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Review

Phenolic Components and Health Beneficial Properties of Onions †

Beijing Advanced Innovation Center for Food Nutrition and Human Health, Beijing Engineering and Technology Research Center of Food Additives, School of Food and Health, Beijing Technology & Business University (BTBU), Beijing 100048, China
*
Author to whom correspondence should be addressed.
Part of Ph.D Thesis of Effects of pre and post-harvest treatments on the phenolic compounds and antioxidant activity of different onion varieties.
Agriculture 2021, 11(9), 872; https://doi.org/10.3390/agriculture11090872
Submission received: 11 August 2021 / Revised: 2 September 2021 / Accepted: 7 September 2021 / Published: 10 September 2021
(This article belongs to the Section Agricultural Product Quality and Safety)

Abstract

:
Onions are a widely cultivated and consumed vegetable, and contain various bioactive components, which possess various health benefits, such as antioxidant, anti-obesity, and anti-diabetic properties. As the major bioactive constituents in onions, it is essential to study phenolic compounds and the heath beneficial properties of onion and its by-products. The bioactivity of phenolic components in onions can be affected by many factors, including the genotype, different growing environments and food processing methods. Currently, most reviews have focused on an investigation of the chemical compounds or bioactivity of raw onions, but there is a paucity of studies concerning whether pre-harvest (i.e., genotype and growing environment) and post-harvest (i.e., storage) factors can impact its phenolic compounds. This review provides knowledge and guidance to agricultural production on producing high-quality onions and to the food industry on developing functional foods to reduce some chronic diseases such as diabetes. It also promotes research interest in studying bioactive compounds in fruits and vegetables considering different pre-harvest and post-harvest conditions.

1. Introduction

The onion (Allium cepa L.) is a common vegetable and is widely consumed all over the world. It originated in central Asia and is one of the oldest cultivated plants, with cultivation records dating back more than 4000 years [1,2]. Onions are known to contain bioactive compounds related to positive nutritional and health benefits, such as anti-inflammatory, antioxidant, anti-obesity, anti-diabetic, anticancer, anti-allergic, cardiovascular protective, neuroprotective, respiratory protective, and bacteriostatic properties [1,2] (Table 1).
When onions grow to an appropriate stage of maturity, they are harvested. The stage of maturity depends on the planting season, cultivar and conditions of the crop. Before harvest, onion bulbs, along with their tops, are pulled/lifted from the soil in order to stop growth, and are usually kept/cured in the field for a few days to remove excess moisture from the outer skin and neck to avoid excessive shrinkage of the onion, allowing for color development during storage. These fresh onions can then be directly supplied to the market, or further processed into different forms; for example, in dried powders or flakes [3]. It has been reported that the growing international market for onion products has been developed with dehydrated methods such as powder, frozen, or canned onions [4]. One of the drivers to further process fresh onions into other forms was to reduce product loss (20–30%) during storage. Additionally, dehydrated products possess medicinal features, containing higher concentrations of beneficial compounds than fresh onions [5].
The food industry offers commercial onion powder as a nutraceutical or a dietary supplement [5,6]. Onion powders, rich in phenolic compounds, can produce positive effects that combine with other food to improve antioxidant capacity and flavor [5,6,7].
Although the bioactive compounds and certain bioactivities of onion have been discussed in recent reviews [8,9,10], this review can provide a more comprehensive understanding about how pre-harvest and post-harvest factors affect the changes of phenolic compounds in onions. The literature summarized in this review was mainly collected from Web of Science and Scopus databases from 1996 to 2021. We hope that this paper can attract a broader attention to those who are interested in studying bioactive compounds in onions and those who are interested in developing functional foods with the extraction of phenolic compounds in reducing the risk of some chronic diseases.
Table 1. Reported bioactivity of phenolics in onions.
Table 1. Reported bioactivity of phenolics in onions.
Reported BioactivitiesReferences
Preventing cardiovascular diseases [11]
[12]
Antioxidant
Anti-inflammatory[13]
[14]
[15]
[16]
[17]
[18]
[19]
[20]
[21,22,23]
Anti-proliferative
Anti-angiogenic
Pro-apoptotic
Activating Immune destruction
Tumor promoting inflammation
Senescence induction and telomerase inhibition
Preventing the growth of tumors
Apoptosis autophagy[24]
Reducing the risk of death from coronary heart disease[25,26]
Against arteriosclerosis[27]
Antimicrobial activity against fungal, bacterial and viral infections[28]
Anticarcinogenic and antimutagenic activities [29]
Anti-hypertensive effect and reduce blood pressure [30]
Anti-hyperglycemic or anti-diabetic potential and prevention of advanced glycation of collagens, which contributes to the development of cardiovascular complications in diabetic patients [31,32]

2. Phenolic Compounds in Onions

Common fruits and vegetables that are abundant in phenolics include most berry crops, many tree fruit crops and onions. Onion was reported to be one of the vegetables that contains the greatest amount of phenolic compounds contributing to the human daily diet [33,34,35]. Flavonoids are the largest group of phenolic compounds, along with quercetin, and will be summarized and discussed in this section.

2.1. Flavonoids in Onions

Most flavonoids are important polyphenols in foods and they are categorized by their chemical structure, namely: flavonols, flavones, flavanones, isoflavones, flavanols, catechins, flavanonols and anthocyanidins (Figure 1). Many studies have investigated the presence of flavonoids in onions [26,36]. At least 25 different flavonols have been characterized in onions [37]. There are seven major flavonol compounds in onions and they are (i) quercetin aglycone; (ii) quercetin monoglucoside; (iii) quercetin diglucosides; (iv) isorhamnetin, which is a methyl ether of quercetin; (v) isorhamnetin monoglucoside; (vi) rutin; and (vii) kaempferol. Kaempferol is detectable in certain onion varieties but it presents in much smaller quantities than quercetin [38,39].
Even though anthocyanins do not constitute a major flavonoid content in onions, they have frequently been reported to be presented in red onions. Slimestad, Fossen, and Vagen [37] reported that there are at least 25 different anthocyanins in red onions, with the quantitative content being approximately 10% (39–240 mg/kg fresh weight) of the total flavonoid content (TFC). Bystricka et al. [40] also showed that many varieties of red onions contain red anthocyanins in the form of glycosides of cyanidin, peonidin, and pelargonidin. Anthocyanins are also reported to be a source of antioxidant activity [41]. Anthocyanin pigments, concentrated in the outer shell/skin of red onions, are only minor constituents of the edible portion.
However, little is known about the total amount of anthocyanins in red onions. Although some researchers have found about 250 mg/kg (wet weight) anthocyanins in red onions, they did not address which part of the onion they used, the edible part or the whole onion [42,43]. Statistically, the most amount of anthocyanins was found on the dry skin of red onions, ranging from a minimum 109 mg/100 g to a maximum 219 mg/100 g [44].

2.2. Quercetins in Onions

Quercetin is the aglycone form of a number of flavonoid glycosides, such as rutin, found in onions [45,46]. Glycosides can be classified by the type of glycone, by the type of glycosidic bond, or by the aglycone. The aglycone part is the non-sugar part of a glycoside. Quercetin diglucoside (Qdg) and monoglucoside (Qmg) account for up to 93% of the total flavonol content in onions [47]. Sellappan and Akoh [48] also reported that quercetin is the major flavonoid found in onion and is presented in its conjugated form, quercetin 4′ glucoside (4′Qmg), quercetin 3,4′ diaglucoside (3,4′Qdg), and quercetin. Slimestad, Fossen, and Vagen [37] also agreed that quercetin and its derivatives were the most dominant flavonols found in studied onion cultivars. Similarly, Lombard et al. [49] reported that 4′Qmg and 3,4′Qdg are the main flavonols present in onions, accounting for about 80 to 95% of the total flavonol content.

3. Variation of Phenolic Contents in Onions

3.1. Different Onion Cultivars

Onions have the highest quercetin compounds among many other vegetables and fruits [50]. Onions contain 300 mg quercetin/kg fresh weight compared to 100 mg/kg fresh weight in kale, 40 mg/kg fresh weight in blackcurrants, and 30 mg/kg fresh weight in broccoli and apples [51]. Onions provide a good example of the importance of a vegetable genotype on the content of phenolic compounds [52]. Both color and long/short day onion cultivars contribute to the differences in the content of phenolic compounds.
Color is a phenotypical attribute and is closely related to the content of flavonols in onions [53]. Total flavonol contents in onions are usually higher in red onions, and lower in yellow or white varieties [54,55]. In a detailed study of 55 onion cultivars, the level of quercetin was found to be the highest in red, pink, and yellow onion varieties (in the range of 54–286 mg/kg fresh weight (FW), whilst white onions contained low levels of quercetin [56]. Similarly, Pérez-Gregorio and colleagues studied two white and three red onion varieties and the results showed that all the red onions contained the highest levels of flavonols and anthocyanins [36]. Marotti and Piccaglia stated that colored onions showed higher TFC than white ones [52,57]. It seems that color plays an important role in determining the content of flavonols. However, Crozier et al. [58] found that red-skinned onion did not contain a higher level of quercetin content than the white-skinned onions. This could be due to different onion varieties and different growing locations.
Long-day onion cultivars and short-day onion cultivars were studied by Okamoto et al. [59], Yoo, Lee, and Patil [60] and Petropoulos et al. [61], who reported the differences in quercetin content in these two cultivars. Lombard, Geoffriau, and Peffley [62] pointed out that the total quercetin content in long-day cultivars was documented to be higher than in short-day cultivars and this difference did not depend on growing locations. The effects of onion bulb size on quercetin content was also investigated by some researchers. Lee et al. [63] reported that small onions had higher flavonoid contents than larger onions. However, Patil, Pike, and Hamilton [64] demonstrated that bulb size did not show any effect on the quercetin level. Mogren, Olsson, and Gertsson [51] also reported that minor or no differences in quercetin glucoside content were observed between small- and large-sized onions.

3.2. Flavonoid Distribution in Onion Tissue

Flavonoids in onions, mainly consisting of quercetins, accumulate to varying degrees in plant tissues and the levels determined in different plant parts are dependent upon environmental conditions [65]. Onion bulb skin (the non-edible dry peel) is richer in total flavonoids compared to the edible pulp. Grzelak et al. [66] determined a three-fold difference in flavonols presented in the fresh outer scales of the studied onion compared to any other onion part. Lee et al. [63] reported a decrease in the content of flavonoids in onion from the first to the seventh scale, i.e, from the onion skin to the onion pulp. Mogren, Olsson, and Gertsson [51] claimed that about 90% of total flavonols was concentrated and confined to epidermal tissue. Nemeth and Piskula [67] and Slimestad and Vagen [68] suggested that higher flavonol contents in the outer bulb scales, compared to the inner scales, is due to cell aging. However, Beesk et al. [69] found that the total flavonoid content in onions ranked as follows: middle layers > outer layers > inner layers.
Anthocyanin contents in onions were also studied and reported to be rich in the dry skin of onion bulbs (particularly in red and pink onion varieties). It is noteworthy that 63% of red onion anthocyanins are presented in the dry skin, which means that, after bulb peeling, only 27% of the total anthocyanins of red onion will be consumed [70].

4. Bioactivity of Phenolic Compounds in Onions

Onion has been reported to have multiple health functions based on in vitro, in vivo, and human studies [71,72,73,74,75,76] (Table 1). Phenolics, as the major bioactive constituents in onions, not only have strong biological functions such as anti-inflammatory and antioxidant activities [77,78,79,80,81,82,83,84,85,86], which are linked to the prevention of a number of degenerative diseases, but also provide sources for natural food dyes [77]. In this section, antimicrobial activity, antioxidant activity and anticarcinogenic and antimutagenic activities of onion and its by-products are mainly summarized and discussed.

4.1. Antimicrobial Activity of Onions

Pszczola [87] highlighted the fact that onions have been used for centuries against fungal, bacterial and viral infections. Phenolic compounds in onions were reported to contribute to these activities [75]. Due to the great antimicrobial activity that onions appear to possess, it is not surprising that onion-derived phenolic compounds have been investigated for their antimicrobial properties, especially owing to the fact that these compounds appear to be relatively stable. Santas, Almajano and Carbo [88] investigated the antimicrobial activity of flavonol standards and ethyl acetate subfractions of methanolic extracts of three Spanish onion varieties against three different bacterial strains. Among the onion extracts tested, ethyl acetate sub-fractions alone showed microbial inhibition.
It was reported that the major onion flavonoids possessed antiviral activity and enhanced the bioavailability of some antiviral drugs [89]. Chen et al. [90] found that shallots presented the highest antiviral activities, followed by onions. Given the high content of quercetin in onion, it was suspected that quercetin and its derivatives affected antiviral action.
Zohri, Abdel-Gawad, and Saber [91] reported that onion extracts are effective against many yeast species, and their essential oils inhibit dermatophytic fungi. De Souza et al. [92] demonstrated a relationship between the levels of total phenolics in onion and the antifungal activity tested against Rhizopus oryzae.
In sum, accumulated studies have demonstrated that onion inhibits the growth of microbes, showing great potential to be used as a natural preservative in the food industry to maintain food quality.

4.2. Antioxidant Activity of Onions

Onions have shown antioxidant properties due to the presence of polyphenols [93,94,95]. Some research has highlighted the variation that occurs in antioxidant activity in onions, owing to the fluctuation in onion total phenolic content [96,97]. Gokce et al. [98] suggested that red onions had higher antioxidant activities than yellow and white onions. Bora and Sharma [38] indicated that the dry outer layers of onion contained large amounts of quercetin, quercetin glycoside and their oxidative products, which are effective antioxidants against non-enzymatic lipid peroxidation and oxidation of low-density lipoproteins.
A good source of antioxidant polyphenols can be found in onion waste (i.e., residues and surpluses of onion) and by-products [99]. Singh et al. [29] pointed out that extracts from red onion peel contained large amounts of antioxidant polyphenols. Benite et al. [100] reported a higher content of total phenolics and flavonoids from brown skin and top-bottoms of industrial onion wastes had a high antioxidant activity compared with other bioactive compounds, and hence the wastes could be used as functional ingredients. A by-product developed by Roldan et al. [101] derived from two Spanish onion cultivars that were stabilised by thermal treatments are shown to possess good antioxidant activities measured by the DPPH (2,2′-diphenyl-1-picrylhydrazyl radical) assay.
In addition to onion varieties, processing treatments and extraction methods could also affect the antioxidant activities of onion extracts. Widely employed food processing methods on the antioxidant activity of onions include drying [102,103], heating [104], and high-pressure processing [105], which showed a decrease in the antioxidant activity of onions [104].
Singh et al. [29] used several methods to extract polyphenols and found that ethyl acetate (EA) extract obtained large amounts of polyphenols, and hence displayed a stronger antioxidant capacity. Roldan et al. [101] found that obtaining the onion paste from processing the onion wastes, followed by applying mild pasteurization, were the best approach to obtain an increasing stabilized onion by-product with good antioxidant activities. According to Lee et al. [106], onion samples were heated and juiced and the levels of active compounds in onions increased after heating, since the antioxidant activities of the ethyl acetate fraction were higher in onions heated at 120 °C, 130 °C or 140 °C for 2 h than in raw onions, and the higher the processing temperature employed, the greater were the radical and nitrite scavenging activities observed. Similar results were found by Woo et al. [107], who indicated that the optimal heating time and temperature were 2 h at 130 °C. In contrast, Khaki et al. [108] employed acidified water/ethanol-based solvent extraction systems and reported that optimal extraction yields occurred at 6 h, whereas an increasing temperature from 40 °C to 60 °C had a negative effect on yields. Different processing conditions (e.g., temperature, time) may affect the antioxidant activity in onions. The bioactivity of phenolic compounds in onion was reduced by thermal processing, but the use of extraction solvents or extraction techniques could improve the bioactivity of its phenolic compounds under optimal conditions (i.e., temperature and time).

4.3. Anticarcinogenic and Antimutagenic Activities

As highlighted previously, quercetin and its derivatives have been shown to exhibit anticancer properties, including activity against prostate, breast, skin, lung and liver cancers [109]. Jeong et al. [110] reported different anticancer activities from extracts from pulp and peel of white, yellow and red onion. In general, onion peel with the highest amounts of total phenolics and flavonoids inhibited the growth of several human cancer cell lines, including cells from both the stomach and colon, breast and prostate [110], more efficiently than fresh onion pulp. Likewise, several studies have reported that quercetin enhanced the bioavailability of some anticancer drugs, such as Tamoxifen, a non-steroidal antiestrogen for the treatment and prevention of breast cancer, by promoting its intestinal absorption and reducing their metabolism [89].

4.4. Hypotensive and Bradycardic Effects

A study with several rat models of hypertension has indicated that quercetin and its methylated metabolite isorhamnetin can reduce blood pressure [30]. Moreover, Edwards et al. [111] investigated the efficacy of supplementation of quercetin on lowering blood pressure in hypertensive humans and demonstrated that 730 mg of quercetin per day could reduce systolic blood pressure by 7 mm Hg, diastolic blood pressure by 5 mm Hg, and mean arterial pressure by 5 mm Hg in hypertensive patients. Egert, Bosy-Westphal, and Plachta-Danielzik [112] also found that quercetin reduced systolic blood pressure and plasma oxidized low-density lipoproteins concentrations in overweight subjects with a high cardiovascular disease (CVD) risk phenotype. It is believed that more animal studies and clinical trials are required for a better understanding of the cardiovascular protective effects of onion and its phenolic compounds.

4.5. Anti-Hyperglycemic and Anti-Diabetic Potential

An investigation into the effects of quercetin on human diabetic lymphocytes showed an association between an increase in the protection against DNA damage from hydrogen peroxide at the tissue level and the number of consumed flavonols (mostly quercetin) from onions [113]. Likewise, it has been reported that long-term absorption of quercetin could be useful to prevent advanced glycation of collagen, which contributes to the development of cardiovascular complications in diabetic patients [31].

4.6. Anti-Platelet Effect

Quercetin and its derivative showed their beneficial effects on cardiovascular health because of their antioxidant and anti-inflammatory activities [114], through the inhibition of lipid peroxidation and endothelial cell damage, which are involved in the early development of atherosclerosis [115]. An in vitro study carried out by Janssen et al. [116] showed that 2500 μmol/L quercetin isolated from onions inhibited platelet aggregation by 95–97%. However, an in vivo assay from the same authors with 18 human subjects ingesting 114 mg quercetin/day showed no significant effects. They concluded that necessary concentration levels of quercetin for the beneficial effects were too high to be obtained in daily dietary.

5. Pre-Harvest Treatments Influencing the Phenolic Compounds in Onions

Besides intrinsic characteristics such as different onion varieties, many other factors influence the level of phenolic compounds in onions, for example environmental conditions (e.g., soil type, sun exposure, and rainfall) and agronomic conditions (e.g., culture in greenhouses or fields, biological culture, and hydroponic culture) [117,118]. Table 2 lists the pre-harvest factors and their effects on the quercetin content of onions during growing and storage.
Patil, Pike, and Hamilton [64] showed that meteorological factors (including temperature and rainfall patterns) had a stronger influence on quercetin concentration in onion cultivars than soil factors or plant maturity. Mogren, Olsson, and Gertsson [126,130] indicated a strong correlation between total radiation during lifting stages and the quercetin glucoside content of onions. However, Patil, Pike, and Hamilton [64] reported no correlation between onion growth stage and quercetin content in onions. On the other hand, they showed a relationship between the quercetin content of onions and environmental factors such as location and soil type, which played a major role in affecting the levels of quercetins.
Furthermore, there is increasing evidence indicating an impact of genotype, growing environment including the production year, and interactions between the genotype and growing conditions on variations in the bioactive compositions and contents of onion [117,118]. Others have also reported the effect of genotype and environment interaction on the total phenolic contents and antioxidant properties of wheat [114], but little is known about such interactions in onions.

5.1. Light

Light can influence genetic expression that is relevant to enzymes participating in the phenylpropanoid pathway [129]. Light conditions during plant development and/or storage (in light or darkness) could play an important role in the total phenolic content [129]. Quercetins are strong UV-absorbing compounds, and can be accumulated mainly in the epidermal cells of plant tissues after UV-induction [132]. Light stimulates the synthesis of quercetins, and L-phenylalanine ammonia-lyase (PAL) is the major inducible enzyme [133]. The formation of the quercetin glucoside (QG) is normally induced by UV light, which induces PAL activity up to 30-fold [71]. Yoo, Lee, and Patil [134] exposed onions under different lights, and found that the synthesis of QG compounds is enhanced by UV light and, to a lesser extent, by visible light. In the sprouting leaves, 4′Qmg and 3,4′Qdg concentrations increased most when exposed to UV light and, to a lesser extent, when exposed to visible light; however, even the samples in dark conditions showed a slight increase in QG compounds.
Onions grown in full sunlight have been reported to contain higher levels of flavonoids [135]. A five-year study which examined the effect of climatic conditions on flavonoid contents in two Portuguese landrace onion varieties, total quercetin levels varied significantly between years, with the highest quercetin levels observed in dry years [131].
Mogren, Olsson, and Gertsson [51] proposed that global radiation rather than temperature is the determining factor for quercetin glucoside biosynthesis in onions. Rodrigues et al. [127] pointed out that global radiation at the end of the onion production period seemed to be one of the major determinants of annual quercetin glucoside content in the onions. Mogren, Olsson, and Gertsson [51] reported that, during a four-year study, the month with the lowest global radiation corresponded to the lowest levels of quercetin glucosides. Higashio et al. [128] found that quercetin content in onion could be doubled after harvest using UV light lamps to irradiate the onion. Lee et al. [63] conducted a similar study where they exposed onions to fluorescent light for 24 and 48 h and showed that this induced time-dependent increases in quercetin content.
Light can also cause a stress signal, enhancing flavonoid synthesis in some fresh cut foods [129]. Under the light, an increase of flavonols [63] and quercetin has also been found in fresh-cut onions [130]. Pérez-Gregorio et al. [131] also found that, with the light, total flavonoids in fresh-cut onions were increased by 58% and anthocyanins were increased by 39%.

5.2. Soil Status

Patil, Pike, and Hamilton [64] observed higher amounts of quercetin in onions grown in both clay and sandy loam soils with nitrogen limitation. However, the correlation between nitrogen stress and flavonol synthesis could not be verified due to the different growth stages of onions during experiments. On the other hand, they concluded that the site of growth, more so than the growth stage and soil type, is a major environmental factor in determining quercetin concentration in onion.
Application of fertilizer is one of the most dominant factors affecting the level of quercetin in onions [132]. Nitrogen, phosphorus, and potassium are the three major fertilizers required for the optimum growth of plants; however, the amount and the method of fertilizer application also influences the level of quercetins. A decrease in soil nitrogen concentration may be associated with an increase in total quercetin concentration [133], and a limited nitrogen supply was also reported to be associated with higher levels of phenolics in plants [71]. However, either high or low levels of nitrogen fertilizers during the growth of onions did not result in differences in quercetin content after field curing [132].
Fertilizer application methods and nitrogen source (organic and conventional fertilizers) can significantly affect bulb size, without affecting total yield and the quercetin content of dry bulbs [132].

5.3. Agronomic Conditions

Agronomic practices, such as sowing date, fertilization, irrigation, and subsequent harvesting, would affect quercetins content in onions. Previous studies showed that organically grown onions had higher levels of flavonols and antioxidant capacity than conventionally grown onions [126]. However, Søltoft et al. [134] found no significant differences between the conventionally and the organically grown onions in terms of quercetin content.

6. Changes in Content of the Phenolic Compounds in Onions during Post-Harvest

Onion bulbs are normally sown in March and are generally mechanically harvested from late August to mid-September. Before harvest, they are lifted to stop their growth and are cured by air drying at 25–28 °C and 65–75% RH for ten days to six weeks in the UK and Ireland [135] (Figure 2).
Onion bulbs are ready for harvest as soon as the leaves of the plants (‘top’) start to recline (‘fall’). The usual practice is to harvest when 25–80% of tops have fallen, with a consequently significant effect on storage susceptibility and quality of the bulbs. Harvest stage can be essential for sprout incidence, since early lifting can result in a lower sprouting percentage and better storage without negative effects on the initial quercetin content, which remains unchanged during storage [51].
Quercetin content in onions increases after lifting and the lifting time would affect the increase. Mogren, Olsson, and Gertsson [136] pointed out that an early lifting time of onions resulted in a reduced level of quercetin content in onions, probably due to low sprouting and a lighter color in the early lifted onions. On the other hand, late lifting (80% fallen leaves) resulted in up to 45% higher concentrations of quercetin glucosides compared to early lifting (50% fallen leaves).

6.1. Effect of Curing on the Phenolic Compounds

Straight after harvest, bulbs have to be subjected to a drying process (‘curing’) in order to have their outer scales hardened and to reduce skin cracks, and allow the necks to become narrower, thus inhibiting pathogen infections. Curing method (field curing or forced air curing) and conditions (temperature and relative humidity), as well as growing conditions and harvest stage, can be of major importance for maximum quality in dry bulbs and minimum losses due to water losses and pathogen infections [137].
Curing may result in an increase of flavonols in onions, although this phenomenon depends on the year and cultivars [138]. Patil, Pike, and Hamilton [64] indicated that onions cured in the field could accumulate more flavonols. Traditionally, in hot dry climates, onions can be left to cure in the field in windrows or mesh bags and this has been reported to be associated with an increase in quercetin content [51]. Rodrigues et al. [125,129] also reported that field curing increased 4′Qmg and 3,4′Qdg (33–40%) content compared to levels at lifting, particularly when the flavonol concentrations were low at lifting. Light conditions (light or dark condition) during curing, however, did not affect flavonol and anthocyanin contents, regardless of skin color and cultivar.
The effect of cold storage combined with curing or post-curing treatment was studied by many researchers. Downes, Chope, and Terry [131] cured two types of yellow onion and one kind of red onion at 20 °C, 24 °C or 28 °C for six weeks and then stored the onions at 1 °C for seven months. They found that levels of flavonols in red onions cured at 20 °C decreased during cold storage for seven months.
The evolution of onion flavonols during storage after post-curing heat treatment at 36 °C for 24 or 96 h was studied by Olsson, Gustavsson, and Vagen [139]. Three onion varieties were cured in the field for two weeks and then heat treated, followed by subsequent cold storage at 2 °C for up to eight months. The levels of Q 3,4′ D increased in the 24-h. A lower content of total flavonols was found in the three onion varieties after eight months of cold storage following the 96-h heat treatment, possibly due to negative effects of heat treatment on onion metabolism.
Price and Rhodes [133] investigated the levels of flavonols of two onion varieties (‘Red Baron’ and ‘Crossbow’) cured at 28 °C for ten days and stored for six months at ≤4 °C in dark, and found no change in the flavonol levels for the two varieties after storage.

6.2. Evolution of the Phenolic Compounds When Sprouting during Storage

Post-harvest sprouting in onions would occur after long-term storage. Onions may be kept in cold storage at around 1–4 °C in the dark to induce dormancy and prevent sprouting; however, sprouting commonly initiates within one to three weeks after removal from cold storage [140]. Benkeblia and Shiomi [141] indicated that total phenolics content (TPC) in onions began to reduce when internal sprouting began, which can be caused by the temperature change (from cold to room temperature) during storage. In their study, the reduction also happened to onions stored in control conditions (in refrigerators) when internal sprouting began, after seven weeks of storage. Benkeblia et al. [142] also reported that there was an inverse relationship between total phenolic content and sprout development.
However, conflicting results were reported by Sharma et al. [143], who investigated the evolution of total flavonoid content (TFC) of onions during storage (post-storage) at room temperature and relatively humidity (RH) 60–80%, subsequent to a cold storage for eight months. They found that internal sprouting began within the 1st week post-storage, but TFC increased during the post-storage time, and reached a maximum between the 4th and 8th weeks.

6.3. Evolution of the Phenolic Compounds during Storage

Phenolic contents can be changed during storage. Kevers et al. [144] argued that, 23 days after purchasing, both antioxidant activity and the total flavonols of onions increased during storage and became 10 times higher than on purchase from the market. Sharma et al. [143] also reported increased TPC and TFC during storage at room temperature after cold storage. However, due to sprouting and decay after four weeks post-storage, they suggested that the onions thereafter should be used only for, e.g., extraction of nutraceuticals. Rodrigue et al. [145] stored Portuguese red and white onions after harvest for seven months under refrigeration (at 2 °C and 65% relative humidity) or under traditional bulk storage in the field. TFC in both of the two varieties increased up to 64% after six or seven months of storage, especially in the first three months (58% increase), irrespective of the storage temperature. Regarding anthocyanins, after seven months in both conditions (refrigeration and traditional treatment), the anthocyanin content was reduced by more than 40%. Elhassanneen and Sanad [146] reported significant differences in flavonol content between white and red Egyptian onion varieties, with red varieties having a higher content of total flavonols, quercetin and quercetin glucosides after storage for a three-month period. Quercetin glycosides are not significantly affected by storage; however, the fact that these compounds are present mostly in the outer scales, which are severely affected by storage and are usually discarded after the peeling of bulbs, could affect nutritional values and their intake on a daily basis [147].
It is believed that the phenolic compounds in onions could be influenced by storage conditions [35]. Storage conditions, like storage time, temperature and light, have effects on the synthesis, retention or breakdown of quercetins. Sharma et al. [148] examined the effect of storage under aerobic and anaerobic conditions at ambient temperatures, reporting that quercetin content increased significantly during anaerobic condition and that total phenolic and flavonoid contents were positively correlated with antioxidant activity. Light conditions and light quality during storage may affect quercetin and quercetin glucoside profiles. Ko et al. [149] examined the effect of five light wavelengths (dark, white, red, blue and UV-A light) for three days as a post-harvest treatment and found that white light treatment significantly increased quercetin glucoside content in peeled onion bulbs, as well as in bulb skins.

7. Storage Technologies

Storage technologies are employed to prolong onions or its product shelf life. Some studies have been carried out to investigate the effects of these technologies on the levels of phenolics, mainly flavonoid compounds, in onions during storage [150,151].
Drying technological developments are driven by consumers who demand a healthy, fresh, and convenient food. Hence, the effect of dehydration on onion quality was studied [3,152]. Drying can prolong the shelf life of onions, and onions can be marketed as dried powder intended for culinary uses, by applying various drying processes [153,154]. Pérez-Gregorio et al. [131] pointed out that freeze-drying, as an innovative drying technique, used to dry chopped onions could prolong the shelf life of dried powder at room temperature for up to six months without significant quality losses in terms of antioxidant compounds (flavonols and anthocyanins), provided that they are stored under dark conditions and within air-tight containers. The freeze-drying process produces the highest-quality dried food product, since the food structure is not damaged during sublimation; hence, it was verified that onion flavonoid content increases after the freeze-drying process [131]. The stability of flavonoids of freeze-dried onion after long-term storage was mainly due to the inactivation of various enzymes, as well as ethylene activity [145]. Moreover, the implementation of the freeze-drying technique itself resulted in an increase in the extractable flavonoids by 32 and 25% for flavonols and anthocyanins, respectively, because of the structural changes of bulb tissues that made flavonoids more readily available [131].

8. Conclusions

Onion, as an important crop in the Allium family, contains a high amount of phenolics compounds, which to a great extent is attributed to human overall dietary intake. It is worth noting that the content of the phenolic compounds can be varied in different onion cultivars. For example, red onion cultivars generally contain the highest level of flavonoids. In addition, agronomic practices (sowing date, fertilization, and harvesting time) can also affect the phenolic content of onions.
The storage of onions is a complex process that can be influenced by many factors. Pre-harvest conditions that affect the storability of onion bulbs are related to genetic background and growing conditions, including cultivar, fertilizer, and harvest stage. In addition, storage conditions (time, temperature, relative humidity, controlled atmospheres) are important for retaining high quality bulbs as well as for prolonging the life of onions. Optimized storage conditions can subsequently be employed after processing to further reduce the loss of phenolic content in raw and processed onions. Some new techniques such as different drying methods, which are applied in onion production have benefits in retaining quality, and bioactive compounds and increasing storage potential during storage. Most of the studies so far have been performed at a laboratory scale, but further research is necessary to apply the knowledge to industry needs to maintain onion quality.

Author Contributions

Conceptualization, F.R., S.Z.; Writing—original draft preparation, F.R., S.Z.; Writing—review and editing, S.Z.; Supervision, S.Z. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Taglienti, A.; Araniti, F.; Piscopo, A.; Tiberini, A. Characterization of Volatile Organic Compounds in ‘Rossa di Tropea’ Onion by Means of Headspace Solid-Phase Microextraction Gas Chromatography–Mass Spectrometry (HS/SPME GC–MS) and Sensory Analysis. Agronomy 2021, 11, 874. [Google Scholar] [CrossRef]
  2. Kazimierczak, R.; Średnicka-Tober, D.; Barański, M.; Hallmann, E.; Góralska-Walczak, R.; Kopczyńska, K.; Rembiałkowska, E.; Górski, J.; Leifert, C.; Rempelos, L. The Effect of Different Fertilization Regimes on Yield, Selected Nutrients, and Bioactive Compounds Profiles of Onion. Agronomy 2021, 11, 883. [Google Scholar] [CrossRef]
  3. Khan, M.K.I.; Ansar, M.; Nazir, A.; Maan, A.A. Sustainable dehydration of onion slices through novel microwave hydro-diffusion gravity technique. Innov. Food Sci. Emerg. Technol. 2016, 33, 327–332. [Google Scholar] [CrossRef]
  4. Choi, S.M.; Lee, D.-J.; Kim, J.-Y.; Lim, S.-T. Volatile composition and sensory characteristics of onion powders prepared by convective drying. Food Chem. 2017, 231, 386–392. [Google Scholar] [CrossRef]
  5. Arslan, D.; Özcan, M.M. Study the effect of sun, oven and microwave drying on quality of onion slices. LWT-Food Sci. Technol. 2010, 43, 1121–1127. [Google Scholar] [CrossRef]
  6. Debnath, S.; Hemavathy, J.; Bhat, K. Moisture sorption studies on onion powder. Food Chem. 2002, 78, 479–482. [Google Scholar] [CrossRef]
  7. Lanzotti, V. The analysis of onion and garlic. J. Chromatogr. A 2006, 1112, 3–22. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  8. Zhao, X.-X.; Lin, F.-J.; Li, H.; Li, H.-B.; Wu, D.-T.; Geng, F.; Ma, W.; Wang, Y.; Miao, B.-H.; Gan, R.-Y. Recent advances in bioactive compounds, health functions, and safety concerns of onion (Allium cepa L.). Front. Nutr. 2021, 8, 463. [Google Scholar] [CrossRef]
  9. Marrelli, M.; Amodeo, V.; Statti, G.; Conforti, F. Biological properties and bioactive components of Allium cepa L.: Focus on potential benefits in the treatment of obesity and related comorbidities. Molecules 2019, 24, 119. [Google Scholar] [CrossRef] [Green Version]
  10. Moreno-Ortega, A.; Pereira-Caro, G.; Ordóñez, J.L.; Muñoz-Redondo, J.M.; Moreno-Rojas, R.; Pérez-Aparicio, J.; Moreno-Rojas, J.M. Changes in the antioxidant activity and metabolite profile of three onion varieties during the elaboration of ‘black onion’. Food Chem. 2020, 311, 125958. [Google Scholar] [CrossRef] [PubMed]
  11. Lamson, D.W.; Brignall, M.S. Antioxidants and cancer, part 3: Quercetin. Altern. Med. Rev. J. Clin. Pharm. 2000, 5, 196–208. [Google Scholar]
  12. Siddiq, M.; Roidoung, S.; Sogi, D.; Dolan, K. Total phenolics, antioxidant properties and quality of fresh-cut onions (Allium cepa L.) treated with mild-heat. Food Chem. 2013, 136, 803–806. [Google Scholar] [CrossRef]
  13. Hanahan, D.; Weinberg, R.A. The hallmarks of cancer. Cell 2000, 100, 57–70. [Google Scholar] [CrossRef] [Green Version]
  14. Gee, J.M.; Hara, H.; Johnson, I.T. Suppression of intestinal crypt cell proliferation and aberrant crypt foci by dietary quercetin in rats. Nutr. Cancer 2002, 43, 193–201. [Google Scholar] [CrossRef]
  15. Yang, J.; Meyers, K.J.; van der Heide, J.; Liu, R.H. Varietal differences in phenolic content and antioxidant and antiproliferative activities of onions. J. Agric. Food Chem. 2004, 52, 6787–6793. [Google Scholar] [CrossRef]
  16. Ly, T.N.; Hazama, C.; Shimoyamada, M.; Ando, H.; Kato, K.; Yamauchi, R. Antioxidative compounds from the outer scales of onion. J. Agric. Food Chem. 2005, 53, 8183–8189. [Google Scholar] [CrossRef]
  17. Russo, M.; Spagnuolo, C.; Tedesco, I.; Bilotto, S.; Russo, G.L. The flavonoid quercetin in disease prevention and therapy: Facts and fancies. Biochem. Pharmacol. 2012, 83, 6–15. [Google Scholar] [CrossRef] [PubMed]
  18. Lisanti, A.; Formica, V.; Ianni, F.; Albertini, B.; Marinozzi, M.; Sardella, R.; Natalini, B. Antioxidant activity of phenolic extracts from different cultivars of Italian onion (Allium cepa) and relative human immune cell proliferative induction. Pharm. Biol. 2016, 54, 799–806. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  19. Sharma, K.; Lee, Y.R. Effect of different storage temperature on chemical composition of onion (Allium cepa L.) and its enzymes. J. Food Sci. Technol. 2016, 53, 1620–1632. [Google Scholar] [CrossRef] [PubMed]
  20. Valentová, K.; Šíma, P.; Rybková, Z.; Křížan, J.; Malachová, K.; Křen, V. (Anti) mutagenic and immunomodulatory properties of quercetin glycosides. J. Sci. Food Agric. 2016, 96, 1492–1499. [Google Scholar] [CrossRef]
  21. Fredotović, Ž.; Šprung, M.; Soldo, B.; Ljubenkov, I.; Budić-Leto, I.; Bilušić, T.; Čikeš-Čulić, V.; Puizina, J. Chemical composition and biological activity of Allium cepa L. and Allium× cornutum (Clementi ex Visiani 1842) Methanolic extracts. Molecules 2017, 22, 448. [Google Scholar] [CrossRef] [Green Version]
  22. Murayyan, A.I.; Manohar, C.M.; Hayward, G.; Neethirajan, S. Antiproliferative activity of Ontario grown onions against colorectal adenocarcinoma cells. Food Res. Int. 2017, 96, 12–18. [Google Scholar] [CrossRef]
  23. Bahram-Parvar, M.; Lim, L.T. Fresh-Cut Onion: A Review on Processing, Health Benefits, and Shelf-Life. Compr. Rev. Food Sci. Food Saf. 2018, 17, 290–308. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  24. Hanahan, D.; Weinberg, R.A. Hallmarks of cancer: The next generation. Cell 2011, 144, 646–674. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Hertog, M.G.; Feskens, E.J.; Kromhout, D.; Hollman, P.; Katan, M. Dietary antioxidant flavonoids and risk of coronary heart disease: The Zutphen Elderly Study. Lancet 1993, 342, 1007–1011. [Google Scholar] [CrossRef]
  26. Arshad, M.S.; Sohaib, M.; Nadeem, M.; Saeed, F.; Imran, A.; Javed, A.; Amjad, Z.; Batool, S.M. Status and trends of nutraceuticals from onion and onion by-products: A critical review. Cogent Food Agric. 2017, 3, 1280254. [Google Scholar] [CrossRef]
  27. Kleemann, R.; Verschuren, L.; Morrison, M.; Zadelaar, S.; van Erk, M.J.; Wielinga, P.Y.; Kooistra, T. Anti-inflammatory, anti-proliferative and anti-atherosclerotic effects of quercetin in human in vitro and in vivo models. Atherosclerosis 2011, 218, 44–52. [Google Scholar] [CrossRef]
  28. Dozio, E.; Barassi, A.; Ravelli, A.; Angeli, I.; Lodi, F.; Melzi d’Eril, G.V.; Corsi Romanelli, M.M. The “Breme” red onion: Effects of home-storage methods on quercetin and quercetin-glycoside contents. Czech J. Food Sci. 2015, 33, 405–409. [Google Scholar] [CrossRef] [Green Version]
  29. Singh, B.N.; Singh, B.R.; Singh, R.L.; Prakash, D.; Singh, D.P.; Sarma, B.K.; Upadhyay, G.; Singh, H.B. Polyphenolics from various extracts/fractions of red onion (Allium cepa) peel with potent antioxidant and antimutagenic activities. Food Chem. Toxicol. 2009, 47, 1161–1167. [Google Scholar] [CrossRef]
  30. Sanchez, M.; Lodi, F.; Vera, R.; Villar, I.C.; Cogolludo, A.; Jimenez, R.; Moreno, L.; Romero, M.; Tamargo, J.; Perez-Vizcaino, F. Quercetin and isorhamnetin prevent endothelial dysfunction, superoxide production, and overexpression of p47phox induced by angiotensin II in rat aorta. Nutr. J. 2007, 137, 910–915. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  31. Urios, P.; Grigorova-Borsos, A.-M.; Sternberg, M. Flavonoids inhibit the formation of the cross-linking AGE pentosidine in collagen incubated with glucose, according to their structure. Eur. J. Nutr. 2007, 46, 139. [Google Scholar] [CrossRef] [PubMed]
  32. Akash, M.S.H.; Rehman, K.; Chen, S. Spice plant Allium cepa: Dietary supplement for treatment of type 2 diabetes mellitus. Nutrition 2014, 30, 1128–1137. [Google Scholar] [CrossRef]
  33. Hertog, M.; Hollman, P.; Kromhout, D. Determination of Potentially Anticarcinogenic Flavonoids in Foods and Preliminary Results on Daily Intake in The Netherlands. In Food and Cancer Prevention: Chemical and Biological Aspects; Fenwick, G.R., Johnson, I., Waldron, K.W., Eds.; Woodhead Publishing: Sawston, UK, 1993. [Google Scholar]
  34. D Archivio, M.; Filesi, C.; Di Benedetto, R.; Gargiulo, R.; Giovannini, C.; Masella, R. Polyphenols, dietary sources and bioavailability. Ann. Ist. Super. Sanita 2007, 43, 348. [Google Scholar]
  35. Tiwari, U.; Cummins, E. Factors influencing levels of phytochemicals in selected fruit and vegetables during pre-and post-harvest food processing operations. Food Res. Int. 2013, 50, 497–506. [Google Scholar] [CrossRef]
  36. Pérez-Gregorio, R.M.; García-Falcón, M.S.; Simal-Gándara, J.; Rodrigues, A.S.; Almeida, D.P. Identification and quantification of flavonoids in traditional cultivars of red and white onions at harvest. J. Food Compos. Anal. 2010, 23, 592–598. [Google Scholar] [CrossRef]
  37. Slimestad, R.; Fossen, T.; Vågen, I.M. Onions: A source of unique dietary flavonoids. J. Agric. Food Chem. 2007, 55, 10067–10080. [Google Scholar] [CrossRef] [PubMed]
  38. Bora, K.S.S.; Sharma, A. Phytoconstituents and therapeutic potential of Allium cepa Linn.—A review. Pharmacogn. Rev. 2009, 3, 170–180. [Google Scholar]
  39. Ignat, I.; Volf, I.; Popa, V.I. A critical review of methods for characterisation of polyphenolic compounds in fruits and vegetables. Food Chem. 2011, 126, 1821–1835. [Google Scholar] [CrossRef] [PubMed]
  40. Bystrická, J.; Musilová, J.; Vollmannová, A.; Timoracká, M.; Kavalcová, P. Bioactive components of onion (Allium cepa L.)—A review. Acta Aliment. 2013, 42, 11–22. [Google Scholar] [CrossRef]
  41. Geetha, M.; Ponmozhi, P.; Saravanakumar, M.; Suganyadevi, P. Extraction of anthocyanin and analyzing its antioxidant properties from different onion (Allium cepa) varieties. J. Res. Pharm. Sci. 2011, 2, 497–506. [Google Scholar]
  42. Ferreres, F.; Gil, M.I.; Tomas-Barberan, F.A. Anthocyanins and flavonoids from shredded red onion and changes during storage in perforated films. Food Res. Int. 1996, 29, 389–395. [Google Scholar] [CrossRef]
  43. Clifford, M.N. Anthocyanins–nature, occurrence and dietary burden. J. Sci. Food Agric. 2000, 80, 1063–1072. [Google Scholar] [CrossRef]
  44. Donner, H.; Gao, L.; Mazza, G. Separation and characterization of simple and malonylated anthocyanins in red onions, Allium cepa L. Food Res Int. 1997, 30, 637–643. [Google Scholar] [CrossRef]
  45. Juergenliemk, G.; Boje, K.; Huewel, S.; Lohmann, C.; Galla, H.-J.; Nahrstedt, A. In Vitro studies indicate that miquelianin (quercetin 3-O-ß-d-glucuronopyranoside) is able to reach the CNS from the small intestine. Planta Med. 2003, 69, 1013–1017. [Google Scholar]
  46. Brito-Arias, M. Synthesis and Characterization of Glycosides; Springer: Boston, MA, USA, 2007. [Google Scholar]
  47. Lombard, K.A.; Geoffriau, E.; Peffley, E. Flavonoid quantification in onion by spectrophotometric and high performance liquid chromatography analysis. HortScience 2002, 37, 682–685. [Google Scholar] [CrossRef] [Green Version]
  48. Sellappan, S.; Akoh, C.C. Flavonoids and antioxidant capacity of Georgia-grown Vidalia onions. J. Agric. Food Chem. 2002, 50, 5338–5342. [Google Scholar] [CrossRef]
  49. Lombard, K.; Peffley, E.; Geoffriau, E.; Thompson, L.; Herring, A. Quercetin in onion (Allium cepa L.) after heat-treatment simulating home preparation. J. Food Compos. Anal. 2005, 18, 571–581. [Google Scholar] [CrossRef]
  50. Rodríguez Galdón, B.; Rodríguez Rodríguez, E.; Díaz Romero, C. Flavonoids in onion cultivars (Allium cepa L.). J. Food Sci. 2008, 73, C599–C605. [Google Scholar] [CrossRef] [PubMed]
  51. Mogren, L.M.; Olsson, M.E.; Gertsson, U.E. Quercetin content in field-cured onions (Allium cepa L.): Effects of cultivar, lifting time, and nitrogen fertilizer level. J. Agric. Food Chem. 2006, 54, 6185–6191. [Google Scholar] [CrossRef] [PubMed]
  52. Marotti, M.; Piccaglia, R. Characterization of flavonoids in different cultivars of onion (Allium cepa L.). J. Food Sci. 2002, 67, 1229–1232. [Google Scholar] [CrossRef]
  53. Lachman, J.; Pronek, D.; Hejtmánková, A.; Dudjak, J.; Pivec, V.; Faitová, K. Total polyphenol and main flavonoid antioxidants in different onion (Allium cepa L.) varieties. Sci. Hortic. 2003, 30, 142–147. [Google Scholar] [CrossRef] [Green Version]
  54. Desjardins, Y. Horticultural Science Focus-Onion as a Nutraceutical and Functional Food. Chron. Hortic. 2008, 48, 8. [Google Scholar]
  55. Tedesco, I.; Carbone, V.; Spagnuolo, C.; Minasi, P.; Russo, G.L. Identification and quantification of flavonoids from two southern Italian cultivars of Allium cepa L., Tropea (Red Onion) and Montoro (Copper Onion), and their capacity to protect human erythrocytes from oxidative stress. J. Agric. Food Chem. 2015, 63, 5229–5238. [Google Scholar] [CrossRef]
  56. Patil, B.; Pike, L. Distribution of quercetin content in different rings of various coloured onion (Allium cepa L.) cultivars. J. Hortic. Sci. 1995, 70, 643–650. [Google Scholar] [CrossRef]
  57. Kaur, C.; Singh, M.; Walia, S.; Joshi, S.; Munshi, A.D. Variations in phenolics and antioxidants in Indian onions (Allium cepa L.) Genotype selection for breeding. Food Sci. Nutr. 2010, 40, 6–19. [Google Scholar] [CrossRef]
  58. Crozier, A.; Lean, M.E.; McDonald, M.S.; Black, C. Quantitative analysis of the flavonoid content of commercial tomatoes, onions, lettuce, and celery. J. Agric. Food Chem. 1997, 45, 590–595. [Google Scholar] [CrossRef]
  59. Okamoto, D.; Noguchi, Y.; Muro, T.; Morishita, M. Genetic variation of quercetin glucoside content in onion (Allium cepa L.). J. Jpn. Soc. Hortic. Sci. 2006, 75, 100–108. [Google Scholar] [CrossRef] [Green Version]
  60. Yoo, K.S.; Lee, E.J.; Patil, B.S. Quantification of quercetin glycosides in 6 onion cultivars and comparisons of hydrolysis-HPLC and spectrophotometric methods in measuring total quercetin concentrations. J. Food Sci. 2010, 75, C160–C165. [Google Scholar] [CrossRef]
  61. Petropoulos, S.A.; Fernandes, Â.; Barros, L.; Ferreira, I.C.; Ntatsi, G. Morphological, nutritional and chemical description of “Vatikiotiko”, an onion local landrace from Greece. Food Chem. 2015, 182, 156–163. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  62. Lombard, K.A.; Geoffriau, E.; Peffley, E.B. Total quercetin content in onion: Survey of cultivars grown at various locations. HortTechnology 2004, 14, 628–630. [Google Scholar] [CrossRef] [Green Version]
  63. Lee, S.U.; Lee, J.H.; Choi, S.H.; Lee, J.S.; Ohnisi-Kameyama, M.; Kozukue, N.; Levin, C.E.; Friedman, M. Flavonoid content in fresh, home-processed, and light-exposed onions and in dehydrated commercial onion products. J. Agric. Food Chem. 2008, 56, 8541–8548. [Google Scholar] [CrossRef] [PubMed]
  64. Patil, B.; Pike, L.; Hamilton, B. Changes in quercetin concentration in onion (Allium cepa L.) owing to location, growth stage and soil type. New Phytol. 1995, 130, 349–355. [Google Scholar] [CrossRef]
  65. Hichri, I.; Barrieu, F.; Bogs, J.; Kappel, C.; Delrot, S.; Lauvergeat, V. Recent advances in the transcriptional regulation of the flavonoid biosynthetic pathway. J. Exp. Bot. 2011, 62, 2465–2483. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  66. Grzelak, K.; Milala, J.; Król, B.; Adamicki, F.; Badełek, E. Content of quercetin glycosides and fructooligosaccharides in onion stored in a cold room. Eur. Food Res. Technol. 2009, 228, 1001–1007. [Google Scholar] [CrossRef]
  67. Nemeth, K.; Piskula, M. Food content, processing, absorption and metabolism of onion flavonoids. Crit. Rev. Food Sci. Nutr. 2007, 47, 397–409. [Google Scholar] [CrossRef]
  68. Slimestad, R.; Vågen, I.M. Distribution of non-structural carbohydrates, sugars, flavonols and pyruvate in scales of onions, Allium cepa L. J. Food Agric. Environ. 2009, 7, 289–294. [Google Scholar]
  69. Beesk, N.; Perner, H.; Schwarz, D.; George, E.; Kroh, L.W.; Rohn, S. Distribution of quercetin-3,4′-O-diglucoside, quercetin-4′-O-monoglucoside, and quercetin in different parts of the onion bulb (Allium cepa L.) influenced by genotype. Food Chem. 2010, 122, 566–571. [Google Scholar] [CrossRef]
  70. Gennaro, L.; Leonardi, C.; Esposito, F.; Salucci, M.; Maiani, G.; Quaglia, G.; Fogliano, V. Flavonoid and carbohydrate contents in Tropea red onions: Effects of homelike peeling and storage. J. Agric. Food Chem. 2002, 50, 1904–1910. [Google Scholar] [CrossRef]
  71. Erdman, J.W.; Balentine, D.; Arab, L.; Beecher, G.; Dwyer, J.T.; Folts, J.; Harnly, J.; Hollman, P.; Keen, C.L.; Mazza, G. Flavonoids and heart health: Proceedings of the ILSI North America flavonoids workshop, May 31–June 1, 2005, Washington, DC. J. Nutr. 2007, 137, 718S–737S. [Google Scholar] [CrossRef] [Green Version]
  72. Hertog, M.G.; Kromhout, D.; Aravanis, C.; Blackburn, H.; Buzina, R.; Fidanza, F.; Giampaoli, S.; Jansen, A.; Menotti, A.; Nedeljkovic, S. Flavonoid intake and long-term risk of coronary heart disease and cancer in the seven countries study. Arch. Intern. Med. 1995, 155, 381–386. [Google Scholar] [CrossRef]
  73. Harwood, M.; Danielewska-Nikiel, B.; Borzelleca, J.; Flamm, G.; Williams, G.; Lines, T. A critical review of the data related to the safety of quercetin and lack of evidence of in vivo toxicity, including lack of genotoxic/carcinogenic properties. Food Chem. Toxicol. 2007, 45, 2179–2205. [Google Scholar] [CrossRef] [PubMed]
  74. Hollman, P.C.; de Vries, J.H.; van Leeuwen, S.D.; Mengelers, M.J.; Katan, M.B. Absorption of dietary quercetin glycosides and quercetin in healthy ileostomy volunteers. Am. J. Clin. Nutr. 1995, 62, 1276–1282. [Google Scholar] [CrossRef] [Green Version]
  75. Wiczkowski, W.; Romaszko, J.; Bucinski, A.; Szawara-Nowak, D.; Honke, J.; Zielinski, H.; Piskula, M.K. Quercetin from shallots (Allium cepa L. var. aggregatum) is more bioavailable than its glucosides. J. Nutr. 2008, 138, 885–888. [Google Scholar] [CrossRef] [PubMed]
  76. Hidalgo, M.; Sánchez-Moreno, C.; de Pascual-Teresa, S. Flavonoid–flavonoid interaction and its effect on their antioxidant activity. Food Chem. 2010, 121, 691–696. [Google Scholar] [CrossRef]
  77. Parr, A.J.; Bolwell, G.P. Phenols in the plant and in man. The potential for possible nutritional enhancement of the diet by modifying the phenols content or profile. J. Sci. Food Agric. 2000, 80, 985–1012. [Google Scholar] [CrossRef]
  78. Ślusarczyk, S.; Hajnos, M.; Skalicka-Woźniak, K.; Matkowski, A. Antioxidant activity of polyphenols from Lycopus lucidus Turcz. Food Chem. 2009, 113, 134–138. [Google Scholar] [CrossRef]
  79. Prakash, D.; Singh, B.N.; Upadhyay, G. Antioxidant and free radical scavenging activities of phenols from onion (Allium cepa). Food Chem. 2007, 102, 1389–1393. [Google Scholar] [CrossRef]
  80. Özyürek, M.; Bener, M.; Güçlü, K.; Apak, R. Antioxidant/antiradical properties of microwave-assisted extracts of three wild edible mushrooms. Food Chem. 2014, 157, 323–331. [Google Scholar] [CrossRef]
  81. Griffiths, G.; Trueman, L.; Crowther, T.; Thomas, B.; Smith, B. Onions—A global benefit to health. Phytother. Res. 2002, 16, 603–615. [Google Scholar] [CrossRef]
  82. Kong, J.-M.; Chia, L.-S.; Goh, N.-K.; Chia, T.-F.; Brouillard, R. Analysis and biological activities of anthocyanins. Phytochemistry 2003, 64, 923–933. [Google Scholar] [CrossRef]
  83. Bleve, M.; Ciurlia, L.; Erroi, E.; Lionetto, G.; Longoc, L.; Rescioa, L. An innovative method for the purification of anthocyanins from grape skin extracts by using liquid and sub-critical carbon dioxide. Sep. Purif. Technol. 2008, 64, 192–197. [Google Scholar] [CrossRef]
  84. Jan, A.T.; Kamli, M.R.; Murtaza, I.; Singh, J.B.; Ali, A.; Haq, Q. Dietary flavonoid quercetin and associated health benefits—An overview. Food Rev. Int. 2010, 26, 302–317. [Google Scholar] [CrossRef]
  85. Harris, S.; Brunton, N.; Tiwari, U.; Cummins, E. Human exposure modelling of quercetin in onions (Allium cepa L.) following thermal processing. Food Chem. 2015, 187, 135–139. [Google Scholar] [CrossRef] [PubMed]
  86. O’Reilly, J.D.; Mallet, A.I.; McAnlis, G.T.; Young, I.S.; Halliwell, B.; Sanders, T.A.; Wiseman, H. Consumption of flavonoids in onions and black tea: Lack of effect on F2-isoprostanes and autoantibodies to oxidized LDL in healthy humans. Am. J. Clin. Nutr. 2001, 73, 1040–1044. [Google Scholar] [CrossRef] [Green Version]
  87. Pszczola, D.E. Antimicrobials: Setting up additional hurdles to ensure food safety. Food Technol. 2002, 56, 99–108. [Google Scholar]
  88. Santas, J.; Almajano, M.P.; Carbó, R. Antimicrobial and antioxidant activity of crude onion (Allium cepa L.) extracts. Int. J. Food Sci. 2010, 45, 403–409. [Google Scholar] [CrossRef]
  89. Wu, C.P.; Calcagno, A.M.; Hladky, S.B.; Ambudkar, S.V.; Barrand, M.A. Modulatory effects of plant phenols on human multidrug-resistance proteins 1, 4 and 5 (ABCC1, 4 and 5). FEBS J. 2005, 272, 4725–4740. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  90. Chen, C.-H.; Chou, T.-W.; Cheng, L.-H.; Ho, C.-W. In vitro anti-adenoviral activity of five Allium plants. J. Taiwan Inst. Chem. Eng. 2011, 42, 228–232. [Google Scholar] [CrossRef]
  91. Zohri, A.-N.; Abdel-Gawad, K.; Saber, S. Antibacterial, antidermatophytic and antitoxigenic activities of onion (Allium cepa L.) oil. Microbiol. Res. 1995, 150, 167–172. [Google Scholar] [CrossRef]
  92. Souza, M.M.d.; Oliveira, M.d.S.; Rocha, M.d.; Furlong, E.B. Antifungal activity evaluation in phenolic extracts from onion, rice bran, and Chlorella phyrenoidosa. Food Sci. Technol. 2010, 30, 680–685. [Google Scholar] [CrossRef] [Green Version]
  93. Ames, B.N.; Shigenaga, M.K.; Hagen, T.M. Oxidants, antioxidants, and the degenerative diseases of aging. Proc. Natl. Acad. Sci. USA 1993, 90, 7915–7922. [Google Scholar] [CrossRef] [Green Version]
  94. Stajner, D.; Varga, I.S. An evaluation of the antioxidant abilities of Allium species. Acta Biol. Szeged. 2003, 47, 103–106. [Google Scholar]
  95. Sanderson, J.; McLauchlan, W.R.; Williamson, G. Quercetin inhibits hydrogen peroxide-induced oxidation of the rat lens. Free Radic. Biol. Med. 1999, 26, 639–645. [Google Scholar] [CrossRef]
  96. Rice-evans, C.A.; Miller, N.J.; Bolwell, P.G.; Bramley, P.M.; Pridham, J.B. The relative antioxidant activities of plant-derived polyphenolic flavonoids. Free Radic. Res. 1995, 22, 375–383. [Google Scholar] [CrossRef]
  97. Sidhu, J.S.; Ali, M.; Al-Rashdan, A.; Ahmed, N. Onion (Allium cepa L.) is potentially a good source of important antioxidants. J. Food Sci. Technol. 2019, 56, 1811–1819. [Google Scholar] [CrossRef] [PubMed]
  98. Gökçe, A.F.; Kaya, C.; Serçe, S.; Özgen, M. Effect of scale color on the antioxidant capacity of onions. Sci. Hortic. 2010, 123, 431–435. [Google Scholar] [CrossRef]
  99. Choi, I.S.; Cho, E.J.; Moon, J.-H.; Bae, H.-J. Onion skin waste as a valorization resource for the by-products quercetin and biosugar. Food Chem. 2015, 188, 537–542. [Google Scholar] [CrossRef] [PubMed]
  100. Benítez, V.; Mollá, E.; Martín-Cabrejas, M.; López-Andréu, J.F.; Downes, K.; Terry, L.; Esteba, R. Study of bioactive compound content in different onion sections. Plant Foods Hum. Nutr. 2011, 66, 48–57. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  101. Roldán, E.; Sánchez-Moreno, C.; de Ancos, B.; Cano, M.P. Characterisation of onion (Allium cepa L.) by-products as food ingredients with antioxidant and antibrowning properties. Food Chem. 2008, 108, 907–916. [Google Scholar] [CrossRef] [PubMed]
  102. Wang, Y.Y.; Duan, X.; Ren, G.Y.; Liu, Y.H. Comparative study on the flavonoids extraction rate and antioxidant activity of onions treated by three different drying methods. Dry. Technol. 2019, 37, 245–252. [Google Scholar] [CrossRef]
  103. Salamatullah, A.M.; Uslu, N.; Özcan, M.M.; Alkaltham, M.S.; Hayat, K. The effect of oven drying on bioactive compounds, antioxidant activity, and phenolic compounds of white and red-skinned onion slices. J. Food Proc. Preserv. 2021, 45, e15173. [Google Scholar] [CrossRef]
  104. Cubukcu, H.C.; Kilicaslan, N.S.D.; Durak, I. Different effects of heating andfreezing treatments on the antioxidant properties of broccoli, cauliflower, garlic and onion. An experimental in vitro study. São Paulo Med. J. 2019, 137, 407–413. [Google Scholar] [CrossRef] [Green Version]
  105. Fernandez-Jalao, I.; Sanchez-Moreno, C.; De Ancos, B. Influence of food matrix and high-pressure processing on onion flavonols and antioxidant activity during gastrointestinal digestion. J. Food Eng. 2017, 213, 60–68. [Google Scholar] [CrossRef]
  106. Lee, Y.R.; Hwang, I.G.; Woo, K.S.; Kim, D.J.; Hong, J.T.; Jeong, H.S. Antioxidative activities of the ethyl acetate fraction from heated onion (Allium cepa). Food Sci. Biotechnol. 2007, 16, 1041. [Google Scholar]
  107. Woo, K.S.; Hwang, I.G.; Kim, T.M.; Kim, D.J.; Hong, J.T.; Jeong, H.S. Changes in the antioxidant activity of onion (Allium cepa) extracts with heat treatment. Food Sci. Biotechnol. 2007, 16, 828–831. [Google Scholar]
  108. Khaki, A.; Fathiazad, F.; Nouri, M.; Khaki, A.; Khamenehi, H.; Hamadeh, M. Evaluation of androgenic activity of allium cepa on spermatogenesis in the rat. Folia Morphol. 2009, 68, 45–51. [Google Scholar]
  109. Arung, E.T.; Furuta, S.; Ishikawa, H.; Kusuma, I.W.; Shimizu, K.; Kondo, R. Anti-melanogenesis properties of quercetin and its derivate extract from Allium cepa. Food Chem. 2011, 124, 1024–1028. [Google Scholar] [CrossRef]
  110. Jeong, C.-H.; Heo, H.J.; Choi, S.-G.; Shim, K.-H. Antioxidant and anticancer properties of methanolic extracts from different parts of white, yellow, and red onion. Food Sci. Biotechnol. 2009, 18, 108–112. [Google Scholar]
  111. Edwards, R.L.; Lyon, T.; Litwin, S.E.; Rabovsky, A.; Symons, J.D.; Jalili, T. Quercetin reduces blood pressure in hypertensive subjects. J. Nutr. 2007, 137, 2405–2411. [Google Scholar] [CrossRef]
  112. Egert, S.; Bosy-Westphal, A.; Seiberl, J.; Kürbitz, C.; Settler, U.; Plachta-Danielzik, S.; Wagner, A.E.; Frank, J.; Schrezenmeir, J.; Rimbach, G. Quercetin reduces systolic blood pressure and plasma oxidised low-density lipoprotein concentrations in overweight subjects with a high-cardiovascular disease risk phenotype: A double-blinded, placebo-controlled cross-over study. Br. J. Nutr. 2009, 102, 1065–1074. [Google Scholar] [CrossRef] [Green Version]
  113. Lean, M.; Noroozi, M.; Kelly, I.; Burns, J.; Talwar, D.; Sattar, N.; Crozier, A. Dietary flavonols protect diabetic human lymphocytes against oxidative damage to DNA. Diabetes 1999, 48, 176–181. [Google Scholar] [CrossRef]
  114. Kuhlmann, M.; Burkhardt, G.; Horsch, E.; Wagner, M.; Köhler, H. Inhibition of oxidant-induced lipid peroxidation in cultured renal tubular epithelial cells (LLC-PK1) by quercetin. Free Radic. Res. 1998, 29, 451–460. [Google Scholar] [CrossRef]
  115. Kaneko, T. Protective effect of flavonoids on endothelial cells against linoleic acid hydroperoxide-induced toxicity. Biosci. Biotechnol. Biochem. 1999, 63, 323–328. [Google Scholar] [CrossRef] [PubMed]
  116. Janssen, K.; Mensink, R.P.; Cox, F.; Harryvan, J.L.; Hovenier, R.; Hollman, P.; Katan, M.B. Effects of the flavonoids quercetin and apigenin on hemostasis in healthy volunteers: Results from an in vitro and a dietary supplement study. Am. J. Clin. Nutr. 1998, 67, 255–262. [Google Scholar] [CrossRef] [PubMed]
  117. Ren, F.; Reilly, K.; Gaffney, M.; Kerry, J.P.; Hossain, M.; Rai, D.K. Evaluation of polyphenolic content and antioxidant activity in two onion varieties grown under organic and conventional production systems. J. Sci. Food Agric. 2017, 97, 2982–2990. [Google Scholar] [CrossRef] [PubMed]
  118. Liu, J.; Yu, L.L.; Wu, Y. Bioactive Components and Health Beneficial Properties of Whole Wheat Foods. J. Agric. Food Chem. 2020, 68, 12904–12915. [Google Scholar] [CrossRef]
  119. Kaur, C.; Joshi, S.; Kapoor, H. Antioxidants in onion (Allium Cepa L.) cultivars grown in India. J. Food Biochem. 2009, 33, 184–200. [Google Scholar] [CrossRef]
  120. Lu, X.; Wang, J.; Al-Qadiri, H.M.; Ross, C.F.; Powers, J.R.; Tang, J.; Rasco, B.A. Determination of total phenolic content and antioxidant capacity of onion (Allium cepa) and shallot (Allium oschaninii) using infrared spectroscopy. Food Chem. 2011, 129, 637–644. [Google Scholar] [CrossRef]
  121. Nile, S.H.; Park, S.W. Total phenolics, antioxidant and xanthine oxidase inhibitory activity of three colored onions (Allium cepa L.). Front. Life Sci. 2013, 7, 224–228. [Google Scholar] [CrossRef] [Green Version]
  122. Cheng, A.; Chen, X.; Jin, Q.; Wang, W.; Shi, J.; Liu, Y. Comparison of Phenolic Content and Antioxidant Capacity of Red and Yellow Onions. Czech J. Food Sci. Vol. 2013, 31, 501–508. [Google Scholar] [CrossRef]
  123. Nayak, B.; Liu, R.H.; Tang, J. Effect of processing on phenolic antioxidants of fruits, vegetables, and grains—A review. Crit. Rev. Food Sci. Nutr. 2015, 55, 887–918. [Google Scholar] [CrossRef] [PubMed]
  124. Kwak, J.-H.; Seo, J.M.; Kim, N.-H.; Arasu, M.V.; Kim, S.; Yoon, M.K.; Kim, S.-J. Variation of quercetin glycoside derivatives in three onion (Allium cepa L.) varieties. Saudi J. Biol. Sci. 2017, 24, 1387–1391. [Google Scholar] [CrossRef] [Green Version]
  125. Ren, H.; Endo, H.; Hayashi, T. Antioxidative and antimutagenic activities and polyphenol content of pesticide-free and organically cultivated green vegetables using water-soluble chitosan as a soil modifier and leaf surface spray. J. Sci. Food Agric. 2001, 81, 1426–1432. [Google Scholar] [CrossRef]
  126. Faller, A.L.K.; Fialho, E. Polyphenol content and antioxidant capacity in organic and conventional plant foods. J. Food Compos. Anal. 2010, 23, 561–568. [Google Scholar] [CrossRef]
  127. Mogren, L.; Gertsson, U.; Olsson, M.E. Effect of cultivation factors on flavonoid content in yellow onion (Allium cepa L.). Acta Hortic. 2008, 765, 191. [Google Scholar] [CrossRef]
  128. Higashio, H.; Hirokane, H.; Sato, F.; Tokuda, S.; Uragami, A. Enhancement of Functional Compounds in Allium Vegetables with UV Radiation. Acta Hortic. 2007, 744, 357–361. [Google Scholar] [CrossRef]
  129. Jaakola, L.; Määttä-Riihinen, K.; Kärenlampi, S.; Hohtola, A. Activation of flavonoid biosynthesis by solar radiation in bilberry (Vaccinium myrtillus L.) leaves. Planta 2004, 218, 721–728. [Google Scholar]
  130. Dixon, R.A.; Paiva, N.L. Stress-induced phenylpropanoid metabolism. Plant Cell 1995, 7, 1085. [Google Scholar] [CrossRef] [PubMed]
  131. Yoo, K.S.; Lee, E.J.; Patil, B.S. Changes in quercetin glucoside concentrations of onion bulbs by scales, during storage, and in sprouting leaves exposed to UV. Postharvest Biol. Technol. 2013, 83, 65–71. [Google Scholar] [CrossRef]
  132. Rodrigues, A.S.; Pérez-Gregorio, M.R.; García-Falcón, M.S.; Simal-Gándara, J.; Almeida, D.P.F. Effect of meteorological conditions on antioxidant flavonoids in Portuguese cultivars of white and red onions. Food Chem. 2011, 124, 303–308. [Google Scholar] [CrossRef]
  133. Price, K.; Rhodes, M. Analysis of the major flavonol glycosides present in four varieties of onion (Allium cepa) and changes in composition resulting from autolysis. J. Sci. Food Agric. 1997, 74, 331–339. [Google Scholar] [CrossRef]
  134. Søltoft, M.; Nielsen, J.; Holst Laursen, K.; Husted, S.; Halekoh, U.; Knuthsen, P. Effects of organic and conventional growth systems on the content of flavonoids in onions and phenolic acids in carrots and potatoes. J. Agric. Food Chem. 2010, 58, 10323–10329. [Google Scholar] [CrossRef]
  135. Reilly, K.; Cullen, E.; Lola-Luz, T.; Stone, D.; Valverde, J.; Gaffney, M.; Brunton, N.; Grant, J.; Griffiths, B.S. Effect of organic, conventional and mixed cultivation practices on soil microbial community structure and nematode abundance in a cultivated onion crop. J. Sci. Food Agric. 2013, 93, 3700–3709. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  136. Mogren, L.M.; Olsson, M.E.; Gertsson, U.E. Effects of cultivar, lifting time and nitrogen fertiliser level on quercetin content in onion (Allium cepa L.) at lifting. J. Sci. Food Agric. 2007, 87, 470–476. [Google Scholar] [CrossRef]
  137. Eshel, D.; Teper-Bamnolker, P.; Vinokur, Y.; Saad, I.; Zutahy, Y.; Rodov, V. Fast curing: A method to improve postharvest quality of onions in hot climate harvest. Postharvest Biol. Technol. 2014, 88, 34–39. [Google Scholar] [CrossRef]
  138. Sharma, K.; Asnin, L.; Ko, E.Y.; Lee, E.T.; Park, S.W. Phytochemical composition of onion during long-term storage. Acta Agric. Scand. B Soil Plant Sci. 2015, 65, 150–160. [Google Scholar] [CrossRef]
  139. Olsson, M.E.; Gustavsson, K.E.; Vagen, I.M. Quercetin and isorhamnetin in sweet and red cultivars of onion (Allium cepa L.) at harvest, after field curing, heat treatment, and storage. J. Agric. Food Chem. 2010, 58, 2323–2330. [Google Scholar] [CrossRef]
  140. Sorensen, J.; Grevsen, K. Sprouting in bulb onions (Allium cepa L.) as influenced by nitrogen and water stress. J. Hortic. Sci. 2001, 76, 501–506. [Google Scholar]
  141. Benkeblia, N.; Shiomi, N. Chilling effect on soluble sugars, respiration rate, total phenolics, peroxidase activity and dormancy of onion bulbs. Sci. Agric. 2004, 61, 281–285. [Google Scholar] [CrossRef] [Green Version]
  142. Benkeblia, N. Phenylalanine ammonia-lyase, peroxidase, piruvic acid and total phenolics variations in onion bulbs during long-term storage. Lebensm. Wiss. Technol. 2000, 33, 112–116. [Google Scholar] [CrossRef] [Green Version]
  143. Sharma, K.; Assefa, A.D.; Ko, E.Y.; Lee, E.T.; Park, S.W. Quantitative analysis of flavonoids, sugars, phenylalanine and tryptophan in onion scales during storage under ambient conditions. J. Food Sci. Technol. 2015, 52, 2157–2165. [Google Scholar] [CrossRef] [Green Version]
  144. Kevers, C.; Falkowski, M.; Tabart, J.; Defraigne, J.-O.; Dommes, J.; Pincemail, J. Evolution of antioxidant capacity during storage of selected fruits and vegetables. J. Agric. Food Chem. 2007, 55, 8596–8603. [Google Scholar] [CrossRef]
  145. Rodrigues, A.S.; Pérez-Gregorio, M.R.; García-Falcón, M.S.; Simal-Gándara, J.; Almeida, D.P. Effect of post-harvest practices on flavonoid content of red and white onion cultivars. Food Control 2010, 21, 878–884. [Google Scholar] [CrossRef]
  146. Elhassaneen, Y.; Sanad, M. Phenolics, selenium, vitamin C, amino acids and pungency levels and antioxidant activities of two Egyptian onion varieties. Am. J. Food Technol. 2009, 4, 241–254. [Google Scholar] [CrossRef]
  147. Lee, J.; Mitchell, A.E. Quercetin and isorhamnetin glycosides in onion (Allium cepa L.): Varietal comparison, physical distribution, coproduct evaluation, and long-term storage stability. J. Agric. Food Chem. 2011, 59, 857–863. [Google Scholar] [CrossRef]
  148. Sharma, K.; Ko, E.Y.; Assefa, A.D.; Nile, S.H.; Park, S.W. A comparative study of anaerobic and aerobic decomposition of quercetin glucosides and sugars in onion at an ambient temperature. Front. Life Sci. 2015, 8, 117–123. [Google Scholar] [CrossRef] [Green Version]
  149. Ko, E.Y.; Nile, S.H.; Sharma, K.; Li, G.H.; Park, S.W. Effect of different exposed lights on quercetin and quercetin glucoside content in onion (Allium cepa L.). Saudi J. Biol. Sci. 2015, 22, 398–403. [Google Scholar] [CrossRef] [Green Version]
  150. Berno, N.D.; Tezotto-Uliana, J.V.; dos Santos Dias, C.T.; Kluge, R.A. Storage temperature and type of cut affect the biochemical and physiological characteristics of fresh-cut purple onions. Postharvest Biol. Technol. 2014, 93, 91–96. [Google Scholar] [CrossRef]
  151. Zudaire, L.; Viñas, I.; Abadias, M.; Simó, J.; Echeverria, G.; Plaza, L.; Aguiló-Aguayo, I. Quality and bioaccessibility of total phenols and antioxidant activity of calçots (Allium cepa L.) stored under controlled atmosphere conditions. Postharvest Biol. Technol. 2017, 129, 118–128. [Google Scholar] [CrossRef] [Green Version]
  152. Sahoo, N.R.; Bal, L.M.; S Pal, U.; Sahoo, D. Impact of pretreatment and drying methods on quality attributes of onion shreds. Food Technol. Biotechnol. 2015, 53, 57–65. [Google Scholar] [CrossRef]
  153. Alezandro, M.R.; Lui, M.C.Y.; Lajolo, F.M.; Genovese, M.I. Commercial spices and industrial ingredients: Evaluation of antioxidant capacity and flavonoids content for functional foods development. Food Sci. Technol. 2011, 31, 527–533. [Google Scholar] [CrossRef] [Green Version]
  154. Mitra, J.; Shrivastava, S.L.; Rao, P.S. Non-enzymatic browning and flavour kinetics of vacuum dried onion slices. Int. Agrophys. 2015, 29, 91–100. [Google Scholar] [CrossRef] [Green Version]
Figure 1. Examples of flavonoid structures.
Figure 1. Examples of flavonoid structures.
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Figure 2. Post-harvest factor changes in the contents of the phenolic compounds in onions.
Figure 2. Post-harvest factor changes in the contents of the phenolic compounds in onions.
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Table 2. Studied factors influencing the content of quercetins during pre-harvest in onions.
Table 2. Studied factors influencing the content of quercetins during pre-harvest in onions.
FactorsEffect on Quercetins ContentReferences
Variety of onionRank of quercetins content: Red > Yellow > White[49,53,60,119,120,121,122,123,124]
Rank of quercetins content: small > large[51,63]
Bulb partsRank of quercetins content: dry outer skins > inner skins[37]
Organic/Conventional
varieties onions
Rank of quercetins content: organic > conventional[125,126]
LightRank of quercetins content:
Exposure to sun light during production period> less sun light during production period of onion
UV light lamps after harvest > no UV treated onion
Fluorescent light after harvest > no UV treated onion
[63,127,128]
CuringRank of quercetins content: after curing > at lifting[63]
Rank of quercetins content: Field curing > dark environment[51,129]
LiftingRank of quercetins content: late lifting time > early lifting time[130,131]
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Ren, F.; Zhou, S. Phenolic Components and Health Beneficial Properties of Onions. Agriculture 2021, 11, 872. https://doi.org/10.3390/agriculture11090872

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Ren F, Zhou S. Phenolic Components and Health Beneficial Properties of Onions. Agriculture. 2021; 11(9):872. https://doi.org/10.3390/agriculture11090872

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Ren, Feiyue, and Sumei Zhou. 2021. "Phenolic Components and Health Beneficial Properties of Onions" Agriculture 11, no. 9: 872. https://doi.org/10.3390/agriculture11090872

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Ren, F., & Zhou, S. (2021). Phenolic Components and Health Beneficial Properties of Onions. Agriculture, 11(9), 872. https://doi.org/10.3390/agriculture11090872

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