and cultured with various concentrations of the different flavonoids for 72 hours at 37°C. After the treatment, each cell was treated with an MTT solution to a final concentration 500 μg/mL, and the plates were then incubated for 4 hours at 37°C. At the end of the incubation period, the media was carefully removed from each well and replaced with 100 μL of DMSO. The resulting mixtures were then gently agitated to allow for the solubilization of the precipitated formazan crystals, and the absorbance values of the cells were then measured at 570 nm using a Bio-Rad model 680 microplate reader (Richmond, CA, USA). The absorbance values of the treated cells were compared with those of the controls, where the cells were considered to be 100% viable. The rate of inhibition could then be calculated using the following equation.

Inhibition rate (%) = (1 - absorbance of treatment groups / absorbance of control groups) × 100%.


Results

Structures of isolated compounds

Seven flavonoids were isolated from the dry onion skins evaluated in the current study (Figure 1). The structures of these compounds were elucidated as follows:

Compound 1: Physical form, yellow powder; hydrochloric acid-Mg reaction, positive; Molisch reaction, negative. These results suggested that compound 1 was a flavonoid without any glycosidic groups. ESI-MS (Agilent 1100 LC-MSD-Trap-XCT, Agilent, Agilent Technologies Inc. SantaClara, California, USA) in the negative ion mode displayed a pseudomolecular ion peaks with an m/z value of 315, corresponding to [M–H]. Elemental analysis (Flash EA1112 elemental analyzer, Thermo Electron SPA Company, USA) showed that the amounts of C and H in compound 1 were 60.44 and 3.83%, respectively. Taken together with the NMR results (Avance-300 NMR spectrometer, Bruker, Bruker Optics, Germany), the molecular formula of compound 1 was determined to be C16H12O7. The Fourier transform infrared (FT-IR) spectrum (Nexus470 Fourier transform infrared spectrometer, Nicolet Instrument Company, USA) spectrum of compound 1 contained a broad peak at 3238 cm-1, as well as a much narrower C-O peak in the range of 1250–1050 cm-1, which were consistent with the presence of hydroxyl groups. Another peak was observed at 1656 cm-1, which was attributed to the stretching vibration of a carbonyl group. Several other peaks were observed at 1616, 1560, 1509 and 1446 cm-1, together with broader peaks over 3000 cm-1, which were attributed to an entitative phenyl ring structure. The peaks at 1616, 1509 and 1383 cm-1 could also be indicative of the presence of an oxygen heterocycle.

NMR data: 1H-NMR (300 MHz, DMSO-d6) δ: 12.48 (1H, s, 5-OH), 10.74 (1H, s, 7-OH),9.75 (2H, s, -OH), 7.76 (1H, d, J = 1.7 Hz, H-2′), 7.69 (1H, dd, J = 1.7, 8.1 Hz, H-6′), 6.95 (1H, d, J = 8.5 Hz, H-5′), 6.49 (1H, d, J = 2.0 Hz, H-8), 6.20 (1H, d, J = 1.7 Hz, H-6), 3.85 (3H, s, -OCH3); 13C-NMR (75 MHz, MeOD) d: 175.8 (C-4), 164.1 (C-7)), 161.1 (C-9), 156.2 (C-5), 148.4 (C-3′), 147.6 (C-2), 146.8 (C-4′), 135.8 (C-3), 122.2 (C-1′), 120.8 (C-6′), 115.6 (C-2′), 111.8 (C-5′), 102.8 (C-10), 98.8 (C-6), 94.0 (C-8), 55.2 (3-OCH3). These data were found to be consistent with those reported in the literature for isorhamnetin (Park and Lee, 1996; Bonaccorsi et al., 2005; Ning, 2000; Fossen and Abdersen, 2006; Markham and Geiger, 1994; Stochmal et al., 2001), and so compound 1 was identified as isorhamnetin.

Compound 2: Physical form, yellow powder; hydrochloric acid-Mg reaction, positive; Molisch reaction, negative. The results suggested that compound 2 could be a flavonoid without any glycoside functionality. ESI-MS analysis of compound 2 in the negative ion mode revealed a pseudomolecular ion peak with an m/z value of 301, corresponding to [M+H]. Elemental analysis showed that the amounts of C and H in compound 2 were 59.61 and 3.32%, respectively. Taken together with the NMR results, these data suggested that the molecular formula of compound 2 was C15H10O7. FT-IR analysis revealed peaks at 3318 and 1250–1050 cm-1, which were consistent with the presence of hydroxyl groups. The peak at 1663 cm-1 was attributed to the stretching vibration of a carbonyl group. Several other peaks were observed at 1611, 1561, 1522 and 1450 cm-1, which were consistent with the presence of a phenyl ring skeleton. The peaks observed at 1611, 1522 and 1408 cm-1 also suggested the presence of an oxygen-containing heterocycle.

NMR data: 1H-NMR (300 MHz, DMSO-d6) δ: 12.50 (1H, s, 5-OH), 10.83 (1H, s, 7-OH), 9.38 (3H, s, -OH), 7.67 (1H, d, J = 2.1 Hz, H-2′), 7.53 (1H, dd, J = 7.2, 1.9 Hz, H-6′), 6.88 (1H, d, J = 8.5 Hz, H-5′), 6.40 (1H, d, J = 1.7 Hz, H-8), 6.18 (1H, d, J = 1.7 Hz, H-6); 13C-NMR (75 MHz, MeOD) δ: 175.9 (C-4), 164.2 (C-7), 161.1 (C-9), 156.8 (C-5), 147.4 (C-2), 146.6 (C-4′), 144.8 (C-3′), 135.7 (C-3), 122.7 (C-1′), 120.3 (C-6′), 114.8 (C-5′), 114.5 (C-2′), 103.1 (C-10), 97.8 (C-6), 93.0 (C-8). These data were consistent with those reported in the literature for quercetin (Rhodes and Price, 1996; Fossen et al., 1998; Lee et al., 2008; Ly et al., 2005; Ning, 2000; Fossen and Andersen, 2006; Markham and Geiger, 1994; Stochmal et al., 2001), and so compound 2 was identified as quercetin.

Compound 3: Physical form, yellow powder; hydrochloric acid-Mg reaction, positive; Molisch reaction, negative. These results suggested that compound 3 was a flavonoid without any glycoside functionality. ESI-MS analysis in the negative ion mode revealed a pseudomolecular ion peaks with anm/z value of 285, corresponding to [M–H]. Elemental analysis showed that the amounts of C and H in compound 3 were 61.91 and 3.63%, respectively. Taken together with the NMR results, these data suggested that the molecular formula of compound 3 was C15H10O6. The FT-IR spectrum of compound 3 contained peaks at 3318 and 1250–1050 cm-1, which were consistent with the existence of hydroxyl groups. A peak was also observed at 1661 cm-1, which was attributed to the stretching vibration of a carbonyl group. The vibrational absorption peaks observed at 1613, 1569, 1508 and 1438 cm-1 were consistent with the presence of a phenyl ring skeleton, and the peaks at 1611, 1522 and 1408 cm-1 indicated the presence of an oxygen-containing heterocycle.

NMR data: 1H-NMR (300 MHz, DMSO-d6) δ: 12.50 (1H, s, 5-OH), 10.83 (1H, s, 7-OH-7), 9.38 (3H, s, -OH), 7.67 (1H, d, J = 2.1 Hz, H-2′), 7.53 (1H, dd, J = 7.2, 1.9 Hz, H-6′), 6.88 (1H, d, J = 8.5 Hz, H-5′), 6.40 (1H, d, J = 1.7 Hz, H-8), 6.18 (1H, d, J = 1.7 Hz, H-6); 13C-NMR (75 MHz, MeOD) δ: 175.9 (C-4), 164.2 (C-7), 161.1 (C-9), 156.8 (C-5), 147.4 (C-2), 146.6 (C-4′), 144.8 (C-3′), 135.7 (C-3), 122.7 (C-1′), 120.3 (C-6′), 114.8 (C-5′), 114.5 (C-2′), 103.1 (C-10), 97.8 (C-6), 93.0 (C-8). These data were found to be consistent with those reported in the literature for kaempferol (Ning, 2000; Fossen and Andersen, 2006; Markham and Geiger, 1994; Stochmal et al., 2001), and so compound 3 was identified as kaempferol.

Compound 4: Physical appearance, yellow powder; hydrochloric acid-Mg reaction, positive; Molisch reac-tion, positive. These results suggested that compound 4 was a flavonoid glycoside.

NMR data: 1H-NMR (300 MHz, DMSO-d6) δ: 7.97 (2H, d, J = 9.4 Hz, H-2′,6′), 6.95 (2H, d, J = 8.3 Hz, H-3′,5′), 6.88 (1H, s, H-3), 6.83 (1H, s, H-8), 6.44 (1H, s, H-6), 5.09 (2H, d, J = 6.9 Hz, H-1″); 13C-NMR (75 MHz, DMSO-d6) δ: 182.1 (C-4), 164.4 (C-2), 163.0 (C-7), 161.5 (C-5), 161.2 (C-4′), 157.0 (C-9), 128.7 (C-6′), 128.7 (C-2′), 121.1 (C-1′), 116.1 (C-3′), 116.1 (C-5′), 105.4 (C-10), 103.2 (C-3), 100.0 (C-1″), 99.6 (C-6), 94.9 (C-8), 77.3 (C-3″), 76.4 (C-5″), 73.2 (C-2″), 69.6 (C-4″), 60.7 (C-6″). These data were discovered to be consistent with those reported in the literature of apigenin-7-O-β-D-glucopyranoside (Ning, 2000; Fossen and Andersen, 2006; Markham and Geiger, 1994; Stochmal et al., 2001), and so compound 4 was identified as apigenin-7-O-β-D-glucopyranoside.

Compound 5: Physical form, yellow powder; hydrochloric acid-Mg reaction, positive; Molisch reaction, positive. These results suggested that compound 5 could be a flavonoid glycoside.

NMR data: 1H-NMR (300 MHz, DMSO-d6) δ: 12.65 (1H, s, 5-OH-5), 9.0–11.0 (3H, br, -OH), 7.59 (2H, d, J = 5.9 Hz, H-2′, 6′), 6.85 (1H, d, J = 8.9 Hz, H-5′), 6.41 (1H, s, H-8), 6.20 (1H, d, J = 1.4 Hz, H-6), 5.48 (1H, d, J = 6.9 Hz, H-1″); 13C-NMR (75 MHz, DMSO-d6) δ:177.5 (C-4), 164.3 (C-7), 161.3 (C-5), 156.4 (C-2), 156.3 (C-9), 148.6 (C-4′), 144.9 (C-3′), 133.4 (C-3), 121.7 (C-6′), 121.3 (C-1′), 116.3 (C-5′), 115.3 (C-2′), 104.1 (C-10), 100.9 (C-1″), 98.8 (C-6), 93.6 (C-8), 77.7 (C-3″), 76.6 (C-5″), 74.2(C-2″), 70.0 (C-4″), 61.1 (C-6″). These data were found to be consistent with those reported in the literature for quercetin 3-O-β-D-glucopyranoside (Park and Lee, 1996; Bonaccorsi et al., 2005; Lee et al., 2008; Ning, 2000; Fossen and Andersen, 2006; Markham and Geiger, 1994; Stochmal et al., 2001), and so compound 5 was identified as quercetin 3-O-β-D-glucopyranoside.

Compound 6: Physical form, yellow powder; hydrochloric acid-Mg reaction, positive; Molisch reaction, positive. These results suggested that compound 6 could be a flavonoid glycoside.

NMR data: 1H-NMR (300 MHz, DMSO-d6) δ: 12.51 (1H, s, -OH), 10.16 (1H, s, -OH), 9.56 (1H, s, -OH), 8.09 (2H, d, J = 8.8 Hz, H-2′,6′), 6.95 (2H, d, J = 8.8 Hz, H-3′,5′), 6.82 (1H, d, J = 1.5 Hz, 8-H), 6.44 (1H, d, J = 1.7 Hz, H-6), 5.08 (1H, d, J = 6.3 Hz, H-1″); 13C-NMR (75 MHz, DMSO-d6) 176.1 (C-4), 162.8 (C-7), 160.4 (C-5), 159.4 (C-4′), 155.8 (C-9), 147.6 (C-2), 136.1 (C-3), 129.7 (C-2′), 129.7 (C-6′), 115.5 (C-3′), 115.5 (C-5′), 104.8 (C-10), 100.9 (C-1″), 100.0 (C-1′), 98.8 (C-6), 94.5 (C-8), 77.2 (C-3″), 76.5 (C-5″), 73.2(C-2″), 69.7 (C-4″), 60.7 (C-6″). These data were found to be consistent with those reported in the litera-ture for kaempferol-7-O-β-D-glucopyranoside (Ning, 2000; Fossen and Andersen, 2006; Markham and Geiger, 1994; Stochmal et al., 2001), and so compound 6 was identified as kaempferol-7-O-β-D-glucopyranoside.

Compound 7: Physical form, yellow powder; hydrochloric acid-Mg reaction, positive; Molisch reaction, positive. These results therefore suggested that compound 7 could be a flavonoid glycoside. ESI-MS analysis of compound 7 in the negative ion mode revealed a pseudomolecular ion peak with anm/z value of 609, corresponding to [M–H]. Elemental analysis showed that the amounts of C and H in compound 7 were 53.22 and 4.86%, respectively. Taken together with the NMR results, these data suggested that the molecular formula of compound 7 was C27H30O16. The FT-IR spectrum of compound 7 contained a broad peak at 3423 cm-1 and a second peak at 1250–1050 cm-1, which indicated the presence of hydroxyl groups. A peak was also observed at 1656 cm-1, which was attributed to the stretching vibration of a carbonyl group. Several other vibrational absorption peaks were observed at 1601, 1574, 1505 and 1456 cm-1, together with a shoulder peak at 3000 cm-1, which were consistent with an entitative phenyl ring skeleton. The peaks at 1601 and 1505 cm-1 were indicative of the presence of an oxygen-containing heterocycle. The peak at 1363 cm-1 was attributed to the stretching vibration of a methyl group.

NMR data: 1H-NMR (300 MHz, DMSO-d6) δ: 12.61 (1H, s, 5-OH), 8.5–11.5 (1H, br, -OH), 7.54 (2H, d, J = 7.5 Hz, H-2′,6′), 6.84 (1H, d, J = 8.4 Hz, H-5′), 6.38 (1H, s, H-8), 6.19 (1H, s, H-6), 5.34 (2H, d, J = 7.1 Hz, H-1″), 4.38 (1H, s, H-1‴), 0.99 (3H, d, J = 6.1 Hz, H-6‴); 13C-NMR (75 MHz, DMSO-d6) δ: 177.5 (C-4), 164.3 (C-7), 161.4 (C-5), 156.8 (C-9), 156.8 (C-4′), 156.6(C-2), 144.9 (C-3′), 133.5 (C-3), 121.8 (C-6′), 121.3 (C-1′), 116.4 (C-5′), 115.4 (C-2′), 104.1 (C-10), 101.3 (C-1″), 100.9 (C-1‴), 98.9 (C-6), 93.8 (C-8), 76.6 (C-3″), 76.1 (C-5″), 74.2 (C-2″), 72.0 (C-4‴), 70.7 (C-3″), 70.5(C-3‴), 70.2 (C-2‴), 68.4 (C-5‴), 67.2 (C-6″), 17.9 (C-6″). These data were found to be consistent with those reported in the literature of rutin (Park and Lee, 1996; Ning, 2000; Fossen and Andersen, 2006; Markham et al., 1994; Stochmal et al., 2001), and so compound 7 was identified as rutin.

Isorhamnetin (17 mg), quercetin (64 mg), kaempferol (14 mg), apigenin-7-O-β-D-glucopyranoside (3 mg), quercetin 3-O-β-D-glucopyranoside (3 mg), kaempferol-7-O-β-D-glucopyranoside (2 mg) and rutin (11 mg) were obtained from 200 g of dry onion skins using the extraction and isolation methods described above.

Inhibitory effects of the flavonoids from onion skins towards the proliferation of K562 cells

Although a wide range of flavonoids have recently reported to exhibit antitumor activities, inhibit the proliferation of leukemia cells, and induce cell apoptosis, none of these flavonoids have been reported to be nontoxic or even weakly toxic to normal human cells (Cárdenas et al., 2006; Shen et al., 2007). To evaluate the anti-proliferative activities of the flavonoids isolated from onion skins in the current study, we investigated the effects of isorhamnetin, rutin, quercetin, and kaempferol on the viability of chronic myelogenous leukemia K562 cells.

As shown in Figure 2, quercetin and kaempferol led to a significant reduction in the proliferation of the K562 cells. Furthermore, the anti-proliferative activity of quercetin was stronger than that of kaempferol when they were administered at the same concentration. Interestingly, however, isorhamnetin and rutin led to an increase in viability of the K562 cells.


Discussion

In this study, seven flavonoids were isolated from dry onion skins and evaluated in terms of their anti-proliferative activity towards K562 cells. Although isorhamnetin and rutin exhibited certain proliferation-promoting effects, quercetin and kaempferol led to a significant decrease in the viability of K562 cells, with quercetin exhibiting the stronger effect of the two compounds. In terms of the structural features of these flavonols, the presence of an ortho hydroxyl group on the B ring or hydroxyl and carbonyl groups at the 3- and 4-positions, respectively, were critical to the anti-proliferative activity towards K562 cells.

As mentioned above, the mono- and diglucosides of quercetin account for up to 80% of the total flavonol content of onion skins (Rhodes and Price, 1996). Fossen et al. (1998) reported the isolation quercetin, quercetin 3,7,4′-triglucopyranoside, quercetin 4′-O-b-glucopyranoside and quercetin 3,4′-O-b-digluco-pyranoside from the pigmented scales of red onion. Seven flavonols were identified by high-performance liquid chromatography (HPLC) diode array detector coupled with ESI-MS from southern Italian red onions (Bonaccorsi et al., 2005). In this case, quercetin-4′-glucoside and quercetin-3,4′-diglucoside were found to be the most abundant components, whereas quercetin-3-glucoside, quercetin-7,4′-digluco-side, quercetin-3,7,4′-triglucoside, isorhamnetin 4′-gluco-side and isorhamnetin 3,4′-diglucoside were identified as the minor flavonoid components. Furthermore, only trace amounts of free quercetin and isorhamnetin 3-glucoside were detected during this particular study. Although no quercetin diglucosides or quercetin triglu-cosides were isolatedfrom the onion skins used in the current study, a large amount of free quercetin was obtained, as well as a minor amount of quercetin-3-O-β-D-glucopyranoside. Suh et al. (1999) reported similar results to those of the current study, when they identified quercetin and quercetin 4′-glucoside from onion skins by fast atom bombardment. Suh et al. (1999) also reported the isolation of substantial amounts of isorhamnetin, kaempferol and rutin from onion skins, but only managed to isolate a trace amount of kaempferol-7-O-β-D-glucopyranoside. Furthermore, no diglucosides or triglucosides of any other flavonols were isolated from onion skins during this study. Taken together, these results suggest that dry onion skins are an abundant source of free flavonols, as well as containing small amounts of flavonol mono-glucosides, and tracequantities of flavonol di- and triglucosides. Rutin was separated from red Spirit onions by sephadex LH-20 chromatography (Park and Lee, 1996). Three major flavonoids, including kaempferol, myricetin, and quercetin, were identified and quantified using the HPLC method developed for the analysis of Georgia-grown Vidalia onions (Sellappan and Akoh, 2002). In the current study, 11 mg of rutin was isolated from 200 g of dry onion skins, although no myricetin was detected. It is noteworthy that apigenin-7-O-β-D-glucopyranoside was isolated from onion skins in the current study. It is well known that garlic is an abundant source of apigenin (Miean and Mohamed, 2001). However, to the best of our knowledge, this report represents the first report account of isolation of apigenin-7-O-β-D-glucopyranoside from onions.

The anti-proliferative effects of flavonoids towards tumor cells are closely related to their molecular struc-tures. In this sense, specific substituents or structural features could be essential for these flavonoids to exhibit specific pharmacological effects (Cárdenas et al., 2006; Shen et al., 2007). Chang et al. ( 2007) compared the effects of 23 different flavonoids on the proliferation of human leukemia HL-60 cells in terms of their structures. The results of this study indicated that an appropriate number of hydroxyl groups, including a hydroxyls at the 3-position and the ortho position of the B ring, was critical to enhancing the inhibitory effects of plant flavonoids towards HL-60 cell proliferation. Plochmann et al. (Plochmann et al., 2007; Kamei et al., 1996) conduced a similar study, and compared the cytotoxic activities of 23 different flavonoids towards the human leukemia cell line Jurkat E6-1. The results of this study showed that the presence of a 4-carbonyl group and an ortho-hydroxyl group on the B ring were important for enhanced cytotoxicity. Furthermore, flavonoids bearing a 3-hydroxyl group were found to be less cytotoxic towards Jurkat E6-1 cells than their nonhydroxylated counterparts. In the current study, quercetin with an ortho-hydroxyl group on its B ring showed greater antiproliferative activity towards K562 cells than kaempferol, while isorhamnetin appeared to enhance the viability of the K562 cells. The weak promotional effect of rutin towards the viability of the K562 cells was attributed to its 3-hydroxyl and 4-carbonyl groups being sheltered by the 3-glycoside unit. These effects therefore showed that flavonoids with different structural features can exhibit different cytotoxic effects towards different leukemia cell lines.


Conclusion

Onion is a suitable source of flavonoids, its quercetin and kaempferol have good anti-proliferative activities on leukemia K562 cell line.


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